<?xml version="1.0"?>
<!DOCTYPE SupplementalRecordSet SYSTEM "https://www.nlm.nih.gov/databases/dtd/nlmsupplementalrecordset_20210101.dtd">
<SupplementalRecordSet LanguageCode = "eng">
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C114158</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>quantum dye macrocyclic europium-chelate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>09</Month>
   <Day>14</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>a macrocyclic europium-chelate; structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005063</DescriptorUI>
     <DescriptorName>
      <String>Europium</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009942</DescriptorUI>
     <DescriptorName>
      <String>Organometallic Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Glycobiology 1998 Sep;8(9):849-56</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0294520</ConceptUI>
    <ConceptName>
     <String>quantum dye macrocyclic europium-chelate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T324525</TermUI>
      <String>quantum dye macrocyclic europium-chelate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T324524</TermUI>
      <String>QD macrocyclic</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008718</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>osteoclast activating factor</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>found in supernatants of cultured human leukocytes; assayed by ability to stimulate bone resorption in organ culture in mechanism of localized bone loss
  </Note>
  <Frequency>82</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008222</DescriptorUI>
     <DescriptorName>
      <String>Lymphokines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D001862</DescriptorUI>
     <DescriptorName>
      <String>Bone Resorption</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D010010</DescriptorUI>
     <DescriptorName>
      <String>Osteoclasts</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Ann N Y Acad Sci 230(0):474;1974</Source>
   <Source>Ann N Y Acad Sci 256(0):133;1975</Source>
   <Source>Calcif Tissue Int 1979;29(3):201</Source>
   <Source>Calcif Tissue Res 1979;28(1):23</Source>
   <Source>Cell Immunol 1980;49(1):74</Source>
   <Source>Eur J Immunol 6:732;1976</Source>
   <Source>J Clin Invest 64(1):337;1979</Source>
   <Source>J Exp Med 149(1):279;1979</Source>
   <Source>J Lab Clin Med 92(5):772;1978</Source>
   <Source>Surg Clin North America 57(3):543;1977</Source>
   <Source>WE 200 M486:127;1977</Source>
   <Source>WE 200 M486:13;1977</Source>
   <Source>WE 200 M486:319;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0052808</ConceptUI>
    <ConceptName>
     <String>osteoclast activating factor</String>
    </ConceptName>
    <RegistryNumber>64060-24-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T082811</TermUI>
      <String>osteoclast activating factor</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008720</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>otoline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1995</Year>
   <Month>07</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>analog of cpd 48-80; oligomeric product (n-6-8); Russian drug
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011108</DescriptorUI>
     <DescriptorName>
      <String>Polymers</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D006636</DescriptorUI>
     <DescriptorName>
      <String>Histamine Release</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000187</QualifierUI>
     <QualifierName>
      <String>drug effects</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Farmakol Toksikol 36(5):614;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0052812</ConceptUI>
    <ConceptName>
     <String>otoline</String>
    </ConceptName>
    <RegistryNumber>50643-04-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T082815</TermUI>
      <String>otoline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002540</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>miracil A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ETHYLENEDIAMINES (72-75)</PreviousIndexing>
   <PreviousIndexing>*XANTHENES (72-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008154</DescriptorUI>
     <DescriptorName>
      <String>Lucanthone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Prog Drug Res 16:11;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043189</ConceptUI>
    <ConceptName>
     <String>miracil A</String>
    </ConceptName>
    <CASN1Name>9H-Xanthen-9-one, 1-((2-(diethylamino)ethyl)amino)-4-methyl-</CASN1Name>
    <RegistryNumber>3569-84-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073192</TermUI>
      <String>miracil A</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C055240</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Leakadine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1988</Year>
   <Month>04</Month>
   <Day>20</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>may contain 2-carbamoylaziridine
  </Note>
  <Frequency>8</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001388</DescriptorUI>
     <DescriptorName>
      <String>Aziridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Vopr Onkol 1988;34(2):192</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0155620</ConceptUI>
    <ConceptName>
     <String>Leakadine</String>
    </ConceptName>
    <RegistryNumber>91433-16-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="TRD"  RecordPreferredTermYN="Y">
      <TermUI>T185625</TermUI>
      <String>Leakadine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T185624</TermUI>
      <String>Leakadin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T185623</TermUI>
      <String>Leacadin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C060863</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>conduritol aziridine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1989</Year>
   <Month>10</Month>
   <Day>04</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>11</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>inhibits both alpha- and beta-glucosidases; structure given in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001388</DescriptorUI>
     <DescriptorName>
      <String>Aziridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007294</DescriptorUI>
     <DescriptorName>
      <String>Inositol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D050112</DescriptorUI>
     <DescriptorName>
      <String>Imino Pyranoses</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D001617</DescriptorUI>
     <DescriptorName>
      <String>beta-Glucosidase</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
     <QualifierName>
      <String>antagonists &amp; inhibitors</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 1989;163(1):495</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0168905</ConceptUI>
    <ConceptName>
     <String>conduritol aziridine</String>
    </ConceptName>
    <CASN1Name>7-Azabicyclo(4.1.0)heptane-2,3,4,5-tetrol, (1alpha,2alpha,3beta,4alpha,5beta,6alpha)-</CASN1Name>
    <RegistryNumber>123788-61-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T198910</TermUI>
      <String>conduritol aziridine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T198909</TermUI>
      <String>1,2-dideoxy-1,2-iminoinositol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T198908</TermUI>
      <String>1,2-dideoxy-1,2-epimino-myo-inositol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008725</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-oxacephalothin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002512</DescriptorUI>
     <DescriptorName>
      <String>Cephalothin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Am Chem Soc 96(24):7582;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0052819</ConceptUI>
    <ConceptName>
     <String>1-oxacephalothin</String>
    </ConceptName>
    <CASN1Name>5-Oxa-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid, 3-((acetyloxy)methyl)-8-oxo-7-((2-thienylacetyl)amino)-, monosodium salt, trans-(+-)-</CASN1Name>
    <RegistryNumber>54214-84-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T082822</TermUI>
      <String>1-oxacephalothin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008727</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>oxaluric acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Frequency>12</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*OXALATES (74-75)</PreviousIndexing>
   <PreviousIndexing>AMIDES (74-75)</PreviousIndexing>
   <PreviousIndexing>CARBAMATES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010072</DescriptorUI>
     <DescriptorName>
      <String>Oxamic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Bacteriol 117(3):1240;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0052823</ConceptUI>
    <ConceptName>
     <String>oxaluric acid</String>
    </ConceptName>
    <RegistryNumber>585-05-7</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0052823</Concept1UI>
     <Concept2UI>M0052821</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0052823</Concept1UI>
     <Concept2UI>M0052822</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T082826</TermUI>
      <String>oxaluric acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0052821</ConceptUI>
    <ConceptName>
     <String>carbamoyloxamic acid</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0052823</Concept1UI>
     <Concept2UI>M0052821</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T082824</TermUI>
      <String>carbamoyloxamic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0052822</ConceptUI>
    <ConceptName>
     <String>oxalurate</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0052823</Concept1UI>
     <Concept2UI>M0052822</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T082825</TermUI>
      <String>oxalurate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008736</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6-oxomestranol-6-(O-carboxymethyl)oxime</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>03</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*NORPREGNANES (74-79)</PreviousIndexing>
   <PreviousIndexing>*PREGNATRIENES (74-79)</PreviousIndexing>
   <PreviousIndexing>KETOSTEROIDS (74-79)</PreviousIndexing>
   <PreviousIndexing>OXIMES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008656</DescriptorUI>
     <DescriptorName>
      <String>Mestranol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Steroids 22(3):327;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0052843</ConceptUI>
    <ConceptName>
     <String>6-oxomestranol-6-(O-carboxymethyl)oxime</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T082846</TermUI>
      <String>6-oxomestranol-6-(O-carboxymethyl)oxime</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008737</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-oxo-3-phenyl-1,2,3,4-tetrahydropyrido(2,3-c)pyrazine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PYRIDINES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011719</DescriptorUI>
     <DescriptorName>
      <String>Pyrazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 16(11):1296;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0052844</ConceptUI>
    <ConceptName>
     <String>2-oxo-3-phenyl-1,2,3,4-tetrahydropyrido(2,3-c)pyrazine</String>
    </ConceptName>
    <CASN1Name>3,4-dihydro-3-phenylpyrido(3,4-b)pyrazin-2(1H)-one</CASN1Name>
    <RegistryNumber>43064-15-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T082847</TermUI>
      <String>2-oxo-3-phenyl-1,2,3,4-tetrahydropyrido(2,3-c)pyrazine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008738</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>9-oxoprostanoic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PROSTAGLANDINS (74-75)</PreviousIndexing>
   <PreviousIndexing>CYCLOPENTANES (74-75)</PreviousIndexing>
   <PreviousIndexing>FATTY ACIDS (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011466</DescriptorUI>
     <DescriptorName>
      <String>Prostanoic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Experientia 29(8):990;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0052845</ConceptUI>
    <ConceptName>
     <String>9-oxoprostanoic acid</String>
    </ConceptName>
    <RegistryNumber>64122-56-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T082848</TermUI>
      <String>9-oxoprostanoic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008739</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>7-oxo-delta(1)-tetrahydrocannabinol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>aldehydic intermediate in metabolism of tetrahydrocannabinol; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*TETRAHYDROCANNABINOL (74-75)</PreviousIndexing>
   <PreviousIndexing>ALDEHYDES (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013759</DescriptorUI>
     <DescriptorName>
      <String>Dronabinol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Res Commun Chem Pathol Pharmacol 8(2):223;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0052846</ConceptUI>
    <ConceptName>
     <String>7-oxo-delta(1)-tetrahydrocannabinol</String>
    </ConceptName>
    <RegistryNumber>52663-85-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T082849</TermUI>
      <String>7-oxo-delta(1)-tetrahydrocannabinol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008722</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>methyl 6-(1,2,2-trichloroethenyl)imidazo(1,2-a)pyridine-2-carbamate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1982</Year>
   <Month>01</Month>
   <Day>26</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001562</DescriptorUI>
     <DescriptorName>
      <String>Benzimidazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 1981;24(12):1518</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0052817</ConceptUI>
    <ConceptName>
     <String>methyl 6-(1,2,2-trichloroethenyl)imidazo(1,2-a)pyridine-2-carbamate</String>
    </ConceptName>
    <CASN1Name>Carbamic acid, (6-(trichloroethenyl)imidazo(1,2-a)pyridin-2-yl)-, methyl ester</CASN1Name>
    <RegistryNumber>71820-94-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T082820</TermUI>
      <String>methyl 6-(1,2,2-trichloroethenyl)imidazo(1,2-a)pyridine-2-carbamate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T082819</TermUI>
      <String>MTCE-IPC</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008746</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>30-oxyethylated t-octyl phenol formaldehyde tetramer</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>08</Month>
   <Day>13</Day>
  </DateRevised>
  <Note>reduces thromboatherosclerosis &amp; cholesterol atherosclerosis; structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011092</DescriptorUI>
     <DescriptorName>
      <String>Polyethylene Glycols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D001161</DescriptorUI>
     <DescriptorName>
      <String>Arteriosclerosis</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000188</QualifierUI>
     <QualifierName>
      <String>drug therapy</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Exp Mol Pathol 20(2):154;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0052859</ConceptUI>
    <ConceptName>
     <String>30-oxyethylated t-octyl phenol formaldehyde tetramer</String>
    </ConceptName>
    <RegistryNumber>12584-89-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T082862</TermUI>
      <String>30-oxyethylated t-octyl phenol formaldehyde tetramer</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009879</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>estane plastic</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>estane is urethane rubber
  </Note>
  <Frequency>8</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011140</DescriptorUI>
     <DescriptorName>
      <String>Polyurethanes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Obstet Gynecol 45(3):287;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054951</ConceptUI>
    <ConceptName>
     <String>estane plastic</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0054951</Concept1UI>
     <Concept2UI>M0054950</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084954</TermUI>
      <String>estane plastic</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0054950</ConceptUI>
    <ConceptName>
     <String>Estane 5714 F1</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0054951</Concept1UI>
     <Concept2UI>M0054950</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T084953</TermUI>
      <String>Estane 5714 F1</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008765</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>paracoccidioidin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1993</Year>
   <Month>02</Month>
   <Day>10</Day>
  </DateRevised>
  <Frequency>36</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ANTIGENS, FUNGAL (74-79)</PreviousIndexing>
   <PreviousIndexing>*COCCIDIOIDIN (74-92)</PreviousIndexing>
   <PreviousIndexing>PARACOCCIDIOIDES (74-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005656</DescriptorUI>
     <DescriptorName>
      <String>Fungal Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Am J Trop Med Hyg 23(1):87;1974</Source>
   <Source>Sabouraudia 16(2):93;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0052899</ConceptUI>
    <ConceptName>
     <String>paracoccidioidin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T082902</TermUI>
      <String>paracoccidioidin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C419503</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>plutonium hydroxide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>06</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011005</DescriptorUI>
     <DescriptorName>
      <String>Plutonium</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Health Phys. 2001 Feb;80(2) :164-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0378031</ConceptUI>
    <ConceptName>
     <String>plutonium hydroxide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T435350</TermUI>
      <String>plutonium hydroxide</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>02</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T435352</TermUI>
      <String>(239)Pu-hydroxide</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>02</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T435351</TermUI>
      <String>(239)plutonium hydroxide</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>02</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C084722</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3,6-dimethyl-2,5-diaziridinylhydroquinone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>01</Month>
   <Day>07</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>hydroquinone form of the aziridinylbenzoquinone MeDZQ
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001388</DescriptorUI>
     <DescriptorName>
      <String>Aziridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006873</DescriptorUI>
     <DescriptorName>
      <String>Hydroquinones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 1993 Nov 30;32(47):12857-63</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0225024</ConceptUI>
    <ConceptName>
     <String>3,6-dimethyl-2,5-diaziridinylhydroquinone</String>
    </ConceptName>
    <RegistryNumber>152923-07-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T255029</TermUI>
      <String>3,6-dimethyl-2,5-diaziridinylhydroquinone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T255028</TermUI>
      <String>MeDZHQ</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T255027</TermUI>
      <String>3,6-dimethyl-2,5-diaziridinyl-hydroquinone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008784</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>pentafluorobenzylimine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>14</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>IMINES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005464</DescriptorUI>
     <DescriptorName>
      <String>Fluorobenzenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Chromatogr Sci 12(7):411;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0052947</ConceptUI>
    <ConceptName>
     <String>pentafluorobenzylimine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T082950</TermUI>
      <String>pentafluorobenzylimine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008786</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3,5,5,O-3',5'-pentamethyl-2'-deoxydihydrouridine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>08</Month>
   <Day>22</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DEOXYURIDINE (74-75)</PreviousIndexing>
   <PreviousIndexing>METHYL ETHERS (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003857</DescriptorUI>
     <DescriptorName>
      <String>Deoxyuridine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 331(2):147;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0052954</ConceptUI>
    <ConceptName>
     <String>3,5,5,O-3',5'-pentamethyl-2'-deoxydihydrouridine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0052954</Concept1UI>
     <Concept2UI>M0052953</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T082957</TermUI>
      <String>3,5,5,O-3',5'-pentamethyl-2'-deoxydihydrouridine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0052953</ConceptUI>
    <ConceptName>
     <String>2'-deoxy-3,5,5,O-3',5'-pentamethyldihydrouridine</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0052954</Concept1UI>
     <Concept2UI>M0052953</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T082956</TermUI>
      <String>2'-deoxy-3,5,5,O-3',5'-pentamethyldihydrouridine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008796</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>S-pentyl-L-cysteine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CYSTEINE (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003545</DescriptorUI>
     <DescriptorName>
      <String>Cysteine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Xenobiotica 3(4):207;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0052966</ConceptUI>
    <ConceptName>
     <String>S-pentyl-L-cysteine</String>
    </ConceptName>
    <RegistryNumber>4080-25-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T082969</TermUI>
      <String>S-pentyl-L-cysteine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008801</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>peptide PV</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010456</DescriptorUI>
     <DescriptorName>
      <String>Peptides, Cyclic</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Gen Physiol 63(4):492;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0052971</ConceptUI>
    <ConceptName>
     <String>peptide PV</String>
    </ConceptName>
    <CASN1Name>Cyclic(D-prolyl-D-valyl-L-prolyl-L-valyl-D-prolyl-D-valyl-L-prolyl-L-valyl-D-prolyl-D-valyl-L-prolyl-L-valyl)</CASN1Name>
    <RegistryNumber>38249-87-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T082974</TermUI>
      <String>peptide PV</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008878</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>phosphatidylkojibiosyl diglyceride</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PHOSPHOLIPIDS (75-76)</PreviousIndexing>
   <PreviousIndexing>DIGLYCERIDES (75-76)</PreviousIndexing>
   <PreviousIndexing>DISACCHARIDES (75-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006017</DescriptorUI>
     <DescriptorName>
      <String>Glycolipids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010715</DescriptorUI>
     <DescriptorName>
      <String>Phosphatidylglycerols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 250(2):702;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0053107</ConceptUI>
    <ConceptName>
     <String>phosphatidylkojibiosyl diglyceride</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T083110</TermUI>
      <String>phosphatidylkojibiosyl diglyceride</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T083109</TermUI>
      <String>phosphatidylkojibiosyl diacylglycerol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008826</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>phenacid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>RN given refers to parent cpd; structure
  </Note>
  <Frequency>18</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PHENYLACETATES (72-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009588</DescriptorUI>
     <DescriptorName>
      <String>Nitrogen Mustard Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biofizika 24(2):230;1979</Source>
   <Source>Steroids 19(6):771;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0053015</ConceptUI>
    <ConceptName>
     <String>phenacid</String>
    </ConceptName>
    <RegistryNumber>10477-72-2</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>40068-28-8 (Na salt)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0053015</Concept1UI>
     <Concept2UI>M0310481</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T083018</TermUI>
      <String>phenacid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T083017</TermUI>
      <String>phenylacetic mustard</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T083016</TermUI>
      <String>p-(N,N-bis(2-chloroethyl)amino)phenylacetic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T083014</TermUI>
      <String>4-(N,N-bis(2-chloroethyl)amino)phenylacetic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T083015</TermUI>
      <String>chlorphenacyl</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0310481</ConceptUI>
    <ConceptName>
     <String>phenacid, sodium salt</String>
    </ConceptName>
    <RegistryNumber>40068-28-8</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0053015</Concept1UI>
     <Concept2UI>M0310481</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T340481</TermUI>
      <String>phenacid, sodium salt</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008814</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>peroben</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>hypnosedative combination of diphenhydramine &amp; pyrithyldione
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004155</DescriptorUI>
     <DescriptorName>
      <String>Diphenhydramine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011728</DescriptorUI>
     <DescriptorName>
      <String>Pyridones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Dermatologica 158(6):417;1979</Source>
   <Source>Praxis 63(6):157;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0052994</ConceptUI>
    <ConceptName>
     <String>peroben</String>
    </ConceptName>
    <CASN1Name>2,4(1H,3H)-Pyridinedione, 3,3-diethyl-, mixt. with 2-(diphenylmethoxy)-N,N-dimethylethanamine</CASN1Name>
    <RegistryNumber>78371-63-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T082997</TermUI>
      <String>peroben</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C054080</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>lipid-associated sialic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1987</Year>
   <Month>12</Month>
   <Day>14</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>elevated in patients with metastatic spread of laryngeal cancer; plasma levels of LASA-P may be correlated to alteration of cancer cells' surface membranes and thus may serve as a useful marker for malignant melanoma
  </Note>
  <Frequency>68</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SIALIC ACIDS (87-96)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008055</DescriptorUI>
     <DescriptorName>
      <String>Lipids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D019158</DescriptorUI>
     <DescriptorName>
      <String>N-Acetylneuraminic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D014408</DescriptorUI>
     <DescriptorName>
      <String>Biomarkers, Tumor</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Clin Otolaryngol 1987;12(4):303</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0152917</ConceptUI>
    <ConceptName>
     <String>lipid-associated sialic acid</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T182922</TermUI>
      <String>lipid-associated sialic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T182921</TermUI>
      <String>LASA-P</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T182920</TermUI>
      <String>LASA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C069989</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>serine containing aminolipid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1991</Year>
   <Month>08</Month>
   <Day>21</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>analog of ornithine containing aminolipid; rarely present in bacteria; protects mice form lethal endotoxemia
  </Note>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008055</DescriptorUI>
     <DescriptorName>
      <String>Lipids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D012694</DescriptorUI>
     <DescriptorName>
      <String>Serine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Infect Immun 1991;59(8):2560</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0190832</ConceptUI>
    <ConceptName>
     <String>serine containing aminolipid</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T220837</TermUI>
      <String>serine containing aminolipid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T220836</TermUI>
      <String>serine-containing lipid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T220835</TermUI>
      <String>Ser-L</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012409</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>lonetil M3</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>Russian Drug; structure
  </Note>
  <Frequency>11</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008702</DescriptorUI>
     <DescriptorName>
      <String>Methaqualone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Act Nerv Super (Praha) 18(3):198;1976</Source>
   <Source>Eksp Med Morfol 15(2):79;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059417</ConceptUI>
    <ConceptName>
     <String>lonetil M3</String>
    </ConceptName>
    <RegistryNumber>1897-96-7</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0059417</Concept1UI>
     <Concept2UI>M0059415</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0059417</Concept1UI>
     <Concept2UI>M0059416</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089420</TermUI>
      <String>lonetil M3</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0059415</ConceptUI>
    <ConceptName>
     <String>2-methyl-3(4-ethoxy)phenyl-4-quinazolone</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0059417</Concept1UI>
     <Concept2UI>M0059415</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T089418</TermUI>
      <String>2-methyl-3(4-ethoxy)phenyl-4-quinazolone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0059416</ConceptUI>
    <ConceptName>
     <String>lonetil</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0059417</Concept1UI>
     <Concept2UI>M0059416</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T089419</TermUI>
      <String>lonetil</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012411</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>lysometra</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>polypeptide preparation; low MW polypeptides obtained from hydrolysis of animal organs
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010455</DescriptorUI>
     <DescriptorName>
      <String>Peptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Curr Med Res Opin 4(2):151;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059425</ConceptUI>
    <ConceptName>
     <String>lysometra</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089428</TermUI>
      <String>lysometra</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012413</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>mastodynon</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>plant extract used therapeutically in breast diseases; mastodynon composition: 100 g Agnus castus D1, 20 g Caulophyllum thalictroides D4, 10 g Cyclamen D4, 10 g Ignatia D6, 10 g Iris D2, 20 g Lillum tigrinum D3, 10 g Lupulinum D8, 10 g Tinctura Condurango, 10 g Hersteller: Bionorica KG. 85 Nurnberg 1
  </Note>
  <Frequency>15</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010936</DescriptorUI>
     <DescriptorName>
      <String>Plant Extracts</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Fortschr Med 95(17):1175;1977</Source>
   <Source>Med Welt 27(12):591;1976</Source>
   <Source>ZFA (Stuttgart) 1979;55(22):1239</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059426</ConceptUI>
    <ConceptName>
     <String>mastodynon</String>
    </ConceptName>
    <CASN1Name>Mastodynon</CASN1Name>
    <RegistryNumber>78200-25-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089429</TermUI>
      <String>mastodynon</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012421</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-methoxy-abeo-estrone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>10</Month>
   <Day>07</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>HOMOSTEROIDS (76-83)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004970</DescriptorUI>
     <DescriptorName>
      <String>Estrone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Steroids 27(2):261;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059440</ConceptUI>
    <ConceptName>
     <String>3-methoxy-abeo-estrone</String>
    </ConceptName>
    <CASN1Name>3-methoxy-9(10-19)abeo-1,3,5(10)-estratrien- 17-one</CASN1Name>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089443</TermUI>
      <String>3-methoxy-abeo-estrone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012424</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3 beta-methoxy-dinor-5-cholen-22-ol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>metabolite of cholesteryl methyl ether; structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002770</DescriptorUI>
     <DescriptorName>
      <String>Cholenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Microbiol 22(4):447;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059443</ConceptUI>
    <ConceptName>
     <String>3 beta-methoxy-dinor-5-cholen-22-ol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089446</TermUI>
      <String>3 beta-methoxy-dinor-5-cholen-22-ol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012428</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>20-methylcholesterol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002784</DescriptorUI>
     <DescriptorName>
      <String>Cholesterol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 41(13):2288;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059449</ConceptUI>
    <ConceptName>
     <String>20-methylcholesterol</String>
    </ConceptName>
    <CASN1Name>Cholest-5-en-3-ol, 20-methyl-, (3beta)-</CASN1Name>
    <RegistryNumber>58958-29-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089452</TermUI>
      <String>20-methylcholesterol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012431</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-O-methyl-D-glucuronic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>12</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>METHYLGLYCOSIDES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005965</DescriptorUI>
     <DescriptorName>
      <String>Glucuronates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem J 155(1):181;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059454</ConceptUI>
    <ConceptName>
     <String>2-O-methyl-D-glucuronic acid</String>
    </ConceptName>
    <CASN1Name>D-Glucuronic acid, 2-O-methyl-</CASN1Name>
    <RegistryNumber>59894-02-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089457</TermUI>
      <String>2-O-methyl-D-glucuronic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012432</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-methyl-6-hydroxyquinazoline-2,4-dione</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011799</DescriptorUI>
     <DescriptorName>
      <String>Quinazolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>C R Soc Biol (Paris) 169(5):1151;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059455</ConceptUI>
    <ConceptName>
     <String>3-methyl-6-hydroxyquinazoline-2,4-dione</String>
    </ConceptName>
    <RegistryNumber>17730-75-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089458</TermUI>
      <String>3-methyl-6-hydroxyquinazoline-2,4-dione</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012433</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-methylinosine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>11</Month>
   <Day>29</Day>
  </DateRevised>
  <Frequency>25</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007288</DescriptorUI>
     <DescriptorName>
      <String>Inosine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer 41(5):1685;1978</Source>
   <Source>Clin Chim Acta 1979;97(2-3):159</Source>
   <Source>J Am Chem Soc 98(9):2641;1976</Source>
   <Source>Monogr Hum Genet 10:135;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059456</ConceptUI>
    <ConceptName>
     <String>1-methylinosine</String>
    </ConceptName>
    <RegistryNumber>2140-73-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089459</TermUI>
      <String>1-methylinosine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012441</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-methyl-alpha-tocopheramine nitroxide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1995</Year>
   <Month>03</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*VITAMIN E (83-95)</PreviousIndexing>
   <PreviousIndexing>NITROGEN OXIDES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014810</DescriptorUI>
     <DescriptorName>
      <String>Vitamin E</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Lipids 11(4):296;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059462</ConceptUI>
    <ConceptName>
     <String>N-methyl-alpha-tocopheramine nitroxide</String>
    </ConceptName>
    <CASN1Name>Nitroxide, 3,4-dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-2H-1-benzopyran-6-yl methyl</CASN1Name>
    <RegistryNumber>78249-60-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089465</TermUI>
      <String>N-methyl-alpha-tocopheramine nitroxide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C498281</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cdc16 protein, S pombe</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateCreated>
  <Note>required both for maintenance of p34(cdc2) kinase activity &amp; regulation of septum formation
  </Note>
  <Frequency>16</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*FUNGAL PROTEINS (1993-1995)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D018797</DescriptorUI>
     <DescriptorName>
      <String>Cell Cycle Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029702</DescriptorUI>
     <DescriptorName>
      <String>Schizosaccharomyces pombe Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0465925</ConceptUI>
    <ConceptName>
     <String>cdc16 protein, S pombe</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T586913</TermUI>
      <String>cdc16 protein, S pombe</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>05</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T586915</TermUI>
      <String>SPAC6F6.08c protein, S pombe</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>05</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T586914</TermUI>
      <String>bub2 protein, S pombe</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>05</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012468</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-oximino-4-chromanone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*OXIMES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002867</DescriptorUI>
     <DescriptorName>
      <String>Chromones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 65(3):397;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059507</ConceptUI>
    <ConceptName>
     <String>3-oximino-4-chromanone</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089510</TermUI>
      <String>3-oximino-4-chromanone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012471</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>oxyglucocycline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>carboxamido derivative of oxytetracycline
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010118</DescriptorUI>
     <DescriptorName>
      <String>Oxytetracycline</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Antibiotiki 21(10):933;1976</Source>
   <Source>Antibiotiki 22(2):172;1977</Source>
   <Source>Vestn Khir 119(12):53;1977</Source>
   <Source>Z Eksp Klin Med 15(6):66;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059514</ConceptUI>
    <ConceptName>
     <String>oxyglucocycline</String>
    </ConceptName>
    <RegistryNumber>11140-93-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089517</TermUI>
      <String>oxyglucocycline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012478</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>alpha-(N-1-phenethyl)urea</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>03</Month>
   <Day>27</Day>
  </DateRevised>
  <Note>RN given refers to (+)-isomer
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PHENYLUREA COMPOUNDS (76-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014508</DescriptorUI>
     <DescriptorName>
      <String>Urea</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Science 193(4247):66;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059524</ConceptUI>
    <ConceptName>
     <String>alpha-(N-1-phenethyl)urea</String>
    </ConceptName>
    <RegistryNumber>16849-91-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089527</TermUI>
      <String>alpha-(N-1-phenethyl)urea</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C018754</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>(acyl-carrier-protein) phosphodiesterase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>01</Month>
   <Day>10</Day>
  </DateRevised>
  <Frequency>8</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ACYL CARRIER PROTEIN (79-81)</PreviousIndexing>
   <PreviousIndexing>CARRIER PROTEINS (75-79)</PreviousIndexing>
   <PreviousIndexing>PANTETHEINE/analogs (79-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010727</DescriptorUI>
     <DescriptorName>
      <String>Phosphoric Diester Hydrolases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Biochem Biophys 168(2):490;1975</Source>
   <Source>Methods Enzymol 62:249;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0070603</ConceptUI>
    <ConceptName>
     <String>(acyl-carrier-protein) phosphodiesterase</String>
    </ConceptName>
    <RegistryNumber>EC 3.1.4.14</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T100606</TermUI>
      <String>(acyl-carrier-protein) phosphodiesterase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T100605</TermUI>
      <String>holo-(acyl carrier protein) hydrolase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T100603</TermUI>
      <String>4'-phosphopantetheine-holofatty acid synthetase hydrolase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T100602</TermUI>
      <String>4'-phosphopantetheine hydrolase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T100604</TermUI>
      <String>acyl carrier protein phosphodiesterase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012483</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>phenylhydrazone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>55</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006835</DescriptorUI>
     <DescriptorName>
      <String>Hydrazones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Folia Microbiol 23(4):304;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059540</ConceptUI>
    <ConceptName>
     <String>phenylhydrazone</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089543</TermUI>
      <String>phenylhydrazone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012485</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-phenyl-2-indolinon-1,3-diacetic acid amide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>02</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>AMIDES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007210</DescriptorUI>
     <DescriptorName>
      <String>Indoleacetic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Farm Zh 31(1):29;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059543</ConceptUI>
    <ConceptName>
     <String>3-phenyl-2-indolinon-1,3-diacetic acid amide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089546</TermUI>
      <String>3-phenyl-2-indolinon-1,3-diacetic acid amide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012486</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>20-phenyl-5-pregnene-3 beta,20-diol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>20-aryl analog of 20-hydroxycholesterol; structure
  </Note>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>HYDROXYSTEROIDS (76-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011283</DescriptorUI>
     <DescriptorName>
      <String>Pregnenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 251(3):7336;1976</Source>
   <Source>J Biol Chem 251(7):2087;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059544</ConceptUI>
    <ConceptName>
     <String>20-phenyl-5-pregnene-3 beta,20-diol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089547</TermUI>
      <String>20-phenyl-5-pregnene-3 beta,20-diol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012489</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>phosphorpyridoxyltrifluoroethylamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011732</DescriptorUI>
     <DescriptorName>
      <String>Pyridoxal Phosphate</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 251(7):1853;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059551</ConceptUI>
    <ConceptName>
     <String>phosphorpyridoxyltrifluoroethylamine</String>
    </ConceptName>
    <CASN1Name>3-Pyridinemethanol, 5-hydroxy-6-methyl-4-(((2,2,2-trifluoroethyl)amino)methyl)-, alpha-(dihydrogen phosphate)</CASN1Name>
    <RegistryNumber>59087-16-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089554</TermUI>
      <String>phosphorpyridoxyltrifluoroethylamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012492</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>phthalonic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010795</DescriptorUI>
     <DescriptorName>
      <String>Phthalic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 430(1):53;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059554</ConceptUI>
    <ConceptName>
     <String>phthalonic acid</String>
    </ConceptName>
    <CASN1Name>2-carboxy-alpha-oxobenzeneacetic acid</CASN1Name>
    <RegistryNumber>528-46-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089557</TermUI>
      <String>phthalonic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C018777</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-phenylacetoaminomethylene-DL-p-nitrophenylalanine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>01</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010649</DescriptorUI>
     <DescriptorName>
      <String>Phenylalanine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>JNCI 62(3):565;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0070679</ConceptUI>
    <ConceptName>
     <String>N-phenylacetoaminomethylene-DL-p-nitrophenylalanine</String>
    </ConceptName>
    <CASN1Name>DL-Phenylalanine, 4-nitro-N-(((phenylacetyl)amino)methyl)-</CASN1Name>
    <RegistryNumber>70172-42-8</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0070679</Concept1UI>
     <Concept2UI>M0070680</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T100682</TermUI>
      <String>N-phenylacetoaminomethylene-DL-p-nitrophenylalanine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0070680</ConceptUI>
    <ConceptName>
     <String>A-101</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0070679</Concept1UI>
     <Concept2UI>M0070680</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T100683</TermUI>
      <String>A-101</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T100681</TermUI>
      <String>A 101</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012507</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-pregnen-3 beta-ol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>04</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>C-20 deoxy-analog
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011284</DescriptorUI>
     <DescriptorName>
      <String>Pregnenolone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 251(11):3320;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059572</ConceptUI>
    <ConceptName>
     <String>5-pregnen-3 beta-ol</String>
    </ConceptName>
    <CASN1Name>(3 beta)-pregn-5-en-3-ol</CASN1Name>
    <RegistryNumber>2862-58-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089575</TermUI>
      <String>5-pregnen-3 beta-ol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012510</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>prospan</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>extract from Hedera helix with bronchosecretolytic &amp; antitussive qualities
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010936</DescriptorUI>
     <DescriptorName>
      <String>Plant Extracts</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Z Allgemeinmed 52(10):546;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059580</ConceptUI>
    <ConceptName>
     <String>prospan</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089583</TermUI>
      <String>prospan</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C069172</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,3-bis(palmitoyloxy)-2-propyl-1-palmitoylcysteine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1991</Year>
   <Month>07</Month>
   <Day>09</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>intermediate for immunogen preparation
  </Note>
  <Frequency>46</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003545</DescriptorUI>
     <DescriptorName>
      <String>Cysteine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008074</DescriptorUI>
     <DescriptorName>
      <String>Lipoproteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Int J Pept Protein Res 1991;37(1):46</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0188867</ConceptUI>
    <ConceptName>
     <String>2,3-bis(palmitoyloxy)-2-propyl-1-palmitoylcysteine</String>
    </ConceptName>
    <RegistryNumber>87420-41-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T218872</TermUI>
      <String>2,3-bis(palmitoyloxy)-2-propyl-1-palmitoylcysteine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T218871</TermUI>
      <String>Pam3Cys-OH</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T218870</TermUI>
      <String>N-palmitoyl-2,3-bis(palmitoyloxy)-2-propylcysteine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012634</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>AB 74</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>related to &amp; may be identical with destomycin C
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>AMINOGLYCOSIDES (76-87)</PreviousIndexing>
   <PreviousIndexing>ANTIBIOTICS (76-87)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000617</DescriptorUI>
     <DescriptorName>
      <String>Aminoglycosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiot (Tokyo) 29(5):590;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059807</ConceptUI>
    <ConceptName>
     <String>AB 74</String>
    </ConceptName>
    <RegistryNumber>59794-19-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T089810</TermUI>
      <String>AB 74</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T089808</TermUI>
      <String>AB-74</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T089809</TermUI>
      <String>antibiotic AB 74</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012520</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>D-psicose-6-phosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>16</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005636</DescriptorUI>
     <DescriptorName>
      <String>Fructosephosphates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 251(10):2983;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059600</ConceptUI>
    <ConceptName>
     <String>D-psicose-6-phosphate</String>
    </ConceptName>
    <RegistryNumber>4300-29-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089603</TermUI>
      <String>D-psicose-6-phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C081249</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tissue factor pathway inhibitor (1-161)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1993</Year>
   <Month>06</Month>
   <Day>16</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>05</Day>
  </DateRevised>
  <Frequency>8</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008074</DescriptorUI>
     <DescriptorName>
      <String>Lipoproteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010446</DescriptorUI>
     <DescriptorName>
      <String>Peptide Fragments</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D011994</DescriptorUI>
     <DescriptorName>
      <String>Recombinant Proteins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Haemostasis 1993 Mar;23 Suppl 1:112-7</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0216749</ConceptUI>
    <ConceptName>
     <String>tissue factor pathway inhibitor (1-161)</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T246754</TermUI>
      <String>tissue factor pathway inhibitor (1-161)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T246752</TermUI>
      <String>TFPI (1-161)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T246753</TermUI>
      <String>rTFPI (1-161)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C092528</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>S-(2,3-bis-(palmitoyloxy)propyl)-N-palmitoyl-cysteinyl-alanyl-lysine(4)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>04</Month>
   <Day>14</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>05</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008074</DescriptorUI>
     <DescriptorName>
      <String>Lipoproteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 1995 Mar 11;270(11):6017-21</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0244226</ConceptUI>
    <ConceptName>
     <String>S-(2,3-bis-(palmitoyloxy)propyl)-N-palmitoyl-cysteinyl-alanyl-lysine(4)</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0244226</Concept1UI>
     <Concept2UI>M0244225</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T274231</TermUI>
      <String>S-(2,3-bis-(palmitoyloxy)propyl)-N-palmitoyl-cysteinyl-alanyl-lysine(4)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T274229</TermUI>
      <String>Pam-Cys-Ala-Lys(4)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0244225</ConceptUI>
    <ConceptName>
     <String>S-(2,3-bis(palmitoyloxy)-(2R,2S)-propyl)-N-palmytoyl-(R)-Cys-Ala-Lys(4)</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0244226</Concept1UI>
     <Concept2UI>M0244225</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T274230</TermUI>
      <String>S-(2,3-bis(palmitoyloxy)-(2R,2S)-propyl)-N-palmytoyl-(R)-Cys-Ala-Lys(4)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012528</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>quinaldofur</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1988</Year>
   <Month>09</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>used in treatment of bovine mastitis; structure
  </Note>
  <Frequency>6</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*NITROFURANS (76-82)</PreviousIndexing>
   <PreviousIndexing>*QUINALDINES (76-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011804</DescriptorUI>
     <DescriptorName>
      <String>Quinolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Tijdschr Diergeneeskd 103(2):122;1978</Source>
   <Source>Zentralbl Veterinaermed (B) 23(4):301;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059617</ConceptUI>
    <ConceptName>
     <String>quinaldofur</String>
    </ConceptName>
    <RegistryNumber>57474-29-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0059617</Concept1UI>
     <Concept2UI>M0059615</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0059617</Concept1UI>
     <Concept2UI>M0059616</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089620</TermUI>
      <String>quinaldofur</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0059615</ConceptUI>
    <ConceptName>
     <String>4-(5'-nitrofuryl)quinaldinic acid N-oxide</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0059617</Concept1UI>
     <Concept2UI>M0059615</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T089618</TermUI>
      <String>4-(5'-nitrofuryl)quinaldinic acid N-oxide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0059616</ConceptUI>
    <ConceptName>
     <String>abimasten</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0059617</Concept1UI>
     <Concept2UI>M0059616</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T089619</TermUI>
      <String>abimasten</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012531</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>resistoflavin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*FLAVONES (76-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001580</DescriptorUI>
     <DescriptorName>
      <String>Benzopyrenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Antibiotiki 21(2):105;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059620</ConceptUI>
    <ConceptName>
     <String>resistoflavin</String>
    </ConceptName>
    <CASN1Name>(-)-3,5,7,11b-tetrahydroxy-1,1,9-trimethyl-2H-benzo(cd)pyrene-2,6,10(1H,11bH)-trione</CASN1Name>
    <RegistryNumber>29706-96-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089623</TermUI>
      <String>resistoflavin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012534</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-(beta-D-ribofuranosyl)-2,3-dihydro-6H-1,3-oxazine-2,6-dione</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>01</Month>
   <Day>18</Day>
  </DateRevised>
  <Note>pyrimidine nucleoside analog related to uridine; structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010078</DescriptorUI>
     <DescriptorName>
      <String>Oxazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012263</DescriptorUI>
     <DescriptorName>
      <String>Ribonucleosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 19(5):643;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059625</ConceptUI>
    <ConceptName>
     <String>3-(beta-D-ribofuranosyl)-2,3-dihydro-6H-1,3-oxazine-2,6-dione</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089628</TermUI>
      <String>3-(beta-D-ribofuranosyl)-2,3-dihydro-6H-1,3-oxazine-2,6-dione</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012542</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ruscorectal (combination)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>combination of ruscogenin &amp; neoruscogenin
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013150</DescriptorUI>
     <DescriptorName>
      <String>Spirostans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Munch Med Wochenschr 118(11):339;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059633</ConceptUI>
    <ConceptName>
     <String>ruscorectal (combination)</String>
    </ConceptName>
    <RegistryNumber>50933-59-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089636</TermUI>
      <String>ruscorectal (combination)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C113382</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>coat protein, Cowpea aphid-borne mosaic virus</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>07</Month>
   <Day>31</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>02</Month>
   <Day>26</Day>
  </DateRevised>
  <Note>from a potyvirus infecting sesame (Sesamum indicum); amino acid sequence in first source
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CAPSID (1998-2003)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D036022</DescriptorUI>
     <DescriptorName>
      <String>Capsid Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D017800</DescriptorUI>
     <DescriptorName>
      <String>Potyvirus</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Arch Virol 1997;142(9):1919-27</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0292840</ConceptUI>
    <ConceptName>
     <String>coat protein, Cowpea aphid-borne mosaic virus</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0292840</Concept1UI>
     <Concept2UI>M0461464</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T462602</TermUI>
      <String>coat protein, Cowpea aphid-borne mosaic virus</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>09</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0461464</ConceptUI>
    <ConceptName>
     <String>coat protein, Sesame mosaic potyvirus</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0292840</Concept1UI>
     <Concept2UI>M0461464</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T574483</TermUI>
      <String>coat protein, Sesame mosaic potyvirus</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>02</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T322843</TermUI>
      <String>SeMV coat protein, Sesame mosaic potyvirus</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T322845</TermUI>
      <String>coat protein, sesame potyvirus</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012549</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Silufol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1993</Year>
   <Month>09</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>10</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SILICONES (76-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012822</DescriptorUI>
     <DescriptorName>
      <String>Silicon Dioxide</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D005782</DescriptorUI>
     <DescriptorName>
      <String>Gels</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Biokhimiia 44(2):368;1979</Source>
   <Source>Cesk Farm 25(2):64;1976</Source>
   <Source>Cesk Farm 25(6):213;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059648</ConceptUI>
    <ConceptName>
     <String>Silufol</String>
    </ConceptName>
    <CASN1Name>Silufol</CASN1Name>
    <RegistryNumber>62253-50-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089651</TermUI>
      <String>Silufol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012560</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Streptotriad</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1995</Year>
   <Month>06</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>combination of above used in prevention of diarrhea
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013307</DescriptorUI>
     <DescriptorName>
      <String>Streptomycin</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013411</DescriptorUI>
     <DescriptorName>
      <String>Sulfadiazine</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013418</DescriptorUI>
     <DescriptorName>
      <String>Sulfamethazine</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013432</DescriptorUI>
     <DescriptorName>
      <String>Sulfathiazoles</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Lancet 2(7977):143;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059659</ConceptUI>
    <ConceptName>
     <String>Streptotriad</String>
    </ConceptName>
    <CASN1Name>D-Streptamine, O- 2-deoxy-2-(methylamino)-alpha-L-glucopyranosyl-(1-2)-O-5-deoxy-3-C-formyl-alpha-L-lyxofuranosyl-(1-4)-N,N'-bis(aminoiminomethyl)-, sulfate (2:3) (salt), mixt. with 4-amino-N-(4,6-dimethyl-2-pyrimidinyl)benzenesulfonamide, 4-amino-N-2-pyrimidinylbenzenesulfonamide and 4-amino-N-2-thiazolylbenzenesulfonamide</CASN1Name>
    <RegistryNumber>79028-52-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089662</TermUI>
      <String>Streptotriad</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012930</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dimethyl-3,3'-(dithiahexamethylenedioxy)dipropionimidate</String>
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  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>05</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>reagent suitable for cross-linking of proteins; structure; RN given refers to HCl
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*IMIDES (76-80)</PreviousIndexing>
   <PreviousIndexing>DISULFIDES (76-82)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007096</DescriptorUI>
     <DescriptorName>
      <String>Imidoesters</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Hoppe-Seyler's Z Physiol Chem 357(3):477;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060299</ConceptUI>
    <ConceptName>
     <String>dimethyl-3,3'-(dithiahexamethylenedioxy)dipropionimidate</String>
    </ConceptName>
    <CASN1Name>Propanimidic acid, 3,3'-(dithiobis(2,1-ethanediyloxy))bis-, dimethyl ester, dihydrochloride</CASN1Name>
    <RegistryNumber>59759-98-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090302</TermUI>
      <String>dimethyl-3,3'-(dithiahexamethylenedioxy)dipropionimidate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012933</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3,8-dimethyl-N-methylphenanthrolinium</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010618</DescriptorUI>
     <DescriptorName>
      <String>Phenanthrolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biophys Struct Mech 2(1):13;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060302</ConceptUI>
    <ConceptName>
     <String>3,8-dimethyl-N-methylphenanthrolinium</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090305</TermUI>
      <String>3,8-dimethyl-N-methylphenanthrolinium</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012937</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,2-dioleoyl-3-(alpha-1-adamantoyl)-sn-glycerol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>pancreatic lipase inhibitor
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ADAMANTANE/analogs (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014280</DescriptorUI>
     <DescriptorName>
      <String>Triglycerides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 65(8):1243;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060310</ConceptUI>
    <ConceptName>
     <String>1,2-dioleoyl-3-(alpha-1-adamantoyl)-sn-glycerol</String>
    </ConceptName>
    <CASN1Name>Tricyclo(3.3.1.13,7)decane-1-carboxylic-14C acid, 2,3-bis((1-oxo-9-octadecenyl)oxy)propyl ester, (R-(Z,Z))-</CASN1Name>
    <RegistryNumber>61199-79-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090313</TermUI>
      <String>1,2-dioleoyl-3-(alpha-1-adamantoyl)-sn-glycerol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C582002</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>migracin B</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>07</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>from the culture broth of Streptomyces sp. MI264-NF2.; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001547</DescriptorUI>
     <DescriptorName>
      <String>Benzaldehydes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiot (Tokyo). 2013 Apr;66(4):225-3</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0585962</ConceptUI>
    <ConceptName>
     <String>migracin B</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T846400</TermUI>
      <String>migracin B</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>07</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012940</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,2'-diphenylene chlorophosphonate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>03</Month>
   <Day>24</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BIPHENYL COMPOUNDS</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009943</DescriptorUI>
     <DescriptorName>
      <String>Organophosphorus Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Experientia 32(9):1111;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060313</ConceptUI>
    <ConceptName>
     <String>2,2'-diphenylene chlorophosphonate</String>
    </ConceptName>
    <CASN1Name>Dibenzo(d,f)(1,3,2)dioxaphosphepin, 6-chloro-, 6-oxide</CASN1Name>
    <RegistryNumber>52258-06-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090316</TermUI>
      <String>2,2'-diphenylene chlorophosphonate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012942</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4,6-diphenylthieno(3,4-d)(1,3)dioxol-2-one-5,5-dioxide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>02</Month>
   <Day>13</Day>
  </DateRevised>
  <Note>activating agent for peptide synthesis; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*THIOPHENES</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004149</DescriptorUI>
     <DescriptorName>
      <String>Dioxoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Angew Chem Int Ed Engl 15(7):444;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060315</ConceptUI>
    <ConceptName>
     <String>4,6-diphenylthieno(3,4-d)(1,3)dioxol-2-one-5,5-dioxide</String>
    </ConceptName>
    <RegistryNumber>54714-11-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090318</TermUI>
      <String>4,6-diphenylthieno(3,4-d)(1,3)dioxol-2-one-5,5-dioxide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012943</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3',4'-dipropionylhelveticosol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>30</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CARDANOLIDES (76-77)</PreviousIndexing>
   <PreviousIndexing>*CARDENOLIDES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004071</DescriptorUI>
     <DescriptorName>
      <String>Digitalis Glycosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Inner Med 31(13):501;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060316</ConceptUI>
    <ConceptName>
     <String>3',4'-dipropionylhelveticosol</String>
    </ConceptName>
    <RegistryNumber>20045-25-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090319</TermUI>
      <String>3',4'-dipropionylhelveticosol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C523072</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>DB359</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>09</Month>
   <Day>27</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001550</DescriptorUI>
     <DescriptorName>
      <String>Benzamidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Am Chem Soc 2007 Jul 4;129(26):8389-95</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0513902</ConceptUI>
    <ConceptName>
     <String>DB359</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T706630</TermUI>
      <String>DB359</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>09</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012945</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,2'-dipyridyl diselenide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1994</Year>
   <Month>01</Month>
   <Day>28</Day>
  </DateRevised>
  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PYRIDINES (76-77)</PreviousIndexing>
   <PreviousIndexing>SELENIUM (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D015082</DescriptorUI>
     <DescriptorName>
      <String>2,2'-Dipyridyl</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D016566</DescriptorUI>
     <DescriptorName>
      <String>Organoselenium Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nucleic acid Res 3(5):1233;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060325</ConceptUI>
    <ConceptName>
     <String>2,2'-dipyridyl diselenide</String>
    </ConceptName>
    <CASN1Name>Pyridine, 2,2'-diselenobis-</CASN1Name>
    <RegistryNumber>59957-75-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090328</TermUI>
      <String>2,2'-dipyridyl diselenide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C582001</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>paecilin C</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>07</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>from marine gorgonian coral-associated fungus Penicillium sp.; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D047309</DescriptorUI>
     <DescriptorName>
      <String>Flavones</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D061065</DescriptorUI>
     <DescriptorName>
      <String>Polyketides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiot (Tokyo). 2013 Apr;66(4):219-23</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0585961</ConceptUI>
    <ConceptName>
     <String>paecilin C</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T846397</TermUI>
      <String>paecilin C</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>07</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
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   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C582000</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6,8,5'6'-tetrahydroxy-3'-methylflavone</String>
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  <DateCreated>
   <Year>2013</Year>
   <Month>07</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2013</Year>
   <Month>07</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>from marine gorgonian coral-associated fungus Penicillium sp.; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D047309</DescriptorUI>
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      <String>Flavones</String>
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   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D061065</DescriptorUI>
     <DescriptorName>
      <String>Polyketides</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiot (Tokyo). 2013 Apr;66(4):219-23</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0585960</ConceptUI>
    <ConceptName>
     <String>6,8,5'6'-tetrahydroxy-3'-methylflavone</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T846396</TermUI>
      <String>6,8,5'6'-tetrahydroxy-3'-methylflavone</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>07</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012949</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dithiophosgene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>dimeric thiophosgene; inactivates cathepsin D; structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*HETEROCYCLIC COMPOUNDS (76-77)</PreviousIndexing>
   <PreviousIndexing>SULFIDES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010705</DescriptorUI>
     <DescriptorName>
      <String>Phosgene</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem J 153(3):737;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060328</ConceptUI>
    <ConceptName>
     <String>dithiophosgene</String>
    </ConceptName>
    <CASN1Name>2,2,4,4-tetrachloro-1,3-dithiacyclobutane</CASN1Name>
    <RegistryNumber>20464-23-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090331</TermUI>
      <String>dithiophosgene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C582003</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>migracin A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>07</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>from the culture broth of Streptomyces sp. MI264-NF2.; structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001547</DescriptorUI>
     <DescriptorName>
      <String>Benzaldehydes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiot (Tokyo). 2013 Apr;66(4):225-3</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0585963</ConceptUI>
    <ConceptName>
     <String>migracin A</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T846401</TermUI>
      <String>migracin A</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>07</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C523071</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>PDZ-RhoGEF, rat</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>09</Month>
   <Day>27</Day>
  </DateCreated>
  <Note>an increased PDZ-RhoGEF/RhoA/Rho kinase signaling in small mesenteric arteries of angiotensin II-induced hypertensive rats is reported
  </Note>
  <Frequency>7</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D020662</DescriptorUI>
     <DescriptorName>
      <String>Guanine Nucleotide Exchange Factors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Hypertens 2007 Aug;25(8):1687-97</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0513899</ConceptUI>
    <ConceptName>
     <String>PDZ-RhoGEF, rat</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T706626</TermUI>
      <String>PDZ-RhoGEF, rat</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>09</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012979</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>fluorophenindione</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010630</DescriptorUI>
     <DescriptorName>
      <String>Phenindione</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Europ J Clin Pharmacol 10:139;1976</Source>
   <Source>Europ J Clin Pharmacol 8:271;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060386</ConceptUI>
    <ConceptName>
     <String>fluorophenindione</String>
    </ConceptName>
    <RegistryNumber>52892-82-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090389</TermUI>
      <String>fluorophenindione</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012983</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-formyluridine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014529</DescriptorUI>
     <DescriptorName>
      <String>Uridine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nucleic Acid Res 3(7):1791;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060398</ConceptUI>
    <ConceptName>
     <String>5-formyluridine</String>
    </ConceptName>
    <CASN1Name>Uridine, 5-formyl-</CASN1Name>
    <RegistryNumber>3180-21-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090401</TermUI>
      <String>5-formyluridine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C582004</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>monodeacettphomoxanthone B</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>07</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>from Phomopsis longicolla; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D044004</DescriptorUI>
     <DescriptorName>
      <String>Xanthones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiot (Tokyo). 2013 Apr;66(4):231-3</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0585964</ConceptUI>
    <ConceptName>
     <String>monodeacettphomoxanthone B</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T846402</TermUI>
      <String>monodeacettphomoxanthone B</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>07</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C582008</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ICM0301B</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>07</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004852</DescriptorUI>
     <DescriptorName>
      <String>Epoxy Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006576</DescriptorUI>
     <DescriptorName>
      <String>Heterocyclic Compounds, 4 or More Rings</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiot (Tokyo). 2013 Apr;66(4):243-6</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0585968</ConceptUI>
    <ConceptName>
     <String>ICM0301B</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T846406</TermUI>
      <String>ICM0301B</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>07</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C059112</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-isopropyl-3-amino-2-(3,4-dihydroxyphenyl)-2-hydroxybicyclo(2.2.1)heptane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1989</Year>
   <Month>05</Month>
   <Day>12</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>RN &amp; structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001643</DescriptorUI>
     <DescriptorName>
      <String>Bridged Bicyclo Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 1989;32(4):856</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0164542</ConceptUI>
    <ConceptName>
     <String>N-isopropyl-3-amino-2-(3,4-dihydroxyphenyl)-2-hydroxybicyclo(2.2.1)heptane</String>
    </ConceptName>
    <RegistryNumber>118891-95-5</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>118891-93-3 (HCl)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0164542</Concept1UI>
     <Concept2UI>M0324103</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T194547</TermUI>
      <String>N-isopropyl-3-amino-2-(3,4-dihydroxyphenyl)-2-hydroxybicyclo(2.2.1)heptane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T194546</TermUI>
      <String>N-IADHH</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0324103</ConceptUI>
    <ConceptName>
     <String>N-isopropyl-3-amino-2-(3,4-dihydroxyphenyl)-2-hydroxybicyclo(2.2.1)heptane hydrochloride</String>
    </ConceptName>
    <RegistryNumber>118891-93-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0164542</Concept1UI>
     <Concept2UI>M0324103</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T354103</TermUI>
      <String>N-isopropyl-3-amino-2-(3,4-dihydroxyphenyl)-2-hydroxybicyclo(2.2.1)heptane hydrochloride</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013004</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>glycerol 1,2 cyclic phosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1987</Year>
   <Month>10</Month>
   <Day>20</Day>
  </DateRevised>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005994</DescriptorUI>
     <DescriptorName>
      <String>Glycerophosphates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem J 153(3):745;1976</Source>
   <Source>Biochem J 173(2):579;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060425</ConceptUI>
    <ConceptName>
     <String>glycerol 1,2 cyclic phosphate</String>
    </ConceptName>
    <RegistryNumber>5695-96-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090428</TermUI>
      <String>glycerol 1,2 cyclic phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013005</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>glycyladenylate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>06</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>GLYCINE (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000249</DescriptorUI>
     <DescriptorName>
      <String>Adenosine Monophosphate</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem J 175(2):461;1978</Source>
   <Source>J Theor Biol 57(2):407;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060426</ConceptUI>
    <ConceptName>
     <String>glycyladenylate</String>
    </ConceptName>
    <CASN1Name>Glycine, monoanhydride with 5'-adenylic acid</CASN1Name>
    <RegistryNumber>35985-26-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090429</TermUI>
      <String>glycyladenylate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013051</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>17-hydroxypregnanolone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1970</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>RN given refers to cpd without isomeric designation
  </Note>
  <Frequency>17</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011280</DescriptorUI>
     <DescriptorName>
      <String>Pregnanolone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Endocrinology 98(1):179;1976</Source>
   <Source>J Endocrinol 70(1):117;1976</Source>
   <Source>J Steroid Biochem 8:1197;1977</Source>
   <Source>Z Geburtsch Perinatol 181:294;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060496</ConceptUI>
    <ConceptName>
     <String>17-hydroxypregnanolone</String>
    </ConceptName>
    <RegistryNumber>40248-23-5</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>570-51-4 ((3beta,5alpha,14beta,17alpha)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>570-52-5 ((3alpha,5beta)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>570-53-6 ((3beta,5beta)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>570-54-7 ((3beta,5alpha,17alpha)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>6609-97-8 ((3alpha)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>6890-65-9 ((3alpha,5alpha,17alpha)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0060496</Concept1UI>
     <Concept2UI>M0312062</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0060496</Concept1UI>
     <Concept2UI>M0312058</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0060496</Concept1UI>
     <Concept2UI>M0060495</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0060496</Concept1UI>
     <Concept2UI>M0312060</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0060496</Concept1UI>
     <Concept2UI>M0312059</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0060496</Concept1UI>
     <Concept2UI>M0060490</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0060496</Concept1UI>
     <Concept2UI>M0060493</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0060496</Concept1UI>
     <Concept2UI>M0312061</Concept2UI>
     </ConceptRelation>
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      <TermUI>T090499</TermUI>
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      <ThesaurusIDlist>
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      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T090494</TermUI>
      <String>17-OH-Polone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
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    <RegistryNumber>6890-65-9</RegistryNumber>
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      <TermUI>T342062</TermUI>
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      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
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      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T090495</TermUI>
      <String>3 alpha,17 alpha-dihydroxy-5 alpha-pregnan-20-one</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
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   <Concept PreferredConceptYN="N">
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    <RegistryNumber>570-52-5</RegistryNumber>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342058</TermUI>
      <String>17-hydroxypregnanolone, (3alpha,5beta)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
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     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0060495</ConceptUI>
    <ConceptName>
     <String>allopregnane-3 beta,17 alpha-diol-20-one</String>
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     <Concept1UI>M0060496</Concept1UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T090498</TermUI>
      <String>allopregnane-3 beta,17 alpha-diol-20-one</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
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     </Term>
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   </Concept>
   <Concept PreferredConceptYN="N">
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    <ConceptName>
     <String>17-hydroxypregnanolone, (3beta,5alpha,17alpha)-isomer</String>
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    <RegistryNumber>570-54-7</RegistryNumber>
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     <Concept1UI>M0060496</Concept1UI>
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    <TermList>
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      <TermUI>T342060</TermUI>
      <String>17-hydroxypregnanolone, (3beta,5alpha,17alpha)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312059</ConceptUI>
    <ConceptName>
     <String>17-hydroxypregnanolone, (3beta,5beta)-isomer</String>
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    <RegistryNumber>570-53-6</RegistryNumber>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0060496</Concept1UI>
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    <TermList>
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      <TermUI>T342059</TermUI>
      <String>17-hydroxypregnanolone, (3beta,5beta)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0060490</ConceptUI>
    <ConceptName>
     <String>17-(1-ketoethyl)androstane-3,17-diol</String>
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    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0060496</Concept1UI>
     <Concept2UI>M0060490</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T090493</TermUI>
      <String>17-(1-ketoethyl)androstane-3,17-diol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
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   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0060493</ConceptUI>
    <ConceptName>
     <String>3 alpha,17 alpha-dihydroxy-5 beta-pregnan-20-one</String>
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    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0060496</Concept1UI>
     <Concept2UI>M0060493</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T090496</TermUI>
      <String>3 alpha,17 alpha-dihydroxy-5 beta-pregnan-20-one</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T090497</TermUI>
      <String>5 beta-pregnane-3 alpha,17alpha-diol-20-one</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312061</ConceptUI>
    <ConceptName>
     <String>17-hydroxypregnanolone, (3alpha)-isomer</String>
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    <RegistryNumber>6609-97-8</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0060496</Concept1UI>
     <Concept2UI>M0312061</Concept2UI>
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    <TermList>
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      <TermUI>T342061</TermUI>
      <String>17-hydroxypregnanolone, (3alpha)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312057</ConceptUI>
    <ConceptName>
     <String>17-hydroxypregnanolone, (3beta,5alpha,14beta,17alpha)-isomer</String>
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    <RegistryNumber>570-51-4</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0060496</Concept1UI>
     <Concept2UI>M0312057</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342057</TermUI>
      <String>17-hydroxypregnanolone, (3beta,5alpha,14beta,17alpha)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C113617</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Trp-Lys-Tyr-Met-Val-Met</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>08</Month>
   <Day>13</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>a synthetic peptide, stimulates phosphoinositide hyrolysis in human leukocytes
  </Note>
  <Frequency>90</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009842</DescriptorUI>
     <DescriptorName>
      <String>Oligopeptides</String>
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   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D002630</DescriptorUI>
     <DescriptorName>
      <String>Chemotactic Factors</String>
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     </DescriptorReferredTo>
   </IndexingInformation>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D013237</DescriptorUI>
     <DescriptorName>
      <String>Stereoisomerism</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Clin Biochem 1998 Apr;31(3):137-41</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0293353</ConceptUI>
    <ConceptName>
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    <RegistryNumber>0</RegistryNumber>
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     <Concept1UI>M0293353</Concept1UI>
     <Concept2UI>M0359486</Concept2UI>
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    <TermList>
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      <TermUI>T323358</TermUI>
      <String>Trp-Lys-Tyr-Met-Val-Met</String>
      <ThesaurusIDlist>
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      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T323356</TermUI>
      <String>WKYMVM</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T323357</TermUI>
      <String>tryptophyl-lysyl-tyrosyl-methionyl-valyl-methionyl</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
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   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0359486</ConceptUI>
    <ConceptName>
     <String>Trp-Lys-Tyr-Met-Val-DMet</String>
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     <Concept1UI>M0293353</Concept1UI>
     <Concept2UI>M0359486</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T410316</TermUI>
      <String>Trp-Lys-Tyr-Met-Val-DMet</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>03</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
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   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C098564</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>MAPEP1 protein, Microcystis aeruginosa</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>04</Month>
   <Day>12</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>04</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>putative peptide synthetase isolated from the cyanobacterium Microcystis aeruginosa; amino acid sequence in first source; GenBank Z28338
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  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
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   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010453</DescriptorUI>
     <DescriptorName>
      <String>Peptide Synthases</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>FEMS Microbiol Lett 1996 Jan 15;135(2-3):295-303</Source>
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  <ConceptList>
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    <ConceptUI>M0258907</ConceptUI>
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    <RegistryNumber>EC 6.3.2.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T537202</TermUI>
      <String>MAPEP1 protein, Microcystis aeruginosa</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>04</Month>
       <Day>02</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C411848</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Nik related kinase</String>
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  <DateCreated>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>11</Day>
  </DateCreated>
  <DateRevised>
   <Year>2007</Year>
   <Month>09</Month>
   <Day>27</Day>
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  <Note>RefSeq NM_198465
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  <Frequency>16</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D017346</DescriptorUI>
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      <String>Protein-Serine-Threonine Kinases</String>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D047908</DescriptorUI>
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  <SourceList>
   <Source>J Biol Chem 2000 Jul 7;275(27):20533-9</Source>
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      <DateCreated>
       <Year>2007</Year>
       <Month>09</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T421449</TermUI>
      <String>NESK kinase</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>08</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
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      <TermUI>T560099</TermUI>
      <String>Nrk protein, mouse</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>11</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T560102</TermUI>
      <String>NIK related kinase, mouse</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>11</Month>
       <Day>25</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
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    <TermList>
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      <TermUI>T706628</TermUI>
      <String>Nrk protein, rat</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>09</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T706629</TermUI>
      <String>Nik related kinase, rat</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>09</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
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    <ConceptUI>M0513900</ConceptUI>
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    <RegistryNumber>EC 2.7.1.11</RegistryNumber>
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     <Concept1UI>M0367661</Concept1UI>
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     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T706624</TermUI>
      <String>NRK protein, human</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>09</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T706625</TermUI>
      <String>Nik related kinase, human</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>09</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C063478</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-chloroacetal</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1990</Year>
   <Month>04</Month>
   <Day>27</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000080</DescriptorUI>
     <DescriptorName>
      <String>Acetals</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 1990;167(2):457</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0175198</ConceptUI>
    <ConceptName>
     <String>2-chloroacetal</String>
    </ConceptName>
    <RegistryNumber>621-62-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T205203</TermUI>
      <String>2-chloroacetal</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013743</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>TB 68</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010936</DescriptorUI>
     <DescriptorName>
      <String>Plant Extracts</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eksp Med Morphol 15(4):228;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061751</ConceptUI>
    <ConceptName>
     <String>TB 68</String>
    </ConceptName>
    <CASN1Name>TV 68</CASN1Name>
    <RegistryNumber>62683-44-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T091754</TermUI>
      <String>TB 68</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T091753</TermUI>
      <String>TB-68</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C065895</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>methyl 2,3-4,5-di-O-isopropylidine-glucoseptanoside</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1990</Year>
   <Month>11</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000080</DescriptorUI>
     <DescriptorName>
      <String>Acetals</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005960</DescriptorUI>
     <DescriptorName>
      <String>Glucosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Carbohydr Res 1990;201(1):150</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0180999</ConceptUI>
    <ConceptName>
     <String>methyl 2,3-4,5-di-O-isopropylidine-glucoseptanoside</String>
    </ConceptName>
    <RegistryNumber>26784-78-1</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0180999</Concept1UI>
     <Concept2UI>M0180998</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T211004</TermUI>
      <String>methyl 2,3-4,5-di-O-isopropylidine-glucoseptanoside</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T211002</TermUI>
      <String>methyl 2,3-4,5-di-O-isopropylidine-alpha-glucoseptanoside</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T211001</TermUI>
      <String>2,3-DIGSP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0180998</ConceptUI>
    <ConceptName>
     <String>methyl 2,3-4,5-di-O-isopropylidine-beta-glucoseptanoside</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0180999</Concept1UI>
     <Concept2UI>M0180998</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T211003</TermUI>
      <String>methyl 2,3-4,5-di-O-isopropylidine-beta-glucoseptanoside</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013027</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hydroperoxidobutyloleate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*OLEIC ACIDS (76-82)</PreviousIndexing>
   <PreviousIndexing>*PEROXIDES (76-80)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008054</DescriptorUI>
     <DescriptorName>
      <String>Lipid Peroxides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nahrung 20(1):1;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060458</ConceptUI>
    <ConceptName>
     <String>hydroperoxidobutyloleate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090461</TermUI>
      <String>hydroperoxidobutyloleate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C582005</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>JBIR-130</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>07</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2013</Year>
   <Month>07</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>from Isaria sp. NBRC 104353; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011728</DescriptorUI>
     <DescriptorName>
      <String>Pyridones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D000470</DescriptorUI>
     <DescriptorName>
      <String>Alkaloids</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Antibiot (Tokyo). 2013 Apr;66(4):235-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0585965</ConceptUI>
    <ConceptName>
     <String>JBIR-130</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T846403</TermUI>
      <String>JBIR-130</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>07</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013034</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-hydroxy-diaminopimelic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>analog of diaminopimelic acid only partially replacing it during synthesis of murein
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003960</DescriptorUI>
     <DescriptorName>
      <String>Diaminopimelic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Folia Microbiol 21(3):161;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060465</ConceptUI>
    <ConceptName>
     <String>4-hydroxy-diaminopimelic acid</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090468</TermUI>
      <String>4-hydroxy-diaminopimelic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013036</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>15 alpha-hydroxyestradiol 3-sulfate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004958</DescriptorUI>
     <DescriptorName>
      <String>Estradiol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Clin Endocrinol Metab 43(1):144;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060468</ConceptUI>
    <ConceptName>
     <String>15 alpha-hydroxyestradiol 3-sulfate</String>
    </ConceptName>
    <CASN1Name>Estra-1,3,5(10)-triene-3,15,17-triol, 3-(hydrogen sulfate), (15alpha,17beta)-</CASN1Name>
    <RegistryNumber>2524-23-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090471</TermUI>
      <String>15 alpha-hydroxyestradiol 3-sulfate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013037</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-hydroxy-1,3,5(10)-estratriene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>HYDROXYSTEROIDS (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004963</DescriptorUI>
     <DescriptorName>
      <String>Estrenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Steroids 28(3):325;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060469</ConceptUI>
    <ConceptName>
     <String>1-hydroxy-1,3,5(10)-estratriene</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090472</TermUI>
      <String>1-hydroxy-1,3,5(10)-estratriene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C582007</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>JBIR-131</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>07</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>from Isaria sp. NBRC 104353; structure in first sourc
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011728</DescriptorUI>
     <DescriptorName>
      <String>Pyridones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D000470</DescriptorUI>
     <DescriptorName>
      <String>Alkaloids</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Antibiot (Tokyo). 2013 Apr;66(4):235-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0585967</ConceptUI>
    <ConceptName>
     <String>JBIR-131</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T846405</TermUI>
      <String>JBIR-131</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>07</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013041</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>17 beta-hydroxy-7 alpha-methylestr-5-en-3-one acetate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1991</Year>
   <Month>06</Month>
   <Day>03</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>KETOSTEROIDS (76-77)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004963</DescriptorUI>
     <DescriptorName>
      <String>Estrenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Steroids 27(6):759;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060476</ConceptUI>
    <ConceptName>
     <String>17 beta-hydroxy-7 alpha-methylestr-5-en-3-one acetate</String>
    </ConceptName>
    <RegistryNumber>54793-00-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090479</TermUI>
      <String>17 beta-hydroxy-7 alpha-methylestr-5-en-3-one acetate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013043</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hydroxymethylinulin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007444</DescriptorUI>
     <DescriptorName>
      <String>Inulin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Clin Invest 57(4):885;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060481</ConceptUI>
    <ConceptName>
     <String>hydroxymethylinulin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090484</TermUI>
      <String>hydroxymethylinulin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C582006</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>JBIR-132</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>07</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2013</Year>
   <Month>07</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>from Isaria sp. NBRC 104353; structure in first sourc
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011728</DescriptorUI>
     <DescriptorName>
      <String>Pyridones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D000470</DescriptorUI>
     <DescriptorName>
      <String>Alkaloids</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Antibiot (Tokyo). 2013 Apr;66(4):235-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0585966</ConceptUI>
    <ConceptName>
     <String>JBIR-132</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T846404</TermUI>
      <String>JBIR-132</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>07</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013045</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6-hydroxymethyllaudanosine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007546</DescriptorUI>
     <DescriptorName>
      <String>Isoquinolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Pharm Acta Helv 51(6):164;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060483</ConceptUI>
    <ConceptName>
     <String>6-hydroxymethyllaudanosine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090486</TermUI>
      <String>6-hydroxymethyllaudanosine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013049</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hydroxypepstatin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>05</Month>
   <Day>20</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010436</DescriptorUI>
     <DescriptorName>
      <String>Pepstatins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Proteases Biol Control W3 C162N:439;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060487</ConceptUI>
    <ConceptName>
     <String>hydroxypepstatin</String>
    </ConceptName>
    <RegistryNumber>52329-53-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090490</TermUI>
      <String>hydroxypepstatin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C069602</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-bromo-2-methoxypropional dimethylacetal</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1991</Year>
   <Month>08</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000080</DescriptorUI>
     <DescriptorName>
      <String>Acetals</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Gig Sanit 1991(1):74</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0189891</ConceptUI>
    <ConceptName>
     <String>1-bromo-2-methoxypropional dimethylacetal</String>
    </ConceptName>
    <RegistryNumber>759-97-7</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0189891</Concept1UI>
     <Concept2UI>M0189890</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T219896</TermUI>
      <String>1-bromo-2-methoxypropional dimethylacetal</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T219894</TermUI>
      <String>1-BMPDA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0189890</ConceptUI>
    <ConceptName>
     <String>alpha-bromo-beta-methoxypropionic aldehyde dimethylacetal</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0189891</Concept1UI>
     <Concept2UI>M0189890</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T219895</TermUI>
      <String>alpha-bromo-beta-methoxypropionic aldehyde dimethylacetal</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013054</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-hydroxysuccinimidyl 3-(4'-hydroxy-(3',5'-125I)- diiodophenyl)propionate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>used for labeling enzymes; no RN found for labeled or unlabeled cpd; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SUCCINIMIDES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010666</DescriptorUI>
     <DescriptorName>
      <String>Phenylpropionates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D007457</DescriptorUI>
     <DescriptorName>
      <String>Iodine Radioisotopes</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Clin Chem 22(8):1277;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060504</ConceptUI>
    <ConceptName>
     <String>N-hydroxysuccinimidyl 3-(4'-hydroxy-(3',5'-125I)- diiodophenyl)propionate</String>
    </ConceptName>
    <CASN1Name>2,5-Pyrrolidinedione, 1-(3-(4-hydroxy-3,5-di(iodo-125I)phenyl)-1-oxopropoxy)-</CASN1Name>
    <RegistryNumber>60285-92-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090507</TermUI>
      <String>N-hydroxysuccinimidyl 3-(4'-hydroxy-(3',5'-125I)- diiodophenyl)propionate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013060</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>immunoglobulin Kol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007074</DescriptorUI>
     <DescriptorName>
      <String>Immunoglobulin G</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009194</DescriptorUI>
     <DescriptorName>
      <String>Myeloma Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Hoppe-Seyler's Z Physiol Chem 357:795;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060520</ConceptUI>
    <ConceptName>
     <String>immunoglobulin Kol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090523</TermUI>
      <String>immunoglobulin Kol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013061</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>immunopeptide 1</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1992</Year>
   <Month>09</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>no other information available 11/19/76
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010455</DescriptorUI>
     <DescriptorName>
      <String>Peptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ann Allergy 37(4):267;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060521</ConceptUI>
    <ConceptName>
     <String>immunopeptide 1</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090524</TermUI>
      <String>immunopeptide 1</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C076323</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>deaminotri-O-isopropylidene tunicamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1992</Year>
   <Month>09</Month>
   <Day>24</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000080</DescriptorUI>
     <DescriptorName>
      <String>Acetals</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014312</DescriptorUI>
     <DescriptorName>
      <String>Trisaccharides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Carbohydr Res 1992 Apr 10;228(1):205-16</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0205329</ConceptUI>
    <ConceptName>
     <String>deaminotri-O-isopropylidene tunicamine</String>
    </ConceptName>
    <RegistryNumber>142010-67-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T235334</TermUI>
      <String>deaminotri-O-isopropylidene tunicamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T235332</TermUI>
      <String>5-C-(6-deoxy-1,2-3,4-di-O-isopropylidene-D-galactopyranos-6-yl)-2,3-O-isopropylidene-D-pentofuranose</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T235333</TermUI>
      <String>DAI-tunicamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013076</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>isoxazolin-5-one</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>8</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007555</DescriptorUI>
     <DescriptorName>
      <String>Isoxazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Int Physiol Biochim 84(1):169;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060548</ConceptUI>
    <ConceptName>
     <String>isoxazolin-5-one</String>
    </ConceptName>
    <CASN1Name>5(2H)-Isoxazolone</CASN1Name>
    <RegistryNumber>43228-53-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090551</TermUI>
      <String>isoxazolin-5-one</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C416764</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-(1-(2-(1-(cyclopropylmethyl)-3-(3,4-dichlorophenyl)-6-oxo-3-piperidyl)ethyl)azetidin-3-yl)-1-piperazine sulfamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>12</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>02</Month>
   <Day>24</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001384</DescriptorUI>
     <DescriptorName>
      <String>Azetidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010879</DescriptorUI>
     <DescriptorName>
      <String>Piperazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D018041</DescriptorUI>
     <DescriptorName>
      <String>Receptors, Neurokinin-2</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
     <QualifierName>
      <String>antagonists &amp; inhibitors</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Xenobiotica 2000 Jun;30(6):627-42</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0374454</ConceptUI>
    <ConceptName>
     <String>4-(1-(2-(1-(cyclopropylmethyl)-3-(3,4-dichlorophenyl)-6-oxo-3-piperidyl)ethyl)azetidin-3-yl)-1-piperazine sulfamide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0374454</Concept1UI>
     <Concept2UI>M0374456</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0374454</Concept1UI>
     <Concept2UI>M0374455</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T430811</TermUI>
      <String>4-(1-(2-(1-(cyclopropylmethyl)-3-(3,4-dichlorophenyl)-6-oxo-3-piperidyl)ethyl)azetidin-3-yl)-1-piperazine sulfamide</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>12</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T528809</TermUI>
      <String>4-(1-(2-(1-(cyclopropylmethyl)-3-(3,4-dichlorophenyl)-6-oxopiperidinyl)ethyl)-3-azetidinyl)-1-piperazinesulfonamide</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>12</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0374456</ConceptUI>
    <ConceptName>
     <String>UK 224671</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0374454</Concept1UI>
     <Concept2UI>M0374456</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T430813</TermUI>
      <String>UK 224671</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>12</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T528807</TermUI>
      <String>UK-224671</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>12</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T528808</TermUI>
      <String>UK224671</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>12</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0374455</ConceptUI>
    <ConceptName>
     <String>(S)-(+)-4-(1-(2-(1-(cyclopropylmethyl)-3-(3,4-dichlorophenyl)-6-oxo-3-piperidyl)ethyl)azetidin-3-yl)-1-piperazine sulfamide</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0374454</Concept1UI>
     <Concept2UI>M0374455</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T430812</TermUI>
      <String>(S)-(+)-4-(1-(2-(1-(cyclopropylmethyl)-3-(3,4-dichlorophenyl)-6-oxo-3-piperidyl)ethyl)azetidin-3-yl)-1-piperazine sulfamide</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>12</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C471326</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-piperazinyl carbamoyl tetrahydropapaverine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>02</Month>
   <Day>24</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007546</DescriptorUI>
     <DescriptorName>
      <String>Isoquinolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Pharm Bull (Tokyo) 2002 Sep;50(9):1223-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0445957</ConceptUI>
    <ConceptName>
     <String>N-piperazinyl carbamoyl tetrahydropapaverine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T533378</TermUI>
      <String>N-piperazinyl carbamoyl tetrahydropapaverine</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>02</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T533379</TermUI>
      <String>N-PCTHP</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>02</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013090</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ligatin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>06</Month>
   <Day>30</Day>
  </DateRevised>
  <Frequency>28</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>GLYCOPROTEINS (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008565</DescriptorUI>
     <DescriptorName>
      <String>Membrane Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Membranes and Diseases W3 IN169J:263;1975m</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060582</ConceptUI>
    <ConceptName>
     <String>ligatin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090585</TermUI>
      <String>ligatin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013094</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>lymphocyte effector molecules</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1989</Year>
   <Month>08</Month>
   <Day>02</Day>
  </DateRevised>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008233</DescriptorUI>
     <DescriptorName>
      <String>Lymphotoxin-alpha</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cell Immunol 24(2):277;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060590</ConceptUI>
    <ConceptName>
     <String>lymphocyte effector molecules</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090593</TermUI>
      <String>lymphocyte effector molecules</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C513071</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Apba1 protein, rat</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>09</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>09</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>RefSeq NM_031779
  </Note>
  <Frequency>28</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008565</DescriptorUI>
     <DescriptorName>
      <String>Membrane Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D048868</DescriptorUI>
     <DescriptorName>
      <String>Adaptor Proteins, Signal Transducing</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0284502</ConceptUI>
    <ConceptName>
     <String>Apba1 protein, rat</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T601987</TermUI>
      <String>Apba1 protein, rat</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>05</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T601988</TermUI>
      <String>Mint1 protein, rat</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>05</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T601989</TermUI>
      <String>X11alpha protein, rat</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>05</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T601990</TermUI>
      <String>amyloid beta (A4) precursor protein-binding, family A, member 1 protein, rat</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>05</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C469681</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-(1-(2-(4-(2-(3,5-bis(trifluoromethyl)phenyl)acetyl)-2-(3,4-dichlorophenyl)-2-morpholinyl)ethyl)-4-piperidinyl)-2-methylpropanamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>12</Month>
   <Day>20</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>02</Month>
   <Day>24</Day>
  </DateRevised>
  <Note>SSR-240600 is the (R)-isomer; structure in first source
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009025</DescriptorUI>
     <DescriptorName>
      <String>Morpholines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010880</DescriptorUI>
     <DescriptorName>
      <String>Piperidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharmacol Exp Ther 2002 Dec;303(3):1171-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0443921</ConceptUI>
    <ConceptName>
     <String>2-(1-(2-(4-(2-(3,5-bis(trifluoromethyl)phenyl)acetyl)-2-(3,4-dichlorophenyl)-2-morpholinyl)ethyl)-4-piperidinyl)-2-methylpropanamide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0443921</Concept1UI>
     <Concept2UI>M0443922</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T528973</TermUI>
      <String>2-(1-(2-(4-(2-(3,5-bis(trifluoromethyl)phenyl)acetyl)-2-(3,4-dichlorophenyl)-2-morpholinyl)ethyl)-4-piperidinyl)-2-methylpropanamide</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>12</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0443922</ConceptUI>
    <ConceptName>
     <String>SSR 240600</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0443921</Concept1UI>
     <Concept2UI>M0443922</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T528974</TermUI>
      <String>SSR 240600</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>12</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T528976</TermUI>
      <String>SSR240600</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>12</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T528975</TermUI>
      <String>SSR-240600</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>12</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C414127</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SB 253514</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>10</Month>
   <Day>10</Day>
  </DateCreated>
  <Note>inhibitor of lipoprotein-associated phospholipase A2; structure in first source
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011714</DescriptorUI>
     <DescriptorName>
      <String>Pyrans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D019086</DescriptorUI>
     <DescriptorName>
      <String>Bridged Bicyclo Compounds, Heterocyclic</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiot (Tokyo) 2000 Jul;53(7):664-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0370915</ConceptUI>
    <ConceptName>
     <String>SB 253514</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T426197</TermUI>
      <String>SB 253514</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>10</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C471328</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>acetyltetrahydropapaverine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>02</Month>
   <Day>24</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007546</DescriptorUI>
     <DescriptorName>
      <String>Isoquinolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Pharm Bull (Tokyo) 2002 Sep;50(9):1223-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0445959</ConceptUI>
    <ConceptName>
     <String>acetyltetrahydropapaverine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T533383</TermUI>
      <String>acetyltetrahydropapaverine</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>02</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T533384</TermUI>
      <String>ATHP cpd</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>02</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013113</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-methoxy-7-oxaestra-1,3,5(10),8-tetraen-17(e)-ol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>09</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>STEROIDS, HETEROCYCLIC (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004963</DescriptorUI>
     <DescriptorName>
      <String>Estrenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Steroids 28(2):197;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060630</ConceptUI>
    <ConceptName>
     <String>3-methoxy-7-oxaestra-1,3,5(10),8-tetraen-17(e)-ol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090633</TermUI>
      <String>3-methoxy-7-oxaestra-1,3,5(10),8-tetraen-17(e)-ol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013115</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>9-methyladenine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>53</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000225</DescriptorUI>
     <DescriptorName>
      <String>Adenine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Proc Natl Acad Sci USA 73(9):2966;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060633</ConceptUI>
    <ConceptName>
     <String>9-methyladenine</String>
    </ConceptName>
    <RegistryNumber>700-00-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090636</TermUI>
      <String>9-methyladenine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013117</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-methyl-7-amino-cis-decahydroisoquinoline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007546</DescriptorUI>
     <DescriptorName>
      <String>Isoquinolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Yakugaku Zasshi 96(2):180;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060635</ConceptUI>
    <ConceptName>
     <String>2-methyl-7-amino-cis-decahydroisoquinoline</String>
    </ConceptName>
    <CASN1Name>7-Isoquinolinamine, decahydro-2-methyl-, (4aalpha,7alpha,8aalpha)-</CASN1Name>
    <RegistryNumber>59320-70-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090638</TermUI>
      <String>2-methyl-7-amino-cis-decahydroisoquinoline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000318</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-bromopyrazole</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1970</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>BROMINE (72-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011720</DescriptorUI>
     <DescriptorName>
      <String>Pyrazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040414</ConceptUI>
    <ConceptName>
     <String>4-bromopyrazole</String>
    </ConceptName>
    <RegistryNumber>2075-45-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070416</TermUI>
      <String>4-bromopyrazole</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C551953</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-(4-(4-chloro-1-methyl-1H-pyrazole-3-carbonyl)piperazin-1-yl)-1-(4-fluorophenyl)ethanone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2010</Year>
   <Month>09</Month>
   <Day>07</Day>
  </DateCreated>
  <Note>a 5-HT2A receptor antagonist and anti-insomnia agent; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010879</DescriptorUI>
     <DescriptorName>
      <String>Piperazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011720</DescriptorUI>
     <DescriptorName>
      <String>Pyrazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D044402</DescriptorUI>
     <DescriptorName>
      <String>Receptor, Serotonin, 5-HT2A</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Med Chem 2010 Aug 12;53(15):5696-706</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0549671</ConceptUI>
    <ConceptName>
     <String>2-(4-(4-chloro-1-methyl-1H-pyrazole-3-carbonyl)piperazin-1-yl)-1-(4-fluorophenyl)ethanone</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T776913</TermUI>
      <String>2-(4-(4-chloro-1-methyl-1H-pyrazole-3-carbonyl)piperazin-1-yl)-1-(4-fluorophenyl)ethanone</String>
      <DateCreated>
       <Year>2010</Year>
       <Month>09</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2010)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T776914</TermUI>
      <String>2-CMPCP-FP-ethanone</String>
      <DateCreated>
       <Year>2010</Year>
       <Month>09</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2010)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C038153</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>CMESA-sepharose</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1983</Year>
   <Month>06</Month>
   <Day>21</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>17</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SEPHAROSE/analogs (83-83)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D012685</DescriptorUI>
     <DescriptorName>
      <String>Sepharose</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 1983;22(10):2537</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0114988</ConceptUI>
    <ConceptName>
     <String>CMESA-sepharose</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T144991</TermUI>
      <String>CMESA-sepharose</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T144992</TermUI>
      <String>O-carboxymethylagarose ethylenediamine-succinyl-17 beta-O-4,6-androstadien-3-one</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C038613</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>citrullinase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>17</Day>
  </DateRevised>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000581</DescriptorUI>
     <DescriptorName>
      <String>Amidohydrolases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>MGG 1983;190(2):278</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0116135</ConceptUI>
    <ConceptName>
     <String>citrullinase</String>
    </ConceptName>
    <RegistryNumber>EC 3.5.1.20</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T146139</TermUI>
      <String>citrullinase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T146138</TermUI>
      <String>citrulline hydrolase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000334</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>butanediol divinylether</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>07</Month>
   <Day>11</Day>
  </DateRevised>
  <Note>VINYL ETHER (72-85) is no longer an active MH
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BUTANEDIOLS (75-81)</PreviousIndexing>
   <PreviousIndexing>*GLYCOLS (72-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002072</DescriptorUI>
     <DescriptorName>
      <String>Butylene Glycols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004987</DescriptorUI>
     <DescriptorName>
      <String>Ethers</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Europ J Biochem 25(1):129;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040429</ConceptUI>
    <ConceptName>
     <String>butanediol divinylether</String>
    </ConceptName>
    <RegistryNumber>3891-33-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070431</TermUI>
      <String>butanediol divinylether</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C432870</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>palicoside</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>17</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000470</DescriptorUI>
     <DescriptorName>
      <String>Alkaloids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009005</DescriptorUI>
     <DescriptorName>
      <String>Monosaccharides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Phytochemistry 2001 Jul;57(5):653-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0395793</ConceptUI>
    <ConceptName>
     <String>palicoside</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T457785</TermUI>
      <String>palicoside</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>08</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000357</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cannabivarin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CANNABIS (71-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002186</DescriptorUI>
     <DescriptorName>
      <String>Cannabinoids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nature 232(5312):579;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040456</ConceptUI>
    <ConceptName>
     <String>cannabivarin</String>
    </ConceptName>
    <RegistryNumber>33745-21-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070458</TermUI>
      <String>cannabivarin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C418762</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>9,12-dioxo-10-dodecenoic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>08</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005229</DescriptorUI>
     <DescriptorName>
      <String>Fatty Acids, Monounsaturated</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Lipids 2000 Sep;35(9):953-60</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0377130</ConceptUI>
    <ConceptName>
     <String>9,12-dioxo-10-dodecenoic acid</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0377130</Concept1UI>
     <Concept2UI>M0488653</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0377130</Concept1UI>
     <Concept2UI>M0488652</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T434047</TermUI>
      <String>9,12-dioxo-10-dodecenoic acid</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>01</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T434048</TermUI>
      <String>9,12-DD acid</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>01</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0488653</ConceptUI>
    <ConceptName>
     <String>9,12-dioxo-10(E)-dodecenoic acid</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0377130</Concept1UI>
     <Concept2UI>M0488653</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T650010</TermUI>
      <String>9,12-dioxo-10(E)-dodecenoic acid</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>08</Month>
       <Day>31</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0488652</ConceptUI>
    <ConceptName>
     <String>9,12-dioxo-10(Z)-dodecenoic acid</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0377130</Concept1UI>
     <Concept2UI>M0488652</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T650009</TermUI>
      <String>9,12-dioxo-10(Z)-dodecenoic acid</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>08</Month>
       <Day>31</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000364</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Captostibone (g)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1987</Year>
   <Month>03</Month>
   <Day>18</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>SULFIDES (71-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009942</DescriptorUI>
     <DescriptorName>
      <String>Organometallic Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D000965</DescriptorUI>
     <DescriptorName>
      <String>Antimony</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040463</ConceptUI>
    <ConceptName>
     <String>Captostibone (g)</String>
    </ConceptName>
    <CASN1Name>sodium 2-(carboxymethylmercapto)benzene stibonate</CASN1Name>
    <RegistryNumber>36524-24-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070465</TermUI>
      <String>Captostibone (g)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C432871</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dolichantoside</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>17</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000470</DescriptorUI>
     <DescriptorName>
      <String>Alkaloids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009005</DescriptorUI>
     <DescriptorName>
      <String>Monosaccharides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Phytochemistry 2001 Jul;57(5):653-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0395795</ConceptUI>
    <ConceptName>
     <String>dolichantoside</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T457787</TermUI>
      <String>dolichantoside</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>08</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000390</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>carnitylcholine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CARNITINE (72-75)</PreviousIndexing>
   <PreviousIndexing>*CHOLINE (72-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002331</DescriptorUI>
     <DescriptorName>
      <String>Carnitine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002794</DescriptorUI>
     <DescriptorName>
      <String>Choline</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Pharmacol 20(12):3385;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040488</ConceptUI>
    <ConceptName>
     <String>carnitylcholine</String>
    </ConceptName>
    <RegistryNumber>34566-86-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070490</TermUI>
      <String>carnitylcholine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000402</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>chinophene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CARBOXYLIC ACIDS (72-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011804</DescriptorUI>
     <DescriptorName>
      <String>Quinolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040497</ConceptUI>
    <ConceptName>
     <String>chinophene</String>
    </ConceptName>
    <RegistryNumber>11139-62-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070499</TermUI>
      <String>chinophene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C511820</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-methylimidazol-4-yl-methylideneamino-2-ethylpyridine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>07</Month>
   <Day>18</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007093</DescriptorUI>
     <DescriptorName>
      <String>Imidazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011725</DescriptorUI>
     <DescriptorName>
      <String>Pyridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Inorg Chem. 2005 Dec 12;44(25):9288-92</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0499951</ConceptUI>
    <ConceptName>
     <String>2-methylimidazol-4-yl-methylideneamino-2-ethylpyridine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T678063</TermUI>
      <String>2-methylimidazol-4-yl-methylideneamino-2-ethylpyridine</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>07</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T678064</TermUI>
      <String>HLMe cpd</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>07</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C024125</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>feto-specific proteins</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateRevised>
  <Note>proteins that find principal quantitative expression in prenatal state
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005326</DescriptorUI>
     <DescriptorName>
      <String>Fetal Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Soc Trans 7(6):1179;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0082080</ConceptUI>
    <ConceptName>
     <String>feto-specific proteins</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T112083</TermUI>
      <String>feto-specific proteins</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T112082</TermUI>
      <String>foeto-specific proteins</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006815</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>551-D-1</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>piperidineacetyl deriv of dihydrobenzoxazole cpd
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*OXAZINES (75-80)</PreviousIndexing>
   <PreviousIndexing>PIPERIDINES (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010080</DescriptorUI>
     <DescriptorName>
      <String>Oxazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arzneim Forsch 24(12):2053;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049590</ConceptUI>
    <ConceptName>
     <String>551-D-1</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079593</TermUI>
      <String>551-D-1</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C497399</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SMAD1 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>11</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>RefSeq NM_005900
  </Note>
  <Frequency>320</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D051898</DescriptorUI>
     <DescriptorName>
      <String>Smad1 Protein</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0261787</ConceptUI>
    <ConceptName>
     <String>SMAD1 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T611218</TermUI>
      <String>SMAD1 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T611216</TermUI>
      <String>MAD, mothers against decapentaplegic homolog 1 (Drosophila) protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T611217</TermUI>
      <String>TGF-beta signaling protein-1, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T424348</TermUI>
      <String>MADH1 protein, human</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>09</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T611219</TermUI>
      <String>MADR1 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T424347</TermUI>
      <String>MAD homolog 1, human</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>09</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T611220</TermUI>
      <String>MAD-related 1 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006818</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>alpha-bromohydrin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>07</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>BROMINE (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011409</DescriptorUI>
     <DescriptorName>
      <String>Propylene Glycols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Res 36(9):3369;1976</Source>
   <Source>J Reprod Fert 38(2):379;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049594</ConceptUI>
    <ConceptName>
     <String>alpha-bromohydrin</String>
    </ConceptName>
    <RegistryNumber>4704-77-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079597</TermUI>
      <String>alpha-bromohydrin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C497782</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SMAD2 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>11</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>RefSeq NM_005901
  </Note>
  <Frequency>1583</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D051899</DescriptorUI>
     <DescriptorName>
      <String>Smad2 Protein</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0482099</ConceptUI>
    <ConceptName>
     <String>SMAD2 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T633655</TermUI>
      <String>SMAD2 protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T633656</TermUI>
      <String>SMAD, mothers against DPP homolog 2 (Drosophila) protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T633657</TermUI>
      <String>MADH2 protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T633658</TermUI>
      <String>MADR2 protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T633660</TermUI>
      <String>JV18-1 protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T633659</TermUI>
      <String>MAD-related 2 protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C497790</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SMAD3 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>11</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>RefSeq NM_005902
  </Note>
  <Frequency>1825</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D051900</DescriptorUI>
     <DescriptorName>
      <String>Smad3 Protein</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0265157</ConceptUI>
    <ConceptName>
     <String>SMAD3 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T633672</TermUI>
      <String>SMAD3 protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T633674</TermUI>
      <String>MADH3 protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T633673</TermUI>
      <String>SMAD, mothers against DPP homolog 3 (Drosophila) protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000605031</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>STP1 protein, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2016</Year>
   <Month>02</Month>
   <Day>18</Day>
  </DateCreated>
  <DateRevised>
   <Year>2016</Year>
   <Month>02</Month>
   <Day>18</Day>
  </DateRevised>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009004</DescriptorUI>
     <DescriptorName>
      <String>Monosaccharide Transport Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>EMBO J. 1990 Oct;9(10):3045-50.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M000614779</ConceptUI>
    <ConceptName>
     <String>STP1 protein, Arabidopsis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T000895542</TermUI>
      <String>STP1 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2016</Year>
       <Month>02</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2016)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T000895544</TermUI>
      <String>SUGAR TRANSPORTER PROTEIN 1, Arabidopsis</String>
      <DateCreated>
       <Year>2016</Year>
       <Month>02</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2016)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T000895545</TermUI>
      <String>At1g11260 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2016</Year>
       <Month>02</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2016)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T000895543</TermUI>
      <String>AtSTP1 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2016</Year>
       <Month>02</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2016)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C087033</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>thioxoalanylproline 4-nitroanilide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>05</Month>
   <Day>30</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000813</DescriptorUI>
     <DescriptorName>
      <String>Anilides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004151</DescriptorUI>
     <DescriptorName>
      <String>Dipeptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Biochem 1994 Apr 1;221(1):455-61</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0230599</ConceptUI>
    <ConceptName>
     <String>thioxoalanylproline 4-nitroanilide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T260604</TermUI>
      <String>thioxoalanylproline 4-nitroanilide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T260602</TermUI>
      <String>Ala-psi(CS-N)-Pro-NH-Np</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T260603</TermUI>
      <String>thioxoalanyl-proline 4-nitroanilide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C497796</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SMAD4 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>11</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>RefSeq NM_005359
  </Note>
  <Frequency>1490</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D051901</DescriptorUI>
     <DescriptorName>
      <String>Smad4 Protein</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0256839</ConceptUI>
    <ConceptName>
     <String>SMAD4 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T611016</TermUI>
      <String>SMAD4 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T611018</TermUI>
      <String>MADH4 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T611017</TermUI>
      <String>SMAD, mothers against DPP homolog 4 (Drosophila) protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T611019</TermUI>
      <String>DPC4 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006835</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bufarenogin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>12</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>HYDROXSTERIODS (74-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002018</DescriptorUI>
     <DescriptorName>
      <String>Bufanolides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Helv Chim Acta 56(1):2827;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049626</ConceptUI>
    <ConceptName>
     <String>bufarenogin</String>
    </ConceptName>
    <RegistryNumber>17008-65-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079629</TermUI>
      <String>bufarenogin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006849</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>alpha-((tert-butylamino)methyl)-3,4-dihydroxybenzyl alcohol-3,4-di(4-toluate)methanesulfonate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>11</Month>
   <Day>06</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>TOSYL COMPOUNDS (75-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000605</DescriptorUI>
     <DescriptorName>
      <String>Amino Alcohols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Int Arch Allergy 47(5):633;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049651</ConceptUI>
    <ConceptName>
     <String>alpha-((tert-butylamino)methyl)-3,4-dihydroxybenzyl alcohol-3,4-di(4-toluate)methanesulfonate</String>
    </ConceptName>
    <CASN1Name>Benzoic acid, 4-methyl-, 4-(2-((1,1-dimethylethyl)amino)-1-((methylsulfonyl)oxy)ethyl)-1,2-phenylene ester</CASN1Name>
    <RegistryNumber>76741-89-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079654</TermUI>
      <String>alpha-((tert-butylamino)methyl)-3,4-dihydroxybenzyl alcohol-3,4-di(4-toluate)methanesulfonate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T079653</TermUI>
      <String>alpha-((tert-butylamino)methyl)-3,4-dihydroxybenzyl alcohol-3,4-di(p-toluate)methanesulfonate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C094891</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>prothoracicostatic hormone, Neobellieria bullata</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>08</Month>
   <Day>31</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>02</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>a folliculostatin isolated from the gray fleshfly Neobellieria bullata
  </Note>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007301</DescriptorUI>
     <DescriptorName>
      <String>Insect Hormones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009842</DescriptorUI>
     <DescriptorName>
      <String>Oligopeptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Insect Biochem Mol Biol 1995 Jun;25(6):661-7</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0249940</ConceptUI>
    <ConceptName>
     <String>prothoracicostatic hormone, Neobellieria bullata</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T279945</TermUI>
      <String>prothoracicostatic hormone, Neobellieria bullata</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T279942</TermUI>
      <String>Neb-PTSH protein, Sarcophaga bullata</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T279943</TermUI>
      <String>Neb-TMOF protein, Sarcophaga bullata</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T279944</TermUI>
      <String>asparagyl-prolyl-threonyl-asparaginyl-leucyl-histidine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C090597</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>succinic acid mono-3-amino-2,4,6-triiodo-N-ethylanilide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>12</Month>
   <Day>26</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000813</DescriptorUI>
     <DescriptorName>
      <String>Anilides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013386</DescriptorUI>
     <DescriptorName>
      <String>Succinates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D007462</DescriptorUI>
     <DescriptorName>
      <String>Iodobenzenes</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Invest Radiol 1994 Jul;29(7):689-94</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0239376</ConceptUI>
    <ConceptName>
     <String>succinic acid mono-3-amino-2,4,6-triiodo-N-ethylanilide</String>
    </ConceptName>
    <RegistryNumber>1634-73-7</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>2666-11-7 (Na salt)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0239376</Concept1UI>
     <Concept2UI>M0326779</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T269381</TermUI>
      <String>succinic acid mono-3-amino-2,4,6-triiodo-N-ethylanilide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T269380</TermUI>
      <String>MATEA-succinic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0326779</ConceptUI>
    <ConceptName>
     <String>succinic acid mono-3-amino-2,4,6-triiodo-N-ethylanilide, sodium salt</String>
    </ConceptName>
    <RegistryNumber>2666-11-7</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0239376</Concept1UI>
     <Concept2UI>M0326779</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T356779</TermUI>
      <String>succinic acid mono-3-amino-2,4,6-triiodo-N-ethylanilide, sodium salt</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C497797</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SMAD5 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>11</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>RefSeq NM_005903
  </Note>
  <Frequency>175</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D051902</DescriptorUI>
     <DescriptorName>
      <String>Smad5 Protein</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0482116</ConceptUI>
    <ConceptName>
     <String>SMAD5 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T633730</TermUI>
      <String>SMAD5 protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T633732</TermUI>
      <String>MADH5 protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T633731</TermUI>
      <String>SMAD, mothers against DPP homolog 5 (Drosophila) protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T633742</TermUI>
      <String>Dwf-C protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C497802</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SMAD6 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>11</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>RefSeq NM_005585
  </Note>
  <Frequency>124</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D051905</DescriptorUI>
     <DescriptorName>
      <String>Smad6 Protein</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0482125</ConceptUI>
    <ConceptName>
     <String>SMAD6 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T633750</TermUI>
      <String>SMAD6 protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T633751</TermUI>
      <String>SMAD, mothers against DPP homolog 6 (Drosophila) protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C497806</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SMAD7 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>11</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>RefSeq NM_005904
  </Note>
  <Frequency>604</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D051906</DescriptorUI>
     <DescriptorName>
      <String>Smad7 Protein</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0482128</ConceptUI>
    <ConceptName>
     <String>SMAD7 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T633760</TermUI>
      <String>SMAD7 protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T633761</TermUI>
      <String>SMAD, mothers against DPP homolog 7 (Drosophila) protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C092092</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>alanyl-phenylalanyl-psi(CS-N)-prolyl-phenylalanyl-4-nitroanilide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>03</Month>
   <Day>17</Day>
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  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>01</Day>
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  <Note>amino acid sequence in first source
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  <Frequency>1</Frequency>
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    <DescriptorReferredTo>
     <DescriptorUI>*D000813</DescriptorUI>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009842</DescriptorUI>
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  <SourceList>
   <Source>Electrophoresis 1994 Aug-Sep;15(8-9):1151-7</Source>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T273150</TermUI>
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   <String>coronarin E</String>
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  <DateCreated>
   <Year>2004</Year>
   <Month>03</Month>
   <Day>22</Day>
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  <Note>structure in first source
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    <DescriptorReferredTo>
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      <String>Diterpenes</String>
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  <SourceList>
   <Source>J Nat Prod 2003 Dec;66(12):1623-7</Source>
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      <TermUI>T578288</TermUI>
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      <DateCreated>
       <Year>2004</Year>
       <Month>03</Month>
       <Day>22</Day>
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      <ThesaurusIDlist>
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   <Concept PreferredConceptYN="N">
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    <ConceptName>
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     <Concept2UI>M0462752</Concept2UI>
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      <TermUI>T578289</TermUI>
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      <DateCreated>
       <Year>2004</Year>
       <Month>03</Month>
       <Day>22</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
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  <SupplementalRecordUI>C006851</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-n-butylbarbital</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
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  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001463</DescriptorUI>
     <DescriptorName>
      <String>Barbiturates</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharmacol Exp Therap 190(2):384;1974</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049652</ConceptUI>
    <ConceptName>
     <String>N-n-butylbarbital</String>
    </ConceptName>
    <CASN1Name>1-n-butyl-5,5-diethylbarbituric acid</CASN1Name>
    <RegistryNumber>15517-26-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079655</TermUI>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
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   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C093089</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>glycylproline 3,5-dibromo-4-hydroxyanilide</String>
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  <DateCreated>
   <Year>1995</Year>
   <Month>05</Month>
   <Day>17</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure given in first source
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000813</DescriptorUI>
     <DescriptorName>
      <String>Anilides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004151</DescriptorUI>
     <DescriptorName>
      <String>Dipeptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
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  </HeadingMappedToList>
  <SourceList>
   <Source>J Clin Lab Anal 1995;9(2):113-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0245548</ConceptUI>
    <ConceptName>
     <String>glycylproline 3,5-dibromo-4-hydroxyanilide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T275553</TermUI>
      <String>glycylproline 3,5-dibromo-4-hydroxyanilide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T275552</TermUI>
      <String>glycyl-L-proline 3,5-dibromo-4-hydroxyanilide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T275551</TermUI>
      <String>Gly-Pro-DBAP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006856</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>butyletharine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>1994</Year>
   <Month>06</Month>
   <Day>15</Day>
  </DateRevised>
  <Note>N-t-butyl analog of isoetharine; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AMINO ALCOHOLS (74-75)</PreviousIndexing>
   <PreviousIndexing>CATECHOL (74-75)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007528</DescriptorUI>
     <DescriptorName>
      <String>Isoetharine</String>
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    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
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    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Int Pharmacod 205(1):144;1973</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049660</ConceptUI>
    <ConceptName>
     <String>butyletharine</String>
    </ConceptName>
    <CASN1Name>1-(3,4-dihydroxyphenyl)-2-tert-butyl-1-butanol.HCl</CASN1Name>
    <RegistryNumber>51264-24-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079663</TermUI>
      <String>butyletharine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
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 </SupplementalRecord>
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  <SupplementalRecordUI>C419307</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>n-(3-chloro-2-hydroxypropyl)trimethylammonium</String>
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  <DateCreated>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>01</Day>
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  <Frequency>3</Frequency>
  <HeadingMappedToList>
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    <DescriptorReferredTo>
     <DescriptorUI>*D000644</DescriptorUI>
     <DescriptorName>
      <String>Quaternary Ammonium Compounds</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Appl Biochem Biotechnol. 2000 Jun;87(3):233-45</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0377675</ConceptUI>
    <ConceptName>
     <String>n-(3-chloro-2-hydroxypropyl)trimethylammonium</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T434877</TermUI>
      <String>n-(3-chloro-2-hydroxypropyl)trimethylammonium</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>02</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T434879</TermUI>
      <String>n-(3-chloro-2-hydroxypropyl)-trimethylammonium chloride</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>02</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T434878</TermUI>
      <String>Cl-HPTMA</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>02</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006861</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>butyl(2-oxopropyl)nitrosamine</String>
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  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
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     <DescriptorName>
      <String>Nitrosamines</String>
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  <SourceList>
   <Source>Gann 65(1):13;1974</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049667</ConceptUI>
    <ConceptName>
     <String>butyl(2-oxopropyl)nitrosamine</String>
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    <RegistryNumber>51938-15-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079670</TermUI>
      <String>butyl(2-oxopropyl)nitrosamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C100669</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>UC 82</String>
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  <DateCreated>
   <Year>1996</Year>
   <Month>08</Month>
   <Day>30</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>a thiocarboxanilide pentenyloxy ether derivative; structure given in first source
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000813</DescriptorUI>
     <DescriptorName>
      <String>Anilides</String>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013876</DescriptorUI>
     <DescriptorName>
      <String>Thiophenes</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Pharmacol 1996 Aug;50(2):394-401</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0264152</ConceptUI>
    <ConceptName>
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    <RegistryNumber>0</RegistryNumber>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
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    <ConceptUI>M0264150</ConceptUI>
    <ConceptName>
     <String>2-chloro-5-(((2-methyl-3-thienyl)carbonothioyl)amino)phenyl 3-methyl-2-butenyl ether</String>
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    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0264152</Concept1UI>
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      <TermUI>T294155</TermUI>
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       <ThesaurusID>NLM (1996)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
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  <SupplementalRecordName>
   <String>MON 0856</String>
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  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>01</Day>
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  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>MALONATES (72-76)</PreviousIndexing>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000814</DescriptorUI>
     <DescriptorName>
      <String>Aniline Compounds</String>
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  <SourceList>
   <Source>J Econ Entomol 165(1):48;1972</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041201</ConceptUI>
    <ConceptName>
     <String>MON 0856</String>
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    <CASN1Name>propanedinitrile, (((3,5-bis(trifluoromethyl)phenyl)ethylamino)methylene)-</CASN1Name>
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    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0041201</Concept1UI>
     <Concept2UI>M0041199</Concept2UI>
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      <TermUI>T071204</TermUI>
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       <ThesaurusID>NLM (1972)</ThesaurusID>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T071203</TermUI>
      <String>MON-0856</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
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   <Concept PreferredConceptYN="N">
    <ConceptUI>M0041199</ConceptUI>
    <ConceptName>
     <String>(3,5-di(alpha,alpha,alpha-trifluoromethyl)-N-ethylanilino)methylenemalononitrile</String>
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    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
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      <TermUI>T071202</TermUI>
      <String>(3,5-di(alpha,alpha,alpha-trifluoromethyl)-N-ethylanilino)methylenemalononitrile</String>
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       <ThesaurusID>NLM (1972)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
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  <SupplementalRecordName>
   <String>camphidine</String>
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  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>01</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>structure
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  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>AZA COMPOUNDS (75-81)</PreviousIndexing>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001892</DescriptorUI>
     <DescriptorName>
      <String>Camphanes</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>Farmaco(Sci) 29(1):37;1974</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049697</ConceptUI>
    <ConceptName>
     <String>camphidine</String>
    </ConceptName>
    <CASN1Name>1,8,8-trimethyl-3-azabicyclo(3.2.1)octane</CASN1Name>
    <RegistryNumber>465-49-6</RegistryNumber>
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      <TermUI>T079700</TermUI>
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       <ThesaurusID>NLM (1975)</ThesaurusID>
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  <DateCreated>
   <Year>1994</Year>
   <Month>03</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>2001</Year>
   <Month>07</Month>
   <Day>20</Day>
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    <DescriptorReferredTo>
     <DescriptorUI>D011341</DescriptorUI>
     <DescriptorName>
      <String>Probucol</String>
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    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013141</DescriptorUI>
     <DescriptorName>
      <String>Spiro Compounds</String>
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  <SourceList>
   <Source>Eur J Pharmacol 1993 Oct 1;248(3):263-72</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0227045</ConceptUI>
    <ConceptName>
     <String>S 12340</String>
    </ConceptName>
    <CASN1Name>1-Oxa-3,8-diazaspiro(4.5)decan-2-one, 8-(3-((3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl)thio)propyl)-</CASN1Name>
    <RegistryNumber>144754-35-8</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0227045</Concept1UI>
     <Concept2UI>M0227041</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T257050</TermUI>
      <String>S 12340</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T257049</TermUI>
      <String>S12340</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T257048</TermUI>
      <String>S-12340</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
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    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0227041</ConceptUI>
    <ConceptName>
     <String>8-(3-(3,5-di-tert-butyl-4-hydroxyphenylthio)propyl)-1-oxa-2-oxo-3,8-diazaspiro(4.5)decane</String>
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    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0227045</Concept1UI>
     <Concept2UI>M0227041</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T257046</TermUI>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T257047</TermUI>
      <String>8-(3-(3,5-diterbutyl-4-hydroxyphenylthio)propyl)-1-oxa-2-oxo-3,8-diazaspiro(4.5)decane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012173</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-amino-N-acetyl-N-methylaniline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000814</DescriptorUI>
     <DescriptorName>
      <String>Aniline Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Res 36(5):1568;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059054</ConceptUI>
    <ConceptName>
     <String>4-amino-N-acetyl-N-methylaniline</String>
    </ConceptName>
    <RegistryNumber>119-63-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089057</TermUI>
      <String>4-amino-N-acetyl-N-methylaniline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T089056</TermUI>
      <String>para-amino-N-acetyl-N-methylaniline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T089055</TermUI>
      <String>p-amino-N-acetyl-N-methylaniline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006890</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>caracurine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>24</Day>
  </DateRevised>
  <Note>calabash curarine; structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003472</DescriptorUI>
     <DescriptorName>
      <String>Curare</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Biol Interactions 6(6):355;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049709</ConceptUI>
    <ConceptName>
     <String>caracurine</String>
    </ConceptName>
    <RegistryNumber>466-85-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079712</TermUI>
      <String>caracurine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C419308</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cetearyl alcohol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>14</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005233</DescriptorUI>
     <DescriptorName>
      <String>Fatty Alcohols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D017449</DescriptorUI>
     <DescriptorName>
      <String>Dermatitis, Allergic Contact</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Contact Dermatitis. 2000 Sep;43(3):174-5</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0377676</ConceptUI>
    <ConceptName>
     <String>cetearyl alcohol</String>
    </ConceptName>
    <RegistryNumber>67762-27-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T434880</TermUI>
      <String>cetearyl alcohol</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>02</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T434882</TermUI>
      <String>1-octadecanol, mixed with 1-hexadecanol</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>02</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T434881</TermUI>
      <String>cetyl-stearyl alcohol</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>02</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006911</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>S-carboxymethyl-thiopyruvate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>17</Day>
  </DateRevised>
  <Note>oxidative deamination product of S-carboxymethylcysteine; structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>SULFIDES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003998</DescriptorUI>
     <DescriptorName>
      <String>Dicarboxylic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Cell Biochem 3(1):3;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049754</ConceptUI>
    <ConceptName>
     <String>S-carboxymethyl-thiopyruvate</String>
    </ConceptName>
    <CASN1Name>Propanoic acid, 3-((carboxymethyl)thio)-2-oxo-</CASN1Name>
    <RegistryNumber>51783-05-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079757</TermUI>
      <String>S-carboxymethyl-thiopyruvate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C482833</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>isoschizandrin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>03</Month>
   <Day>22</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011083</DescriptorUI>
     <DescriptorName>
      <String>Polycyclic Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D034242</DescriptorUI>
     <DescriptorName>
      <String>Cyclooctanes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem. 2003 Dec 12;68(25):9533-40</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0462755</ConceptUI>
    <ConceptName>
     <String>isoschizandrin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T578292</TermUI>
      <String>isoschizandrin</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>03</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006915</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Cardioplegin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>pharmacoplegic agent for producing cardiac standstill in open-heart surgery; contains procaine, magnesium L-asparaginate &amp; sorbitol
  </Note>
  <Frequency>9</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ASPARAGINE (74-79)</PreviousIndexing>
   <PreviousIndexing>*MAGNESIUM (74-78)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D001224</DescriptorUI>
     <DescriptorName>
      <String>Aspartic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011343</DescriptorUI>
     <DescriptorName>
      <String>Procaine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013012</DescriptorUI>
     <DescriptorName>
      <String>Sorbitol</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D002314</DescriptorUI>
     <DescriptorName>
      <String>Cardioplegic Solutions</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Cardiovasc Surg 19(2):193;1978</Source>
   <Source>Kard Pol 16(4):299;1973</Source>
   <Source>Khirurgiia(Sofia) 1979;32(4):290</Source>
   <Source>Langenbecks Arch Chir suppl 1979;p.29</Source>
   <Source>Langenbecks Arch Chir:99;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049761</ConceptUI>
    <ConceptName>
     <String>Cardioplegin</String>
    </ConceptName>
    <CASN1Name>Magnesate(2-), bis(L-aspartato(2-)-N,O1)-, (T-4)-, dihydrogen, mixt. with 2-(diethylamino)ethyl 4-aminobenzoate monohydrochloride</CASN1Name>
    <RegistryNumber>68245-15-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079764</TermUI>
      <String>Cardioplegin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006918</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>carococculine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>06</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>alkaloid from Cocculus carolinus (sinomenine type); structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*MORPHINANS (75-81)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000470</DescriptorUI>
     <DescriptorName>
      <String>Alkaloids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 37(3):488;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049762</ConceptUI>
    <ConceptName>
     <String>carococculine</String>
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    <RegistryNumber>54302-44-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079765</TermUI>
      <String>carococculine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006920</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>caroxin F</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>fluorocarbon liquid
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*HYDROCARBONS, FLUORINATED (74-76)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005466</DescriptorUI>
     <DescriptorName>
      <String>Fluorocarbons</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Anesthesiol 40(6):566;1974</Source>
   <Source>J Appl Physiol 39(4):603;1975</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049767</ConceptUI>
    <ConceptName>
     <String>caroxin F</String>
    </ConceptName>
    <CASN1Name>perfluoro-1-isopropoxy-hexane</CASN1Name>
    <RegistryNumber>37340-18-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079770</TermUI>
      <String>caroxin F</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C482834</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1beta,3beta-dihydroxyurs-12-en-27-oic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>03</Month>
   <Day>22</Day>
  </DateCreated>
  <Note>from Caiophora coronata; structure in first source
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014315</DescriptorUI>
     <DescriptorName>
      <String>Triterpenes</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2003 Dec;66(12):1628-31</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0462758</ConceptUI>
    <ConceptName>
     <String>1beta,3beta-dihydroxyurs-12-en-27-oic acid</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T578300</TermUI>
      <String>1beta,3beta-dihydroxyurs-12-en-27-oic acid</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>03</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C091408</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>MDL 73975</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>02</Month>
   <Day>06</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>07</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>a 5-HT(1A) receptor agonist
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013141</DescriptorUI>
     <DescriptorName>
      <String>Spiro Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Pharmacol 1994 Sep 12;262(3):205-15</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0241385</ConceptUI>
    <ConceptName>
     <String>MDL 73975</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0241385</Concept1UI>
     <Concept2UI>M0241381</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T271390</TermUI>
      <String>MDL 73975</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T271388</TermUI>
      <String>MDL-73,975</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T271389</TermUI>
      <String>MDL-73975</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T271387</TermUI>
      <String>MDL 73,975</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0241381</ConceptUI>
    <ConceptName>
     <String>8-(2-(2,3-dihydro-8-methoxy-1,4-benzodoxin-2-yl)methylamino)ethyl-8-azaspiro(4,5)decane-7,9-dione hydrochloride</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0241385</Concept1UI>
     <Concept2UI>M0241381</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T271386</TermUI>
      <String>8-(2-(2,3-dihydro-8-methoxy-1,4-benzodoxin-2-yl)methylamino)ethyl-8-azaspiro(4,5)decane-7,9-dione hydrochloride</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010477</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>kosotoxin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>toxins from Hagenia abyssinica
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>BUTYROPHENONES (75-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010696</DescriptorUI>
     <DescriptorName>
      <String>Phloroglucinol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D014118</DescriptorUI>
     <DescriptorName>
      <String>Toxins, Biological</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Acta Chem Scand (B) 28(10):1200-09;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055998</ConceptUI>
    <ConceptName>
     <String>kosotoxin</String>
    </ConceptName>
    <CASN1Name>Kosotoxin</CASN1Name>
    <RegistryNumber>1400-16-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086001</TermUI>
      <String>kosotoxin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010478</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>lacto-N-fucoheptaose</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>01</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>heptasaccharide isolated from human milk; contains galactose, fucose, &amp; N-acetylglucosamine in 3:1:1:2 ratio
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009844</DescriptorUI>
     <DescriptorName>
      <String>Oligosaccharides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>FEBS Lett 54(2):221;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055999</ConceptUI>
    <ConceptName>
     <String>lacto-N-fucoheptaose</String>
    </ConceptName>
    <RegistryNumber>56501-25-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086002</TermUI>
      <String>lacto-N-fucoheptaose</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C499867</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>protein S Heerlen</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>04</Month>
   <Day>25</Day>
  </DateCreated>
  <Note>has Ser460Pro mutation which does not affect its APC-cofactor and APC-independent anticoagulant activities
  </Note>
  <Frequency>7</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D017293</DescriptorUI>
     <DescriptorName>
      <String>Protein S</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Thromb Haemost 2004 Jun;91(6):1105-14</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0483732</ConceptUI>
    <ConceptName>
     <String>protein S Heerlen</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T637645</TermUI>
      <String>protein S Heerlen</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>04</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010486</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>16 beta-methyl-16 alpha,17 alpha-epoxyprogesterone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>12</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>EPOXY COMPOUNDS (75-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011374</DescriptorUI>
     <DescriptorName>
      <String>Progesterone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Pharmazie 30(1):22;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056013</ConceptUI>
    <ConceptName>
     <String>16 beta-methyl-16 alpha,17 alpha-epoxyprogesterone</String>
    </ConceptName>
    <RegistryNumber>34182-56-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086016</TermUI>
      <String>16 beta-methyl-16 alpha,17 alpha-epoxyprogesterone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010490</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>neotizol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1994</Year>
   <Month>11</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>consists of neomycin sulfate, ethyl cellulose, castor oil, absolute alcohol, freons
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002368</DescriptorUI>
     <DescriptorName>
      <String>Castor Oil</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002482</DescriptorUI>
     <DescriptorName>
      <String>Cellulose</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005617</DescriptorUI>
     <DescriptorName>
      <String>Chlorofluorocarbons, Methane</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009355</DescriptorUI>
     <DescriptorName>
      <String>Neomycin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Klin Khir 3:55;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056017</ConceptUI>
    <ConceptName>
     <String>neotizol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086020</TermUI>
      <String>neotizol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010493</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-nitro-9-aminoacridine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Frequency>4</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ACRIDINES (75-80)</PreviousIndexing>
   <PreviousIndexing>*AMINOACRIDINES (80-81)</PreviousIndexing>
   <PreviousIndexing>AMINES (75-80)</PreviousIndexing>
   <PreviousIndexing>NITRO COMPOUNDS (75-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000585</DescriptorUI>
     <DescriptorName>
      <String>Aminacrine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Biochim Pol 22(2):119;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056020</ConceptUI>
    <ConceptName>
     <String>1-nitro-9-aminoacridine</String>
    </ConceptName>
    <RegistryNumber>21914-54-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086023</TermUI>
      <String>1-nitro-9-aminoacridine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010501</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-(3-phenyl-5-(1,2,3,4-oxatriazolio))phenylamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014230</DescriptorUI>
     <DescriptorName>
      <String>Triazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Chem Scand 29(1):45;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056034</ConceptUI>
    <ConceptName>
     <String>N-(3-phenyl-5-(1,2,3,4-oxatriazolio))phenylamide</String>
    </ConceptName>
    <CASN1Name>1,2,3,4-Oxatriazolium, 3-phenyl-5-(phenylamino)-, hydroxide, inner salt</CASN1Name>
    <RegistryNumber>55717-75-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086037</TermUI>
      <String>N-(3-phenyl-5-(1,2,3,4-oxatriazolio))phenylamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010524</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>vitamin Q</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>11</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>prevents hemorrhagic state
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*VITAMINS (1975-2005)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009930</DescriptorUI>
     <DescriptorName>
      <String>Organic Chemicals</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D014815</DescriptorUI>
     <DescriptorName>
      <String>Vitamins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Life Sci 16(7):1017;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056067</ConceptUI>
    <ConceptName>
     <String>vitamin Q</String>
    </ConceptName>
    <RegistryNumber>55127-92-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086070</TermUI>
      <String>vitamin Q</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C029873</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tris-boric-polyol buffer</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>06</Month>
   <Day>16</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001888</DescriptorUI>
     <DescriptorName>
      <String>Boric Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011108</DescriptorUI>
     <DescriptorName>
      <String>Polymers</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014325</DescriptorUI>
     <DescriptorName>
      <String>Tromethamine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D002021</DescriptorUI>
     <DescriptorName>
      <String>Buffers</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Lab Delo 1981;(4):232</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0094967</ConceptUI>
    <ConceptName>
     <String>tris-boric-polyol buffer</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T124970</TermUI>
      <String>tris-boric-polyol buffer</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T124969</TermUI>
      <String>tris-boric acid-polyol buffer</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013052</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>16 alpha-hydroxypregnenolone 7-(O-carboxymethyl)oxime</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>OXIMES (77-78)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D006907</DescriptorUI>
     <DescriptorName>
      <String>17-alpha-Hydroxypregnenolone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Steroid Biochem 7(9):697;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060498</ConceptUI>
    <ConceptName>
     <String>16 alpha-hydroxypregnenolone 7-(O-carboxymethyl)oxime</String>
    </ConceptName>
    <CASN1Name>Acetic acid, ((((3beta,16alpha)-3,16-dihydroxy-20-oxopregn-5-en-7-ylidene)amino)oxy)-</CASN1Name>
    <RegistryNumber>61192-54-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090501</TermUI>
      <String>16 alpha-hydroxypregnenolone 7-(O-carboxymethyl)oxime</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T090500</TermUI>
      <String>3 beta,16 alpha-dihydroxy-5-pregnene-7,20-dione 7- (O-carboxymethyl)oxime</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010519</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>thiohydroximic acid ester</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>10</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*MERCAPTOETHYLAMINES (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010091</DescriptorUI>
     <DescriptorName>
      <String>Oximes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biokhimiia 39(6):1163;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056060</ConceptUI>
    <ConceptName>
     <String>thiohydroximic acid ester</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086063</TermUI>
      <String>thiohydroximic acid ester</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010520</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>threosaminitol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>10</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AMINO SUGARS (75-82)</PreviousIndexing>
   <PreviousIndexing>*THREOSE/analogs (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013780</DescriptorUI>
     <DescriptorName>
      <String>Tetroses</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>FEBS Lett 54(2):135;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056061</ConceptUI>
    <ConceptName>
     <String>threosaminitol</String>
    </ConceptName>
    <CASN1Name>1,2,4-Butanetriol, 3-amino-, (R-(R*,S*))-</CASN1Name>
    <RegistryNumber>62397-88-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086064</TermUI>
      <String>threosaminitol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C087080</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tumor-associated protein kinase p40</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>06</Month>
   <Day>03</Day>
  </DateCreated>
  <DateRevised>
   <Year>2007</Year>
   <Month>09</Month>
   <Day>14</Day>
  </DateRevised>
  <Note>preferentially phosphorylates seryl residues in protein substrates; highly active in squamous cell carcinomas and adenocarcinomas of the lung; MW 40 kDa
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D017346</DescriptorUI>
     <DescriptorName>
      <String>Protein-Serine-Threonine Kinases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D009363</DescriptorUI>
     <DescriptorName>
      <String>Neoplasm Proteins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Cancer Res 1994 Apr 15;54(8):2262-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0230715</ConceptUI>
    <ConceptName>
     <String>tumor-associated protein kinase p40</String>
    </ConceptName>
    <RegistryNumber>EC 2.7.1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T260720</TermUI>
      <String>tumor-associated protein kinase p40</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T260719</TermUI>
      <String>p40(TAK)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C033000</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Trikolpon</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1982</Year>
   <Month>01</Month>
   <Day>06</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>contains boric acid, sulfanilamide &amp; carbarson
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D001147</DescriptorUI>
     <DescriptorName>
      <String>Arsanilic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001888</DescriptorUI>
     <DescriptorName>
      <String>Boric Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013424</DescriptorUI>
     <DescriptorName>
      <String>Sulfanilamides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ned Tijdschr Geneeskd 1981;125(42):1718</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0102590</ConceptUI>
    <ConceptName>
     <String>Trikolpon</String>
    </ConceptName>
    <CASN1Name>Arsonic acid, (4-((aminocarbonyl)amino)phenyl)-, mixt. with 4-aminobenzenesulfonamide and boric acid (H3BO3)</CASN1Name>
    <RegistryNumber>81219-14-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="TRD"  RecordPreferredTermYN="Y">
      <TermUI>T132594</TermUI>
      <String>Trikolpon</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010533</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>8-aminoadenosine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>15</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000241</DescriptorUI>
     <DescriptorName>
      <String>Adenosine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Mol Biol 94(1):1;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056091</ConceptUI>
    <ConceptName>
     <String>8-aminoadenosine</String>
    </ConceptName>
    <RegistryNumber>3868-33-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086094</TermUI>
      <String>8-aminoadenosine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010539</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-(9-anthroyl)palmitic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1996</Year>
   <Month>03</Month>
   <Day>12</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ANTHRACENES (75-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010169</DescriptorUI>
     <DescriptorName>
      <String>Palmitic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem J 146(2):473;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056099</ConceptUI>
    <ConceptName>
     <String>2-(9-anthroyl)palmitic acid</String>
    </ConceptName>
    <CASN1Name>9-Anthracenepropanoic acid, beta-oxo-alpha-tetradecyl-</CASN1Name>
    <RegistryNumber>62498-77-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086102</TermUI>
      <String>2-(9-anthroyl)palmitic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010541</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>7-azaaminopterin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>AZA COMPOUNDS (75-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000630</DescriptorUI>
     <DescriptorName>
      <String>Aminopterin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 40(15):2205;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056101</ConceptUI>
    <ConceptName>
     <String>7-azaaminopterin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086104</TermUI>
      <String>7-azaaminopterin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010547</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-(bis(2-chloroethyl)amino)-1,3-phenylene biscarbamate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>potentially cytotoxic cpd; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CARBAMATES (75-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009588</DescriptorUI>
     <DescriptorName>
      <String>Nitrogen Mustard Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 40(11):1556;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056113</ConceptUI>
    <ConceptName>
     <String>5-(bis(2-chloroethyl)amino)-1,3-phenylene biscarbamate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086116</TermUI>
      <String>5-(bis(2-chloroethyl)amino)-1,3-phenylene biscarbamate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010553</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-(2-chloro-2-deoxy-D-arabinofuranosyl)cytosine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003561</DescriptorUI>
     <DescriptorName>
      <String>Cytarabine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Carbohydrate Res 39(2):227;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056118</ConceptUI>
    <ConceptName>
     <String>1-(2-chloro-2-deoxy-D-arabinofuranosyl)cytosine</String>
    </ConceptName>
    <RegistryNumber>58461-30-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086121</TermUI>
      <String>1-(2-chloro-2-deoxy-D-arabinofuranosyl)cytosine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010562</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>crofilcon A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>06</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>METHYLMETHACRYLATE/*analogs (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008768</DescriptorUI>
     <DescriptorName>
      <String>Methylmethacrylates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Am J Ophthalmol 80(1):139;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056132</ConceptUI>
    <ConceptName>
     <String>crofilcon A</String>
    </ConceptName>
    <CASN1Name>2-Propenoic acid, 2-methyl-, 2,3-dihydroxypropyl ester, polymer with methyl 2-methyl-2-propenoate</CASN1Name>
    <RegistryNumber>50450-03-8</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0056132</Concept1UI>
     <Concept2UI>M0056131</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086135</TermUI>
      <String>crofilcon A</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0056131</ConceptUI>
    <ConceptName>
     <String>CS 151</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0056132</Concept1UI>
     <Concept2UI>M0056131</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T086134</TermUI>
      <String>CS 151</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010558</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cocytotaxin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>02</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CHEMOTAXIS (75-80)</PreviousIndexing>
   <PreviousIndexing>*PEPTIDES (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002630</DescriptorUI>
     <DescriptorName>
      <String>Chemotactic Factors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Antibiotics Chemother 19:443;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056126</ConceptUI>
    <ConceptName>
     <String>cocytotaxin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086129</TermUI>
      <String>cocytotaxin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010560</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>copper tetraphenylporphyrin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>02</Day>
  </DateRevised>
  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PORPHYRINS (75-82)</PreviousIndexing>
   <PreviousIndexing>COPPER (79-82)</PreviousIndexing>
   <PreviousIndexing>ORGANOMETALLIC COMPOUNDS (75-79)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008665</DescriptorUI>
     <DescriptorName>
      <String>Metalloporphyrins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Proc Nat Acad Sci 72(6):2340;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056129</ConceptUI>
    <ConceptName>
     <String>copper tetraphenylporphyrin</String>
    </ConceptName>
    <RegistryNumber>14172-91-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086132</TermUI>
      <String>copper tetraphenylporphyrin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013064</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-iodoacetamidomethyl-2'-deoxyuridine 5'-phosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>selective inhibitor of thymidylate synthetase
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*URACIL NUCLEOTIDES (76-78)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007460</DescriptorUI>
     <DescriptorName>
      <String>Iodoacetamide</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013942</DescriptorUI>
     <DescriptorName>
      <String>Thymine Nucleotides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 473:73;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060527</ConceptUI>
    <ConceptName>
     <String>5-iodoacetamidomethyl-2'-deoxyuridine 5'-phosphate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090530</TermUI>
      <String>5-iodoacetamidomethyl-2'-deoxyuridine 5'-phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T090529</TermUI>
      <String>IA-DUMP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C087170</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,3,4,5,6-pentafluorobenzyl alcohol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>06</Month>
   <Day>07</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>08</Day>
  </DateRevised>
  <Frequency>9</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001592</DescriptorUI>
     <DescriptorName>
      <String>Benzyl Alcohols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 1994 May 3;33(17):5230-7</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0230926</ConceptUI>
    <ConceptName>
     <String>2,3,4,5,6-pentafluorobenzyl alcohol</String>
    </ConceptName>
    <RegistryNumber>440-60-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T260931</TermUI>
      <String>2,3,4,5,6-pentafluorobenzyl alcohol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T260930</TermUI>
      <String>pentafluorobenzyl alcohol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T260929</TermUI>
      <String>5FBzOH</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C522862</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>NT020 formula</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>09</Month>
   <Day>20</Day>
  </DateCreated>
  <Note>a proprietary dietary supplement formula of blueberry, green tea, carnosine and vitamin D3
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  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002336</DescriptorUI>
     <DescriptorName>
      <String>Carnosine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002762</DescriptorUI>
     <DescriptorName>
      <String>Cholecalciferol</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010936</DescriptorUI>
     <DescriptorName>
      <String>Plant Extracts</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Rejuvenation Res 2007 Jun;10(2):173-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0513601</ConceptUI>
    <ConceptName>
     <String>NT020 formula</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T706027</TermUI>
      <String>NT020 formula</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>09</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010566</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cyclo-sarcosyl-sarcosine-epitetrasulfide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>13</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D012521</DescriptorUI>
     <DescriptorName>
      <String>Sarcosine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D009183</DescriptorUI>
     <DescriptorName>
      <String>Mycotoxins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Arzneim Forsch 25(3):397;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056140</ConceptUI>
    <ConceptName>
     <String>cyclo-sarcosyl-sarcosine-epitetrasulfide</String>
    </ConceptName>
    <RegistryNumber>31964-23-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086143</TermUI>
      <String>cyclo-sarcosyl-sarcosine-epitetrasulfide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010568</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-deazaguanosine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1985</Year>
   <Month>09</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>21</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D006151</DescriptorUI>
     <DescriptorName>
      <String>Guanosine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Antimicrob Ag Chemother 12(1):114;1977</Source>
   <Source>J Am Chem Soc 97(10):2916;1975</Source>
   <Source>J Am Chem Soc 98(6):1492;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056144</ConceptUI>
    <ConceptName>
     <String>3-deazaguanosine</String>
    </ConceptName>
    <CASN1Name>6-amino-beta-D-ribofuranosylimidazo(4,5-c)pyridin- 4(5H)-one</CASN1Name>
    <RegistryNumber>56039-11-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0056144</Concept1UI>
     <Concept2UI>M0056143</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0056144</Concept1UI>
     <Concept2UI>M0056142</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086147</TermUI>
      <String>3-deazaguanosine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0056143</ConceptUI>
    <ConceptName>
     <String>7-ribosyl-3-deazaguanine</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0056144</Concept1UI>
     <Concept2UI>M0056143</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T086146</TermUI>
      <String>7-ribosyl-3-deazaguanine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0056142</ConceptUI>
    <ConceptName>
     <String>7-(beta-D-ribofuranosyl-3-deazaguanine)</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0056144</Concept1UI>
     <Concept2UI>M0056142</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T086145</TermUI>
      <String>7-(beta-D-ribofuranosyl-3-deazaguanine)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010569</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-deazaguanylic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1993</Year>
   <Month>05</Month>
   <Day>26</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*GUANYLIC ACIDS (75-78)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D006157</DescriptorUI>
     <DescriptorName>
      <String>Guanosine Monophosphate</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Antimicrob Ag Chemother 12(1):114;1977</Source>
   <Source>J Am Chem Soc 97(10):2916;1975</Source>
   <Source>J Am Chem Soc 98(6):1492;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056145</ConceptUI>
    <ConceptName>
     <String>3-deazaguanylic acid</String>
    </ConceptName>
    <CASN1Name>3-deazaguanosine-5'-phosphate</CASN1Name>
    <RegistryNumber>56039-13-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086148</TermUI>
      <String>3-deazaguanylic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C522863</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>LY980503</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>09</Month>
   <Day>20</Day>
  </DateCreated>
  <Note>a benflumetol derivative, structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004983</DescriptorUI>
     <DescriptorName>
      <String>Ethanolamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005449</DescriptorUI>
     <DescriptorName>
      <String>Fluorenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>World J Gastroenterol 2007 Apr 21;13(15):2234-7</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0513602</ConceptUI>
    <ConceptName>
     <String>LY980503</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T706028</TermUI>
      <String>LY980503</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>09</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010575</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>disulphane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013424</DescriptorUI>
     <DescriptorName>
      <String>Sulfanilamides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Oftalmolog ZH 30(4):309;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056157</ConceptUI>
    <ConceptName>
     <String>disulphane</String>
    </ConceptName>
    <CASN1Name>Benzenesulfonamide, 4-amino-N-(4-(aminosulfonyl)phenyl)-</CASN1Name>
    <RegistryNumber>547-52-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086160</TermUI>
      <String>disulphane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010578</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,N(6)-etheno-2-azaadenosine 2',3'-monophosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1993</Year>
   <Month>09</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>structure
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  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>AZA COMPOUNDS (76-82)</PreviousIndexing>
   <PreviousIndexing>IMIDAZOLES (75-76)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000242</DescriptorUI>
     <DescriptorName>
      <String>Cyclic AMP</String>
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    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Neurochem 25(2):181;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056158</ConceptUI>
    <ConceptName>
     <String>1,N(6)-etheno-2-azaadenosine 2',3'-monophosphate</String>
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    <CASN1Name>3H-Diimidazo(1,2-c 4',5'-e)(1,2,3)triazine, 3-(2,3-O-phosphinico-beta-D-ribofuranosyl)-</CASN1Name>
    <RegistryNumber>56875-63-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086161</TermUI>
      <String>1,N(6)-etheno-2-azaadenosine 2',3'-monophosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
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     </Term>
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  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C444900</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>zampanolide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>01</Month>
   <Day>24</Day>
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  <Note>structure in first source
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  <Frequency>29</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D018942</DescriptorUI>
     <DescriptorName>
      <String>Macrolides</String>
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  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D013237</DescriptorUI>
     <DescriptorName>
      <String>Stereoisomerism</String>
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     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Am Chem Soc 2001 Dec 12;123(49):12426-7</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0412190</ConceptUI>
    <ConceptName>
     <String>zampanolide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T479243</TermUI>
      <String>zampanolide</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>01</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T479244</TermUI>
      <String>(+)-zampanolide</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>01</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C514899</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>PREP protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>11</Month>
   <Day>19</Day>
  </DateCreated>
  <DateRevised>
   <Year>2007</Year>
   <Month>06</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>RefSeq NM_002726
  </Note>
  <Frequency>22</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012697</DescriptorUI>
     <DescriptorName>
      <String>Serine Endopeptidases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D024101</DescriptorUI>
     <DescriptorName>
      <String>Mitochondrial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 2006 Sep 29;281(39):29096-104</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0504040</ConceptUI>
    <ConceptName>
     <String>PREP protein, human</String>
    </ConceptName>
    <RegistryNumber>EC 2.4.21.25</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T686330</TermUI>
      <String>PREP protein, human</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>11</Month>
       <Day>19</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T695692</TermUI>
      <String>prolyl endopeptidase, human</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>04</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T686331</TermUI>
      <String>PreP peptidasome, human</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>11</Month>
       <Day>19</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C032222</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3,N(4)-ethenodeoxycytidine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>11</Month>
   <Day>27</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>13</Day>
  </DateRevised>
  <Frequency>46</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003841</DescriptorUI>
     <DescriptorName>
      <String>Deoxycytidine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Biol Interact 1981;37(1-2):219</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0100691</ConceptUI>
    <ConceptName>
     <String>3,N(4)-ethenodeoxycytidine</String>
    </ConceptName>
    <CASN1Name>Imidazo(1,2-c)pyrimidin-5(6H)-one, 6-(2-deoxy-beta-D-erythro-pentofuranosyl)-</CASN1Name>
    <RegistryNumber>68498-26-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T130695</TermUI>
      <String>3,N(4)-ethenodeoxycytidine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T130694</TermUI>
      <String>3,N(4)-etheno-2'-deoxycytidine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C064068</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Thomsen-Friedenreich antigen, cryptic</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1990</Year>
   <Month>06</Month>
   <Day>12</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>07</Month>
   <Day>26</Day>
  </DateRevised>
  <Note>detected in rat fetuses with amaranthin
  </Note>
  <Frequency>18</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014312</DescriptorUI>
     <DescriptorName>
      <String>Trisaccharides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D007519</DescriptorUI>
     <DescriptorName>
      <String>Isoantigens</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Histochem Cytochem 1990;38(6):763</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0176642</ConceptUI>
    <ConceptName>
     <String>Thomsen-Friedenreich antigen, cryptic</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T206647</TermUI>
      <String>Thomsen-Friedenreich antigen, cryptic</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T206645</TermUI>
      <String>NeuAc(alpha)(2-3)-Gal(beta)(1-3)-GalNac(alpha)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T206643</TermUI>
      <String>CTF-antigen</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T206646</TermUI>
      <String>cryptic Thomsen-Friedenreich antigen</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T206644</TermUI>
      <String>N-acetylneuraminyl-(2-3)-beta-galactosyl (1-3)-N-acetylgalactosamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007867</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>glycerol-1,3-diphosphonic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DIPHOSPHOGLYCERIC ACIDS (76-79)</PreviousIndexing>
   <PreviousIndexing>*GLYCERIN (74-76)</PreviousIndexing>
   <PreviousIndexing>*ORGANOPHOSPHORUS CPDS (74-76)</PreviousIndexing>
   <PreviousIndexing>PHOSPHONIC ACIDS (74-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005994</DescriptorUI>
     <DescriptorName>
      <String>Glycerophosphates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Can J Biochem 51(8):1203;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051313</ConceptUI>
    <ConceptName>
     <String>glycerol-1,3-diphosphonic acid</String>
    </ConceptName>
    <CASN1Name>1,2,3-propanetriol 1,3-bis(dihydrogen phosphate)</CASN1Name>
    <RegistryNumber>2075-06-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081316</TermUI>
      <String>glycerol-1,3-diphosphonic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C518487</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>HY2 protein, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>03</Month>
   <Day>31</Day>
  </DateCreated>
  <DateRevised>
   <Year>2007</Year>
   <Month>06</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>GenBank AB045112
  </Note>
  <Frequency>7</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010088</DescriptorUI>
     <DescriptorName>
      <String>Oxidoreductases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Plant Cell 2001 Feb;13(2):425-36</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0508306</ConceptUI>
    <ConceptName>
     <String>HY2 protein, Arabidopsis</String>
    </ConceptName>
    <RegistryNumber>EC 1.3.7.4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T694723</TermUI>
      <String>HY2 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>03</Month>
       <Day>31</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T694724</TermUI>
      <String>phytochromobilin synthase, Arabidopsis</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>03</Month>
       <Day>31</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C083788</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>S-(4-bromophenyl)cysteine sulfoxide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1993</Year>
   <Month>11</Month>
   <Day>19</Day>
  </DateCreated>
  <DateRevised>
   <Year>2007</Year>
   <Month>06</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003545</DescriptorUI>
     <DescriptorName>
      <String>Cysteine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013454</DescriptorUI>
     <DescriptorName>
      <String>Sulfoxides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Pharmacol 1993 Oct 5;46(7):1113-7</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0222818</ConceptUI>
    <ConceptName>
     <String>S-(4-bromophenyl)cysteine sulfoxide</String>
    </ConceptName>
    <RegistryNumber>152406-99-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0222818</Concept1UI>
     <Concept2UI>M0222816</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T252823</TermUI>
      <String>S-(4-bromophenyl)cysteine sulfoxide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T252822</TermUI>
      <String>S-BPCS</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0222816</ConceptUI>
    <ConceptName>
     <String>S-(p-bromophenyl)-L-cysteine sulfoxide</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0222818</Concept1UI>
     <Concept2UI>M0222816</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T252821</TermUI>
      <String>S-(p-bromophenyl)-L-cysteine sulfoxide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C531288</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SE5-OH</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2008</Year>
   <Month>09</Month>
   <Day>11</Day>
  </DateCreated>
  <Note>an equol-rich product produced by Lactococcus garvieae; toxic in rats
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007529</DescriptorUI>
     <DescriptorName>
      <String>Isoflavones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Food Chem Toxicol 2008 Aug;46(8):2713-20</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0524680</ConceptUI>
    <ConceptName>
     <String>SE5-OH</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T725523</TermUI>
      <String>SE5-OH</String>
      <DateCreated>
       <Year>2008</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2008)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C531289</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Lodyne P208E</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2008</Year>
   <Month>09</Month>
   <Day>11</Day>
  </DateCreated>
  <Note>less toxic than diacetyl and did not induce a mutagenic response
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006845</DescriptorUI>
     <DescriptorName>
      <String>Hydrocarbons, Fluorinated</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Food Chem Toxicol 2008 Aug;46(8):2928-33</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0524682</ConceptUI>
    <ConceptName>
     <String>Lodyne P208E</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="TRD"  RecordPreferredTermYN="Y">
      <TermUI>T725526</TermUI>
      <String>Lodyne P208E</String>
      <DateCreated>
       <Year>2008</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2008)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011500</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>oxytocin, 1 beta-mercapto-beta, beta-diethylpropionic acid-(3,5-dibromo-Tyr)(2)-</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>23</Day>
  </DateRevised>
  <Note>inhibitor of oxytocin
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>TYROSINE/analogs (76-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010121</DescriptorUI>
     <DescriptorName>
      <String>Oxytocin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 18(12):1262;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057843</ConceptUI>
    <ConceptName>
     <String>oxytocin, 1 beta-mercapto-beta, beta-diethylpropionic acid-(3,5-dibromo-Tyr)(2)-</String>
    </ConceptName>
    <CASN1Name>Oxytocin, 1-(3-ethyl-3-mercaptopentanoic acid)-2-(3,5-dibromo-L-tyrosine)-</CASN1Name>
    <RegistryNumber>57292-38-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087846</TermUI>
      <String>oxytocin, 1 beta-mercapto-beta, beta-diethylpropionic acid-(3,5-dibromo-Tyr)(2)-</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T087845</TermUI>
      <String>oxytocin, 1 beta-mercapto-beta, beta-diethylpropionic acid-(3,5-dibromotyrosine)(2)-</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T087844</TermUI>
      <String>1 beta-mercapto-beta, beta-diethylpropionic acid-2-(3,5-dibromo-Tyr)-oxytocin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011412</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bronchodilat</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>10</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>combination of pragman and polycaine
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010627</DescriptorUI>
     <DescriptorName>
      <String>Phenethylamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011437</DescriptorUI>
     <DescriptorName>
      <String>Propylamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Gruzlica 43(11):995;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057707</ConceptUI>
    <ConceptName>
     <String>bronchodilat</String>
    </ConceptName>
    <CASN1Name>Benzenepropanamine, N,N,4-trimethyl-gamma-phenyl-, hydrochloride, mixt. with N,N-dimethyl-beta-phenylbenzeneethanamine hydrochloride</CASN1Name>
    <RegistryNumber>76986-90-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087710</TermUI>
      <String>bronchodilat</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011422</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cimigol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014315</DescriptorUI>
     <DescriptorName>
      <String>Triterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Soc Jap 95(10):1133;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057725</ConceptUI>
    <ConceptName>
     <String>cimigol</String>
    </ConceptName>
    <RegistryNumber>57943-48-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087728</TermUI>
      <String>cimigol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011424</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>crassin acetate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>principle antineoplastic agent in four gorgonians (marine invertebrates) of Pseudoplexaura genus; structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004224</DescriptorUI>
     <DescriptorName>
      <String>Diterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 38(5):378;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057730</ConceptUI>
    <ConceptName>
     <String>crassin acetate</String>
    </ConceptName>
    <RegistryNumber>28028-68-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087733</TermUI>
      <String>crassin acetate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011427</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cyclohexylammonium-3,6-pyridazinediolate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>has effect on cardiovascular system; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CYCLOHEXYLAMINES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011724</DescriptorUI>
     <DescriptorName>
      <String>Pyridazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Formosan Med Assoc 74(7):20;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057731</ConceptUI>
    <ConceptName>
     <String>cyclohexylammonium-3,6-pyridazinediolate</String>
    </ConceptName>
    <RegistryNumber>58380-90-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087734</TermUI>
      <String>cyclohexylammonium-3,6-pyridazinediolate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011432</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-decynedioic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>03</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>DICARBOXYLIC ACIDS (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005231</DescriptorUI>
     <DescriptorName>
      <String>Fatty Acids, Unsaturated</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Clin Chem 21(13):1964;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057738</ConceptUI>
    <ConceptName>
     <String>5-decynedioic acid</String>
    </ConceptName>
    <RegistryNumber>3646-44-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087741</TermUI>
      <String>5-decynedioic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011435</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6-deoxy-gulose</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003837</DescriptorUI>
     <DescriptorName>
      <String>Deoxy Sugars</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Carbohydrate Res 44(1):116;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057740</ConceptUI>
    <ConceptName>
     <String>6-deoxy-gulose</String>
    </ConceptName>
    <RegistryNumber>5158-61-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087743</TermUI>
      <String>6-deoxy-gulose</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011438</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4',4'-diacetamido stilbene-2,2'-disulfonic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>disulfonic acid which produces a reversible inhibition of sulfate equilibrium exchange in human red blood cells; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BENZENESULFONATES (76-82)</PreviousIndexing>
   <PreviousIndexing>*STILBENES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D012856</DescriptorUI>
     <DescriptorName>
      <String>4-Acetamido-4'-isothiocyanatostilbene-2,2'-disulfonic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>FEBS Lett 62(2):182;1976</Source>
   <Source>J Cell Physiol 86(3):471;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057745</ConceptUI>
    <ConceptName>
     <String>4',4'-diacetamido stilbene-2,2'-disulfonic acid</String>
    </ConceptName>
    <RegistryNumber>5968-56-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087748</TermUI>
      <String>4',4'-diacetamido stilbene-2,2'-disulfonic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011439</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,2-diacylglycerol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>726</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004075</DescriptorUI>
     <DescriptorName>
      <String>Diglycerides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nature 258(5533):348;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057746</ConceptUI>
    <ConceptName>
     <String>1,2-diacylglycerol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087749</TermUI>
      <String>1,2-diacylglycerol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C076692</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Baypamun HK</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1992</Year>
   <Month>10</Month>
   <Day>14</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>tradename; each ml (1 dose) HK contains inactivated parapox virus ovis with &gt;4.4 million TCID50 (tissue culture infectious dose 50%); used in dogs &amp; cats for immunization against parapox
  </Note>
  <Frequency>19</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014765</DescriptorUI>
     <DescriptorName>
      <String>Viral Vaccines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Berl Munch Tierarztl Wochenschr 1992 Aug 1;105(8):253-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0206175</ConceptUI>
    <ConceptName>
     <String>Baypamun HK</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="TRD"  RecordPreferredTermYN="Y">
      <TermUI>T236180</TermUI>
      <String>Baypamun HK</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="TRD"  RecordPreferredTermYN="N">
      <TermUI>T236179</TermUI>
      <String>Baypamun</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011448</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>10,11-dihydro-10,11-dihydroxyprotriptyline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011530</DescriptorUI>
     <DescriptorName>
      <String>Protriptyline</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Farmaco(Sci)30(11):904;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057762</ConceptUI>
    <ConceptName>
     <String>10,11-dihydro-10,11-dihydroxyprotriptyline</String>
    </ConceptName>
    <RegistryNumber>29785-65-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087765</TermUI>
      <String>10,11-dihydro-10,11-dihydroxyprotriptyline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011449</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3,4-dimethoxybenzylidenaminoacetal</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1986</Year>
   <Month>01</Month>
   <Day>06</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001597</DescriptorUI>
     <DescriptorName>
      <String>Benzylidene Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Soc Jpn 95(9):1038;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057763</ConceptUI>
    <ConceptName>
     <String>3,4-dimethoxybenzylidenaminoacetal</String>
    </ConceptName>
    <CASN1Name>Ethanamine, N-((3,4-dimethoxyphenyl)methylene)-2,2-diethoxy-</CASN1Name>
    <RegistryNumber>58163-19-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087766</TermUI>
      <String>3,4-dimethoxybenzylidenaminoacetal</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011456</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4,4-dimethylcholesta-1,5-dien-3-one</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002774</DescriptorUI>
     <DescriptorName>
      <String>Cholestadienes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 40(25):3786;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057773</ConceptUI>
    <ConceptName>
     <String>4,4-dimethylcholesta-1,5-dien-3-one</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087776</TermUI>
      <String>4,4-dimethylcholesta-1,5-dien-3-one</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C119888</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>transportin SR</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1999</Year>
   <Month>07</Month>
   <Day>08</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>09</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>import receptor for arginine/serine-rich proteins; amino acid sequence in first source; GenBank AF145029
  </Note>
  <Frequency>11</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*RECEPTORS, CYTOPLASMIC AND NUCLEAR (1999-2001)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D028961</DescriptorUI>
     <DescriptorName>
      <String>beta Karyopherins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Cell Biol 1999 Jun 14;145(6):1145-52</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0306763</ConceptUI>
    <ConceptName>
     <String>transportin SR</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T336768</TermUI>
      <String>transportin SR</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T336767</TermUI>
      <String>transportin-SR</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T336766</TermUI>
      <String>TRN-SR</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T336765</TermUI>
      <String>SR protein import receptor</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011464</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>estriol-16,17-disuccinyl-bovine serum albumin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1993</Year>
   <Month>07</Month>
   <Day>08</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004964</DescriptorUI>
     <DescriptorName>
      <String>Estriol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012710</DescriptorUI>
     <DescriptorName>
      <String>Serum Albumin, Bovine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D004966</DescriptorUI>
     <DescriptorName>
      <String>Estrogens, Conjugated (USP)</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Am J Obstet Gyn 123(7):700;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057779</ConceptUI>
    <ConceptName>
     <String>estriol-16,17-disuccinyl-bovine serum albumin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087782</TermUI>
      <String>estriol-16,17-disuccinyl-bovine serum albumin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C424165</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>transportin SR2</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>09</Month>
   <Day>05</Day>
  </DateCreated>
  <Note>homolog of transportin SR
  </Note>
  <Frequency>12</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*RECEPTORS, CYTOPLASMIC AND NUCLEAR (1999-2001)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D028961</DescriptorUI>
     <DescriptorName>
      <String>beta Karyopherins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0360330</ConceptUI>
    <ConceptName>
     <String>transportin SR2</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T411567</TermUI>
      <String>transportin SR2</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>04</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T443895</TermUI>
      <String>transportin-SR2</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>04</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T443894</TermUI>
      <String>SR2 protein import receptor</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>04</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C040514</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-fluorohexadecanoic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1984</Year>
   <Month>04</Month>
   <Day>03</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>23</Day>
  </DateRevised>
  <Note>inhibits sphingosine base formation &amp; accumulates in membrane lipids of cultured mammalian cells
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010169</DescriptorUI>
     <DescriptorName>
      <String>Palmitic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 1984;792(2):214</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0120615</ConceptUI>
    <ConceptName>
     <String>2-fluorohexadecanoic acid</String>
    </ConceptName>
    <RegistryNumber>16518-94-8</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0120615</Concept1UI>
     <Concept2UI>M0120614</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T150620</TermUI>
      <String>2-fluorohexadecanoic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1984)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T150618</TermUI>
      <String>2-fluoropalmitic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1984)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0120614</ConceptUI>
    <ConceptName>
     <String>DL-alpha-fluoropalmitic acid</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0120615</Concept1UI>
     <Concept2UI>M0120614</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T150619</TermUI>
      <String>DL-alpha-fluoropalmitic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1984)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C046143</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>14-methylhexadecanoic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1985</Year>
   <Month>09</Month>
   <Day>17</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>23</Day>
  </DateRevised>
  <Note>RN given refers to cpd without isomeric designation
  </Note>
  <Frequency>11</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010169</DescriptorUI>
     <DescriptorName>
      <String>Palmitic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Neoplasma 1985;32(3):323</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0133838</ConceptUI>
    <ConceptName>
     <String>14-methylhexadecanoic acid</String>
    </ConceptName>
    <RegistryNumber>5918-29-6</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>5746-59-8 ((+-)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0133838</Concept1UI>
     <Concept2UI>M0322393</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T163843</TermUI>
      <String>14-methylhexadecanoic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T163842</TermUI>
      <String>14-methylpalmitic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0322393</ConceptUI>
    <ConceptName>
     <String>14-methylhexadecanoic acid, (+-)-isomer</String>
    </ConceptName>
    <RegistryNumber>5746-59-8</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0133838</Concept1UI>
     <Concept2UI>M0322393</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T352393</TermUI>
      <String>14-methylhexadecanoic acid, (+-)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011479</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hexadecyl phosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>01</Month>
   <Day>22</Day>
  </DateRevised>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009943</DescriptorUI>
     <DescriptorName>
      <String>Organophosphorus Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Membrane Biol 23(3-4):293;1975</Source>
   <Source>J Pharm Soc Jpn 96(7):912;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057799</ConceptUI>
    <ConceptName>
     <String>hexadecyl phosphate</String>
    </ConceptName>
    <CASN1Name>1-Hexadecanol, dihydrogen phosphate</CASN1Name>
    <RegistryNumber>3539-43-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087802</TermUI>
      <String>hexadecyl phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C026834</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>beta-cell tropin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>11</Month>
   <Day>04</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>peptide of pituitary pars intermedia which stimulates insulin release
  </Note>
  <Frequency>22</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PITUITARY HORMONES (80-86)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000324</DescriptorUI>
     <DescriptorName>
      <String>Adrenocorticotropic Hormone</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010446</DescriptorUI>
     <DescriptorName>
      <String>Peptide Fragments</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>FEBS Lett 1980;117(1):303</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0087751</ConceptUI>
    <ConceptName>
     <String>beta-cell tropin</String>
    </ConceptName>
    <CASN1Name>beta-Cell tropin</CASN1Name>
    <RegistryNumber>75788-99-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T117754</TermUI>
      <String>beta-cell tropin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T117753</TermUI>
      <String>ACTH(22-39)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T117752</TermUI>
      <String>ACTH (22-39)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011496</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-nitro-8-methoxynaphtho(2,1-b)furan</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>02</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>04</Month>
   <Day>15</Day>
  </DateRevised>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009581</DescriptorUI>
     <DescriptorName>
      <String>Nitrofurans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Bull Cancer (Paris) 1981;68(4):328</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057833</ConceptUI>
    <ConceptName>
     <String>2-nitro-8-methoxynaphtho(2,1-b)furan</String>
    </ConceptName>
    <CASN1Name>Naphtho(2,1-b)furan, 8-methoxy-2-nitro-</CASN1Name>
    <RegistryNumber>75965-75-2</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0057833</Concept1UI>
     <Concept2UI>M0057830</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0057833</Concept1UI>
     <Concept2UI>M0057831</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0057833</Concept1UI>
     <Concept2UI>M0057832</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087836</TermUI>
      <String>2-nitro-8-methoxynaphtho(2,1-b)furan</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0057830</ConceptUI>
    <ConceptName>
     <String>8-methoxy-2-nitronaphtho(2,1-b)furan</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0057833</Concept1UI>
     <Concept2UI>M0057830</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T087833</TermUI>
      <String>8-methoxy-2-nitronaphtho(2,1-b)furan</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0057831</ConceptUI>
    <ConceptName>
     <String>R 6998</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0057833</Concept1UI>
     <Concept2UI>M0057831</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T087834</TermUI>
      <String>R 6998</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0057832</ConceptUI>
    <ConceptName>
     <String>R6998</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0057833</Concept1UI>
     <Concept2UI>M0057832</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T087835</TermUI>
      <String>R6998</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011502</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-(4-methoxycinnamoyl)-4-(5-phenyl-4-oxo-2- oxazolin-2-yl)piperazine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>OXAZOLES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010879</DescriptorUI>
     <DescriptorName>
      <String>Piperazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 18(12):1216;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057846</ConceptUI>
    <ConceptName>
     <String>1-(4-methoxycinnamoyl)-4-(5-phenyl-4-oxo-2- oxazolin-2-yl)piperazine</String>
    </ConceptName>
    <RegistryNumber>51314-69-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087849</TermUI>
      <String>1-(4-methoxycinnamoyl)-4-(5-phenyl-4-oxo-2- oxazolin-2-yl)piperazine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C077914</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>BNC1 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1992</Year>
   <Month>12</Month>
   <Day>07</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>RefSeq NM_001717
  </Note>
  <Frequency>34</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PHOSPHOPROTEINS (1992-2006)</PreviousIndexing>
   <PreviousIndexing>*PROTEINS (1992-2005)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004268</DescriptorUI>
     <DescriptorName>
      <String>DNA-Binding Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014157</DescriptorUI>
     <DescriptorName>
      <String>Transcription Factors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D015603</DescriptorUI>
     <DescriptorName>
      <String>Keratinocytes</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D016335</DescriptorUI>
     <DescriptorName>
      <String>Zinc Fingers</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Proc Natl Acad Sci U S A 1992 Nov 1;89(21):10311-5</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0209016</ConceptUI>
    <ConceptName>
     <String>BNC1 protein, human</String>
    </ConceptName>
    <RegistryNumber>148814-46-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T647475</TermUI>
      <String>BNC1 protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>07</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T647477</TermUI>
      <String>basonuclin protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>07</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T647476</TermUI>
      <String>basonuclin 1 protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>07</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013343</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cyclo 3</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>extract of Ruscus used therapeutically for venous insufficiency in leg
  </Note>
  <Frequency>24</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010936</DescriptorUI>
     <DescriptorName>
      <String>Plant Extracts</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Med Chir Dig 1979;8(4):365</Source>
   <Source>Phlebologie 29(1):77;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061022</ConceptUI>
    <ConceptName>
     <String>cyclo 3</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061022</Concept1UI>
     <Concept2UI>M0061021</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091025</TermUI>
      <String>cyclo 3</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0061021</ConceptUI>
    <ConceptName>
     <String>Cyclo 3 fort</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061022</Concept1UI>
     <Concept2UI>M0061021</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="TRD"  RecordPreferredTermYN="N">
      <TermUI>T091024</TermUI>
      <String>Cyclo 3 fort</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011516</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-nitro-3,4-diphenyl-2-furaldehyde</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*NITROFURANS (76-79)</PreviousIndexing>
   <PreviousIndexing>NITROFURANS (79-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005662</DescriptorUI>
     <DescriptorName>
      <String>Furaldehyde</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Soc Jpn 95(10):1218;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057867</ConceptUI>
    <ConceptName>
     <String>5-nitro-3,4-diphenyl-2-furaldehyde</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087870</TermUI>
      <String>5-nitro-3,4-diphenyl-2-furaldehyde</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C511595</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Bnc1 protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateCreated>
  <Note>RefSeq NM_007562
  </Note>
  <Frequency>21</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004268</DescriptorUI>
     <DescriptorName>
      <String>DNA-Binding Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014157</DescriptorUI>
     <DescriptorName>
      <String>Transcription Factors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0487469</ConceptUI>
    <ConceptName>
     <String>Bnc1 protein, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T647478</TermUI>
      <String>Bnc1 protein, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>07</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T647479</TermUI>
      <String>basonuclin 1 protein, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>07</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011525</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>(14Z)-9-oxo-13-hydroxyprost-14-enoic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1987</Year>
   <Month>07</Month>
   <Day>09</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*FATTY ACIDS, UNSATURATED (76-87)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005229</DescriptorUI>
     <DescriptorName>
      <String>Fatty Acids, Monounsaturated</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Prostaglandins 10(3):503;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057875</ConceptUI>
    <ConceptName>
     <String>(14Z)-9-oxo-13-hydroxyprost-14-enoic acid</String>
    </ConceptName>
    <CASN1Name>(14Z)-13-hydroxy-9-oxoprost-14-en-1-oic acid</CASN1Name>
    <RegistryNumber>57755-79-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087878</TermUI>
      <String>(14Z)-9-oxo-13-hydroxyprost-14-enoic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011526</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>9-oxo-13-hydroxyprost-14-ynoic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1984</Year>
   <Month>08</Month>
   <Day>15</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005231</DescriptorUI>
     <DescriptorName>
      <String>Fatty Acids, Unsaturated</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Prostaglandins 10(3):503;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057876</ConceptUI>
    <ConceptName>
     <String>9-oxo-13-hydroxyprost-14-ynoic acid</String>
    </ConceptName>
    <CASN1Name>13-hydroxy-9-oxoprost-14-yn-1-oic acid</CASN1Name>
    <RegistryNumber>57755-78-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087879</TermUI>
      <String>9-oxo-13-hydroxyprost-14-ynoic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011527</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>paliclavine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>metabolite of strain of Claviceps paspali; structure
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ERGOT ALKALOIDS (76-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004873</DescriptorUI>
     <DescriptorName>
      <String>Ergolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Helv Chim Acta 58(8):2484;1975</Source>
   <Source>Helv Chim Acta 58(8):2492;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057877</ConceptUI>
    <ConceptName>
     <String>paliclavine</String>
    </ConceptName>
    <CASN1Name>(4R)-(4 alpha,5 beta(R*)))-1,3,4,5-tetrahydro-4-(methylamino)-alpha-(1-methylethenyl)benz(cd) indole-5-methanol</CASN1Name>
    <RegistryNumber>52052-66-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087880</TermUI>
      <String>paliclavine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013357</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>FZ 560</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001286</DescriptorUI>
     <DescriptorName>
      <String>Atropine Derivatives</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003685</DescriptorUI>
     <DescriptorName>
      <String>Dehydrocholic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007792</DescriptorUI>
     <DescriptorName>
      <String>Lactulose</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010194</DescriptorUI>
     <DescriptorName>
      <String>Pancreatin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Int J Clin Pharmacol 14(1):40;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061058</ConceptUI>
    <ConceptName>
     <String>FZ 560</String>
    </ConceptName>
    <CASN1Name>Cholan-24-oic acid, 3,7,12-trioxo-, (5beta)-, mixt. with (3(S)-endo)-8-(2-(1,1'-biphenyl)-4-yl-2-oxoethyl)-3-(3-hydroxy-1-oxo-2-phenylpropoxy)-8-methyl-8-azoniabicyclo(3.2.1)octane bromide, 4-O-beta-D-galactopyranosyl-D-fructose and pancreatin</CASN1Name>
    <RegistryNumber>77416-73-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T091061</TermUI>
      <String>FZ 560</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T091060</TermUI>
      <String>FZ-560</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011532</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>(platinum(ethylenediamine)(guanosine)(2))(2+) cation</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1995</Year>
   <Month>01</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>model for Pt-DNA interaction; RN given refers to chloride iodide (2:3:1),tetrahydrate,(SP-4-2)
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PLATINUM (76-79)</PreviousIndexing>
   <PreviousIndexing>ETHYLENEDIAMINES (76-79)</PreviousIndexing>
   <PreviousIndexing>GUANOSINE/*analogs</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009944</DescriptorUI>
     <DescriptorName>
      <String>Organoplatinum Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D002413</DescriptorUI>
     <DescriptorName>
      <String>Cations, Divalent</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Am Chem Soc 97(25):7379;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057884</ConceptUI>
    <ConceptName>
     <String>(platinum(ethylenediamine)(guanosine)(2))(2+) cation</String>
    </ConceptName>
    <CASN1Name>Platinum(2+), (1,2-ethanediamine-N,N')bis(guanosine-N(7))-, chloride iodide (2:3:1), tetrahydrate, (SP-4-2)-</CASN1Name>
    <RegistryNumber>57574-64-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087887</TermUI>
      <String>(platinum(ethylenediamine)(guanosine)(2))(2+) cation</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013369</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>AH 6696</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>gastric acid secretion inhibitor
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>BENZOPYRANS (77-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011725</DescriptorUI>
     <DescriptorName>
      <String>Pyridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Br J Pharmacol 57(3):440P;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061088</ConceptUI>
    <ConceptName>
     <String>AH 6696</String>
    </ConceptName>
    <CASN1Name>5H-(1)benzopyrano(2,3-b)pyridin-5-ol</CASN1Name>
    <RegistryNumber>6722-09-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T091091</TermUI>
      <String>AH 6696</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T091090</TermUI>
      <String>AH-6696</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013377</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>UP 507-04</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011759</DescriptorUI>
     <DescriptorName>
      <String>Pyrrolidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Brit J Pharmacol 58(3):437;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061109</ConceptUI>
    <ConceptName>
     <String>UP 507-04</String>
    </ConceptName>
    <CASN1Name>cyclopropyl-2 p-chlorophenyl-4 methyl-5 pyrrolidine succinate</CASN1Name>
    <RegistryNumber>62510-57-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T091112</TermUI>
      <String>UP 507-04</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T091111</TermUI>
      <String>UP-507-04</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011543</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>san ch'i</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1988</Year>
   <Month>11</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>hemostatic from herb roots; well-known drug in Chinese materia medica
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011134</DescriptorUI>
     <DescriptorName>
      <String>Polysaccharides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D004365</DescriptorUI>
     <DescriptorName>
      <String>Drugs, Chinese Herbal</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Mikrokhim Acta 4-5(2):455;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057902</ConceptUI>
    <ConceptName>
     <String>san ch'i</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087905</TermUI>
      <String>san ch'i</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011549</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>supinidine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011763</DescriptorUI>
     <DescriptorName>
      <String>Pyrrolizidine Alkaloids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 40(26):3866;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057911</ConceptUI>
    <ConceptName>
     <String>supinidine</String>
    </ConceptName>
    <RegistryNumber>551-59-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087914</TermUI>
      <String>supinidine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013381</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N(alpha)-acetoxyethyl-N-ethylnitrosamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004052</DescriptorUI>
     <DescriptorName>
      <String>Diethylnitrosamine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Res 36(12):4504;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061119</ConceptUI>
    <ConceptName>
     <String>N(alpha)-acetoxyethyl-N-ethylnitrosamine</String>
    </ConceptName>
    <CASN1Name>Ethanol, 1-(ethylnitrosoamino)-, acetate (ester)</CASN1Name>
    <RegistryNumber>58431-24-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091122</TermUI>
      <String>N(alpha)-acetoxyethyl-N-ethylnitrosamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T091121</TermUI>
      <String>N-alpha-acetoxyethyl-N-ethylnitrosamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013386</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-acetylprolinamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>RN given refers to (S)-isomer
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011392</DescriptorUI>
     <DescriptorName>
      <String>Proline</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biopolymers 15(12):2523;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061124</ConceptUI>
    <ConceptName>
     <String>N-acetylprolinamide</String>
    </ConceptName>
    <CASN1Name>2-Pyrrolidinecarboxamide, 1-acetyl-, (S)-</CASN1Name>
    <RegistryNumber>16395-58-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091127</TermUI>
      <String>N-acetylprolinamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T091126</TermUI>
      <String>N-acetyl-L-prolinamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011553</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tetrahydrosecamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>06</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>from Amsonia elliptica; structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*INDOLES (76-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000470</DescriptorUI>
     <DescriptorName>
      <String>Alkaloids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Yakugaku Zasshi 95(10):1152;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057920</ConceptUI>
    <ConceptName>
     <String>tetrahydrosecamine</String>
    </ConceptName>
    <CASN1Name>Pyrido(1,2-a)indole-6,9-dicarboxylic acid, 10-(2-(3-ethyl-1-piperidinyl)ethyl)-6-(3-(2-(3-ethyl-1-piperidinyl)ethyl)-1H-indol-2-yl)-6,7,8,9-tetrahydro-, dimethyl ester</CASN1Name>
    <RegistryNumber>33633-19-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087923</TermUI>
      <String>tetrahydrosecamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011560</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>triisopropyl phosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>07</Month>
   <Day>17</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ORGANOPHOSPHORUS CPDS (76-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010755</DescriptorUI>
     <DescriptorName>
      <String>Organophosphates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Exp Cell Res 94(2):292;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057935</ConceptUI>
    <ConceptName>
     <String>triisopropyl phosphate</String>
    </ConceptName>
    <CASN1Name>phosphoric acid, tris(1-methylethyl) ester</CASN1Name>
    <RegistryNumber>513-02-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087938</TermUI>
      <String>triisopropyl phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C083622</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Pla2g3 protein, rat</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1993</Year>
   <Month>11</Month>
   <Day>08</Day>
  </DateCreated>
  <DateRevised>
   <Year>2007</Year>
   <Month>08</Month>
   <Day>13</Day>
  </DateRevised>
  <Note>RefSeq XM_223553
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PHOSPHOLIPASES A (1993-2007)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D054520</DescriptorUI>
     <DescriptorName>
      <String>Group III Phospholipases A2</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Toxicon 1993 Aug;31(8):957-67</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0222408</ConceptUI>
    <ConceptName>
     <String>Pla2g3 protein, rat</String>
    </ConceptName>
    <RegistryNumber>EC 3.1.1.4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T689883</TermUI>
      <String>Pla2g3 protein, rat</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>01</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T689884</TermUI>
      <String>phospholipase A2, group III, rat</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>01</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T252412</TermUI>
      <String>PLA2-III protein, rat</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T252413</TermUI>
      <String>phospholipase A2 III protein, rat</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T252411</TermUI>
      <String>PLA(2)-III protein, rat</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C450899</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Salinum</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>04</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>linseed extract
  </Note>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010936</DescriptorUI>
     <DescriptorName>
      <String>Plant Extracts</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D012464</DescriptorUI>
     <DescriptorName>
      <String>Saliva, Artificial</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D019597</DescriptorUI>
     <DescriptorName>
      <String>Flax</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Gerodontology 2001 Dec;18(2):87-94</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0419331</ConceptUI>
    <ConceptName>
     <String>Salinum</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="TRD"  RecordPreferredTermYN="Y">
      <TermUI>T488204</TermUI>
      <String>Salinum</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>04</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C042390</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>alpha-methylserotonin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1984</Year>
   <Month>09</Month>
   <Day>19</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>06</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>potent agonist at M &amp; D receptors of serotonin; RN given refers to parent cpd
  </Note>
  <Frequency>157</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D012701</DescriptorUI>
     <DescriptorName>
      <String>Serotonin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
    <PharmacologicalActionList>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D017366</DescriptorUI>
        <DescriptorName>
         <String>Serotonin Receptor Agonists</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
    </PharmacologicalActionList>
  <SourceList>
   <Source>Life Sci 1984;35(5):477</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0125210</ConceptUI>
    <ConceptName>
     <String>alpha-methylserotonin</String>
    </ConceptName>
    <RegistryNumber>22965-81-7</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>78263-92-0 ((Z)-2-butenedioate)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0125210</Concept1UI>
     <Concept2UI>M0459909</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0125210</Concept1UI>
     <Concept2UI>M0321748</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T155215</TermUI>
      <String>alpha-methylserotonin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1984)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T570613</TermUI>
      <String>alpha-methyl-5-HT</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>01</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T155214</TermUI>
      <String>alpha-methyl-5-hydroxytryptamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1984)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0459909</ConceptUI>
    <ConceptName>
     <String>alpha-methyl-5-HT maleate</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0125210</Concept1UI>
     <Concept2UI>M0459909</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T570614</TermUI>
      <String>alpha-methyl-5-HT maleate</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>01</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0321748</ConceptUI>
    <ConceptName>
     <String>alpha-methylserotonin, (Z)-2-butenedioate</String>
    </ConceptName>
    <RegistryNumber>78263-92-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0125210</Concept1UI>
     <Concept2UI>M0321748</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T351748</TermUI>
      <String>alpha-methylserotonin, (Z)-2-butenedioate</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1984)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011577</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>compound 5.4</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>pregnenolone isomer with gas chromatographic retention time of 5.4 min
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011284</DescriptorUI>
     <DescriptorName>
      <String>Pregnenolone</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D007536</DescriptorUI>
     <DescriptorName>
      <String>Isomerism</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Tijdschr Diergeneeskd 101(2):83;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057966</ConceptUI>
    <ConceptName>
     <String>compound 5.4</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087969</TermUI>
      <String>compound 5.4</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011586</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>42M-9</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>02</Month>
   <Day>20</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003503</DescriptorUI>
     <DescriptorName>
      <String>Cyclobutanes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006846</DescriptorUI>
     <DescriptorName>
      <String>Hydrocarbons, Halogenated</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Rec Prog Anesth Resusc W3 EX 89 No. 347:205;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057996</ConceptUI>
    <ConceptName>
     <String>42M-9</String>
    </ConceptName>
    <CASN1Name>1-bromo-1,2,2-trifluorocyclobutane</CASN1Name>
    <RegistryNumber>38310-71-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087999</TermUI>
      <String>42M-9</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C114001</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-(2-deoxy-2-fluoro-4-thio-arabinofuranosyl)cytosine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>09</Month>
   <Day>04</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003561</DescriptorUI>
     <DescriptorName>
      <String>Cytarabine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Lett 1998 Jul 3;129(1):103-10</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0294190</ConceptUI>
    <ConceptName>
     <String>1-(2-deoxy-2-fluoro-4-thio-arabinofuranosyl)cytosine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T324195</TermUI>
      <String>1-(2-deoxy-2-fluoro-4-thio-arabinofuranosyl)cytosine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T324194</TermUI>
      <String>2-F-4-Thio-arabinofuranosyl-C</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T324193</TermUI>
      <String>1-(2-deoxy-2-fluoro-4-thio-beta-D-arabinofuranosyl)cytosine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C450900</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-O-methylfunicone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>04</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>derived from Penicillium pinophilum; structure in first source
  </Note>
  <Frequency>12</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011753</DescriptorUI>
     <DescriptorName>
      <String>Pyrones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Altern Lab Anim 2002 Jan-Feb;30(1):69-75</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0419332</ConceptUI>
    <ConceptName>
     <String>3-O-methylfunicone</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T488205</TermUI>
      <String>3-O-methylfunicone</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>04</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C038645</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>lodyne S</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>12</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>09</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>RN given refers to lodyne S 100
  </Note>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SURFACE-ACTIVE AGENTS (1983-2003)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008055</DescriptorUI>
     <DescriptorName>
      <String>Lipids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Caries Res 1983;17(4):304</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0116218</ConceptUI>
    <ConceptName>
     <String>lodyne S</String>
    </ConceptName>
    <RegistryNumber>66039-00-7</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>66039-02-9 (lodyne S 112)</RelatedRegistryNumber>
     <RelatedRegistryNumber>84069-89-6 (lodyne S 110)</RelatedRegistryNumber>
     <RelatedRegistryNumber>85087-50-9 (lodyne S 107)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0116218</Concept1UI>
     <Concept2UI>M0321012</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0116218</Concept1UI>
     <Concept2UI>M0321013</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0116218</Concept1UI>
     <Concept2UI>M0116216</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0116218</Concept1UI>
     <Concept2UI>M0321014</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T146222</TermUI>
      <String>lodyne S</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0321012</ConceptUI>
    <ConceptName>
     <String>lodyne S 112</String>
    </ConceptName>
    <RegistryNumber>66039-02-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0116218</Concept1UI>
     <Concept2UI>M0321012</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T351012</TermUI>
      <String>lodyne S 112</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0321013</ConceptUI>
    <ConceptName>
     <String>lodyne S 110</String>
    </ConceptName>
    <RegistryNumber>84069-89-6</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0116218</Concept1UI>
     <Concept2UI>M0321013</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T351013</TermUI>
      <String>lodyne S 110</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0116216</ConceptUI>
    <ConceptName>
     <String>lodyne S 100</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0116218</Concept1UI>
     <Concept2UI>M0116216</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T146220</TermUI>
      <String>lodyne S 100</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T146221</TermUI>
      <String>lodyne S-100</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0321014</ConceptUI>
    <ConceptName>
     <String>lodyne S 107</String>
    </ConceptName>
    <RegistryNumber>85087-50-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0116218</Concept1UI>
     <Concept2UI>M0321014</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T351014</TermUI>
      <String>lodyne S 107</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011668</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>S-aristeromycinylhomocysteine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>11</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>RN given refers to (1S-(1alpha,2beta,3beta,4alpha))-isomer; structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D012435</DescriptorUI>
     <DescriptorName>
      <String>S-Adenosylhomocysteine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 19(1):197;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058150</ConceptUI>
    <ConceptName>
     <String>S-aristeromycinylhomocysteine</String>
    </ConceptName>
    <RegistryNumber>57884-84-1</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>50700-45-3 ((L-(1alpha,2beta,3beta,4alpha))-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0058150</Concept1UI>
     <Concept2UI>M0311541</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088153</TermUI>
      <String>S-aristeromycinylhomocysteine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T088152</TermUI>
      <String>S-aristeromycinyl-L-homocysteine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0311541</ConceptUI>
    <ConceptName>
     <String>S-aristeromycinylhomocysteine, (L-(1alpha,2beta,3beta,4alpha))-isomer</String>
    </ConceptName>
    <RegistryNumber>50700-45-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0058150</Concept1UI>
     <Concept2UI>M0311541</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T341541</TermUI>
      <String>S-aristeromycinylhomocysteine, (L-(1alpha,2beta,3beta,4alpha))-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C416520</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>8-hydroxyoxomatairesinol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>05</Day>
  </DateCreated>
  <Note>a lignan isolated from the sapwood of Tsuga heterophylla; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005663</DescriptorUI>
     <DescriptorName>
      <String>Furans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Phytochemistry 2000 Jun;54(4):439-44</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0374117</ConceptUI>
    <ConceptName>
     <String>8-hydroxyoxomatairesinol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T430350</TermUI>
      <String>8-hydroxyoxomatairesinol</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>12</Month>
       <Day>05</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011619</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Ro 7-9957</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001570</DescriptorUI>
     <DescriptorName>
      <String>Benzodiazepinones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Clin Chem 24(10):1838;1978</Source>
   <Source>J Chromatogr 118(3):371;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058073</ConceptUI>
    <ConceptName>
     <String>Ro 7-9957</String>
    </ConceptName>
    <CASN1Name>7-iodo-1,3-dihydro-1-methyl-5(2'-fluorophenyl) -2H-1,4-benzodiazepin-2-one</CASN1Name>
    <RegistryNumber>34932-78-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088076</TermUI>
      <String>Ro 7-9957</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011630</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ameletin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1986</Year>
   <Month>08</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>habituation-induced brain peptide (sound stimulus)
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BRAIN (76-79)</PreviousIndexing>
   <PreviousIndexing>*NERVE TISSUE PROTEINS (76-86)</PreviousIndexing>
   <PreviousIndexing>*PEPTIDES (76-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009479</DescriptorUI>
     <DescriptorName>
      <String>Neuropeptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Anal Biochem 70(2):359;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058088</ConceptUI>
    <ConceptName>
     <String>ameletin</String>
    </ConceptName>
    <RegistryNumber>53664-65-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088091</TermUI>
      <String>ameletin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011631</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-acetylgalactosaminitol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000116</DescriptorUI>
     <DescriptorName>
      <String>Acetylgalactosamine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Hoppe-Seyler's Z Physiol Chem 359(6):646;1978</Source>
   <Source>Method Struct Metab Glycoconjuges W3:SY3915;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058089</ConceptUI>
    <ConceptName>
     <String>N-acetylgalactosaminitol</String>
    </ConceptName>
    <RegistryNumber>10486-91-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088092</TermUI>
      <String>N-acetylgalactosaminitol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011632</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>acetyl phosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>08</Month>
   <Day>13</Day>
  </DateRevised>
  <Frequency>212</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ORGANOPHOSPHORUS COMPOUNDS (76-81)</PreviousIndexing>
   <PreviousIndexing>ACETIC ACIDS (76-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010755</DescriptorUI>
     <DescriptorName>
      <String>Organophosphates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 1980;596(1):94</Source>
   <Source>J Am Chem Soc 100(1):304;1978</Source>
   <Source>J Biol Chem 252(12):4210;1977</Source>
   <Source>Life Sci 21(5):713;1977</Source>
   <Source>Z Naturforsch 30(6):771;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058090</ConceptUI>
    <ConceptName>
     <String>acetyl phosphate</String>
    </ConceptName>
    <RegistryNumber>590-54-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088093</TermUI>
      <String>acetyl phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011633</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>acridan</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>8</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000166</DescriptorUI>
     <DescriptorName>
      <String>Acridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Rational Psychopharmacotherapy QV 77 T244r:5;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058091</ConceptUI>
    <ConceptName>
     <String>acridan</String>
    </ConceptName>
    <CASN1Name>9,10-dihydroacridine</CASN1Name>
    <RegistryNumber>92-81-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088094</TermUI>
      <String>acridan</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C416521</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>neoxanthin synthase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>05</Day>
  </DateCreated>
  <Note>catalyzes the conversion of violaxanthin to neoxanthin; amino acid sequence in first source; GenBank Y18297
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010088</DescriptorUI>
     <DescriptorName>
      <String>Oxidoreductases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Biochem 2000 Nov;267(21):6346-52</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0374118</ConceptUI>
    <ConceptName>
     <String>neoxanthin synthase</String>
    </ConceptName>
    <RegistryNumber>EC 1.97.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T430351</TermUI>
      <String>neoxanthin synthase</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>12</Month>
       <Day>05</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T430352</TermUI>
      <String>NSY enzyme</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>12</Month>
       <Day>05</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C416522</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Smt3-specific isopeptidase 1</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>05</Day>
  </DateCreated>
  <Note>a nucleolar protein; amino acid sequence in first source; GenBank AF194031
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010450</DescriptorUI>
     <DescriptorName>
      <String>Endopeptidases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D009687</DescriptorUI>
     <DescriptorName>
      <String>Nuclear Proteins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Eur J Biochem 2000 Nov;267(21):6423-7</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0374119</ConceptUI>
    <ConceptName>
     <String>Smt3-specific isopeptidase 1</String>
    </ConceptName>
    <RegistryNumber>EC 3.4.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T430353</TermUI>
      <String>Smt3-specific isopeptidase 1</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>12</Month>
       <Day>05</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T430354</TermUI>
      <String>SMT3IP1</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>12</Month>
       <Day>05</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012561</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>styrylglycine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>05</Month>
   <Day>27</Day>
  </DateRevised>
  <Note>structure; RN given refers to (E)-(+-)-isomer
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>STYRENES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005998</DescriptorUI>
     <DescriptorName>
      <String>Glycine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 41(8):1466;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059660</ConceptUI>
    <ConceptName>
     <String>styrylglycine</String>
    </ConceptName>
    <CASN1Name>3-Butenoic acid, 2-amino-4-phenyl-, (E)-(+-)-</CASN1Name>
    <RegistryNumber>58207-08-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089663</TermUI>
      <String>styrylglycine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C097405</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>mannose-glucose-binding lectin, Cladrastis lutea</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>02</Month>
   <Day>02</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>08</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>from the bark of yellow wood C. lutea; CLAI is the major Cladrastis bark lectin; CLAII is a minor protein; amino acid sequence given in first source; GenBank U21940
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*LECTINS (1996-2002)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D037121</DescriptorUI>
     <DescriptorName>
      <String>Plant Lectins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Plant Mol Biol 1995 Nov;29(3):579-98</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0256052</ConceptUI>
    <ConceptName>
     <String>mannose-glucose-binding lectin, Cladrastis lutea</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0256052</Concept1UI>
     <Concept2UI>M0256049</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0256052</Concept1UI>
     <Concept2UI>M0256048</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T286057</TermUI>
      <String>mannose-glucose-binding lectin, Cladrastis lutea</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0256049</ConceptUI>
    <ConceptName>
     <String>Cladrastis lutea agglutinin II</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0256052</Concept1UI>
     <Concept2UI>M0256049</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T286054</TermUI>
      <String>Cladrastis lutea agglutinin II</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T286056</TermUI>
      <String>LECLAII</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T286052</TermUI>
      <String>CLAII lectin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0256048</ConceptUI>
    <ConceptName>
     <String>Cladrastis lutea agglutinin I</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0256052</Concept1UI>
     <Concept2UI>M0256048</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T286053</TermUI>
      <String>Cladrastis lutea agglutinin I</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T286055</TermUI>
      <String>LECLAI</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T286051</TermUI>
      <String>CLAI lectin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012569</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,2,6,6-tetramethylpiperidone-1-oxyl (6-purinyl)hydrazone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>06</Month>
   <Day>15</Day>
  </DateRevised>
  <Note>RN is from 9th CI; stable nitroxide radical; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PURINES (76-79)</PreviousIndexing>
   <PreviousIndexing>PIPERIDONES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003497</DescriptorUI>
     <DescriptorName>
      <String>Cyclic N-Oxides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Z Naturforsch (C) 31(1-2):101;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059679</ConceptUI>
    <ConceptName>
     <String>2,2,6,6-tetramethylpiperidone-1-oxyl (6-purinyl)hydrazone</String>
    </ConceptName>
    <RegistryNumber>59225-19-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089682</TermUI>
      <String>2,2,6,6-tetramethylpiperidone-1-oxyl (6-purinyl)hydrazone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012678</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Sch 20656</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>AMINOGLYCOSIDES (77-87)</PreviousIndexing>
   <PreviousIndexing>ANTIBIOTICS (77-87)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000617</DescriptorUI>
     <DescriptorName>
      <String>Aminoglycosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Antimicrob Ag Chemotherap 10(2):382;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059919</ConceptUI>
    <ConceptName>
     <String>Sch 20656</String>
    </ConceptName>
    <RegistryNumber>60617-33-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T089922</TermUI>
      <String>Sch 20656</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T089921</TermUI>
      <String>Sch-20656</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012573</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>thioasparagine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000603</DescriptorUI>
     <DescriptorName>
      <String>Amino Acids, Sulfur</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D001216</DescriptorUI>
     <DescriptorName>
      <String>Asparagine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 41(8):1336;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059688</ConceptUI>
    <ConceptName>
     <String>thioasparagine</String>
    </ConceptName>
    <CASN1Name>Butanoic acid, 2,4-diamino-4-thioxo-, (S)-</CASN1Name>
    <RegistryNumber>58208-26-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089691</TermUI>
      <String>thioasparagine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012575</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3 beta-thiocyanato-14 beta-hydroxy-5 beta-card-20(22)-enolide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>12</Month>
   <Day>28</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CARDANOLIDES (76-77)</PreviousIndexing>
   <PreviousIndexing>THIOCYANATES (76-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002298</DescriptorUI>
     <DescriptorName>
      <String>Cardenolides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 65(5):765;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059690</ConceptUI>
    <ConceptName>
     <String>3 beta-thiocyanato-14 beta-hydroxy-5 beta-card-20(22)-enolide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089693</TermUI>
      <String>3 beta-thiocyanato-14 beta-hydroxy-5 beta-card-20(22)-enolide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012577</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>thiophenyl acetate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010648</DescriptorUI>
     <DescriptorName>
      <String>Phenylacetates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Pharmucol 25(6):701;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059691</ConceptUI>
    <ConceptName>
     <String>thiophenyl acetate</String>
    </ConceptName>
    <RegistryNumber>934-87-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089694</TermUI>
      <String>thiophenyl acetate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013685</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>sorbistins</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>complex of closely related aminoglycoside antibiotics produced by Pseudomonas sorbicinii; RN given refers to cpd with unknown MF
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>AMINOGLYCOSIDES (77-87)</PreviousIndexing>
   <PreviousIndexing>ANTIBIOTICS (77-87)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000617</DescriptorUI>
     <DescriptorName>
      <String>Aminoglycosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Pharm Bull (Tokyo) 26(4):1075;1978</Source>
   <Source>Chem Pharm Bull (Tokyo) 27(1):65;1979</Source>
   <Source>J Antibiot (Tokyo) 29(11):1137;1976</Source>
   <Source>J Antibiot (Tokyo) 29(11):1147;1976</Source>
   <Source>J Antibiot (Tokyo) 29(11):1152;1976</Source>
   <Source>J Antibiot (Tokyo) 29(12):1286;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061635</ConceptUI>
    <ConceptName>
     <String>sorbistins</String>
    </ConceptName>
    <CASN1Name>Sorbistin</CASN1Name>
    <RegistryNumber>75635-19-7</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>60502-98-9 (sorbistin D)</RelatedRegistryNumber>
     <RelatedRegistryNumber>60502-99-0 (sorbistin B)</RelatedRegistryNumber>
     <RelatedRegistryNumber>60534-69-2 (sorbistin A2)</RelatedRegistryNumber>
     <RelatedRegistryNumber>61566-57-2 (sorbistin C)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061635</Concept1UI>
     <Concept2UI>M0312283</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061635</Concept1UI>
     <Concept2UI>M0312284</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061635</Concept1UI>
     <Concept2UI>M0312286</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061635</Concept1UI>
     <Concept2UI>M0061634</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061635</Concept1UI>
     <Concept2UI>M0312285</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091638</TermUI>
      <String>sorbistins</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312283</ConceptUI>
    <ConceptName>
     <String>sorbistins, sorbistin D</String>
    </ConceptName>
    <RegistryNumber>60502-98-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061635</Concept1UI>
     <Concept2UI>M0312283</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342283</TermUI>
      <String>sorbistins, sorbistin D</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312284</ConceptUI>
    <ConceptName>
     <String>sorbistins, sorbistin B</String>
    </ConceptName>
    <RegistryNumber>60502-99-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061635</Concept1UI>
     <Concept2UI>M0312284</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342284</TermUI>
      <String>sorbistins, sorbistin B</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312286</ConceptUI>
    <ConceptName>
     <String>sorbistins, sorbistin C</String>
    </ConceptName>
    <RegistryNumber>61566-57-2</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061635</Concept1UI>
     <Concept2UI>M0312286</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342286</TermUI>
      <String>sorbistins, sorbistin C</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0061634</ConceptUI>
    <ConceptName>
     <String>P-2563</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061635</Concept1UI>
     <Concept2UI>M0061634</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T091637</TermUI>
      <String>P-2563</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312285</ConceptUI>
    <ConceptName>
     <String>sorbistins, sorbistin A2</String>
    </ConceptName>
    <RegistryNumber>60534-69-2</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061635</Concept1UI>
     <Concept2UI>M0312285</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342285</TermUI>
      <String>sorbistins, sorbistin A2</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C104569</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>BfrA protein, Bordetella bronchiseptica</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1997</Year>
   <Month>03</Month>
   <Day>18</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>02</Month>
   <Day>26</Day>
  </DateRevised>
  <Note>homologous to ferric siderophore receptors; GenBank U56084
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001425</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Outer Membrane Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011956</DescriptorUI>
     <DescriptorName>
      <String>Receptors, Cell Surface</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Microbiology 1997 Jan;143( Pt 1):135-45</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0273075</ConceptUI>
    <ConceptName>
     <String>BfrA protein, Bordetella bronchiseptica</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T497162</TermUI>
      <String>BfrA protein, Bordetella bronchiseptica</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>06</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T574484</TermUI>
      <String>ferric iron repressed outer-membrane protein, Bordetella bronchiseptica</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>02</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012588</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,2,2-trifluoroethyl ethyl ether</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1994</Year>
   <Month>06</Month>
   <Day>15</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>FLUROXENE/*analogs (76-94)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005019</DescriptorUI>
     <DescriptorName>
      <String>Ethyl Ethers</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Pharmacol 25(7):773;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059709</ConceptUI>
    <ConceptName>
     <String>2,2,2-trifluoroethyl ethyl ether</String>
    </ConceptName>
    <CASN1Name>2-ethoxy-1,1,1-trifluoroethane</CASN1Name>
    <RegistryNumber>461-24-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089712</TermUI>
      <String>2,2,2-trifluoroethyl ethyl ether</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C034476</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>muconaldehyde</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1982</Year>
   <Month>06</Month>
   <Day>16</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>09</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>potential toxic intermediate in benzene metabolism; structure given in first source
  </Note>
  <Frequency>54</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000447</DescriptorUI>
     <DescriptorName>
      <String>Aldehydes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
    <PharmacologicalActionList>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D000935</DescriptorUI>
        <DescriptorName>
         <String>Antifungal Agents</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
    </PharmacologicalActionList>
  <SourceList>
   <Source>Adv Exp Med Biol 1981;136(A):331</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0106201</ConceptUI>
    <ConceptName>
     <String>muconaldehyde</String>
    </ConceptName>
    <CASN1Name>2,4-Hexadienedial</CASN1Name>
    <RegistryNumber>3249-28-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T136205</TermUI>
      <String>muconaldehyde</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012605</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>vesiculin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009419</DescriptorUI>
     <DescriptorName>
      <String>Nerve Tissue Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Brain Res 75:115;1974</Source>
   <Source>W3 N1355:585;1974m</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059738</ConceptUI>
    <ConceptName>
     <String>vesiculin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089741</TermUI>
      <String>vesiculin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012612</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>yohimbinic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D015016</DescriptorUI>
     <DescriptorName>
      <String>Yohimbine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biopolymers 15(5):977;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059750</ConceptUI>
    <ConceptName>
     <String>yohimbinic acid</String>
    </ConceptName>
    <CASN1Name>Yohimban-16-carboxylic acid, 17-hydroxy-, (16alpha,17alpha)-</CASN1Name>
    <RegistryNumber>522-87-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089753</TermUI>
      <String>yohimbinic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C104070</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>beta-lactamase IRT-3</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1997</Year>
   <Month>02</Month>
   <Day>25</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001618</DescriptorUI>
     <DescriptorName>
      <String>beta-Lactamases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Antimicrob Agents Chemother 1996 Oct;40(10):2434-6</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0271938</ConceptUI>
    <ConceptName>
     <String>beta-lactamase IRT-3</String>
    </ConceptName>
    <RegistryNumber>EC 3.5.2.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T301943</TermUI>
      <String>beta-lactamase IRT-3</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T301942</TermUI>
      <String>TEM-32 beta-lactamase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T301941</TermUI>
      <String>IRT-3 beta-lactamase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012615</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>P.GU 1</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>12</Month>
   <Day>31</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011134</DescriptorUI>
     <DescriptorName>
      <String>Polysaccharides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Folia Pharmacol Jpn 72(1):77;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059754</ConceptUI>
    <ConceptName>
     <String>P.GU 1</String>
    </ConceptName>
    <CASN1Name>PGU 1</CASN1Name>
    <RegistryNumber>74967-08-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089757</TermUI>
      <String>P.GU 1</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C053205</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-(diisopropylaminoethylamino)-2',6'-dimethylpropionanilide, diphosphoric acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1987</Year>
   <Month>08</Month>
   <Day>21</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>10</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000813</DescriptorUI>
     <DescriptorName>
      <String>Anilides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005029</DescriptorUI>
     <DescriptorName>
      <String>Ethylenediamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Rohoku J Exp Med 1987;151(4):443</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0150777</ConceptUI>
    <ConceptName>
     <String>3-(diisopropylaminoethylamino)-2',6'-dimethylpropionanilide, diphosphoric acid</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0150777</Concept1UI>
     <Concept2UI>M0150779</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T180782</TermUI>
      <String>3-(diisopropylaminoethylamino)-2',6'-dimethylpropionanilide, diphosphoric acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0150779</ConceptUI>
    <ConceptName>
     <String>AN 132</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0150777</Concept1UI>
     <Concept2UI>M0150779</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T180784</TermUI>
      <String>AN 132</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T180783</TermUI>
      <String>AN-132</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C081375</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>gp21 morphogenetic proteinase, phage T4</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1993</Year>
   <Month>06</Month>
   <Day>24</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>involved in delivery of encapsidated fusion proteins into bacteria
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010450</DescriptorUI>
     <DescriptorName>
      <String>Endopeptidases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Virology 1993 Jun; 194(2):481-90</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0217092</ConceptUI>
    <ConceptName>
     <String>gp21 morphogenetic proteinase, phage T4</String>
    </ConceptName>
    <RegistryNumber>EC 3.4.99.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T247097</TermUI>
      <String>gp21 morphogenetic proteinase, phage T4</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T247096</TermUI>
      <String>gp21 proteinase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C482094</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>agglutinin-A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>03</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>a lectin from the cnidarian Bunodeopsis antillienis
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D037102</DescriptorUI>
     <DescriptorName>
      <String>Lectins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Toxicon. 2003 Oct;42(5):525-32</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0461581</ConceptUI>
    <ConceptName>
     <String>agglutinin-A</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T574809</TermUI>
      <String>agglutinin-A</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>03</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C515559</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Txn1 protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>12</Month>
   <Day>16</Day>
  </DateCreated>
  <DateRevised>
   <Year>2007</Year>
   <Month>01</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>RefSeq NM_011660
  </Note>
  <Frequency>82</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013879</DescriptorUI>
     <DescriptorName>
      <String>Thioredoxins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Endocrinology 2004 Dec;145(12):5485-92</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0504827</ConceptUI>
    <ConceptName>
     <String>Txn1 protein, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T689084</TermUI>
      <String>Txn1 protein, mouse</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>01</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T687963</TermUI>
      <String>TRX protein, mouse</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>12</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T689085</TermUI>
      <String>thioredoxin 1 protein, mouse</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>01</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T687962</TermUI>
      <String>thioredoxin-1 protein, mouse</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>12</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C482095</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>agglutinin-B</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>03</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>a lectin from the cnidarian Bunodeopsis antillienis
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D037102</DescriptorUI>
     <DescriptorName>
      <String>Lectins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Toxicon. 2003 Oct;42(5):525-32</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0461582</ConceptUI>
    <ConceptName>
     <String>agglutinin-B</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T574810</TermUI>
      <String>agglutinin-B</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>03</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012658</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>S 1592</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>RN &amp; NM refers to mono-HCl; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SALICYLAMIDES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010880</DescriptorUI>
     <DescriptorName>
      <String>Piperidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arzneim Forsch 26(4):516;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059875</ConceptUI>
    <ConceptName>
     <String>S 1592</String>
    </ConceptName>
    <CASN1Name>2-hydroxy-N-((4-hydroxy-1-(2-phenylethyl)-4-piperidinyl)methyl)benzamide, monohydrochloride</CASN1Name>
    <RegistryNumber>25552-58-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0059875</Concept1UI>
     <Concept2UI>M0059873</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T089878</TermUI>
      <String>S 1592</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T089877</TermUI>
      <String>S-1592</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0059873</ConceptUI>
    <ConceptName>
     <String>1-phenethyl-4-hydroxysalicylamido-4-methylpiperidine hydrochloride</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0059875</Concept1UI>
     <Concept2UI>M0059873</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T089876</TermUI>
      <String>1-phenethyl-4-hydroxysalicylamido-4-methylpiperidine hydrochloride</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C475583</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-((3-iodo-5-(3-trifluoromethyl-3H-diazirin-3-yl))benzyl)dantrolene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>07</Month>
   <Day>16</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003620</DescriptorUI>
     <DescriptorName>
      <String>Dantrolene</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Bioorg Med Chem Lett. 2002 Nov 18;12(22):3259-61</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0451665</ConceptUI>
    <ConceptName>
     <String>N-((3-iodo-5-(3-trifluoromethyl-3H-diazirin-3-yl))benzyl)dantrolene</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T546068</TermUI>
      <String>N-((3-iodo-5-(3-trifluoromethyl-3H-diazirin-3-yl))benzyl)dantrolene</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>07</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T546069</TermUI>
      <String>GIF-0276</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>07</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C119448</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>piperidinyl-3-phosphinic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1999</Year>
   <Month>06</Month>
   <Day>21</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010721</DescriptorUI>
     <DescriptorName>
      <String>Phosphinic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010880</DescriptorUI>
     <DescriptorName>
      <String>Piperidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D005680</DescriptorUI>
     <DescriptorName>
      <String>gamma-Aminobutyric Acid</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Bioorg Med Chem Lett 1999 Mar 22;9(6):811-4</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0305801</ConceptUI>
    <ConceptName>
     <String>piperidinyl-3-phosphinic acid</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T335806</TermUI>
      <String>piperidinyl-3-phosphinic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T335805</TermUI>
      <String>3-PPPA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C079105</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dihydronitidine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1993</Year>
   <Month>02</Month>
   <Day>05</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>molecular structure given in first source
  </Note>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PHENANTHRIDINES (1993-2006)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D053119</DescriptorUI>
     <DescriptorName>
      <String>Benzophenanthridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Sci China B 1992 Sep;35(9):1101-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0211857</ConceptUI>
    <ConceptName>
     <String>dihydronitidine</String>
    </ConceptName>
    <RegistryNumber>13063-06-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T241862</TermUI>
      <String>dihydronitidine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T241861</TermUI>
      <String>nitidine, dihydro-</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C497562</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>RFC3 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2008</Year>
   <Month>09</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>RefSeq NM_002915
  </Note>
  <Frequency>24</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D051818</DescriptorUI>
     <DescriptorName>
      <String>Replication Protein C</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0481932</ConceptUI>
    <ConceptName>
     <String>RFC3 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T633238</TermUI>
      <String>RFC3 protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>14</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T633239</TermUI>
      <String>replication factor C (activator 1) 3, 38kDa protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>14</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C416969</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>glutathione transferase M3-3</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>18</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>04</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>functions as prostaglandin E synthase
  </Note>
  <Frequency>17</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005982</DescriptorUI>
     <DescriptorName>
      <String>Glutathione Transferase</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007527</DescriptorUI>
     <DescriptorName>
      <String>Isoenzymes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Neurochem Res 2000 May;25(5):733-6</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0374778</ConceptUI>
    <ConceptName>
     <String>glutathione transferase M3-3</String>
    </ConceptName>
    <RegistryNumber>EC 2.5.1.18</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T431255</TermUI>
      <String>glutathione transferase M3-3</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>12</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T638633</TermUI>
      <String>GSTM3 glutathione transferase</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>04</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000011</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-(n-acetaminophenylazo)-8-oxyquinoline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1991</Year>
   <Month>07</Month>
   <Day>10</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*QUINOLINES (71-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D015125</DescriptorUI>
     <DescriptorName>
      <String>Oxyquinoline</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040023</ConceptUI>
    <ConceptName>
     <String>5-(n-acetaminophenylazo)-8-oxyquinoline</String>
    </ConceptName>
    <CASN1Name>5-(p-acetamidophenylazo)-8-hydroxyquinoline</CASN1Name>
    <RegistryNumber>26424-51-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070023</TermUI>
      <String>5-(n-acetaminophenylazo)-8-oxyquinoline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000024</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>flavophosphine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1970</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>05</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000166</DescriptorUI>
     <DescriptorName>
      <String>Acridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Histochem 35(1):86;1970</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040037</ConceptUI>
    <ConceptName>
     <String>flavophosphine</String>
    </ConceptName>
    <CASN1Name>3-amino-9-(p-aminophenyl)-7-methylacridine</CASN1Name>
    <RegistryNumber>10134-60-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070037</TermUI>
      <String>flavophosphine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000032</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>adenosine arabinose</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ADENOSINE (72-75)</PreviousIndexing>
   <PreviousIndexing>*ARABINOSE (71-75)</PreviousIndexing>
   <PreviousIndexing>ARABINOSE/*analogs (75-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000241</DescriptorUI>
     <DescriptorName>
      <String>Adenosine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001087</DescriptorUI>
     <DescriptorName>
      <String>Arabinonucleosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040045</ConceptUI>
    <ConceptName>
     <String>adenosine arabinose</String>
    </ConceptName>
    <RegistryNumber>2006-02-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070045</TermUI>
      <String>adenosine arabinose</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000039</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>alpha-amino-4-isothiazolylacetic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>27</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ACETIC ACIDS (72-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013844</DescriptorUI>
     <DescriptorName>
      <String>Thiazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040050</ConceptUI>
    <ConceptName>
     <String>alpha-amino-4-isothiazolylacetic acid</String>
    </ConceptName>
    <CASN1Name>4-Isothiazoleacetic acid, alpha-amino-</CASN1Name>
    <RegistryNumber>34653-48-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070050</TermUI>
      <String>alpha-amino-4-isothiazolylacetic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C045521</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dinitrophenol-ovalbumin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1985</Year>
   <Month>07</Month>
   <Day>09</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>18</Day>
  </DateRevised>
  <Frequency>32</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004140</DescriptorUI>
     <DescriptorName>
      <String>Dinitrophenols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010047</DescriptorUI>
     <DescriptorName>
      <String>Ovalbumin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D006241</DescriptorUI>
     <DescriptorName>
      <String>Haptens</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Respiration 1985;47(2):138</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0132317</ConceptUI>
    <ConceptName>
     <String>dinitrophenol-ovalbumin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T162322</TermUI>
      <String>dinitrophenol-ovalbumin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T162320</TermUI>
      <String>DNP-ovalbumin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T162321</TermUI>
      <String>dinitrophenylovalbumin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000047</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>albitocin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>27</Day>
  </DateRevised>
  <Note>saponin consisting of a triterpene glycoside of glucose, rhamnose, xylose &amp; arabinose
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>SAPONINS (71-82)</PreviousIndexing>
   <PreviousIndexing>TRITERPENES (74-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006027</DescriptorUI>
     <DescriptorName>
      <String>Glycosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Pharmacol 15:816;1963</Source>
   <Source>Pathology 2(4):251;1970</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040053</ConceptUI>
    <ConceptName>
     <String>albitocin</String>
    </ConceptName>
    <RegistryNumber>39301-00-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070053</TermUI>
      <String>albitocin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000056</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>264 CP</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>11</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PIPERIDINES (73-76)</PreviousIndexing>
   <PreviousIndexing>ALLYL COMPOUNDS (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001549</DescriptorUI>
     <DescriptorName>
      <String>Benzamides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040061</ConceptUI>
    <ConceptName>
     <String>264 CP</String>
    </ConceptName>
    <CASN1Name>2-allyloxy-4-chloro-N-(2-piperidinoethyl)benzamide</CASN1Name>
    <RegistryNumber>25709-16-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070061</TermUI>
      <String>264 CP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000059</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ametohepazone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1994</Year>
   <Month>04</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CYCLOHEPTANES (71-85)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007093</DescriptorUI>
     <DescriptorName>
      <String>Imidazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040064</ConceptUI>
    <ConceptName>
     <String>ametohepazone</String>
    </ConceptName>
    <CASN1Name>2(1H)-Cycloheptimidazolone, 1-(2-(dimethylamino)ethyl)-</CASN1Name>
    <RegistryNumber>1019-19-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070064</TermUI>
      <String>ametohepazone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000060</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>9-(3-(aden-9-yl)propyl)-2-dimethylaminopurin-6-one</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ADENINE (72-75)</PreviousIndexing>
   <PreviousIndexing>*HYPOXANTHINES (72-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000225</DescriptorUI>
     <DescriptorName>
      <String>Adenine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040065</ConceptUI>
    <ConceptName>
     <String>9-(3-(aden-9-yl)propyl)-2-dimethylaminopurin-6-one</String>
    </ConceptName>
    <RegistryNumber>28077-96-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070065</TermUI>
      <String>9-(3-(aden-9-yl)propyl)-2-dimethylaminopurin-6-one</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000063</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>thiozamin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>10</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SULFONES (71-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013882</DescriptorUI>
     <DescriptorName>
      <String>Thiosemicarbazones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D007918</DescriptorUI>
     <DescriptorName>
      <String>Leprosy</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000188</QualifierUI>
     <QualifierName>
      <String>drug therapy</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040070</ConceptUI>
    <ConceptName>
     <String>thiozamin</String>
    </ConceptName>
    <CASN1Name>p-(p'-aminobenzenesulfonyl)benzaldehyde thiosemicarbazone</CASN1Name>
    <RegistryNumber>4094-36-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070070</TermUI>
      <String>thiozamin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000064</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>putreanine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>11</Month>
   <Day>10</Day>
  </DateRevised>
  <Frequency>9</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AMINO ACIDS (71-78)</PreviousIndexing>
   <PreviousIndexing>PROPIONATES (72-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000599</DescriptorUI>
     <DescriptorName>
      <String>Amino Acids, Diamino</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Seishin Shinkeigaku Zasshi 1979;81(2):141</Source>
   <Source>Tetrahedron 26:4307</Source>
   <Source>Vopr Neirokhir 6:48;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040071</ConceptUI>
    <ConceptName>
     <String>putreanine</String>
    </ConceptName>
    <CASN1Name>N-(4-aminobutyl)-3-aminopropionic acid</CASN1Name>
    <RegistryNumber>25887-39-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070071</TermUI>
      <String>putreanine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000066</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>aminocinnamonitrile</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>10</Month>
   <Day>29</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>NITRILES (71-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002934</DescriptorUI>
     <DescriptorName>
      <String>Cinnamates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040073</ConceptUI>
    <ConceptName>
     <String>aminocinnamonitrile</String>
    </ConceptName>
    <RegistryNumber>1823-99-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070073</TermUI>
      <String>aminocinnamonitrile</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005165</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,1-diphenyl-1-methoxy-3-benzylaminopropane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PROPYLAMINES (73-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001559</DescriptorUI>
     <DescriptorName>
      <String>Benzhydryl Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Wien Klin Wochenschr 85(27):503;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0046517</ConceptUI>
    <ConceptName>
     <String>1,1-diphenyl-1-methoxy-3-benzylaminopropane</String>
    </ConceptName>
    <CASN1Name>Benzenepropanamine, gamma-methoxy-gamma-phenyl-N-(phenylmethyl)-</CASN1Name>
    <RegistryNumber>14089-87-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0046517</Concept1UI>
     <Concept2UI>M0046519</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T076520</TermUI>
      <String>1,1-diphenyl-1-methoxy-3-benzylaminopropane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0046519</ConceptUI>
    <ConceptName>
     <String>St 4250</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0046517</Concept1UI>
     <Concept2UI>M0046519</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T076522</TermUI>
      <String>St 4250</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T076521</TermUI>
      <String>St-4250</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000077</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>amylosubtilin G10x</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>12</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>no other information available 1/1/79
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000681</DescriptorUI>
     <DescriptorName>
      <String>Amylases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ukr Biokhim Zh 51(4):374;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040076</ConceptUI>
    <ConceptName>
     <String>amylosubtilin G10x</String>
    </ConceptName>
    <RegistryNumber>EC 3.2.1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070076</TermUI>
      <String>amylosubtilin G10x</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C020669</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Glycerate dehydrogenase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>11</Month>
   <Day>21</Day>
  </DateRevised>
  <Frequency>34</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ALCOHOL OXIDOREDUCTASES (74-75)</PreviousIndexing>
   <PreviousIndexing>GLYCERIC ACIDS (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002237</DescriptorUI>
     <DescriptorName>
      <String>Carbohydrate Dehydrogenases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 566(1):21;1979</Source>
   <Source>J Nutr 104(8):1018;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0074625</ConceptUI>
    <ConceptName>
     <String>Glycerate dehydrogenase</String>
    </ConceptName>
    <RegistryNumber>EC 1.1.1.29</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>9028-37-9 (CRN)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T104628</TermUI>
      <String>Glycerate dehydrogenase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T202495</TermUI>
      <String>NADH-dependent hydroxypyruvate reductase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T202494</TermUI>
      <String>NDH-reductase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000096</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,5-anhydroglucitol-6-phosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>11</Month>
   <Day>18</Day>
  </DateRevised>
  <Frequency>7</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>SORBITAL/analogs (75-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006600</DescriptorUI>
     <DescriptorName>
      <String>Hexosephosphates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 242(1):89;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040097</ConceptUI>
    <ConceptName>
     <String>1,5-anhydroglucitol-6-phosphate</String>
    </ConceptName>
    <RegistryNumber>17659-59-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070097</TermUI>
      <String>1,5-anhydroglucitol-6-phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000100</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>aquayamycin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateRevised>
  <Frequency>7</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BENZANTHRACENES (71-81)</PreviousIndexing>
   <PreviousIndexing>BENZANTHRACENES (81-82)</PreviousIndexing>
   <PreviousIndexing>PYRANS (71-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000880</DescriptorUI>
     <DescriptorName>
      <String>Anthraquinones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040099</ConceptUI>
    <ConceptName>
     <String>aquayamycin</String>
    </ConceptName>
    <CASN1Name>9-(tetrahydro-4',5'-dihydroxy-6'-methyl-2'H-pyran-2'-yl)-3,4,4a,12b-tetrahydro-3,4a,8,12b-tetrahydroxy-3-methyl-benz(a)anthracene-1,7,12(2H)-trione</CASN1Name>
    <RegistryNumber>26055-63-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070099</TermUI>
      <String>aquayamycin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000102</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Arachin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1993</Year>
   <Month>06</Month>
   <Day>18</Day>
  </DateRevised>
  <Frequency>25</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010940</DescriptorUI>
     <DescriptorName>
      <String>Plant Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D010367</DescriptorUI>
     <DescriptorName>
      <String>Arachis</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Int J Peptide Protein Res 11(4):305;1978</Source>
   <Source>Int J Peptide Protein Res 1980;15(1):67</Source>
   <Source>Int J Peptide Protein Res 7:155;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040104</ConceptUI>
    <ConceptName>
     <String>Arachin</String>
    </ConceptName>
    <RegistryNumber>1398-00-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070105</TermUI>
      <String>Arachin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000105</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>arylid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1970</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SALICYLATES (70-75)</PreviousIndexing>
   <PreviousIndexing>ANILIDES (70-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012457</DescriptorUI>
     <DescriptorName>
      <String>Salicylamides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Pneumonol Pol 44(2):125;1976</Source>
   <Source>Pneumonol Pol 45(8):529;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040105</ConceptUI>
    <ConceptName>
     <String>arylid</String>
    </ConceptName>
    <CASN1Name>4',5-dichlorosalicylanilide</CASN1Name>
    <RegistryNumber>1147-98-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070106</TermUI>
      <String>arylid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000109</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>azabicyclane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1970</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1995</Year>
   <Month>08</Month>
   <Day>18</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BICYCLO COMPOUNDS (80-95)</PreviousIndexing>
   <PreviousIndexing>*BRIDGED CPDS (70-79)</PreviousIndexing>
   <PreviousIndexing>AZA CPDS (74-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D019086</DescriptorUI>
     <DescriptorName>
      <String>Bridged Bicyclo Compounds, Heterocyclic</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 19(1):184;1976</Source>
   <Source>Psychopharmacology 1979;66(1):19</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040114</ConceptUI>
    <ConceptName>
     <String>azabicyclane</String>
    </ConceptName>
    <RegistryNumber>21650-02-2</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0040114</Concept1UI>
     <Concept2UI>M0040113</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070115</TermUI>
      <String>azabicyclane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0040113</ConceptUI>
    <ConceptName>
     <String>azabicyclane citrate</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0040114</Concept1UI>
     <Concept2UI>M0040113</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T070114</TermUI>
      <String>azabicyclane citrate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008973</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>polyornithine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>07</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>RN given refers to (L)-isomer
  </Note>
  <Frequency>173</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ORNITHINE (74-75)</PreviousIndexing>
   <PreviousIndexing>ORNITHINE/analogs (79-80)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010455</DescriptorUI>
     <DescriptorName>
      <String>Peptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
    <PharmacologicalActionList>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D013501</DescriptorUI>
        <DescriptorName>
         <String>Surface-Active Agents</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
    </PharmacologicalActionList>
  <SourceList>
   <Source>Biopolymers 12(9):1997;1973</Source>
   <Source>J Biochem (Tokyo) 83(2):519;1978</Source>
   <Source>JNCI 58(5):1229;1977</Source>
   <Source>Microbiol Immunol 1979;23(11):1067</Source>
   <Source>Thromb Res 1980;17(3-4):481</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0053308</ConceptUI>
    <ConceptName>
     <String>polyornithine</String>
    </ConceptName>
    <RegistryNumber>25104-12-5</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>26445-53-4 ((DL)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>27378-49-0 (HBr(L)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>59166-85-7 (methyl sulfate(L)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0053308</Concept1UI>
     <Concept2UI>M0310542</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0053308</Concept1UI>
     <Concept2UI>M0310543</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0053308</Concept1UI>
     <Concept2UI>M0310541</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T083311</TermUI>
      <String>polyornithine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T083310</TermUI>
      <String>poly-L-ornithine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0310542</ConceptUI>
    <ConceptName>
     <String>polyornithine, hydrobromide, (L)-isomer</String>
    </ConceptName>
    <RegistryNumber>27378-49-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0053308</Concept1UI>
     <Concept2UI>M0310542</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T340542</TermUI>
      <String>polyornithine, hydrobromide, (L)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0310543</ConceptUI>
    <ConceptName>
     <String>polyornithine, methyl sulfate, (L)-isomer</String>
    </ConceptName>
    <RegistryNumber>59166-85-7</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0053308</Concept1UI>
     <Concept2UI>M0310543</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T340543</TermUI>
      <String>polyornithine, methyl sulfate, (L)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0310541</ConceptUI>
    <ConceptName>
     <String>polyornithine, (DL)-isomer</String>
    </ConceptName>
    <RegistryNumber>26445-53-4</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0053308</Concept1UI>
     <Concept2UI>M0310541</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T340541</TermUI>
      <String>polyornithine, (DL)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000115</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>jaligonic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1986</Year>
   <Month>07</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CARBOXYLIC ACIDS (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014315</DescriptorUI>
     <DescriptorName>
      <String>Triterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 36(3):326;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040119</ConceptUI>
    <ConceptName>
     <String>jaligonic acid</String>
    </ConceptName>
    <CASN1Name>(2 beta,3 beta,4 alpha,20 beta)-2,3,23-trihydroxy- olean-12-ene-28,29-dioic acid</CASN1Name>
    <RegistryNumber>51776-39-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070120</TermUI>
      <String>jaligonic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000146</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bactoprenol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>14</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013729</DescriptorUI>
     <DescriptorName>
      <String>Terpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem J 122(5):45;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040160</ConceptUI>
    <ConceptName>
     <String>bactoprenol</String>
    </ConceptName>
    <RegistryNumber>12777-41-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070161</TermUI>
      <String>bactoprenol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000150</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-azacyclononanone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>affects CNS activity
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CYCLOPARAFFINS (73-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001372</DescriptorUI>
     <DescriptorName>
      <String>Aza Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 60(7):1053;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040167</ConceptUI>
    <ConceptName>
     <String>2-azacyclononanone</String>
    </ConceptName>
    <RegistryNumber>935-30-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070168</TermUI>
      <String>2-azacyclononanone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "2">
  <SupplementalRecordUI>C414670</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>CN3OP regimen</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>10</Month>
   <Day>26</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>11</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>chemotherapy protocol consisting of the above compounds; used in the treatment of relapsed/refractory Hodgkin's lymphoma
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000971</DescriptorUI>
     <DescriptorName>
      <String>Antineoplastic Combined Chemotherapy Protocols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003520</DescriptorUI>
     <DescriptorName>
      <String>Cyclophosphamide</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008942</DescriptorUI>
     <DescriptorName>
      <String>Mitoxantrone</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011241</DescriptorUI>
     <DescriptorName>
      <String>Prednisone</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014750</DescriptorUI>
     <DescriptorName>
      <String>Vincristine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Med Oncol 2000 Aug;17(3):195-202</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0371565</ConceptUI>
    <ConceptName>
     <String>CN3OP regimen</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T427243</TermUI>
      <String>CN3OP regimen</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>10</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000156</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-acetylglucosaminuronic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ACETYLGLUCOSAMINE/*analogs (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014574</DescriptorUI>
     <DescriptorName>
      <String>Uronic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nature (New Biol)233(43):259;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040176</ConceptUI>
    <ConceptName>
     <String>N-acetylglucosaminuronic acid</String>
    </ConceptName>
    <CASN1Name>D-Glucuronic acid, 2-(acetylamino)-2-deoxy-</CASN1Name>
    <RegistryNumber>34047-66-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070177</TermUI>
      <String>N-acetylglucosaminuronic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000164</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-benzylindole</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>BENZYL COMPOUNDS (72-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007211</DescriptorUI>
     <DescriptorName>
      <String>Indoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Yakugaku Zasshi 91(8):818;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040180</ConceptUI>
    <ConceptName>
     <String>1-benzylindole</String>
    </ConceptName>
    <RegistryNumber>3377-71-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070181</TermUI>
      <String>1-benzylindole</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000165</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>EX-10-542A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PIPERIDINES (73-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003984</DescriptorUI>
     <DescriptorName>
      <String>Dibenzazepines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040181</ConceptUI>
    <ConceptName>
     <String>EX-10-542A</String>
    </ConceptName>
    <CASN1Name>5-benzyl-11-(4-n-methyl piperidylene)-5,6-dihydromorphanthridine hydrogen maleate</CASN1Name>
    <RegistryNumber>23239-59-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070182</TermUI>
      <String>EX-10-542A</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006505</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-aminobicyclo(2,2,2)octane-1-carboxylic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>07</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AMINO ACIDS (1982-2000)</PreviousIndexing>
   <PreviousIndexing>*BRIDGED COMPOUNDS (1974-1975)</PreviousIndexing>
   <PreviousIndexing>BICYCLO COMPOUNDS (1975-1981)</PreviousIndexing>
   <PreviousIndexing>CARBOXYLIC ACIDS (1974-1975)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000598</DescriptorUI>
     <DescriptorName>
      <String>Amino Acids, Cyclic</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Phys Chem 77(18):2191;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049109</ConceptUI>
    <ConceptName>
     <String>4-aminobicyclo(2,2,2)octane-1-carboxylic acid</String>
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    <RegistryNumber>13595-17-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079112</TermUI>
      <String>4-aminobicyclo(2,2,2)octane-1-carboxylic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000443</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-(4-chlorophenyl)-1-phenyl-2-propynylcarbamate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2019</Year>
   <Month>04</Month>
   <Day>08</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ALKYNES (72-76)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002219</DescriptorUI>
     <DescriptorName>
      <String>Carbamates</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Toxicology Applied Pharmacology 21(3):414;1972</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040562</ConceptUI>
    <ConceptName>
     <String>1-(4-chlorophenyl)-1-phenyl-2-propynylcarbamate</String>
    </ConceptName>
    <RegistryNumber>10473-70-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070564</TermUI>
      <String>1-(4-chlorophenyl)-1-phenyl-2-propynylcarbamate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T000954939</TermUI>
      <String>1-(4-chlorophenyl)-1-phenyl-2-propynyl carbamate</String>
      <DateCreated>
       <Year>2019</Year>
       <Month>04</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2019)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C072221</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>mitochondrial protein mtDBP-C, Xenopus</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1992</Year>
   <Month>02</Month>
   <Day>13</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>02</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>from Xenopus laevis; amino terminal amino acid sequence given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004268</DescriptorUI>
     <DescriptorName>
      <String>DNA-Binding Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029867</DescriptorUI>
     <DescriptorName>
      <String>Xenopus Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochimie 1991;73(5):615</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0195742</ConceptUI>
    <ConceptName>
     <String>mitochondrial protein mtDBP-C, Xenopus</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T225747</TermUI>
      <String>mitochondrial protein mtDBP-C, Xenopus</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T225746</TermUI>
      <String>mtDBP-C protein, Xenopus</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000459</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4,8-anhydro-3-deoxy-octulosonic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2019</Year>
   <Month>04</Month>
   <Day>08</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>SUGAR ACIDS (74-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007661</DescriptorUI>
     <DescriptorName>
      <String>Ketoses</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 247(12):3881;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040578</ConceptUI>
    <ConceptName>
     <String>4,8-anhydro-3-deoxy-octulosonic acid</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T000954941</TermUI>
      <String>4,8-anhydro-3-deoxy-octulosonic acid</String>
      <DateCreated>
       <Year>2019</Year>
       <Month>04</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2019)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C092223</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>HSP22.0 protein, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>03</Month>
   <Day>26</Day>
  </DateCreated>
  <DateRevised>
   <Year>2019</Year>
   <Month>04</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>isolated from Arabidopsis thaliana; 195 amino acid residues, MW 22 kDa; amino acid sequence has been determined; GenBank U11501
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PLANT PROTEINS (1995-2002)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006360</DescriptorUI>
     <DescriptorName>
      <String>Heat-Shock Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Plant Physiol 1995 Jan;107(1):287-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0243447</ConceptUI>
    <ConceptName>
     <String>HSP22.0 protein, Arabidopsis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T273451</TermUI>
      <String>HSP22.0 protein, Arabidopsis</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T273452</TermUI>
      <String>AtHSP22.0 protein, Arabidopsis</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T000954963</TermUI>
      <String>At4g10250 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2019</Year>
       <Month>04</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2019)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C060953</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>flavonol 2'-O-glucosyltransferase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1989</Year>
   <Month>10</Month>
   <Day>10</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>transfers glucose from UDPG to position 2' of partially methylated flavonols
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005964</DescriptorUI>
     <DescriptorName>
      <String>Glucosyltransferases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D044948</DescriptorUI>
     <DescriptorName>
      <String>Flavonols</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Biochem Cell Biol 1989;67(4-5):210</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0169109</ConceptUI>
    <ConceptName>
     <String>flavonol 2'-O-glucosyltransferase</String>
    </ConceptName>
    <RegistryNumber>EC 2.4.1-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T199114</TermUI>
      <String>flavonol 2'-O-glucosyltransferase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C414671</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-ethylestrone-3-O-sulfamate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>10</Month>
   <Day>26</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004970</DescriptorUI>
     <DescriptorName>
      <String>Estrone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Res 2000 Oct 1;60(19):5441-50</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0371566</ConceptUI>
    <ConceptName>
     <String>2-ethylestrone-3-O-sulfamate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T427246</TermUI>
      <String>2-ethylestrone-3-O-sulfamate</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>10</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T427247</TermUI>
      <String>2-EtEMATE</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>10</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000190</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>allerglobulin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>human gamma globulin preparation selected for their histamino-protectant potency; for drug therapy of asthma &amp; eczema
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005719</DescriptorUI>
     <DescriptorName>
      <String>gamma-Globulins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Lyon Med 226(20):891;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040218</ConceptUI>
    <ConceptName>
     <String>allerglobulin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070219</TermUI>
      <String>allerglobulin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C062190</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>brain-associated small-cell lung cancer antigen</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1990</Year>
   <Month>01</Month>
   <Day>30</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>02</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>124 kDa cell surface antigen, probably containing 3 epitopes
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000951</DescriptorUI>
     <DescriptorName>
      <String>Antigens, Neoplasm</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Histochem Cytochem 1990;38(1):51</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0172222</ConceptUI>
    <ConceptName>
     <String>brain-associated small-cell lung cancer antigen</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T202227</TermUI>
      <String>brain-associated small-cell lung cancer antigen</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T202226</TermUI>
      <String>BASCA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C026772</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>chloroacetyl coenzyme A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>10</Month>
   <Day>27</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>24</Day>
  </DateRevised>
  <Frequency>6</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ACETYL COENZYME A/*analogs (80-92)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000105</DescriptorUI>
     <DescriptorName>
      <String>Acetyl Coenzyme A</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 1980;95(4):1642</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0087600</ConceptUI>
    <ConceptName>
     <String>chloroacetyl coenzyme A</String>
    </ConceptName>
    <RegistryNumber>34201-15-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T117603</TermUI>
      <String>chloroacetyl coenzyme A</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T117602</TermUI>
      <String>coenzyme A, chloroacetyl</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T117601</TermUI>
      <String>chloroacetyl CoA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C033104</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-bromoacetyl coenzyme A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1982</Year>
   <Month>01</Month>
   <Day>18</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>24</Day>
  </DateRevised>
  <Frequency>4</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ACETYL COENZYME A/*analogs (82-92)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000105</DescriptorUI>
     <DescriptorName>
      <String>Acetyl Coenzyme A</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Methods Enzymol 1981;72:578</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0102887</ConceptUI>
    <ConceptName>
     <String>2-bromoacetyl coenzyme A</String>
    </ConceptName>
    <RegistryNumber>7303-38-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T132891</TermUI>
      <String>2-bromoacetyl coenzyme A</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T132890</TermUI>
      <String>coenzyme A, 2-bromoacetyl</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T132889</TermUI>
      <String>2-bromoacetyl-CoA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C101348</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>vinylacetyl-coenzyme A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>10</Month>
   <Day>21</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>24</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000105</DescriptorUI>
     <DescriptorName>
      <String>Acetyl Coenzyme A</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 1996 Sep 10;35(36):11710-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0265731</ConceptUI>
    <ConceptName>
     <String>vinylacetyl-coenzyme A</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T295736</TermUI>
      <String>vinylacetyl-coenzyme A</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T295735</TermUI>
      <String>vinylacetyl-CoA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T295734</TermUI>
      <String>coenzyme A, vinylacetyl-</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C414673</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,1,1,3,3,3-hexafluoropropane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>10</Month>
   <Day>26</Day>
  </DateCreated>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006845</DescriptorUI>
     <DescriptorName>
      <String>Hydrocarbons, Fluorinated</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Inhal Toxicol. 2000 Aug;12(8):751-63</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0371568</ConceptUI>
    <ConceptName>
     <String>1,1,1,3,3,3-hexafluoropropane</String>
    </ConceptName>
    <RegistryNumber>690-39-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T427250</TermUI>
      <String>1,1,1,3,3,3-hexafluoropropane</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>10</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T427251</TermUI>
      <String>1,1,1,3,3,3-HFP</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>10</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000630624</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>EC-7012</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2019</Year>
   <Month>04</Month>
   <Day>09</Day>
  </DateCreated>
  <DateRevised>
   <Year>2019</Year>
   <Month>04</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>indolocarbazole analog that have demonstrated a robust ability to inhibit a wide range of pro-survival kinases
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002227</DescriptorUI>
     <DescriptorName>
      <String>Carbazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007211</DescriptorUI>
     <DescriptorName>
      <String>Indoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Cancer Ther. 2018 Mar;17(3):614-624.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M000648477</ConceptUI>
    <ConceptName>
     <String>EC-7012</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T000954953</TermUI>
      <String>EC-7012</String>
      <DateCreated>
       <Year>2019</Year>
       <Month>04</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2019)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000212</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ammoniacal silver</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>11</Month>
   <Day>13</Day>
  </DateRevised>
  <Frequency>55</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>AMMONIA (75-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012834</DescriptorUI>
     <DescriptorName>
      <String>Silver</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Adv Neurol Sci (Tokyo) 15(4):927;1971</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040269</ConceptUI>
    <ConceptName>
     <String>ammoniacal silver</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070271</TermUI>
      <String>ammoniacal silver</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C053445</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>S-trichlorovinyl-N-acetylcysteine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1987</Year>
   <Month>09</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>24</Day>
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  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000111</DescriptorUI>
     <DescriptorName>
      <String>Acetylcysteine</String>
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    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Pharmacol 1987;36(17):2741</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0151432</ConceptUI>
    <ConceptName>
     <String>S-trichlorovinyl-N-acetylcysteine</String>
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    <RegistryNumber>111348-61-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T181437</TermUI>
      <String>S-trichlorovinyl-N-acetylcysteine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T181436</TermUI>
      <String>TCVAC</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T181435</TermUI>
      <String>N-acetyl-S-(trichlorovinyl)cysteine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C055229</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>S-(2-bromophenyl)mercapturic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1988</Year>
   <Month>04</Month>
   <Day>19</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>24</Day>
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000111</DescriptorUI>
     <DescriptorName>
      <String>Acetylcysteine</String>
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    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Anal Toxicol 1988;12(1):42</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0155594</ConceptUI>
    <ConceptName>
     <String>S-(2-bromophenyl)mercapturic acid</String>
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    <RegistryNumber>113276-92-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T185599</TermUI>
      <String>S-(2-bromophenyl)mercapturic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T185597</TermUI>
      <String>O-BPMA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T185598</TermUI>
      <String>ortho-bromophenylmercapturic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C055230</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>S-(3-bromophenyl)mercapturic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1988</Year>
   <Month>04</Month>
   <Day>19</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>24</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000111</DescriptorUI>
     <DescriptorName>
      <String>Acetylcysteine</String>
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    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
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  <SourceList>
   <Source>J Anal Toxicol 1988;12(1):42</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0155597</ConceptUI>
    <ConceptName>
     <String>S-(3-bromophenyl)mercapturic acid</String>
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    <RegistryNumber>113276-93-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T185602</TermUI>
      <String>S-(3-bromophenyl)mercapturic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T185601</TermUI>
      <String>meta-bromophenylmercapturic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T185600</TermUI>
      <String>M-BPMA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
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  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000231</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>azacrin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>27</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PYRIDINES (72-82)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011804</DescriptorUI>
     <DescriptorName>
      <String>Quinolines</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Toxicol Appl Pharmacol 21(4):482;1972</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040299</ConceptUI>
    <ConceptName>
     <String>azacrin</String>
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    <CASN1Name>2-methoxy-7-chloro-10-(4-(diethylamino-1-methyl)butylamino)pyrido(3,2-b)quinoline</CASN1Name>
    <RegistryNumber>34957-04-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070301</TermUI>
      <String>azacrin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000249</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>benzylsuccinic acid</String>
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  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>01</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>inhibitor of carboxypeptidase A
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  <Frequency>19</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>BENZYL COMPOUNDS (72-75)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013386</DescriptorUI>
     <DescriptorName>
      <String>Succinates</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 247(2):606;1972</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040318</ConceptUI>
    <ConceptName>
     <String>benzylsuccinic acid</String>
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    <RegistryNumber>884-33-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070320</TermUI>
      <String>benzylsuccinic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
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 </SupplementalRecord>
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  <SupplementalRecordUI>C000630626</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Gm12185 protein, mouse</String>
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  <DateCreated>
   <Year>2019</Year>
   <Month>04</Month>
   <Day>09</Day>
  </DateCreated>
  <DateRevised>
   <Year>2019</Year>
   <Month>04</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>RefSeq NM_001045540
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  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D020558</DescriptorUI>
     <DescriptorName>
      <String>GTP Phosphohydrolases</String>
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  <SourceList>
   <Source>Nat Commun. 2019 Mar 15;10(1):1233.</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M000648480</ConceptUI>
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     <String>Gm12185 protein, mouse</String>
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    <RegistryNumber>EC 3.6.1.-</RegistryNumber>
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     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T000954960</TermUI>
      <String>Gm12185 protein, mouse</String>
      <DateCreated>
       <Year>2019</Year>
       <Month>04</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2019)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T000954962</TermUI>
      <String>predicted gene 12185 protein, mouse</String>
      <DateCreated>
       <Year>2019</Year>
       <Month>04</Month>
       <Day>09</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2019)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T000954961</TermUI>
      <String>Irgb2b1 protein, mouse</String>
      <DateCreated>
       <Year>2019</Year>
       <Month>04</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2019)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000261</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-acetylethyleneimine</String>
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  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <Frequency>7</Frequency>
  <HeadingMappedToList>
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    <DescriptorReferredTo>
     <DescriptorUI>*D001389</DescriptorUI>
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  <SourceList>
   <Source>Lab Pract 24(6):404;1975</Source>
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   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040333</ConceptUI>
    <ConceptName>
     <String>N-acetylethyleneimine</String>
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    <RegistryNumber>460-07-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070335</TermUI>
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       <ThesaurusID>NLM (1975)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C080714</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>iodonium dicollidine</String>
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  <DateCreated>
   <Year>1993</Year>
   <Month>05</Month>
   <Day>13</Day>
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  <DateRevised>
   <Year>2004</Year>
   <Month>02</Month>
   <Day>02</Day>
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  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009861</DescriptorUI>
     <DescriptorName>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011725</DescriptorUI>
     <DescriptorName>
      <String>Pyridines</String>
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  <SourceList>
   <Source>Carbohydr Res 1993 Mar 17;241:153-64</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0215542</ConceptUI>
    <ConceptName>
     <String>iodonium dicollidine</String>
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    <RegistryNumber>69417-67-0</RegistryNumber>
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      <TermUI>T245547</TermUI>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T245546</TermUI>
      <String>iodonium di-sym-collidine</String>
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       <ThesaurusID>NLM (1993)</ThesaurusID>
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   <Concept PreferredConceptYN="N">
    <ConceptUI>M0441153</ConceptUI>
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     <String>bis(collidine)iodine hexafluorophosphate</String>
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      <TermUI>T524953</TermUI>
      <String>bis(collidine)iodine hexafluorophosphate</String>
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       <Year>2002</Year>
       <Month>10</Month>
       <Day>31</Day>
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      <ThesaurusIDlist>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T524954</TermUI>
      <String>BCIH cpd</String>
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       <Year>2002</Year>
       <Month>10</Month>
       <Day>31</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
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  <DateCreated>
   <Year>2011</Year>
   <Month>01</Month>
   <Day>12</Day>
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  <DateRevised>
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   <Month>04</Month>
   <Day>09</Day>
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  <Note>structure in first source
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  <SourceList>
   <Source>Acta Crystallogr C. 2010 Dec;66(Pt 12):o627-30</Source>
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      <TermUI>T783702</TermUI>
      <String>2-(((dodecylsulfanyl)carbonothioyl)sulfanyl)-2-methylpropanoic acid</String>
      <DateCreated>
       <Year>2011</Year>
       <Month>01</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2011)</ThesaurusID>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T783703</TermUI>
      <String>2-DCS-MPA cpd</String>
      <DateCreated>
       <Year>2011</Year>
       <Month>01</Month>
       <Day>12</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2011)</ThesaurusID>
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   <Concept PreferredConceptYN="N">
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      <String>2-(dodecylthiocarbonothioylthio)-2-methylpropionic acid</String>
      <DateCreated>
       <Year>2019</Year>
       <Month>04</Month>
       <Day>09</Day>
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      <ThesaurusIDlist>
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       <Month>11</Month>
       <Day>23</Day>
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       <Month>11</Month>
       <Day>23</Day>
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   <Month>04</Month>
   <Day>09</Day>
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   <Year>2019</Year>
   <Month>04</Month>
   <Day>09</Day>
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       <Day>09</Day>
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       <Month>04</Month>
       <Day>09</Day>
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  <SupplementalRecordUI>C082714</SupplementalRecordUI>
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   <String>glucagon-like peptide 1 (7-36), Ala(36)-</String>
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  <DateCreated>
   <Year>1993</Year>
   <Month>09</Month>
   <Day>17</Day>
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  <DateRevised>
   <Year>2006</Year>
   <Month>08</Month>
   <Day>04</Day>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005934</DescriptorUI>
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      <String>Glucagon</String>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010446</DescriptorUI>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D052216</DescriptorUI>
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   <Source>Electrophoresis 1993 May-Jun;14(5-6):486-91</Source>
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      <TermUI>T250311</TermUI>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T250310</TermUI>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T250308</TermUI>
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       <ThesaurusID>NLM (1993)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T250309</TermUI>
      <String>Ala(36)-GLP-1 (7-36)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000414</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-chloro-3-tert-butyl-2'-nitrososalicylanilide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SALICYLAMIDES (75-79)</PreviousIndexing>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012458</DescriptorUI>
     <DescriptorName>
      <String>Salicylanilides</String>
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  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040519</ConceptUI>
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     <String>5-chloro-3-tert-butyl-2'-nitrososalicylanilide</String>
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    <RegistryNumber>21889-00-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070521</TermUI>
      <String>5-chloro-3-tert-butyl-2'-nitrososalicylanilide</String>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000415</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2'-chloro-2'-cyanoethyl-1-thio-beta-D-galactopyranoside</String>
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  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>11</Month>
   <Day>09</Day>
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  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*GLYCOSIDES (72-74)</PreviousIndexing>
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   <PreviousIndexing>*THIOGLYCOSIDES (74-75)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009150</DescriptorUI>
     <DescriptorName>
      <String>Mustard Compounds</String>
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   <Source>Nature (New Biology) 234(49):183;1971</Source>
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    <CASN1Name>Propanenitrile, 2-chloro-3-(beta-D-galactopyranosylthio)-</CASN1Name>
    <RegistryNumber>36373-29-2</RegistryNumber>
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     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070522</TermUI>
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   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000417</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Ro 5-5807</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BENZAZEPINES (71-74)</PreviousIndexing>
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     <DescriptorUI>*D001570</DescriptorUI>
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      <String>Benzodiazepinones</String>
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   <Concept PreferredConceptYN="Y">
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    <CASN1Name>7-chloro-2,3-dihydro-N-methyl-2-oxo-5- phenyl-lH-1-benzodiazepin-1-acetamide</CASN1Name>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C551952</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-(4-(4-bromo-1-methyl-1H-pyrazole-3-carbonyl)piperazin-1-yl)-1-(4-fluorophenyl)ethanone</String>
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  <DateCreated>
   <Year>2010</Year>
   <Month>09</Month>
   <Day>07</Day>
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  <DateRevised>
   <Year>2010</Year>
   <Month>09</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>a 5-HT2A receptor antagonist and anti-insomnia agent; structure in first source
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010879</DescriptorUI>
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     <DescriptorUI>*D011720</DescriptorUI>
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   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D044402</DescriptorUI>
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   <Source>J Med Chem 2010 Aug 12;53(15):5696-706</Source>
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   <Year>2004</Year>
   <Month>05</Month>
   <Day>25</Day>
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   <Year>2006</Year>
   <Month>08</Month>
   <Day>04</Day>
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       <Month>05</Month>
       <Day>25</Day>
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       <Year>2004</Year>
       <Month>05</Month>
       <Day>25</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T588024</TermUI>
      <String>pGlu-GLP-1</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>05</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T588023</TermUI>
      <String>N-pyroglutamyl-GLP-1</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>05</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C082119</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>NGR1 protein, S cerevisiae</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1993</Year>
   <Month>08</Month>
   <Day>10</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>11</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>involved in growth &amp; developmental regulation; amino acid sequence in first source
  </Note>
  <Frequency>19</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*FUNGAL PROTEINS (93-98)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D016601</DescriptorUI>
     <DescriptorName>
      <String>RNA-Binding Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029701</DescriptorUI>
     <DescriptorName>
      <String>Saccharomyces cerevisiae Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 1993 Jul 15;268(20):15080-7</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0218903</ConceptUI>
    <ConceptName>
     <String>NGR1 protein, S cerevisiae</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T456838</TermUI>
      <String>NGR1 protein, S cerevisiae</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>08</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T456840</TermUI>
      <String>RNA-binding protein 1, S cerevisiae</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>08</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T686467</TermUI>
      <String>RBP1 protein, S cerevisiae</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>11</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T456839</TermUI>
      <String>negative growth regulatory protein, S cerevisiae</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>08</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C515877</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>BAL 19403</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>01</Month>
   <Day>03</Day>
  </DateCreated>
  <Note>an antimicrobial agent
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D018942</DescriptorUI>
     <DescriptorName>
      <String>Macrolides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>IDrugs 2006 Nov;9(11):771-3</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0505217</ConceptUI>
    <ConceptName>
     <String>BAL 19403</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T688733</TermUI>
      <String>BAL 19403</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>01</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T688735</TermUI>
      <String>BAL19403</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>01</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T688734</TermUI>
      <String>BAL-19403</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>01</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C113291</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-acetamido-2,6-dideoxy-glucose (N-acetyl-quinovosamine)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>07</Month>
   <Day>28</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateRevised>
  <Note>a neutral Proteus penneri O-antigen
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000117</DescriptorUI>
     <DescriptorName>
      <String>Acetylglucosamine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Biochem 1998 May 1;253(3):730-3</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0292645</ConceptUI>
    <ConceptName>
     <String>2-acetamido-2,6-dideoxy-glucose (N-acetyl-quinovosamine)</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T322650</TermUI>
      <String>2-acetamido-2,6-dideoxy-glucose (N-acetyl-quinovosamine)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T322649</TermUI>
      <String>L-QuiNAc</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T322648</TermUI>
      <String>2-acetamido-2,6-dideoxy-L-glucose (N-acetyl-L-quinovosamine)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C114468</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>uridine 5'-(2-trifluoroacetamido-2-deoxyglucopyranosyl diphosphate)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000117</DescriptorUI>
     <DescriptorName>
      <String>Acetylglucosamine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014530</DescriptorUI>
     <DescriptorName>
      <String>Uridine Diphosphate</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Carbohydr Res 1998 Jan;306(1-2):127-36</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0295187</ConceptUI>
    <ConceptName>
     <String>uridine 5'-(2-trifluoroacetamido-2-deoxyglucopyranosyl diphosphate)</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T325192</TermUI>
      <String>uridine 5'-(2-trifluoroacetamido-2-deoxyglucopyranosyl diphosphate)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T325191</TermUI>
      <String>UDP-N-trifluoroacetylglucosamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T325190</TermUI>
      <String>UDP-GlcNAc-F(3)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C474232</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>LiF-Mg,Cu,P</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>05</Month>
   <Day>28</Day>
  </DateCreated>
  <Note>LiF:Mg,Cu,P (GR-200 P)
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003300</DescriptorUI>
     <DescriptorName>
      <String>Copper</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008274</DescriptorUI>
     <DescriptorName>
      <String>Magnesium</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010758</DescriptorUI>
     <DescriptorName>
      <String>Phosphorus</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D018020</DescriptorUI>
     <DescriptorName>
      <String>Lithium Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Health Phys 2003 Apr;84(4):483-91</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0449837</ConceptUI>
    <ConceptName>
     <String>LiF-Mg,Cu,P</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T541756</TermUI>
      <String>LiF-Mg,Cu,P</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>05</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T541757</TermUI>
      <String>GR-200 P</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>05</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C505724</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Yip3 protein, S cerevisiae</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>11</Month>
   <Day>30</Day>
  </DateCreated>
  <Note>a GDI displacement factor for Rab proteins; involved in vesicular transport between the ER and Golgi; GenBank X97400
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029701</DescriptorUI>
     <DescriptorName>
      <String>Saccharomyces cerevisiae Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D033921</DescriptorUI>
     <DescriptorName>
      <String>Vesicular Transport Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eukaryot Cell 2005 Jul;4(7):1166-74</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0492199</ConceptUI>
    <ConceptName>
     <String>Yip3 protein, S cerevisiae</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T660483</TermUI>
      <String>Yip3 protein, S cerevisiae</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>11</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000455</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-chlorouridine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>4</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*URIDINE (72-75)</PreviousIndexing>
   <PreviousIndexing>CHLORINE (72-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014529</DescriptorUI>
     <DescriptorName>
      <String>Uridine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Proc Natl Acad Sci 68(9):2008;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040576</ConceptUI>
    <ConceptName>
     <String>5-chlorouridine</String>
    </ConceptName>
    <RegistryNumber>2880-89-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070578</TermUI>
      <String>5-chlorouridine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000461</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-bromoacetazolamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ACETAZOLAMIDE (72-75)</PreviousIndexing>
   <PreviousIndexing>BROMINE (72-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000086</DescriptorUI>
     <DescriptorName>
      <String>Acetazolamide</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 247(12):3810;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040579</ConceptUI>
    <ConceptName>
     <String>N-bromoacetazolamide</String>
    </ConceptName>
    <RegistryNumber>17124-38-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070581</TermUI>
      <String>N-bromoacetazolamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C505725</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Rtn1 protein, S cerevisiae</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>11</Month>
   <Day>30</Day>
  </DateCreated>
  <Note>ga reticulon protein; GenBank AY164798
  </Note>
  <Frequency>14</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029701</DescriptorUI>
     <DescriptorName>
      <String>Saccharomyces cerevisiae Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eukaryot Cell 2005 Jul;4(7):1166-74</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0492200</ConceptUI>
    <ConceptName>
     <String>Rtn1 protein, S cerevisiae</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T660484</TermUI>
      <String>Rtn1 protein, S cerevisiae</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>11</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000630635</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>STP7 protein, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2019</Year>
   <Month>04</Month>
   <Day>09</Day>
  </DateCreated>
  <DateRevised>
   <Year>2019</Year>
   <Month>04</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>RefSeq NM_116436.6
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009004</DescriptorUI>
     <DescriptorName>
      <String>Monosaccharide Transport Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Plant Physiol. 2018 Mar;176(3):2330-2350.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M000648489</ConceptUI>
    <ConceptName>
     <String>STP7 protein, Arabidopsis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T000954982</TermUI>
      <String>STP7 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2019</Year>
       <Month>04</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2019)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T000954984</TermUI>
      <String>hexose transporter 7 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2019</Year>
       <Month>04</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2019)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T000954985</TermUI>
      <String>At4g02050 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2019</Year>
       <Month>04</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2019)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T000954983</TermUI>
      <String>sugar transport protein 7, Arabidopsis</String>
      <DateCreated>
       <Year>2019</Year>
       <Month>04</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2019)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000467</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>chelidimerine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>06</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PHENANTHRIDINES (72-81)</PreviousIndexing>
   <PreviousIndexing>ACETONE (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000470</DescriptorUI>
     <DescriptorName>
      <String>Alkaloids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Natural Prod 35(1):87;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040584</ConceptUI>
    <ConceptName>
     <String>chelidimerine</String>
    </ConceptName>
    <CASN1Name>1,3-bis(11-hydrosanquinarinyl)acetone</CASN1Name>
    <RegistryNumber>39110-99-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070586</TermUI>
      <String>chelidimerine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C505727</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>poly(epsilon-caprolactone-co-lactide)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>11</Month>
   <Day>30</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>28</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011091</DescriptorUI>
     <DescriptorName>
      <String>Polyesters</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biomater Sci Polym Ed 2005;16(8):1009-21</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0492202</ConceptUI>
    <ConceptName>
     <String>poly(epsilon-caprolactone-co-lactide)</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0492202</Concept1UI>
     <Concept2UI>M0492203</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T660487</TermUI>
      <String>poly(epsilon-caprolactone-co-lactide)</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>11</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0492203</ConceptUI>
    <ConceptName>
     <String>star-poly(epsilon-caprolactone-co-D,L-lactide)</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0492202</Concept1UI>
     <Concept2UI>M0492203</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T660488</TermUI>
      <String>star-poly(epsilon-caprolactone-co-D,L-lactide)</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>11</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000480</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Cibacron Blue-amylose</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>01</Month>
   <Day>05</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AMYLOSE (74-75)</PreviousIndexing>
   <PreviousIndexing>*ANTHRACENES (74-83)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000688</DescriptorUI>
     <DescriptorName>
      <String>Amylose</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014227</DescriptorUI>
     <DescriptorName>
      <String>Triazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040614</ConceptUI>
    <ConceptName>
     <String>Cibacron Blue-amylose</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070616</TermUI>
      <String>Cibacron Blue-amylose</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C515879</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>FcRH3 protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>01</Month>
   <Day>03</Day>
  </DateCreated>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011961</DescriptorUI>
     <DescriptorName>
      <String>Receptors, Fc</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Immunol 2006 Nov 15;177(10):6815-23</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0505219</ConceptUI>
    <ConceptName>
     <String>FcRH3 protein, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T688739</TermUI>
      <String>FcRH3 protein, mouse</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>01</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T688741</TermUI>
      <String>Fc receptor-like 5 protein, mouse</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>01</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T688740</TermUI>
      <String>FCRL5 protein, mouse</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>01</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000483</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cinnabarinic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1970</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>28</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CARBOXYLIC ACIDS (72-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010078</DescriptorUI>
     <DescriptorName>
      <String>Oxazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem J 161(3):551;1977</Source>
   <Source>Biochem Pharmacol 25(6):643;1976</Source>
   <Source>Hoppe-Seyler's Z Physiol Chem 358:1161;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040617</ConceptUI>
    <ConceptName>
     <String>cinnabarinic acid</String>
    </ConceptName>
    <CASN1Name>2-amino-3H-phenoxazin-one-1,9-dicarboxylic acid</CASN1Name>
    <RegistryNumber>606-59-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070619</TermUI>
      <String>cinnabarinic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C505729</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SLH1 protein, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>11</Month>
   <Day>30</Day>
  </DateCreated>
  <Note>a disease resistance protein; GenBank AB188827
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004268</DescriptorUI>
     <DescriptorName>
      <String>DNA-Binding Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Plant J 2005 Sep;43(6):873-88</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0492205</ConceptUI>
    <ConceptName>
     <String>SLH1 protein, Arabidopsis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T660491</TermUI>
      <String>SLH1 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>11</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T660492</TermUI>
      <String>sensitive to low humidity 1 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>11</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000509</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>corchoroside B</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>17</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CARDANOLIDES (72-77)</PreviousIndexing>
   <PreviousIndexing>GLYCOSIDES (72-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002298</DescriptorUI>
     <DescriptorName>
      <String>Cardenolides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D002301</DescriptorUI>
     <DescriptorName>
      <String>Cardiac Glycosides</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Helv Chim Acta 54(7):1960;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040665</ConceptUI>
    <ConceptName>
     <String>corchoroside B</String>
    </ConceptName>
    <RegistryNumber>35536-76-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070667</TermUI>
      <String>corchoroside B</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C515880</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3'-demethylnobiletin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>01</Month>
   <Day>03</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D047309</DescriptorUI>
     <DescriptorName>
      <String>Flavones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biomed Chromatogr 2006 Nov;20(11):1206-15</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0505220</ConceptUI>
    <ConceptName>
     <String>3'-demethylnobiletin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T688742</TermUI>
      <String>3'-demethylnobiletin</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>01</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C036027</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>L-fuculosephosphate aldolase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1982</Year>
   <Month>11</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>10</Month>
   <Day>31</Day>
  </DateRevised>
  <Frequency>24</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000446</DescriptorUI>
     <DescriptorName>
      <String>Aldehyde-Lyases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Bacteriol 1982;152(1):120</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0110012</ConceptUI>
    <ConceptName>
     <String>L-fuculosephosphate aldolase</String>
    </ConceptName>
    <RegistryNumber>EC 4.1.2.17</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>9024-54-8 (CRN)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T140016</TermUI>
      <String>L-fuculosephosphate aldolase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T140015</TermUI>
      <String>L-fuculose-1-phosphate aldolase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000521</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cutin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>01</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>Cutin is meshwork of polymerized cross-esterified hydroxy fatty acids found in plant cuticles
  </Note>
  <Frequency>278</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*LIPIDS (71-78)</PreviousIndexing>
   <PreviousIndexing>FATTY ACIDS (71-75)</PreviousIndexing>
   <PreviousIndexing>HYDROXY ACIDS (71-82)</PreviousIndexing>
   <PreviousIndexing>POLYMERS (71-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008563</DescriptorUI>
     <DescriptorName>
      <String>Membrane Lipids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Biochem Biophys 190(1):17;1978</Source>
   <Source>Biochem Soc 5(5):1263;1977</Source>
   <Source>J Agr Food Chem 26(5):1263;1978</Source>
   <Source>J Bacteriol 133(2):942;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040694</ConceptUI>
    <ConceptName>
     <String>cutin</String>
    </ConceptName>
    <CASN1Name>Cutin</CASN1Name>
    <RegistryNumber>54990-88-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070696</TermUI>
      <String>cutin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C515881</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4'-demethylnobiletin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>01</Month>
   <Day>03</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>7</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D047309</DescriptorUI>
     <DescriptorName>
      <String>Flavones</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biomed Chromatogr 2006 Nov;20(11):1206-15</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0505221</ConceptUI>
    <ConceptName>
     <String>4'-demethylnobiletin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T688743</TermUI>
      <String>4'-demethylnobiletin</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>01</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005661</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>beta,beta-difluoroamphetamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>07</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>RN given refers to parent cpd; structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AMPHETAMINE (74-75)</PreviousIndexing>
   <PreviousIndexing>AMPHETAMINE/*analogs (75-78)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000662</DescriptorUI>
     <DescriptorName>
      <String>Amphetamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Pharmacol 22(16):2059;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0047331</ConceptUI>
    <ConceptName>
     <String>beta,beta-difluoroamphetamine</String>
    </ConceptName>
    <RegistryNumber>39038-72-7</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>35651-89-9 (HCl(+-)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0047331</Concept1UI>
     <Concept2UI>M0309192</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T077334</TermUI>
      <String>beta,beta-difluoroamphetamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0309192</ConceptUI>
    <ConceptName>
     <String>beta,beta-difluoroamphetamine, hydrochloride(+-)-isomer</String>
    </ConceptName>
    <RegistryNumber>35651-89-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0047331</Concept1UI>
     <Concept2UI>M0309192</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T339192</TermUI>
      <String>beta,beta-difluoroamphetamine, hydrochloride(+-)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C049958</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6-O-(3-hydroxy-2-docosylhexacosanoyl)muramyl dipeptide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1986</Year>
   <Month>10</Month>
   <Day>14</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000119</DescriptorUI>
     <DescriptorName>
      <String>Acetylmuramyl-Alanyl-Isoglutamine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Infect Immunol 1986;53(3):517</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0142913</ConceptUI>
    <ConceptName>
     <String>6-O-(3-hydroxy-2-docosylhexacosanoyl)muramyl dipeptide</String>
    </ConceptName>
    <RegistryNumber>81649-55-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T172918</TermUI>
      <String>6-O-(3-hydroxy-2-docosylhexacosanoyl)muramyl dipeptide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1986)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T172917</TermUI>
      <String>BH48-MDP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1986)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T172916</TermUI>
      <String>6-O-(3-hydroxy-2-docosylhexacosanoyl)-N-acetylmuramyl-L-alanyl-D-isoglutamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1986)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C060520</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-palmitoylmuramyl-alanyl-isoglutamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1989</Year>
   <Month>08</Month>
   <Day>30</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000119</DescriptorUI>
     <DescriptorName>
      <String>Acetylmuramyl-Alanyl-Isoglutamine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Jpn J Exp Med 1988;58(6):243</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0168121</ConceptUI>
    <ConceptName>
     <String>N-palmitoylmuramyl-alanyl-isoglutamine</String>
    </ConceptName>
    <RegistryNumber>78408-99-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T198126</TermUI>
      <String>N-palmitoylmuramyl-alanyl-isoglutamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T198125</TermUI>
      <String>NP-MDP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T198124</TermUI>
      <String>N-PA-Mur-Ala-isoGln</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000857</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>deca-glycerol deca-oleate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateRevised>
  <Note>polyglycerol ester
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*GLYCEROL (72-75)</PreviousIndexing>
   <PreviousIndexing>*POLYMERS (72-75)</PreviousIndexing>
   <PreviousIndexing>OLEIC ACIDS (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005990</DescriptorUI>
     <DescriptorName>
      <String>Glycerol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Toxicol Appl Pharmacol 20(3):327;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040814</ConceptUI>
    <ConceptName>
     <String>deca-glycerol deca-oleate</String>
    </ConceptName>
    <CASN1Name>9-Octadecenoic acid (Z)-, decaester with decaglycerol</CASN1Name>
    <RegistryNumber>11094-60-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0040814</Concept1UI>
     <Concept2UI>M0040813</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070816</TermUI>
      <String>deca-glycerol deca-oleate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0040813</ConceptUI>
    <ConceptName>
     <String>Drewpol</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0040814</Concept1UI>
     <Concept2UI>M0040813</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="TRD"  RecordPreferredTermYN="N">
      <TermUI>T070815</TermUI>
      <String>Drewpol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000539</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cyclonerodiol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>7</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CYCLOPENTANES (75-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012717</DescriptorUI>
     <DescriptorName>
      <String>Sesquiterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040707</ConceptUI>
    <ConceptName>
     <String>cyclonerodiol</String>
    </ConceptName>
    <RegistryNumber>28834-06-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070709</TermUI>
      <String>cyclonerodiol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000552</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>rubrosterone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ANDROSTANES (72-80)</PreviousIndexing>
   <PreviousIndexing>HYDROXYSTEROIDS (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000732</DescriptorUI>
     <DescriptorName>
      <String>Androstanols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015068</DescriptorUI>
     <DescriptorName>
      <String>17-Ketosteroids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D007447</DescriptorUI>
     <DescriptorName>
      <String>Invertebrate Hormones</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Pharm Soc Jpn 91(9):916;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040723</ConceptUI>
    <ConceptName>
     <String>rubrosterone</String>
    </ConceptName>
    <RegistryNumber>19466-41-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070725</TermUI>
      <String>rubrosterone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000553</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>9-(3-(cytos-1-yl)propyl)-2-dimethylaminopurin-6-one</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1970</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>10</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CYTOSINE (70-75)</PreviousIndexing>
   <PreviousIndexing>*PURINONES (70-82)</PreviousIndexing>
   <PreviousIndexing>DIMETHYLAMINES (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003596</DescriptorUI>
     <DescriptorName>
      <String>Cytosine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040724</ConceptUI>
    <ConceptName>
     <String>9-(3-(cytos-1-yl)propyl)-2-dimethylaminopurin-6-one</String>
    </ConceptName>
    <RegistryNumber>28098-44-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070726</TermUI>
      <String>9-(3-(cytos-1-yl)propyl)-2-dimethylaminopurin-6-one</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000578</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>exo-bicyclo(3.1.0)hexane-6-carboxylic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>BICYCLO COMPOUNDS (75-76)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003509</DescriptorUI>
     <DescriptorName>
      <String>Cyclohexanecarboxylic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 15(4):424;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040731</ConceptUI>
    <ConceptName>
     <String>exo-bicyclo(3.1.0)hexane-6-carboxylic acid</String>
    </ConceptName>
    <RegistryNumber>4971-24-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070733</TermUI>
      <String>exo-bicyclo(3.1.0)hexane-6-carboxylic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C054064</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-acetylmuramyl-threonyl-isoglutamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1987</Year>
   <Month>12</Month>
   <Day>11</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateRevised>
  <Frequency>7</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000119</DescriptorUI>
     <DescriptorName>
      <String>Acetylmuramyl-Alanyl-Isoglutamine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Vaccine 1987;5(3):223</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0152879</ConceptUI>
    <ConceptName>
     <String>N-acetylmuramyl-threonyl-isoglutamine</String>
    </ConceptName>
    <RegistryNumber>66112-59-2</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0152879</Concept1UI>
     <Concept2UI>M0152877</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T182884</TermUI>
      <String>N-acetylmuramyl-threonyl-isoglutamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T182883</TermUI>
      <String>THR-MDP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0152877</ConceptUI>
    <ConceptName>
     <String>SAF-m</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0152879</Concept1UI>
     <Concept2UI>M0152877</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T182882</TermUI>
      <String>SAF-m</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000668</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-carboxymethyluridine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>08</Month>
   <Day>12</Day>
  </DateRevised>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*URIDINE (72-75)</PreviousIndexing>
   <PreviousIndexing>CARBOXYLIC ACIDS (72-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014529</DescriptorUI>
     <DescriptorName>
      <String>Uridine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 262(3):275;1972</Source>
   <Source>Biochim Biophys Acta 518:530;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040758</ConceptUI>
    <ConceptName>
     <String>5-carboxymethyluridine</String>
    </ConceptName>
    <RegistryNumber>20964-06-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070760</TermUI>
      <String>5-carboxymethyluridine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C068282</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-(2-O-(2-acetamido-1,2,3,5-tetradeoxy-1,5-iminoglucitol-3-yl)lactoyl)alanyl-isoglutamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1991</Year>
   <Month>05</Month>
   <Day>13</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000119</DescriptorUI>
     <DescriptorName>
      <String>Acetylmuramyl-Alanyl-Isoglutamine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Carbohydr Res 1990;208:267</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0186814</ConceptUI>
    <ConceptName>
     <String>N-(2-O-(2-acetamido-1,2,3,5-tetradeoxy-1,5-iminoglucitol-3-yl)lactoyl)alanyl-isoglutamine</String>
    </ConceptName>
    <RegistryNumber>131432-97-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T216819</TermUI>
      <String>N-(2-O-(2-acetamido-1,2,3,5-tetradeoxy-1,5-iminoglucitol-3-yl)lactoyl)alanyl-isoglutamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T216818</TermUI>
      <String>N-(2-O-(2-acetamido-1,2,3,5-tetradeoxy-1,5-imino-D-glucitol-3-yl)-D-lactoyl)-L-alanyl-D-isoglutamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T216817</TermUI>
      <String>ATIGLAI</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000899</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-hydroxycadaverine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AMINO ALCOHOLS (74-75)</PreviousIndexing>
   <PreviousIndexing>*POLYAMINES (72-74)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002103</DescriptorUI>
     <DescriptorName>
      <String>Cadaverine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Enzymologia 42(4):303;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040872</ConceptUI>
    <ConceptName>
     <String>3-hydroxycadaverine</String>
    </ConceptName>
    <RegistryNumber>38595-00-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070874</TermUI>
      <String>3-hydroxycadaverine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T070873</TermUI>
      <String>1,5-diamino-3-pentanol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000674</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>datiscoside</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>10</Month>
   <Day>07</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CHOLESTANES (72-73)</PreviousIndexing>
   <PreviousIndexing>*CHOLESTENES (73-74)</PreviousIndexing>
   <PreviousIndexing>*GLYCOSIDES (72-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002775</DescriptorUI>
     <DescriptorName>
      <String>Cholestadienols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Am Chem Soc 94(4):1353;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040768</ConceptUI>
    <ConceptName>
     <String>datiscoside</String>
    </ConceptName>
    <RegistryNumber>36067-56-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070770</TermUI>
      <String>datiscoside</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000795</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>StC 407</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*HYDROCORTISONE (72-74)</PreviousIndexing>
   <PreviousIndexing>*PREGNADIENETRIOLS (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D006854</DescriptorUI>
     <DescriptorName>
      <String>Hydrocortisone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arzneim Forsch 21(10):1510;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040789</ConceptUI>
    <ConceptName>
     <String>StC 407</String>
    </ConceptName>
    <CASN1Name>6-dehydro-16-methylene hydrocortisone</CASN1Name>
    <RegistryNumber>17332-61-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070791</TermUI>
      <String>StC 407</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000852</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-deazacytidine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>08</Month>
   <Day>14</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>6</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CYTIDINE (72-75)</PreviousIndexing>
   <PreviousIndexing>PYRIDINES (72-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003562</DescriptorUI>
     <DescriptorName>
      <String>Cytidine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D003564</DescriptorUI>
     <DescriptorName>
      <String>Cytidine Deaminase</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
     <QualifierName>
      <String>antagonists &amp; inhibitors</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Biochem Pharmacol 21(8):1063;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040810</ConceptUI>
    <ConceptName>
     <String>3-deazacytidine</String>
    </ConceptName>
    <RegistryNumber>28307-19-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070812</TermUI>
      <String>3-deazacytidine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000862</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dehydrocapaurimine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1970</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>05</Month>
   <Day>14</Day>
  </DateRevised>
  <Note>structure; RN given refers to chloride
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>QUINOLIZINES (70-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000470</DescriptorUI>
     <DescriptorName>
      <String>Alkaloids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040822</ConceptUI>
    <ConceptName>
     <String>dehydrocapaurimine</String>
    </ConceptName>
    <CASN1Name>Dibenzo(a,g)quinolizinium, 5,6-dihydro-1,10-dihydroxy-2,3,9-trimethoxy-, chloride</CASN1Name>
    <RegistryNumber>57499-40-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070824</TermUI>
      <String>dehydrocapaurimine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000864</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dehydrosqualene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>8</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SQUALENE (72-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013185</DescriptorUI>
     <DescriptorName>
      <String>Squalene</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 85(3):867;1978</Source>
   <Source>Biochim Biophys Acta 260(3):482;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040826</ConceptUI>
    <ConceptName>
     <String>dehydrosqualene</String>
    </ConceptName>
    <RegistryNumber>11051-27-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070828</TermUI>
      <String>dehydrosqualene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000866</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-demethoxyubiquinone-9</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>intermediate in biosynthesis of ubiquinone
  </Note>
  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*UBIQUINONE (72-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014451</DescriptorUI>
     <DescriptorName>
      <String>Ubiquinone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 247(8):2499;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040827</ConceptUI>
    <ConceptName>
     <String>5-demethoxyubiquinone-9</String>
    </ConceptName>
    <RegistryNumber>7200-28-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070829</TermUI>
      <String>5-demethoxyubiquinone-9</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000874</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>deoxynybomycin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1970</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>4</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PYRIDINES (70-75)</PreviousIndexing>
   <PreviousIndexing>QUINOLINES (70-88)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D015363</DescriptorUI>
     <DescriptorName>
      <String>Quinolones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040842</ConceptUI>
    <ConceptName>
     <String>deoxynybomycin</String>
    </ConceptName>
    <CASN1Name>6,8,11-trimethyl-2H,4H-oxazolo(5,4,3-IJ)pyrido(3,2-g)quinoline-4,10(11H)-dione</CASN1Name>
    <RegistryNumber>27259-98-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070844</TermUI>
      <String>deoxynybomycin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C047272</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-(N-maleimidopropionyl)biocytin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1986</Year>
   <Month>01</Month>
   <Day>07</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>03</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>thiol-specific biotinylating reagent; structure given in first source
  </Note>
  <Frequency>30</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008239</DescriptorUI>
     <DescriptorName>
      <String>Lysine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008301</DescriptorUI>
     <DescriptorName>
      <String>Maleimides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Anal Biochem 1985;149(2):529</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0136621</ConceptUI>
    <ConceptName>
     <String>3-(N-maleimidopropionyl)biocytin</String>
    </ConceptName>
    <RegistryNumber>98930-71-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T166626</TermUI>
      <String>3-(N-maleimidopropionyl)biocytin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1986)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T166625</TermUI>
      <String>3-MPB</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1986)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T166624</TermUI>
      <String>3-(N-maleimido-propionyl)biocytin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1986)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "2">
  <SupplementalRecordUI>C448581</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>IMAP protocol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>03</Month>
   <Day>05</Day>
  </DateCreated>
  <Note>a chemotherapy protocol consisting of the above compounds; used in the treatment of primary extremity soft tissue sarcomas
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000971</DescriptorUI>
     <DescriptorName>
      <String>Antineoplastic Combined Chemotherapy Protocols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002945</DescriptorUI>
     <DescriptorName>
      <String>Cisplatin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004317</DescriptorUI>
     <DescriptorName>
      <String>Doxorubicin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007069</DescriptorUI>
     <DescriptorName>
      <String>Ifosfamide</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D016685</DescriptorUI>
     <DescriptorName>
      <String>Mitomycin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer 2002 Feb 1;94(3):786-92</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0416571</ConceptUI>
    <ConceptName>
     <String>IMAP protocol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T484543</TermUI>
      <String>IMAP protocol</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>03</Month>
       <Day>05</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005650</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ivosin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>contains a copolymerizate of p-divinyl benzene &amp; dimethylaminomethylstyrene
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*VINYL COMPOUNDS (74-76)</PreviousIndexing>
   <PreviousIndexing>DRUG COMBINATIONS (74-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011145</DescriptorUI>
     <DescriptorName>
      <String>Polyvinyls</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013343</DescriptorUI>
     <DescriptorName>
      <String>Styrenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D007475</DescriptorUI>
     <DescriptorName>
      <String>Ion Exchange Resins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D009824</DescriptorUI>
     <DescriptorName>
      <String>Ointments</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Dermatologica 145(3):176;1972</Source>
   <Source>Przg Dermatol 6:167;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0047314</ConceptUI>
    <ConceptName>
     <String>ivosin</String>
    </ConceptName>
    <CASN1Name>N,N-dimethyl-4-(1-methylethenyl)benzenamine polymer with 1,4-diethenylbenzene hydrochloride</CASN1Name>
    <RegistryNumber>38548-13-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T077317</TermUI>
      <String>ivosin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005651</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>indulona</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1991</Year>
   <Month>07</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>contains salts of EDTA &amp; ascorbic acid
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001205</DescriptorUI>
     <DescriptorName>
      <String>Ascorbic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004492</DescriptorUI>
     <DescriptorName>
      <String>Edetic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D009824</DescriptorUI>
     <DescriptorName>
      <String>Ointments</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Dermatologica 145(3):1175;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0047315</ConceptUI>
    <ConceptName>
     <String>indulona</String>
    </ConceptName>
    <CASN1Name>L-ascorbic acid mixt. with disodium ((N,N'-1,2- ethanediylbis(N-carboxymethyl)glycinato))(4-)- N,N',O,O',O(N),O(N'))calciate(2-) &amp; N,N'-1,2- ethanediylbis(N-(carboxymethyl)glycine) disodium salt</CASN1Name>
    <RegistryNumber>37270-70-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T077318</TermUI>
      <String>indulona</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005652</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>disparalone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ALKENES (74-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005233</DescriptorUI>
     <DescriptorName>
      <String>Fatty Alcohols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Experientia 29(7):783;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0047316</ConceptUI>
    <ConceptName>
     <String>disparalone</String>
    </ConceptName>
    <CASN1Name>7-oxo-10-hexadecen-1-ol</CASN1Name>
    <RegistryNumber>49831-68-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T077319</TermUI>
      <String>disparalone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C043506</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-acetyl-3-O-methyllactosamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1984</Year>
   <Month>12</Month>
   <Day>12</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000606</DescriptorUI>
     <DescriptorName>
      <String>Amino Sugars</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Carbohydr Res 1984;132(1):119</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0128008</ConceptUI>
    <ConceptName>
     <String>N-acetyl-3-O-methyllactosamine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T158013</TermUI>
      <String>N-acetyl-3-O-methyllactosamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1984)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T158012</TermUI>
      <String>Ac-MeLac</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1984)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T158011</TermUI>
      <String>2-acetamido-2-deoxy-4-O-beta-D-galactopyranosyl-3-O-methyl-D-glucopyranose</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1984)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C061684</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>FtsW protein, Bacteria</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1989</Year>
   <Month>12</Month>
   <Day>13</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>01</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>a septum peptidoglycan biosynthesis protein, involved in cell wall formation; plays a role in stabilizing the FtsZ ring during cell division;  amino acid sequence given in first source
  </Note>
  <Frequency>55</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008565</DescriptorUI>
     <DescriptorName>
      <String>Membrane Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Bacteriol 1989;171(11):6375</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0170992</ConceptUI>
    <ConceptName>
     <String>FtsW protein, Bacteria</String>
    </ConceptName>
    <RegistryNumber>125724-13-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T200997</TermUI>
      <String>FtsW protein, Bacteria</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C541164</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-(2,6,6-trimethylcyclohex-1-enyl)ethanol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2009</Year>
   <Month>06</Month>
   <Day>08</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D053138</DescriptorUI>
     <DescriptorName>
      <String>Cyclohexenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Commun (Camb) 2009 Apr 28;(16):2133-5</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0536365</ConceptUI>
    <ConceptName>
     <String>1-(2,6,6-trimethylcyclohex-1-enyl)ethanol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T752477</TermUI>
      <String>1-(2,6,6-trimethylcyclohex-1-enyl)ethanol</String>
      <DateCreated>
       <Year>2009</Year>
       <Month>06</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2009)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005664</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,16 alpha-dihydroxyestrone 3-methyl ether</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ESTRANES (74-75)</PreviousIndexing>
   <PreviousIndexing>ESTRONE/*analogs (75-77)</PreviousIndexing>
   <PreviousIndexing>METHYL ETHERS (74-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006894</DescriptorUI>
     <DescriptorName>
      <String>Hydroxyestrones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Pharm Bull (Tokyo) 21(4):914;1973</Source>
   <Source>Chem Pharm Bull (Tokyo) 23(7):1613;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0047339</ConceptUI>
    <ConceptName>
     <String>2,16 alpha-dihydroxyestrone 3-methyl ether</String>
    </ConceptName>
    <RegistryNumber>42241-06-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T077342</TermUI>
      <String>2,16 alpha-dihydroxyestrone 3-methyl ether</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005665</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>uridine 5'-(alpha-D-apio-D-furanosyl pyrophosphate)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PENTOSES (74-76)</PreviousIndexing>
   <PreviousIndexing>PYROPHOSPHORIC ACIDS (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014539</DescriptorUI>
     <DescriptorName>
      <String>Uridine Diphosphate Sugars</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem J 133(2):227;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0047340</ConceptUI>
    <ConceptName>
     <String>uridine 5'-(alpha-D-apio-D-furanosyl pyrophosphate)</String>
    </ConceptName>
    <CASN1Name>uridine 5'-(trihydrogen diphosphate), mono-D- apio-D-furanosyl ester</CASN1Name>
    <RegistryNumber>20230-91-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T077343</TermUI>
      <String>uridine 5'-(alpha-D-apio-D-furanosyl pyrophosphate)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007034</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>chlorzymine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>RN given refers to parent cpd; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ALKYNES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001596</DescriptorUI>
     <DescriptorName>
      <String>Benzylamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Farmakol Toksikol 36(5):548;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049960</ConceptUI>
    <ConceptName>
     <String>chlorzymine</String>
    </ConceptName>
    <CASN1Name>2-chloro-N-methyl-N-(2-propynyl)benzenemethanamine</CASN1Name>
    <RegistryNumber>2520-91-4</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>5220-94-0 (HCl)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0049960</Concept1UI>
     <Concept2UI>M0309805</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079963</TermUI>
      <String>chlorzymine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0309805</ConceptUI>
    <ConceptName>
     <String>chlorzymine hydrochloride</String>
    </ConceptName>
    <RegistryNumber>5220-94-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0049960</Concept1UI>
     <Concept2UI>M0309805</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T339805</TermUI>
      <String>chlorzymine hydrochloride</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005669</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>11 alpha-bromoacetoxyprogesterone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>01</Month>
   <Day>02</Day>
  </DateRevised>
  <Frequency>7</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PREGNENEDIONES (74-75)</PreviousIndexing>
   <PreviousIndexing>STEROIDS, BROMINATED (75-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006908</DescriptorUI>
     <DescriptorName>
      <String>Hydroxyprogesterones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 248(16):5641;1973</Source>
   <Source>J Biol Chem 250(19):7656;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0047346</ConceptUI>
    <ConceptName>
     <String>11 alpha-bromoacetoxyprogesterone</String>
    </ConceptName>
    <RegistryNumber>36049-50-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T077349</TermUI>
      <String>11 alpha-bromoacetoxyprogesterone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C084030</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>EXP 631</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1993</Year>
   <Month>12</Month>
   <Day>03</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>07</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>a centrally-acting non-opioid analgesic; exhibits serotonin and norepinephrine reuptake inhibiting activities; structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010880</DescriptorUI>
     <DescriptorName>
      <String>Piperidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013876</DescriptorUI>
     <DescriptorName>
      <String>Thiophenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biopharm Drug Dispos 1993 Aug;14(6):519-31</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0223411</ConceptUI>
    <ConceptName>
     <String>EXP 631</String>
    </ConceptName>
    <CASN1Name>4-Piperidinemethanol, alpha,alpha,1-trimethyl-4-(3-thienyl)-, (Z)-2-butenedioate (2:1) (salt)</CASN1Name>
    <RegistryNumber>151656-58-5</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0223411</Concept1UI>
     <Concept2UI>M0223408</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T253416</TermUI>
      <String>EXP 631</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T253415</TermUI>
      <String>EXP631</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T253414</TermUI>
      <String>EXP-631</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0223408</ConceptUI>
    <ConceptName>
     <String>4-(3-thienyl)-alpha,alpha,1-trimethyl-4-piperidinemethanol hemi-fumarate salt</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0223411</Concept1UI>
     <Concept2UI>M0223408</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T253413</TermUI>
      <String>4-(3-thienyl)-alpha,alpha,1-trimethyl-4-piperidinemethanol hemi-fumarate salt</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C431670</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-amino-1,2,4-benzotriazine 4-oxide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>07</Month>
   <Day>31</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>07</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014227</DescriptorUI>
     <DescriptorName>
      <String>Triazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 2001 Jan 12;66(1):107-14</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0394510</ConceptUI>
    <ConceptName>
     <String>3-amino-1,2,4-benzotriazine 4-oxide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T455851</TermUI>
      <String>3-amino-1,2,4-benzotriazine 4-oxide</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>07</Month>
       <Day>31</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T455852</TermUI>
      <String>3-A-BTAO</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>07</Month>
       <Day>31</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C480339</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>munroniamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>01</Month>
   <Day>12</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014315</DescriptorUI>
     <DescriptorName>
      <String>Triterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Agric Food Chem. 2003 Nov 19;51(24):6949-52</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0458699</ConceptUI>
    <ConceptName>
     <String>munroniamide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T568232</TermUI>
      <String>munroniamide</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>01</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C581075</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>curcamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>05</Month>
   <Day>15</Day>
  </DateCreated>
  <Note>antibiotic from the seed cake of Jatropha curcas L; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002934</DescriptorUI>
     <DescriptorName>
      <String>Cinnamates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003958</DescriptorUI>
     <DescriptorName>
      <String>Diamide</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0584777</ConceptUI>
    <ConceptName>
     <String>curcamide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T844180</TermUI>
      <String>curcamide</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>05</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T844181</TermUI>
      <String>(E)-N-(3-acetamidopropyl)cinnamamide</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>05</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C064085</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tev protein p28, Human immunodeficiency virus 1</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1990</Year>
   <Month>06</Month>
   <Day>12</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>03</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>28 kDa protein; contains tat, env, &amp; rev sequences; probably a 4th regulatory factor of HIV-1
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014760</DescriptorUI>
     <DescriptorName>
      <String>Viral Fusion Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015534</DescriptorUI>
     <DescriptorName>
      <String>Trans-Activators</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D015497</DescriptorUI>
     <DescriptorName>
      <String>HIV-1</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Virol 1990;64(6):2505</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0176684</ConceptUI>
    <ConceptName>
     <String>tev protein p28, Human immunodeficiency virus 1</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0176684</Concept1UI>
     <Concept2UI>M0176683</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T206687</TermUI>
      <String>tev protein p28, Human immunodeficiency virus 1</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T206686</TermUI>
      <String>p28(tev) protein, Human immunodeficiency virus 1</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T206689</TermUI>
      <String>p28(tev) protein, HIV-1</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0176683</ConceptUI>
    <ConceptName>
     <String>tnv protein, HIV-1</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0176684</Concept1UI>
     <Concept2UI>M0176683</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T206688</TermUI>
      <String>tnv protein, HIV-1</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010585</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>HEOM</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>20</Day>
  </DateRevised>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DIELDRIN (75-86)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004026</DescriptorUI>
     <DescriptorName>
      <String>Dieldrin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Environ Physiol Biochem 5(1):58;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056173</ConceptUI>
    <ConceptName>
     <String>HEOM</String>
    </ConceptName>
    <CASN1Name>1,2,3,4,9,9-hexachloro-6,7-epoxy-1,4,4a,5,6, 7,8,8a-octahydro-1,4-methanonaphthalene</CASN1Name>
    <RegistryNumber>25967-06-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086176</TermUI>
      <String>HEOM</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010586</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,2-heptadecanediol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006018</DescriptorUI>
     <DescriptorName>
      <String>Glycols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 250(13):4877;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056174</ConceptUI>
    <ConceptName>
     <String>1,2-heptadecanediol</String>
    </ConceptName>
    <CASN1Name>1,2-Heptadecanediol</CASN1Name>
    <RegistryNumber>34719-63-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086177</TermUI>
      <String>1,2-heptadecanediol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010588</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-O-2'-hydroxyheptadecyl-rac-glycerol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1987</Year>
   <Month>07</Month>
   <Day>22</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*GLYCERIDES (82-87)</PreviousIndexing>
   <PreviousIndexing>FATTY ALCOHOLS (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005995</DescriptorUI>
     <DescriptorName>
      <String>Glyceryl Ethers</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 250(13):4877;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056176</ConceptUI>
    <ConceptName>
     <String>1-O-2'-hydroxyheptadecyl-rac-glycerol</String>
    </ConceptName>
    <CASN1Name>1,2-Propanediol, 3-((2-hydroxyheptadecyl)oxy)-</CASN1Name>
    <RegistryNumber>34719-62-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086179</TermUI>
      <String>1-O-2'-hydroxyheptadecyl-rac-glycerol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C444901</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-(2-fluorophenyl)-3-phenyl-3H-naphtho(2,1-b)pyran</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>01</Month>
   <Day>24</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009281</DescriptorUI>
     <DescriptorName>
      <String>Naphthalenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011714</DescriptorUI>
     <DescriptorName>
      <String>Pyrans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Photochem Photobiol 2001 Nov;74(5):694-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0412191</ConceptUI>
    <ConceptName>
     <String>3-(2-fluorophenyl)-3-phenyl-3H-naphtho(2,1-b)pyran</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T479245</TermUI>
      <String>3-(2-fluorophenyl)-3-phenyl-3H-naphtho(2,1-b)pyran</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>01</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T479246</TermUI>
      <String>F-Py cpd</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>01</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010591</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hypophysin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>posterior pituitary lobe extracts
  </Note>
  <Frequency>20</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010909</DescriptorUI>
     <DescriptorName>
      <String>Pituitary Hormones, Posterior</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mater Med Polon 7(2):133;1975</Source>
   <Source>Vet Med Nauki 15(3):36;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056184</ConceptUI>
    <ConceptName>
     <String>hypophysin</String>
    </ConceptName>
    <RegistryNumber>54577-94-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086187</TermUI>
      <String>hypophysin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C113591</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>trimethyl-1,3,5-benzenetrimethanol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>08</Month>
   <Day>11</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001592</DescriptorUI>
     <DescriptorName>
      <String>Benzyl Alcohols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Crystallogr C 1998 June 15;54 (Pt 6):792-5</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0293296</ConceptUI>
    <ConceptName>
     <String>trimethyl-1,3,5-benzenetrimethanol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T323301</TermUI>
      <String>trimethyl-1,3,5-benzenetrimethanol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T323300</TermUI>
      <String>alpha-TMBz</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T323299</TermUI>
      <String>alpha,alpha',alpha''-trimethyl-1,3,5-benzenetrimethanol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C416932</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>imidazolium imidazoletetrachlororuthenate(III)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>16</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>01</Month>
   <Day>24</Day>
  </DateRevised>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009942</DescriptorUI>
     <DescriptorName>
      <String>Organometallic Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D012428</DescriptorUI>
     <DescriptorName>
      <String>Ruthenium</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Pharmacol Exp Ther 2000 Dec;295(3):927-33</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0374720</ConceptUI>
    <ConceptName>
     <String>imidazolium imidazoletetrachlororuthenate(III)</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T431148</TermUI>
      <String>imidazolium imidazoletetrachlororuthenate(III)</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>12</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T431150</TermUI>
      <String>ICR ruthenium complex</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>12</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T431149</TermUI>
      <String>H(Im)(transRuCl4(Im)2)</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>12</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010608</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-methoxyuridine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014529</DescriptorUI>
     <DescriptorName>
      <String>Uridine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Am Chem Soc 97(15):4386;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056206</ConceptUI>
    <ConceptName>
     <String>4-methoxyuridine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086209</TermUI>
      <String>4-methoxyuridine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010610</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>mollisin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>14</Day>
  </DateRevised>
  <Note>halometabolite of Mollisia caesia; structure
  </Note>
  <Frequency>4</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>QUINONES (75-90)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009285</DescriptorUI>
     <DescriptorName>
      <String>Naphthoquinones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>CRC Crit Rev Microbiol 3(4):337-51;1975</Source>
   <Source>J Am Chem Soc 98(9):2636;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056209</ConceptUI>
    <ConceptName>
     <String>mollisin</String>
    </ConceptName>
    <RegistryNumber>667-92-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086212</TermUI>
      <String>mollisin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010613</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>nickel tetraphenylporphyrin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>nickel an integral part of cpd
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PORPHYRINS (75-82)</PreviousIndexing>
   <PreviousIndexing>ORGANOMETALLIC COMPOUNDS (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008665</DescriptorUI>
     <DescriptorName>
      <String>Metalloporphyrins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Proc Natl Acad Sci USA 72(6):2340;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056211</ConceptUI>
    <ConceptName>
     <String>nickel tetraphenylporphyrin</String>
    </ConceptName>
    <RegistryNumber>14172-92-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086214</TermUI>
      <String>nickel tetraphenylporphyrin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C098551</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>NupG protein, E coli</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>04</Month>
   <Day>12</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>11</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>transports nucleosides across inner membrane of E. coli; a member of the CytR regulon; has been sequenced
  </Note>
  <Frequency>11</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CARRIER PROTEINS (1996-2001)</PreviousIndexing>
   <PreviousIndexing>*MEMBRANE PROTEINS (1996-2001)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D026901</DescriptorUI>
     <DescriptorName>
      <String>Membrane Transport Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029968</DescriptorUI>
     <DescriptorName>
      <String>Escherichia coli Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Microbiol 1995 Sep;17(5):843-53</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0258872</ConceptUI>
    <ConceptName>
     <String>NupG protein, E coli</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T463503</TermUI>
      <String>NupG protein, E coli</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>09</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010617</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-norzoanthoxanthin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>01</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CYCLOHEPTANES (75-82)</PreviousIndexing>
   <PreviousIndexing>DIMETHYLAMINES (75-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007093</DescriptorUI>
     <DescriptorName>
      <String>Imidazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Biol Interact 11(2):91;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056219</ConceptUI>
    <ConceptName>
     <String>3-norzoanthoxanthin</String>
    </ConceptName>
    <RegistryNumber>53941-25-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086222</TermUI>
      <String>3-norzoanthoxanthin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C479722</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6,11-dihydro-2-methoxy-11-(2-(1-piperidinyl))ethyl</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>12</Month>
   <Day>17</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010880</DescriptorUI>
     <DescriptorName>
      <String>Piperidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Biomed Anal. 2003 Apr 1;31(5):1021-6</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0457662</ConceptUI>
    <ConceptName>
     <String>6,11-dihydro-2-methoxy-11-(2-(1-piperidinyl))ethyl</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T564184</TermUI>
      <String>6,11-dihydro-2-methoxy-11-(2-(1-piperidinyl))ethyl</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T564185</TermUI>
      <String>6,11-DMP-E</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010622</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>platinum pyrimidine blues</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>10</Month>
   <Day>04</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PLATINUM (75-79)</PreviousIndexing>
   <PreviousIndexing>*PYRIMIDINES (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009944</DescriptorUI>
     <DescriptorName>
      <String>Organoplatinum Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Chemother Rep (Pt 1) 59(2):287;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056227</ConceptUI>
    <ConceptName>
     <String>platinum pyrimidine blues</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086230</TermUI>
      <String>platinum pyrimidine blues</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010623</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>polyisoprenol N-acetylglucosaminyl pyrophosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>13</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*HEXOSEDIPHOSPHATES (75-78)</PreviousIndexing>
   <PreviousIndexing>ACETYLGLUCOSAMINE/analogs (75-82)</PreviousIndexing>
   <PreviousIndexing>TERPENES (75-78)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011103</DescriptorUI>
     <DescriptorName>
      <String>Polyisoprenyl Phosphate Monosaccharides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 65(1):248;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056228</ConceptUI>
    <ConceptName>
     <String>polyisoprenol N-acetylglucosaminyl pyrophosphate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086231</TermUI>
      <String>polyisoprenol N-acetylglucosaminyl pyrophosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010646</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>zexbrevin A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>11</Month>
   <Day>18</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>LACTONES (75-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012717</DescriptorUI>
     <DescriptorName>
      <String>Sesquiterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Agents Actions 5(1):64;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056276</ConceptUI>
    <ConceptName>
     <String>zexbrevin A</String>
    </ConceptName>
    <CASN1Name>(3R-(3R*,3AS*,4S*,6R*,10S*,11AR*))-2-methylpropanoic acid 2,3,3a,4,5,6,7,10,11,11a-decahydro-3,6,10- trimethyl-2,7-dioxo-6,9-epoxycyclodeca(b)furan-4-yl ester</CASN1Name>
    <RegistryNumber>28644-87-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086279</TermUI>
      <String>zexbrevin A</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010647</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>zexbrevin B</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>11</Month>
   <Day>18</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>LACTONES (75-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012717</DescriptorUI>
     <DescriptorName>
      <String>Sesquiterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Agents Actions 5(1):64;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056277</ConceptUI>
    <ConceptName>
     <String>zexbrevin B</String>
    </ConceptName>
    <CASN1Name>(3-AR-(3AR*,4S*,6R*,7S*,9S*,11AR*))-2-methyl-2- propenoic acid 2,3,3a,4,5,6,7,8,9,11a-decahydro- 7,9-dihydroxy-6,10-dimethyl-3-methylene-2-oxo-6,9- epoxycyclodeca(b)furan-4-yl ester</CASN1Name>
    <RegistryNumber>34302-19-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086280</TermUI>
      <String>zexbrevin B</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C030913</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-methylbenzylsulfate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>08</Month>
   <Day>14</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>08</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001593</DescriptorUI>
     <DescriptorName>
      <String>Benzyl Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mutat Res 1981;88(3):273</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0097510</ConceptUI>
    <ConceptName>
     <String>2-methylbenzylsulfate</String>
    </ConceptName>
    <CASN1Name>Benzenemethanol, 2-methyl-, hydrogen sulfate</CASN1Name>
    <RegistryNumber>76773-80-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T127514</TermUI>
      <String>2-methylbenzylsulfate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T127513</TermUI>
      <String>ortho-methylbenzyl sulfate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T127512</TermUI>
      <String>o-methylbenzylsulfate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C087119</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>LI637 protein, Chlamydomonas eugametos</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>06</Month>
   <Day>03</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>10</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>a chloroplast hemoglobin associated with nonphotosynthetic photoreceptors; isolated from the green alga Chlamydomonas eugametos; amino acid sequence in first source; GenBank X72916
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006454</DescriptorUI>
     <DescriptorName>
      <String>Hemoglobins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010940</DescriptorUI>
     <DescriptorName>
      <String>Plant Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Gen Genet 1994 Apr;243(2):185-97</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0230800</ConceptUI>
    <ConceptName>
     <String>LI637 protein, Chlamydomonas eugametos</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T510766</TermUI>
      <String>LI637 protein, Chlamydomonas eugametos</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>08</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010678</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>aminotrideoxybutirosin A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>07</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BUTIROSINS (75-95)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002076</DescriptorUI>
     <DescriptorName>
      <String>Butirosin Sulfate</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiotics 28(7):530;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056372</ConceptUI>
    <ConceptName>
     <String>aminotrideoxybutirosin A</String>
    </ConceptName>
    <CASN1Name>D-Streptamine, O-5- amino-5-deoxy-beta-D-xylofuranosyl-(1-5)-O-(2,6-diamino-2,3,4,6-tetradeoxy-alpha-D-erythro-hexopyranosyl-(1-4))-N(1)-(4-amino-2-hydroxy-1-oxobutyl)-2-deoxy-, (S)-</CASN1Name>
    <RegistryNumber>56182-07-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086375</TermUI>
      <String>aminotrideoxybutirosin A</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T086374</TermUI>
      <String>5''-amino-3',4',5''-trideoxybutirosin A</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C479723</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>(1R,2S,4S,5S,6R,7R,8S,9S,10S)-1,2-diacetoxy-9-benzoyloxy-15-(2-methylbutyroyloxy)-4,6,8-trihydroxydihydro-beta-agarofuran</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>12</Month>
   <Day>17</Day>
  </DateCreated>
  <Note>have a dihydro-beta-agarofuran skeleton;  from Crossopetalum tonduzii; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012717</DescriptorUI>
     <DescriptorName>
      <String>Sesquiterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2003 Aug;66(8):1047-50</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0457663</ConceptUI>
    <ConceptName>
     <String>(1R,2S,4S,5S,6R,7R,8S,9S,10S)-1,2-diacetoxy-9-benzoyloxy-15-(2-methylbutyroyloxy)-4,6,8-trihydroxydihydro-beta-agarofuran</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T564186</TermUI>
      <String>(1R,2S,4S,5S,6R,7R,8S,9S,10S)-1,2-diacetoxy-9-benzoyloxy-15-(2-methylbutyroyloxy)-4,6,8-trihydroxydihydro-beta-agarofuran</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T564187</TermUI>
      <String>DBMTA cpd</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C089942</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>collagen alpha3(IV) 185-203</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>11</Month>
   <Day>15</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>08</Month>
   <Day>09</Day>
  </DateRevised>
  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*Collagen (1995-2002)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010446</DescriptorUI>
     <DescriptorName>
      <String>Peptide Fragments</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D024141</DescriptorUI>
     <DescriptorName>
      <String>Collagen Type IV</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 1994 Oct 14;269(14):25475-82</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0237733</ConceptUI>
    <ConceptName>
     <String>collagen alpha3(IV) 185-203</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T267738</TermUI>
      <String>collagen alpha3(IV) 185-203</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T267737</TermUI>
      <String>type IV collagen alpha3 185-203</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T267736</TermUI>
      <String>alpha3(IV) 185-203 peptide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010701</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>crotonyl-coenzyme A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>14</Day>
  </DateRevised>
  <Frequency>84</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>COENZYME A/*analogs (75-82)</PreviousIndexing>
   <PreviousIndexing>CROTONIC ACIDS (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000214</DescriptorUI>
     <DescriptorName>
      <String>Acyl Coenzyme A</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Tohoku J Exp Med 116(2):133;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056416</ConceptUI>
    <ConceptName>
     <String>crotonyl-coenzyme A</String>
    </ConceptName>
    <RegistryNumber>992-67-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086419</TermUI>
      <String>crotonyl-coenzyme A</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T086418</TermUI>
      <String>crotonyl-CoA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T086417</TermUI>
      <String>coenzyme A, crotonyl-</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010668</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>17-acetoxy-11-oxaprogesterone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>HYDROXYPROGESTERONE/*analogs (75-78)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006908</DescriptorUI>
     <DescriptorName>
      <String>Hydroxyprogesterones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013260</DescriptorUI>
     <DescriptorName>
      <String>Steroids, Heterocyclic</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Steroids 25(6):781;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056356</ConceptUI>
    <ConceptName>
     <String>17-acetoxy-11-oxaprogesterone</String>
    </ConceptName>
    <RegistryNumber>57170-48-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086359</TermUI>
      <String>17-acetoxy-11-oxaprogesterone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C479724</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6,11-dihydro-2-methoxy-5H-benzo(a)carbazole</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>12</Month>
   <Day>17</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002227</DescriptorUI>
     <DescriptorName>
      <String>Carbazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Biomed Anal. 2003 Apr 1;31(5):1021-6</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0457664</ConceptUI>
    <ConceptName>
     <String>6,11-dihydro-2-methoxy-5H-benzo(a)carbazole</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T564188</TermUI>
      <String>6,11-dihydro-2-methoxy-5H-benzo(a)carbazole</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T564189</TermUI>
      <String>6,11-DMB-C</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C053061</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3,4-dichlorobenzyloxyacetic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1987</Year>
   <Month>08</Month>
   <Day>20</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001593</DescriptorUI>
     <DescriptorName>
      <String>Benzyl Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Drug Metab Dispos 1987;15(3):305</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0150408</ConceptUI>
    <ConceptName>
     <String>3,4-dichlorobenzyloxyacetic acid</String>
    </ConceptName>
    <RegistryNumber>82513-28-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T180413</TermUI>
      <String>3,4-dichlorobenzyloxyacetic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T180412</TermUI>
      <String>3,4-DCBAA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T180411</TermUI>
      <String>((3,4-dichlorobenzyl)oxy)acetic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C456923</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>LGI2 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>06</Month>
   <Day>19</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>06</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>RefSeq NM_018176
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011506</DescriptorUI>
     <DescriptorName>
      <String>Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D004827</DescriptorUI>
     <DescriptorName>
      <String>Epilepsy</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>FEBS Lett 2002 May 22;519(1-3):71-6</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0427514</ConceptUI>
    <ConceptName>
     <String>LGI2 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T499293</TermUI>
      <String>LGI2 protein, human</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>06</Month>
       <Day>19</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T499290</TermUI>
      <String>leucine-rich, glioma-inactivated 2 protein, human</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>06</Month>
       <Day>19</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C506777</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>upain-1 peptide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>01</Month>
   <Day>08</Day>
  </DateCreated>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010456</DescriptorUI>
     <DescriptorName>
      <String>Peptides, Cyclic</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D014568</DescriptorUI>
     <DescriptorName>
      <String>Urokinase-Type Plasminogen Activator</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
     <QualifierName>
      <String>antagonists &amp; inhibitors</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Biol Chem 2005 Nov 18;280(46):38424-37</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0493710</ConceptUI>
    <ConceptName>
     <String>upain-1 peptide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T663910</TermUI>
      <String>upain-1 peptide</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>01</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T663912</TermUI>
      <String>Cys-Ser-Trp-Arg-Gly-Leu-Glu-Asn-His-Arg-Met-Cys cyclic (1-12) disulfide</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>01</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T663913</TermUI>
      <String>CSWRGLENHRMC cyclic (1-12) disulfide</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>01</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T663911</TermUI>
      <String>cysteinyl-seryl-tryptophyl-arginyl-glycyl-leucyl-glutamyl-asparagyl-histidyl-arginyl-methionyl-cysteine cyclic (1-12) disulfide</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>01</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C506778</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>At2g32040 protein, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>01</Month>
   <Day>08</Day>
  </DateCreated>
  <Note>a folate transporter; GenBank AY081306
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029382</DescriptorUI>
     <DescriptorName>
      <String>Dicarboxylic Acid Transporters</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 2005 Nov 18;280(46):38457-63</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0493711</ConceptUI>
    <ConceptName>
     <String>At2g32040 protein, Arabidopsis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T663914</TermUI>
      <String>At2g32040 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>01</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010687</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,2-bis(beta-L-aspartyl)hydrazine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>12</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>antileukemic; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*HYDRAZINES (75-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D001224</DescriptorUI>
     <DescriptorName>
      <String>Aspartic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Neoplasma 22(1):69;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056398</ConceptUI>
    <ConceptName>
     <String>1,2-bis(beta-L-aspartyl)hydrazine</String>
    </ConceptName>
    <RegistryNumber>37055-61-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086401</TermUI>
      <String>1,2-bis(beta-L-aspartyl)hydrazine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014091</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>methyl-5-bromovalerimidate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>protein cross-linking reagent; structure
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*IMIDES (77-80)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007096</DescriptorUI>
     <DescriptorName>
      <String>Imidoesters</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 252(4):1505;1977</Source>
   <Source>J Biol Chem 254(4):1022;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062332</ConceptUI>
    <ConceptName>
     <String>methyl-5-bromovalerimidate</String>
    </ConceptName>
    <CASN1Name>Pentanimidic acid, 5-bromo-, methyl ester, hydrochloride</CASN1Name>
    <RegistryNumber>62287-98-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092335</TermUI>
      <String>methyl-5-bromovalerimidate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014094</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>methylcladinoside</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008759</DescriptorUI>
     <DescriptorName>
      <String>Methylglycosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Chromatogr 132(2):309;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062335</ConceptUI>
    <ConceptName>
     <String>methylcladinoside</String>
    </ConceptName>
    <RegistryNumber>18423-88-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092338</TermUI>
      <String>methylcladinoside</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C101164</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>7-(1-propynyl)-7-deaza-2'-deoxyguanosine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>10</Month>
   <Day>05</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003849</DescriptorUI>
     <DescriptorName>
      <String>Deoxyguanosine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nucleic Acids Res 1996 Aug 1;24(15):2974-80</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0265288</ConceptUI>
    <ConceptName>
     <String>7-(1-propynyl)-7-deaza-2'-deoxyguanosine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T295293</TermUI>
      <String>7-(1-propynyl)-7-deaza-2'-deoxyguanosine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T295292</TermUI>
      <String>pdG cpd</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014103</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-methylpentyne-3,4-diol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>13</Day>
  </DateRevised>
  <Note>metabolite of methylpentynol carbamate
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ALKYNES (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006018</DescriptorUI>
     <DescriptorName>
      <String>Glycols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Chromatogr 133(2):267;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062356</ConceptUI>
    <ConceptName>
     <String>3-methylpentyne-3,4-diol</String>
    </ConceptName>
    <RegistryNumber>62386-32-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092359</TermUI>
      <String>3-methylpentyne-3,4-diol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014120</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>neooncinotine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000470</DescriptorUI>
     <DescriptorName>
      <String>Alkaloids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Helv Chim Acta 59(8):3013;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062397</ConceptUI>
    <ConceptName>
     <String>neooncinotine</String>
    </ConceptName>
    <RegistryNumber>53602-28-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092400</TermUI>
      <String>neooncinotine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014183</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>sambicyanin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000872</DescriptorUI>
     <DescriptorName>
      <String>Anthocyanins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Pharmazie 32(1):40;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062509</ConceptUI>
    <ConceptName>
     <String>sambicyanin</String>
    </ConceptName>
    <RegistryNumber>33012-73-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092512</TermUI>
      <String>sambicyanin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T092511</TermUI>
      <String>3,5,7,3',4'-pentahydroxyflavylium-3-O-beta-D-xylopyranosyl-(1-2)-beta-D-glucopyranoside</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C033822</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-chloroisoprenaline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1982</Year>
   <Month>04</Month>
   <Day>14</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>RN given refers to (+-)-isomer
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007545</DescriptorUI>
     <DescriptorName>
      <String>Isoproterenol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Naunyn Schmiedebergs Arch Pharmacol 1982;318(3):192</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0104691</ConceptUI>
    <ConceptName>
     <String>4-chloroisoprenaline</String>
    </ConceptName>
    <RegistryNumber>77145-71-2</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>33584-94-0 (HCl)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0104691</Concept1UI>
     <Concept2UI>M0319935</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T134695</TermUI>
      <String>4-chloroisoprenaline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T134694</TermUI>
      <String>p-chloroisoprenaline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0319935</ConceptUI>
    <ConceptName>
     <String>4-chloroisoprenaline hydrochloride</String>
    </ConceptName>
    <RegistryNumber>33584-94-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0104691</Concept1UI>
     <Concept2UI>M0319935</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T349935</TermUI>
      <String>4-chloroisoprenaline hydrochloride</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C047299</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-(3,4-diacetoxyphenyl)-2-chloro-N-isopropyl-1-ethanamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1986</Year>
   <Month>01</Month>
   <Day>14</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>RN &amp; structure given in first source; RN given refers to parent cpd
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007545</DescriptorUI>
     <DescriptorName>
      <String>Isoproterenol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 1985;28(12):1962</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0136678</ConceptUI>
    <ConceptName>
     <String>2-(3,4-diacetoxyphenyl)-2-chloro-N-isopropyl-1-ethanamine</String>
    </ConceptName>
    <RegistryNumber>98634-91-4</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>98651-83-3 (HCl)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0136678</Concept1UI>
     <Concept2UI>M0322579</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T166683</TermUI>
      <String>2-(3,4-diacetoxyphenyl)-2-chloro-N-isopropyl-1-ethanamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1986)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T166682</TermUI>
      <String>2-DPCIE</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1986)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0322579</ConceptUI>
    <ConceptName>
     <String>2-(3,4-diacetoxyphenyl)-2-chloro-N-isopropyl-1-ethanamine hydrochloride</String>
    </ConceptName>
    <RegistryNumber>98651-83-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0136678</Concept1UI>
     <Concept2UI>M0322579</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T352579</TermUI>
      <String>2-(3,4-diacetoxyphenyl)-2-chloro-N-isopropyl-1-ethanamine hydrochloride</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1986)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C509497</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>mde2 protein, S. pombe</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>04</Month>
   <Day>14</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>04</Month>
   <Day>14</Day>
  </DateRevised>
  <Note>a forkhead homologue isolated from Schizosaccharomyces pombe; has been sequenced
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029702</DescriptorUI>
     <DescriptorName>
      <String>Schizosaccharomyces pombe Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D051858</DescriptorUI>
     <DescriptorName>
      <String>Forkhead Transcription Factors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Curr Biol. 2005 Sep 20;15(18):1663-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0497063</ConceptUI>
    <ConceptName>
     <String>mde2 protein, S. pombe</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T671428</TermUI>
      <String>mde2 protein, S. pombe</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>04</Month>
       <Day>14</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014135</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Novo-Helisen Depot</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>27</Day>
  </DateRevised>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010936</DescriptorUI>
     <DescriptorName>
      <String>Plant Extracts</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D006255</DescriptorUI>
     <DescriptorName>
      <String>Rhinitis, Allergic, Seasonal</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000188</QualifierUI>
     <QualifierName>
      <String>drug therapy</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Praxis 66(9):260;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062432</ConceptUI>
    <ConceptName>
     <String>Novo-Helisen Depot</String>
    </ConceptName>
    <CASN1Name>Novo-Helisen Depot</CASN1Name>
    <RegistryNumber>78355-44-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092435</TermUI>
      <String>Novo-Helisen Depot</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014143</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-(3-oxo-7 alpha-methylsulfonyl-6 beta,17 beta- dihydroxy-4-androsten-17 alpha-yl)propionic acid gamma-lactone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>spironolactone metabolite
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>SULFONES (77-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013148</DescriptorUI>
     <DescriptorName>
      <String>Spironolactone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Steroids 28(4):467;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062442</ConceptUI>
    <ConceptName>
     <String>3-(3-oxo-7 alpha-methylsulfonyl-6 beta,17 beta- dihydroxy-4-androsten-17 alpha-yl)propionic acid gamma-lactone</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092445</TermUI>
      <String>3-(3-oxo-7 alpha-methylsulfonyl-6 beta,17 beta- dihydroxy-4-androsten-17 alpha-yl)propionic acid gamma-lactone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007408</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3,4-dihydro-1-isoquinolineacetamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>RN given refers to parent cpd
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ACETAMIDES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007546</DescriptorUI>
     <DescriptorName>
      <String>Isoquinolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Antimicrob Agents Chemother 4(6):612;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050592</ConceptUI>
    <ConceptName>
     <String>3,4-dihydro-1-isoquinolineacetamide</String>
    </ConceptName>
    <RegistryNumber>19622-86-7</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>3639-53-0 (HCl)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0050592</Concept1UI>
     <Concept2UI>M0309937</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080595</TermUI>
      <String>3,4-dihydro-1-isoquinolineacetamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0309937</ConceptUI>
    <ConceptName>
     <String>3,4-dihydro-1-isoquinolineacetamide hydrochloride</String>
    </ConceptName>
    <RegistryNumber>3639-53-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0050592</Concept1UI>
     <Concept2UI>M0309937</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T339937</TermUI>
      <String>3,4-dihydro-1-isoquinolineacetamide hydrochloride</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T080594</TermUI>
      <String>3,4-dihydro-1-isoquinolineacetamide, monohydrochloride</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C480021</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ALDH3A1 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>12</Month>
   <Day>31</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>05</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>RefSeq NM_000691
  </Note>
  <Frequency>76</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000444</DescriptorUI>
     <DescriptorName>
      <String>Aldehyde Dehydrogenase</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D005136</DescriptorUI>
     <DescriptorName>
      <String>Eye Proteins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Biochem J 2003 Dec 15;376(Pt 3):615-23</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0458198</ConceptUI>
    <ConceptName>
     <String>ALDH3A1 protein, human</String>
    </ConceptName>
    <RegistryNumber>EC 1.2.1.3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T566461</TermUI>
      <String>ALDH3A1 protein, human</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>31</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T566460</TermUI>
      <String>aldehyde dehydrogenase 3A1, human</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>31</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014150</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>phytylplastoquinone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010971</DescriptorUI>
     <DescriptorName>
      <String>Plastoquinone</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Vitam Horm 34:96;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062453</ConceptUI>
    <ConceptName>
     <String>phytylplastoquinone</String>
    </ConceptName>
    <RegistryNumber>1177-24-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092456</TermUI>
      <String>phytylplastoquinone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C101263</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>chloro(5,10,15,20-tetraphenylporphyrinato)manganese(III)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>10</Month>
   <Day>11</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>RN given for (SP-5-12)-isomer; structure in first source
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009942</DescriptorUI>
     <DescriptorName>
      <String>Organometallic Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011166</DescriptorUI>
     <DescriptorName>
      <String>Porphyrins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D008345</DescriptorUI>
     <DescriptorName>
      <String>Manganese</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Acta Crystallogr C 1996 Feb 15;52 Pt 2:361-3</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0265529</ConceptUI>
    <ConceptName>
     <String>chloro(5,10,15,20-tetraphenylporphyrinato)manganese(III)</String>
    </ConceptName>
    <RegistryNumber>32195-55-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T295534</TermUI>
      <String>chloro(5,10,15,20-tetraphenylporphyrinato)manganese(III)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T295533</TermUI>
      <String>Mn(TPP)Cl</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C101264</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,3,4,5-tetra-O-acetyl-1,6-di-O-(triphenylmethyl)mannitol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>10</Month>
   <Day>11</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008353</DescriptorUI>
     <DescriptorName>
      <String>Mannitol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Crystallogr C 1996 Feb 15;52 Pt 2:381-3</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0265531</ConceptUI>
    <ConceptName>
     <String>2,3,4,5-tetra-O-acetyl-1,6-di-O-(triphenylmethyl)mannitol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T295536</TermUI>
      <String>2,3,4,5-tetra-O-acetyl-1,6-di-O-(triphenylmethyl)mannitol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T295535</TermUI>
      <String>TADTPM-mannitol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014156</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>polychlorinated styrene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>06</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*HYDROCARBONS, CHLORINATED (77-82)</PreviousIndexing>
   <PreviousIndexing>*STYRENES (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011137</DescriptorUI>
     <DescriptorName>
      <String>Polystyrenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Assoc Off Anal Chem 60(1):60;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062467</ConceptUI>
    <ConceptName>
     <String>polychlorinated styrene</String>
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    <RegistryNumber>9022-52-0</RegistryNumber>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062467</Concept1UI>
     <Concept2UI>M0062466</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092470</TermUI>
      <String>polychlorinated styrene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0062466</ConceptUI>
    <ConceptName>
     <String>poly(chlorostyrene)</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062467</Concept1UI>
     <Concept2UI>M0062466</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T092469</TermUI>
      <String>poly(chlorostyrene)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014161</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>portensterol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>hydroxyergosterol
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004875</DescriptorUI>
     <DescriptorName>
      <String>Ergosterol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ann Pharm Fr 34(9-10):383;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062471</ConceptUI>
    <ConceptName>
     <String>portensterol</String>
    </ConceptName>
    <CASN1Name>Ergosta-5,8,22-triene-3,11-diol, (3beta,22E)-</CASN1Name>
    <RegistryNumber>62005-66-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092474</TermUI>
      <String>portensterol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014167</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-propyldihydrolipoamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>07</Month>
   <Day>17</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008063</DescriptorUI>
     <DescriptorName>
      <String>Thioctic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 453:277;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062481</ConceptUI>
    <ConceptName>
     <String>N-propyldihydrolipoamide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092484</TermUI>
      <String>N-propyldihydrolipoamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014170</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>protofradin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>protease preparation from Actinomyces fradiae
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010447</DescriptorUI>
     <DescriptorName>
      <String>Peptide Hydrolases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biokhimiia 41(10):1753;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062493</ConceptUI>
    <ConceptName>
     <String>protofradin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092496</TermUI>
      <String>protofradin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014180</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>resorufin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>02</Month>
   <Day>25</Day>
  </DateRevised>
  <Frequency>275</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010078</DescriptorUI>
     <DescriptorName>
      <String>Oxazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Res 37(2):460;1977</Source>
   <Source>Med Biol 1979;57(5):287</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062502</ConceptUI>
    <ConceptName>
     <String>resorufin</String>
    </ConceptName>
    <RegistryNumber>635-78-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092505</TermUI>
      <String>resorufin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C101266</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-(4-iodobenzoyl)-5-methoxy-2-methyl-3-indoleacetic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>10</Month>
   <Day>11</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007213</DescriptorUI>
     <DescriptorName>
      <String>Indomethacin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Crystallogr C 1996 Feb 15;52 Pt 2:455-7</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0265535</ConceptUI>
    <ConceptName>
     <String>1-(4-iodobenzoyl)-5-methoxy-2-methyl-3-indoleacetic acid</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T295540</TermUI>
      <String>1-(4-iodobenzoyl)-5-methoxy-2-methyl-3-indoleacetic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T295539</TermUI>
      <String>1-IBz-MMIAA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C101267</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>phenyl 2-phenyl-1,6-dioxa-2-azaspiro(4.4)non-3-yl ketone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>10</Month>
   <Day>11</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007555</DescriptorUI>
     <DescriptorName>
      <String>Isoxazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013141</DescriptorUI>
     <DescriptorName>
      <String>Spiro Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Crystallogr C 1996 Feb 15;52 Pt 2:486-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0265537</ConceptUI>
    <ConceptName>
     <String>phenyl 2-phenyl-1,6-dioxa-2-azaspiro(4.4)non-3-yl ketone</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T295542</TermUI>
      <String>phenyl 2-phenyl-1,6-dioxa-2-azaspiro(4.4)non-3-yl ketone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T295541</TermUI>
      <String>phenyl PDAN ketone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C069138</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>BM 20.1140</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1991</Year>
   <Month>07</Month>
   <Day>08</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>07</Month>
   <Day>17</Day>
  </DateRevised>
  <Note>structure given in first source; RN given refers to the (+-)-isomer
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011725</DescriptorUI>
     <DescriptorName>
      <String>Pyridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011759</DescriptorUI>
     <DescriptorName>
      <String>Pyrrolidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 1991;266(17):10787</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0188807</ConceptUI>
    <ConceptName>
     <String>BM 20.1140</String>
    </ConceptName>
    <RegistryNumber>135357-95-8</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>134893-56-4 ((R)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>134893-57-5 ((S)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0188807</Concept1UI>
     <Concept2UI>M0325271</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0188807</Concept1UI>
     <Concept2UI>M0188806</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0188807</Concept1UI>
     <Concept2UI>M0325270</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T218812</TermUI>
      <String>BM 20.1140</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T218810</TermUI>
      <String>BM-20.1140</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T218809</TermUI>
      <String>BM 201140</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0325271</ConceptUI>
    <ConceptName>
     <String>BM 20.1140, (S)-isomer</String>
    </ConceptName>
    <RegistryNumber>134893-57-5</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0188807</Concept1UI>
     <Concept2UI>M0325271</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T355271</TermUI>
      <String>BM 20.1140, (S)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0188806</ConceptUI>
    <ConceptName>
     <String>ethyl-2,2-diphenyl-4-(1-pyrrolidino)-5-(2-picolyl)oxyvalerate</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0188807</Concept1UI>
     <Concept2UI>M0188806</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T218811</TermUI>
      <String>ethyl-2,2-diphenyl-4-(1-pyrrolidino)-5-(2-picolyl)oxyvalerate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0325270</ConceptUI>
    <ConceptName>
     <String>BM 20.1140, (R)-isomer</String>
    </ConceptName>
    <RegistryNumber>134893-56-4</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0188807</Concept1UI>
     <Concept2UI>M0325270</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T355270</TermUI>
      <String>BM 20.1140, (R)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014185</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>seldomycin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>07</Month>
   <Day>17</Day>
  </DateRevised>
  <Note>complex consisting of factors 1,2,3,5 from a soil isolate named Streptomyces hofunensis sp. nov; RN given refers to cpd with unknown MF; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ANTIBIOTICS (77-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011714</DescriptorUI>
     <DescriptorName>
      <String>Pyrans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiot (Tokyo) 30(1):17-39;1977</Source>
   <Source>J Antibiot (Tokyo) 30(10):890;1977</Source>
   <Source>J Antibiot (Tokyo) 30(11):1025;1977</Source>
   <Source>J Antibiot (Tokyo) 31(5):441;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062516</ConceptUI>
    <ConceptName>
     <String>seldomycin</String>
    </ConceptName>
    <CASN1Name>Seldomycin</CASN1Name>
    <RegistryNumber>75635-18-6</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>54333-78-7 (seldomycin factor 2)</RelatedRegistryNumber>
     <RelatedRegistryNumber>56276-04-1 (seldomycin factor 1)</RelatedRegistryNumber>
     <RelatedRegistryNumber>56276-05-2 (seldomycin factor 3)</RelatedRegistryNumber>
     <RelatedRegistryNumber>56276-26-7 (seldomycin factor 5)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062516</Concept1UI>
     <Concept2UI>M0312419</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062516</Concept1UI>
     <Concept2UI>M0312418</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062516</Concept1UI>
     <Concept2UI>M0312417</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062516</Concept1UI>
     <Concept2UI>M0312416</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092519</TermUI>
      <String>seldomycin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312419</ConceptUI>
    <ConceptName>
     <String>seldomycin factor 5</String>
    </ConceptName>
    <RegistryNumber>56276-26-7</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062516</Concept1UI>
     <Concept2UI>M0312419</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342419</TermUI>
      <String>seldomycin factor 5</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312418</ConceptUI>
    <ConceptName>
     <String>seldomycin factor 3</String>
    </ConceptName>
    <RegistryNumber>56276-05-2</RegistryNumber>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062516</Concept1UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342418</TermUI>
      <String>seldomycin factor 3</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312417</ConceptUI>
    <ConceptName>
     <String>seldomycin factor 1</String>
    </ConceptName>
    <RegistryNumber>56276-04-1</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062516</Concept1UI>
     <Concept2UI>M0312417</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342417</TermUI>
      <String>seldomycin factor 1</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312416</ConceptUI>
    <ConceptName>
     <String>seldomycin factor 2</String>
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    <RegistryNumber>54333-78-7</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062516</Concept1UI>
     <Concept2UI>M0312416</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342416</TermUI>
      <String>seldomycin factor 2</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
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     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014188</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>sirohydrochlorin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>03</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>chromophore of desulfoviridin; structure
  </Note>
  <Frequency>17</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DESULFOVIRIDINS</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014578</DescriptorUI>
     <DescriptorName>
      <String>Uroporphyrins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Am Chem Soc 100(1):316;1978</Source>
   <Source>J Biochem (Tokyo) 86(1):273;1979</Source>
   <Source>Porphyrins in human diseases W3 IN862:459;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062521</ConceptUI>
    <ConceptName>
     <String>sirohydrochlorin</String>
    </ConceptName>
    <CASN1Name>21H,23H-Porphine-2,7,12,18-tetrapropanoic acid, 3,8,13,17-tetrakis(carboxymethyl)-7,8,12,13-tetrahydro-8,13-dimethyl-, (7S-(7alpha,8beta,12alpha,13beta))-</CASN1Name>
    <RegistryNumber>65207-12-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092524</TermUI>
      <String>sirohydrochlorin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014192</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>spiro(indan-2,2'-pyrrolidine)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>RN is from CA, 87, Chem Subs Index
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011759</DescriptorUI>
     <DescriptorName>
      <String>Pyrrolidines</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013141</DescriptorUI>
     <DescriptorName>
      <String>Spiro Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Pharmacol 28 Suppl:83P;1976</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062526</ConceptUI>
    <ConceptName>
     <String>spiro(indan-2,2'-pyrrolidine)</String>
    </ConceptName>
    <RegistryNumber>62778-57-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092529</TermUI>
      <String>spiro(indan-2,2'-pyrrolidine)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
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   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014193</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>spiro(tetralin-2,2'-pyrrolidine)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>06</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>RN given refers to HCl salt
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011759</DescriptorUI>
     <DescriptorName>
      <String>Pyrrolidines</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013141</DescriptorUI>
     <DescriptorName>
      <String>Spiro Compounds</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Pharmacol 28 Suppl:83P;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062527</ConceptUI>
    <ConceptName>
     <String>spiro(tetralin-2,2'-pyrrolidine)</String>
    </ConceptName>
    <RegistryNumber>62594-46-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092530</TermUI>
      <String>spiro(tetralin-2,2'-pyrrolidine)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014197</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Suczulen</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1992</Year>
   <Month>03</Month>
   <Day>17</Day>
  </DateRevised>
  <Note>combination of licorice, guaiazulene, &amp; bicyclophenamine
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  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PYRROLIDINES (77-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001643</DescriptorUI>
     <DescriptorName>
      <String>Bridged Bicyclo Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012717</DescriptorUI>
     <DescriptorName>
      <String>Sesquiterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D006035</DescriptorUI>
     <DescriptorName>
      <String>Glycyrrhiza</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>ZFA (Stuttgart) 53(3):170;1977</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062538</ConceptUI>
    <ConceptName>
     <String>Suczulen</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092541</TermUI>
      <String>Suczulen</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014213</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tetrahydrojateorrhizine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001600</DescriptorUI>
     <DescriptorName>
      <String>Berberine Alkaloids</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Folia Pharmacol Jpn 72(7):909;1976</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062567</ConceptUI>
    <ConceptName>
     <String>tetrahydrojateorrhizine</String>
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    <CASN1Name>6H-Dibenzo(a,g)quinolizin-3-ol, 5,8,13,13a-tetrahydro-2,9,10-trimethoxy-</CASN1Name>
    <RegistryNumber>13063-54-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092570</TermUI>
      <String>tetrahydrojateorrhizine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
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   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014217</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tetramethyl-2-tetrazene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001391</DescriptorUI>
     <DescriptorName>
      <String>Azo Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>IARC Sci Publ 14:255;1976</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062575</ConceptUI>
    <ConceptName>
     <String>tetramethyl-2-tetrazene</String>
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    <RegistryNumber>6130-87-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092578</TermUI>
      <String>tetramethyl-2-tetrazene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014220</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>thallium malonic formate</String>
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  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009942</DescriptorUI>
     <DescriptorName>
      <String>Organometallic Compounds</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D013793</DescriptorUI>
     <DescriptorName>
      <String>Thallium</String>
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     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Gig Tr 8:35;1976</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062578</ConceptUI>
    <ConceptName>
     <String>thallium malonic formate</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092581</TermUI>
      <String>thallium malonic formate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
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   </Concept>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014221</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-thiageranic acid ethyl ester</String>
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  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>06</Month>
   <Day>16</Day>
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  <Note>structure
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  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>SULFIDES (77-82)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013729</DescriptorUI>
     <DescriptorName>
      <String>Terpenes</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Pharm 309(12):1019;1976</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062579</ConceptUI>
    <ConceptName>
     <String>4-thiageranic acid ethyl ester</String>
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    <CASN1Name>4-thia-3,7-dimethyl-2,6-octadiene-1-carboxylic acid ethyl ester</CASN1Name>
    <RegistryNumber>0</RegistryNumber>
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     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092582</TermUI>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014301</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>acetoxymethylbenzylnitrosamine</String>
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  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>09</Day>
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009602</DescriptorUI>
     <DescriptorName>
      <String>Nitrosamines</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Lett 2(6):305;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062748</ConceptUI>
    <ConceptName>
     <String>acetoxymethylbenzylnitrosamine</String>
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    <CASN1Name>Benzenemethanamine, N-((acetyloxy)methyl)-N-nitroso-</CASN1Name>
    <RegistryNumber>63531-81-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092751</TermUI>
      <String>acetoxymethylbenzylnitrosamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T092750</TermUI>
      <String>N-nitroso-N-methyl-N-alpha-acetoxybenzylamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C422302</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-((2S)-2-mercapto-1-oxo-4-(3,4,4- trimethyl-2,5-dioxo-1-imidazolidinyl)butyl)-L-leucyl-N,3- dimethyl-L-Valinamide</String>
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  <DateCreated>
   <Year>2001</Year>
   <Month>03</Month>
   <Day>22</Day>
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  <DateRevised>
   <Year>2006</Year>
   <Month>02</Month>
   <Day>22</Day>
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  <Note>matrix metalloproteinase inhibitor
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  <Frequency>14</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ANTINEOPLASTIC AGENTS (2001-2003)</PreviousIndexing>
   <PreviousIndexing>*ORGANIS CHEMICALS (2004-2006)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007093</DescriptorUI>
     <DescriptorName>
      <String>Imidazoles</String>
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  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D020782</DescriptorUI>
     <DescriptorName>
      <String>Matrix Metalloproteinases</String>
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     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Natl Cancer Inst 2001 Feb 7;93(3):178-93</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0381870</ConceptUI>
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     <String>N-((2S)-2-mercapto-1-oxo-4-(3,4,4- trimethyl-2,5-dioxo-1-imidazolidinyl)butyl)-L-leucyl-N,3- dimethyl-L-Valinamide</String>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0381870</Concept1UI>
     <Concept2UI>M0492923</Concept2UI>
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      <TermUI>T662204</TermUI>
      <String>N-((2S)-2-mercapto-1-oxo-4-(3,4,4- trimethyl-2,5-dioxo-1-imidazolidinyl)butyl)-L-leucyl-N,3- dimethyl-L-Valinamide</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>12</Month>
       <Day>14</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
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   <Concept PreferredConceptYN="N">
    <ConceptUI>M0492924</ConceptUI>
    <ConceptName>
     <String>D-2163</String>
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      <TermUI>T662205</TermUI>
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       <Year>2005</Year>
       <Month>12</Month>
       <Day>14</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0492923</ConceptUI>
    <ConceptName>
     <String>BMS-275291</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0381870</Concept1UI>
     <Concept2UI>M0492923</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T440261</TermUI>
      <String>BMS-275291</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>03</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014231</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4,6,7-trimethoxy-5-methylchromen-2-one</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003374</DescriptorUI>
     <DescriptorName>
      <String>Coumarins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Chem Soc (Perkin Trans I):2594;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062599</ConceptUI>
    <ConceptName>
     <String>4,6,7-trimethoxy-5-methylchromen-2-one</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092602</TermUI>
      <String>4,6,7-trimethoxy-5-methylchromen-2-one</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014239</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>undofen</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>aerosol prep of the above combination
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004003</DescriptorUI>
     <DescriptorName>
      <String>Dichlorophen</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006582</DescriptorUI>
     <DescriptorName>
      <String>Hexachlorophene</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014476</DescriptorUI>
     <DescriptorName>
      <String>Undecylenic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ann Acad Med Stetin 22:381;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062604</ConceptUI>
    <ConceptName>
     <String>undofen</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092607</TermUI>
      <String>undofen</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014240</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>17 beta-ureido-1,4-androstadien-3-one</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1996</Year>
   <Month>09</Month>
   <Day>13</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000730</DescriptorUI>
     <DescriptorName>
      <String>Androstadienes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D013254</DescriptorUI>
     <DescriptorName>
      <String>Steroid 17-alpha-Hydroxylase</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
     <QualifierName>
      <String>antagonists &amp; inhibitors</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Endocrinol 71(3):289;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062605</ConceptUI>
    <ConceptName>
     <String>17 beta-ureido-1,4-androstadien-3-one</String>
    </ConceptName>
    <CASN1Name>Urea, ((17beta)-3-oxoandrosta-1,4-dien-17-yl)-</CASN1Name>
    <RegistryNumber>32012-41-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092608</TermUI>
      <String>17 beta-ureido-1,4-androstadien-3-one</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014245</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-vinylguaiacol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>03</Month>
   <Day>04</Day>
  </DateRevised>
  <Frequency>55</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>VINYL COMPOUNDS</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D006139</DescriptorUI>
     <DescriptorName>
      <String>Guaiacol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Science 195(4278):575;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062611</ConceptUI>
    <ConceptName>
     <String>4-vinylguaiacol</String>
    </ConceptName>
    <CASN1Name>4-ethenyl-2- methoxyphenol</CASN1Name>
    <RegistryNumber>7786-61-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062611</Concept1UI>
     <Concept2UI>M0062610</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092614</TermUI>
      <String>4-vinylguaiacol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0062610</ConceptUI>
    <ConceptName>
     <String>4-hydroxy-3-methoxystyrene</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062611</Concept1UI>
     <Concept2UI>M0062610</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T092613</TermUI>
      <String>4-hydroxy-3-methoxystyrene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C016681</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>poly(dG).poly(dC)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>see also poly(dC-dG): 29855-95-6
  </Note>
  <Frequency>108</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>POLY C (78-81)</PreviousIndexing>
   <PreviousIndexing>POLY G (78-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011089</DescriptorUI>
     <DescriptorName>
      <String>Polydeoxyribonucleotides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Mol Biol 125(4):535;1978</Source>
   <Source>Nucleic Acids Res 5(3):1017;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0066856</ConceptUI>
    <ConceptName>
     <String>poly(dG).poly(dC)</String>
    </ConceptName>
    <RegistryNumber>25512-84-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T096859</TermUI>
      <String>poly(dG).poly(dC)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T096858</TermUI>
      <String>poly(dC).poly(dG)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014283</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>CD 3400</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>RN given refers to (3beta,16beta,17alpha,18beta,20alpha)-isomer
  </Note>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*RESERPINE DERIVATIVES (77-78)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D012110</DescriptorUI>
     <DescriptorName>
      <String>Reserpine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Folia Pharmacol Jpn 72(8):969;1976</Source>
   <Source>Folia Pharmacol Jpn 73(7):734;1977</Source>
   <Source>Jpn J Pharmacol 27:87;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062714</ConceptUI>
    <ConceptName>
     <String>CD 3400</String>
    </ConceptName>
    <CASN1Name>yohimban-16-carboxylic acid, 18-((3-(4-hydroxy-3-methoxyphenyl)-1-oxo-2-propenyl)oxy)-11,17-dimethoxy-, methyl ester, (3 beta,16 beta,17 alpha,18 beta,20 alpha)-</CASN1Name>
    <RegistryNumber>35440-49-4</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>73573-42-9 ((3beta,16beta,17alpha,18beta(E),20alpha)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0062714</Concept1UI>
     <Concept2UI>M0062713</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062714</Concept1UI>
     <Concept2UI>M0312457</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T092717</TermUI>
      <String>CD 3400</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T092715</TermUI>
      <String>CD-3400</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0062713</ConceptUI>
    <ConceptName>
     <String>methyl O-(4-hydroxy-3-methoxycinnamoyl)reserpate</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0062714</Concept1UI>
     <Concept2UI>M0062713</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T092716</TermUI>
      <String>methyl O-(4-hydroxy-3-methoxycinnamoyl)reserpate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312457</ConceptUI>
    <ConceptName>
     <String>CD 3400, (3beta,16beta,17alpha,18beta(E),20alpha)-isomer</String>
    </ConceptName>
    <RegistryNumber>73573-42-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062714</Concept1UI>
     <Concept2UI>M0312457</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342457</TermUI>
      <String>CD 3400, (3beta,16beta,17alpha,18beta(E),20alpha)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C094467</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>PSK6 protein, Petunia x hybrida</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>08</Month>
   <Day>07</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>09</Month>
   <Day>22</Day>
  </DateRevised>
  <Note>GenBank X83620
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010940</DescriptorUI>
     <DescriptorName>
      <String>Plant Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D017346</DescriptorUI>
     <DescriptorName>
      <String>Protein-Serine-Threonine Kinases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Plant J 1995 Jun;7(6):897-911</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0248892</ConceptUI>
    <ConceptName>
     <String>PSK6 protein, Petunia x hybrida</String>
    </ConceptName>
    <RegistryNumber>EC 2.7.1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T278897</TermUI>
      <String>PSK6 protein, Petunia x hybrida</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T560276</TermUI>
      <String>petunia shaggy kinase 6 protein, Petunia x hybrida</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>11</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011645</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>aminomalononitrile</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>09</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>HCN trimer; structure
  </Note>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>MALONATES (76-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009570</DescriptorUI>
     <DescriptorName>
      <String>Nitriles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Molec Evol 7(1):65;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058115</ConceptUI>
    <ConceptName>
     <String>aminomalononitrile</String>
    </ConceptName>
    <RegistryNumber>5181-05-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088118</TermUI>
      <String>aminomalononitrile</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011646</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6-amino-NAD</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009243</DescriptorUI>
     <DescriptorName>
      <String>NAD</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Teratology 13(1):85;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058116</ConceptUI>
    <ConceptName>
     <String>6-amino-NAD</String>
    </ConceptName>
    <RegistryNumber>652-81-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088119</TermUI>
      <String>6-amino-NAD</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011652</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-aminoselenoazoline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1992</Year>
   <Month>05</Month>
   <Day>14</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PYRROLES (76-81)</PreviousIndexing>
   <PreviousIndexing>SELENIUM (76-92)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D016566</DescriptorUI>
     <DescriptorName>
      <String>Organoselenium Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Strahlentherapie 150(6):590;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058132</ConceptUI>
    <ConceptName>
     <String>2-aminoselenoazoline</String>
    </ConceptName>
    <RegistryNumber>15267-04-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088135</TermUI>
      <String>2-aminoselenoazoline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011662</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>anisilbutamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013453</DescriptorUI>
     <DescriptorName>
      <String>Sulfonylurea Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Farmaco(Ed Prat) 31(2):95;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058145</ConceptUI>
    <ConceptName>
     <String>anisilbutamide</String>
    </ConceptName>
    <CASN1Name>1-butyl-3-(p-methoxyphenylsulfonyl)urea</CASN1Name>
    <RegistryNumber>24535-67-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088148</TermUI>
      <String>anisilbutamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011663</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>anthrazoline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>09</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PYRIDINES (76-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011804</DescriptorUI>
     <DescriptorName>
      <String>Quinolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Proc Int Sym Macromol QU 55:102-1643;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058146</ConceptUI>
    <ConceptName>
     <String>anthrazoline</String>
    </ConceptName>
    <CASN1Name>pyrido(2,3-g)quinoline</CASN1Name>
    <RegistryNumber>260-69-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088149</TermUI>
      <String>anthrazoline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C514006</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>7,14-epoxyazedarachin B</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>10</Month>
   <Day>07</Day>
  </DateCreated>
  <Note>isolated from Melia azedarach; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013256</DescriptorUI>
     <DescriptorName>
      <String>Steroids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Pharm Bull (Tokyo) 2006 Aug;54(8):1219-22</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0502605</ConceptUI>
    <ConceptName>
     <String>7,14-epoxyazedarachin B</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T683186</TermUI>
      <String>7,14-epoxyazedarachin B</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>10</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C492152</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>DED1 protein, S cerevisiae</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>11</Month>
   <Day>02</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>a DEAD box RNA helicase required for translation initiation; amino acid sequence in first source
  </Note>
  <Frequency>62</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CELL CYCLE PROTEINS (2004-2006)</PreviousIndexing>
   <PreviousIndexing>*RNA HELICASES (2004-2006)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029701</DescriptorUI>
     <DescriptorName>
      <String>Saccharomyces cerevisiae Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D053487</DescriptorUI>
     <DescriptorName>
      <String>DEAD-box RNA Helicases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0459539</ConceptUI>
    <ConceptName>
     <String>DED1 protein, S cerevisiae</String>
    </ConceptName>
    <RegistryNumber>EC 3.6.1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T569764</TermUI>
      <String>DED1 protein, S cerevisiae</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>01</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T678002</TermUI>
      <String>SPP81 protein, S cerevisiae</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>07</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T569765</TermUI>
      <String>YOR204W protein, S cerevisiae</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>01</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C525106</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>8-nitroguanosine 3',5'-cyclic monophosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>12</Month>
   <Day>20</Day>
  </DateCreated>
  <Note>a signal for protein S-guanylation; structure in first source
  </Note>
  <Frequency>55</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D006152</DescriptorUI>
     <DescriptorName>
      <String>Cyclic GMP</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nat Chem Biol 2007 Nov;3(11):727-35</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0516695</ConceptUI>
    <ConceptName>
     <String>8-nitroguanosine 3',5'-cyclic monophosphate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T711504</TermUI>
      <String>8-nitroguanosine 3',5'-cyclic monophosphate</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>12</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T711505</TermUI>
      <String>8-nitro-cGMP</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>12</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C525107</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Sod-3 protein, C elegans</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>12</Month>
   <Day>20</Day>
  </DateCreated>
  <Note>GenBank X85790
  </Note>
  <Frequency>44</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013482</DescriptorUI>
     <DescriptorName>
      <String>Superoxide Dismutase</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029742</DescriptorUI>
     <DescriptorName>
      <String>Caenorhabditis elegans Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 1997 Nov 7;272(45):28652-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0516696</ConceptUI>
    <ConceptName>
     <String>Sod-3 protein, C elegans</String>
    </ConceptName>
    <RegistryNumber>EC 1.15.1.1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T711506</TermUI>
      <String>Sod-3 protein, C elegans</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>12</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C445083</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>DHH1 protein, S cerevisiae</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>a DEAD box helicase involved in mRNA decapping; GenBank X66057
  </Note>
  <Frequency>70</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*FUNGAL PROTEINS (2002-2004)</PreviousIndexing>
   <PreviousIndexing>*RNA HELICASES (2002-2006)</PreviousIndexing>
   <PreviousIndexing>*RNA-BINDING PROTEINS (2002-2006)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029701</DescriptorUI>
     <DescriptorName>
      <String>Saccharomyces cerevisiae Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D053487</DescriptorUI>
     <DescriptorName>
      <String>DEAD-box RNA Helicases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Genomics 1998 Feb;148(2):571-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0412380</ConceptUI>
    <ConceptName>
     <String>DHH1 protein, S cerevisiae</String>
    </ConceptName>
    <RegistryNumber>EC 3.6.1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T582438</TermUI>
      <String>DHH1 protein, S cerevisiae</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>04</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T479454</TermUI>
      <String>YDL160C protein, S cerevisiae</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>01</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C100168</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>chloroacetol phosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1985</Year>
   <Month>06</Month>
   <Day>14</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>minor descriptor (75-85); on-line &amp; Index Medicus search ORGANOPHOSPHORUS COMPOUNDS (75-85); RN given refers to parent cpd
  </Note>
  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>minor descriptor (75-85); file-maintained to ORGANOPHOSPHORUS COMPOUNDS</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009943</DescriptorUI>
     <DescriptorName>
      <String>Organophosphorus Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0262878</ConceptUI>
    <ConceptName>
     <String>chloroacetol phosphate</String>
    </ConceptName>
    <RegistryNumber>23743-97-7</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>55765-29-2 (mono-Na salt)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0262878</Concept1UI>
     <Concept2UI>M0327362</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T292883</TermUI>
      <String>chloroacetol phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T292882</TermUI>
      <String>1-chloro-3-hydroxy-2-propanone dihydrogen phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0327362</ConceptUI>
    <ConceptName>
     <String>chloroacetol phosphate, monosodium salt</String>
    </ConceptName>
    <RegistryNumber>55765-29-2</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0262878</Concept1UI>
     <Concept2UI>M0327362</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T357362</TermUI>
      <String>chloroacetol phosphate, monosodium salt</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014563</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>formylvaline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014633</DescriptorUI>
     <DescriptorName>
      <String>Valine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biochem 81(1):269;1977</Source>
   <Source>J Biochem 83:1219;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063151</ConceptUI>
    <ConceptName>
     <String>formylvaline</String>
    </ConceptName>
    <RegistryNumber>4289-97-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093154</TermUI>
      <String>formylvaline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014566</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>17 beta-(3-furyl)-5 beta,14 beta-androstane-3 beta,14 beta-diol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>12</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ANDROSTANEDIOL/analogs (77-80)</PreviousIndexing>
   <PreviousIndexing>FURANS (77-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000732</DescriptorUI>
     <DescriptorName>
      <String>Androstanols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Pharm Bull 24(12):3216;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063155</ConceptUI>
    <ConceptName>
     <String>17 beta-(3-furyl)-5 beta,14 beta-androstane-3 beta,14 beta-diol</String>
    </ConceptName>
    <CASN1Name>24-Norchola-20,22-diene-3,14-diol, 21,23-epoxy-, (3beta,5beta,14beta)-</CASN1Name>
    <RegistryNumber>1919-02-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093158</TermUI>
      <String>17 beta-(3-furyl)-5 beta,14 beta-androstane-3 beta,14 beta-diol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014571</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>glucosyl diacylglycerol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1993</Year>
   <Month>08</Month>
   <Day>31</Day>
  </DateRevised>
  <Frequency>33</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006017</DescriptorUI>
     <DescriptorName>
      <String>Glycolipids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 252(12):4395;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063186</ConceptUI>
    <ConceptName>
     <String>glucosyl diacylglycerol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0063186</Concept1UI>
     <Concept2UI>M0063185</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0063186</Concept1UI>
     <Concept2UI>M0063184</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0063186</Concept1UI>
     <Concept2UI>M0063183</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0063186</Concept1UI>
     <Concept2UI>M0063182</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093189</TermUI>
      <String>glucosyl diacylglycerol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0063185</ConceptUI>
    <ConceptName>
     <String>monoglucosyl diglyceride</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0063186</Concept1UI>
     <Concept2UI>M0063185</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T093188</TermUI>
      <String>monoglucosyl diglyceride</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0063184</ConceptUI>
    <ConceptName>
     <String>monoglucosyl diacylglycerol</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0063186</Concept1UI>
     <Concept2UI>M0063184</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T093187</TermUI>
      <String>monoglucosyl diacylglycerol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0063183</ConceptUI>
    <ConceptName>
     <String>MGlcDAG</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0063186</Concept1UI>
     <Concept2UI>M0063183</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T093186</TermUI>
      <String>MGlcDAG</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0063182</ConceptUI>
    <ConceptName>
     <String>1,2-diacyl-3-O-(alpha-D-glucopyranosyl)-sn-glycerol</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0063186</Concept1UI>
     <Concept2UI>M0063182</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T093185</TermUI>
      <String>1,2-diacyl-3-O-(alpha-D-glucopyranosyl)-sn-glycerol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014576</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>grandiflorenic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>05</Month>
   <Day>24</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>13</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CARBOXYLIC ACIDS (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004224</DescriptorUI>
     <DescriptorName>
      <String>Diterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arzneim Forsch 27(5):999;1977</Source>
   <Source>Arzneim Forsch 27(6):1162;1977</Source>
   <Source>Arzneim Forsch 27(7):1384;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063194</ConceptUI>
    <ConceptName>
     <String>grandiflorenic acid</String>
    </ConceptName>
    <CASN1Name>Kaura-9(11),16-dien-18-oic acid</CASN1Name>
    <RegistryNumber>22338-67-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093197</TermUI>
      <String>grandiflorenic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C525108</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>apoptosis-induced regulator protein</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>12</Month>
   <Day>20</Day>
  </DateCreated>
  <Note>a patented protein derived from a 3564 bp cDNA from okadaic acid-treated Jurkat cells; GenBank AX538681, AX538682, and AC538684
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D051017</DescriptorUI>
     <DescriptorName>
      <String>Apoptosis Regulatory Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Leukemia 2007 Dec;21(12):2557-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0516697</ConceptUI>
    <ConceptName>
     <String>apoptosis-induced regulator protein</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T711507</TermUI>
      <String>apoptosis-induced regulator protein</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>12</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T711508</TermUI>
      <String>AIR synthetic protein</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>12</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014579</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hematodeanol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>complex formed by the above two molecules
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003642</DescriptorUI>
     <DescriptorName>
      <String>Deanol</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006415</DescriptorUI>
     <DescriptorName>
      <String>Hematoporphyrins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arzneim Forsch 27(5):1015;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063198</ConceptUI>
    <ConceptName>
     <String>hematodeanol</String>
    </ConceptName>
    <CASN1Name>21H,23H-Porphine-2,18-dipropanoic acid, 7,12-bis(1-hydroxyethyl)-3,8,13,17-tetramethyl-, compd. with 2-(dimethylamino)ethanol (1:1)</CASN1Name>
    <RegistryNumber>63958-65-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093201</TermUI>
      <String>hematodeanol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014582</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hernandalinol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001060</DescriptorUI>
     <DescriptorName>
      <String>Aporphines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 20(7):914;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063201</ConceptUI>
    <ConceptName>
     <String>hernandalinol</String>
    </ConceptName>
    <RegistryNumber>62874-90-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093204</TermUI>
      <String>hernandalinol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C473365</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>FITC-tyramide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>04</Month>
   <Day>25</Day>
  </DateCreated>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014439</DescriptorUI>
     <DescriptorName>
      <String>Tyramine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D016650</DescriptorUI>
     <DescriptorName>
      <String>Fluorescein-5-isothiocyanate</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Immunol 2003 Feb;33(2):483-93</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0448675</ConceptUI>
    <ConceptName>
     <String>FITC-tyramide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T539252</TermUI>
      <String>FITC-tyramide</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>04</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C433897</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>pannosanol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>09</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>from the Malaysian Laurencia pannosa (Rhodomelaceae, Ceramiales); structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012717</DescriptorUI>
     <DescriptorName>
      <String>Sesquiterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2001 May;64(5):597-602</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0397198</ConceptUI>
    <ConceptName>
     <String>pannosanol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T459953</TermUI>
      <String>pannosanol</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>09</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014589</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hippomannin A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>08</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>toxic principle from Hippomane mancinella; structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D047348</DescriptorUI>
     <DescriptorName>
      <String>Hydrolyzable Tannins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 40(2):169;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063226</ConceptUI>
    <ConceptName>
     <String>hippomannin A</String>
    </ConceptName>
    <CASN1Name>D-Glucose, cyclic 4,6-(4,4',5,5',6,6'-hexahydroxy(1,1'-biphenyl)-2,2'-dicarboxylate) 2-(3,4,5-trihydroxybenzoate)</CASN1Name>
    <RegistryNumber>52934-78-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093229</TermUI>
      <String>hippomannin A</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014598</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-hydroxy-4-isopropylaminochroman</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PROPYLAMINES (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002839</DescriptorUI>
     <DescriptorName>
      <String>Chromans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Pharm Suec 14:21;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063247</ConceptUI>
    <ConceptName>
     <String>3-hydroxy-4-isopropylaminochroman</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093250</TermUI>
      <String>3-hydroxy-4-isopropylaminochroman</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014603</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-hydroxy-3-oxobutyrate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006885</DescriptorUI>
     <DescriptorName>
      <String>Hydroxybutyrates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Med 17(3):284;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063255</ConceptUI>
    <ConceptName>
     <String>4-hydroxy-3-oxobutyrate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093258</TermUI>
      <String>4-hydroxy-3-oxobutyrate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C433899</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>pannosane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>09</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>from the Malaysian Laurencia pannosa (Rhodomelaceae, Ceramiales); structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012717</DescriptorUI>
     <DescriptorName>
      <String>Sesquiterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2001 May;64(5):597-602</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0397201</ConceptUI>
    <ConceptName>
     <String>pannosane</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T459956</TermUI>
      <String>pannosane</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>09</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014619</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N'-isobutyryl-N-benzyl-N-nitrosophenylalaninamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>chymotrypsin preferential inhibitor; structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PHENYLALANINE/analogs (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009602</DescriptorUI>
     <DescriptorName>
      <String>Nitrosamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Am Chem Soc 99(9):3171;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063276</ConceptUI>
    <ConceptName>
     <String>N'-isobutyryl-N-benzyl-N-nitrosophenylalaninamide</String>
    </ConceptName>
    <CASN1Name>Benzenepropanamide, alpha-((2-methyl-1-oxopropyl)amino)-N-nitroso-N-(phenylmethyl)-, (R)-</CASN1Name>
    <RegistryNumber>62886-02-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093279</TermUI>
      <String>N'-isobutyryl-N-benzyl-N-nitrosophenylalaninamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014620</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>isochroman-4-spiro-4'-piperidine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CHROMANS (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010880</DescriptorUI>
     <DescriptorName>
      <String>Piperidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Farmaco(Sci) 32(3):212;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063277</ConceptUI>
    <ConceptName>
     <String>isochroman-4-spiro-4'-piperidine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093280</TermUI>
      <String>isochroman-4-spiro-4'-piperidine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C094779</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>HTLV-II(G12) TaxII protein (337-356)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>08</Month>
   <Day>28</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>13</Day>
  </DateRevised>
  <Note>a human lymphotropic virus (HTLV) type IIb-restricted epitope; amino acid sequence given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010446</DescriptorUI>
     <DescriptorName>
      <String>Peptide Fragments</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D016356</DescriptorUI>
     <DescriptorName>
      <String>Gene Products, tax</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D000939</DescriptorUI>
     <DescriptorName>
      <String>Epitopes</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D015367</DescriptorUI>
     <DescriptorName>
      <String>Human T-lymphotropic virus 2</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Infect Dis 1995 Aug;172(2):554-7</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0249694</ConceptUI>
    <ConceptName>
     <String>HTLV-II(G12) TaxII protein (337-356)</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T279699</TermUI>
      <String>HTLV-II(G12) TaxII protein (337-356)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T279698</TermUI>
      <String>G12Tax24</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014630</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>jodonal A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007466</DescriptorUI>
     <DescriptorName>
      <String>Iodophors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Vet Med (Cesk) 21(11):649-55;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063303</ConceptUI>
    <ConceptName>
     <String>jodonal A</String>
    </ConceptName>
    <CASN1Name>iodonal A</CASN1Name>
    <RegistryNumber>56833-12-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093306</TermUI>
      <String>jodonal A</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C467119</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>roraimine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>10</Month>
   <Day>29</Day>
  </DateCreated>
  <Note>a bisbenzylisoquinoline alkaloid from Cissampelos sympodialis (Menispermaceae) roots; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000470</DescriptorUI>
     <DescriptorName>
      <String>Alkaloids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007546</DescriptorUI>
     <DescriptorName>
      <String>Isoquinolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Fitoterapia 2002 Jul;73(4):356-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0440894</ConceptUI>
    <ConceptName>
     <String>roraimine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T524514</TermUI>
      <String>roraimine</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>10</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C467120</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-hydroxyethyl-N-ethyl-3-methyl-p-phenylenediamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>10</Month>
   <Day>29</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010655</DescriptorUI>
     <DescriptorName>
      <String>Phenylenediamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Rapid Commun Mass Spectrom 2002;16(17):1622-30</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0440895</ConceptUI>
    <ConceptName>
     <String>N-hydroxyethyl-N-ethyl-3-methyl-p-phenylenediamine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T524515</TermUI>
      <String>N-hydroxyethyl-N-ethyl-3-methyl-p-phenylenediamine</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>10</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T524516</TermUI>
      <String>N-HEMP cpd</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>10</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C094744</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>light-harvesting complex 1, Rhodospirillum</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>08</Month>
   <Day>25</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>02</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>partial amino acid sequence given in first source
  </Note>
  <Frequency>98</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PHOTOSYNTHETIC REACTION CENTER, BACTERIAL (1995-2003)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D045342</DescriptorUI>
     <DescriptorName>
      <String>Light-Harvesting Protein Complexes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 1995 Jun 30;1230(3):147-54</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0249599</ConceptUI>
    <ConceptName>
     <String>light-harvesting complex 1, Rhodospirillum</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0249599</Concept1UI>
     <Concept2UI>M0190125</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0249599</Concept1UI>
     <Concept2UI>M0235503</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0249599</Concept1UI>
     <Concept2UI>M0449720</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T279604</TermUI>
      <String>light-harvesting complex 1, Rhodospirillum</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T541467</TermUI>
      <String>LH1 protein, Rhodospirillum</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>05</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0190125</ConceptUI>
    <ConceptName>
     <String>LHIalpha polypeptide, Rhodospirillum</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0249599</Concept1UI>
     <Concept2UI>M0190125</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T220130</TermUI>
      <String>LHIalpha polypeptide, Rhodospirillum</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T220127</TermUI>
      <String>LHI alpha polypeptide, Rhodospirillum</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0235503</ConceptUI>
    <ConceptName>
     <String>LHIbeta polypeptide, Rhodospirillum</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0249599</Concept1UI>
     <Concept2UI>M0235503</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T265508</TermUI>
      <String>LHIbeta polypeptide, Rhodospirillum</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T265505</TermUI>
      <String>B875-beta protein, Rhodospirillum</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0449720</ConceptUI>
    <ConceptName>
     <String>light-harvesting complex 1, Rhodobacter</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0249599</Concept1UI>
     <Concept2UI>M0449720</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T541468</TermUI>
      <String>light-harvesting complex 1, Rhodobacter</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>05</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014643</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>lipopeptidophosphoglycan</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1992</Year>
   <Month>09</Month>
   <Day>18</Day>
  </DateRevised>
  <Note>complex carbohydrate isolated from Trypanosoma cruzi, Entamoeba histolytica, and Acanthamoeba
  </Note>
  <Frequency>28</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010457</DescriptorUI>
     <DescriptorName>
      <String>Peptidoglycan</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010743</DescriptorUI>
     <DescriptorName>
      <String>Phospholipids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D000953</DescriptorUI>
     <DescriptorName>
      <String>Antigens, Protozoan</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D000954</DescriptorUI>
     <DescriptorName>
      <String>Antigens, Surface</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 85(4):1268;1978</Source>
   <Source>Eur J Biochem 74(2):263;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063335</ConceptUI>
    <ConceptName>
     <String>lipopeptidophosphoglycan</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093338</TermUI>
      <String>lipopeptidophosphoglycan</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C503937</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-acetyl-2-carboxymethylbenzenesulfonamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>09</Month>
   <Day>21</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>09</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D001241</DescriptorUI>
     <DescriptorName>
      <String>Aspirin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013449</DescriptorUI>
     <DescriptorName>
      <String>Sulfonamides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Bioorg Med Chem. 2005 Aug 1;13(15):4694-703</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0489564</ConceptUI>
    <ConceptName>
     <String>N-acetyl-2-carboxymethylbenzenesulfonamide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0489564</Concept1UI>
     <Concept2UI>M0489565</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T652604</TermUI>
      <String>N-acetyl-2-carboxymethylbenzenesulfonamide</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>09</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0489565</ConceptUI>
    <ConceptName>
     <String>N-acetyl-3-carboxymethylbenzenesulfonamide</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0489564</Concept1UI>
     <Concept2UI>M0489565</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T652605</TermUI>
      <String>N-acetyl-3-carboxymethylbenzenesulfonamide</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>09</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C039468</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Biolite</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1983</Year>
   <Month>11</Month>
   <Day>17</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>carbon coating biocompatible material; no other information available
  </Note>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002244</DescriptorUI>
     <DescriptorName>
      <String>Carbon</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Octolaryngol Head Neck Surg 1983;91(4):437</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0118165</ConceptUI>
    <ConceptName>
     <String>Biolite</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="TRD"  RecordPreferredTermYN="Y">
      <TermUI>T148169</TermUI>
      <String>Biolite</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014662</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N beta-methyl-beta-arginine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D001120</DescriptorUI>
     <DescriptorName>
      <String>Arginine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 42(8):1282;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063372</ConceptUI>
    <ConceptName>
     <String>N beta-methyl-beta-arginine</String>
    </ConceptName>
    <CASN1Name>Pentanoic acid, 5-((aminoiminomethyl)amino)-3-(methylamino)-, hydrochloride, (S)-</CASN1Name>
    <RegistryNumber>61394-78-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093375</TermUI>
      <String>N beta-methyl-beta-arginine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014670</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>methylethylthiophos</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*INSECTICIDES, ORGANOTHIOPHOSPHATE (77-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009946</DescriptorUI>
     <DescriptorName>
      <String>Organothiophosphorus Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Farmatsiia 26(5):44;1977</Source>
   <Source>Farmatsiia 26(6):67;1977</Source>
   <Source>Sud Med Ekspert 2:48;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063383</ConceptUI>
    <ConceptName>
     <String>methylethylthiophos</String>
    </ConceptName>
    <CASN1Name>Phosphorothioic acid, O-ethyl O-methyl O-(4-nitrophenyl) ester</CASN1Name>
    <RegistryNumber>2591-57-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093386</TermUI>
      <String>methylethylthiophos</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014676</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-methyl-4-nitrofuroxan</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>12</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005664</DescriptorUI>
     <DescriptorName>
      <String>Furazolidone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Pharmacol Res Commun 8(3):253;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063395</ConceptUI>
    <ConceptName>
     <String>3-methyl-4-nitrofuroxan</String>
    </ConceptName>
    <RegistryNumber>5570-27-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093398</TermUI>
      <String>3-methyl-4-nitrofuroxan</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014683</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>micordilin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>11</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>isolated from West Indian medicinal plant Mikania cordifolia.; structure
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*LACTONES (77-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001578</DescriptorUI>
     <DescriptorName>
      <String>Benzopyrans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 42(10):1720;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063403</ConceptUI>
    <ConceptName>
     <String>micordilin</String>
    </ConceptName>
    <CASN1Name>6,9-Epoxyfuro(2,3-h)(3)benzoxepin-2(3H)-one, 9a-((acetyloxy)methyl)decahydro-8-hydroxy-3,5-bis(methylene)-, (3aR-(3aalpha,4aalpha,6beta,8beta,9beta,9abeta,10aalpha))-</CASN1Name>
    <RegistryNumber>61701-92-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093406</TermUI>
      <String>micordilin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C059727</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N,N-diethyl-2-chloroacetamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1989</Year>
   <Month>06</Month>
   <Day>23</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>07</Day>
  </DateRevised>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000081</DescriptorUI>
     <DescriptorName>
      <String>Acetamides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Gig Tr Prof Zabol 1989;(2):51</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0166067</ConceptUI>
    <ConceptName>
     <String>N,N-diethyl-2-chloroacetamide</String>
    </ConceptName>
    <RegistryNumber>2315-36-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T196072</TermUI>
      <String>N,N-diethyl-2-chloroacetamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T196071</TermUI>
      <String>N,N-diethyl-alpha-chloroacetamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014695</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>neocidol powder</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>vet dusting powder containing dimpylat(diazinon) &amp; dichloroxylenol; in Chemline neocidol is synonym for diazinon
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002733</DescriptorUI>
     <DescriptorName>
      <String>Chlorophenols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003976</DescriptorUI>
     <DescriptorName>
      <String>Diazinon</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Veterinariia 10:50;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063433</ConceptUI>
    <ConceptName>
     <String>neocidol powder</String>
    </ConceptName>
    <CASN1Name>Phosphorothioic aicd, O,O-diethyl O-(6-methyl-2-(1-methylethyl)-4-pyrimidinyl) ester, mixt. with 2,4-dichloro-3,5-dimethylphenol</CASN1Name>
    <RegistryNumber>78232-15-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093436</TermUI>
      <String>neocidol powder</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C061655</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ethylbutylacetamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1989</Year>
   <Month>12</Month>
   <Day>12</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000081</DescriptorUI>
     <DescriptorName>
      <String>Acetamides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Pharm Res 1989;6(8):683</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0170905</ConceptUI>
    <ConceptName>
     <String>ethylbutylacetamide</String>
    </ConceptName>
    <RegistryNumber>4164-92-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T200910</TermUI>
      <String>ethylbutylacetamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T200909</TermUI>
      <String>2-ethylhexanamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014702</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6-nitro-1,2,3-benzothiadiazole</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013830</DescriptorUI>
     <DescriptorName>
      <String>Thiadiazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Int Arch Occup Environ Health 39(1):27;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063439</ConceptUI>
    <ConceptName>
     <String>6-nitro-1,2,3-benzothiadiazole</String>
    </ConceptName>
    <RegistryNumber>29241-16-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093442</TermUI>
      <String>6-nitro-1,2,3-benzothiadiazole</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014703</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>disulfide reductase (NADH)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>13</Day>
  </DateRevised>
  <Note>specific for disulfides containing pantethine 4',4''-diphosphate moieties
  </Note>
  <Frequency>29</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>DISULFIDES (79-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009247</DescriptorUI>
     <DescriptorName>
      <String>NADH, NADPH Oxidoreductases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 254(15):6835;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063440</ConceptUI>
    <ConceptName>
     <String>disulfide reductase (NADH)</String>
    </ConceptName>
    <RegistryNumber>EC 1.6.4.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093443</TermUI>
      <String>disulfide reductase (NADH)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C064696</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>kaempferol 3-O-alpha-rhamnopyranosyl(1-2)-beta-galactopyranoside-7-O-beta-glucopyranoside</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1990</Year>
   <Month>07</Month>
   <Day>31</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>flavonol triglycoside from Blackstonia peroliata
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BIOFLAVONOIDS (1980-2002)</PreviousIndexing>
   <PreviousIndexing>TRISACCHARIDES(1990-2001)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D044949</DescriptorUI>
     <DescriptorName>
      <String>Kaempferols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D010944</DescriptorUI>
     <DescriptorName>
      <String>Plants</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Phytochemistry 1990;29(4):1283</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0178151</ConceptUI>
    <ConceptName>
     <String>kaempferol 3-O-alpha-rhamnopyranosyl(1-2)-beta-galactopyranoside-7-O-beta-glucopyranoside</String>
    </ConceptName>
    <RegistryNumber>128988-58-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T208156</TermUI>
      <String>kaempferol 3-O-alpha-rhamnopyranosyl(1-2)-beta-galactopyranoside-7-O-beta-glucopyranoside</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T208155</TermUI>
      <String>kaempferol-Rha-Gal-Glu</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C112956</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SP protein, Lycopersicon esculentum</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>07</Month>
   <Day>09</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>01</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>ortholog of CEN and TFL1; regulates switching from vegetative to reproductive cycle; isolated from tomato; amino acid sequence in first source
  </Note>
  <Frequency>10</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010940</DescriptorUI>
     <DescriptorName>
      <String>Plant Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Development 1998 Jun 125(11):1979-89</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0291914</ConceptUI>
    <ConceptName>
     <String>SP protein, Lycopersicon esculentum</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T517721</TermUI>
      <String>SP protein, Lycopersicon esculentum</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>08</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T321919</TermUI>
      <String>SELF-PRUNING protein, Lycopersicon esculentum</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014709</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>nitrosomethoxymethylamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009602</DescriptorUI>
     <DescriptorName>
      <String>Nitrosamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Z Krebsforsch 89(1):31;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063454</ConceptUI>
    <ConceptName>
     <String>nitrosomethoxymethylamine</String>
    </ConceptName>
    <RegistryNumber>16339-12-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093457</TermUI>
      <String>nitrosomethoxymethylamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C432107</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>TatC protein, plant</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>07</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>01</Month>
   <Day>23</Day>
  </DateRevised>
  <Note>plays a direct role in thylakoid (Delta)pH-dependent protein transport; amino acid sequence in first source
  </Note>
  <Frequency>18</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008565</DescriptorUI>
     <DescriptorName>
      <String>Membrane Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010940</DescriptorUI>
     <DescriptorName>
      <String>Plant Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>FEBS Lett 2001 Jul 13;501(1):65-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0394969</ConceptUI>
    <ConceptName>
     <String>TatC protein, plant</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0394969</Concept1UI>
     <Concept2UI>M0459661</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T456502</TermUI>
      <String>TatC protein, plant</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>08</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0459661</ConceptUI>
    <ConceptName>
     <String>TatC protein, Pisum sativum</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0394969</Concept1UI>
     <Concept2UI>M0459661</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T570049</TermUI>
      <String>TatC protein, Pisum sativum</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>01</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014718</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Nyloprint</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000180</DescriptorUI>
     <DescriptorName>
      <String>Acrylic Resins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Contact Dermatitis 1(5):334;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063471</ConceptUI>
    <ConceptName>
     <String>Nyloprint</String>
    </ConceptName>
    <CASN1Name>Nyloprint</CASN1Name>
    <RegistryNumber>53124-98-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093474</TermUI>
      <String>Nyloprint</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C064704</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>kaempferol 3-O-alpha-rhamnopyranosyl-(1-2)-beta-galactopyranoside</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1990</Year>
   <Month>07</Month>
   <Day>31</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>flavonol diglycoside from Blackstonia peroliata
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BIOFLAVONOIDS (1990-2002)</PreviousIndexing>
   <PreviousIndexing>QUERCETIN/*AA (1990-2002)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D044949</DescriptorUI>
     <DescriptorName>
      <String>Kaempferols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D010944</DescriptorUI>
     <DescriptorName>
      <String>Plants</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Phytochemistry 1990;29(4):1345</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0178164</ConceptUI>
    <ConceptName>
     <String>kaempferol 3-O-alpha-rhamnopyranosyl-(1-2)-beta-galactopyranoside</String>
    </ConceptName>
    <RegistryNumber>108906-96-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T208169</TermUI>
      <String>kaempferol 3-O-alpha-rhamnopyranosyl-(1-2)-beta-galactopyranoside</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T501221</TermUI>
      <String>kaempferol-Rha-Gal</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>06</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C119755</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>CRC protein, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1999</Year>
   <Month>07</Month>
   <Day>02</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>01</Month>
   <Day>23</Day>
  </DateRevised>
  <Note>regulates carpel and nectary development; GenBank AF132606
  </Note>
  <Frequency>21</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PLANT PROTEINS (1999-2004)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014157</DescriptorUI>
     <DescriptorName>
      <String>Transcription Factors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D016335</DescriptorUI>
     <DescriptorName>
      <String>Zinc Fingers</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Development 1999 Jun;126(11):2387-96</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0306476</ConceptUI>
    <ConceptName>
     <String>CRC protein, Arabidopsis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T336480</TermUI>
      <String>CRC protein, Arabidopsis</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T569823</TermUI>
      <String>CRABS CLAW protein, Arabidopsis</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>01</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C470474</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>pipersintenamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>01</Month>
   <Day>22</Day>
  </DateCreated>
  <Note>a plant extract; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000475</DescriptorUI>
     <DescriptorName>
      <String>Alkenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010880</DescriptorUI>
     <DescriptorName>
      <String>Piperidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D031701</DescriptorUI>
     <DescriptorName>
      <String>Piper</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Planta Med 2002 Nov;68(11):980-5</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0444932</ConceptUI>
    <ConceptName>
     <String>pipersintenamide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T530765</TermUI>
      <String>pipersintenamide</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>01</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C412108</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-(1-,3-dithian-2-yl)benzaldehyde</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>17</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001547</DescriptorUI>
     <DescriptorName>
      <String>Benzaldehydes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Crystallogr C 2000 Jun;56 ( Pt 6):705-7</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0368143</ConceptUI>
    <ConceptName>
     <String>2-(1-,3-dithian-2-yl)benzaldehyde</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0368143</Concept1UI>
     <Concept2UI>M0368144</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T421982</TermUI>
      <String>2-(1-,3-dithian-2-yl)benzaldehyde</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>08</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0368144</ConceptUI>
    <ConceptName>
     <String>2-(D)-benzaldehyde</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0368143</Concept1UI>
     <Concept2UI>M0368144</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T421983</TermUI>
      <String>2-(D)-benzaldehyde</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>08</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014739</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>phallisin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010590</DescriptorUI>
     <DescriptorName>
      <String>Phalloidine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Angew Chem (Engl):16(4):267;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063512</ConceptUI>
    <ConceptName>
     <String>phallisin</String>
    </ConceptName>
    <RegistryNumber>19774-69-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093515</TermUI>
      <String>phallisin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014740</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>phenanthridinium</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>46</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010617</DescriptorUI>
     <DescriptorName>
      <String>Phenanthridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>C R Acad Sci (D) (Paris) 283(12):1453;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063513</ConceptUI>
    <ConceptName>
     <String>phenanthridinium</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093516</TermUI>
      <String>phenanthridinium</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C047219</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-((4'-mercapto)butylthio)-1,1,1-trifluoropropan-2-one</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1985</Year>
   <Month>12</Month>
   <Day>18</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>17</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000096</DescriptorUI>
     <DescriptorName>
      <String>Acetone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013438</DescriptorUI>
     <DescriptorName>
      <String>Sulfhydryl Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Biochem Biophys 1985;243(1):206</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0136477</ConceptUI>
    <ConceptName>
     <String>3-((4'-mercapto)butylthio)-1,1,1-trifluoropropan-2-one</String>
    </ConceptName>
    <RegistryNumber>99541-29-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T166482</TermUI>
      <String>3-((4'-mercapto)butylthio)-1,1,1-trifluoropropan-2-one</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T166481</TermUI>
      <String>MBTFP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014744</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>phenoplasts</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010636</DescriptorUI>
     <DescriptorName>
      <String>Phenols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011108</DescriptorUI>
     <DescriptorName>
      <String>Polymers</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Zh Ushn Nos Gorl Bolezn 3:47;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063526</ConceptUI>
    <ConceptName>
     <String>phenoplasts</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0063526</Concept1UI>
     <Concept2UI>M0063525</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093529</TermUI>
      <String>phenoplasts</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0063525</ConceptUI>
    <ConceptName>
     <String>phenol condensation products</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0063526</Concept1UI>
     <Concept2UI>M0063525</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T093528</TermUI>
      <String>phenol condensation products</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C474553</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>excoecarin R1</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>06</Month>
   <Day>10</Day>
  </DateCreated>
  <Note>bis-secolabdane diterpenoid from the resinous wood of Excoecaria agallocha; sructure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004224</DescriptorUI>
     <DescriptorName>
      <String>Diterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2003 Jan;66(1):108-11</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0450264</ConceptUI>
    <ConceptName>
     <String>excoecarin R1</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T542912</TermUI>
      <String>excoecarin R1</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>06</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014750</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>beta-phenylpropionyl-L-phenylalanine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010649</DescriptorUI>
     <DescriptorName>
      <String>Phenylalanine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 16(11):2506;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063539</ConceptUI>
    <ConceptName>
     <String>beta-phenylpropionyl-L-phenylalanine</String>
    </ConceptName>
    <RegistryNumber>21888-30-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093542</TermUI>
      <String>beta-phenylpropionyl-L-phenylalanine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014764</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>poly(2'-methyl) U</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>POLY U/*analogs (77-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011072</DescriptorUI>
     <DescriptorName>
      <String>Poly U</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 16(11):2410;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063561</ConceptUI>
    <ConceptName>
     <String>poly(2'-methyl) U</String>
    </ConceptName>
    <RegistryNumber>28451-02-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093564</TermUI>
      <String>poly(2'-methyl) U</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014767</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>polypectate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1986</Year>
   <Month>05</Month>
   <Day>13</Day>
  </DateRevised>
  <Note>RN given refers to K salt
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010368</DescriptorUI>
     <DescriptorName>
      <String>Pectins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ital J Biochem 26(1):59;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063564</ConceptUI>
    <ConceptName>
     <String>polypectate</String>
    </ConceptName>
    <CASN1Name>Pectic acid, potassium salt</CASN1Name>
    <RegistryNumber>37251-70-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093567</TermUI>
      <String>polypectate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014768</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>polytrifluoropropylmethylvinylsiloxane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011145</DescriptorUI>
     <DescriptorName>
      <String>Polyvinyls</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012833</DescriptorUI>
     <DescriptorName>
      <String>Siloxanes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biomed Mater Res 11(4):471;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063565</ConceptUI>
    <ConceptName>
     <String>polytrifluoropropylmethylvinylsiloxane</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093568</TermUI>
      <String>polytrifluoropropylmethylvinylsiloxane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014771</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>preproalbumin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>11</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>compared to prealbumin, it contains 18 additional amino acids at the NH2 terminal
  </Note>
  <Frequency>12</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011228</DescriptorUI>
     <DescriptorName>
      <String>Prealbumin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011498</DescriptorUI>
     <DescriptorName>
      <String>Protein Precursors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 76(2):469;1977</Source>
   <Source>Biochem Biophys Res Commun 77(4):1224;1977</Source>
   <Source>Eur J Biochem 1979;98(2):477</Source>
   <Source>J Biol Chem 252(19):6846;1977</Source>
   <Source>J Biol Chem 253(17):6270;1978</Source>
   <Source>Proc Natl Acad Sci 74(4):1358;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063567</ConceptUI>
    <ConceptName>
     <String>preproalbumin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093570</TermUI>
      <String>preproalbumin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014772</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>presocyl</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>contains above three compounds
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001241</DescriptorUI>
     <DescriptorName>
      <String>Aspirin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002738</DescriptorUI>
     <DescriptorName>
      <String>Chloroquine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011239</DescriptorUI>
     <DescriptorName>
      <String>Prednisolone</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Pediatriia (11):70;1978</Source>
   <Source>Vestn Dermatol Venerol 1:74;1978</Source>
   <Source>Vestn Dermatol Venerol 2:54;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063568</ConceptUI>
    <ConceptName>
     <String>presocyl</String>
    </ConceptName>
    <CASN1Name>Pregna-1,4-diene-3,20-dione, 11,17,21-trihydroxy-, (11beta)-, mixt. with 2-(acetyloxy)benzoic acid and N4-(7-chloro-4-quinolinyl)-N1,N1-diethyl-1,4-pentanediamine</CASN1Name>
    <RegistryNumber>78456-99-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093571</TermUI>
      <String>presocyl</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003463</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>thymidinediphosphomycarose</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1985</Year>
   <Month>08</Month>
   <Day>06</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*NUCLEOSIDE DIPHOSPHATE SUGARS (73-75)</PreviousIndexing>
   <PreviousIndexing>*THYMIDINE DIPHOSPHATE SUGARS (75-85)</PreviousIndexing>
   <PreviousIndexing>THYMIDINE (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009702</DescriptorUI>
     <DescriptorName>
      <String>Nucleoside Diphosphate Sugars</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Mikrobiol 88(1):25;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044518</ConceptUI>
    <ConceptName>
     <String>thymidinediphosphomycarose</String>
    </ConceptName>
    <CASN1Name>Thymidine 5'-(trihydrogen diphosphate), mono(2,6-dideoxy-3-C-methyl-L-ribo-hexopyranosyl) ester</CASN1Name>
    <RegistryNumber>39950-81-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074521</TermUI>
      <String>thymidinediphosphomycarose</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C031464</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>CF 19415</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>09</Month>
   <Day>22</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>27</Day>
  </DateRevised>
  <Note>RN given refers to cpd without isomeric designation
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000097</DescriptorUI>
     <DescriptorName>
      <String>Acetonitriles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Pharmacol 1981;33(6):348</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0098838</ConceptUI>
    <ConceptName>
     <String>CF 19415</String>
    </ConceptName>
    <CASN1Name>Pyrazineacetonitrile, alpha-(methoxyimino)-</CASN1Name>
    <RegistryNumber>79378-26-0</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>67936-63-4 ((Z)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>67936-76-9 ((E)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0098838</Concept1UI>
     <Concept2UI>M0319269</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0098838</Concept1UI>
     <Concept2UI>M0319268</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0098838</Concept1UI>
     <Concept2UI>M0098837</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T128842</TermUI>
      <String>CF 19415</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0319269</ConceptUI>
    <ConceptName>
     <String>CF 19415, (E)-isomer</String>
    </ConceptName>
    <RegistryNumber>67936-76-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0098838</Concept1UI>
     <Concept2UI>M0319269</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T349269</TermUI>
      <String>CF 19415, (E)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0319268</ConceptUI>
    <ConceptName>
     <String>CF 19415, (Z)-isomer</String>
    </ConceptName>
    <RegistryNumber>67936-63-4</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0098838</Concept1UI>
     <Concept2UI>M0319268</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T349268</TermUI>
      <String>CF 19415, (Z)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0098837</ConceptUI>
    <ConceptName>
     <String>2-alpha-methoxyiminopyrazine acetonitrile</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0098838</Concept1UI>
     <Concept2UI>M0098837</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T128841</TermUI>
      <String>2-alpha-methoxyiminopyrazine acetonitrile</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C581078</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>(S)-5,7,3',5'-tetrahydroxy-flavanone-7-O-(6''-galloyl)-beta-D-glucopyranose</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>05</Month>
   <Day>15</Day>
  </DateCreated>
  <Note>BACE (beta-secretase) inhibitory flavanone from Balanophora involucrata; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D044950</DescriptorUI>
     <DescriptorName>
      <String>Flavanones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Fitoterapia. 2012 Dec;83(8):1386-90</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0584780</ConceptUI>
    <ConceptName>
     <String>(S)-5,7,3',5'-tetrahydroxy-flavanone-7-O-(6''-galloyl)-beta-D-glucopyranose</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T844184</TermUI>
      <String>(S)-5,7,3',5'-tetrahydroxy-flavanone-7-O-(6''-galloyl)-beta-D-glucopyranose</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>05</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C090248</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>LF 7-0156</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>12</Month>
   <Day>02</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>a nonpeptide antagonist radioligand for the type 1 angiotensin II receptor; structure given in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001565</DescriptorUI>
     <DescriptorName>
      <String>Benzoates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007093</DescriptorUI>
     <DescriptorName>
      <String>Imidazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Pharmacol 1994 Oct;46(4):693-701</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0238497</ConceptUI>
    <ConceptName>
     <String>LF 7-0156</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0238497</Concept1UI>
     <Concept2UI>M0238495</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T268502</TermUI>
      <String>LF 7-0156</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T268501</TermUI>
      <String>LF-7-0156</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0238495</ConceptUI>
    <ConceptName>
     <String>2-(((2-butyl-1-((4-carboxyphenyl)methyl)-1H-imidazol-5-yl)methyl)amino)benzoic acid</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0238497</Concept1UI>
     <Concept2UI>M0238495</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T268500</TermUI>
      <String>2-(((2-butyl-1-((4-carboxyphenyl)methyl)-1H-imidazol-5-yl)methyl)amino)benzoic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C560485</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>malaysianol A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2011</Year>
   <Month>08</Month>
   <Day>22</Day>
  </DateCreated>
  <DateRevised>
   <Year>2013</Year>
   <Month>05</Month>
   <Day>15</Day>
  </DateRevised>
  <Note>resveratrol trimer from the stem bark of Dryobalanops aromatica; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013267</DescriptorUI>
     <DescriptorName>
      <String>Stilbenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Fitoterapia. 2011 Jun;82(4):676-81</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0560352</ConceptUI>
    <ConceptName>
     <String>malaysianol A</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T795701</TermUI>
      <String>malaysianol A</String>
      <DateCreated>
       <Year>2011</Year>
       <Month>08</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2011)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C118339</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SycD protein, bacteria</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1999</Year>
   <Month>04</Month>
   <Day>16</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>04</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>a chaperone for YopB and YopD; isolated from Yersinia pestis; amino acid sequence in first source
  </Note>
  <Frequency>25</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D018832</DescriptorUI>
     <DescriptorName>
      <String>Molecular Chaperones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Infect Immun 1989 May;57(5):1491-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0303342</ConceptUI>
    <ConceptName>
     <String>SycD protein, bacteria</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T333347</TermUI>
      <String>SycD protein, bacteria</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T333345</TermUI>
      <String>lcrH protein, bacteria</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005753</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ethyl 6-chlorochroman-2-carboxylate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>06</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>chroman analog of clofibrate; structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BENZOPYRANS (74-75)</PreviousIndexing>
   <PreviousIndexing>CARBOXYLIC ACIDS (74-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002839</DescriptorUI>
     <DescriptorName>
      <String>Chromans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Lipids 8(7):378;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0047507</ConceptUI>
    <ConceptName>
     <String>ethyl 6-chlorochroman-2-carboxylate</String>
    </ConceptName>
    <CASN1Name>6-chloro-2-chromancarboxylic acid ethyl ester</CASN1Name>
    <RegistryNumber>33533-96-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T077510</TermUI>
      <String>ethyl 6-chlorochroman-2-carboxylate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005754</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ethyl 2,3-dihydrobenzofuran-2-carboxylate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>dihydrobenzofuran analog of clofibrate; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CARBOXYLIC ACIDS (74-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001572</DescriptorUI>
     <DescriptorName>
      <String>Benzofurans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Lipids 8(7):378;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0047508</ConceptUI>
    <ConceptName>
     <String>ethyl 2,3-dihydrobenzofuran-2-carboxylate</String>
    </ConceptName>
    <RegistryNumber>43119-53-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T077511</TermUI>
      <String>ethyl 2,3-dihydrobenzofuran-2-carboxylate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005755</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ethyl 1,4-benzodioxane-2-carboxylate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DIOXINS (74-75)</PreviousIndexing>
   <PreviousIndexing>CARBOXYLIC ACIDS (74-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004146</DescriptorUI>
     <DescriptorName>
      <String>Dioxanes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Lipids 8(7):378;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0047509</ConceptUI>
    <ConceptName>
     <String>ethyl 1,4-benzodioxane-2-carboxylate</String>
    </ConceptName>
    <RegistryNumber>4739-94-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T077512</TermUI>
      <String>ethyl 1,4-benzodioxane-2-carboxylate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C581079</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>alstilobanine A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>05</Month>
   <Day>15</Day>
  </DateCreated>
  <Note>from the leaves of the Malayan plant Alstonia angustiloba; structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D046948</DescriptorUI>
     <DescriptorName>
      <String>Secologanin Tryptamine Alkaloids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Angew Chem Int Ed Engl. 2012 Dec 14;51(51):12846-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0584782</ConceptUI>
    <ConceptName>
     <String>alstilobanine A</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T844187</TermUI>
      <String>alstilobanine A</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>05</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005762</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>7-oxo-7H-benzo(d,e)pyrrolo(1,2-a)quinoline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PYRROLES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011804</DescriptorUI>
     <DescriptorName>
      <String>Quinolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Farmaco (Sci) 27(9):786;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0047527</ConceptUI>
    <ConceptName>
     <String>7-oxo-7H-benzo(d,e)pyrrolo(1,2-a)quinoline</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T077530</TermUI>
      <String>7-oxo-7H-benzo(d,e)pyrrolo(1,2-a)quinoline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005763</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>11-oxo-11H-benzo(e)pyrrolo(1,2-a)indole</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PYRROLES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007211</DescriptorUI>
     <DescriptorName>
      <String>Indoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Farmaco (Sci) 27(9):786;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0047528</ConceptUI>
    <ConceptName>
     <String>11-oxo-11H-benzo(e)pyrrolo(1,2-a)indole</String>
    </ConceptName>
    <CASN1Name>11H-Benzo(e)pyrrolo(1,2-a)indol-11-one</CASN1Name>
    <RegistryNumber>38040-61-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T077531</TermUI>
      <String>11-oxo-11H-benzo(e)pyrrolo(1,2-a)indole</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C093512</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SAD1 protein, S pombe</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>06</Month>
   <Day>12</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>02</Month>
   <Day>24</Day>
  </DateRevised>
  <Note>a 58 kDa product of the spindle formation gene that associates with the fission yeast spindle pole body &amp; is essential for viability; amino acid sequence given in first source; GenBank X85105
  </Note>
  <Frequency>24</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*FUNGAL PROTEINS (1995-2003)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029702</DescriptorUI>
     <DescriptorName>
      <String>Schizosaccharomyces pombe Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Cell Biol 1995 May;129(4):1033-47</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0246602</ConceptUI>
    <ConceptName>
     <String>SAD1 protein, S pombe</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T533055</TermUI>
      <String>SAD1 protein, S pombe</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>02</Month>
       <Day>19</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T533479</TermUI>
      <String>spindle architecture defective protein 1, S pombe</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>02</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005771</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4',5'-dihydropsoralen</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>11</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*FICUSIN/analogs (75-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011564</DescriptorUI>
     <DescriptorName>
      <String>Furocoumarins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Can J Biochem 51(7):965;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0047539</ConceptUI>
    <ConceptName>
     <String>4',5'-dihydropsoralen</String>
    </ConceptName>
    <RegistryNumber>7535-48-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T077542</TermUI>
      <String>4',5'-dihydropsoralen</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005773</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N(6)-(3-hydroxy-3-methylbutyl)adenine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>substrate for xanthine oxidase
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ADENINE (74-75)</PreviousIndexing>
   <PreviousIndexing>ALCOHOLS, AMYL (74-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000225</DescriptorUI>
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      <String>Adenine</String>
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     <QualifierUI>*Q000031</QualifierUI>
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  <SourceList>
   <Source>Can J Biochem 51(7):1123;1973</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0047540</ConceptUI>
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     <String>N(6)-(3-hydroxy-3-methylbutyl)adenine</String>
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    <CASN1Name>2-methyl-4-(1H-purin-6-ylamino)-2-butanol</CASN1Name>
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  <DateCreated>
   <Year>2000</Year>
   <Month>03</Month>
   <Day>31</Day>
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  <DateRevised>
   <Year>2004</Year>
   <Month>04</Month>
   <Day>07</Day>
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  <Note>cyclic AMP binding protein from Synechocystis sp. PCC 6803; amino acid sequence in first source
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   <HeadingMappedTo>
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   <Source>J Biol Chem 2000 Mar 3;275(9):6241-5</Source>
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       <Month>03</Month>
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  <SupplementalRecordUI>C085268</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Re 80</String>
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  <DateCreated>
   <Year>1994</Year>
   <Month>02</Month>
   <Day>11</Day>
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  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>19</Day>
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  <Note>structure given in first source; an anti-angiogenic agent
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  <Frequency>8</Frequency>
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    <DescriptorReferredTo>
     <DescriptorUI>*D001565</DescriptorUI>
     <DescriptorName>
      <String>Benzoates</String>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013764</DescriptorUI>
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  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D012176</DescriptorUI>
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      <String>Retinoids</String>
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  <SourceList>
   <Source>Eur J Pharmacol 1993 Nov 2;249(1):113-6</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0226365</ConceptUI>
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     <String>Re 80</String>
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     <ConceptRelation RelationName="BRD">
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     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T256370</TermUI>
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      <ThesaurusIDlist>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
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       <ThesaurusID>NLM (1994)</ThesaurusID>
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   <Concept PreferredConceptYN="N">
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   <Month>05</Month>
   <Day>31</Day>
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   <Year>2013</Year>
   <Month>05</Month>
   <Day>15</Day>
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   <Source>Adv Exp Med Biol 2009;611:269-70</Source>
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       <Month>05</Month>
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      <DateCreated>
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       <Month>05</Month>
       <Day>31</Day>
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      <ThesaurusIDlist>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
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      <DateCreated>
       <Year>2009</Year>
       <Month>05</Month>
       <Day>31</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2009)</ThesaurusID>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
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      <DateCreated>
       <Year>2009</Year>
       <Month>05</Month>
       <Day>31</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2009)</ThesaurusID>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
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      <DateCreated>
       <Year>2009</Year>
       <Month>05</Month>
       <Day>31</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2009)</ThesaurusID>
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     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T844195</TermUI>
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      <DateCreated>
       <Year>2013</Year>
       <Month>05</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
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  <SupplementalRecordUI>C581567</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-amino-6-hydroxy-2-mercaptopyrimidine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>09</Day>
  </DateCreated>
  <Note>a capping ligand for gold nanoparticles used in the determination of tannic acid
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011743</DescriptorUI>
     <DescriptorName>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013438</DescriptorUI>
     <DescriptorName>
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  <SourceList>
   <Source>Bioelectrochemistry. 2013 Feb;89:1-10.</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0585418</ConceptUI>
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    <RegistryNumber>0</RegistryNumber>
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      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>09</Day>
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  <SupplementalRecordUI>C093629</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SNG1 protein, S cerevisiae</String>
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  <DateCreated>
   <Year>1995</Year>
   <Month>06</Month>
   <Day>20</Day>
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  <DateRevised>
   <Year>2003</Year>
   <Month>02</Month>
   <Day>24</Day>
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  <Note>a 547-amino acid polypeptide; contains 7 transmembrane-spanning regions; involved in nitrosoguanidine resistance in Saccharomyces cerevisiae; amino acid sequence given in first source
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   <Source>Mutat Res 1995 Apr;346(4):207-14</Source>
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       <Month>02</Month>
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  <DateCreated>
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   <Month>06</Month>
   <Day>09</Day>
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
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   <HeadingMappedTo>
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     <DescriptorUI>*D029681</DescriptorUI>
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      <String>Arabidopsis Proteins</String>
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  <SourceList>
   <Source>Am J Bot. 2013 Jan;100(1):183-93.</Source>
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  <ConceptList>
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       <Day>09</Day>
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       <Year>2013</Year>
       <Month>06</Month>
       <Day>09</Day>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
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       <Year>2013</Year>
       <Month>06</Month>
       <Day>09</Day>
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       <Month>06</Month>
       <Day>09</Day>
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       <ThesaurusID>NLM (2013)</ThesaurusID>
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  <SupplementalRecordUI>C581569</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>poly(caprolactone-co-ethylethylene phosphate)</String>
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  <DateCreated>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>09</Day>
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    <DescriptorReferredTo>
     <DescriptorUI>*D010755</DescriptorUI>
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   <Source>Acta Biomater. 2013 Jan;9(1):4513-24.</Source>
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  <DateCreated>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>09</Day>
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      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C581570</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>oligo(benzylethylenimine)-b-polyethylenimine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>09</Day>
  </DateCreated>
  <DateRevised>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>used in gene delivery; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011094</DescriptorUI>
     <DescriptorName>
      <String>Polyethyleneimine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D004337</DescriptorUI>
     <DescriptorName>
      <String>Drug Carriers</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Acta Biomater. 2013 Feb;9(2):4985-93.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0585421</ConceptUI>
    <ConceptName>
     <String>oligo(benzylethylenimine)-b-polyethylenimine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T845339</TermUI>
      <String>oligo(benzylethylenimine)-b-polyethylenimine</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T845340</TermUI>
      <String>OBzEI-PEI</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C581573</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6-(2,4-dichlorophenyl)-8-ethyl-2-(3-fluoro-4-(piperazin-1-yl)phenylamino)pyrido(2,3-d)pyrimidin-7(8H)-one</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>09</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011728</DescriptorUI>
     <DescriptorName>
      <String>Pyridones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011743</DescriptorUI>
     <DescriptorName>
      <String>Pyrimidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D054462</DescriptorUI>
     <DescriptorName>
      <String>p21-Activated Kinases</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
     <QualifierName>
      <String>antagonists &amp; inhibitors</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Proc Natl Acad Sci U S A. 2013 Apr 2;110(14):5671-6.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0585424</ConceptUI>
    <ConceptName>
     <String>6-(2,4-dichlorophenyl)-8-ethyl-2-(3-fluoro-4-(piperazin-1-yl)phenylamino)pyrido(2,3-d)pyrimidin-7(8H)-one</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0585424</Concept1UI>
     <Concept2UI>M0585425</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T845344</TermUI>
      <String>6-(2,4-dichlorophenyl)-8-ethyl-2-(3-fluoro-4-(piperazin-1-yl)phenylamino)pyrido(2,3-d)pyrimidin-7(8H)-one</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0585425</ConceptUI>
    <ConceptName>
     <String>FRAX486</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0585424</Concept1UI>
     <Concept2UI>M0585425</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T845345</TermUI>
      <String>FRAX486</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C581574</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-(1H-pyrrolo(2,3-b)pyridin-3-ylmethyl)-N-((4-(trifluoromethyl)phenyl)methyl)pyridin-2-amine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>09</Day>
  </DateCreated>
  <Note>a dual FMS and KIT kinase inhibitor; structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000631</DescriptorUI>
     <DescriptorName>
      <String>Aminopyridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011758</DescriptorUI>
     <DescriptorName>
      <String>Pyrroles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Proc Natl Acad Sci U S A. 2013 Apr 2;110(14):5689-94.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0585426</ConceptUI>
    <ConceptName>
     <String>5-(1H-pyrrolo(2,3-b)pyridin-3-ylmethyl)-N-((4-(trifluoromethyl)phenyl)methyl)pyridin-2-amine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0585426</Concept1UI>
     <Concept2UI>M0585427</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T845346</TermUI>
      <String>5-(1H-pyrrolo(2,3-b)pyridin-3-ylmethyl)-N-((4-(trifluoromethyl)phenyl)methyl)pyridin-2-amine</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0585427</ConceptUI>
    <ConceptName>
     <String>PLX647</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0585426</Concept1UI>
     <Concept2UI>M0585427</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T845347</TermUI>
      <String>PLX647</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007117</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>copper 2,2'-bicinchoninate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>reagent for determining uric acid in blood
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>COPPER (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011804</DescriptorUI>
     <DescriptorName>
      <String>Quinolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Clin Chem 19(10):1184;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050097</ConceptUI>
    <ConceptName>
     <String>copper 2,2'-bicinchoninate</String>
    </ConceptName>
    <CASN1Name>Copper, ((2,2'-biquinoline)-4,4'-dicarboxylato(2-)-N(1),N(1)')-</CASN1Name>
    <RegistryNumber>76109-99-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080100</TermUI>
      <String>copper 2,2'-bicinchoninate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T080099</TermUI>
      <String>Cu(II)-2,2'-bicinchoninate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C581575</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>MTG1 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>09</Day>
  </DateCreated>
  <Note>RefSeq NM_138384
  </Note>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D020558</DescriptorUI>
     <DescriptorName>
      <String>GTP Phosphohydrolases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Biol Cell. 2003 Jun;14(6):2292-302.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0585428</ConceptUI>
    <ConceptName>
     <String>MTG1 protein, human</String>
    </ConceptName>
    <RegistryNumber>EC 3.6.1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T845348</TermUI>
      <String>MTG1 protein, human</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C050456</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>nickel-palladium alloy</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1987</Year>
   <Month>01</Month>
   <Day>15</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>used for magnetic induction of hyperthermia as a brain implant for therapy of brain neoplasms
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009532</DescriptorUI>
     <DescriptorName>
      <String>Nickel</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010165</DescriptorUI>
     <DescriptorName>
      <String>Palladium</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D000497</DescriptorUI>
     <DescriptorName>
      <String>Alloys</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Neurooncol 1986;4(2):175</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0144058</ConceptUI>
    <ConceptName>
     <String>nickel-palladium alloy</String>
    </ConceptName>
    <RegistryNumber>106747-79-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T174063</TermUI>
      <String>nickel-palladium alloy</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T174062</TermUI>
      <String>Ni-Pd alloy</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C071586</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>araloside D</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1991</Year>
   <Month>12</Month>
   <Day>13</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>08</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>structure given in first source; isolated from the root bark of Aralia chinesis L.
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009828</DescriptorUI>
     <DescriptorName>
      <String>Oleanolic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012503</DescriptorUI>
     <DescriptorName>
      <String>Saponins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D004365</DescriptorUI>
     <DescriptorName>
      <String>Drugs, Chinese Herbal</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Yao Hsueh Hsueh Pao 1991;26(3):197</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0194371</ConceptUI>
    <ConceptName>
     <String>araloside D</String>
    </ConceptName>
    <CASN1Name>Olean-12-en-28-oic-acid, 3-((O-beta-D-glucopyranosyl-(1-2)-O-beta-D-xylopyranosyl-(1-2)-alpha-L-arabinopyranosyl)oxy)-, (3beta)-</CASN1Name>
    <RegistryNumber>135560-19-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T224376</TermUI>
      <String>araloside D</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007125</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cordycepin-C</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>the C-C nucleoside analog of cordycepin; structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003839</DescriptorUI>
     <DescriptorName>
      <String>Deoxyadenosines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Carb. Res. 29(2):525;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050112</ConceptUI>
    <ConceptName>
     <String>cordycepin-C</String>
    </ConceptName>
    <CASN1Name>8-(3'-deoxy-beta-D-erythro-ribofuranosyl)adenine</CASN1Name>
    <RegistryNumber>51771-54-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080115</TermUI>
      <String>cordycepin-C</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T080114</TermUI>
      <String>cordycepin C</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005909</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tetrahydrotriamcinolone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>07</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>RN given is for cpd named as tetrahydro deriv of a pregnadiene
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*TRIAMCINOLONE (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014221</DescriptorUI>
     <DescriptorName>
      <String>Triamcinolone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Med Clin North Am 57(5):1167;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0047772</ConceptUI>
    <ConceptName>
     <String>tetrahydrotriamcinolone</String>
    </ConceptName>
    <RegistryNumber>51855-44-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T077775</TermUI>
      <String>tetrahydrotriamcinolone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C409566</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>CSEA protein, E coli</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>06</Month>
   <Day>20</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>01</Month>
   <Day>23</Day>
  </DateRevised>
  <Note>a human enterotoxigenic E. coli adhesin, related to CS15; amino acid sequence in first source
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BACTERIAL PROTEINS (2000-2002)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D018829</DescriptorUI>
     <DescriptorName>
      <String>Adhesins, Bacterial</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029968</DescriptorUI>
     <DescriptorName>
      <String>Escherichia coli Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Infect Immun 2000 Jun;68(6):3280-5</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0364461</ConceptUI>
    <ConceptName>
     <String>CSEA protein, E coli</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T521691</TermUI>
      <String>CSEA protein, E coli</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>10</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T417152</TermUI>
      <String>CS22 protein, E coli</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>06</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C528967</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>YM753 compound</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2008</Year>
   <Month>05</Month>
   <Day>19</Day>
  </DateCreated>
  <DateRevised>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>12</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010456</DescriptorUI>
     <DescriptorName>
      <String>Peptides, Cyclic</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D000970</DescriptorUI>
     <DescriptorName>
      <String>Antineoplastic Agents</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D056572</DescriptorUI>
     <DescriptorName>
      <String>Histone Deacetylase Inhibitors</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Int J Oncol. 2008 Mar;32(3):545-55</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0521525</ConceptUI>
    <ConceptName>
     <String>YM753 compound</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0521525</Concept1UI>
     <Concept2UI>M0585468</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T720033</TermUI>
      <String>YM753 compound</String>
      <DateCreated>
       <Year>2008</Year>
       <Month>05</Month>
       <Day>19</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2008)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0585468</ConceptUI>
    <ConceptName>
     <String>OBP-801</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0521525</Concept1UI>
     <Concept2UI>M0585468</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T845385</TermUI>
      <String>OBP-801</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005914</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>DONS</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>new impurity in Schaeffer's salt; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ETHERS (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009282</DescriptorUI>
     <DescriptorName>
      <String>Naphthalenesulfonates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Assoc Anal Chem 54(1):137;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0047785</ConceptUI>
    <ConceptName>
     <String>DONS</String>
    </ConceptName>
    <CASN1Name>6,6'-oxybis(2-naphthalenesulfonic acid)</CASN1Name>
    <RegistryNumber>31034-03-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T077788</TermUI>
      <String>DONS</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005919</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>9-oxo-9H-pyrrolo(1,2-a)indole</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PYRROLES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007211</DescriptorUI>
     <DescriptorName>
      <String>Indoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Farmaco 27(1):60;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0047791</ConceptUI>
    <ConceptName>
     <String>9-oxo-9H-pyrrolo(1,2-a)indole</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T077794</TermUI>
      <String>9-oxo-9H-pyrrolo(1,2-a)indole</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005920</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-hydroxyimidazole-3-oxide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CYCLIC N-OXIDES (74-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007093</DescriptorUI>
     <DescriptorName>
      <String>Imidazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Farmaco 27(1):46;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0047792</ConceptUI>
    <ConceptName>
     <String>1-hydroxyimidazole-3-oxide</String>
    </ConceptName>
    <CASN1Name>1H-Imidazole, 1-hydroxy-, 3-oxide</CASN1Name>
    <RegistryNumber>35321-46-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T077795</TermUI>
      <String>1-hydroxyimidazole-3-oxide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005922</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>daphnetin-8-glucoside</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>04</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>RN given refers to (beta)-isomer
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*COUMARINS (74-79)</PreviousIndexing>
   <PreviousIndexing>*GLYCOSIDES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014468</DescriptorUI>
     <DescriptorName>
      <String>Umbelliferones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 62(8):1360;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0047794</ConceptUI>
    <ConceptName>
     <String>daphnetin-8-glucoside</String>
    </ConceptName>
    <CASN1Name>2H-1-Benzopyran-2-one, 8-(beta-D-glucopyranosyloxy)-7-hydroxy-</CASN1Name>
    <RegistryNumber>20853-56-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T077797</TermUI>
      <String>daphnetin-8-glucoside</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C060634</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-(9-acridinylamino)-N-(glycyl-histidyl-lysyl-glycyl)aniline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1989</Year>
   <Month>09</Month>
   <Day>11</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000609</DescriptorUI>
     <DescriptorName>
      <String>Aminoacridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009842</DescriptorUI>
     <DescriptorName>
      <String>Oligopeptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Anticancer Drug Des 1989;4(1):37</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0168389</ConceptUI>
    <ConceptName>
     <String>4-(9-acridinylamino)-N-(glycyl-histidyl-lysyl-glycyl)aniline</String>
    </ConceptName>
    <RegistryNumber>121034-91-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T198394</TermUI>
      <String>4-(9-acridinylamino)-N-(glycyl-histidyl-lysyl-glycyl)aniline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T198392</TermUI>
      <String>4-AGHLGA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T198393</TermUI>
      <String>4-AcA-Gly-His-Lys-Gly-A</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005929</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>14-dehydro-19-nortestosterone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*NANDROLONE (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009277</DescriptorUI>
     <DescriptorName>
      <String>Nandrolone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Steroids 22(1):99;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0047807</ConceptUI>
    <ConceptName>
     <String>14-dehydro-19-nortestosterone</String>
    </ConceptName>
    <RegistryNumber>35644-61-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T077810</TermUI>
      <String>14-dehydro-19-nortestosterone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005931</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>7 alpha-methyl-14-dehydro-19-nortestosterone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ANDROSTENOLS (74-75)</PreviousIndexing>
   <PreviousIndexing>KETOSTEROIDS (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009277</DescriptorUI>
     <DescriptorName>
      <String>Nandrolone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Steroids 22(1):99;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0047808</ConceptUI>
    <ConceptName>
     <String>7 alpha-methyl-14-dehydro-19-nortestosterone</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T077811</TermUI>
      <String>7 alpha-methyl-14-dehydro-19-nortestosterone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C546349</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>MIRN517 microRNA, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2010</Year>
   <Month>01</Month>
   <Day>13</Day>
  </DateCreated>
  <DateRevised>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>RefSeq NR_030201
  </Note>
  <Frequency>17</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D035683</DescriptorUI>
     <DescriptorName>
      <String>MicroRNAs</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biol Reprod 2009 Oct;81(4):717-29</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0542665</ConceptUI>
    <ConceptName>
     <String>MIRN517 microRNA, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0542665</Concept1UI>
     <Concept2UI>M0581363</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0542665</Concept1UI>
     <Concept2UI>M0585470</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0542665</Concept1UI>
     <Concept2UI>M0542666</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T764115</TermUI>
      <String>MIRN517 microRNA, human</String>
      <DateCreated>
       <Year>2010</Year>
       <Month>01</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2010)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T764118</TermUI>
      <String>microRNA-517, human</String>
      <DateCreated>
       <Year>2010</Year>
       <Month>01</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2010)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T764117</TermUI>
      <String>miR-517, human</String>
      <DateCreated>
       <Year>2010</Year>
       <Month>01</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2010)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T764116</TermUI>
      <String>hsa-mir-517</String>
      <DateCreated>
       <Year>2010</Year>
       <Month>01</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2010)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0581363</ConceptUI>
    <ConceptName>
     <String>MIR517c, human</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0542665</Concept1UI>
     <Concept2UI>M0581363</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T837267</TermUI>
      <String>MIR517c, human</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>02</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0585470</ConceptUI>
    <ConceptName>
     <String>miR-517b, human</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0542665</Concept1UI>
     <Concept2UI>M0585470</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T845388</TermUI>
      <String>miR-517b, human</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0542666</ConceptUI>
    <ConceptName>
     <String>MIR517A, human</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0542665</Concept1UI>
     <Concept2UI>M0542666</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T764119</TermUI>
      <String>MIR517A, human</String>
      <DateCreated>
       <Year>2010</Year>
       <Month>01</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2010)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C546194</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>MIRN519 microRNA, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2010</Year>
   <Month>01</Month>
   <Day>09</Day>
  </DateCreated>
  <DateRevised>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>10</Day>
  </DateRevised>
  <Frequency>91</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D035683</DescriptorUI>
     <DescriptorName>
      <String>MicroRNAs</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Cancer Ther 2009 Oct;8(10):2959-68</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0542488</ConceptUI>
    <ConceptName>
     <String>MIRN519 microRNA, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0542488</Concept1UI>
     <Concept2UI>M0542489</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0542488</Concept1UI>
     <Concept2UI>M0580439</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0542488</Concept1UI>
     <Concept2UI>M0585471</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T763787</TermUI>
      <String>MIRN519 microRNA, human</String>
      <DateCreated>
       <Year>2010</Year>
       <Month>01</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2010)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T763790</TermUI>
      <String>microRNA-519, human</String>
      <DateCreated>
       <Year>2010</Year>
       <Month>01</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2010)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T763788</TermUI>
      <String>hsa-mir-519</String>
      <DateCreated>
       <Year>2010</Year>
       <Month>01</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2010)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T763789</TermUI>
      <String>miR-519, human</String>
      <DateCreated>
       <Year>2010</Year>
       <Month>01</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2010)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0542489</ConceptUI>
    <ConceptName>
     <String>hsa-mir-519c</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0542488</Concept1UI>
     <Concept2UI>M0542489</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T763791</TermUI>
      <String>hsa-mir-519c</String>
      <DateCreated>
       <Year>2010</Year>
       <Month>01</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2010)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T763792</TermUI>
      <String>miR-519c, human</String>
      <DateCreated>
       <Year>2010</Year>
       <Month>01</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2010)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0580439</ConceptUI>
    <ConceptName>
     <String>miR-519b, human</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0542488</Concept1UI>
     <Concept2UI>M0580439</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T835893</TermUI>
      <String>miR-519b, human</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>01</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T835894</TermUI>
      <String>oncomir miR-519b, human</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>01</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0585471</ConceptUI>
    <ConceptName>
     <String>miR-519a, human</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0542488</Concept1UI>
     <Concept2UI>M0585471</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T845389</TermUI>
      <String>miR-519a, human</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009343</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>sucrose 6,6'-dimycolate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*GLYCOLIPIDS (74-75)</PreviousIndexing>
   <PreviousIndexing>*SUCROSE (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009171</DescriptorUI>
     <DescriptorName>
      <String>Mycolic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013395</DescriptorUI>
     <DescriptorName>
      <String>Sucrose</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Infect Immun 7(4):632;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0053951</ConceptUI>
    <ConceptName>
     <String>sucrose 6,6'-dimycolate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T083954</TermUI>
      <String>sucrose 6,6'-dimycolate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010143</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>GEA 968</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008012</DescriptorUI>
     <DescriptorName>
      <String>Lidocaine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharmacol Exp Ther 195(2):25;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055437</ConceptUI>
    <ConceptName>
     <String>GEA 968</String>
    </ConceptName>
    <CASN1Name>N,N-diethylglycyl-N-(2,6-dimethylphenyl)glycinamide</CASN1Name>
    <RegistryNumber>50333-29-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085440</TermUI>
      <String>GEA 968</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085439</TermUI>
      <String>GEA-968</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009347</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6-sulfanilamidoindazole</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>06</Month>
   <Day>23</Day>
  </DateRevised>
  <Note>induces acute arthritis &amp; periarticular inflammation in rats
  </Note>
  <Frequency>14</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>INDAZOLES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013424</DescriptorUI>
     <DescriptorName>
      <String>Sulfanilamides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Pharmacol 27(20):2395;1978</Source>
   <Source>Infect Immun 25(1):337;1979</Source>
   <Source>Z Rheumatol 35(11-12):403;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0053957</ConceptUI>
    <ConceptName>
     <String>6-sulfanilamidoindazole</String>
    </ConceptName>
    <RegistryNumber>13744-68-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T083960</TermUI>
      <String>6-sulfanilamidoindazole</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C531294</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>aplysinoplide A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2008</Year>
   <Month>09</Month>
   <Day>11</Day>
  </DateCreated>
  <Note>isolated from the marine sponge Aplysinopsis digitata; exhibited cytotoxic activity against P388 mouse leukemia cells; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D054830</DescriptorUI>
     <DescriptorName>
      <String>Sesterterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2008 Jun;71(6):1089-91</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0524687</ConceptUI>
    <ConceptName>
     <String>aplysinoplide A</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T725532</TermUI>
      <String>aplysinoplide A</String>
      <DateCreated>
       <Year>2008</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2008)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009367</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>O-Syl</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>09</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>p-tert butylphenol is active ingredient
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005998</DescriptorUI>
     <DescriptorName>
      <String>Glycine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010636</DescriptorUI>
     <DescriptorName>
      <String>Phenols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Dermatol 108(6):848;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0053999</ConceptUI>
    <ConceptName>
     <String>O-Syl</String>
    </ConceptName>
    <RegistryNumber>64726-60-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084002</TermUI>
      <String>O-Syl</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009371</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>syringomyelin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010743</DescriptorUI>
     <DescriptorName>
      <String>Phospholipids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Crit Care Med 2(4):221;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054006</ConceptUI>
    <ConceptName>
     <String>syringomyelin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084009</TermUI>
      <String>syringomyelin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C053925</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Hoxb5 protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1987</Year>
   <Month>11</Month>
   <Day>23</Day>
  </DateCreated>
  <DateRevised>
   <Year>2013</Year>
   <Month>10</Month>
   <Day>24</Day>
  </DateRevised>
  <Note>RefSeq NM_008268
  </Note>
  <Frequency>41</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DNA-BINDING PROTEINS (87-95)</PreviousIndexing>
   <PreviousIndexing>*PROTEINS (87-90)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D018398</DescriptorUI>
     <DescriptorName>
      <String>Homeodomain Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Development 1987;99(4):603</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0152577</ConceptUI>
    <ConceptName>
     <String>Hoxb5 protein, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T606367</TermUI>
      <String>Hoxb5 protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T606370</TermUI>
      <String>hoxb-5 protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T606371</TermUI>
      <String>Hox2.1 protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T606368</TermUI>
      <String>homeo box B5 protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T606369</TermUI>
      <String>Hox-2.1 protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009398</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>teration</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>06</Month>
   <Day>15</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>SULFIDES (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009946</DescriptorUI>
     <DescriptorName>
      <String>Organothiophosphorus Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Lab Delo 12:719;1974</Source>
   <Source>Med Dosw Mikrobiol 25(4):351;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054042</ConceptUI>
    <ConceptName>
     <String>teration</String>
    </ConceptName>
    <CASN1Name>O-ethyl-S-(2-(ethylthio)ethyl)-O-methyl phosphorodithioic acid ester</CASN1Name>
    <RegistryNumber>7421-50-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084045</TermUI>
      <String>teration</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009399</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-terphenylhemicholinium 3</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>14</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*HEMICHOLINIUM 3 (74-75)</PreviousIndexing>
   <PreviousIndexing>BENZENE DERIVATIVES (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D006426</DescriptorUI>
     <DescriptorName>
      <String>Hemicholinium 3</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Br J Pharmacol 44(2):324P;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054045</ConceptUI>
    <ConceptName>
     <String>4-terphenylhemicholinium 3</String>
    </ConceptName>
    <RegistryNumber>29605-98-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0054045</Concept1UI>
     <Concept2UI>M0054043</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0054045</Concept1UI>
     <Concept2UI>M0054044</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084048</TermUI>
      <String>4-terphenylhemicholinium 3</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0054043</ConceptUI>
    <ConceptName>
     <String>p-terphenylhemicholinium 3</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0054045</Concept1UI>
     <Concept2UI>M0054043</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T084046</TermUI>
      <String>p-terphenylhemicholinium 3</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0054044</ConceptUI>
    <ConceptName>
     <String>para-terphenyl hemicholinium 3</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0054045</Concept1UI>
     <Concept2UI>M0054044</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T084047</TermUI>
      <String>para-terphenyl hemicholinium 3</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009626</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Uridion</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*INDENES (74-75)</PreviousIndexing>
   <PreviousIndexing>BROMINE (74-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007189</DescriptorUI>
     <DescriptorName>
      <String>Indans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Wien Klin Wochenschr 85(42):697;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054483</ConceptUI>
    <ConceptName>
     <String>Uridion</String>
    </ConceptName>
    <CASN1Name>5-bromo-2- phenyl-1H-indene-1,3(2H)-dione</CASN1Name>
    <RegistryNumber>1470-35-5</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0054483</Concept1UI>
     <Concept2UI>M0054482</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="TRD"  RecordPreferredTermYN="Y">
      <TermUI>T084486</TermUI>
      <String>Uridion</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0054482</ConceptUI>
    <ConceptName>
     <String>5-bromo-2-phenyl-1,3-indanedione</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0054483</Concept1UI>
     <Concept2UI>M0054482</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T084485</TermUI>
      <String>5-bromo-2-phenyl-1,3-indanedione</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009401</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>terremutin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>isolated from cultures of Aspergillus cervinus Massee (Moniliaceae); RN from 9th CI; cpd not in Chemline 8/83; structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>EPOXY COMPOUNDS (75-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011809</DescriptorUI>
     <DescriptorName>
      <String>Quinones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 63(10):1632;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054048</ConceptUI>
    <ConceptName>
     <String>terremutin</String>
    </ConceptName>
    <RegistryNumber>18746-82-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084051</TermUI>
      <String>terremutin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C477836</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>CpsR protein, Vibrio parahaemolyticus</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>10</Month>
   <Day>09</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>08</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>GenBank AY216912
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CARRIER PROTEINS (2003-2004)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014157</DescriptorUI>
     <DescriptorName>
      <String>Transcription Factors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Bacteriol 2003 Sep;185(18):5431-41</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0454658</ConceptUI>
    <ConceptName>
     <String>CpsR protein, Vibrio parahaemolyticus</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T552865</TermUI>
      <String>CpsR protein, Vibrio parahaemolyticus</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>10</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009406</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tetrabutylammonium permanganate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>08</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>reagent for oxidizing &amp; determining DDT residues
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AMMONIUM COMPOUNDS (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009942</DescriptorUI>
     <DescriptorName>
      <String>Organometallic Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D008345</DescriptorUI>
     <DescriptorName>
      <String>Manganese</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Bull Environ Contam Toxicol 11(5):451;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054061</ConceptUI>
    <ConceptName>
     <String>tetrabutylammonium permanganate</String>
    </ConceptName>
    <RegistryNumber>35638-41-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084064</TermUI>
      <String>tetrabutylammonium permanganate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C077550</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>vitelline protein B1, Fasciola hepatica</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1992</Year>
   <Month>11</Month>
   <Day>23</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>06</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>amino acid sequence given in first source; isolated from Fasciola hepatica; a 31-kDa eggshell protein; GenBank M93024
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004527</DescriptorUI>
     <DescriptorName>
      <String>Egg Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015801</DescriptorUI>
     <DescriptorName>
      <String>Helminth Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Biochem Parasitol 1992 Sep;54(2):129-42</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0208177</ConceptUI>
    <ConceptName>
     <String>vitelline protein B1, Fasciola hepatica</String>
    </ConceptName>
    <RegistryNumber>148591-67-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T543285</TermUI>
      <String>vitelline protein B1, Fasciola hepatica</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>06</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C097538</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>eilatine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>02</Month>
   <Day>08</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>08</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>isolated from the Red Sea purple tunicate Eudistoma sp.; structure given in first source
  </Note>
  <Frequency>11</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010618</DescriptorUI>
     <DescriptorName>
      <String>Phenanthrolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D000470</DescriptorUI>
     <DescriptorName>
      <String>Alkaloids</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D013237</DescriptorUI>
     <DescriptorName>
      <String>Stereoisomerism</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Exp Hematol 1995 Dec;23(14):1439-44</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0256387</ConceptUI>
    <ConceptName>
     <String>eilatine</String>
    </ConceptName>
    <RegistryNumber>120154-96-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0256387</Concept1UI>
     <Concept2UI>M0470196</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T286392</TermUI>
      <String>eilatine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T286391</TermUI>
      <String>eilatin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0470196</ConceptUI>
    <ConceptName>
     <String>isoeilatin</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0256387</Concept1UI>
     <Concept2UI>M0470196</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T601383</TermUI>
      <String>isoeilatin</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C108753</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>manuifolin F</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1997</Year>
   <Month>11</Month>
   <Day>13</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>an isoflavonoid from root of Maackia tenuifolia; structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*FLAVONOIDS (1997-2003)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007529</DescriptorUI>
     <DescriptorName>
      <String>Isoflavones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 1997 Sep;60(9):918-20</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0282450</ConceptUI>
    <ConceptName>
     <String>manuifolin F</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T312455</TermUI>
      <String>manuifolin F</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T312454</TermUI>
      <String>5'-(1-isopropylethenyl)-8-(3-methyl-2-butenyl)-7,2',4'-trihydroxyisoflavan</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009414</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tetrahydrofurfuryl mercaptan</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>10</Month>
   <Day>04</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SULFHYDRYL COMPOUNDS (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005663</DescriptorUI>
     <DescriptorName>
      <String>Furans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biochem 74(4):733;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054102</ConceptUI>
    <ConceptName>
     <String>tetrahydrofurfuryl mercaptan</String>
    </ConceptName>
    <CASN1Name>2-Furanmethanethiol, tetrahydro-</CASN1Name>
    <RegistryNumber>5069-94-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084105</TermUI>
      <String>tetrahydrofurfuryl mercaptan</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C055127</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Lrp2 protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1988</Year>
   <Month>04</Month>
   <Day>08</Day>
  </DateCreated>
  <DateRevised>
   <Year>2013</Year>
   <Month>10</Month>
   <Day>24</Day>
  </DateRevised>
  <Note>RefSeq NM_001081088
  </Note>
  <Frequency>96</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*Membrane Glycoproteins (1988-2005)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D026561</DescriptorUI>
     <DescriptorName>
      <String>Low Density Lipoprotein Receptor-Related Protein-2</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ann Inst Pasteur Immunol 1987;138(5):707</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0155341</ConceptUI>
    <ConceptName>
     <String>Lrp2 protein, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T654273</TermUI>
      <String>Lrp2 protein, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>10</Month>
       <Day>04</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T654275</TermUI>
      <String>megalin protein, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>10</Month>
       <Day>04</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T654274</TermUI>
      <String>brushin protein, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>10</Month>
       <Day>04</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T654276</TermUI>
      <String>low density lipoprotein receptor-related protein 2, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>10</Month>
       <Day>04</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009419</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6,7,8,9-tetrahydropyrimido(2,1-f)purine-2,4-(1H,3H)-dione</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>11</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PURINES (74-79)</PreviousIndexing>
   <PreviousIndexing>PYRIMIDINES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014970</DescriptorUI>
     <DescriptorName>
      <String>Xanthines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Pol J Pharmacol Pharm 25(2):171;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054108</ConceptUI>
    <ConceptName>
     <String>6,7,8,9-tetrahydropyrimido(2,1-f)purine-2,4-(1H,3H)-dione</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084111</TermUI>
      <String>6,7,8,9-tetrahydropyrimido(2,1-f)purine-2,4-(1H,3H)-dione</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009420</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,2,3,4-tetrahydropyrimido(1,2-c)quinazoline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>06</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>RN given refers to mono-HBr with configuration labeled as (2,1-b)
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PYRIMIDINES (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011799</DescriptorUI>
     <DescriptorName>
      <String>Quinazolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Yakugaku Zasshi 94(4):417;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054109</ConceptUI>
    <ConceptName>
     <String>1,2,3,4-tetrahydropyrimido(1,2-c)quinazoline</String>
    </ConceptName>
    <RegistryNumber>41363-26-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084112</TermUI>
      <String>1,2,3,4-tetrahydropyrimido(1,2-c)quinazoline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009422</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,3,4,5-tetrahydroxycyclohexanemethanol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ALCOHOL, METHYL (74-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003511</DescriptorUI>
     <DescriptorName>
      <String>Cyclohexanols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biotechnol Bioeng 15(6):1075;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054111</ConceptUI>
    <ConceptName>
     <String>2,3,4,5-tetrahydroxycyclohexanemethanol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084114</TermUI>
      <String>2,3,4,5-tetrahydroxycyclohexanemethanol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009426</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,5,7,8-tetramethyl-2-(4',8'-dimethylnonyl)-6- hydroxychromane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CHROMONES (75-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002839</DescriptorUI>
     <DescriptorName>
      <String>Chromans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Am J Clin Nutr 27(9):1005;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054118</ConceptUI>
    <ConceptName>
     <String>2,5,7,8-tetramethyl-2-(4',8'-dimethylnonyl)-6- hydroxychromane</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084121</TermUI>
      <String>2,5,7,8-tetramethyl-2-(4',8'-dimethylnonyl)-6- hydroxychromane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009431</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,2,6,6-tetramethylpiperidine 4-amino-(N,N-dichlorotriazine)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>07</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>TRIAZINES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010880</DescriptorUI>
     <DescriptorName>
      <String>Piperidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D013113</DescriptorUI>
     <DescriptorName>
      <String>Spin Labels</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>FEBS Lett 35(2):306;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054123</ConceptUI>
    <ConceptName>
     <String>2,2,6,6-tetramethylpiperidine 4-amino-(N,N-dichlorotriazine)</String>
    </ConceptName>
    <CASN1Name>1,3,5-Triazin-2-amine, 4,6-dichloro-N-(2,2,6,6-tetramethyl-4-piperidinyl)-</CASN1Name>
    <RegistryNumber>78717-59-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084126</TermUI>
      <String>2,2,6,6-tetramethylpiperidine 4-amino-(N,N-dichlorotriazine)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009432</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,2,6,6-tetramethylpiperidine N-oxyl 4-iodoacetate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>03</Month>
   <Day>02</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>IODOACETATES (74-79)</PreviousIndexing>
   <PreviousIndexing>PIPERIDINES (74-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003497</DescriptorUI>
     <DescriptorName>
      <String>Cyclic N-Oxides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D013113</DescriptorUI>
     <DescriptorName>
      <String>Spin Labels</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Biochim Biophys Acta 327(1):57;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054124</ConceptUI>
    <ConceptName>
     <String>2,2,6,6-tetramethylpiperidine N-oxyl 4-iodoacetate</String>
    </ConceptName>
    <CASN1Name>1-Piperidinyloxy, 4-((iodoacetyl)oxy)-2,2,6,6-tetramethyl-</CASN1Name>
    <RegistryNumber>36775-20-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084127</TermUI>
      <String>2,2,6,6-tetramethylpiperidine N-oxyl 4-iodoacetate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C111531</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>NTE 122</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>04</Month>
   <Day>22</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>11</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>7</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000814</DescriptorUI>
     <DescriptorName>
      <String>Aniline Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003510</DescriptorUI>
     <DescriptorName>
      <String>Cyclohexanes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D002785</DescriptorUI>
     <DescriptorName>
      <String>Sterol O-Acyltransferase</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
     <QualifierName>
      <String>antagonists &amp; inhibitors</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 1998 Mar 17;244(2):347-52</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0288752</ConceptUI>
    <ConceptName>
     <String>NTE 122</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0288752</Concept1UI>
     <Concept2UI>M0288749</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T318757</TermUI>
      <String>NTE 122</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T318756</TermUI>
      <String>NTE122</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T318755</TermUI>
      <String>NTE-122</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0288749</ConceptUI>
    <ConceptName>
     <String>1,4-bis-((1-cyclohexyl-3-(4-dimethylaminophenyl)ureido)methyl)cyclohexane</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0288752</Concept1UI>
     <Concept2UI>M0288749</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T318754</TermUI>
      <String>1,4-bis-((1-cyclohexyl-3-(4-dimethylaminophenyl)ureido)methyl)cyclohexane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009435</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tetramic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>132</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011760</DescriptorUI>
     <DescriptorName>
      <String>Pyrrolidinones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Biochem 40(1):163;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054134</ConceptUI>
    <ConceptName>
     <String>tetramic acid</String>
    </ConceptName>
    <CASN1Name>1,5-dihydro-4-hydroxy-2H-pyrrol-2-one</CASN1Name>
    <RegistryNumber>503-83-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084137</TermUI>
      <String>tetramic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009448</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-thiaisoleucine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>07</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ISOLEUCINE (74-75)</PreviousIndexing>
   <PreviousIndexing>AMINO ACIDS, SULFUR (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007532</DescriptorUI>
     <DescriptorName>
      <String>Isoleucine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>J Bacteriol 116(2):564;1973</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054154</ConceptUI>
    <ConceptName>
     <String>4-thiaisoleucine</String>
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    <RegistryNumber>443-80-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084157</TermUI>
      <String>4-thiaisoleucine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C464584</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>sulfoscanate</String>
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  <DateCreated>
   <Year>2002</Year>
   <Month>08</Month>
   <Day>29</Day>
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  <Note>structure in first source
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  <Frequency>1</Frequency>
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    <DescriptorReferredTo>
     <DescriptorUI>*D017879</DescriptorUI>
     <DescriptorName>
      <String>Isothiocyanates</String>
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  <SourceList>
   <Source>Mutat Res 2002 Jul 25;518(2):155-61</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0437824</ConceptUI>
    <ConceptName>
     <String>sulfoscanate</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T517870</TermUI>
      <String>sulfoscanate</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>08</Month>
       <Day>29</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T517871</TermUI>
      <String>4-isothiocyanate-4'-nitrodiphenyl sulphide</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>08</Month>
       <Day>29</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
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  <SupplementalRecordName>
   <String>2,2'-thiobis(4-methyl-6-tert-butylphenol)</String>
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  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>1994</Year>
   <Month>05</Month>
   <Day>26</Day>
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  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CRESOLS (75-80)</PreviousIndexing>
   <PreviousIndexing>SULFIDES (75-82)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002084</DescriptorUI>
     <DescriptorName>
      <String>Butylated Hydroxytoluene</String>
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    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>Vopr Onkol 20(7):47;1974</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054174</ConceptUI>
    <ConceptName>
     <String>2,2'-thiobis(4-methyl-6-tert-butylphenol)</String>
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    <CASN1Name>Phenol, 2,2'-thiobis(6-(1,1-dimethylethyl)-4-methyl-</CASN1Name>
    <RegistryNumber>90-66-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084177</TermUI>
      <String>2,2'-thiobis(4-methyl-6-tert-butylphenol)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
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   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009459</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,2'-thiobis-(4-methyl-6-alpha-phenylethylphenol)</String>
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  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>1994</Year>
   <Month>05</Month>
   <Day>26</Day>
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  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>SULFIDES (75-82)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003408</DescriptorUI>
     <DescriptorName>
      <String>Cresols</String>
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  <SourceList>
   <Source>Vopr Onkol 20(7):47;1974</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054175</ConceptUI>
    <ConceptName>
     <String>2,2'-thiobis-(4-methyl-6-alpha-phenylethylphenol)</String>
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    <RegistryNumber>13314-00-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084178</TermUI>
      <String>2,2'-thiobis-(4-methyl-6-alpha-phenylethylphenol)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
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   </Concept>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
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  <SupplementalRecordName>
   <String>4-thio-2'-deoxyuridylate</String>
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  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>RN in Chemline for 5-thio-isomer: 22456-57-7
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  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DEOXYRIBONUCLEOTIDES (74-78)</PreviousIndexing>
   <PreviousIndexing>*THIOURACIL (74-78)</PreviousIndexing>
   <PreviousIndexing>THIOURIDINE/analogs (78-79)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003856</DescriptorUI>
     <DescriptorName>
      <String>Deoxyuracil Nucleotides</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013873</DescriptorUI>
     <DescriptorName>
      <String>Thionucleotides</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 55(1):210;1973</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054177</ConceptUI>
    <ConceptName>
     <String>4-thio-2'-deoxyuridylate</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084180</TermUI>
      <String>4-thio-2'-deoxyuridylate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C439828</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>26-fluoroepothilone B</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>11</Month>
   <Day>28</Day>
  </DateCreated>
  <Note>a fluorinated epothilone compound with antitumor activity against human prostate cancer xenografts; structure in first source
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D018942</DescriptorUI>
     <DescriptorName>
      <String>Macrolides</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Chemother Pharmacol 2001 Oct;48(4):319-26</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0405810</ConceptUI>
    <ConceptName>
     <String>26-fluoroepothilone B</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T471404</TermUI>
      <String>26-fluoroepothilone B</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>11</Month>
       <Day>28</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
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    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009472</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>thiothenoyltrifluoroacetone</String>
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  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>08</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>used in spectrophotometric determination of silver
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  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ACETONE (74-75)</PreviousIndexing>
   <PreviousIndexing>THIONES (74-75)</PreviousIndexing>
   <PreviousIndexing>THIOPHENES (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013804</DescriptorUI>
     <DescriptorName>
      <String>Thenoyltrifluoroacetone</String>
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    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Soc Jpn 93(10):1394;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054206</ConceptUI>
    <ConceptName>
     <String>thiothenoyltrifluoroacetone</String>
    </ConceptName>
    <CASN1Name>2-Butanone, 1,1,1-trifluoro-4-(2-thienyl)-4-thioxo-</CASN1Name>
    <RegistryNumber>13801-41-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084209</TermUI>
      <String>thiothenoyltrifluoroacetone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009481</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>thymidylyl-(3'-5')-uridine</String>
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  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1988</Year>
   <Month>08</Month>
   <Day>10</Day>
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  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*THYMIDINE MONOPHOSPHATE/analogs (80-88)</PreviousIndexing>
   <PreviousIndexing>*THYMINE NUCLEOTIDES (73-79)</PreviousIndexing>
   <PreviousIndexing>*URIDINE (73-79)</PreviousIndexing>
   <PreviousIndexing>URIDINE/*analogs (80-88)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015226</DescriptorUI>
     <DescriptorName>
      <String>Dinucleoside Phosphates</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biokhimiia 38(6):1115;1973</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054221</ConceptUI>
    <ConceptName>
     <String>thymidylyl-(3'-5')-uridine</String>
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    <CASN1Name>Thymidine, uridylyl-(5'-3')-</CASN1Name>
    <RegistryNumber>15737-45-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084224</TermUI>
      <String>thymidylyl-(3'-5')-uridine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
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     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C439830</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>10,15,20-tritolylporphyrin-5-(4-amidophenyl)-(5-(4-phenyl)-10,15,20-tritolylporphyrin)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>11</Month>
   <Day>28</Day>
  </DateCreated>
  <Note>a tritolylporphyrin dimer as a new potent hydrophobic sensitizer for photodynamic therapy of melanoma; structure in first source
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011166</DescriptorUI>
     <DescriptorName>
      <String>Porphyrins</String>
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   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Biochim Pol 2001;48(1):277-82</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0405814</ConceptUI>
    <ConceptName>
     <String>10,15,20-tritolylporphyrin-5-(4-amidophenyl)-(5-(4-phenyl)-10,15,20-tritolylporphyrin)</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T471408</TermUI>
      <String>10,15,20-tritolylporphyrin-5-(4-amidophenyl)-(5-(4-phenyl)-10,15,20-tritolylporphyrin)</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>11</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T471409</TermUI>
      <String>TAPT dimer</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>11</Month>
       <Day>28</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009492</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tingenone</String>
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  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <Note>quinonoid triterpene isolated from Euonymus tingens; structure
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  <Frequency>12</Frequency>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014315</DescriptorUI>
     <DescriptorName>
      <String>Triterpenes</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>J Chem Soc Perkin I 22:2725;1973</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
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    <ConceptName>
     <String>tingenone</String>
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    <RegistryNumber>50802-21-6</RegistryNumber>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0054242</Concept1UI>
     <Concept2UI>M0054240</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
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      <String>tingenone</String>
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   <Concept PreferredConceptYN="N">
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    <ConceptName>
     <String>maitenine</String>
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    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0054242</Concept1UI>
     <Concept2UI>M0054241</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T084244</TermUI>
      <String>maitenine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
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     </Term>
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   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0054240</ConceptUI>
    <ConceptName>
     <String>20-decarboxy-20-oxocelastrol</String>
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    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0054242</Concept1UI>
     <Concept2UI>M0054240</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T084243</TermUI>
      <String>20-decarboxy-20-oxocelastrol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
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     </Term>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009506</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-tosylamido-2-phenylethyldiazomethylketone</String>
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  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>05</Day>
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  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AZO COMPOUNDS (73-80)</PreviousIndexing>
   <PreviousIndexing>*PHENYLALANINE (74-80)</PreviousIndexing>
   <PreviousIndexing>*TOSYL COMPOUNDS (74-80)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003979</DescriptorUI>
     <DescriptorName>
      <String>Diazonium Compounds</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>FEBS Lett 37(2):200;1973</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054293</ConceptUI>
    <ConceptName>
     <String>1-tosylamido-2-phenylethyldiazomethylketone</String>
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    <CASN1Name>Benzenesulfonamide, N-(3-diazo-2-oxo-1-(phenylmethyl)propyl)-4-methyl-, (S)-</CASN1Name>
    <RegistryNumber>10119-00-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084296</TermUI>
      <String>1-tosylamido-2-phenylethyldiazomethylketone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T084295</TermUI>
      <String>TPDK</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009499</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>togal</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>07</Month>
   <Day>24</Day>
  </DateRevised>
  <Note>contains 1.5 mg quinine.di-HCl, 42 mg lithium citrate, 250 mg acetylsalicylic acid
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001241</DescriptorUI>
     <DescriptorName>
      <String>Aspirin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002951</DescriptorUI>
     <DescriptorName>
      <String>Citrates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011803</DescriptorUI>
     <DescriptorName>
      <String>Quinine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D008094</DescriptorUI>
     <DescriptorName>
      <String>Lithium</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Arzneim Forsch 24(9):1305;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054263</ConceptUI>
    <ConceptName>
     <String>togal</String>
    </ConceptName>
    <RegistryNumber>8064-38-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084266</TermUI>
      <String>togal</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C058992</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Tagln protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1989</Year>
   <Month>05</Month>
   <Day>04</Day>
  </DateCreated>
  <DateRevised>
   <Year>2013</Year>
   <Month>10</Month>
   <Day>24</Day>
  </DateRevised>
  <Note>RefSeq NM_011526
  </Note>
  <Frequency>356</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008840</DescriptorUI>
     <DescriptorName>
      <String>Microfilament Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009124</DescriptorUI>
     <DescriptorName>
      <String>Muscle Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Exp Cell Res 1989;181(1):518</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0164278</ConceptUI>
    <ConceptName>
     <String>Tagln protein, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T588083</TermUI>
      <String>Tagln protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>05</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T607865</TermUI>
      <String>Sm22a protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T588084</TermUI>
      <String>transgelin protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>05</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T607866</TermUI>
      <String>SM-22 alpha protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T607867</TermUI>
      <String>smooth muscle protein 22-alpha, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C084276</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>TOM 92 protein, Lycopersicon esculentum</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1993</Year>
   <Month>12</Month>
   <Day>16</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>10</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>a polypeptide with high homology to several bacterial pyridoxal phosphate requiring histidine decarboxylases; involved in tomato fruit ripening; aa sequence given in first source; GenBank X71900
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010940</DescriptorUI>
     <DescriptorName>
      <String>Plant Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D006640</DescriptorUI>
     <DescriptorName>
      <String>Histidine Decarboxylase</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Plant Mol Biol 1993 Nov;23(3):627-31</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0223980</ConceptUI>
    <ConceptName>
     <String>TOM 92 protein, Lycopersicon esculentum</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T517994</TermUI>
      <String>TOM 92 protein, Lycopersicon esculentum</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>08</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C423631</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>PtsN protein, Pseudomonas putida</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>13</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>04</Month>
   <Day>13</Day>
  </DateRevised>
  <Note>required for C source inhibition of the Pu promotor of the TOL plasmid pWW0; isolated from Pseudomonas putida
  </Note>
  <Frequency>15</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010731</DescriptorUI>
     <DescriptorName>
      <String>Phosphoenolpyruvate Sugar Phosphotransferase System</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Bacteriol 2001 Feb;183(3):1032-7</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0384064</ConceptUI>
    <ConceptName>
     <String>PtsN protein, Pseudomonas putida</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T442987</TermUI>
      <String>PtsN protein, Pseudomonas putida</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>04</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T442989</TermUI>
      <String>IIA(Ntr) protein, Pseudomonas putida</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>04</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009511</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>toyocamycin 3',5'-cyclic phosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*NUCLEOTIDES, CYCLIC (74-80)</PreviousIndexing>
   <PreviousIndexing>*RIBONUCLEOTIDES (74-80)</PreviousIndexing>
   <PreviousIndexing>NITRILES (74-80)</PreviousIndexing>
   <PreviousIndexing>PYRROLES (74-80)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014127</DescriptorUI>
     <DescriptorName>
      <String>Toyocamycin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 55(3):843;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054302</ConceptUI>
    <ConceptName>
     <String>toyocamycin 3',5'-cyclic phosphate</String>
    </ConceptName>
    <CASN1Name>7H-Pyrrolo(2,3-d)pyrimidine-5-carbonitrile, 4-amino-7-(3,5-O-phosphinico-beta-D-ribofuranosyl)-</CASN1Name>
    <RegistryNumber>52134-58-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084305</TermUI>
      <String>toyocamycin 3',5'-cyclic phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009517</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>trans-n-(N,N,N-trimethylamino)cinnamoyltrypsin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>09</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CINNAMATES (74-82)</PreviousIndexing>
   <PreviousIndexing>METHYLAMINES (74-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014357</DescriptorUI>
     <DescriptorName>
      <String>Trypsin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biokhimiia 38(3):601;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054304</ConceptUI>
    <ConceptName>
     <String>trans-n-(N,N,N-trimethylamino)cinnamoyltrypsin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084307</TermUI>
      <String>trans-n-(N,N,N-trimethylamino)cinnamoyltrypsin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C523093</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-diphenylphosphinoaniline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>09</Month>
   <Day>27</Day>
  </DateCreated>
  <DateRevised>
   <Year>2007</Year>
   <Month>09</Month>
   <Day>27</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000814</DescriptorUI>
     <DescriptorName>
      <String>Aniline Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Commun (Camb) 2007 May 21;(19):1951-3</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0513926</ConceptUI>
    <ConceptName>
     <String>2-diphenylphosphinoaniline</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T706674</TermUI>
      <String>2-diphenylphosphinoaniline</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>09</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009526</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>(tricarbonyltechnetium(I))-mu-(mesoporphyrin IX dimethyl esterato)(tricarbonylrhenium(I))</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>first heterodinuclear metalloporphyrin; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PORPHYRINS (74-80)</PreviousIndexing>
   <PreviousIndexing>*RHENIUM (74-80)</PreviousIndexing>
   <PreviousIndexing>*TECHNETIUM (74-80)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008665</DescriptorUI>
     <DescriptorName>
      <String>Metalloporphyrins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Am Chem Soc 95(17):5777;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054317</ConceptUI>
    <ConceptName>
     <String>(tricarbonyltechnetium(I))-mu-(mesoporphyrin IX dimethyl esterato)(tricarbonylrhenium(I))</String>
    </ConceptName>
    <CASN1Name>Rhenium, tricarbonyl(mu-(dimethyl 7,12-diethyl-3,8,13,17-tetramethyl-21H,23H-porphine-2,18-dipropanoato(2-)))(tricarbonyltechnetium)-</CASN1Name>
    <RegistryNumber>39452-96-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084320</TermUI>
      <String>(tricarbonyltechnetium(I))-mu-(mesoporphyrin IX dimethyl esterato)(tricarbonylrhenium(I))</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C416807</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>polyaniline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>12</Day>
  </DateCreated>
  <Note>struct in first source
  </Note>
  <Frequency>1359</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000814</DescriptorUI>
     <DescriptorName>
      <String>Aniline Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D011108</DescriptorUI>
     <DescriptorName>
      <String>Polymers</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Biomed Mater Sci 2000 Dec 5:52(3):467-78</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0374496</ConceptUI>
    <ConceptName>
     <String>polyaniline</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T430854</TermUI>
      <String>polyaniline</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>12</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009542</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tridigal</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>isolated complex of glucosides from leaves of Digitalis lanata (Bulgarian)
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004071</DescriptorUI>
     <DescriptorName>
      <String>Digitalis Glycosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Vutr Boles 13(3):63-70;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054338</ConceptUI>
    <ConceptName>
     <String>tridigal</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084341</TermUI>
      <String>tridigal</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009548</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>triethylene glycol dinitrate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ETHERS (74-75)</PreviousIndexing>
   <PreviousIndexing>*NITRATES (74-80)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005026</DescriptorUI>
     <DescriptorName>
      <String>Ethylene Glycols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Am Ind Hyg Assoc J 34(12):526;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054350</ConceptUI>
    <ConceptName>
     <String>triethylene glycol dinitrate</String>
    </ConceptName>
    <CASN1Name>2,2'-(1,2-ethanediylbis(oxy))bisethanol, dinitrate</CASN1Name>
    <RegistryNumber>111-22-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084353</TermUI>
      <String>triethylene glycol dinitrate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009555</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-trifluoromethyl-2'-deoxyuridine 5'-triphosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DEOXYRIBONUCLEOTIDES (74-78)</PreviousIndexing>
   <PreviousIndexing>*URACIL NUCLEOTIDES (74-78)</PreviousIndexing>
   <PreviousIndexing>HYDROCARBONS, FLUORINATED (74-78)</PreviousIndexing>
   <PreviousIndexing>TRIFLUOROTHYMIDINE/analogs (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013942</DescriptorUI>
     <DescriptorName>
      <String>Thymine Nucleotides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Pharmacol 1973;9(6):783</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054360</ConceptUI>
    <ConceptName>
     <String>5-trifluoromethyl-2'-deoxyuridine 5'-triphosphate</String>
    </ConceptName>
    <CASN1Name>alpha,alpha,alpha-trifluorothymidine 5'-(tetrahydrogen triphosphate)</CASN1Name>
    <RegistryNumber>345-03-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084363</TermUI>
      <String>5-trifluoromethyl-2'-deoxyuridine 5'-triphosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C423802</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>TgMIC10 protein, Toxoplasma gondii</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>18</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>04</Month>
   <Day>13</Day>
  </DateRevised>
  <Note>a 18-kDa secretory antigen ; amino acid sequence in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000953</DescriptorUI>
     <DescriptorName>
      <String>Antigens, Protozoan</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D014122</DescriptorUI>
     <DescriptorName>
      <String>Toxoplasma</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Exp Parasitol 2001 Feb;97(2):77-88</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0384293</ConceptUI>
    <ConceptName>
     <String>TgMIC10 protein, Toxoplasma gondii</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T443285</TermUI>
      <String>TgMIC10 protein, Toxoplasma gondii</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>04</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T443284</TermUI>
      <String>TgMIC10 antigen, Toxoplasma gondii</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>04</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C523094</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hemoglobin Hagley Park</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>09</Month>
   <Day>27</Day>
  </DateCreated>
  <Note>has (alpha82Ala--&gt;Thr) substitution; identified in an infant with severe hemolytic anemia
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006455</DescriptorUI>
     <DescriptorName>
      <String>Hemoglobins, Abnormal</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Clin Chem 2007 Sep;53(9):1718-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0513927</ConceptUI>
    <ConceptName>
     <String>hemoglobin Hagley Park</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T706682</TermUI>
      <String>hemoglobin Hagley Park</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>09</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T706683</TermUI>
      <String>Hb Hagley Park</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>09</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013120</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>O(2)'-methyl-5-carbamoylmethyluridine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>Constituent of yeast tRNA; structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014529</DescriptorUI>
     <DescriptorName>
      <String>Uridine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 15(14):3046;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060641</ConceptUI>
    <ConceptName>
     <String>O(2)'-methyl-5-carbamoylmethyluridine</String>
    </ConceptName>
    <CASN1Name>Uridine, 5-(2-amino-2-oxoethyl)-2'-O-methyl-</CASN1Name>
    <RegistryNumber>60197-30-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090644</TermUI>
      <String>O(2)'-methyl-5-carbamoylmethyluridine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C079091</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>APBA1 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1993</Year>
   <Month>02</Month>
   <Day>04</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>09</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>RefSeq NM_001163
  </Note>
  <Frequency>102</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009419</DescriptorUI>
     <DescriptorName>
      <String>Nerve Tissue Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D048868</DescriptorUI>
     <DescriptorName>
      <String>Adaptor Proteins, Signal Transducing</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D005621</DescriptorUI>
     <DescriptorName>
      <String>Friedreich Ataxia</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Proc Natl Acad Sci U S A 1993 Jan 1;90(1):109-13</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0470347</ConceptUI>
    <ConceptName>
     <String>APBA1 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T601991</TermUI>
      <String>APBA1 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>05</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T601992</TermUI>
      <String>amyloid beta (A4) precursor protein-binding, family A, member 1 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>05</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T601993</TermUI>
      <String>MINT1 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>05</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T601994</TermUI>
      <String>neuronal munc18-1-interacting protein 1, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>05</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T601996</TermUI>
      <String>X11 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>05</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T601995</TermUI>
      <String>adaptor protein X11alpha, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>05</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T660662</TermUI>
      <String>Neuron-specific X11 protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>12</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C098872</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>alpha-conotoxin MII</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>05</Month>
   <Day>06</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>inhibits alpha3beta2 nicotinic acetylcholine receptors; isolated from Conus magus; amino acid sequence in first source
  </Note>
  <Frequency>94</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*Peptides (1996-1999)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D020916</DescriptorUI>
     <DescriptorName>
      <String>Conotoxins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
    <PharmacologicalActionList>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D018733</DescriptorUI>
        <DescriptorName>
         <String>Nicotinic Antagonists</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
    </PharmacologicalActionList>
  <SourceList>
   <Source>J Biol Chem 1996 Mar 29;271(13):7522-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0259656</ConceptUI>
    <ConceptName>
     <String>alpha-conotoxin MII</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T289661</TermUI>
      <String>alpha-conotoxin MII</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T289660</TermUI>
      <String>MII alpha-conotoxin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C098875</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>delta-latroinsectotoxin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>05</Month>
   <Day>06</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>isolated from the black widow spider Latrodectus mactans tredecimguttatus; amino acid sequence in first source; GenBank X92679
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013111</DescriptorUI>
     <DescriptorName>
      <String>Spider Venoms</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 1996 Mar 29;271(13):7535-43</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0259667</ConceptUI>
    <ConceptName>
     <String>delta-latroinsectotoxin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T289672</TermUI>
      <String>delta-latroinsectotoxin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T289671</TermUI>
      <String>delta-LIT</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013127</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-methyl-5-hydroxyvaleric acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>12</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PENTANOIC ACIDS (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006880</DescriptorUI>
     <DescriptorName>
      <String>Hydroxy Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Experientia 32(9):1138;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060657</ConceptUI>
    <ConceptName>
     <String>4-methyl-5-hydroxyvaleric acid</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090660</TermUI>
      <String>4-methyl-5-hydroxyvaleric acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013128</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>divezid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>11</Month>
   <Day>21</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004049</DescriptorUI>
     <DescriptorName>
      <String>Diethylcarbamazine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006834</DescriptorUI>
     <DescriptorName>
      <String>Hydrazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Veterinariia 12:48;1976</Source>
   <Source>Veterinariia 3:69;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060658</ConceptUI>
    <ConceptName>
     <String>divezid</String>
    </ConceptName>
    <RegistryNumber>52109-02-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090661</TermUI>
      <String>divezid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013130</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2'(3')-O-L-(O-methyl-3-phenyllactyl)adenosine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000241</DescriptorUI>
     <DescriptorName>
      <String>Adenosine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 442(1):71;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060661</ConceptUI>
    <ConceptName>
     <String>2'(3')-O-L-(O-methyl-3-phenyllactyl)adenosine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090664</TermUI>
      <String>2'(3')-O-L-(O-methyl-3-phenyllactyl)adenosine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013133</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-methyl-4-thia-cyclohexylsulfamic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003494</DescriptorUI>
     <DescriptorName>
      <String>Cyclamates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Z Lebensm Unters Forsch 161(3):275;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060663</ConceptUI>
    <ConceptName>
     <String>3-methyl-4-thia-cyclohexylsulfamic acid</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090666</TermUI>
      <String>3-methyl-4-thia-cyclohexylsulfamic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013134</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-methylthioacrylic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>13</Day>
  </DateRevised>
  <Note>formed from methionine by Streptomyces lincolnensis; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>SULFIDES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008689</DescriptorUI>
     <DescriptorName>
      <String>Methacrylates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiot (Tokyo) 29(6):646;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060664</ConceptUI>
    <ConceptName>
     <String>3-methylthioacrylic acid</String>
    </ConceptName>
    <RegistryNumber>26398-93-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090667</TermUI>
      <String>3-methylthioacrylic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013137</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>microhelenins</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>05</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>from Helenium microcephalum; RN given refers to microhelenin A in Chemline; RN given refers to (3aR-(3aalpha,4aalpha,7alpha,7aalpha,8alpha,9aalpha))-isomer
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>LACTONES (76-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012717</DescriptorUI>
     <DescriptorName>
      <String>Sesquiterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 65(9):1410;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060670</ConceptUI>
    <ConceptName>
     <String>microhelenins</String>
    </ConceptName>
    <CASN1Name>5H-4a,7-Ethano-4H-cyclohepta(1,2-b:4,5-c')difuran-2,11(3H)-dione, hexahydro-8-methyl-3-methylene-, (3aR-(3aalpha,4aalpha,7alpha,7aalpha,8alpha,9aalpha))-</CASN1Name>
    <RegistryNumber>61490-63-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0060670</Concept1UI>
     <Concept2UI>M0060667</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0060670</Concept1UI>
     <Concept2UI>M0060665</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0060670</Concept1UI>
     <Concept2UI>M0060669</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0060670</Concept1UI>
     <Concept2UI>M0060666</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0060670</Concept1UI>
     <Concept2UI>M0060668</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090673</TermUI>
      <String>microhelenins</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0060667</ConceptUI>
    <ConceptName>
     <String>microhelenin C</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0060670</Concept1UI>
     <Concept2UI>M0060667</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T090670</TermUI>
      <String>microhelenin C</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0060665</ConceptUI>
    <ConceptName>
     <String>microhelenin A</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0060670</Concept1UI>
     <Concept2UI>M0060665</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T090668</TermUI>
      <String>microhelenin A</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0060669</ConceptUI>
    <ConceptName>
     <String>microhelenin E</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0060670</Concept1UI>
     <Concept2UI>M0060669</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T090672</TermUI>
      <String>microhelenin E</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0060666</ConceptUI>
    <ConceptName>
     <String>microhelenin B</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0060670</Concept1UI>
     <Concept2UI>M0060666</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T090669</TermUI>
      <String>microhelenin B</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0060668</ConceptUI>
    <ConceptName>
     <String>microhelenin D</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0060670</Concept1UI>
     <Concept2UI>M0060668</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T090671</TermUI>
      <String>microhelenin D</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013158</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-nitrosobis(2-acetoxypropyl)amine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>26</Day>
  </DateRevised>
  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PROPYLAMINES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009602</DescriptorUI>
     <DescriptorName>
      <String>Nitrosamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Lett 1:197;1976</Source>
   <Source>Cancer Lett 3(3-4):109;1977</Source>
   <Source>Cancer Res 36(8):2877;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060711</ConceptUI>
    <ConceptName>
     <String>N-nitrosobis(2-acetoxypropyl)amine</String>
    </ConceptName>
    <RegistryNumber>60414-81-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090714</TermUI>
      <String>N-nitrosobis(2-acetoxypropyl)amine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013241</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ribonuclease dimer</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>cross-linked dimer of bovine pancreatic ribonuclease; significantly more effective than monomer in inhibiting tumor development in mice
  </Note>
  <Frequency>7</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*RIBONUCLEASE (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012260</DescriptorUI>
     <DescriptorName>
      <String>Ribonucleases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Res 36(11):4074;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060849</ConceptUI>
    <ConceptName>
     <String>ribonuclease dimer</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090852</TermUI>
      <String>ribonuclease dimer</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T090851</TermUI>
      <String>RNase dimer</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013169</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-O-oleandrosyl-5-O-desosaminylerythronolide A oxime</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009827</DescriptorUI>
     <DescriptorName>
      <String>Oleandomycin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiot 29(7):728;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060732</ConceptUI>
    <ConceptName>
     <String>3-O-oleandrosyl-5-O-desosaminylerythronolide A oxime</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090735</TermUI>
      <String>3-O-oleandrosyl-5-O-desosaminylerythronolide A oxime</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013170</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>oletetrin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Frequency>10</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ANTIBIOTICS, COMBINED (89-93)</PreviousIndexing>
   <PreviousIndexing>DRUG COMBINATIONS (76-88)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009827</DescriptorUI>
     <DescriptorName>
      <String>Oleandomycin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013752</DescriptorUI>
     <DescriptorName>
      <String>Tetracycline</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Przegl Dermatol 6:459;1976</Source>
   <Source>Przegl Lek 63(4):489;1976</Source>
   <Source>Zh Eksp Klin Med 16(2):64;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060733</ConceptUI>
    <ConceptName>
     <String>oletetrin</String>
    </ConceptName>
    <RegistryNumber>8048-44-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090736</TermUI>
      <String>oletetrin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C477257</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>naphthyl phenyl ketone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>09</Month>
   <Day>16</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007659</DescriptorUI>
     <DescriptorName>
      <String>Ketones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nanosci Nanotechnol 2002 Feb;2(1):41-4</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0453749</ConceptUI>
    <ConceptName>
     <String>naphthyl phenyl ketone</String>
    </ConceptName>
    <RegistryNumber>642-29-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T551034</TermUI>
      <String>naphthyl phenyl ketone</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>09</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T551035</TermUI>
      <String>2-naphthylphenylketone</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>09</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013176</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ovoglycopeptide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>glycopeptide prepared from ovalbumin
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006020</DescriptorUI>
     <DescriptorName>
      <String>Glycopeptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Gan 67(2):303;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060743</ConceptUI>
    <ConceptName>
     <String>ovoglycopeptide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090746</TermUI>
      <String>ovoglycopeptide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013183</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-oxosuccinamic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SUCCINATES (77-79)</PreviousIndexing>
   <PreviousIndexing>AMIDES (77-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010071</DescriptorUI>
     <DescriptorName>
      <String>Oxaloacetates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem J 157(3):600;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060749</ConceptUI>
    <ConceptName>
     <String>2-oxosuccinamic acid</String>
    </ConceptName>
    <RegistryNumber>33239-40-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090752</TermUI>
      <String>2-oxosuccinamic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C493728</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>RUNX1 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2013</Year>
   <Month>04</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>RefSeq NM_001001890
  </Note>
  <Frequency>1388</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D050676</DescriptorUI>
     <DescriptorName>
      <String>Core Binding Factor Alpha 2 Subunit</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0461964</ConceptUI>
    <ConceptName>
     <String>RUNX1 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0461964</Concept1UI>
     <Concept2UI>M0573973</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0461964</Concept1UI>
     <Concept2UI>M0583214</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T575930</TermUI>
      <String>RUNX1 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>03</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T575932</TermUI>
      <String>AML1 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>03</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T623711</TermUI>
      <String>core binding factor alpha 2 subunit, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>12</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T622160</TermUI>
      <String>runt-related transcription factor 1 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>12</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T575931</TermUI>
      <String>acute myeloid leukemia 1 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>03</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T575933</TermUI>
      <String>CBFA2 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>03</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0573973</ConceptUI>
    <ConceptName>
     <String>RUNX1b protein, human</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0461964</Concept1UI>
     <Concept2UI>M0573973</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T822689</TermUI>
      <String>RUNX1b protein, human</String>
      <DateCreated>
       <Year>2012</Year>
       <Month>05</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2012)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T822690</TermUI>
      <String>Runt related transcription factor isoform b, human</String>
      <DateCreated>
       <Year>2012</Year>
       <Month>05</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2012)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0583214</ConceptUI>
    <ConceptName>
     <String>RUNX1c protein, human</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0461964</Concept1UI>
     <Concept2UI>M0583214</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T840567</TermUI>
      <String>RUNX1c protein, human</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>04</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C435669</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-piperidinopyridine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateCreated>
  <Note>oxidosqualene cyclase antagonists; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010880</DescriptorUI>
     <DescriptorName>
      <String>Piperidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011725</DescriptorUI>
     <DescriptorName>
      <String>Pyridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Bioorg Med Chem Lett 2001 Aug 20;11(16):2213-6</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0399837</ConceptUI>
    <ConceptName>
     <String>4-piperidinopyridine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T463534</TermUI>
      <String>4-piperidinopyridine</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>09</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013189</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>pequocrin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>08</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>from Bupleurum rotundifolium
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010936</DescriptorUI>
     <DescriptorName>
      <String>Plant Extracts</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Vrach Delo 10:60;1976</Source>
   <Source>Vrach Delo 5:77;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060761</ConceptUI>
    <ConceptName>
     <String>pequocrin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090764</TermUI>
      <String>pequocrin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C501744</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>indotricarbocyanine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>03</Day>
  </DateCreated>
  <Frequency>58</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002232</DescriptorUI>
     <DescriptorName>
      <String>Carbocyanines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Circ Res 2004 Dec 10;95(12):1225-33</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0486567</ConceptUI>
    <ConceptName>
     <String>indotricarbocyanine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T644977</TermUI>
      <String>indotricarbocyanine</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>07</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T644978</TermUI>
      <String>Cy7 dye</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>07</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C477258</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>barium lanthanum hafnium oxide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>09</Month>
   <Day>16</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010087</DescriptorUI>
     <DescriptorName>
      <String>Oxides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nanosci Nanotechnol 2002 Feb;2(1):107-11</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0453750</ConceptUI>
    <ConceptName>
     <String>barium lanthanum hafnium oxide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T551036</TermUI>
      <String>barium lanthanum hafnium oxide</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>09</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T551037</TermUI>
      <String>Ba2LaHfO5.5</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>09</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013194</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>phospholenes</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009943</DescriptorUI>
     <DescriptorName>
      <String>Organophosphorus Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Pharm (Weinheim) 309(9):707;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060772</ConceptUI>
    <ConceptName>
     <String>phospholenes</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090775</TermUI>
      <String>phospholenes</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C501746</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>NARG2 protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>03</Day>
  </DateCreated>
  <Note>GenBank BC068183
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009687</DescriptorUI>
     <DescriptorName>
      <String>Nuclear Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Biochem 2004 Dec;271(23-24):4629-37</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0486569</ConceptUI>
    <ConceptName>
     <String>NARG2 protein, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T644981</TermUI>
      <String>NARG2 protein, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>07</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T644982</TermUI>
      <String>NMDA receptor-regulated protein 2, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>07</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013206</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>poly(2-aminoadenylic acid)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011061</DescriptorUI>
     <DescriptorName>
      <String>Poly A</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 15(17):3783;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060798</ConceptUI>
    <ConceptName>
     <String>poly(2-aminoadenylic acid)</String>
    </ConceptName>
    <CASN1Name>5'-Adenylic acid, 2-amino-, homopolymer</CASN1Name>
    <RegistryNumber>49717-85-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090801</TermUI>
      <String>poly(2-aminoadenylic acid)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013207</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>poly 2'-azido-2'-deoxyAMP</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>20</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*POLYDEOXYRIBONUCLEOTIDES (76-79)</PreviousIndexing>
   <PreviousIndexing>AZIDES (76-79)</PreviousIndexing>
   <PreviousIndexing>DEOXYADENINE NUCLEOTIDES (79-82)</PreviousIndexing>
   <PreviousIndexing>POLY A/analogs (76-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011061</DescriptorUI>
     <DescriptorName>
      <String>Poly A</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Lett 7(1):27;1979</Source>
   <Source>Nucleic Acid Res 3(8):2089;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060799</ConceptUI>
    <ConceptName>
     <String>poly 2'-azido-2'-deoxyAMP</String>
    </ConceptName>
    <CASN1Name>5'-Adenylic acid, 2'-azido-2'-deoxy-, homopolymer</CASN1Name>
    <RegistryNumber>61186-92-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090802</TermUI>
      <String>poly 2'-azido-2'-deoxyAMP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013210</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>poly(5-bromocytidylic acid)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011066</DescriptorUI>
     <DescriptorName>
      <String>Poly C</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nucleic Acid Res 3(6):1591;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060801</ConceptUI>
    <ConceptName>
     <String>poly(5-bromocytidylic acid)</String>
    </ConceptName>
    <RegistryNumber>29692-81-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090804</TermUI>
      <String>poly(5-bromocytidylic acid)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C435670</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>AM132</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007211</DescriptorUI>
     <DescriptorName>
      <String>Indoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011427</DescriptorUI>
     <DescriptorName>
      <String>Propiophenones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Jpn J Cancer Res 2001 Jul;92(7):768-77</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0399838</ConceptUI>
    <ConceptName>
     <String>AM132</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T463535</TermUI>
      <String>AM132</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>09</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T463536</TermUI>
      <String>AM-132</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>09</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013212</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>poly(2'-O-ethylcytidylate)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1995</Year>
   <Month>09</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>inhibitor &amp; poor template for reverse transcriptase
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*POLY C/analogs (76-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011066</DescriptorUI>
     <DescriptorName>
      <String>Poly C</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nucleic Acids Res 3(6):1603;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060804</ConceptUI>
    <ConceptName>
     <String>poly(2'-O-ethylcytidylate)</String>
    </ConceptName>
    <CASN1Name>5'-Cytidylic acid, 2'-O-ethyl-, homopolymer</CASN1Name>
    <RegistryNumber>58998-59-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090807</TermUI>
      <String>poly(2'-O-ethylcytidylate)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013214</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>polysar X 414</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>used in dental impression supports
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BUTADIENES (76-79)</PreviousIndexing>
   <PreviousIndexing>*PLASTICS (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011108</DescriptorUI>
     <DescriptorName>
      <String>Polymers</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Orthod Fr 46:292;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060805</ConceptUI>
    <ConceptName>
     <String>polysar X 414</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090808</TermUI>
      <String>polysar X 414</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C488098</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>NXNL1 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>07</Month>
   <Day>28</Day>
  </DateCreated>
  <DateRevised>
   <Year>2008</Year>
   <Month>09</Month>
   <Day>11</Day>
  </DateRevised>
  <Note>RefSeq NM_138454
  </Note>
  <Frequency>26</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013879</DescriptorUI>
     <DescriptorName>
      <String>Thioredoxins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nat Genet 2004 Jul;36(7):755-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0469899</ConceptUI>
    <ConceptName>
     <String>NXNL1 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T725557</TermUI>
      <String>NXNL1 protein, human</String>
      <DateCreated>
       <Year>2008</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2008)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T725558</TermUI>
      <String>nucleoredoxin-like 1 protein, human</String>
      <DateCreated>
       <Year>2008</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2008)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T600115</TermUI>
      <String>rod-derived cone viability factor, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T695152</TermUI>
      <String>thioredoxin-like 6 rod-derived cone viability factor, human</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>04</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T695151</TermUI>
      <String>TXNL6 protein, human</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>04</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T600116</TermUI>
      <String>RdCVF protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C016706</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>pyridinophane cryptand</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PYRIDINES (78-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004988</DescriptorUI>
     <DescriptorName>
      <String>Ethers, Cyclic</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D007476</DescriptorUI>
     <DescriptorName>
      <String>Ionophores</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D008024</DescriptorUI>
     <DescriptorName>
      <String>Ligands</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Biochim Biophys Acta 508(1):122;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0066891</ConceptUI>
    <ConceptName>
     <String>pyridinophane cryptand</String>
    </ConceptName>
    <RegistryNumber>61696-67-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T096894</TermUI>
      <String>pyridinophane cryptand</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T096893</TermUI>
      <String>1,12-dioxo-2,11-diaza-5,8,21,24-tetraoxa(12.8)(2,6)pyridinophane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C111579</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>CED-5 protein, C elegans</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>04</Month>
   <Day>24</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>11</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>similar to DOCK180; required for cell-corpse engulfment; isolated from Caenorhabditis elegans; amino acid sequence in first source
  </Note>
  <Frequency>23</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*HELMINTH PROTEINS (1998-2002)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008565</DescriptorUI>
     <DescriptorName>
      <String>Membrane Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029742</DescriptorUI>
     <DescriptorName>
      <String>Caenorhabditis elegans Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nature 1998 Apr 2;392(6675):501-4</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0288863</ConceptUI>
    <ConceptName>
     <String>CED-5 protein, C elegans</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T521730</TermUI>
      <String>CED-5 protein, C elegans</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>10</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C078134</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>calpain p94</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1992</Year>
   <Month>12</Month>
   <Day>16</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>amino acid sequence given in first source; a subunit of calpain which is expressed only in skeletal muscle
  </Note>
  <Frequency>35</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002154</DescriptorUI>
     <DescriptorName>
      <String>Calpain</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 1992 Nov 10;1160(1):55-62</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0209519</ConceptUI>
    <ConceptName>
     <String>calpain p94</String>
    </ConceptName>
    <RegistryNumber>EC 3.4.22.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T239524</TermUI>
      <String>calpain p94</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T239523</TermUI>
      <String>p94 calpain</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T239522</TermUI>
      <String>calpain subunit p94</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C016710</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-pyrrolidinecarbothioic acid (2-pyridylmethylene) hydrazide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PYRIDINES (78-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011759</DescriptorUI>
     <DescriptorName>
      <String>Pyrrolidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem J 171:485;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0066901</ConceptUI>
    <ConceptName>
     <String>1-pyrrolidinecarbothioic acid (2-pyridylmethylene) hydrazide</String>
    </ConceptName>
    <CASN1Name>1-Pyrrolidinecarbothioic acid, (2-pyridinylmethylene)hydrazide</CASN1Name>
    <RegistryNumber>16552-99-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T096904</TermUI>
      <String>1-pyrrolidinecarbothioic acid (2-pyridylmethylene) hydrazide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T096903</TermUI>
      <String>1-Pyrrolidinecarbothioic acid, (2-pyridylmethylene)hydrazide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014292</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Ro 03-6061</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>11</Month>
   <Day>17</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003497</DescriptorUI>
     <DescriptorName>
      <String>Cyclic N-Oxides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010880</DescriptorUI>
     <DescriptorName>
      <String>Piperidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Br J Cancer 37(Suppl 3):73;1978</Source>
   <Source>Radiation Res 69:489;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062738</ConceptUI>
    <ConceptName>
     <String>Ro 03-6061</String>
    </ConceptName>
    <CASN1Name>bis(2,2,6,6-tetramethyl-1-oxyl-4-piperidinyl) succinate</CASN1Name>
    <RegistryNumber>2516-88-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092741</TermUI>
      <String>Ro 03-6061</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014294</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>80.647</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>03</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*HYDRAZONES</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010879</DescriptorUI>
     <DescriptorName>
      <String>Piperazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Tropenmed Parasit 28(1):51;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062741</ConceptUI>
    <ConceptName>
     <String>80.647</String>
    </ConceptName>
    <CASN1Name>2-chloro-4-(1)-piperazinopenzalazin</CASN1Name>
    <RegistryNumber>51419-60-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092744</TermUI>
      <String>80.647</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014295</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Ro 8-1998</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003986</DescriptorUI>
     <DescriptorName>
      <String>Dibenzocycloheptenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Int Pharmacopsychiatr 12(1):38;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062742</ConceptUI>
    <ConceptName>
     <String>Ro 8-1998</String>
    </ConceptName>
    <CASN1Name>N,N-dimethyl-3-(1-methyl-5H-dibenzo(a,d)cycloheptene-5-ylidene)propylamine N-oxide.HCl</CASN1Name>
    <RegistryNumber>27747-18-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092745</TermUI>
      <String>Ro 8-1998</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014365</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bis(1-methylbenzimidazol-2-yl)methane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>04</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001562</DescriptorUI>
     <DescriptorName>
      <String>Benzimidazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Angew Chem Eng 16(3):189;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062845</ConceptUI>
    <ConceptName>
     <String>bis(1-methylbenzimidazol-2-yl)methane</String>
    </ConceptName>
    <CASN1Name>1H-Benzimidazole, 2,2'-methylenebis(1-methyl)-</CASN1Name>
    <RegistryNumber>55514-10-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092848</TermUI>
      <String>bis(1-methylbenzimidazol-2-yl)methane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014311</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-amidinobenzylphthalimide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>11</Month>
   <Day>05</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>AMIDINES (77-78)</PreviousIndexing>
   <PreviousIndexing>BENZAMIDINES (78-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010797</DescriptorUI>
     <DescriptorName>
      <String>Phthalimides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Pharmazie 32(2):76;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062767</ConceptUI>
    <ConceptName>
     <String>N-amidinobenzylphthalimide</String>
    </ConceptName>
    <CASN1Name>Benzenecarboximidamide, 4-((1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)methyl)-, monohydrochloride</CASN1Name>
    <RegistryNumber>62898-74-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092770</TermUI>
      <String>N-amidinobenzylphthalimide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014312</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-amidinophenylphthalimide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>11</Month>
   <Day>05</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>AMIDINES (77-78)</PreviousIndexing>
   <PreviousIndexing>BENZAMIDINES (78-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010797</DescriptorUI>
     <DescriptorName>
      <String>Phthalimides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Pharmazie 32(2):76;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062768</ConceptUI>
    <ConceptName>
     <String>N-amidinophenylphthalimide</String>
    </ConceptName>
    <CASN1Name>Benzenecarboximidamide, 3-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-, monohydrochloride</CASN1Name>
    <RegistryNumber>78249-59-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092771</TermUI>
      <String>N-amidinophenylphthalimide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014315</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-amino-5H-1,3,4-benzotriazepin-5-one</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001552</DescriptorUI>
     <DescriptorName>
      <String>Benzazepines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 66(4):605;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062770</ConceptUI>
    <ConceptName>
     <String>2-amino-5H-1,3,4-benzotriazepin-5-one</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092773</TermUI>
      <String>2-amino-5H-1,3,4-benzotriazepin-5-one</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014396</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cellulose acetate-butyrate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>10</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>68</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002482</DescriptorUI>
     <DescriptorName>
      <String>Cellulose</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D010969</DescriptorUI>
     <DescriptorName>
      <String>Plastics</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D011108</DescriptorUI>
     <DescriptorName>
      <String>Polymers</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Am J Optomet Physiolog Optics 54(12):826;1977</Source>
   <Source>Anal Biochem 86:417;1978</Source>
   <Source>Annals Ophthalmol 9(9):1085;1977</Source>
   <Source>Bull Soc Ophtalmol Fr 1980;80(3):269</Source>
   <Source>J Am Opt Assoc 48(3):387;1977</Source>
   <Source>J Am Opt Assoc 49(3):299;1978</Source>
   <Source>J Am Optom Assoc 49(8):927;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062901</ConceptUI>
    <ConceptName>
     <String>cellulose acetate-butyrate</String>
    </ConceptName>
    <CASN1Name>cellulose, acetate butanoate</CASN1Name>
    <RegistryNumber>9004-36-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092904</TermUI>
      <String>cellulose acetate-butyrate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T092903</TermUI>
      <String>cellulose aceto-butyrate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T092902</TermUI>
      <String>cabufocon</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T092901</TermUI>
      <String>C.A.B.</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C518813</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>zirconium tetra(tert-butoxide)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>04</Month>
   <Day>15</Day>
  </DateCreated>
  <DateRevised>
   <Year>2007</Year>
   <Month>04</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009942</DescriptorUI>
     <DescriptorName>
      <String>Organometallic Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D015040</DescriptorUI>
     <DescriptorName>
      <String>Zirconium</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Am Chem Soc 2007 Jan 10;129(1):93-7</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0508760</ConceptUI>
    <ConceptName>
     <String>zirconium tetra(tert-butoxide)</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T695548</TermUI>
      <String>zirconium tetra(tert-butoxide)</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>04</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T695549</TermUI>
      <String>Zr(OtBu)4</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>04</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014326</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>alpha-aminolaurophenone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>05</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>structure; RN given refers to HCL
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007659</DescriptorUI>
     <DescriptorName>
      <String>Ketones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cesk Farm 26(1):27;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062794</ConceptUI>
    <ConceptName>
     <String>alpha-aminolaurophenone</String>
    </ConceptName>
    <CASN1Name>1-Dodecanone, 2-amino-1-phenyl-, hydrochloride</CASN1Name>
    <RegistryNumber>63544-79-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092797</TermUI>
      <String>alpha-aminolaurophenone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014341</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>argyrophilic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>03</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>34</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004224</DescriptorUI>
     <DescriptorName>
      <String>Diterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D004365</DescriptorUI>
     <DescriptorName>
      <String>Drugs, Chinese Herbal</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D009032</DescriptorUI>
     <DescriptorName>
      <String>Mosquito Control</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Rev Inst Antibiot(Recife) 14(1/2):83;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062814</ConceptUI>
    <ConceptName>
     <String>argyrophilic acid</String>
    </ConceptName>
    <RegistryNumber>20316-84-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092817</TermUI>
      <String>argyrophilic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T092815</TermUI>
      <String>ent-kaur-16-en-19-oic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T092816</TermUI>
      <String>kaur-16-en-19-oic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014329</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>aminopolystyrene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011137</DescriptorUI>
     <DescriptorName>
      <String>Polystyrenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Vop Med Khimii 22(2):187;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062801</ConceptUI>
    <ConceptName>
     <String>aminopolystyrene</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092804</TermUI>
      <String>aminopolystyrene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014332</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>aminotricycline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>07</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>BRIDGED COMPOUNDS (78-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013729</DescriptorUI>
     <DescriptorName>
      <String>Terpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Farmaco (Sci) 32(3):180;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062803</ConceptUI>
    <ConceptName>
     <String>aminotricycline</String>
    </ConceptName>
    <CASN1Name>Tricyclo(2.2.1.0(2,6))heptane-3-methanamine, 2,3-dimethyl-</CASN1Name>
    <RegistryNumber>76740-71-1</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062803</Concept1UI>
     <Concept2UI>M0062802</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092806</TermUI>
      <String>aminotricycline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0062802</ConceptUI>
    <ConceptName>
     <String>7-methylamino-1,7-dimethyltricyclo(2,2,1,0)heptane</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062803</Concept1UI>
     <Concept2UI>M0062802</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T092805</TermUI>
      <String>7-methylamino-1,7-dimethyltricyclo(2,2,1,0)heptane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002319</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>phenylthiodiphenylpenicillin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>SULFIDES (73-76)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010406</DescriptorUI>
     <DescriptorName>
      <String>Penicillins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Can J Physiol Pharmacol 50(10):986;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0042875</ConceptUI>
    <ConceptName>
     <String>phenylthiodiphenylpenicillin</String>
    </ConceptName>
    <RegistryNumber>38964-63-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T072878</TermUI>
      <String>phenylthiodiphenylpenicillin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C426829</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Sm2 protein, Archaeoglobus fulgidus</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>05</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>12</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>binds RNA and forms heptameric and hexameric complexes
  </Note>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*RNA-BINDING PROTEINS (2001-2002)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D017411</DescriptorUI>
     <DescriptorName>
      <String>Ribonucleoproteins, Small Nuclear</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D019843</DescriptorUI>
     <DescriptorName>
      <String>Archaeal Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>EMBO J 2001 May 1;20(9):2293-303</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0388409</ConceptUI>
    <ConceptName>
     <String>Sm2 protein, Archaeoglobus fulgidus</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T448363</TermUI>
      <String>Sm2 protein, Archaeoglobus fulgidus</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>05</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C032506</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>somatotropin (1-134)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>12</Month>
   <Day>14</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>23</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010446</DescriptorUI>
     <DescriptorName>
      <String>Peptide Fragments</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013006</DescriptorUI>
     <DescriptorName>
      <String>Growth Hormone</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Endocrinology 1981;109(5):1663</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0101441</ConceptUI>
    <ConceptName>
     <String>somatotropin (1-134)</String>
    </ConceptName>
    <CASN1Name>1-134-Somatotropin</CASN1Name>
    <RegistryNumber>53528-53-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T131445</TermUI>
      <String>somatotropin (1-134)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T131444</TermUI>
      <String>human growth hormone (1-134)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T131443</TermUI>
      <String>HGH (1-134)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C032507</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>somatotropin (135-191)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>12</Month>
   <Day>14</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>23</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010446</DescriptorUI>
     <DescriptorName>
      <String>Peptide Fragments</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013006</DescriptorUI>
     <DescriptorName>
      <String>Growth Hormone</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Endocrinology 1981;109(5):1663</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0101444</ConceptUI>
    <ConceptName>
     <String>somatotropin (135-191)</String>
    </ConceptName>
    <RegistryNumber>80738-38-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T131448</TermUI>
      <String>somatotropin (135-191)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T131447</TermUI>
      <String>human growth hormone (135-191)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T131446</TermUI>
      <String>HGH (135-191)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C114290</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-methyl-2-thietaniumcarboxylic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>09</Month>
   <Day>18</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>07</Month>
   <Day>24</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002264</DescriptorUI>
     <DescriptorName>
      <String>Carboxylic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006571</DescriptorUI>
     <DescriptorName>
      <String>Heterocyclic Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Res Toxicol 1998 Jul;11(7):794-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0294819</ConceptUI>
    <ConceptName>
     <String>1-methyl-2-thietaniumcarboxylic acid</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T324824</TermUI>
      <String>1-methyl-2-thietaniumcarboxylic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C032835</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>alpha-N-acetyl beta-endorphin (1-26)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>12</Month>
   <Day>31</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>23</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ENDORPHINS (81-87)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D001615</DescriptorUI>
     <DescriptorName>
      <String>beta-Endorphin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010446</DescriptorUI>
     <DescriptorName>
      <String>Peptide Fragments</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 1981;102(3):897</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0102183</ConceptUI>
    <ConceptName>
     <String>alpha-N-acetyl beta-endorphin (1-26)</String>
    </ConceptName>
    <CASN1Name>beta-Endorphin, N-acetyl-27-de-L-histidine-28-de-L-lysine-29-de-L-lysine-30-deglycine-31-de-L-glutamine-</CASN1Name>
    <RegistryNumber>78325-28-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T132187</TermUI>
      <String>alpha-N-acetyl beta-endorphin (1-26)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T132186</TermUI>
      <String>alpha-N-acetyl beta-endorphin(1-26)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T132185</TermUI>
      <String>ANAC-BE26</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C110292</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-O-(indole-3-acetyl)glucose</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>02</Month>
   <Day>16</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>07</Month>
   <Day>24</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005960</DescriptorUI>
     <DescriptorName>
      <String>Glucosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007211</DescriptorUI>
     <DescriptorName>
      <String>Indoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Biochim Pol 1997;44(2):215-20</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0285970</ConceptUI>
    <ConceptName>
     <String>1-O-(indole-3-acetyl)glucose</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T315975</TermUI>
      <String>1-O-(indole-3-acetyl)glucose</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002353</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6-methyluridine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*URIDINE (72-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014529</DescriptorUI>
     <DescriptorName>
      <String>Uridine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nature (London) 235(333);1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0042899</ConceptUI>
    <ConceptName>
     <String>6-methyluridine</String>
    </ConceptName>
    <RegistryNumber>16710-13-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T072902</TermUI>
      <String>6-methyluridine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002356</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Mexaform</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1992</Year>
   <Month>06</Month>
   <Day>18</Day>
  </DateRevised>
  <Note>contains 4,7-phenanthroline-5,6-dione &amp; iodochlorhydroxyquin; used in treatment of non-specific enteritis; structure
  </Note>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007464</DescriptorUI>
     <DescriptorName>
      <String>Clioquinol</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010618</DescriptorUI>
     <DescriptorName>
      <String>Phenanthrolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D010115</DescriptorUI>
     <DescriptorName>
      <String>Oxyphenonium</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Curr Ther Res 18(4):546;1975</Source>
   <Source>J Assoc Physicians India 24(2):95;1976</Source>
   <Source>Pediatriia 7:38;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0042900</ConceptUI>
    <ConceptName>
     <String>Mexaform</String>
    </ConceptName>
    <RegistryNumber>8056-07-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T072903</TermUI>
      <String>Mexaform</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002357</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Mexase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1992</Year>
   <Month>06</Month>
   <Day>18</Day>
  </DateRevised>
  <Note>contains bromelain, pancreatin, dehydrocholic acid, iodochlorhydroquin, 4,7-phenanthroline-5,6-dione used in treatment of non-specific enteritis
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001963</DescriptorUI>
     <DescriptorName>
      <String>Bromelains</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003685</DescriptorUI>
     <DescriptorName>
      <String>Dehydrocholic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007464</DescriptorUI>
     <DescriptorName>
      <String>Clioquinol</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010194</DescriptorUI>
     <DescriptorName>
      <String>Pancreatin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010618</DescriptorUI>
     <DescriptorName>
      <String>Phenanthrolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Vrach Delo 5:137;1977</Source>
   <Source>Vrach Delo 6:78;1976</Source>
   <Source>Z Allgemeinmed 46(9):482;1970</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0042901</ConceptUI>
    <ConceptName>
     <String>Mexase</String>
    </ConceptName>
    <CASN1Name>Cholan-24-oic acid, 3,7,12-trioxo-, (5beta)-, mixt. with 5-chloro-7-iodo-8-quinolinol, pancreatin, 4,7-phenanthroline-5,6-dione and stem bromelain</CASN1Name>
    <RegistryNumber>99753-54-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T072904</TermUI>
      <String>Mexase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C493186</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Fuji VII</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>11</Month>
   <Day>21</Day>
  </DateCreated>
  <DateRevised>
   <Year>2007</Year>
   <Month>05</Month>
   <Day>29</Day>
  </DateRevised>
  <Frequency>35</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005899</DescriptorUI>
     <DescriptorName>
      <String>Glass Ionomer Cements</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Indian Soc Pedod Prev Dent 2004 Jun;22(2):56-62</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0475824</ConceptUI>
    <ConceptName>
     <String>Fuji VII</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T618693</TermUI>
      <String>Fuji VII</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>11</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T618695</TermUI>
      <String>GC VII</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>11</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T618694</TermUI>
      <String>Fuji GC VII</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>11</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000602737</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>amantelide A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2015</Year>
   <Month>11</Month>
   <Day>18</Day>
  </DateCreated>
  <DateRevised>
   <Year>2015</Year>
   <Month>11</Month>
   <Day>18</Day>
  </DateRevised>
  <Note>Cytotoxic cpd from a Guamanian marine Cyanobacterium; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D018942</DescriptorUI>
     <DescriptorName>
      <String>Macrolides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod. 2015 Aug 28;78(8):1957-62</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M000611744</ConceptUI>
    <ConceptName>
     <String>amantelide A</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T000890600</TermUI>
      <String>amantelide A</String>
      <DateCreated>
       <Year>2015</Year>
       <Month>11</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2016)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002383</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>morpholinomethylphenol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>12</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*MORPHOLINES (71-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010636</DescriptorUI>
     <DescriptorName>
      <String>Phenols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0042929</ConceptUI>
    <ConceptName>
     <String>morpholinomethylphenol</String>
    </ConceptName>
    <CASN1Name>4-(3-methyl-2-morpholinyl)phenol</CASN1Name>
    <RegistryNumber>54804-09-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T072932</TermUI>
      <String>morpholinomethylphenol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C492913</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>BRCA1 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>11</Month>
   <Day>07</Day>
  </DateCreated>
  <DateRevised>
   <Year>2007</Year>
   <Month>05</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>RefSeq NM_007305
  </Note>
  <Frequency>3368</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CHROMOSOMAL PROTEINS, NON-HISTONE (2004-2007)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D019313</DescriptorUI>
     <DescriptorName>
      <String>BRCA1 Protein</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nat Cell Biol 2004 Oct;6(10):954-67</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0475257</ConceptUI>
    <ConceptName>
     <String>BRCA1 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0475257</Concept1UI>
     <Concept2UI>M0509994</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T698438</TermUI>
      <String>BRCA1 protein, human</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>05</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T698439</TermUI>
      <String>breast cancer 1, early onset protein, human</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>05</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T698440</TermUI>
      <String>BRCC1 protein, human</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>05</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0509994</ConceptUI>
    <ConceptName>
     <String>BRCA1-IRIS protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0475257</Concept1UI>
     <Concept2UI>M0509994</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T617458</TermUI>
      <String>BRCA1-IRIS protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>11</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C519893</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,6-bis(L-alpha, beta-diaminopropionic acid) oxytocin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>05</Month>
   <Day>29</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010121</DescriptorUI>
     <DescriptorName>
      <String>Oxytocin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Sheng Wu Yi Xue Gong Cheng Xue Za Zhi. 2006 Aug;23(4):818-21</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0509995</ConceptUI>
    <ConceptName>
     <String>1,6-bis(L-alpha, beta-diaminopropionic acid) oxytocin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T698442</TermUI>
      <String>1,6-bis(L-alpha, beta-diaminopropionic acid) oxytocin</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>05</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T698443</TermUI>
      <String>1,6-b(DAPA)O cpd</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>05</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C071899</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>130k protein, Tobacco mosaic virus</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1992</Year>
   <Month>01</Month>
   <Day>06</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>01</Month>
   <Day>13</Day>
  </DateRevised>
  <Note>126-kDa protein encoded by same ORF as 130-kDa form; possesses methyltransferase and helicase-like domains
  </Note>
  <Frequency>12</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014764</DescriptorUI>
     <DescriptorName>
      <String>Viral Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D014027</DescriptorUI>
     <DescriptorName>
      <String>Tobacco Mosaic Virus</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Virology 1991;185(2)580</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0195035</ConceptUI>
    <ConceptName>
     <String>130k protein, Tobacco mosaic virus</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0195035</Concept1UI>
     <Concept2UI>M0365111</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T225039</TermUI>
      <String>130k protein, Tobacco mosaic virus</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T225040</TermUI>
      <String>TMV 130k protein, Tobacco mosaic virus</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0365111</ConceptUI>
    <ConceptName>
     <String>126-kDa protein, Tobacco mosaic virus</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0195035</Concept1UI>
     <Concept2UI>M0365111</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T418009</TermUI>
      <String>126-kDa protein, Tobacco mosaic virus</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>06</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T418008</TermUI>
      <String>TMV 126-kDa protein, Tobacco mosaic virus</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>06</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002459</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>D 048</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>26</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PHENOLS (73-74)</PreviousIndexing>
   <PreviousIndexing>SULFITES (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010647</DescriptorUI>
     <DescriptorName>
      <String>Phenyl Ethers</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Ag Food Chem 21(1):98;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043058</ConceptUI>
    <ConceptName>
     <String>D 048</String>
    </ConceptName>
    <CASN1Name>1-(2-butynyl)-1-(p-tert-butylphenoxy)-2-butyl sulfite</CASN1Name>
    <RegistryNumber>40642-27-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T073061</TermUI>
      <String>D 048</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073060</TermUI>
      <String>D-048</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C418973</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>pronapsin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>27</Day>
  </DateCreated>
  <Note>amino acid sequence in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004792</DescriptorUI>
     <DescriptorName>
      <String>Enzyme Precursors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D016282</DescriptorUI>
     <DescriptorName>
      <String>Aspartic Acid Endopeptidases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Biochem 2000 Dec;267(23):6921-30</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0377330</ConceptUI>
    <ConceptName>
     <String>pronapsin</String>
    </ConceptName>
    <RegistryNumber>EC 3.4.23.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T434346</TermUI>
      <String>pronapsin</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>01</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "3">
  <SupplementalRecordUI>C565176</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Corneal Dystrophy, Posterior Polymorphous, 2</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2012</Year>
   <Month>11</Month>
   <Day>05</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003317</DescriptorUI>
     <DescriptorName>
      <String>Corneal Dystrophies, Hereditary</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0565476</ConceptUI>
    <ConceptName>
     <String>Corneal Dystrophy, Posterior Polymorphous, 2</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T806289</TermUI>
      <String>Corneal Dystrophy, Posterior Polymorphous, 2</String>
      <DateCreated>
       <Year>2011</Year>
       <Month>11</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>OMIM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002423</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>mannophosphoinositide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1993</Year>
   <Month>08</Month>
   <Day>19</Day>
  </DateRevised>
  <Frequency>12</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PHOSPHOINOSITIDES (77-93)</PreviousIndexing>
   <PreviousIndexing>MANNOSE (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010716</DescriptorUI>
     <DescriptorName>
      <String>Phosphatidylinositols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Am Rev Respir Dis 106(6):892;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043002</ConceptUI>
    <ConceptName>
     <String>mannophosphoinositide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073005</TermUI>
      <String>mannophosphoinositide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C088094</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>chlorophyll a-b-binding protein, Ginkgo biloba</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>isolated from Ginkgo biloba; amino acid sequence in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D045332</DescriptorUI>
     <DescriptorName>
      <String>Photosystem II Protein Complex</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D045342</DescriptorUI>
     <DescriptorName>
      <String>Light-Harvesting Protein Complexes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Plant Physiol 1993 Nov;103(3):727-32</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0233192</ConceptUI>
    <ConceptName>
     <String>chlorophyll a-b-binding protein, Ginkgo biloba</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T263197</TermUI>
      <String>chlorophyll a-b-binding protein, Ginkgo biloba</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014578</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hawkinsin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>10</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000603</DescriptorUI>
     <DescriptorName>
      <String>Amino Acids, Sulfur</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D053138</DescriptorUI>
     <DescriptorName>
      <String>Cyclohexenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Clin Chim Acta 76:345;1977</Source>
   <Source>Clin Chim Acta 90(2):195;1978</Source>
   <Source>J Chromatogr 146(2):207;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063197</ConceptUI>
    <ConceptName>
     <String>hawkinsin</String>
    </ConceptName>
    <CASN1Name>2-Cyclohexene-1-acetic acid, 6-((2-amino-2-carboxyethyl)thio)-1,4-dihydroxy-</CASN1Name>
    <RegistryNumber>63224-90-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093200</TermUI>
      <String>hawkinsin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T093199</TermUI>
      <String>(2-L-cystein-S-yl-1,4-dihydroxycyclohex-5-en-1- yl)acetic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C088752</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>fucoxanthin-, chlorophyll a-c-containing protein</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>09</Month>
   <Day>07</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>a light-harvesting protein; amino acid sequence given in first source; GenBank X77333
  </Note>
  <Frequency>33</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D045342</DescriptorUI>
     <DescriptorName>
      <String>Light-Harvesting Protein Complexes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Plant Mol Biol 1994 Jun;25(3):355-68</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0234819</ConceptUI>
    <ConceptName>
     <String>fucoxanthin-, chlorophyll a-c-containing protein</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T264824</TermUI>
      <String>fucoxanthin-, chlorophyll a-c-containing protein</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T264823</TermUI>
      <String>fucoxanthin-chlorophyll protein (FCP)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002432</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-methyl-4-dimethylaminoazobenzene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>12</Day>
  </DateRevised>
  <Frequency>10</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DIMETHYLAMINOAZOBENZENE (73-75)</PreviousIndexing>
   <PreviousIndexing>METHANE (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008749</DescriptorUI>
     <DescriptorName>
      <String>Methyldimethylaminoazobenzene</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D007536</DescriptorUI>
     <DescriptorName>
      <String>Isomerism</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Cancer Res 32(9):1878;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043018</ConceptUI>
    <ConceptName>
     <String>2-methyl-4-dimethylaminoazobenzene</String>
    </ConceptName>
    <RegistryNumber>54-88-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073021</TermUI>
      <String>2-methyl-4-dimethylaminoazobenzene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002437</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-(4'-hydroxyazobenzene)benzoic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>09</Month>
   <Day>02</Day>
  </DateRevised>
  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>BENZOATES (73-82)</PreviousIndexing>
   <PreviousIndexing>PHENOLS (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001391</DescriptorUI>
     <DescriptorName>
      <String>Azo Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Clin Biochem 8(4):273;1975</Source>
   <Source>Clin Chem 18(12):1537;1972</Source>
   <Source>J Pediatr 90(4):642;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043020</ConceptUI>
    <ConceptName>
     <String>2-(4'-hydroxyazobenzene)benzoic acid</String>
    </ConceptName>
    <RegistryNumber>29533-13-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073023</TermUI>
      <String>2-(4'-hydroxyazobenzene)benzoic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002438</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-methyl-3-carbethoxy-4-(3-propionic acid)pyrrole</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>09</Month>
   <Day>02</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PROPIONATES (73-75)</PreviousIndexing>
   <PreviousIndexing>PROPIONIC ACIDS (75-83)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011758</DescriptorUI>
     <DescriptorName>
      <String>Pyrroles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Clin Chem 18(12):1534;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043021</ConceptUI>
    <ConceptName>
     <String>2-methyl-3-carbethoxy-4-(3-propionic acid)pyrrole</String>
    </ConceptName>
    <RegistryNumber>38664-16-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073024</TermUI>
      <String>2-methyl-3-carbethoxy-4-(3-propionic acid)pyrrole</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C083513</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>PurC protein, Bacteria</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1993</Year>
   <Month>11</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>01</Month>
   <Day>15</Day>
  </DateRevised>
  <Note>Phosphoribosylaminoimidazole-succinocarboxamide synthase
  </Note>
  <Frequency>14</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010453</DescriptorUI>
     <DescriptorName>
      <String>Peptide Synthases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Bacteriol 1993 Oct 1;175(19):6364-67</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0222177</ConceptUI>
    <ConceptName>
     <String>PurC protein, Bacteria</String>
    </ConceptName>
    <RegistryNumber>EC 6.3.2.6</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0222177</Concept1UI>
     <Concept2UI>M0222175</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T252182</TermUI>
      <String>PurC protein, Bacteria</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0222175</ConceptUI>
    <ConceptName>
     <String>PurC protein, Streptococcus pneumoniae</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0222177</Concept1UI>
     <Concept2UI>M0222175</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T252180</TermUI>
      <String>PurC protein, Streptococcus pneumoniae</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C097590</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>GW 3600</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>02</Month>
   <Day>12</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>a selective inhibitor of cAMP-specific phosphodiesterase type IV (PDE4); structure given in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011759</DescriptorUI>
     <DescriptorName>
      <String>Pyrrolidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D010726</DescriptorUI>
     <DescriptorName>
      <String>Phosphodiesterase Inhibitors</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Med Chem 1995 Dec 22;38(26):4972-5</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0256516</ConceptUI>
    <ConceptName>
     <String>GW 3600</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0256516</Concept1UI>
     <Concept2UI>M0256515</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T286521</TermUI>
      <String>GW 3600</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T286519</TermUI>
      <String>GW3600</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T286518</TermUI>
      <String>GW-3600</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0256515</ConceptUI>
    <ConceptName>
     <String>methyl 3-acetyl-4-(3-(cyclopentyloxy)-4-methoxyphenyl)-3-methyl-1-pyrrolidinecarboxylate</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0256516</Concept1UI>
     <Concept2UI>M0256515</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T286520</TermUI>
      <String>methyl 3-acetyl-4-(3-(cyclopentyloxy)-4-methoxyphenyl)-3-methyl-1-pyrrolidinecarboxylate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002451</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,3-dimethyluracil</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>21</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*URACIL (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014498</DescriptorUI>
     <DescriptorName>
      <String>Uracil</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biophys Chem 8:151;1978</Source>
   <Source>Photochem Photobiol 16(6):465;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043050</ConceptUI>
    <ConceptName>
     <String>1,3-dimethyluracil</String>
    </ConceptName>
    <RegistryNumber>874-14-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073053</TermUI>
      <String>1,3-dimethyluracil</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002457</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>polyoxin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1994</Year>
   <Month>06</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>antifungal antibiotics produced by Streptomyces cacaoi var asoensis; group of peptide-pyrimidine nucleoside antibiotics
  </Note>
  <Frequency>50</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PEPTIDES (73-93)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011741</DescriptorUI>
     <DescriptorName>
      <String>Pyrimidine Nucleosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 16(14):3121;1977</Source>
   <Source>Chem Pharm Bull (Tokyo) 25(7):1740;1977</Source>
   <Source>Environ Qual Saf 5:49;1976</Source>
   <Source>J Am Chem Soc 91:7490;1969</Source>
   <Source>J Chem Soc (Perkin I) 12:1472;1977</Source>
   <Source>J Org Chem 37(26):4391;1972</Source>
   <Source>Pesticides 3:439;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043055</ConceptUI>
    <ConceptName>
     <String>polyoxin</String>
    </ConceptName>
    <RegistryNumber>11113-80-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073058</TermUI>
      <String>polyoxin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002464</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tetrodamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>intermediate in synthesis of tetrodotoxin; RN from 9th CI; cpd not in Chemline 8/83; structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*TETRODOTOXIN (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013779</DescriptorUI>
     <DescriptorName>
      <String>Tetrodotoxin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Am Chem Soc 94(26):9217;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043060</ConceptUI>
    <ConceptName>
     <String>tetrodamine</String>
    </ConceptName>
    <RegistryNumber>41963-49-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073063</TermUI>
      <String>tetrodamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002469</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>fusarenon-X</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>mycotoxin isolated from Fusarium nivale; belongs to 12,13-epoxytrichothecene group; structure
  </Note>
  <Frequency>73</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SESQUITERPENES (74-75)</PreviousIndexing>
   <PreviousIndexing>FUSARIUM (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014255</DescriptorUI>
     <DescriptorName>
      <String>Trichothecenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D009183</DescriptorUI>
     <DescriptorName>
      <String>Mycotoxins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Biochim Biophys Acta 287(3):520;1972</Source>
   <Source>Biochim Biophys Acta 383(2):207;1975</Source>
   <Source>Eur J Biochem 84:103;1978</Source>
   <Source>IARC Monogr Eval Carcinog Risk Chem Man 11:169;1976</Source>
   <Source>Jpn Med Sci Biol 1979;32(4):189</Source>
   <Source>Toxicol Appl Pharmacol 1979;50(1):87</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043065</ConceptUI>
    <ConceptName>
     <String>fusarenon-X</String>
    </ConceptName>
    <CASN1Name>12,13-epoxy-3 alpha,4 beta,7 beta,15-tetrahydroxytrichothec-9-en-8-one 4-acetate</CASN1Name>
    <RegistryNumber>23255-69-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073068</TermUI>
      <String>fusarenon-X</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002481</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>isohomofolic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1984</Year>
   <Month>08</Month>
   <Day>15</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*FOLIC ACID (72-75)</PreviousIndexing>
   <PreviousIndexing>*HOMOFOLIC ACID (75-84)</PreviousIndexing>
   <PreviousIndexing>ISOMERISM (72-74)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005492</DescriptorUI>
     <DescriptorName>
      <String>Folic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Pharmacol 8(6):740;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043084</ConceptUI>
    <ConceptName>
     <String>isohomofolic acid</String>
    </ConceptName>
    <CASN1Name>N-(4-((((2-amino-1,4-dihydro-4-oxo-6-pteridinyl)methyl)amino)methyl)benzoyl)-L-glutamic acid</CASN1Name>
    <RegistryNumber>24960-28-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073087</TermUI>
      <String>isohomofolic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002482</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>isohomoaminopterin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AMINOPTERIN (73-75)</PreviousIndexing>
   <PreviousIndexing>ISOMERISM (73-74)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000630</DescriptorUI>
     <DescriptorName>
      <String>Aminopterin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Pharmacol 8(6):740;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043085</ConceptUI>
    <ConceptName>
     <String>isohomoaminopterin</String>
    </ConceptName>
    <CASN1Name>N-(4-((((2,4-diamino-6-pteridinyl)methyl)amino)methyl)benzoyl)-L-glutamic acid</CASN1Name>
    <RegistryNumber>39271-61-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073088</TermUI>
      <String>isohomoaminopterin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002495</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Ro 4-1398</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1995</Year>
   <Month>09</Month>
   <Day>15</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011807</DescriptorUI>
     <DescriptorName>
      <String>Quinolizines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arzneim Forsch 22(9):1474;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043116</ConceptUI>
    <ConceptName>
     <String>Ro 4-1398</String>
    </ConceptName>
    <CASN1Name>2-hydroxy-2-(3'-methoxybutyl)-3-isobutyl-9,10-dimethoxy-1,3,4,6,7,11b-hexahydro-2H-benzoquinolizine.HCl</CASN1Name>
    <RegistryNumber>37819-46-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073119</TermUI>
      <String>Ro 4-1398</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002507</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bracteoline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>METHYL ETHER (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001060</DescriptorUI>
     <DescriptorName>
      <String>Aporphines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Ber 105(2):609;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043134</ConceptUI>
    <ConceptName>
     <String>bracteoline</String>
    </ConceptName>
    <RegistryNumber>25651-04-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073137</TermUI>
      <String>bracteoline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002585</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-hydroxyphytanic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>26</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>7</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*FATTY ACIDS (73-75)</PreviousIndexing>
   <PreviousIndexing>FATTY ALCOHOLS (74-75)</PreviousIndexing>
   <PreviousIndexing>HYDROXY ACIDS (75-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010831</DescriptorUI>
     <DescriptorName>
      <String>Phytanic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 248(3):1091;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043244</ConceptUI>
    <ConceptName>
     <String>2-hydroxyphytanic acid</String>
    </ConceptName>
    <CASN1Name>2-hydroxy-3,7,11,15-tetramethylhexadecanoic acid</CASN1Name>
    <RegistryNumber>14721-68-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073247</TermUI>
      <String>2-hydroxyphytanic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073246</TermUI>
      <String>alpha-hydroxyphytanic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C041205</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>aflatoxin Q2a-bovine serum albumin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1984</Year>
   <Month>05</Month>
   <Day>23</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000348</DescriptorUI>
     <DescriptorName>
      <String>Aflatoxins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012710</DescriptorUI>
     <DescriptorName>
      <String>Serum Albumin, Bovine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D000941</DescriptorUI>
     <DescriptorName>
      <String>Antigens</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Appl Environ Microbiol 1984;47(3):526</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0122311</ConceptUI>
    <ConceptName>
     <String>aflatoxin Q2a-bovine serum albumin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T152316</TermUI>
      <String>aflatoxin Q2a-bovine serum albumin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1984)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T152314</TermUI>
      <String>AFQ2a-BSA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1984)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T152315</TermUI>
      <String>AFQ2a-bovine serum albumin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1984)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002513</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-(2-chloro-1-naphthylidene)-3-amino-2,6-lutidine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1991</Year>
   <Month>06</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PIPERIDINES (73-79)</PreviousIndexing>
   <PreviousIndexing>*PYRIDINES (73-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009281</DescriptorUI>
     <DescriptorName>
      <String>Naphthalenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Reprod Fertil 31(3):383;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043143</ConceptUI>
    <ConceptName>
     <String>N-(2-chloro-1-naphthylidene)-3-amino-2,6-lutidine</String>
    </ConceptName>
    <RegistryNumber>38641-70-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073146</TermUI>
      <String>N-(2-chloro-1-naphthylidene)-3-amino-2,6-lutidine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002519</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dimethialium propyldisulfide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DISULFIDES (73-76)</PreviousIndexing>
   <PreviousIndexing>AMIDES (73-74)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011743</DescriptorUI>
     <DescriptorName>
      <String>Pyrimidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Jap Circulation J 36(9):935;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043146</ConceptUI>
    <ConceptName>
     <String>dimethialium propyldisulfide</String>
    </ConceptName>
    <RegistryNumber>7244-66-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073149</TermUI>
      <String>dimethialium propyldisulfide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002520</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-dimethylaminopropyldiphenylphosphine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>CNS depressant; structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PHOSPHINES (73-76)</PreviousIndexing>
   <PreviousIndexing>PROPYLAMINES (73-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009943</DescriptorUI>
     <DescriptorName>
      <String>Organophosphorus Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Pharmacol 21(24):3235;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043147</ConceptUI>
    <ConceptName>
     <String>3-dimethylaminopropyldiphenylphosphine</String>
    </ConceptName>
    <RegistryNumber>961-04-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073150</TermUI>
      <String>3-dimethylaminopropyldiphenylphosphine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C063347</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>javanicin D</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1990</Year>
   <Month>04</Month>
   <Day>11</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>08</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>quassinoid from Picrasma javinica; structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>GLAUCARUBIN/*AA (1990-2002)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D036702</DescriptorUI>
     <DescriptorName>
      <String>Quassins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D032270</DescriptorUI>
     <DescriptorName>
      <String>Picrasma</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Chem Pharm Bull 1989;37(11):2991</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0174917</ConceptUI>
    <ConceptName>
     <String>javanicin D</String>
    </ConceptName>
    <CASN1Name>18-Norpicrasan-1-one, 2,12-bis(acetyloxy)-11-((1,3-benzodioxol-5-ylcarbonyl)oxy)-13-hydroxy-16-methoxy-, (2alpha,11alpha,12beta,16beta)-</CASN1Name>
    <RegistryNumber>126167-89-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T204922</TermUI>
      <String>javanicin D</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002529</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1 alpha-hydroxycorticosterone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>13</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*HYDROCORTISONE (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003345</DescriptorUI>
     <DescriptorName>
      <String>Corticosterone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Comp Biochem Physiol 44B(1):179;1973</Source>
   <Source>J Chem Soc Perkins I 22:2371;1975</Source>
   <Source>Steroids 31(4):573;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043166</ConceptUI>
    <ConceptName>
     <String>1 alpha-hydroxycorticosterone</String>
    </ConceptName>
    <CASN1Name>1 alpha,11 beta,21-trihydroxypregn-4-ene-3,20- dione</CASN1Name>
    <RegistryNumber>10163-49-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073169</TermUI>
      <String>1 alpha-hydroxycorticosterone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C106314</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>PIG2 protein, Uromyces</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1997</Year>
   <Month>06</Month>
   <Day>25</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>10</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>PIG2 - Planta-Induced Gene 2; a putative amino acid transporter expressed in haustoria of the rust fungus, Uromyces fabae; GenBank U81794
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*Carrier Proteins (1997-2004)</PreviousIndexing>
   <PreviousIndexing>*Membrane Proteins (1997-2004)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005656</DescriptorUI>
     <DescriptorName>
      <String>Fungal Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D026905</DescriptorUI>
     <DescriptorName>
      <String>Amino Acid Transport Systems</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Plant Microbe Interact 1997 May;10(4):438-45</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0277073</ConceptUI>
    <ConceptName>
     <String>PIG2 protein, Uromyces</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T307078</TermUI>
      <String>PIG2 protein, Uromyces</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002538</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>methylene dimethanesulfonate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>11</Month>
   <Day>08</Day>
  </DateRevised>
  <Frequency>10</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*METHANESULFONATES (74-75)</PreviousIndexing>
   <PreviousIndexing>*METHYL METHANESULFONATE/analogs (75-80)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008741</DescriptorUI>
     <DescriptorName>
      <String>Methyl Methanesulfonate</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D013091</DescriptorUI>
     <DescriptorName>
      <String>Spermatogenesis</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000187</QualifierUI>
     <QualifierName>
      <String>drug effects</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Br Med Bull 26(1):83;1970</Source>
   <Source>Chem Biol Interact 11(3):163;1975</Source>
   <Source>Chem Biol Interact 14(1-2):93;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043187</ConceptUI>
    <ConceptName>
     <String>methylene dimethanesulfonate</String>
    </ConceptName>
    <RegistryNumber>156-72-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073190</TermUI>
      <String>methylene dimethanesulfonate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002543</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>alumicrocin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>ferrichrome analog
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*HYDROXAMIC ACIDS (73-76)</PreviousIndexing>
   <PreviousIndexing>*PEPTIDES, CYCLIC (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005291</DescriptorUI>
     <DescriptorName>
      <String>Ferrichrome</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 248(3):924;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043191</ConceptUI>
    <ConceptName>
     <String>alumicrocin</String>
    </ConceptName>
    <RegistryNumber>39028-06-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073194</TermUI>
      <String>alumicrocin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002544</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>alumichrysin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>ferrichrome analog
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PEPTIDES, CYCLIC (73-75)</PreviousIndexing>
   <PreviousIndexing>HYDROXAMIC ACIDS (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005291</DescriptorUI>
     <DescriptorName>
      <String>Ferrichrome</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 248(3):924;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043192</ConceptUI>
    <ConceptName>
     <String>alumichrysin</String>
    </ConceptName>
    <RegistryNumber>39028-07-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073195</TermUI>
      <String>alumichrysin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002548</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>asebotin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*GLYCOSIDES (73-78)</PreviousIndexing>
   <PreviousIndexing>PLANT EXTRACTS (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005960</DescriptorUI>
     <DescriptorName>
      <String>Glucosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Soc Jap 92(9):1173;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043201</ConceptUI>
    <ConceptName>
     <String>asebotin</String>
    </ConceptName>
    <RegistryNumber>11075-15-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073204</TermUI>
      <String>asebotin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C481826</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>phosphate translocator 1, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>02</Month>
   <Day>23</Day>
  </DateCreated>
  <Note>phosphoenolpyruvate/phosphate translocator (PPT), may be involved in the provision of signals for correct mesophyll development
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D026901</DescriptorUI>
     <DescriptorName>
      <String>Membrane Transport Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Plant J 2003 Nov;36(3);411-20</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0461215</ConceptUI>
    <ConceptName>
     <String>phosphate translocator 1, Arabidopsis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T573845</TermUI>
      <String>phosphate translocator 1, Arabidopsis</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>02</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T573846</TermUI>
      <String>PPT1 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>02</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C103952</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>lipoprotein lp6.6, Borrelia burgdorferi</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1997</Year>
   <Month>02</Month>
   <Day>20</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>02</Month>
   <Day>23</Day>
  </DateRevised>
  <Note>expression of lp6.6 protein is downregulated during experimental Lyme disease in mice; amino acid sequence given in first source; GenBank U59857, U59858, U59859
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001425</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Outer Membrane Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008074</DescriptorUI>
     <DescriptorName>
      <String>Lipoproteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D008193</DescriptorUI>
     <DescriptorName>
      <String>Lyme Disease</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Infect Immun 1997 Feb;65(2):412-21</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0271662</ConceptUI>
    <ConceptName>
     <String>lipoprotein lp6.6, Borrelia burgdorferi</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T301667</TermUI>
      <String>lipoprotein lp6.6, Borrelia burgdorferi</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T301666</TermUI>
      <String>Lp6.6 protein, Borrelia burgdorferi</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003489</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-methylpiperidine-4-yl-2-cyclohexyl-2-hydroxy-2- phenylacetate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>acetylcholine antagonists; structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CYCLOHEXANES (72-76)</PreviousIndexing>
   <PreviousIndexing>PIPERIDINES (72-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010648</DescriptorUI>
     <DescriptorName>
      <String>Phenylacetates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Pharmacol 23(10):745;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044543</ConceptUI>
    <ConceptName>
     <String>N-methylpiperidine-4-yl-2-cyclohexyl-2-hydroxy-2- phenylacetate</String>
    </ConceptName>
    <RegistryNumber>33445-17-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074546</TermUI>
      <String>N-methylpiperidine-4-yl-2-cyclohexyl-2-hydroxy-2- phenylacetate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C491988</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Epm2a protein, rat</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>11</Month>
   <Day>02</Day>
  </DateCreated>
  <DateRevised>
   <Year>2007</Year>
   <Month>10</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>GenBank AF347030
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PROTEIN TYROSINE PHOSPHATASES (2004-2007)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D054637</DescriptorUI>
     <DescriptorName>
      <String>Dual-Specificity Phosphatases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0471077</ConceptUI>
    <ConceptName>
     <String>Epm2a protein, rat</String>
    </ConceptName>
    <RegistryNumber>EC 3.1.3.48</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>EC 3.1.3.18</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T604395</TermUI>
      <String>Epm2a protein, rat</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T604397</TermUI>
      <String>laforin protein, rat</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T604396</TermUI>
      <String>epilepsy, progressive myoclonic epilepsy, type 2 gene alpha protein, rat</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C580814</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>EUK-172</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>04</Month>
   <Day>30</Day>
  </DateCreated>
  <DateRevised>
   <Year>2013</Year>
   <Month>04</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>an antioxidant with catalase activity; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D056831</DescriptorUI>
     <DescriptorName>
      <String>Coordination Complexes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D008345</DescriptorUI>
     <DescriptorName>
      <String>Manganese</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D018696</DescriptorUI>
     <DescriptorName>
      <String>Neuroprotective Agents</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Eur J Pharmacol. 2012 Dec 15;697(1-3):47-52.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0584362</ConceptUI>
    <ConceptName>
     <String>EUK-172</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T843416</TermUI>
      <String>EUK-172</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>04</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003522</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>17-aminopregn-4-ene-3,20-dione</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>17-amino deriv of progesterone
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PROGESTERONE (73-75)</PreviousIndexing>
   <PreviousIndexing>AMINES (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011374</DescriptorUI>
     <DescriptorName>
      <String>Progesterone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044566</ConceptUI>
    <ConceptName>
     <String>17-aminopregn-4-ene-3,20-dione</String>
    </ConceptName>
    <CASN1Name>Pregn-4-ene-3,20-dione, 17-amino-</CASN1Name>
    <RegistryNumber>18211-54-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074569</TermUI>
      <String>17-aminopregn-4-ene-3,20-dione</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003523</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>androsta-3,5-diene-3,17-diol diacetate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>27</Day>
  </DateRevised>
  <Note>enol deriv of testosterone
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*TESTOSTERONE (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013739</DescriptorUI>
     <DescriptorName>
      <String>Testosterone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044567</ConceptUI>
    <ConceptName>
     <String>androsta-3,5-diene-3,17-diol diacetate</String>
    </ConceptName>
    <CASN1Name>Androsta-3,5-diene-3,17-diol, diacetate, (17beta)-</CASN1Name>
    <RegistryNumber>1778-93-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074570</TermUI>
      <String>androsta-3,5-diene-3,17-diol diacetate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006448</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>aldrin-transdiol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>07</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>dieldrin metabolite suggested as active neurotoxic form; RN refers to (1 alpha,2 alpha,3 beta,4 alpha,4a beta,5 alpha,8 alpha,8a beta)-isomer
  </Note>
  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ALDRIN (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000452</DescriptorUI>
     <DescriptorName>
      <String>Aldrin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Int Pharmacodyn Ther 206(2):363;1973</Source>
   <Source>Drug Metab Dispos 2(4):333;1974</Source>
   <Source>Eur J Pharmacol 31(2):166;1975</Source>
   <Source>Eur J Pharmacol 34(1):133;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049034</ConceptUI>
    <ConceptName>
     <String>aldrin-transdiol</String>
    </ConceptName>
    <CASN1Name>trans-6,7-dihydroxydihydroaldrin</CASN1Name>
    <RegistryNumber>3106-29-4</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>30460-74-3 ((1alpha,2alpha,3alpha,4alpha,4abeta,5alpha,8alpha,8abeta)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0049034</Concept1UI>
     <Concept2UI>M0309561</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079037</TermUI>
      <String>aldrin-transdiol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T079036</TermUI>
      <String>dihydroaldrindiol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0309561</ConceptUI>
    <ConceptName>
     <String>aldrin-transdiol, (1alpha,2alpha,3alpha,4alpha,4abeta,5alpha,8alpha,8abeta)-isomer</String>
    </ConceptName>
    <RegistryNumber>30460-74-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0049034</Concept1UI>
     <Concept2UI>M0309561</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T339561</TermUI>
      <String>aldrin-transdiol, (1alpha,2alpha,3alpha,4alpha,4abeta,5alpha,8alpha,8abeta)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C035588</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>fatty acyl amidases</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1982</Year>
   <Month>10</Month>
   <Day>04</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>amidases I &amp; II act sequentially on lipopolysaccharides cleaving hydroxymyristyl groups
  </Note>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000581</DescriptorUI>
     <DescriptorName>
      <String>Amidohydrolases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 1982;257(17):10222</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0108967</ConceptUI>
    <ConceptName>
     <String>fatty acyl amidases</String>
    </ConceptName>
    <RegistryNumber>EC 3.5.1.-</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0108967</Concept1UI>
     <Concept2UI>M0108966</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0108967</Concept1UI>
     <Concept2UI>M0108965</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T138971</TermUI>
      <String>fatty acyl amidases</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0108966</ConceptUI>
    <ConceptName>
     <String>fatty acyl amidase II</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0108967</Concept1UI>
     <Concept2UI>M0108966</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T138970</TermUI>
      <String>fatty acyl amidase II</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0108965</ConceptUI>
    <ConceptName>
     <String>fatty acyl amidase I</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0108967</Concept1UI>
     <Concept2UI>M0108965</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T138969</TermUI>
      <String>fatty acyl amidase I</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003547</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>16 alpha-cyanoestradiol 3-methyl ether</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>08</Month>
   <Day>24</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ESTRANES (73-75)</PreviousIndexing>
   <PreviousIndexing>METHYL ETHERS (73-81)</PreviousIndexing>
   <PreviousIndexing>NITRILES (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004958</DescriptorUI>
     <DescriptorName>
      <String>Estradiol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044582</ConceptUI>
    <ConceptName>
     <String>16 alpha-cyanoestradiol 3-methyl ether</String>
    </ConceptName>
    <CASN1Name>Estra-1,3,5(10)-triene-16-carbonitrile, 17-hydroxy-3-methoxy-, (16alpha,17beta)-</CASN1Name>
    <RegistryNumber>69381-96-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074585</TermUI>
      <String>16 alpha-cyanoestradiol 3-methyl ether</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C489236</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tus protein, E coli</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>09</Month>
   <Day>29</Day>
  </DateCreated>
  <Note>inhibits helicases in vitro; component of the E coli termination system
  </Note>
  <Frequency>73</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029968</DescriptorUI>
     <DescriptorName>
      <String>Escherichia coli Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D004268</DescriptorUI>
     <DescriptorName>
      <String>DNA-Binding Proteins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0458701</ConceptUI>
    <ConceptName>
     <String>tus protein, E coli</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T568235</TermUI>
      <String>tus protein, E coli</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>01</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T568237</TermUI>
      <String>terminus-binding protein, E coli</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>01</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T568236</TermUI>
      <String>terminator utilization substance protein, E coli</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>01</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003591</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>16 beta-hydroxy-19-nortestosterone 16,17-acetonide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ESTRANES (74-75)</PreviousIndexing>
   <PreviousIndexing>*TESTOSTERONE (73-74)</PreviousIndexing>
   <PreviousIndexing>ACETALS (73-75)</PreviousIndexing>
   <PreviousIndexing>HYDROXYSTEROIDS (73-76)</PreviousIndexing>
   <PreviousIndexing>KETOSTEROIDS (73-75)</PreviousIndexing>
   <PreviousIndexing>NORSTEROIDS (73-74)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009277</DescriptorUI>
     <DescriptorName>
      <String>Nandrolone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044617</ConceptUI>
    <ConceptName>
     <String>16 beta-hydroxy-19-nortestosterone 16,17-acetonide</String>
    </ConceptName>
    <CASN1Name>Estr-4-en-3-one, 16,17-((1-methylethylidene)bis(oxy))-, (16beta,17beta)-</CASN1Name>
    <RegistryNumber>78592-87-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074620</TermUI>
      <String>16 beta-hydroxy-19-nortestosterone 16,17-acetonide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003593</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>17-hydroxypregnenedione</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PREGNENES (73-74)</PreviousIndexing>
   <PreviousIndexing>HYDROXYSTEROIDS (74-76)</PreviousIndexing>
   <PreviousIndexing>KETOSTEROIDS (73-74)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011282</DescriptorUI>
     <DescriptorName>
      <String>Pregnenediones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044619</ConceptUI>
    <ConceptName>
     <String>17-hydroxypregnenedione</String>
    </ConceptName>
    <CASN1Name>17 alpha-hydroxypregn-5-ene-3,20-dione</CASN1Name>
    <RegistryNumber>641-80-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074622</TermUI>
      <String>17-hydroxypregnenedione</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003597</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1 beta-hydroxytetrahydrocortisone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PREGNANES (73-75)</PreviousIndexing>
   <PreviousIndexing>17-HYDROXYCORTICOSTEROIDS (73-75)</PreviousIndexing>
   <PreviousIndexing>HYDROXYSTEROIDS (73-76)</PreviousIndexing>
   <PreviousIndexing>TETRAHYDROCORTISONE (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013761</DescriptorUI>
     <DescriptorName>
      <String>Tetrahydrocortisone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044621</ConceptUI>
    <ConceptName>
     <String>1 beta-hydroxytetrahydrocortisone</String>
    </ConceptName>
    <CASN1Name>1 beta,3 alpha,17 alpha,21-tetrahydroxy-5 beta- pregnane-11,20-dione</CASN1Name>
    <RegistryNumber>10536-01-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074624</TermUI>
      <String>1 beta-hydroxytetrahydrocortisone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C437483</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bis(1,2-benzisothiazol-3(2H)-one 1,1-dioxido-N:O)bis(1,2-benzisothiazol-3(2H)-one 1,1-dioxido-N)bis(imidazole)copper(II)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>10</Month>
   <Day>22</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>10</Month>
   <Day>22</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009942</DescriptorUI>
     <DescriptorName>
      <String>Organometallic Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013844</DescriptorUI>
     <DescriptorName>
      <String>Thiazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D003300</DescriptorUI>
     <DescriptorName>
      <String>Copper</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Acta Crystallogr C 2001 Sep;57(Pt 9):1016-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0402583</ConceptUI>
    <ConceptName>
     <String>bis(1,2-benzisothiazol-3(2H)-one 1,1-dioxido-N:O)bis(1,2-benzisothiazol-3(2H)-one 1,1-dioxido-N)bis(imidazole)copper(II)</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T467272</TermUI>
      <String>bis(1,2-benzisothiazol-3(2H)-one 1,1-dioxido-N:O)bis(1,2-benzisothiazol-3(2H)-one 1,1-dioxido-N)bis(imidazole)copper(II)</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>10</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T467273</TermUI>
      <String>bis(mu-1,2-benzisothiazol-3(2H)-one 1,1-dioxido-kappa(2)N:O)bis(1,2-benzisothiazol-3(2H)-one 1,1-dioxido-kappaN)bis(imidazole)copper(II)</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>10</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T467274</TermUI>
      <String>B(BIT)-ODK-B(BIT)ODK-B(I)Cu(II)</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>10</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C061910</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tus protein, Bacteria</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1990</Year>
   <Month>01</Month>
   <Day>04</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>09</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>inhibits helicases in vitro
  </Note>
  <Frequency>45</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D004268</DescriptorUI>
     <DescriptorName>
      <String>DNA-Binding Proteins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Cell 1989;59(4):581</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0171550</ConceptUI>
    <ConceptName>
     <String>tus protein, Bacteria</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T201555</TermUI>
      <String>tus protein, Bacteria</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T201552</TermUI>
      <String>terminator utilization substance protein, Bacteria</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T201553</TermUI>
      <String>terminus-binding protein, Bacteria</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C437544</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>lacticin BH5</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>10</Month>
   <Day>22</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001430</DescriptorUI>
     <DescriptorName>
      <String>Bacteriocins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D013294</DescriptorUI>
     <DescriptorName>
      <String>Lactococcus lactis</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Food Prot 2000 Dec;63(12):1707-12</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0402644</ConceptUI>
    <ConceptName>
     <String>lacticin BH5</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T467334</TermUI>
      <String>lacticin BH5</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>10</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C105043</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Evi5 protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1997</Year>
   <Month>04</Month>
   <Day>09</Day>
  </DateCreated>
  <DateRevised>
   <Year>2019</Year>
   <Month>12</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>RefSeq NM_007964
  </Note>
  <Frequency>8</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*Transcription Factors (2014-2020)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D018797</DescriptorUI>
     <DescriptorName>
      <String>Cell Cycle Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D020690</DescriptorUI>
     <DescriptorName>
      <String>GTPase-Activating Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D016335</DescriptorUI>
     <DescriptorName>
      <String>Zinc Fingers</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Oncogene 1997 Mar 6;14(6):1023-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0274176</ConceptUI>
    <ConceptName>
     <String>Evi5 protein, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T304181</TermUI>
      <String>Evi5 protein, mouse</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T567849</TermUI>
      <String>ecotropic viral integration site 5 protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>01</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003622</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Tranquo-Buscopan</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>11</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>combination drug of buscopan &amp; oxazepam
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SCOPOLAMINE (71-80)</PreviousIndexing>
   <PreviousIndexing>BROMINE (71-73)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002086</DescriptorUI>
     <DescriptorName>
      <String>Butylscopolammonium Bromide</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010076</DescriptorUI>
     <DescriptorName>
      <String>Oxazepam</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044664</ConceptUI>
    <ConceptName>
     <String>Tranquo-Buscopan</String>
    </ConceptName>
    <CASN1Name>3-Oxa-9-azoniatricyclo(3.3.1.02,4)nonane, 9-butyl-7-(3-hydroxy-1-oxo-2-phenylpropoxy)-9-methyl-, bromide, (7(S)-(1alpha,2beta,4beta,5alpha,7beta))-, mixt. with 7-chloro-1,3-dihydro-3-hydroxy-5-phenyl-2H-1,4-benzodiazepin-2-one</CASN1Name>
    <RegistryNumber>78940-00-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074667</TermUI>
      <String>Tranquo-Buscopan</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003635</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3,4-10,11-12,13-tribenzofluoranthene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1970</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>RN &amp; Nl from 9th CI; cpd not in Chemline 8/4/83
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>BENZENE DERIVATIVES (70-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005449</DescriptorUI>
     <DescriptorName>
      <String>Fluorenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044683</ConceptUI>
    <ConceptName>
     <String>3,4-10,11-12,13-tribenzofluoranthene</String>
    </ConceptName>
    <CASN1Name>phenanthro(9,10-e)acephenanthrylene</CASN1Name>
    <RegistryNumber>13579-05-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074686</TermUI>
      <String>3,4-10,11-12,13-tribenzofluoranthene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003638</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,2,3-tricarboxy-1-cyclopentene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>inhibitor of cis-aconitase
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CYCLOPENTANES (72-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014233</DescriptorUI>
     <DescriptorName>
      <String>Tricarboxylic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Biochem Biophys 147(2):772;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044693</ConceptUI>
    <ConceptName>
     <String>1,2,3-tricarboxy-1-cyclopentene</String>
    </ConceptName>
    <CASN1Name>1-Cyclopentene-1,2,3-tricarboxylic acid</CASN1Name>
    <RegistryNumber>31602-26-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074696</TermUI>
      <String>1,2,3-tricarboxy-1-cyclopentene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003639</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>trichloroiodopyridine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CHLORINE (72-74)</PreviousIndexing>
   <PreviousIndexing>IODINE (72-74)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011725</DescriptorUI>
     <DescriptorName>
      <String>Pyridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Roum Pathol Exp Microbiol 29(3):385;1970</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044694</ConceptUI>
    <ConceptName>
     <String>trichloroiodopyridine</String>
    </ConceptName>
    <CASN1Name>Pyridine, trichloroiodo-</CASN1Name>
    <RegistryNumber>26856-63-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074697</TermUI>
      <String>trichloroiodopyridine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C499596</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>desat1 protein, Bombyx mori</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateCreated>
  <Note>desat 1 and desat 2 are 98% identical; may be either a delta(11) or delta(10,12) desaturase; GenBank AF157627
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D044943</DescriptorUI>
     <DescriptorName>
      <String>Fatty Acid Desaturases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0459934</ConceptUI>
    <ConceptName>
     <String>desat1 protein, Bombyx mori</String>
    </ConceptName>
    <RegistryNumber>EC 1.14.99.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T570661</TermUI>
      <String>desat1 protein, Bombyx mori</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>01</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000621508</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>F2RL1 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2017</Year>
   <Month>07</Month>
   <Day>27</Day>
  </DateCreated>
  <DateRevised>
   <Year>2019</Year>
   <Month>12</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>RefSeq NM_005242
  </Note>
  <Frequency>72</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*Receptors, G-Protein-Coupled (2017-2020)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D044464</DescriptorUI>
     <DescriptorName>
      <String>Receptor, PAR-2</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Cancer. 2016 Aug 24;15(1)54</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M000634578</ConceptUI>
    <ConceptName>
     <String>F2RL1 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T000929179</TermUI>
      <String>F2RL1 protein, human</String>
      <DateCreated>
       <Year>2017</Year>
       <Month>07</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2017)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T000929181</TermUI>
      <String>PAR2 protein, human</String>
      <DateCreated>
       <Year>2017</Year>
       <Month>07</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2017)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T000929182</TermUI>
      <String>GPR11 protein, human</String>
      <DateCreated>
       <Year>2017</Year>
       <Month>07</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2017)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T000929180</TermUI>
      <String>F2R like trypsin receptor 1, human</String>
      <DateCreated>
       <Year>2017</Year>
       <Month>07</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2017)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C499597</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>desat2 protein, Bombyx mori</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateCreated>
  <Note>desat 1 and desat 2 are 98% identical; may be either a delta(11) or delta(10,12) desaturase; GenBank AF182405
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D044943</DescriptorUI>
     <DescriptorName>
      <String>Fatty Acid Desaturases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0459935</ConceptUI>
    <ConceptName>
     <String>desat2 protein, Bombyx mori</String>
    </ConceptName>
    <RegistryNumber>EC 1.14.99.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T570662</TermUI>
      <String>desat2 protein, Bombyx mori</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>01</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003669</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>pregn-5-ene-3,20-dione</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>15</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PREGNENEDIONES (75-78)</PreviousIndexing>
   <PreviousIndexing>*PROGESTERONE (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011374</DescriptorUI>
     <DescriptorName>
      <String>Progesterone</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D007536</DescriptorUI>
     <DescriptorName>
      <String>Isomerism</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Reprod Fertil 36(1):83;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044729</ConceptUI>
    <ConceptName>
     <String>pregn-5-ene-3,20-dione</String>
    </ConceptName>
    <RegistryNumber>1236-09-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074732</TermUI>
      <String>pregn-5-ene-3,20-dione</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C031632</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ependymins</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>09</Month>
   <Day>30</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>goldfish brain proteins involved in behavioral plasticity
  </Note>
  <Frequency>56</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009419</DescriptorUI>
     <DescriptorName>
      <String>Nerve Tissue Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Neurochem 1981;36(4):1368</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0099227</ConceptUI>
    <ConceptName>
     <String>ependymins</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0099227</Concept1UI>
     <Concept2UI>M0099226</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0099227</Concept1UI>
     <Concept2UI>M0099225</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T129231</TermUI>
      <String>ependymins</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0099226</ConceptUI>
    <ConceptName>
     <String>ependymin gamma</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0099227</Concept1UI>
     <Concept2UI>M0099226</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T129230</TermUI>
      <String>ependymin gamma</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0099225</ConceptUI>
    <ConceptName>
     <String>ependymin beta</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0099227</Concept1UI>
     <Concept2UI>M0099225</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T129229</TermUI>
      <String>ependymin beta</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C045140</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>visinin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1985</Year>
   <Month>05</Month>
   <Day>31</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>MW 24,000 protein; found in chick retina &amp; rat brain
  </Note>
  <Frequency>42</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009419</DescriptorUI>
     <DescriptorName>
      <String>Nerve Tissue Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D005136</DescriptorUI>
     <DescriptorName>
      <String>Eye Proteins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Neuroscience 1985;14(2):547</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0131417</ConceptUI>
    <ConceptName>
     <String>visinin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T161422</TermUI>
      <String>visinin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005006</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>glycarbylamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1969</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Frequency>6</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>DICARBOXYLIC ACIDS (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007093</DescriptorUI>
     <DescriptorName>
      <String>Imidazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Parazitologiia 12(4):366;1978</Source>
   <Source>Parazitologiia 9(1):82;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0046273</ConceptUI>
    <ConceptName>
     <String>glycarbylamide</String>
    </ConceptName>
    <CASN1Name>imidazole-4,5-dicarboxamide</CASN1Name>
    <RegistryNumber>83-39-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T076276</TermUI>
      <String>glycarbylamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1969)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T076275</TermUI>
      <String>glycamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1969)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C490780</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>FAF1 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>09</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2019</Year>
   <Month>12</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>potentiates Fas-mediated apoptosis; similar to FADD protein; RefSeq NM_007051
  </Note>
  <Frequency>69</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CARRIER PROTEINS (2004-2005)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D048868</DescriptorUI>
     <DescriptorName>
      <String>Adaptor Proteins, Signal Transducing</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D051017</DescriptorUI>
     <DescriptorName>
      <String>Apoptosis Regulatory Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D017209</DescriptorUI>
     <DescriptorName>
      <String>Apoptosis</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0469935</ConceptUI>
    <ConceptName>
     <String>FAF1 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T600191</TermUI>
      <String>FAF1 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T600532</TermUI>
      <String>TNFRSF6-associated factor 1, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T600194</TermUI>
      <String>TNFRSF6-associated factor 1 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T600192</TermUI>
      <String>Fas (TNFRSF6) associated factor 1 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T600193</TermUI>
      <String>FAS-associated factor 1 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003696</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>trilead tetroxide formalin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>05</Month>
   <Day>28</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*FORMALDEHYDE (72-75)</PreviousIndexing>
   <PreviousIndexing>OXIDES (72-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005557</DescriptorUI>
     <DescriptorName>
      <String>Formaldehyde</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009942</DescriptorUI>
     <DescriptorName>
      <String>Organometallic Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D007854</DescriptorUI>
     <DescriptorName>
      <String>Lead</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Tokyo Dent Coll Soc 71(10):2096;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044762</ConceptUI>
    <ConceptName>
     <String>trilead tetroxide formalin</String>
    </ConceptName>
    <CASN1Name>(carbonato(2-))dioxotrilead</CASN1Name>
    <RegistryNumber>12287-01-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074765</TermUI>
      <String>trilead tetroxide formalin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C046788</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cerebellin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1985</Year>
   <Month>11</Month>
   <Day>15</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>cerebellum-specific hexadecapeptide marker for Purkinje cells
  </Note>
  <Frequency>43</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009419</DescriptorUI>
     <DescriptorName>
      <String>Nerve Tissue Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D002531</DescriptorUI>
     <DescriptorName>
      <String>Cerebellum</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Proc Natl Acad Sci USA 1985;82(20):7145</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0135420</ConceptUI>
    <ConceptName>
     <String>cerebellin</String>
    </ConceptName>
    <RegistryNumber>94071-26-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T165425</TermUI>
      <String>cerebellin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T165424</TermUI>
      <String>NH2-Ser-Gly-Ser-Ala-Lys-Val-Ala-Phe-Ser-Ala-Ile-Arg-Ser-Thr-Asn-His-OH</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C437563</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-hydroxy-1-(2-hydroxy-3,4-dimethoxyphenyl)-2-methylpropanone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>10</Month>
   <Day>23</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D006910</DescriptorUI>
     <DescriptorName>
      <String>Hydroxypropiophenone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Bioorg Med Chem 2001 Oct;9(10):2643-52</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0402664</ConceptUI>
    <ConceptName>
     <String>3-hydroxy-1-(2-hydroxy-3,4-dimethoxyphenyl)-2-methylpropanone</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T467353</TermUI>
      <String>3-hydroxy-1-(2-hydroxy-3,4-dimethoxyphenyl)-2-methylpropanone</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>10</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T467354</TermUI>
      <String>3-HHDM cpd</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>10</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003708</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>trimethyl-3,4-dihydropyrimidine-2-thiol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>inhibitor of dopamine beta-hydroxylase
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>SULFHYDRYL CPDS (71-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011743</DescriptorUI>
     <DescriptorName>
      <String>Pyrimidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044780</ConceptUI>
    <ConceptName>
     <String>trimethyl-3,4-dihydropyrimidine-2-thiol</String>
    </ConceptName>
    <CASN1Name>3,4-dihydro-4,4,6-trimethyl-2(1H)-pyrimidinethione</CASN1Name>
    <RegistryNumber>5392-23-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074783</TermUI>
      <String>trimethyl-3,4-dihydropyrimidine-2-thiol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C509694</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>FAM20A protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>04</Month>
   <Day>23</Day>
  </DateCreated>
  <DateRevised>
   <Year>2019</Year>
   <Month>12</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>expressed in the early stages of hematopoietic development; GenBank GenBank BC029169
  </Note>
  <Frequency>7</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*Proteins (2006-2020)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003746</DescriptorUI>
     <DescriptorName>
      <String>Dental Enamel Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>BMC Genomics 2005;6(1):11</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0497314</ConceptUI>
    <ConceptName>
     <String>FAM20A protein, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T672184</TermUI>
      <String>FAM20A protein, mouse</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>04</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003778</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>yemenimycin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>isolated from Streptomyces AS-Y-52
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PEPTIDES (72-93)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010455</DescriptorUI>
     <DescriptorName>
      <String>Peptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Treat Rep 60(7):937;1976</Source>
   <Source>J Antibiot (Tokyo) 24(9):593;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044894</ConceptUI>
    <ConceptName>
     <String>yemenimycin</String>
    </ConceptName>
    <RegistryNumber>12764-56-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074897</TermUI>
      <String>yemenimycin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003800</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>PH.3</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>11</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>contains licorice extract, bismuth subnitrate, aminoacetic acid, frangula extract
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PLANT EXTRACTS (72-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001729</DescriptorUI>
     <DescriptorName>
      <String>Bismuth</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005998</DescriptorUI>
     <DescriptorName>
      <String>Glycine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044914</ConceptUI>
    <ConceptName>
     <String>PH.3</String>
    </ConceptName>
    <CASN1Name>PH 3</CASN1Name>
    <RegistryNumber>37341-77-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074917</TermUI>
      <String>PH.3</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C519095</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-(2-(1,3-benzodioxol-5-yl)ethyl)-1-(2-(1H-imidazol-1-yl)-6-methyl-4-pyrimidinyl)-2-pyrrolidinecarboxamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>04</Month>
   <Day>25</Day>
  </DateCreated>
  <Note>inhibits dimerization of iNOS; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011743</DescriptorUI>
     <DescriptorName>
      <String>Pyrimidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D052117</DescriptorUI>
     <DescriptorName>
      <String>Benzodioxoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D052247</DescriptorUI>
     <DescriptorName>
      <String>Nitric Oxide Synthase Type II</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
     <QualifierName>
      <String>antagonists &amp; inhibitors</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Med Chem 2007 Mar 22;50(6):1146-57</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0509091</ConceptUI>
    <ConceptName>
     <String>N-(2-(1,3-benzodioxol-5-yl)ethyl)-1-(2-(1H-imidazol-1-yl)-6-methyl-4-pyrimidinyl)-2-pyrrolidinecarboxamide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T696215</TermUI>
      <String>N-(2-(1,3-benzodioxol-5-yl)ethyl)-1-(2-(1H-imidazol-1-yl)-6-methyl-4-pyrimidinyl)-2-pyrrolidinecarboxamide</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>04</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T696216</TermUI>
      <String>BDE-IMPPCNH2</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>04</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C584240</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>FAM21 protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>11</Month>
   <Day>07</Day>
  </DateCreated>
  <DateRevised>
   <Year>2019</Year>
   <Month>12</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>RefSeq NM_026585
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*Carrier Proteins (2013-2020)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D028044</DescriptorUI>
     <DescriptorName>
      <String>Phosphate-Binding Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biol Cell. 2013 May;105(5):191-207.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0588781</ConceptUI>
    <ConceptName>
     <String>FAM21 protein, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T850780</TermUI>
      <String>FAM21 protein, mouse</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>11</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C042312</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Young's cardioplegic solution</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1984</Year>
   <Month>08</Month>
   <Day>23</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>contains 0.8% potassium citrate, 2.46% magnesium sulfate &amp; neostigmine
  </Note>
  <Frequency>8</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CITRATES (84-96)</PreviousIndexing>
   <PreviousIndexing>*MAGNESIUM SULFATE (84-96)</PreviousIndexing>
   <PreviousIndexing>*NEOSTIGMINE (84-96)</PreviousIndexing>
   <PreviousIndexing>*POTASSIUM COMPOUNDS (94-96)</PreviousIndexing>
   <PreviousIndexing>POTASSIUM (84-93)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008278</DescriptorUI>
     <DescriptorName>
      <String>Magnesium Sulfate</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009388</DescriptorUI>
     <DescriptorName>
      <String>Neostigmine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D019357</DescriptorUI>
     <DescriptorName>
      <String>Potassium Citrate</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D002314</DescriptorUI>
     <DescriptorName>
      <String>Cardioplegic Solutions</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Jpn Heart J 1984;25(2):207</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0125021</ConceptUI>
    <ConceptName>
     <String>Young's cardioplegic solution</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T155026</TermUI>
      <String>Young's cardioplegic solution</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1984)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T155025</TermUI>
      <String>Young's solution</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1984)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C112689</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>TAC 101</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>06</Month>
   <Day>25</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>inhibits liver metastasis; structure in first source
  </Note>
  <Frequency>25</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001565</DescriptorUI>
     <DescriptorName>
      <String>Benzoates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014297</DescriptorUI>
     <DescriptorName>
      <String>Trimethylsilyl Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biol Pharm Bull 1996 Oct;19(10):1322-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0291325</ConceptUI>
    <ConceptName>
     <String>TAC 101</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0291325</Concept1UI>
     <Concept2UI>M0291321</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0291325</Concept1UI>
     <Concept2UI>M0291320</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T321330</TermUI>
      <String>TAC 101</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T321329</TermUI>
      <String>TAC-101</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0291321</ConceptUI>
    <ConceptName>
     <String>Am 555S</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0291325</Concept1UI>
     <Concept2UI>M0291321</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T321326</TermUI>
      <String>Am 555S</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T321328</TermUI>
      <String>Am555S</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T321327</TermUI>
      <String>Am-555S</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0291320</ConceptUI>
    <ConceptName>
     <String>4-(3,5-bis(trimethylsilyl)benzamido)benzoic acid</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0291325</Concept1UI>
     <Concept2UI>M0291320</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T321325</TermUI>
      <String>4-(3,5-bis(trimethylsilyl)benzamido)benzoic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003750</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>vallarose</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>RN is from 9th CI; cpd not found in Chemline 8/83
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*GLYCOSIDES (72-74)</PreviousIndexing>
   <PreviousIndexing>DEOXY SUGARS (74-76)</PreviousIndexing>
   <PreviousIndexing>HEXOSES (72-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008759</DescriptorUI>
     <DescriptorName>
      <String>Methylglycosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Chem Soc 22(0):3762;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044850</ConceptUI>
    <ConceptName>
     <String>vallarose</String>
    </ConceptName>
    <CASN1Name>6-deoxy-3-O-methylaltrose</CASN1Name>
    <RegistryNumber>25374-97-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074853</TermUI>
      <String>vallarose</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003755</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Vascularin-Gel</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1994</Year>
   <Month>07</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>contains vaculat, sodium heparin &amp; tincture Arnicae
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BAMETHAN (71-94)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004983</DescriptorUI>
     <DescriptorName>
      <String>Ethanolamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006493</DescriptorUI>
     <DescriptorName>
      <String>Heparin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010627</DescriptorUI>
     <DescriptorName>
      <String>Phenethylamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010936</DescriptorUI>
     <DescriptorName>
      <String>Plant Extracts</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044856</ConceptUI>
    <ConceptName>
     <String>Vascularin-Gel</String>
    </ConceptName>
    <CASN1Name>Heparin, sodium salt, mixt. with alpha-((butylamino)methyl)-4-hydroxybenzenemethanol and Arnica ext.</CASN1Name>
    <RegistryNumber>78920-39-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074859</TermUI>
      <String>Vascularin-Gel</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C074160</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>BlaA protein, Bacteria</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1992</Year>
   <Month>05</Month>
   <Day>21</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>02</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>amino acid sequence given in first source; an activator-regulator protein from Streptomyces cacaoi
  </Note>
  <Frequency>10</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004268</DescriptorUI>
     <DescriptorName>
      <String>DNA-Binding Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Bacteriol 1992 May;174(9):2834-42</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0200307</ConceptUI>
    <ConceptName>
     <String>BlaA protein, Bacteria</String>
    </ConceptName>
    <RegistryNumber>142615-56-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T230312</TermUI>
      <String>BlaA protein, Bacteria</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000596972</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Fan1 protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2015</Year>
   <Month>04</Month>
   <Day>18</Day>
  </DateCreated>
  <DateRevised>
   <Year>2019</Year>
   <Month>12</Month>
   <Day>12</Day>
  </DateRevised>
  <Frequency>8</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004706</DescriptorUI>
     <DescriptorName>
      <String>Endodeoxyribonucleases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005090</DescriptorUI>
     <DescriptorName>
      <String>Exodeoxyribonucleases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D064251</DescriptorUI>
     <DescriptorName>
      <String>Multifunctional Enzymes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>DNA Repair (Amst). 2014 Sep;21:55-64.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M000604699</ConceptUI>
    <ConceptName>
     <String>Fan1 protein, mouse</String>
    </ConceptName>
    <RegistryNumber>EC 3.1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T000878402</TermUI>
      <String>Fan1 protein, mouse</String>
      <DateCreated>
       <Year>2015</Year>
       <Month>04</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2015)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C046132</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>development-specific protein (Sclerotinia)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1985</Year>
   <Month>09</Month>
   <Day>12</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>02</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>makes up about 40% of the total protein in sclerotia of Sclerotinia sclerotiorum
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005656</DescriptorUI>
     <DescriptorName>
      <String>Fungal Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Bacteriol 1985;163(2):696</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0133816</ConceptUI>
    <ConceptName>
     <String>development-specific protein (Sclerotinia)</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T163821</TermUI>
      <String>development-specific protein (Sclerotinia)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T163820</TermUI>
      <String>DSP-SC protein, Sclerotinia sclerotiorum</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C519094</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>DRE-1 protein, C elegans</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>04</Month>
   <Day>25</Day>
  </DateCreated>
  <Note>involved in regulation of developmental age; has been sequenced
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029742</DescriptorUI>
     <DescriptorName>
      <String>Caenorhabditis elegans Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D044783</DescriptorUI>
     <DescriptorName>
      <String>F-Box Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Dev Cell 2007 Mar;12(3):443-55</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0509090</ConceptUI>
    <ConceptName>
     <String>DRE-1 protein, C elegans</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T696214</TermUI>
      <String>DRE-1 protein, C elegans</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>04</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003768</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>wobe</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>09</Month>
   <Day>04</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010447</DescriptorUI>
     <DescriptorName>
      <String>Peptide Hydrolases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Wien Tieraerztl Monatsschr 58(5):193;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044871</ConceptUI>
    <ConceptName>
     <String>wobe</String>
    </ConceptName>
    <RegistryNumber>EC 3.4.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074874</TermUI>
      <String>wobe</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003771</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Amberlite XAD-2 resin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>10</Month>
   <Day>11</Day>
  </DateRevised>
  <Note>styrene-divinylbenzene copolymer
  </Note>
  <Frequency>230</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*RESINS (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011137</DescriptorUI>
     <DescriptorName>
      <String>Polystyrenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D007475</DescriptorUI>
     <DescriptorName>
      <String>Ion Exchange Resins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D012117</DescriptorUI>
     <DescriptorName>
      <String>Resins, Synthetic</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>AM Ind Hyg Assn J 39(8):678;1978</Source>
   <Source>Anal Biochem 92(2):447;1979</Source>
   <Source>Biochem Med 7(1):145;1973</Source>
   <Source>Bull Environ Contam Toxicol 1979;22(4-5):561</Source>
   <Source>J Anal Chem 48(13):1854;1976</Source>
   <Source>J Anal Chem 50(3):491;1978</Source>
   <Source>J Assoc Off Anal Chem 62(2):241;1979</Source>
   <Source>J Chromatogr 133(1):214;1977</Source>
   <Source>J Chromatogr 145(3):478;1978</Source>
   <Source>J Forensic Sci 20(4):726;1975</Source>
   <Source>Trans Am Soc Artif Intern Organs 1979;25:480</Source>
   <Source>Vet Hum Toxicol 1979;21(Suppl):185</Source>
   <Source>Vet Hum Toxicol 1979;21(Suppl):193</Source>
   <Source>Vutr Boles 76(2):95;1977</Source>
   <Source>Yonago Acta Med 21(2):76;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044887</ConceptUI>
    <ConceptName>
     <String>Amberlite XAD-2 resin</String>
    </ConceptName>
    <RegistryNumber>9060-05-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0044887</Concept1UI>
     <Concept2UI>M0044882</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0044887</Concept1UI>
     <Concept2UI>M0044885</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0044887</Concept1UI>
     <Concept2UI>M0044886</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0044887</Concept1UI>
     <Concept2UI>M0044881</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0044887</Concept1UI>
     <Concept2UI>M0044884</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0044887</Concept1UI>
     <Concept2UI>M0044880</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0044887</Concept1UI>
     <Concept2UI>M0044883</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074890</TermUI>
      <String>Amberlite XAD-2 resin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0044882</ConceptUI>
    <ConceptName>
     <String>Empore</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0044887</Concept1UI>
     <Concept2UI>M0044882</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T074885</TermUI>
      <String>Empore</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0044885</ConceptUI>
    <ConceptName>
     <String>copoly(styrene-divinylbenzene)</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0044887</Concept1UI>
     <Concept2UI>M0044885</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T074888</TermUI>
      <String>copoly(styrene-divinylbenzene)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0044886</ConceptUI>
    <ConceptName>
     <String>poly(styrene-divinylbenzene)</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0044887</Concept1UI>
     <Concept2UI>M0044886</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T074889</TermUI>
      <String>poly(styrene-divinylbenzene)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0044881</ConceptUI>
    <ConceptName>
     <String>Biobeads</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0044887</Concept1UI>
     <Concept2UI>M0044881</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T074884</TermUI>
      <String>Biobeads</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0044884</ConceptUI>
    <ConceptName>
     <String>XAD-2 resin</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0044887</Concept1UI>
     <Concept2UI>M0044884</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T074887</TermUI>
      <String>XAD-2 resin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0044880</ConceptUI>
    <ConceptName>
     <String>AR-1</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0044887</Concept1UI>
     <Concept2UI>M0044880</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T074883</TermUI>
      <String>AR-1</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0044883</ConceptUI>
    <ConceptName>
     <String>Persorb</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0044887</Concept1UI>
     <Concept2UI>M0044883</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T074886</TermUI>
      <String>Persorb</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C046299</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>herpes simplex virus type 2 protein ICSP 11-12</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1985</Year>
   <Month>10</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>02</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>major HSV-2-specified DNA-binding protein in patients with acute HSV infection or cervical neoplasia
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014764</DescriptorUI>
     <DescriptorName>
      <String>Viral Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D004268</DescriptorUI>
     <DescriptorName>
      <String>DNA-Binding Proteins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D018139</DescriptorUI>
     <DescriptorName>
      <String>Simplexvirus</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Med Virol 1985;16(3):245</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0134231</ConceptUI>
    <ConceptName>
     <String>herpes simplex virus type 2 protein ICSP 11-12</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T164236</TermUI>
      <String>herpes simplex virus type 2 protein ICSP 11-12</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T164235</TermUI>
      <String>ICSP 11-12 protein, Human herpesvirus 2</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T164234</TermUI>
      <String>HSV-2-ICSP-11-12</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C519099</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>laxaphycin B2</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>04</Month>
   <Day>25</Day>
  </DateCreated>
  <Note>has antineoplastic activity; isolated from Anabaena torulosa; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010456</DescriptorUI>
     <DescriptorName>
      <String>Peptides, Cyclic</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 2007 Mar 22;50(6):1266-79</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0509095</ConceptUI>
    <ConceptName>
     <String>laxaphycin B2</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T696223</TermUI>
      <String>laxaphycin B2</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>04</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C112667</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>NC 67722</String>
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  <DateCreated>
   <Year>1998</Year>
   <Month>06</Month>
   <Day>25</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>iodinated nanoparticle suspension used for imaging regional lymph node metastases; structure in second source
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  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CONTRAST MEDIA (98-99)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001565</DescriptorUI>
     <DescriptorName>
      <String>Benzoates</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acad Radiol 1998 Apr;5 Suppl 1:S180-S182</Source>
   <Source>Acad Radiol 1999 Jan;6(1):55-60</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0291278</ConceptUI>
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     <String>NC 67722</String>
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    <RegistryNumber>0</RegistryNumber>
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     <Concept1UI>M0291278</Concept1UI>
     <Concept2UI>M0291276</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T321283</TermUI>
      <String>NC 67722</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T321282</TermUI>
      <String>NC-67722</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0291276</ConceptUI>
    <ConceptName>
     <String>6-(ethoxycarbonyl)hexyl-bis(3,5-acetylamino-2,4,6-triiodobenzoate)</String>
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    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0291278</Concept1UI>
     <Concept2UI>M0291276</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T321281</TermUI>
      <String>6-(ethoxycarbonyl)hexyl-bis(3,5-acetylamino-2,4,6-triiodobenzoate)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003807</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Dona 200</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>combination drug containing lidocaine &amp; D-glucosamine salts in water
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005944</DescriptorUI>
     <DescriptorName>
      <String>Glucosamine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008012</DescriptorUI>
     <DescriptorName>
      <String>Lidocaine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Int Pharmacodyn Ther 192(2):279;1971</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044920</ConceptUI>
    <ConceptName>
     <String>Dona 200</String>
    </ConceptName>
    <CASN1Name>2-amino-2-deoxy-D-glucose hydriodide, mixt. with 2-amino-2-deoxy-D-glucose hydrochloride, 2-amino-2-deoxy-D-glucose sulfate (salt) &amp; 2-(diethylamino)-N-(2,6-dimethylphenyl)acetamide monohydrochloride</CASN1Name>
    <RegistryNumber>8075-86-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074923</TermUI>
      <String>Dona 200</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
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   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C519097</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-(4-fluorophenyl)-4-pyridin-4-ylquinoline-2(1H)-one</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>04</Month>
   <Day>25</Day>
  </DateCreated>
  <DateRevised>
   <Year>2007</Year>
   <Month>04</Month>
   <Day>25</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015363</DescriptorUI>
     <DescriptorName>
      <String>Quinolones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D048051</DescriptorUI>
     <DescriptorName>
      <String>p38 Mitogen-Activated Protein Kinases</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
     <QualifierName>
      <String>antagonists &amp; inhibitors</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Med Chem 2007 Mar 22;50(6):1213-21</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0509093</ConceptUI>
    <ConceptName>
     <String>3-(4-fluorophenyl)-4-pyridin-4-ylquinoline-2(1H)-one</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T696219</TermUI>
      <String>3-(4-fluorophenyl)-4-pyridin-4-ylquinoline-2(1H)-one</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>04</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T696220</TermUI>
      <String>3-FPhPQO</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>04</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007885</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>grandifloric acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>diterpene constituent of Aralia cordata Thunb roots; structure
  </Note>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CARBOXYLIC ACIDS (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004224</DescriptorUI>
     <DescriptorName>
      <String>Diterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Pharm Bull 22(7):1629;1974</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051341</ConceptUI>
    <ConceptName>
     <String>grandifloric acid</String>
    </ConceptName>
    <CASN1Name>15 alpha-hydroxy-ent-kaur-16-en-19-oic acid</CASN1Name>
    <RegistryNumber>22338-69-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081344</TermUI>
      <String>grandifloric acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C435671</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>TK5048</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007211</DescriptorUI>
     <DescriptorName>
      <String>Indoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011427</DescriptorUI>
     <DescriptorName>
      <String>Propiophenones</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Jpn J Cancer Res 2001 Jul;92(7):768-77</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0399839</ConceptUI>
    <ConceptName>
     <String>TK5048</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T463537</TermUI>
      <String>TK5048</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>09</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T463538</TermUI>
      <String>TK-5048</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>09</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C477259</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-acetylcyclohexanone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>09</Month>
   <Day>17</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003512</DescriptorUI>
     <DescriptorName>
      <String>Cyclohexanones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 2003 Apr 4;68(7):2689-97</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0453751</ConceptUI>
    <ConceptName>
     <String>2-acetylcyclohexanone</String>
    </ConceptName>
    <RegistryNumber>874-23-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T551038</TermUI>
      <String>2-acetylcyclohexanone</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>09</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C477260</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>methylomuralide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>09</Month>
   <Day>17</Day>
  </DateCreated>
  <Note>a potent inhibitor of proteasome; structure in first source
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007783</DescriptorUI>
     <DescriptorName>
      <String>Lactones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 2003 Apr 4;68(7):2760-4</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0453752</ConceptUI>
    <ConceptName>
     <String>methylomuralide</String>
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    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0453752</Concept1UI>
     <Concept2UI>M0453753</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T551039</TermUI>
      <String>methylomuralide</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>09</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0453753</ConceptUI>
    <ConceptName>
     <String>alpha-methylomuralide</String>
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    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0453752</Concept1UI>
     <Concept2UI>M0453753</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T551040</TermUI>
      <String>alpha-methylomuralide</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>09</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C501748</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,5-diamino-2-pentyne</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>03</Day>
  </DateCreated>
  <Note>substrate and inactivator of copper amine oxidases
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000480</DescriptorUI>
     <DescriptorName>
      <String>Alkynes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003959</DescriptorUI>
     <DescriptorName>
      <String>Diamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Biochem 2004 Dec;271(23-24):4696-708</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0486571</ConceptUI>
    <ConceptName>
     <String>1,5-diamino-2-pentyne</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T644985</TermUI>
      <String>1,5-diamino-2-pentyne</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>07</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C501749</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>phaiodotoxin, Anuroctonus phaiodactylus</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>03</Day>
  </DateCreated>
  <Note>an insect toxin; amino acid sequence in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012604</DescriptorUI>
     <DescriptorName>
      <String>Scorpion Venoms</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Biochem 2004 Dec;271(23-24):4753-61</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0486572</ConceptUI>
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     <String>phaiodotoxin, Anuroctonus phaiodactylus</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T644986</TermUI>
      <String>phaiodotoxin, Anuroctonus phaiodactylus</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>07</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C578332</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>FARP1 protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>02</Month>
   <Day>15</Day>
  </DateCreated>
  <DateRevised>
   <Year>2019</Year>
   <Month>12</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>RefSeq NM_134082
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*Cytoskeletal Proteins (2013-2020)</PreviousIndexing>
   <PreviousIndexing>*Guanine Nucleotide Exchange Factors (2013-2020)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D064067</DescriptorUI>
     <DescriptorName>
      <String>Rho Guanine Nucleotide Exchange Factors</String>
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   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Cell Biol. 2012 Dec 10;199(6):985-1001</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0581467</ConceptUI>
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    <RegistryNumber>0</RegistryNumber>
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      <TermUI>T837431</TermUI>
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      <DateCreated>
       <Year>2013</Year>
       <Month>02</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T837433</TermUI>
      <String>CDEP protein, mouse</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>02</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T837434</TermUI>
      <String>chondrocyte-derived ezrin-like protein, mouse</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>02</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T837432</TermUI>
      <String>FERMRhoGEF (Arhgef) and pleckstrin domain protein 1, mouse</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>02</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C523476</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Fbxl20 protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>10</Month>
   <Day>15</Day>
  </DateCreated>
  <DateRevised>
   <Year>2019</Year>
   <Month>12</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>RefSeq NM_028149
  </Note>
  <Frequency>7</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*Nerve Tissue Proteins (2007-2020)</PreviousIndexing>
   <PreviousIndexing>*UBIQUITIN-PROTEIN LIGASES (2007-2016)</PreviousIndexing>
   <PreviousIndexing>*Ubiquitin-Protein Ligase Complexes (2007-2020)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D044783</DescriptorUI>
     <DescriptorName>
      <String>F-Box Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cell 2007 Sep 7;130(5):943-57</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0514422</ConceptUI>
    <ConceptName>
     <String>Fbxl20 protein, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T000906848</TermUI>
      <String>Fbxl20 protein, mouse</String>
      <DateCreated>
       <Year>2016</Year>
       <Month>09</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2017)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T707679</TermUI>
      <String>SCRAPPER protein, mouse</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>10</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T000906849</TermUI>
      <String>F-box and leucine-rich repeat protein 20, mouse</String>
      <DateCreated>
       <Year>2016</Year>
       <Month>09</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2017)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C092482</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ACLA protein, Dictyostelium discoideum</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>04</Month>
   <Day>12</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>09</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>belongs to the ARP3 actin-related protein family; from Dictyostelium discoideum; amino acid sequence given in first source; GenBank Z46418
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000199</DescriptorUI>
     <DescriptorName>
      <String>Actins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>FEBS Lett 1995 Mar 6;360(3):235-41</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0244105</ConceptUI>
    <ConceptName>
     <String>ACLA protein, Dictyostelium discoideum</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T549719</TermUI>
      <String>ACLA protein, Dictyostelium discoideum</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>08</Month>
       <Day>31</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013227</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-(5-pyrazolazo)-2-naphthol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>for analysis of bismuth ions
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PYRAZOLES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009284</DescriptorUI>
     <DescriptorName>
      <String>Naphthols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Pol Pharm 33(4):485;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060829</ConceptUI>
    <ConceptName>
     <String>1-(5-pyrazolazo)-2-naphthol</String>
    </ConceptName>
    <RegistryNumber>55435-18-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090832</TermUI>
      <String>1-(5-pyrazolazo)-2-naphthol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013230</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>pyrogel</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>purified macropyroglobulin in aggrgated form from patients with hyperviscosity syndrome (at physiologic temperature)
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>GELS (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011750</DescriptorUI>
     <DescriptorName>
      <String>Pyroglobulins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Am J Med 61(3):321;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060833</ConceptUI>
    <ConceptName>
     <String>pyrogel</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090836</TermUI>
      <String>pyrogel</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013237</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Remanex</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*MERCURY (76-77)</PreviousIndexing>
   <PreviousIndexing>*ORGANOMETALLIC COMPOUNDS (76-77)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006582</DescriptorUI>
     <DescriptorName>
      <String>Hexachlorophene</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010663</DescriptorUI>
     <DescriptorName>
      <String>Phenylmercury Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Pol Przegl Chir 48(7):919;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060844</ConceptUI>
    <ConceptName>
     <String>Remanex</String>
    </ConceptName>
    <RegistryNumber>8066-67-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090847</TermUI>
      <String>Remanex</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C455166</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>poricoic acid H</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>05</Month>
   <Day>26</Day>
  </DateCreated>
  <Note>from Poria cocos (Polyporaceae); structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014315</DescriptorUI>
     <DescriptorName>
      <String>Triterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2002 Apr;65(4):462-5</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0425216</ConceptUI>
    <ConceptName>
     <String>poricoic acid H</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0425216</Concept1UI>
     <Concept2UI>M0425217</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T495351</TermUI>
      <String>poricoic acid H</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>05</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0425217</ConceptUI>
    <ConceptName>
     <String>16alpha-hydroxy-3,4-seco-24-methyllanosta-4(28),8,24(24(1))-triene-3,21-dioic acid</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0425216</Concept1UI>
     <Concept2UI>M0425217</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T495352</TermUI>
      <String>16alpha-hydroxy-3,4-seco-24-methyllanosta-4(28),8,24(24(1))-triene-3,21-dioic acid</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>05</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013248</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>selenocystathionamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1991</Year>
   <Month>05</Month>
   <Day>23</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SELENIUM (76-91)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003959</DescriptorUI>
     <DescriptorName>
      <String>Diamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D016566</DescriptorUI>
     <DescriptorName>
      <String>Organoselenium Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ital J Biochem 25(2):152-9;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060857</ConceptUI>
    <ConceptName>
     <String>selenocystathionamine</String>
    </ConceptName>
    <CASN1Name>1-Propanamine, 3-((2-aminoethyl)seleno)-</CASN1Name>
    <RegistryNumber>58114-52-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090860</TermUI>
      <String>selenocystathionamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013266</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-sulfonamido-4-chlorobenzoic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>06</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SULFONAMIDES (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002723</DescriptorUI>
     <DescriptorName>
      <String>Chlorobenzoates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Clin Pharmacol 10:139;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060876</ConceptUI>
    <ConceptName>
     <String>3-sulfonamido-4-chlorobenzoic acid</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090879</TermUI>
      <String>3-sulfonamido-4-chlorobenzoic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C092570</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>CRS4C protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>04</Month>
   <Day>17</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>09</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>a cryptidin-related sequence protein; CRS4C mRNA 94% identical to cryptdin-1; contains a prepro sequence; CRS4C mRNA isolated from Paneth cells of intestial crypts; amino acid sequence in first source
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011498</DescriptorUI>
     <DescriptorName>
      <String>Protein Precursors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D023082</DescriptorUI>
     <DescriptorName>
      <String>Defensins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Genomics 1994 Nov 1;24(1):99-109</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0244335</ConceptUI>
    <ConceptName>
     <String>CRS4C protein, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T549720</TermUI>
      <String>CRS4C protein, mouse</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>08</Month>
       <Day>31</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T549721</TermUI>
      <String>cryptdin-related protein 4C, mouse</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>08</Month>
       <Day>31</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C455167</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>poricoic acid G</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>05</Month>
   <Day>26</Day>
  </DateCreated>
  <Note>from Poria cocos (Polyporaceae); structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014315</DescriptorUI>
     <DescriptorName>
      <String>Triterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2002 Apr;65(4):462-5</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0425218</ConceptUI>
    <ConceptName>
     <String>poricoic acid G</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0425218</Concept1UI>
     <Concept2UI>M0425219</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T495353</TermUI>
      <String>poricoic acid G</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>05</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0425219</ConceptUI>
    <ConceptName>
     <String>16alpha-hydroxy-3,4-seco-lanosta-4(28),8,24-triene-3,21-dioic acid</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0425218</Concept1UI>
     <Concept2UI>M0425219</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T495354</TermUI>
      <String>16alpha-hydroxy-3,4-seco-lanosta-4(28),8,24-triene-3,21-dioic acid</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>05</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C455168</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-formyl-6-methoxybenzoxazolin-2(3H)-one</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>05</Month>
   <Day>26</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001583</DescriptorUI>
     <DescriptorName>
      <String>Benzoxazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2002 Apr;65(4):466-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0425220</ConceptUI>
    <ConceptName>
     <String>3-formyl-6-methoxybenzoxazolin-2(3H)-one</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0425220</Concept1UI>
     <Concept2UI>M0425221</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T495355</TermUI>
      <String>3-formyl-6-methoxybenzoxazolin-2(3H)-one</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>05</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T495356</TermUI>
      <String>FMBOA cpd</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>05</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0425221</ConceptUI>
    <ConceptName>
     <String>(13)C-labeled FMBOA</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0425220</Concept1UI>
     <Concept2UI>M0425221</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T495357</TermUI>
      <String>(13)C-labeled FMBOA</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>05</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013285</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-(3,4,5,6-tetrahydrophthalyl)glutarimide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>06</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PIPERIDONES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010797</DescriptorUI>
     <DescriptorName>
      <String>Phthalimides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Pharm (Weinheim) 309(6):520;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060924</ConceptUI>
    <ConceptName>
     <String>N-(3,4,5,6-tetrahydrophthalyl)glutarimide</String>
    </ConceptName>
    <CASN1Name>1H-Isoindole-1,3(2H)-dione, 2-(2,6-dioxo-3-piperidinyl)-4,5,6,7-tetrahydro-, (S)-</CASN1Name>
    <RegistryNumber>60242-08-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090927</TermUI>
      <String>N-(3,4,5,6-tetrahydrophthalyl)glutarimide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013287</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3,6,11,14-tetramethoxydibenzo(g,p)chrysene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002911</DescriptorUI>
     <DescriptorName>
      <String>Chrysenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mutat Res 40(3):225;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060927</ConceptUI>
    <ConceptName>
     <String>3,6,11,14-tetramethoxydibenzo(g,p)chrysene</String>
    </ConceptName>
    <RegistryNumber>60223-52-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090930</TermUI>
      <String>3,6,11,14-tetramethoxydibenzo(g,p)chrysene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C455169</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>muricin H</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>05</Month>
   <Day>26</Day>
  </DateCreated>
  <Note>from the seeds of Annona muricata; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005663</DescriptorUI>
     <DescriptorName>
      <String>Furans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2002 Apr;65(4):470-5</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0425223</ConceptUI>
    <ConceptName>
     <String>muricin H</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T495359</TermUI>
      <String>muricin H</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>05</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C455170</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>muricin I</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>05</Month>
   <Day>26</Day>
  </DateCreated>
  <Note>from the seeds of Annona muricata; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005663</DescriptorUI>
     <DescriptorName>
      <String>Furans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2002 Apr;65(4):470-5</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0425224</ConceptUI>
    <ConceptName>
     <String>muricin I</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T495360</TermUI>
      <String>muricin I</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>05</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C579708</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>phenylurea formaldehyde resin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>04</Month>
   <Day>14</Day>
  </DateCreated>
  <DateRevised>
   <Year>2013</Year>
   <Month>04</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>has antimicrobial activity; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009757</DescriptorUI>
     <DescriptorName>
      <String>Nylons</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010671</DescriptorUI>
     <DescriptorName>
      <String>Phenylurea Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Spectrochim Acta A Mol Biomol Spectrosc. 2012 Oct;96:179-87.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0583109</ConceptUI>
    <ConceptName>
     <String>phenylurea formaldehyde resin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T840408</TermUI>
      <String>phenylurea formaldehyde resin</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>04</Month>
       <Day>14</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T840573</TermUI>
      <String>phenylurea-formaldehyde resin</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>04</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C507729</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,3-bis(2-benzimidazyl)-2-thiapropane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001562</DescriptorUI>
     <DescriptorName>
      <String>Benzimidazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011407</DescriptorUI>
     <DescriptorName>
      <String>Propane</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Med Chem. 2005 Nov;40(11):1096-102</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0494819</ConceptUI>
    <ConceptName>
     <String>1,3-bis(2-benzimidazyl)-2-thiapropane</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T666063</TermUI>
      <String>1,3-bis(2-benzimidazyl)-2-thiapropane</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>02</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T666064</TermUI>
      <String>1,3-B(2-BI)-2-TP</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>02</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013300</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-(4-thio-beta-D-ribofuranosyl)-1,2,4-triazole-3-carboxamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D012254</DescriptorUI>
     <DescriptorName>
      <String>Ribavirin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 19(6):841;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060952</ConceptUI>
    <ConceptName>
     <String>1-(4-thio-beta-D-ribofuranosyl)-1,2,4-triazole-3-carboxamide</String>
    </ConceptName>
    <RegistryNumber>58928-39-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090955</TermUI>
      <String>1-(4-thio-beta-D-ribofuranosyl)-1,2,4-triazole-3-carboxamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013301</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>thioeserine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1986</Year>
   <Month>07</Month>
   <Day>23</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010830</DescriptorUI>
     <DescriptorName>
      <String>Physostigmine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Pharm 309(8):631;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060953</ConceptUI>
    <ConceptName>
     <String>thioeserine</String>
    </ConceptName>
    <CASN1Name>Carbamothioic acid, methyl-, S-(1,2,3,3a,8,8a-hexahydro-1,3a,8-trimethylpyrrolo(2,3-b)indol-5-yl) ester, (3aS-cis)-</CASN1Name>
    <RegistryNumber>61562-64-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090956</TermUI>
      <String>thioeserine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C455171</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>annocatalin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>05</Month>
   <Day>26</Day>
  </DateCreated>
  <Note>from the seeds of Annona muricata; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005663</DescriptorUI>
     <DescriptorName>
      <String>Furans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2002 Apr;65(4):470-5</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0425225</ConceptUI>
    <ConceptName>
     <String>annocatalin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T495361</TermUI>
      <String>annocatalin</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>05</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013310</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>trichloro(8-azaadeninium)zinc(II)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>06</Month>
   <Day>28</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ZINC (77-82)</PreviousIndexing>
   <PreviousIndexing>AZA CPDS (77-80)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000225</DescriptorUI>
     <DescriptorName>
      <String>Adenine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 447(1):117;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060970</ConceptUI>
    <ConceptName>
     <String>trichloro(8-azaadeninium)zinc(II)</String>
    </ConceptName>
    <CASN1Name>Zincate(1-), trichloro(6H-1,2,3-triazolo(4,5-d)pyrimidin-7-amine-N4)-, hydrogen, (T-4)-</CASN1Name>
    <RegistryNumber>60866-15-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090973</TermUI>
      <String>trichloro(8-azaadeninium)zinc(II)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013317</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>trinervi-2 beta,3 alpha,9 alpha-triol 9-O-acetate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>diterpene from frontal gland of termite soldiers; structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004224</DescriptorUI>
     <DescriptorName>
      <String>Diterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Am Chem Soc 98(19):6061;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060976</ConceptUI>
    <ConceptName>
     <String>trinervi-2 beta,3 alpha,9 alpha-triol 9-O-acetate</String>
    </ConceptName>
    <CASN1Name>1,11-Ethanocyclopentacycloundecene-5,13,14-triol, 1,2,3,3a,4,5,6,7,8,9,10,12a-dodecahydro-1,8,12-trimethyl-4-methylene-, 5-acetate, (1S-(1R*,3aS*,5S*,8S*,12aS*,13S*,14S*))-</CASN1Name>
    <RegistryNumber>60791-30-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090979</TermUI>
      <String>trinervi-2 beta,3 alpha,9 alpha-triol 9-O-acetate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013331</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>vanilglycolic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1985</Year>
   <Month>07</Month>
   <Day>19</Day>
  </DateRevised>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>GLYCOLATES (77-79)</PreviousIndexing>
   <PreviousIndexing>VANILLIN/*analogs (77-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D006719</DescriptorUI>
     <DescriptorName>
      <String>Homovanillic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Clin Chim Acta 72(1):49;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061002</ConceptUI>
    <ConceptName>
     <String>vanilglycolic acid</String>
    </ConceptName>
    <CASN1Name>4-hydroxy-3-methoxy-alpha-oxobenzeneacetic acid</CASN1Name>
    <RegistryNumber>2021-40-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091005</TermUI>
      <String>vanilglycolic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013337</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>xanthobilirubic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>has chromophore very similar to that of bilirubin; structure
  </Note>
  <Frequency>8</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D001663</DescriptorUI>
     <DescriptorName>
      <String>Bilirubin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Photochem Photobiol 24(1):29;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061013</ConceptUI>
    <ConceptName>
     <String>xanthobilirubic acid</String>
    </ConceptName>
    <CASN1Name>5-((3-ethyl-1,5-dihydro-4-methyl-5-oxo-2H-pyrrol-2-ylidene)methyl-2,4-dimethyl-1H-pyrrole- 3-propanoic acid</CASN1Name>
    <RegistryNumber>15770-19-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091016</TermUI>
      <String>xanthobilirubic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013339</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>9-(beta-D-xylofuranosyl)guanine delta 5'-monophosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1993</Year>
   <Month>05</Month>
   <Day>26</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*GUANINE NUCLEOTIDES (77-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D006157</DescriptorUI>
     <DescriptorName>
      <String>Guanosine Monophosphate</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 19(8):1026;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061015</ConceptUI>
    <ConceptName>
     <String>9-(beta-D-xylofuranosyl)guanine delta 5'-monophosphate</String>
    </ConceptName>
    <RegistryNumber>47349-49-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091018</TermUI>
      <String>9-(beta-D-xylofuranosyl)guanine delta 5'-monophosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C118943</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Daphne repellent</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1999</Year>
   <Month>05</Month>
   <Day>24</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>08</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>Daphne is tradename; microencapsulated agrochemical (mixture of vanillin, heliotropin, cyclamaldehyde, methionyl acetaldehyde, citronellol, dimethylphthalate) tested as an animal repellent in deer and rabbits
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009822</DescriptorUI>
     <DescriptorName>
      <String>Oils, Volatile</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D010575</DescriptorUI>
     <DescriptorName>
      <String>Pesticides</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Microencapsul 1999 Mar-Apr;16(2):169-80</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0304665</ConceptUI>
    <ConceptName>
     <String>Daphne repellent</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T464356</TermUI>
      <String>Daphne repellent</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>10</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001141</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>elsholtzidiol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1970</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>BUTANEDIOLS (75-82)</PreviousIndexing>
   <PreviousIndexing>GLYCOLS (70-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005663</DescriptorUI>
     <DescriptorName>
      <String>Furans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041231</ConceptUI>
    <ConceptName>
     <String>elsholtzidiol</String>
    </ConceptName>
    <RegistryNumber>28666-20-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071234</TermUI>
      <String>elsholtzidiol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C490375</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Tic32 protein, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>09</Month>
   <Day>21</Day>
  </DateCreated>
  <Note>involved in chloroplast biogenesis; amino acid sequence in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008565</DescriptorUI>
     <DescriptorName>
      <String>Membrane Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 2004 Aug 13;279(33):34756-62</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0472956</ConceptUI>
    <ConceptName>
     <String>Tic32 protein, Arabidopsis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T610408</TermUI>
      <String>Tic32 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C506002</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ircinin-1</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>12</Month>
   <Day>08</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>02</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>from sponge Sarcotragus sp.; structure in first source
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005663</DescriptorUI>
     <DescriptorName>
      <String>Furans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012717</DescriptorUI>
     <DescriptorName>
      <String>Sesquiterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Carcinog 2005 Nov;44(3):162-73</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0492709</ConceptUI>
    <ConceptName>
     <String>ircinin-1</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T661802</TermUI>
      <String>ircinin-1</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>12</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001164</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>etazocine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1984</Year>
   <Month>08</Month>
   <Day>15</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AZOCINES (71-81)</PreviousIndexing>
   <PreviousIndexing>ALCOHOLS (71-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001575</DescriptorUI>
     <DescriptorName>
      <String>Benzomorphans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041255</ConceptUI>
    <ConceptName>
     <String>etazocine</String>
    </ConceptName>
    <CASN1Name>1,2,3,4,5,6-hexahydro-6,11-diethyl- 3-methyl-2,6-methano-3-benzazocin-8-ol</CASN1Name>
    <RegistryNumber>34254-87-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071258</TermUI>
      <String>etazocine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001171</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ethoxychlor</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*HYDROCARBONS, HALOGENATED (73-75)</PreviousIndexing>
   <PreviousIndexing>*INSECTICIDES, ORGANOCHLORINE (73-75)</PreviousIndexing>
   <PreviousIndexing>ETHYL ETHERS (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008731</DescriptorUI>
     <DescriptorName>
      <String>Methoxychlor</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Agric Food Chem 20(1):1;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041263</ConceptUI>
    <ConceptName>
     <String>ethoxychlor</String>
    </ConceptName>
    <CASN1Name>2,2-bis(p-ethoxyphenyl)-1,1,1-trichloroethane</CASN1Name>
    <RegistryNumber>4329-03-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071266</TermUI>
      <String>ethoxychlor</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001172</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>9-ethyladenine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>28</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ADENINE (72-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000225</DescriptorUI>
     <DescriptorName>
      <String>Adenine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 11(5):816;1972</Source>
   <Source>Photochem Photobiol 22(3-4):97;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041264</ConceptUI>
    <ConceptName>
     <String>9-ethyladenine</String>
    </ConceptName>
    <RegistryNumber>2715-68-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071267</TermUI>
      <String>9-ethyladenine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001174</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-ethyl-4-amino-6-methoxy-s-triazine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>AMINES (72-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014227</DescriptorUI>
     <DescriptorName>
      <String>Triazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041270</ConceptUI>
    <ConceptName>
     <String>2-ethyl-4-amino-6-methoxy-s-triazine</String>
    </ConceptName>
    <CASN1Name>1,3,5-Triazin-2-amine, 4-ethyl-6-methoxy-</CASN1Name>
    <RegistryNumber>701-78-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071273</TermUI>
      <String>2-ethyl-4-amino-6-methoxy-s-triazine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C452874</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6-methyl-2,4-dihydroxyphenyl 4-O-methyl-glucopyranoside</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>04</Month>
   <Day>28</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009005</DescriptorUI>
     <DescriptorName>
      <String>Monosaccharides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Planta Med 2002 Jan;68(1):64-5</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0421887</ConceptUI>
    <ConceptName>
     <String>6-methyl-2,4-dihydroxyphenyl 4-O-methyl-glucopyranoside</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T491365</TermUI>
      <String>6-methyl-2,4-dihydroxyphenyl 4-O-methyl-glucopyranoside</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>04</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T491366</TermUI>
      <String>6-MDP-MGlu</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>04</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C452875</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>terredionol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>04</Month>
   <Day>28</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003512</DescriptorUI>
     <DescriptorName>
      <String>Cyclohexanones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Planta Med 2002 Jan;68(1):64-5</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0421888</ConceptUI>
    <ConceptName>
     <String>terredionol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T491367</TermUI>
      <String>terredionol</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>04</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001183</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ethylene di-11-bromoundecanoate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>BROMINE (72-76)</PreviousIndexing>
   <PreviousIndexing>ETHYLENES (72-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005227</DescriptorUI>
     <DescriptorName>
      <String>Fatty Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Science 176(036):806;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041290</ConceptUI>
    <ConceptName>
     <String>ethylene di-11-bromoundecanoate</String>
    </ConceptName>
    <RegistryNumber>39630-55-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071293</TermUI>
      <String>ethylene di-11-bromoundecanoate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001189</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N'-ethyl-2-methyl-N(3)-(2,6-dimethylphenyl)-4- imidazolidinone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>a metabolite of lidocaine
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>XYLENES (72-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007093</DescriptorUI>
     <DescriptorName>
      <String>Imidazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041294</ConceptUI>
    <ConceptName>
     <String>N'-ethyl-2-methyl-N(3)-(2,6-dimethylphenyl)-4- imidazolidinone</String>
    </ConceptName>
    <RegistryNumber>32845-42-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071297</TermUI>
      <String>N'-ethyl-2-methyl-N(3)-(2,6-dimethylphenyl)-4- imidazolidinone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001195</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-ethylsulfonylnaphthalene-1-sulfonamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>03</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>6</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>SULFONAMIDES</PreviousIndexing>
   <PreviousIndexing>SULFONES (72-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009281</DescriptorUI>
     <DescriptorName>
      <String>Naphthalenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ann Clin Lab Sci 6(3):223;1976</Source>
   <Source>Biochem Med 12(4):313;1975</Source>
   <Source>Br J Cancer 23:772;1969</Source>
   <Source>Br J Cancer 31(5):585;1975</Source>
   <Source>Chem Biol Interact 1(1):49;1969</Source>
   <Source>Clin Toxicol W3 EX89 (417):177;1976</Source>
   <Source>J Natl Cancer Inst 46:337;1971</Source>
   <Source>J Natl Cancer Inst 51:2007;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041297</ConceptUI>
    <ConceptName>
     <String>4-ethylsulfonylnaphthalene-1-sulfonamide</String>
    </ConceptName>
    <RegistryNumber>842-00-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071300</TermUI>
      <String>4-ethylsulfonylnaphthalene-1-sulfonamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001201</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Eupond</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>contains inulin: choline &amp; intybin
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002794</DescriptorUI>
     <DescriptorName>
      <String>Choline</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003508</DescriptorUI>
     <DescriptorName>
      <String>Cycloheptanes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007444</DescriptorUI>
     <DescriptorName>
      <String>Inulin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D009765</DescriptorUI>
     <DescriptorName>
      <String>Obesity</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000188</QualifierUI>
     <QualifierName>
      <String>drug therapy</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Med Monatschr 25(12):554;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041301</ConceptUI>
    <ConceptName>
     <String>Eupond</String>
    </ConceptName>
    <RegistryNumber>77430-01-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071304</TermUI>
      <String>Eupond</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001222</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>flavaspidic acid-N-methylglucaminate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>11</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>AMINO SUGARS (71-76)</PreviousIndexing>
   <PreviousIndexing>GLUCOSE (71-74)</PreviousIndexing>
   <PreviousIndexing>MEGLUMINE/analogs (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002090</DescriptorUI>
     <DescriptorName>
      <String>Butyrophenones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Br J Pharm 27(20):2425;1978</Source>
   <Source>Life Sci 24(7):587;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041328</ConceptUI>
    <ConceptName>
     <String>flavaspidic acid-N-methylglucaminate</String>
    </ConceptName>
    <RegistryNumber>992-18-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071331</TermUI>
      <String>flavaspidic acid-N-methylglucaminate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001252</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>nefurthiazole</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1970</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>7</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*THIAZOLES (70-82)</PreviousIndexing>
   <PreviousIndexing>HYDRAZINES (70-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009581</DescriptorUI>
     <DescriptorName>
      <String>Nitrofurans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Res 33(11):2802;1973</Source>
   <Source>Cancer Res 38:1398;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041365</ConceptUI>
    <ConceptName>
     <String>nefurthiazole</String>
    </ConceptName>
    <CASN1Name>formic acid 2-(4-(5-nitro-2-furyl)-2- thiazolyl)hydrazide</CASN1Name>
    <RegistryNumber>3570-75-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071368</TermUI>
      <String>nefurthiazole</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T071367</TermUI>
      <String>2-FNT</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T071366</TermUI>
      <String>2-(4-(5-nitro-2-furyl)-2-thiazolyl)formic acid hydrazide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001249</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-formamido-1-beta-D-ribofuranosylthioimidazole-4-carboxamide 2',3',5'-triformate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*NUCLEOSIDES (72-73)</PreviousIndexing>
   <PreviousIndexing>IMIDAZOLES (72-82)</PreviousIndexing>
   <PreviousIndexing>THIONES (74-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012263</DescriptorUI>
     <DescriptorName>
      <String>Ribonucleosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Chemother Rep 55(3):229;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041361</ConceptUI>
    <ConceptName>
     <String>5-formamido-1-beta-D-ribofuranosylthioimidazole-4-carboxamide 2',3',5'-triformate</String>
    </ConceptName>
    <RegistryNumber>27115-65-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071364</TermUI>
      <String>5-formamido-1-beta-D-ribofuranosylthioimidazole-4-carboxamide 2',3',5'-triformate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C018247</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>chinoin 123</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>12</Day>
  </DateRevised>
  <Frequency>4</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PYRIDINES (79-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011743</DescriptorUI>
     <DescriptorName>
      <String>Pyrimidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Morphol Acad Sci Hung 1979;27(1-2):38</Source>
   <Source>Acta Pharm Hung 48(Suppl):40;1978</Source>
   <Source>Internat Symp State Prev Ther Hum Arterosclerosis Anim Models: WG 550 I6222i:187;1977</Source>
   <Source>Pharmazie 1979;34(9):551</Source>
   <Source>Ther Hung 26(4):171;1978</Source>
   <Source>Ther Hung 26(4):174;1978</Source>
   <Source>Ther Hung 26(4):178;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0069583</ConceptUI>
    <ConceptName>
     <String>chinoin 123</String>
    </ConceptName>
    <CASN1Name>3-(ethoxycarbonyl)-6,7,8,9-tetrahydro-6-methyl-4-oxo-4H-pyrido(1,2-a)pyrimidine-9-acetic acid</CASN1Name>
    <RegistryNumber>64405-40-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0069583</Concept1UI>
     <Concept2UI>M0069581</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T099586</TermUI>
      <String>chinoin 123</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T099583</TermUI>
      <String>3-carbethoxy-6-methyl-9-carboxymethyl-4-oxo-6,7,8,9-tetrahydro-4H-pyrido(1,2-A)pyrimidine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0069581</ConceptUI>
    <ConceptName>
     <String>CH 123</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0069583</Concept1UI>
     <Concept2UI>M0069581</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T099584</TermUI>
      <String>CH 123</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T099585</TermUI>
      <String>CH-123</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C497563</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>RFC4 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2008</Year>
   <Month>09</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>RefSeq NM_002916
  </Note>
  <Frequency>28</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D051818</DescriptorUI>
     <DescriptorName>
      <String>Replication Protein C</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0481933</ConceptUI>
    <ConceptName>
     <String>RFC4 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T633240</TermUI>
      <String>RFC4 protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>14</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T633241</TermUI>
      <String>replication factor C (activator 1) 4, 37kDa protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>14</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001256</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Fortalidon</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>Contains aminopyrin, aspirin, codeine and barbiturate
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000632</DescriptorUI>
     <DescriptorName>
      <String>Aminopyrine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001241</DescriptorUI>
     <DescriptorName>
      <String>Aspirin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001463</DescriptorUI>
     <DescriptorName>
      <String>Barbiturates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003061</DescriptorUI>
     <DescriptorName>
      <String>Codeine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Med Welt 23(13):468;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041368</ConceptUI>
    <ConceptName>
     <String>Fortalidon</String>
    </ConceptName>
    <RegistryNumber>67797-89-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071371</TermUI>
      <String>Fortalidon</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001258</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>franol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>contains luminal, theophylline, ephderine, thenfadil
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004809</DescriptorUI>
     <DescriptorName>
      <String>Ephedrine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005029</DescriptorUI>
     <DescriptorName>
      <String>Ethylenediamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010634</DescriptorUI>
     <DescriptorName>
      <String>Phenobarbital</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013806</DescriptorUI>
     <DescriptorName>
      <String>Theophylline</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D001249</DescriptorUI>
     <DescriptorName>
      <String>Asthma</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000188</QualifierUI>
     <QualifierName>
      <String>drug therapy</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041370</ConceptUI>
    <ConceptName>
     <String>franol</String>
    </ConceptName>
    <RegistryNumber>8058-86-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071373</TermUI>
      <String>franol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C100155</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>leukoagglutinins, leukocytes</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1984</Year>
   <Month>08</Month>
   <Day>28</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>08</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>agglutinins found on leukocytes
  </Note>
  <Frequency>28</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AGGLUTININS (1984-2005)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007962</DescriptorUI>
     <DescriptorName>
      <String>Leukocytes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011506</DescriptorUI>
     <DescriptorName>
      <String>Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem J 1980;187(2):525</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0262833</ConceptUI>
    <ConceptName>
     <String>leukoagglutinins, leukocytes</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T292838</TermUI>
      <String>leukoagglutinins, leukocytes</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1984)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T292837</TermUI>
      <String>leucoagglutinins, leukocyte</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1984)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C104735</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SJAsg agglutinin, Sophora japonica</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1997</Year>
   <Month>03</Month>
   <Day>24</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>08</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>isolated from Sophora japonica; amino acid sequence in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D037121</DescriptorUI>
     <DescriptorName>
      <String>Plant Lectins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Plant Mol Biol 1997 Feb;33(3):523-36</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0273456</ConceptUI>
    <ConceptName>
     <String>SJAsg agglutinin, Sophora japonica</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T303461</TermUI>
      <String>SJAsg agglutinin, Sophora japonica</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T459522</TermUI>
      <String>seed lectin, Sophora japonica</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>08</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T303459</TermUI>
      <String>GalNAc-specific Sophora japonica seed agglutinin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T459523</TermUI>
      <String>LECSJAsg protein, Sophora japonica</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>08</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001269</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>galactocarolose</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1989</Year>
   <Month>09</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>galactofuranose polymer
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*POLYSACCHARIDES (72-79)</PreviousIndexing>
   <PreviousIndexing>GALACTOSE (72-75)</PreviousIndexing>
   <PreviousIndexing>GALACTOSE/analogs (75-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005685</DescriptorUI>
     <DescriptorName>
      <String>Galactans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem J 122(1):49;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041383</ConceptUI>
    <ConceptName>
     <String>galactocarolose</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071386</TermUI>
      <String>galactocarolose</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001273</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>galactosyl-beta-D-(1-4)-N-acetyllactosamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1995</Year>
   <Month>06</Month>
   <Day>20</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*OLIGOSACCHARIDES (72-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014312</DescriptorUI>
     <DescriptorName>
      <String>Trisaccharides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 247(12):3744;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041384</ConceptUI>
    <ConceptName>
     <String>galactosyl-beta-D-(1-4)-N-acetyllactosamine</String>
    </ConceptName>
    <CASN1Name>D-Glucitol, O-beta-D-galactopyranosyl-(1-4)-O-beta-D-galactopyranosyl-(1-4)-2-(acetylamino)-2-deoxy-</CASN1Name>
    <RegistryNumber>77416-66-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071387</TermUI>
      <String>galactosyl-beta-D-(1-4)-N-acetyllactosamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001274</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Gapona</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>contains Gastrixon &amp; Halidor
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CYCLOHEPTANES (72-75)</PreviousIndexing>
   <PreviousIndexing>*PROPYLAMINES (72-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001537</DescriptorUI>
     <DescriptorName>
      <String>Bencyclane</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014326</DescriptorUI>
     <DescriptorName>
      <String>Tropanes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Therap Hungarica 19(4):156;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041385</ConceptUI>
    <ConceptName>
     <String>Gapona</String>
    </ConceptName>
    <CASN1Name>8-Azoniabicyclo(3.2.1)octane, 8,8-dimethyl-3-((9H-xanthen-9-ylcarbonyl)oxy)-, bromide, endo-, mixt. with N,N-dimethyl-3-((1-(phenylmethyl)cycloheptyl)oxy)-1-propanamine</CASN1Name>
    <RegistryNumber>77416-70-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071388</TermUI>
      <String>Gapona</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001275</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>gaylussacin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1986</Year>
   <Month>05</Month>
   <Day>27</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*GLYCOSIDES (72-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005960</DescriptorUI>
     <DescriptorName>
      <String>Glucosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013267</DescriptorUI>
     <DescriptorName>
      <String>Stilbenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 35(1):49;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041386</ConceptUI>
    <ConceptName>
     <String>gaylussacin</String>
    </ConceptName>
    <CASN1Name>5-(beta-D-glucosyloxy)-3-hydroxy-trans- stilbene-2-carboxylic acid</CASN1Name>
    <RegistryNumber>38232-08-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071389</TermUI>
      <String>gaylussacin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C490823</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>delta sleep-inducing peptide (1-4)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>09</Month>
   <Day>27</Day>
  </DateCreated>
  <Note>a synthetic analog of DSIP &amp; a potential antiepileptic
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003701</DescriptorUI>
     <DescriptorName>
      <String>Delta Sleep-Inducing Peptide</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Pharmacol Biochem Behav 2004 Feb;77(2):227-34</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0473177</ConceptUI>
    <ConceptName>
     <String>delta sleep-inducing peptide (1-4)</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T611045</TermUI>
      <String>delta sleep-inducing peptide (1-4)</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T611046</TermUI>
      <String>DSIP(1-4)</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T611047</TermUI>
      <String>DSIP tetrapeptide (1-4)</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001294</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>glucosoxime</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1970</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>20</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>GLUCOSE (70-75)</PreviousIndexing>
   <PreviousIndexing>GLUCOSE/analogs (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010091</DescriptorUI>
     <DescriptorName>
      <String>Oximes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041399</ConceptUI>
    <ConceptName>
     <String>glucosoxime</String>
    </ConceptName>
    <RegistryNumber>608-81-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071402</TermUI>
      <String>glucosoxime</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C496061</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>PXN protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>06</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>RefSeq NM_002859
  </Note>
  <Frequency>569</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D051419</DescriptorUI>
     <DescriptorName>
      <String>Paxillin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0480419</ConceptUI>
    <ConceptName>
     <String>PXN protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T629983</TermUI>
      <String>PXN protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>02</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T629984</TermUI>
      <String>paxillin protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>02</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001304</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>glyceryl sulfoquinovoside</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*GLYCOSIDES (72-75)</PreviousIndexing>
   <PreviousIndexing>GLYCERIN (72-75)</PreviousIndexing>
   <PreviousIndexing>GLYCERIN/analogs (75-82)</PreviousIndexing>
   <PreviousIndexing>METHANESULFONATES (74-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006017</DescriptorUI>
     <DescriptorName>
      <String>Glycolipids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 261(1):35;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041423</ConceptUI>
    <ConceptName>
     <String>glyceryl sulfoquinovoside</String>
    </ConceptName>
    <CASN1Name>2,3-dihydroxypropyl 6-deoxy-6-sulfo-alpha-D- glucopyranoside</CASN1Name>
    <RegistryNumber>2308-53-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071426</TermUI>
      <String>glyceryl sulfoquinovoside</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001305</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>glycidol phosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>23</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ETHERS, CYCLIC (72-75)</PreviousIndexing>
   <PreviousIndexing>ALCOHOL, PROPYL (72-76)</PreviousIndexing>
   <PreviousIndexing>ORGANOPHOSPHORUS COMPOUNDS (72-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004852</DescriptorUI>
     <DescriptorName>
      <String>Epoxy Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 246(17):5510;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041424</ConceptUI>
    <ConceptName>
     <String>glycidol phosphate</String>
    </ConceptName>
    <RegistryNumber>23815-70-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071427</TermUI>
      <String>glycidol phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C467138</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>godoside D</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>10</Month>
   <Day>29</Day>
  </DateCreated>
  <Note>from Ilex godajam; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012503</DescriptorUI>
     <DescriptorName>
      <String>Saponins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014315</DescriptorUI>
     <DescriptorName>
      <String>Triterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Asian Nat Prod Res 2002 Mar;4(1):25-31</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0440913</ConceptUI>
    <ConceptName>
     <String>godoside D</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T524574</TermUI>
      <String>godoside D</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>10</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C497651</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>FANCC protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2008</Year>
   <Month>09</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>RefSeq NM_000136
  </Note>
  <Frequency>157</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D052218</DescriptorUI>
     <DescriptorName>
      <String>Fanconi Anemia Complementation Group C Protein</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0474920</ConceptUI>
    <ConceptName>
     <String>FANCC protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0474920</Concept1UI>
     <Concept2UI>M0261427</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T616519</TermUI>
      <String>FANCC protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>10</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T616520</TermUI>
      <String>Fanconi anemia, complementation group C protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>10</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T616523</TermUI>
      <String>FACC protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>10</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T616524</TermUI>
      <String>Fanconi anemia group C protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>10</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T616521</TermUI>
      <String>FA3 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>10</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T616522</TermUI>
      <String>FAC protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>10</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0261427</ConceptUI>
    <ConceptName>
     <String>Fanconi anemia group C-related protein, 50-kDa, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0474920</Concept1UI>
     <Concept2UI>M0261427</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T643272</TermUI>
      <String>Fanconi anemia group C-related protein, 50-kDa, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>06</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T291432</TermUI>
      <String>Fanconi anemia group C-related protein, 50-kDa</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T643274</TermUI>
      <String>FRP-50 protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>06</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T643273</TermUI>
      <String>FAC-related protein, 50-kDa, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>06</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001327</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hayatinin methochloride</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1970</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1992</Year>
   <Month>06</Month>
   <Day>22</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000470</DescriptorUI>
     <DescriptorName>
      <String>Alkaloids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041459</ConceptUI>
    <ConceptName>
     <String>hayatinin methochloride</String>
    </ConceptName>
    <RegistryNumber>29900-15-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071462</TermUI>
      <String>hayatinin methochloride</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001328</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hedamycin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>03</Month>
   <Day>31</Day>
  </DateRevised>
  <Frequency>29</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ANTHRAQUINONES (72-95)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000880</DescriptorUI>
     <DescriptorName>
      <String>Anthraquinones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Annu Rev Biochem 40:775;1971</Source>
   <Source>Biochemistry 17(20):4232;1978</Source>
   <Source>Helv Chim Acta 60(3):896;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041460</ConceptUI>
    <ConceptName>
     <String>hedamycin</String>
    </ConceptName>
    <RegistryNumber>11048-97-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071463</TermUI>
      <String>hedamycin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001330</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hellebrigenin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>7</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002018</DescriptorUI>
     <DescriptorName>
      <String>Bufanolides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Molec Pharmacol 8(1):31;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041462</ConceptUI>
    <ConceptName>
     <String>hellebrigenin</String>
    </ConceptName>
    <RegistryNumber>465-90-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071465</TermUI>
      <String>hellebrigenin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001332</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hemichrome</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>06</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>heme protein
  </Note>
  <Frequency>90</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*HEME (72-73)</PreviousIndexing>
   <PreviousIndexing>*PROTEINS (72-73)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006420</DescriptorUI>
     <DescriptorName>
      <String>Hemeproteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Blood 39(6):794;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041463</ConceptUI>
    <ConceptName>
     <String>hemichrome</String>
    </ConceptName>
    <CASN1Name>haemichrome</CASN1Name>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071466</TermUI>
      <String>hemichrome</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C489785</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>PXMP2 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>09</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>06</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>RefSeq NM_018663
  </Note>
  <Frequency>23</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008565</DescriptorUI>
     <DescriptorName>
      <String>Membrane Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D008830</DescriptorUI>
     <DescriptorName>
      <String>Microbodies</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0469605</ConceptUI>
    <ConceptName>
     <String>PXMP2 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T598931</TermUI>
      <String>PXMP2 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T598935</TermUI>
      <String>PMP22 protein, human (peroxosomal)</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T598932</TermUI>
      <String>peroxisomal membrane protein 2, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T598934</TermUI>
      <String>22 kDa peroxisomal membrane protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T598933</TermUI>
      <String>peroxisomal membrane protein 2, 22kDa, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001340</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hexahydrospinamycin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>SUCCINATES (72-83)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010659</DescriptorUI>
     <DescriptorName>
      <String>Phenylhydrazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 15(3):339;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041483</ConceptUI>
    <ConceptName>
     <String>hexahydrospinamycin</String>
    </ConceptName>
    <RegistryNumber>21471-49-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071486</TermUI>
      <String>hexahydrospinamycin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001341</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hexahydroubiquinone-4</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*UBIQUINONE (72-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014451</DescriptorUI>
     <DescriptorName>
      <String>Ubiquinone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Int. Z. Vitaminforsch. 41(2):189;1971</Source>
   <Source>Kardiologiia 17(12):79;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041484</ConceptUI>
    <ConceptName>
     <String>hexahydroubiquinone-4</String>
    </ConceptName>
    <CASN1Name>phytylubiquinone /OD/ hexahydrocoenzyme Q4</CASN1Name>
    <RegistryNumber>362-45-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071487</TermUI>
      <String>hexahydroubiquinone-4</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001442</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N,N'-(iminoditrimethylene)di-p-toluenesulfonamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>therapeutic agent for myocardial necrosis; RN given refers to HCl
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>IMINES (72-82)</PreviousIndexing>
   <PreviousIndexing>TOLUENE (72-73)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013449</DescriptorUI>
     <DescriptorName>
      <String>Sulfonamides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014050</DescriptorUI>
     <DescriptorName>
      <String>Toluene</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ann NY Acad Sci 156(1):294;1969</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041646</ConceptUI>
    <ConceptName>
     <String>N,N'-(iminoditrimethylene)di-p-toluenesulfonamide</String>
    </ConceptName>
    <CASN1Name>N,N'-(iminodi-3,1-propanediyl)bis(4- methylbenzenesulfonamide)</CASN1Name>
    <RegistryNumber>13380-01-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0041646</Concept1UI>
     <Concept2UI>M0041647</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071649</TermUI>
      <String>N,N'-(iminoditrimethylene)di-p-toluenesulfonamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0041647</ConceptUI>
    <ConceptName>
     <String>Ro 5-5340</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0041646</Concept1UI>
     <Concept2UI>M0041647</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T071650</TermUI>
      <String>Ro 5-5340</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C489803</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>RAB9B protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>09</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>06</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>RefSeq NM_016370
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D020691</DescriptorUI>
     <DescriptorName>
      <String>rab GTP-Binding Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0470907</ConceptUI>
    <ConceptName>
     <String>RAB9B protein, human</String>
    </ConceptName>
    <RegistryNumber>EC 3.6.1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T603676</TermUI>
      <String>RAB9B protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T603677</TermUI>
      <String>RAB9B, member RAS oncogene family protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T603678</TermUI>
      <String>RAB9L protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T603679</TermUI>
      <String>RAB9-like protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C497564</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>RFC5 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2008</Year>
   <Month>09</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>RefSeq NM_007370
  </Note>
  <Frequency>17</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D051818</DescriptorUI>
     <DescriptorName>
      <String>Replication Protein C</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0481934</ConceptUI>
    <ConceptName>
     <String>RFC5 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T633246</TermUI>
      <String>RFC5 protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>14</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T633247</TermUI>
      <String>replication factor C (activator 1) 5, 36.5kDa protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>14</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C507749</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cancer-testis antigen P1A, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateCreated>
  <Note>P1A is normally expressed only in a few tumor lines, de novo induction by 5-aza-2'-deoxycytidine augments adoptive immunotherapy in a murine tumor model
  </Note>
  <Frequency>12</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000951</DescriptorUI>
     <DescriptorName>
      <String>Antigens, Neoplasm</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Res 2006 Jan 15;66(2):1105-13</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0494842</ConceptUI>
    <ConceptName>
     <String>cancer-testis antigen P1A, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T666099</TermUI>
      <String>cancer-testis antigen P1A, mouse</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>02</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T666100</TermUI>
      <String>P1A antigen, mouse</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>02</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001769</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>veronamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>has cardiovascular effects; RN given refers to (R)-isomer
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ALKALOIDS (72-76)</PreviousIndexing>
   <PreviousIndexing>*ISOQUINOLINES (1972-2003)</PreviousIndexing>
   <PreviousIndexing>BENZYL CPDS (72-75)</PreviousIndexing>
   <PreviousIndexing>GLYCOSIDES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D044005</DescriptorUI>
     <DescriptorName>
      <String>Tetrahydroisoquinolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Int Pharmacodyn Ther 198(2):392;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0042092</ConceptUI>
    <ConceptName>
     <String>veronamine</String>
    </ConceptName>
    <CASN1Name>(R-)- trimethoxy-1,2,3,4-tetrahydro-5,6,7-trimethoxy-2-methyl-1- 4-((1,2,3,4-tetrahydro-5,6,7-trimethoxy-2-methyl-1-isoquinolinyl)methyl)phenyl 6-deoxy-alpha-L-manno pyranoside</CASN1Name>
    <RegistryNumber>36388-20-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T072095</TermUI>
      <String>veronamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T072094</TermUI>
      <String>1-(4'-alpha-L-rhamnosidobenzyl)-2-methyl-5,6,7- trimethoxy-1,2,3,4-tetrahydroisoquinoline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001365</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-hydroxy-4-acetylaminobiphenyl</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>09</Month>
   <Day>11</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>25</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BIPHENYL CPDS (71-75)</PreviousIndexing>
   <PreviousIndexing>HYDROXAMIC ACIDS (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000611</DescriptorUI>
     <DescriptorName>
      <String>Aminobiphenyl Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Res 1979;39(9):3369</Source>
   <Source>Cancer Res 35(11):2962;1975</Source>
   <Source>Chem Biol Interact 11(6):599;1975</Source>
   <Source>J Natl Cancer Inst 55(2):285;1975</Source>
   <Source>Oncology 36(3):105;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041512</ConceptUI>
    <ConceptName>
     <String>N-hydroxy-4-acetylaminobiphenyl</String>
    </ConceptName>
    <CASN1Name>N-(1,1'- biphenyl)-4-yl-N-hydroxyacetamide</CASN1Name>
    <RegistryNumber>4463-22-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071515</TermUI>
      <String>N-hydroxy-4-acetylaminobiphenyl</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T071514</TermUI>
      <String>N-hydroxy-N-4-biphenylacetamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T071513</TermUI>
      <String>N-hydroxy-N-4-acetylaminobiphenyl</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001373</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hydroxybenzindazole</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>03</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007191</DescriptorUI>
     <DescriptorName>
      <String>Indazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Can J Biochem 50(5):516;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041528</ConceptUI>
    <ConceptName>
     <String>hydroxybenzindazole</String>
    </ConceptName>
    <CASN1Name>1H-Benz(g)indazol-7-ol, 4,5-dihydro-</CASN1Name>
    <RegistryNumber>31184-53-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071531</TermUI>
      <String>hydroxybenzindazole</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C028409</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,7-dimethyl-2,3,6,7-tetrahydro-1H,5H-biscyclopentapyrazine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>03</Month>
   <Day>11</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>15</Day>
  </DateRevised>
  <Note>obtained from browning reaction of cyclotene &amp; ammonia under simulated cooking conditions; RN given refers to (cis)-isomer; structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011719</DescriptorUI>
     <DescriptorName>
      <String>Pyrazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Agric Food Cehm 1980;28(4):883</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0091479</ConceptUI>
    <ConceptName>
     <String>1,7-dimethyl-2,3,6,7-tetrahydro-1H,5H-biscyclopentapyrazine</String>
    </ConceptName>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T121480</TermUI>
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       <ThesaurusID>NLM (1981)</ThesaurusID>
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   <Concept PreferredConceptYN="N">
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     <String>1,7-dimethyl-2,3,6,7-tetrahydro-1H,5H-biscyclopentapyrazine, (trans)-isomer</String>
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    <RegistryNumber>72438-06-3</RegistryNumber>
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    <TermList>
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      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
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  <SupplementalRecordUI>C001385</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>S-(9-hydroxy-9,10-dihydro-10-phenanthryl)-L-cysteine</String>
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  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>17</Day>
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  <Frequency>1</Frequency>
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   <PreviousIndexing>*CYSTEINE (72-75)</PreviousIndexing>
   <PreviousIndexing>PHENANTHRENES (72-82)</PreviousIndexing>
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     <DescriptorUI>D003545</DescriptorUI>
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      <String>Cysteine</String>
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     <QualifierName>
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  <SourceList>
   <Source>Proc Soc Exptl Biol Med 139(1):173;1972</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041546</ConceptUI>
    <ConceptName>
     <String>S-(9-hydroxy-9,10-dihydro-10-phenanthryl)-L-cysteine</String>
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    <RegistryNumber>25331-33-3</RegistryNumber>
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       <ThesaurusID>NLM (1972)</ThesaurusID>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001386</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>25-hydroxydihydrotachysterol(3)</String>
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  <DateCreated>
   <Year>1970</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <Note>structure
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  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*VITAMIN D (70-72)</PreviousIndexing>
   <PreviousIndexing>HYDROXYSTEROIDS (73-76)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004097</DescriptorUI>
     <DescriptorName>
      <String>Dihydrotachysterol</String>
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    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041547</ConceptUI>
    <ConceptName>
     <String>25-hydroxydihydrotachysterol(3)</String>
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    <CASN1Name>9,10-secocholesta-5,7-diene-3 beta,25-diol</CASN1Name>
    <RegistryNumber>25631-39-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071550</TermUI>
      <String>25-hydroxydihydrotachysterol(3)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
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     </Term>
    </TermList>
   </Concept>
  </ConceptList>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C446061</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-(4-(4-(2-(1-hydroxyethyl)pyrimidin-4-yl)-2,6-dimethylpiperazin-1-yl)pyrimidin-2-yl)ethanol</String>
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  <DateCreated>
   <Year>2002</Year>
   <Month>02</Month>
   <Day>06</Day>
  </DateCreated>
  <Note>structure in first source
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010879</DescriptorUI>
     <DescriptorName>
      <String>Piperazines</String>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011743</DescriptorUI>
     <DescriptorName>
      <String>Pyrimidines</String>
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  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D007064</DescriptorUI>
     <DescriptorName>
      <String>L-Iditol 2-Dehydrogenase</String>
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     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
     <QualifierName>
      <String>antagonists &amp; inhibitors</String>
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  <SourceList>
   <Source>J Med Chem 2002 Jan 17;45(2):511-28</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0413617</ConceptUI>
    <ConceptName>
     <String>1-(4-(4-(2-(1-hydroxyethyl)pyrimidin-4-yl)-2,6-dimethylpiperazin-1-yl)pyrimidin-2-yl)ethanol</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T480930</TermUI>
      <String>1-(4-(4-(2-(1-hydroxyethyl)pyrimidin-4-yl)-2,6-dimethylpiperazin-1-yl)pyrimidin-2-yl)ethanol</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>02</Month>
       <Day>06</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T480931</TermUI>
      <String>2002uglycpd15</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>02</Month>
       <Day>06</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
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  <SupplementalRecordUI>C028438</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>17 beta-((1R)-1-hydroxy-2-propynyl)androst-4-en-3-one</String>
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  <DateCreated>
   <Year>1981</Year>
   <Month>03</Month>
   <Day>16</Day>
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  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>15</Day>
  </DateRevised>
  <Note>RN given refers to (17beta)-isomer; structure given in first source
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  <Frequency>2</Frequency>
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    <DescriptorReferredTo>
     <DescriptorUI>*D000737</DescriptorUI>
     <DescriptorName>
      <String>Androstenols</String>
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  <SourceList>
   <Source>Biochemistry 1980;19(22):4950</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0091545</ConceptUI>
    <ConceptName>
     <String>17 beta-((1R)-1-hydroxy-2-propynyl)androst-4-en-3-one</String>
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    <CASN1Name>androst-4-en-3-one, 17-(1-hydroxy-2-propynyl)-, (17 beta(R))-</CASN1Name>
    <RegistryNumber>72012-08-9</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>72012-07-8 ((17beta)-(S)-isomer)</RelatedRegistryNumber>
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    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0091545</Concept1UI>
     <Concept2UI>M0317740</Concept2UI>
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    <TermList>
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      <TermUI>T121548</TermUI>
      <String>17 beta-((1R)-1-hydroxy-2-propynyl)androst-4-en-3-one</String>
      <ThesaurusIDlist>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T121547</TermUI>
      <String>17-HPAO</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
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   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0317740</ConceptUI>
    <ConceptName>
     <String>17 beta-((1R)-1-hydroxy-2-propynyl)androst-4-en-3-one, (17beta)-(S)-isomer</String>
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    <RegistryNumber>72012-07-8</RegistryNumber>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0091545</Concept1UI>
     <Concept2UI>M0317740</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T347740</TermUI>
      <String>17 beta-((1R)-1-hydroxy-2-propynyl)androst-4-en-3-one, (17beta)-(S)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001438</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>imidazo(4,5,1-kl)phenoxazine</String>
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  <DateCreated>
   <Year>1970</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>29</Day>
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  <Note>structure
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  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>IMIDAZOLES (70-82)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010078</DescriptorUI>
     <DescriptorName>
      <String>Oxazines</String>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041634</ConceptUI>
    <ConceptName>
     <String>imidazo(4,5,1-kl)phenoxazine</String>
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    <CASN1Name>Imidazo(4,5,1-kl)phenothiazine</CASN1Name>
    <RegistryNumber>202-25-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071637</TermUI>
      <String>imidazo(4,5,1-kl)phenoxazine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
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   </Concept>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001443</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Immobilizine</String>
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  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ANTIBODIES (71-75)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000907</DescriptorUI>
     <DescriptorName>
      <String>Antibodies, Bacterial</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Res Commun Chem Pathol Pharmacol 11(1):147;1975</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041648</ConceptUI>
    <ConceptName>
     <String>Immobilizine</String>
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    <RegistryNumber>0</RegistryNumber>
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     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071651</TermUI>
      <String>Immobilizine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001451</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Innovar</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>combination drug containing fentanyl citrate &amp; droperidol
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  <Frequency>96</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BENPERIDOL (72-74)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004329</DescriptorUI>
     <DescriptorName>
      <String>Droperidol</String>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005283</DescriptorUI>
     <DescriptorName>
      <String>Fentanyl</String>
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   </HeadingMappedTo>
  </HeadingMappedToList>
    <PharmacologicalActionList>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D000700</DescriptorUI>
        <DescriptorName>
         <String>Analgesics</String>
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     </PharmacologicalAction>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D019162</DescriptorUI>
        <DescriptorName>
         <String>Anesthetics, Combined</String>
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  <SourceList>
   <Source>Anesteziol Reanimatol 4:24;1978</Source>
   <Source>Anesth Analg (Cleve) 1980;59(1):50</Source>
   <Source>Can Anaesth Soc J 26(1):29;1979</Source>
   <Source>Ill Med J 140(3):214;1971</Source>
   <Source>Jpn J Anesthesiol 20(10):965;1071</Source>
   <Source>Jpn J Anesthesiol 20(10):973;1971</Source>
   <Source>Masui 28(4):356;1979</Source>
   <Source>Rev Esp Anestesiol Reanim 23(5):390;1976</Source>
   <Source>West Afr J Pharmacol Drug Res 2(1):73;1975</Source>
   <Source>Z Gastroenterol 16(11):696;1978</Source>
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   <Concept PreferredConceptYN="Y">
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    <ConceptName>
     <String>Innovar</String>
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     <ConceptRelation RelationName="NRW">
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     <ConceptRelation RelationName="NRW">
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     <ConceptRelation RelationName="NRW">
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     <Concept2UI>M0041660</Concept2UI>
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    <TermList>
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      <TermUI>T071662</TermUI>
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   <Concept PreferredConceptYN="N">
    <ConceptUI>M0041663</ConceptUI>
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     <String>talamonal</String>
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    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0041664</Concept1UI>
     <Concept2UI>M0041663</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T071666</TermUI>
      <String>talamonal</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0041660</ConceptUI>
    <ConceptName>
     <String>Thalamonal</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0041664</Concept1UI>
     <Concept2UI>M0041660</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T071663</TermUI>
      <String>Thalamonal</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0041662</ConceptUI>
    <ConceptName>
     <String>leptofen</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0041664</Concept1UI>
     <Concept2UI>M0041662</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T071665</TermUI>
      <String>leptofen</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001535</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>leucylnegamycin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateRevised>
  <Note>from negamycin-producing Streptomyces; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ANTIBIOTICS (72-76)</PreviousIndexing>
   <PreviousIndexing>*DIPEPTIDES (72-76)</PreviousIndexing>
   <PreviousIndexing>*HYDRAZINES (72-76)</PreviousIndexing>
   <PreviousIndexing>AMINOCAPROIC ACID (72-75)</PreviousIndexing>
   <PreviousIndexing>LEUCINE (72-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000599</DescriptorUI>
     <DescriptorName>
      <String>Amino Acids, Diamino</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiot (Tokyo) 24(10):732;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041770</ConceptUI>
    <ConceptName>
     <String>leucylnegamycin</String>
    </ConceptName>
    <RegistryNumber>35663-84-4</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0041770</Concept1UI>
     <Concept2UI>M0041769</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071773</TermUI>
      <String>leucylnegamycin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0041769</ConceptUI>
    <ConceptName>
     <String>(2-(3(R)-amino-5(R)-hydroxy-6-L-leucylaminohexanoyl)-1-methylhydrazino)acetic acid</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0041770</Concept1UI>
     <Concept2UI>M0041769</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T071772</TermUI>
      <String>(2-(3(R)-amino-5(R)-hydroxy-6-L-leucylaminohexanoyl)-1-methylhydrazino)acetic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001527</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Ledermix</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>13</Day>
  </DateRevised>
  <Note>contains above two cpds
  </Note>
  <Frequency>77</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003707</DescriptorUI>
     <DescriptorName>
      <String>Demeclocycline</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014222</DescriptorUI>
     <DescriptorName>
      <String>Triamcinolone Acetonide</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Br Endod Soc 6(1):8;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041756</ConceptUI>
    <ConceptName>
     <String>Ledermix</String>
    </ConceptName>
    <RegistryNumber>8059-68-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="TRD"  RecordPreferredTermYN="Y">
      <TermUI>T071759</TermUI>
      <String>Ledermix</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001463</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>iodoindoxyl phosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>01</Month>
   <Day>05</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>IODIDES (71-72)</PreviousIndexing>
   <PreviousIndexing>IODINE (72-76)</PreviousIndexing>
   <PreviousIndexing>ORGANOPHOSPHORUS COMPOUNDS (71-82)</PreviousIndexing>
   <PreviousIndexing>PHOSPHORIC ACIDS (71-74)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007211</DescriptorUI>
     <DescriptorName>
      <String>Indoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041675</ConceptUI>
    <ConceptName>
     <String>iodoindoxyl phosphate</String>
    </ConceptName>
    <CASN1Name>5-iodo-1H-indol-3-ol dihydrogen phosphate ester</CASN1Name>
    <RegistryNumber>7300-58-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071678</TermUI>
      <String>iodoindoxyl phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005932</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>17-hydroxyprogesterone 17-(9-oxo-10-chlorodecanoate)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>11</Month>
   <Day>09</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>DECANOIC ACIDS (75-76)</PreviousIndexing>
   <PreviousIndexing>FATTY ACIDS (73-75)</PreviousIndexing>
   <PreviousIndexing>KETO ACIDS (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006908</DescriptorUI>
     <DescriptorName>
      <String>Hydroxyprogesterones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Steroids 22(1):139;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0047809</ConceptUI>
    <ConceptName>
     <String>17-hydroxyprogesterone 17-(9-oxo-10-chlorodecanoate)</String>
    </ConceptName>
    <CASN1Name>Pregn-4-ene-3,20-dione, 17-((10-chloro-1,9-dioxodecyl)oxy)-</CASN1Name>
    <RegistryNumber>40946-49-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T077812</TermUI>
      <String>17-hydroxyprogesterone 17-(9-oxo-10-chlorodecanoate)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005935</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Vesitan</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>contains thiopropazate &amp; chlorphencyclan
  </Note>
  <Frequency>6</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ETHYLAMINES (73-79)</PreviousIndexing>
   <PreviousIndexing>*THIOPROPAZATE (73-85)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003510</DescriptorUI>
     <DescriptorName>
      <String>Cyclohexanes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010640</DescriptorUI>
     <DescriptorName>
      <String>Phenothiazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Dtsch Med Wochenschr 98(21):1071;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0047813</ConceptUI>
    <ConceptName>
     <String>Vesitan</String>
    </ConceptName>
    <CASN1Name>1-Piperazineethanol, 4-(3-(2-chloro-10H-phenothiazin-10-yl)propyl)-, acetate (ester), mixt. with 2-((1-(4-chlorophenyl)cyclohexyl)oxy)-N,N-diethylethanamine</CASN1Name>
    <RegistryNumber>8063-62-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T077816</TermUI>
      <String>Vesitan</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005936</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>paromamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>04</Month>
   <Day>22</Day>
  </DateRevised>
  <Note>RN given refers to (D)-isomer
  </Note>
  <Frequency>15</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AMINO SUGARS (73-74)</PreviousIndexing>
   <PreviousIndexing>*GLYCOSIDES (73-74)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000617</DescriptorUI>
     <DescriptorName>
      <String>Aminoglycosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiot (Tokyo) 25(9):530;1972</Source>
   <Source>J Antibiot (Tokyo) 28(8):574;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0047814</ConceptUI>
    <ConceptName>
     <String>paromamine</String>
    </ConceptName>
    <RegistryNumber>534-47-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T077817</TermUI>
      <String>paromamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C410343</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>BLAB3 protein, Flavobacterium meningosepticum</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>07</Month>
   <Day>07</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>01</Month>
   <Day>23</Day>
  </DateRevised>
  <Note>a metallo-beta-lactamase isolated from Chryseobacterium meningosepticum; amino acid sequence in first source; GenBank AF162284
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001618</DescriptorUI>
     <DescriptorName>
      <String>beta-Lactamases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Antimicrob Agents Chemother 2000 Jun;44(6):1448-52</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0365571</ConceptUI>
    <ConceptName>
     <String>BLAB3 protein, Flavobacterium meningosepticum</String>
    </ConceptName>
    <RegistryNumber>EC 3.5.2.6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T520394</TermUI>
      <String>BLAB3 protein, Flavobacterium meningosepticum</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>09</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C455504</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>QseC protein, E coli</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>06</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>01</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>involved in flagella regulation and motility; has been sequenced
  </Note>
  <Frequency>38</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029968</DescriptorUI>
     <DescriptorName>
      <String>Escherichia coli Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Microbiol 2002 Feb;43(3):809-21</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0425676</ConceptUI>
    <ConceptName>
     <String>QseC protein, E coli</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T496211</TermUI>
      <String>QseC protein, E coli</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>06</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T496213</TermUI>
      <String>quorum sensing Escherichia coli regulator C</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>06</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C034671</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>prostaglandin F2alpha receptor</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1982</Year>
   <Month>06</Month>
   <Day>23</Day>
  </DateCreated>
  <DateRevised>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>10</Day>
  </DateRevised>
  <Frequency>459</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011982</DescriptorUI>
     <DescriptorName>
      <String>Receptors, Prostaglandin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D015237</DescriptorUI>
     <DescriptorName>
      <String>Dinoprost</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Arch Biochem Biophys 1982;214(2):431</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0106714</ConceptUI>
    <ConceptName>
     <String>prostaglandin F2alpha receptor</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0106714</Concept1UI>
     <Concept2UI>M0585472</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0106714</Concept1UI>
     <Concept2UI>M0106710</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0106714</Concept1UI>
     <Concept2UI>M0227131</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0106714</Concept1UI>
     <Concept2UI>M0106706</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0106714</Concept1UI>
     <Concept2UI>M0106707</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T136718</TermUI>
      <String>prostaglandin F2alpha receptor</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T136717</TermUI>
      <String>receptor, prostaglandin F2alpha</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T136715</TermUI>
      <String>prostaglandin F2alpha receptors</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T136716</TermUI>
      <String>receptor, PGF2alpha</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T136712</TermUI>
      <String>PGF2alpha receptor</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T136713</TermUI>
      <String>PGF2alpha receptors</String>
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       <ThesaurusID>NLM (1982)</ThesaurusID>
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     </Term>
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   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0585472</ConceptUI>
    <ConceptName>
     <String>PTGFR protein, human</String>
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     <Concept1UI>M0106714</Concept1UI>
     <Concept2UI>M0585472</Concept2UI>
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    <TermList>
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      <TermUI>T845390</TermUI>
      <String>PTGFR protein, human</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>10</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
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   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0106710</ConceptUI>
    <ConceptName>
     <String>prostaglandin F2 receptor</String>
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    <ConceptRelationList>
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     <Concept1UI>M0106714</Concept1UI>
     <Concept2UI>M0106710</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T136714</TermUI>
      <String>prostaglandin F2 receptor</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
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     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0227131</ConceptUI>
    <ConceptName>
     <String>prostanoid FP receptor</String>
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    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0106714</Concept1UI>
     <Concept2UI>M0227131</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T257136</TermUI>
      <String>prostanoid FP receptor</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T257135</TermUI>
      <String>PGF receptor</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T257134</TermUI>
      <String>FP receptor</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0106706</ConceptUI>
    <ConceptName>
     <String>8-epi-PGF2alpha receptor</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0106714</Concept1UI>
     <Concept2UI>M0106706</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T136710</TermUI>
      <String>8-epi-PGF2alpha receptor</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0106707</ConceptUI>
    <ConceptName>
     <String>F2-isoprostane receptor</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0106714</Concept1UI>
     <Concept2UI>M0106707</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T136711</TermUI>
      <String>F2-isoprostane receptor</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C120242</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>aquilegioside A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1999</Year>
   <Month>09</Month>
   <Day>30</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>08</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>cycloartane-type glycoside from Aquilegia flabellata; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012503</DescriptorUI>
     <DescriptorName>
      <String>Saponins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014315</DescriptorUI>
     <DescriptorName>
      <String>Triterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Phytochemistry 1999 Jun;51(3):449-52</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0333064</ConceptUI>
    <ConceptName>
     <String>aquilegioside A</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T364686</TermUI>
      <String>aquilegioside A</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T364687</TermUI>
      <String>22-3beta,16alpha,29-trihydroxy-cycloart-24-en-26,22-olide 3-O-beta-D-glucopyranosyl-(1-6)-beta-D-glucopyranosyl-(1-2)-alpha-L-arabinopyranoside</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006038</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>AB 64</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>new phenolic, indicator-pigment antibiotic isolated from Actinomadura roseoviolacea var. rubescens
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010636</DescriptorUI>
     <DescriptorName>
      <String>Phenols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D010860</DescriptorUI>
     <DescriptorName>
      <String>Pigments, Biological</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Antibiot (Tokyo) 26(9):492;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0048047</ConceptUI>
    <ConceptName>
     <String>AB 64</String>
    </ConceptName>
    <CASN1Name>Antibiotic AB 64</CASN1Name>
    <RegistryNumber>50863-62-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T078050</TermUI>
      <String>AB 64</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T078049</TermUI>
      <String>AB-64</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C475498</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Tub1 protein, S cerevisiae</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>07</Month>
   <Day>11</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>01</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>amino acid sequence in first source
  </Note>
  <Frequency>12</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029701</DescriptorUI>
     <DescriptorName>
      <String>Saccharomyces cerevisiae Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D014404</DescriptorUI>
     <DescriptorName>
      <String>Tubulin</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>EMBO Rep. 2003 Jan;4(1):94-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0451519</ConceptUI>
    <ConceptName>
     <String>Tub1 protein, S cerevisiae</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T545782</TermUI>
      <String>Tub1 protein, S cerevisiae</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>07</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005968</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>carboxymuconolactone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>16</Day>
  </DateRevised>
  <Frequency>4</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>LACTONES (74-81)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014233</DescriptorUI>
     <DescriptorName>
      <String>Tricarboxylic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 12(18):3537;1973</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0047880</ConceptUI>
    <ConceptName>
     <String>carboxymuconolactone</String>
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    <CASN1Name>2-Furanacetic acid, 2-carboxy-2,5-dihydro-5-oxo-</CASN1Name>
    <RegistryNumber>13249-46-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T077883</TermUI>
      <String>carboxymuconolactone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
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   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005971</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-ethyluracil-1-beta-D-xylopyranoside</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>10</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*NUCLEOSIDES (74-75)</PreviousIndexing>
   <PreviousIndexing>*URACIL (74-75)</PreviousIndexing>
   <PreviousIndexing>URACIL/*analogs (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011741</DescriptorUI>
     <DescriptorName>
      <String>Pyrimidine Nucleosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Pharm Bull 21(6):1382;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0047890</ConceptUI>
    <ConceptName>
     <String>5-ethyluracil-1-beta-D-xylopyranoside</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T077893</TermUI>
      <String>5-ethyluracil-1-beta-D-xylopyranoside</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
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   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005972</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-ethyluracil-1-beta-D-galactopyranoside</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>10</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*NUCLEOSIDES (74-75)</PreviousIndexing>
   <PreviousIndexing>*URACIL (74-75)</PreviousIndexing>
   <PreviousIndexing>URACIL/*analogs (75-82)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011741</DescriptorUI>
     <DescriptorName>
      <String>Pyrimidine Nucleosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Pharm Bull 21(6):1382;1973</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0047891</ConceptUI>
    <ConceptName>
     <String>5-ethyluracil-1-beta-D-galactopyranoside</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T077894</TermUI>
      <String>5-ethyluracil-1-beta-D-galactopyranoside</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
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   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C058877</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-(4-isobutylcyclohexyl)-2-oxoethyl benzenesulfonate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1989</Year>
   <Month>04</Month>
   <Day>26</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>structure given in first source; RN from Toxlit
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  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001557</DescriptorUI>
     <DescriptorName>
      <String>Benzenesulfonates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Chromatogr 1988;433:282</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0164015</ConceptUI>
    <ConceptName>
     <String>2-(4-isobutylcyclohexyl)-2-oxoethyl benzenesulfonate</String>
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    <RegistryNumber>84856-18-8</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0164015</Concept1UI>
     <Concept2UI>M0164017</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T194020</TermUI>
      <String>2-(4-isobutylcyclohexyl)-2-oxoethyl benzenesulfonate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0164017</ConceptUI>
    <ConceptName>
     <String>FL 386</String>
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    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0164015</Concept1UI>
     <Concept2UI>M0164017</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T194022</TermUI>
      <String>FL 386</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T194021</TermUI>
      <String>FL-386</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005985</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3,6-dioxohexahydropyrrolo(1,2-a)pyrazine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>isolated from starfish Luidia clathrata; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PYRROLIDINES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010879</DescriptorUI>
     <DescriptorName>
      <String>Piperazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Experientia 29(5):521;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0047917</ConceptUI>
    <ConceptName>
     <String>3,6-dioxohexahydropyrrolo(1,2-a)pyrazine</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T077920</TermUI>
      <String>3,6-dioxohexahydropyrrolo(1,2-a)pyrazine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
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   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006104</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>U 0521</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1969</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>catechol methyltransferase antagonist; structure
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  <Frequency>56</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011427</DescriptorUI>
     <DescriptorName>
      <String>Propiophenones</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Am J Physiol 228(6):1702;1975</Source>
   <Source>Biochem Pharmacol 28(7):1221;1979</Source>
   <Source>Cardiovasc Res 1979;13(12):723</Source>
   <Source>Circ Res 1980;46(1):22</Source>
   <Source>Clin Exp Pharmacol Physiol Suppl 2:39;1975</Source>
   <Source>J Pharm Pharmacol 29(8):502;1977</Source>
   <Source>Naunyn Schmiedebergs Arch Pharmacol 1979;307(3):235</Source>
   <Source>Naunyn Schmiedebergs Arch Pharmacol 286:401;1975</Source>
   <Source>Naunyn Schmiedebergs Arch Pharmacol 292(3):205;1976</Source>
   <Source>Naunyn Schmiedebergs Arch Pharmacol 292(3):219,231;1976</Source>
   <Source>Naunyn Schmiedebergs Arch Pharmacol 293(2):115;1976</Source>
   <Source>Naunyn Schmiedebergs Arch Pharmacol 295(2):141;1976</Source>
   <Source>Naunyn Schmiedebergs Arch Pharmacol 296(3):217,279;1977</Source>
   <Source>Naunyn Schmiedebergs Arch Pharmacol 304(2):147;1978</Source>
   <Source>Pharmacology 18(5):228;1979</Source>
   <Source>Proc Soc Exp Biol Med 156:315;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0048217</ConceptUI>
    <ConceptName>
     <String>U 0521</String>
    </ConceptName>
    <CASN1Name>1-(3,4-dihydroxyphenyl)-2-methyl-1-propanone</CASN1Name>
    <RegistryNumber>5466-89-7</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0048217</Concept1UI>
     <Concept2UI>M0048214</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T078220</TermUI>
      <String>U 0521</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1969)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T078219</TermUI>
      <String>U0521</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1969)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T078218</TermUI>
      <String>U-0521</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1969)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0048214</ConceptUI>
    <ConceptName>
     <String>3',4'-dihydroxy-2-methylpropiophenone</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0048217</Concept1UI>
     <Concept2UI>M0048214</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T078217</TermUI>
      <String>3',4'-dihydroxy-2-methylpropiophenone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1969)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005990</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-(2,4-dinitrophenyl)hexamethylenediamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*NITROBENZENES (74-77)</PreviousIndexing>
   <PreviousIndexing>DIAMINES (74-77)</PreviousIndexing>
   <PreviousIndexing>DINITROBENZENES (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003959</DescriptorUI>
     <DescriptorName>
      <String>Diamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Biochem 35(3):540;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0047928</ConceptUI>
    <ConceptName>
     <String>N-(2,4-dinitrophenyl)hexamethylenediamine</String>
    </ConceptName>
    <CASN1Name>1,6-Hexanediamine, N-(2,4-dinitrophenyl)-</CASN1Name>
    <RegistryNumber>40299-04-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T077931</TermUI>
      <String>N-(2,4-dinitrophenyl)hexamethylenediamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C068569</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>E coli O18 O-specific polysaccharide-cholera toxin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1991</Year>
   <Month>05</Month>
   <Day>26</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>07</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>O-specific polysaccharide isolated from serotype 18 Escherichia coli lipopolysaccharide covalently coupled to cholera toxin
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BACTERIAL VACCINES (1991-2000)</PreviousIndexing>
   <PreviousIndexing>*CHOLERA TOXIN (1991-2000)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000942</DescriptorUI>
     <DescriptorName>
      <String>Antigens, Bacterial</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002772</DescriptorUI>
     <DescriptorName>
      <String>Cholera Toxin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D022121</DescriptorUI>
     <DescriptorName>
      <String>Cholera Vaccines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D004926</DescriptorUI>
     <DescriptorName>
      <String>Escherichia coli</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Infect Dis 1991;163(5):1040</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0187477</ConceptUI>
    <ConceptName>
     <String>E coli O18 O-specific polysaccharide-cholera toxin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T217482</TermUI>
      <String>E coli O18 O-specific polysaccharide-cholera toxin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T217481</TermUI>
      <String>O-PS-cholera toxin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C113425</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cinnamoyl-LIGRLO-amide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>08</Month>
   <Day>03</Day>
  </DateCreated>
  <DateRevised>
   <Year>2007</Year>
   <Month>01</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>a proteinase-activated receptor 2-activating peptide
  </Note>
  <Frequency>10</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009842</DescriptorUI>
     <DescriptorName>
      <String>Oligopeptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Proc Natl Acad Sci U S A 1998 Jun 23;95(13):7766-71</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0292936</ConceptUI>
    <ConceptName>
     <String>cinnamoyl-LIGRLO-amide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0292936</Concept1UI>
     <Concept2UI>M0292935</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T322941</TermUI>
      <String>cinnamoyl-LIGRLO-amide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0292935</ConceptUI>
    <ConceptName>
     <String>trans-cinnamoyl-leucyl-isoleucyl-glycyl-arginyl-leucyl-ornithinamide</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0292936</Concept1UI>
     <Concept2UI>M0292935</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T322940</TermUI>
      <String>trans-cinnamoyl-leucyl-isoleucyl-glycyl-arginyl-leucyl-ornithinamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T322939</TermUI>
      <String>trans-cinnamoyl-LIGRLO-NH2</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T688637</TermUI>
      <String>tc-LIGRLO-NH2</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>01</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T322938</TermUI>
      <String>tc-NH2</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C512648</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>NUDC protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>09</Month>
   <Day>22</Day>
  </DateCreated>
  <Note>RefSeq NM_006600
  </Note>
  <Frequency>37</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009687</DescriptorUI>
     <DescriptorName>
      <String>Nuclear Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D018797</DescriptorUI>
     <DescriptorName>
      <String>Cell Cycle Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0305387</ConceptUI>
    <ConceptName>
     <String>NUDC protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T645186</TermUI>
      <String>NUDC protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>07</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T645188</TermUI>
      <String>nuclear distribution gene C homolog (A. nidulans) protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>07</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T645187</TermUI>
      <String>HNUDC protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>07</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006141</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>MK 940</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>RN given refers to (trans)-isomer; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ANTIDEPRESSIVE AGENTS (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003986</DescriptorUI>
     <DescriptorName>
      <String>Dibenzocycloheptenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Am J Ophthalmol 76(5):641;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0048315</ConceptUI>
    <ConceptName>
     <String>MK 940</String>
    </ConceptName>
    <CASN1Name>(5 alpha,10 alpha,11 beta)-10,11-dihydro-5-(3-(methylamino)propyl)-5,10-epoxy-5H-dibenzo(a,d)cyclohepten-11-0l, (Z)-2-butenedioate (1:1) salt</CASN1Name>
    <RegistryNumber>5154-92-7</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>23239-40-9 (maleate[1:1](5alpha,10alpha,11beta)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>5154-91-6 ((cis)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0048315</Concept1UI>
     <Concept2UI>M0309452</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0048315</Concept1UI>
     <Concept2UI>M0048314</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0048315</Concept1UI>
     <Concept2UI>M0309453</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T078318</TermUI>
      <String>MK 940</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T078316</TermUI>
      <String>MK-940</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0309452</ConceptUI>
    <ConceptName>
     <String>MK 940, maleate (1:1), (5alpha,10alpha,11beta)-isomer</String>
    </ConceptName>
    <RegistryNumber>23239-40-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0048315</Concept1UI>
     <Concept2UI>M0309452</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T339452</TermUI>
      <String>MK 940, maleate (1:1), (5alpha,10alpha,11beta)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0048314</ConceptUI>
    <ConceptName>
     <String>trans-10,11-dihydro-5,10-epoxy-5-(3-(methylamino)propyl)-5H-dibenzo(a,d)cyclohepten-11-ol hydrogen maleate</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0048315</Concept1UI>
     <Concept2UI>M0048314</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T078317</TermUI>
      <String>trans-10,11-dihydro-5,10-epoxy-5-(3-(methylamino)propyl)-5H-dibenzo(a,d)cyclohepten-11-ol hydrogen maleate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0309453</ConceptUI>
    <ConceptName>
     <String>MK 940, (cis)-isomer</String>
    </ConceptName>
    <RegistryNumber>5154-91-6</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0048315</Concept1UI>
     <Concept2UI>M0309453</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T339453</TermUI>
      <String>MK 940, (cis)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C512649</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Nudc protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>09</Month>
   <Day>22</Day>
  </DateCreated>
  <Note>RefSeq NM_010948
  </Note>
  <Frequency>9</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009687</DescriptorUI>
     <DescriptorName>
      <String>Nuclear Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D018797</DescriptorUI>
     <DescriptorName>
      <String>Cell Cycle Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0486685</ConceptUI>
    <ConceptName>
     <String>Nudc protein, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T645189</TermUI>
      <String>Nudc protein, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>07</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T645191</TermUI>
      <String>Silica-induced gene 92 protein, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>07</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T645190</TermUI>
      <String>nuclear distribution gene C homolog (Aspergillus) protein, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>07</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T645192</TermUI>
      <String>SIG-92 protein, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>07</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C482174</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bonactin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>03</Month>
   <Day>02</Day>
  </DateCreated>
  <Note>from the liquid culture of a Streptomyces sp.; structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005663</DescriptorUI>
     <DescriptorName>
      <String>Furans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2003 Sep;66(9):1291-3</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0461667</ConceptUI>
    <ConceptName>
     <String>bonactin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T575046</TermUI>
      <String>bonactin</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>03</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C115691</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>F18 protein, Equus caballus</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>12</Month>
   <Day>03</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>03</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>gene has high sequence similarity to human F18 gene; GenBank U46023
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011506</DescriptorUI>
     <DescriptorName>
      <String>Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Anim Genet 1998 Oct;29(5):381-4</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0297779</ConceptUI>
    <ConceptName>
     <String>F18 protein, Equus caballus</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T521610</TermUI>
      <String>F18 protein, Equus caballus</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>10</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C095642</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>CEL-IV, Cucumaria echinata</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>10</Month>
   <Day>16</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>08</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>a calcium-dependent lectin; from the marine invertebrate Cucumaria echinata; has 157 amino acid residues; MW 17,098 Da; amino acid sequence given in first source
  </Note>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*LECTINS (1995-2002)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D037181</DescriptorUI>
     <DescriptorName>
      <String>Lectins, C-Type</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biosci Biotech Biochem 1995 Jul;59(7):1314-7</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0251812</ConceptUI>
    <ConceptName>
     <String>CEL-IV, Cucumaria echinata</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T495203</TermUI>
      <String>CEL-IV, Cucumaria echinata</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>05</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T281817</TermUI>
      <String>CEL-IV lectin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C403136</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-glycidoxypropyltrimethoxysilane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>01</Month>
   <Day>24</Day>
  </DateCreated>
  <DateRevised>
   <Year>2007</Year>
   <Month>01</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>63</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012821</DescriptorUI>
     <DescriptorName>
      <String>Silanes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Int Arch Occup Environ Health 1999 Nov;72(8):539-45</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0355965</ConceptUI>
    <ConceptName>
     <String>3-glycidoxypropyltrimethoxysilane</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T405644</TermUI>
      <String>3-glycidoxypropyltrimethoxysilane</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>01</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T688639</TermUI>
      <String>glycid-oxi-propyl-trimetil-oxi-silane</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>01</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T405645</TermUI>
      <String>3-GPTMS</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>01</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C037061</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>UDPglucose-glycoprotein glucose-1-phosphotransferase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1983</Year>
   <Month>02</Month>
   <Day>15</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>05</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>from embryonic chicken neural retina; glucose is linked by phosphodiester bonds to mannose of a cell surface glycoprotein; catalyzes the transfer of alpha Glc-1-P from UDP-Glc to mannose residues on acceptor glycoproteins
  </Note>
  <Frequency>10</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PHOSPHOTRANSFERASES (83-93)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D017855</DescriptorUI>
     <DescriptorName>
      <String>Transferases (Other Substituted Phosphate Groups)</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cell 1982;31(2):739</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0112404</ConceptUI>
    <ConceptName>
     <String>UDPglucose-glycoprotein glucose-1-phosphotransferase</String>
    </ConceptName>
    <RegistryNumber>EC 2.7.8.19</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T142408</TermUI>
      <String>UDPglucose-glycoprotein glucose-1-phosphotransferase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T142407</TermUI>
      <String>GlcPTase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T142406</TermUI>
      <String>Glc-phosphotransferase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C037363</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>UDPgalactose - UDP-N-acetylglucosamine galactosephosphotransferase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1983</Year>
   <Month>03</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>05</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>forms UDP N-acetylglucosamine-6-phosphogalactose
  </Note>
  <Frequency>6</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PHOSPHOTRANSFERASES (83-93)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D017855</DescriptorUI>
     <DescriptorName>
      <String>Transferases (Other Substituted Phosphate Groups)</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>FEBS Lett 1983;151(1):15</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0113131</ConceptUI>
    <ConceptName>
     <String>UDPgalactose - UDP-N-acetylglucosamine galactosephosphotransferase</String>
    </ConceptName>
    <RegistryNumber>EC 2.7.8.18</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T143135</TermUI>
      <String>UDPgalactose - UDP-N-acetylglucosamine galactosephosphotransferase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T143133</TermUI>
      <String>UDPgalactose-N-acetylglucosamine galactose-1-phosphotransferase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T143134</TermUI>
      <String>galactose-1-phosphotransferase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006089</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ICR 340</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>ICR acridine half-mustard cpd; RN &amp; NM refer to di-HCl
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ACRIDINES (75-80)</PreviousIndexing>
   <PreviousIndexing>*NAPHTHYRIDINES (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009588</DescriptorUI>
     <DescriptorName>
      <String>Nitrogen Mustard Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Proc Natl Acad Sci USA 71(11):4416;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0048191</ConceptUI>
    <ConceptName>
     <String>ICR 340</String>
    </ConceptName>
    <CASN1Name>N-(2-chloroethyl)-N'-(7-chloro-2-methoxybenzo(b)-1,5-naphthyridin-10-yl)-N-ethyl-1,3-propanediamine, dihydrochloride</CASN1Name>
    <RegistryNumber>38915-28-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T078194</TermUI>
      <String>ICR 340</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T078193</TermUI>
      <String>ICR-340</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C451260</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>PIN4 protein, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>04</Month>
   <Day>05</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>10</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>auxin transporter that mediates sink-driven auxin gradients and root patterning in Arabidopsis; amino acid sequence in first source
  </Note>
  <Frequency>26</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*Carrier Proteins (2002-2004)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D026901</DescriptorUI>
     <DescriptorName>
      <String>Membrane Transport Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cell 2002 Mar 8;108(5):661-73</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0419730</ConceptUI>
    <ConceptName>
     <String>PIN4 protein, Arabidopsis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T488764</TermUI>
      <String>PIN4 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>04</Month>
       <Day>05</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T570679</TermUI>
      <String>PIN-FORMED 4 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>01</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T488765</TermUI>
      <String>AtPIN4 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>04</Month>
       <Day>05</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C071768</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>picrasinoside H</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1991</Year>
   <Month>12</Month>
   <Day>24</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>08</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>from Picrasma ailanthoides; structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>GLAUCARUBIN/*AA (1991-2002)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D036702</DescriptorUI>
     <DescriptorName>
      <String>Quassins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D032270</DescriptorUI>
     <DescriptorName>
      <String>Picrasma</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Nat Prod 1991;54(3):844</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0194812</ConceptUI>
    <ConceptName>
     <String>picrasinoside H</String>
    </ConceptName>
    <CASN1Name>Picras-2-en-1-one, 13-(acetyloxy)-16-(beta-D-glucopyranosyloxy)-2-methoxy-11,12-(methylenebis(oxy))-, (11alpha,12beta,16alpha)-</CASN1Name>
    <RegistryNumber>135638-54-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T224817</TermUI>
      <String>picrasinoside H</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002553</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>caroxin D</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>fluorocarbon liquid C10F2202
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*HYDROCARBONS, HALOGENATED (73-74)</PreviousIndexing>
   <PreviousIndexing>FLUORINE (73-74)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005466</DescriptorUI>
     <DescriptorName>
      <String>Fluorocarbons</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Anesthesiology 38(2):134;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043206</ConceptUI>
    <ConceptName>
     <String>caroxin D</String>
    </ConceptName>
    <RegistryNumber>23228-90-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073209</TermUI>
      <String>caroxin D</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C511026</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>diplobifuranylone A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>06</Month>
   <Day>16</Day>
  </DateCreated>
  <Note>produced by Diplodia corticola, a fungus pathogen of cork oak; structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005663</DescriptorUI>
     <DescriptorName>
      <String>Furans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2006 Apr;69(4):671-4</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0498984</ConceptUI>
    <ConceptName>
     <String>diplobifuranylone A</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T676044</TermUI>
      <String>diplobifuranylone A</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>06</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002557</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cholesterol 7 beta-hydroperoxide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CHOLESTEROL (73-75)</PreviousIndexing>
   <PreviousIndexing>*PEROXIDES (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002784</DescriptorUI>
     <DescriptorName>
      <String>Cholesterol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 38(1):119;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043209</ConceptUI>
    <ConceptName>
     <String>cholesterol 7 beta-hydroperoxide</String>
    </ConceptName>
    <RegistryNumber>35455-44-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073212</TermUI>
      <String>cholesterol 7 beta-hydroperoxide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C479821</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Ear2 protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>12</Month>
   <Day>19</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>06</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>do not confuse with Nr2f6 protein, which is also known as ear-2, RefSeq NM_007895
  </Note>
  <Frequency>9</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*RIBONUCLEASES (2003-2004)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D047208</DescriptorUI>
     <DescriptorName>
      <String>Eosinophil-Derived Neurotoxin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Circ Res. 2003 May 16;92(9):1033-40</Source>
   <Source>Gene 2001 Apr 4;267(1):23-30</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0457819</ConceptUI>
    <ConceptName>
     <String>Ear2 protein, mouse</String>
    </ConceptName>
    <RegistryNumber>EC 3.1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T564954</TermUI>
      <String>Ear2 protein, mouse</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>19</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T647579</TermUI>
      <String>Rnase2 protein, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>07</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T564953</TermUI>
      <String>mEAR2 protein, mouse</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>19</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T564952</TermUI>
      <String>eosinophil-associated RNase 2, mouse</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>19</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T584443</TermUI>
      <String>eosinophil-associated, ribonuclease A family, member 2 protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>04</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006927</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Cassella 7657</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>05</Month>
   <Day>14</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*MORPHOLINES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003374</DescriptorUI>
     <DescriptorName>
      <String>Coumarins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Int Pharmacodyn Ther 206(2):299;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049780</ConceptUI>
    <ConceptName>
     <String>Cassella 7657</String>
    </ConceptName>
    <CASN1Name>3-(gamma-morpholino-beta-(3',4',5'-trimethoxybenzyloxy)propyl-4-methyl-7,8-dimethoxycoumarin.HCl</CASN1Name>
    <RegistryNumber>52591-15-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079783</TermUI>
      <String>Cassella 7657</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006934</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cecekin vitrum</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005768</DescriptorUI>
     <DescriptorName>
      <String>Gastrointestinal Hormones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Gut 14(10):763;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049789</ConceptUI>
    <ConceptName>
     <String>cecekin vitrum</String>
    </ConceptName>
    <RegistryNumber>9012-22-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079792</TermUI>
      <String>cecekin vitrum</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C070827</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-azidoaniline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1991</Year>
   <Month>10</Month>
   <Day>09</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>RN given refers to parent cpd
  </Note>
  <Frequency>8</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000814</DescriptorUI>
     <DescriptorName>
      <String>Aniline Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001391</DescriptorUI>
     <DescriptorName>
      <String>Azo Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 1991;30(35):8605</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0192697</ConceptUI>
    <ConceptName>
     <String>4-azidoaniline</String>
    </ConceptName>
    <RegistryNumber>14860-64-1</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>91159-79-4 (HCl)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0192697</Concept1UI>
     <Concept2UI>M0325431</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T222702</TermUI>
      <String>4-azidoaniline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T222701</TermUI>
      <String>para-azidoaniline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0325431</ConceptUI>
    <ConceptName>
     <String>4-azidoaniline hydrochloride</String>
    </ConceptName>
    <RegistryNumber>91159-79-4</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0192697</Concept1UI>
     <Concept2UI>M0325431</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T355431</TermUI>
      <String>4-azidoaniline hydrochloride</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C074798</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-aminooctoylphenone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1992</Year>
   <Month>06</Month>
   <Day>28</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure given in first source; protects against the effects of cyanide on hemoglobin
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000814</DescriptorUI>
     <DescriptorName>
      <String>Aniline Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007659</DescriptorUI>
     <DescriptorName>
      <String>Ketones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Gen Pharmacol 1992 Jan;23(1):19-25</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0201820</ConceptUI>
    <ConceptName>
     <String>4-aminooctoylphenone</String>
    </ConceptName>
    <RegistryNumber>63884-78-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T231825</TermUI>
      <String>4-aminooctoylphenone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T231823</TermUI>
      <String>4-PAOP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T231824</TermUI>
      <String>para-aminooctoylphenone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006949</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ceramide pentasaccharide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CEREBROSIDES (74-76)</PreviousIndexing>
   <PreviousIndexing>OLIGOSACCHARIDES (74-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006028</DescriptorUI>
     <DescriptorName>
      <String>Glycosphingolipids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 249(4):1022;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049805</ConceptUI>
    <ConceptName>
     <String>ceramide pentasaccharide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079808</TermUI>
      <String>ceramide pentasaccharide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008380</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>metamizil</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>RN given refers to parent cpd; structure
  </Note>
  <Frequency>24</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BENZILATES (74-78)</PreviousIndexing>
   <PreviousIndexing>DIETHYLAMINES (74-78)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D001535</DescriptorUI>
     <DescriptorName>
      <String>Benactyzine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Endodrinologie 71(2):149;1978</Source>
   <Source>Horm Brain Funct:WL300:1601H:243;1971</Source>
   <Source>Klin Med (Mosk) 56(9):113;1978</Source>
   <Source>Klin Med(Mosk) 1979;57(9):59</Source>
   <Source>Pharmacol Biochem Behav 2(1):1;1974</Source>
   <Source>Vestn Dermatol Venerol 1979;9:3</Source>
   <Source>Vrach Delo 3:122;1978</Source>
   <Source>Zh Nevropatol Psikhiatr 78(3):365;1978</Source>
   <Source>Zh Vyssh Nerv Deiat 26(1):181;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0052180</ConceptUI>
    <ConceptName>
     <String>metamizil</String>
    </ConceptName>
    <RegistryNumber>57-36-3</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>10503-18-1 (HCl)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0052180</Concept1UI>
     <Concept2UI>M0310271</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T082183</TermUI>
      <String>metamizil</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T082181</TermUI>
      <String>methamisil</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T082182</TermUI>
      <String>methylbenactyzine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T082180</TermUI>
      <String>metamyzil</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0310271</ConceptUI>
    <ConceptName>
     <String>metamizil hydrochloride</String>
    </ConceptName>
    <RegistryNumber>10503-18-1</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0052180</Concept1UI>
     <Concept2UI>M0310271</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T340271</TermUI>
      <String>metamizil hydrochloride</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T082179</TermUI>
      <String>beta-diethylaminopropylbenzilic acid ester, hydrochloride</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C102373</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>glycoprotein PE2, Sindbis virus</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>12</Month>
   <Day>27</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>03</Month>
   <Day>22</Day>
  </DateRevised>
  <Note>has been sequenced
  </Note>
  <Frequency>11</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008562</DescriptorUI>
     <DescriptorName>
      <String>Membrane Glycoproteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011498</DescriptorUI>
     <DescriptorName>
      <String>Protein Precursors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014764</DescriptorUI>
     <DescriptorName>
      <String>Viral Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Virol 1996 Nov;70(11):7910-20</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0268093</ConceptUI>
    <ConceptName>
     <String>glycoprotein PE2, Sindbis virus</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0268093</Concept1UI>
     <Concept2UI>M0268091</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T298098</TermUI>
      <String>glycoprotein PE2, Sindbis virus</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T298095</TermUI>
      <String>PE(2) glycoprotein, Sindbis virus</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T298097</TermUI>
      <String>glycoprotein PE(2), Sindbis virus</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0268091</ConceptUI>
    <ConceptName>
     <String>glycoprotein E precursor protein, Sindbis virus</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0268093</Concept1UI>
     <Concept2UI>M0268091</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T298096</TermUI>
      <String>glycoprotein E precursor protein, Sindbis virus</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006960</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>chelex</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1970</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Frequency>86</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011137</DescriptorUI>
     <DescriptorName>
      <String>Polystyrenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011145</DescriptorUI>
     <DescriptorName>
      <String>Polyvinyls</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D007475</DescriptorUI>
     <DescriptorName>
      <String>Ion Exchange Resins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
    <PharmacologicalActionList>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D002614</DescriptorUI>
        <DescriptorName>
         <String>Chelating Agents</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
    </PharmacologicalActionList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049822</ConceptUI>
    <ConceptName>
     <String>chelex</String>
    </ConceptName>
    <RegistryNumber>80208-96-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079825</TermUI>
      <String>chelex</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006963</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>chlamydocin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>10</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>18</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ETHERS, CYCLIC (74-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010456</DescriptorUI>
     <DescriptorName>
      <String>Peptides, Cyclic</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Europ J Cancer 10(12):801;1974</Source>
   <Source>Helv Chim Acta 57(3):533;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049826</ConceptUI>
    <ConceptName>
     <String>chlamydocin</String>
    </ConceptName>
    <RegistryNumber>53342-16-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079829</TermUI>
      <String>chlamydocin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006966</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>chlorcolchicine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*COLCHICINE (74-75)</PreviousIndexing>
   <PreviousIndexing>CHLORINE (74-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003078</DescriptorUI>
     <DescriptorName>
      <String>Colchicine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Schweiz Med Wochenschr 104(8):265;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049828</ConceptUI>
    <ConceptName>
     <String>chlorcolchicine</String>
    </ConceptName>
    <RegistryNumber>26279-89-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079831</TermUI>
      <String>chlorcolchicine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C084408</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-methyl-4,6-bis(N,N-dimethylaminophenyl)pyrylium</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1993</Year>
   <Month>12</Month>
   <Day>22</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>RN refers to iodide; structure given in first source
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000814</DescriptorUI>
     <DescriptorName>
      <String>Aniline Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011714</DescriptorUI>
     <DescriptorName>
      <String>Pyrans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nucleic Acids Symp Ser 1993;(29):83-4</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0224255</ConceptUI>
    <ConceptName>
     <String>2-methyl-4,6-bis(N,N-dimethylaminophenyl)pyrylium</String>
    </ConceptName>
    <RegistryNumber>151921-86-7</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0224255</Concept1UI>
     <Concept2UI>M0224254</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T254260</TermUI>
      <String>2-methyl-4,6-bis(N,N-dimethylaminophenyl)pyrylium</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T254258</TermUI>
      <String>2-Me-bis(diMeNHPh)pyrylium</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0224254</ConceptUI>
    <ConceptName>
     <String>2-methyl-4,6-bis(N,N-dimethylaminophenyl)pyrylium iodide</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0224255</Concept1UI>
     <Concept2UI>M0224254</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T254259</TermUI>
      <String>2-methyl-4,6-bis(N,N-dimethylaminophenyl)pyrylium iodide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C084409</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-methyl-4,6-bis-(N,N-dimethylaminophenyl)thiopyrylium</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1993</Year>
   <Month>12</Month>
   <Day>22</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>RN refers to iodide; structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000814</DescriptorUI>
     <DescriptorName>
      <String>Aniline Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013876</DescriptorUI>
     <DescriptorName>
      <String>Thiophenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nucleic Acids Symp Ser 1993;(29):83-4</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0224258</ConceptUI>
    <ConceptName>
     <String>2-methyl-4,6-bis-(N,N-dimethylaminophenyl)thiopyrylium</String>
    </ConceptName>
    <RegistryNumber>151921-87-8</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0224258</Concept1UI>
     <Concept2UI>M0224257</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T254263</TermUI>
      <String>2-methyl-4,6-bis-(N,N-dimethylaminophenyl)thiopyrylium</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T254261</TermUI>
      <String>2-Me-bis(diMeNHPh)thiopyrylium</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0224257</ConceptUI>
    <ConceptName>
     <String>2-methyl-4,6-bis-(N,N-dimethylaminophenyl)thiopyrylium iodide</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0224258</Concept1UI>
     <Concept2UI>M0224257</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T254262</TermUI>
      <String>2-methyl-4,6-bis-(N,N-dimethylaminophenyl)thiopyrylium iodide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006975</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-chloroacetyltyramine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*TYRAMINE (74-75)</PreviousIndexing>
   <PreviousIndexing>ACETIC ACIDS (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014439</DescriptorUI>
     <DescriptorName>
      <String>Tyramine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Am Chem Soc 96(8):2564;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049841</ConceptUI>
    <ConceptName>
     <String>N-chloroacetyltyramine</String>
    </ConceptName>
    <CASN1Name>Acetamide, 2-chloro-N-(2-(4-hydroxyphenyl)ethyl)-</CASN1Name>
    <RegistryNumber>52399-83-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079844</TermUI>
      <String>N-chloroacetyltyramine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C078847</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cycMs2 protein, Medicago sativa</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1993</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>10</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>amino acid sequence given in first source; isolated from alfalfa; shows high homology with type B cyclins; a true cell division marker at the mRNA level; expressed in young leaves but not in mature leaves
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010940</DescriptorUI>
     <DescriptorName>
      <String>Plant Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D016213</DescriptorUI>
     <DescriptorName>
      <String>Cyclins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Plant Cell 1992 Dec;4(12):1531-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0211249</ConceptUI>
    <ConceptName>
     <String>cycMs2 protein, Medicago sativa</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T241253</TermUI>
      <String>cycMs2 protein, Medicago sativa</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006979</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-chloro-ATP</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>new ATP analog; relaxes mammalian gut preparations; structure
  </Note>
  <Frequency>13</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ATP (74-75)</PreviousIndexing>
   <PreviousIndexing>CHLORINE (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000255</DescriptorUI>
     <DescriptorName>
      <String>Adenosine Triphosphate</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 16(10):1188;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049850</ConceptUI>
    <ConceptName>
     <String>2-chloro-ATP</String>
    </ConceptName>
    <CASN1Name>2-chloroadenosine-5-triphosphate</CASN1Name>
    <RegistryNumber>49564-60-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079853</TermUI>
      <String>2-chloro-ATP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006980</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>chlorobactene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>10</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002338</DescriptorUI>
     <DescriptorName>
      <String>Carotenoids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem J 136(2):395;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049851</ConceptUI>
    <ConceptName>
     <String>chlorobactene</String>
    </ConceptName>
    <RegistryNumber>2932-09-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079854</TermUI>
      <String>chlorobactene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006985</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>16-alpha-chloroestrone methyl ether</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ESTRANES (74-75)</PreviousIndexing>
   <PreviousIndexing>17-KETOSTEROIDS (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004970</DescriptorUI>
     <DescriptorName>
      <String>Estrone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049863</ConceptUI>
    <ConceptName>
     <String>16-alpha-chloroestrone methyl ether</String>
    </ConceptName>
    <CASN1Name>16-alpha-chloro-3-methoxy-estra-1,3,5,(10)-trien-17- one</CASN1Name>
    <RegistryNumber>4091-75-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079866</TermUI>
      <String>16-alpha-chloroestrone methyl ether</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006988</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6-chloro-9-(6-deoxy-beta-L-lyxo-hexopyranosylulose)purine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>shows activity against KB cells; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>KETOSES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011684</DescriptorUI>
     <DescriptorName>
      <String>Purine Nucleosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Carbohyd Res 30(1):192;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049865</ConceptUI>
    <ConceptName>
     <String>6-chloro-9-(6-deoxy-beta-L-lyxo-hexopyranosylulose)purine</String>
    </ConceptName>
    <RegistryNumber>50615-82-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079868</TermUI>
      <String>6-chloro-9-(6-deoxy-beta-L-lyxo-hexopyranosylulose)purine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006990</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-chloro-beta,beta-difluoroamphetamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AMPHETAMINE (74-75)</PreviousIndexing>
   <PreviousIndexing>AMPHETAMINE/*analogs (75-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000662</DescriptorUI>
     <DescriptorName>
      <String>Amphetamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Int Pharmacodyn 208(2):274;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049867</ConceptUI>
    <ConceptName>
     <String>4-chloro-beta,beta-difluoroamphetamine</String>
    </ConceptName>
    <RegistryNumber>37410-86-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079870</TermUI>
      <String>4-chloro-beta,beta-difluoroamphetamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C086624</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-(4-N,N-dimethylaminophenyl)but-3-en-2-one</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>05</Month>
   <Day>05</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>RN given refers to compound with no isomeric designation; structure given in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000814</DescriptorUI>
     <DescriptorName>
      <String>Aniline Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002074</DescriptorUI>
     <DescriptorName>
      <String>Butanones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mutat Res 1994 Apr 1;306(1):71-80</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0229644</ConceptUI>
    <ConceptName>
     <String>4-(4-N,N-dimethylaminophenyl)but-3-en-2-one</String>
    </ConceptName>
    <RegistryNumber>5432-53-1</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>30625-58-2 ((E)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0229644</Concept1UI>
     <Concept2UI>M0326522</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T259649</TermUI>
      <String>4-(4-N,N-dimethylaminophenyl)but-3-en-2-one</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T259648</TermUI>
      <String>DMAPB</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0326522</ConceptUI>
    <ConceptName>
     <String>4-(4-N,N-dimethylaminophenyl)but-3-en-2-one, (E)-isomer</String>
    </ConceptName>
    <RegistryNumber>30625-58-2</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0229644</Concept1UI>
     <Concept2UI>M0326522</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T356522</TermUI>
      <String>4-(4-N,N-dimethylaminophenyl)but-3-en-2-one, (E)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C090913</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-benzylidene-4-chloroaniline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>01</Month>
   <Day>12</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000814</DescriptorUI>
     <DescriptorName>
      <String>Aniline Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Pharmacol 1994 Jul;46(7):585-90</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0240212</ConceptUI>
    <ConceptName>
     <String>N-benzylidene-4-chloroaniline</String>
    </ConceptName>
    <RegistryNumber>780-21-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T270217</TermUI>
      <String>N-benzylidene-4-chloroaniline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T270216</TermUI>
      <String>NBE4CA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T270215</TermUI>
      <String>4-chloro-N-(phenylmethylene)benzeneamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006998</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>chloroisobutyronitrile</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>06</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>BUTYRATES (74-82)</PreviousIndexing>
   <PreviousIndexing>HYDROCARBONS, CHLORINATED (74-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009570</DescriptorUI>
     <DescriptorName>
      <String>Nitriles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Soc Jap 93(10):1274;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049886</ConceptUI>
    <ConceptName>
     <String>chloroisobutyronitrile</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079889</TermUI>
      <String>chloroisobutyronitrile</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007001</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-chloromercuri-4,6-dinitrophenol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>13</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DINITROPHENOLS (74-77)</PreviousIndexing>
   <PreviousIndexing>*MERCURY (74-77)</PreviousIndexing>
   <PreviousIndexing>*ORGANOMETALLIC CPDS (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002730</DescriptorUI>
     <DescriptorName>
      <String>Chloromercurinitrophenols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D013439</DescriptorUI>
     <DescriptorName>
      <String>Sulfhydryl Reagents</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Arch Int Physiol Biochem 81(2):366;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049891</ConceptUI>
    <ConceptName>
     <String>2-chloromercuri-4,6-dinitrophenol</String>
    </ConceptName>
    <RegistryNumber>24579-91-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079894</TermUI>
      <String>2-chloromercuri-4,6-dinitrophenol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007003</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>10-chloro-2-methoxy-5-methyl-7H-pyrrolo(3,2,1-d,e)phenanthrid-7-one-4-acetic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1986</Year>
   <Month>08</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>rigid analog of indomethacin; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PYRROLES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010617</DescriptorUI>
     <DescriptorName>
      <String>Phenanthridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 17(2):167;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049892</ConceptUI>
    <ConceptName>
     <String>10-chloro-2-methoxy-5-methyl-7H-pyrrolo(3,2,1-d,e)phenanthrid-7-one-4-acetic acid</String>
    </ConceptName>
    <RegistryNumber>51806-88-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079895</TermUI>
      <String>10-chloro-2-methoxy-5-methyl-7H-pyrrolo(3,2,1-d,e)phenanthrid-7-one-4-acetic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007013</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6-chloro-9-(1,4-oxathian-2-yl)-9H-purine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>potential as antitumor or insecticidal &amp; acaricidal activity; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*HETEROCYCLIC COMPOUNDS (74-79)</PreviousIndexing>
   <PreviousIndexing>OXATHIINS (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011687</DescriptorUI>
     <DescriptorName>
      <String>Purines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Carbohyd Res 30(1):225;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049906</ConceptUI>
    <ConceptName>
     <String>6-chloro-9-(1,4-oxathian-2-yl)-9H-purine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079909</TermUI>
      <String>6-chloro-9-(1,4-oxathian-2-yl)-9H-purine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007014</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6-chloro-9-(1,4-oxathian-3-yl)-9H-purine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>potential as antitumor or insecticidal &amp; acaricidal activity; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*HETEROCYCLIC COMPOUNDS (74-79)</PreviousIndexing>
   <PreviousIndexing>OXATHIINS (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011687</DescriptorUI>
     <DescriptorName>
      <String>Purines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Carbohyd Res 30(1):225;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049907</ConceptUI>
    <ConceptName>
     <String>6-chloro-9-(1,4-oxathian-3-yl)-9H-purine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079910</TermUI>
      <String>6-chloro-9-(1,4-oxathian-3-yl)-9H-purine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C415647</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SGD1 protein, S cerevisiae</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>11</Month>
   <Day>14</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>11</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>an essential nuclear protein of Saccharomyces cerevisiae that affects expression of the GPD1 gene for glycerol 3-phosphate dehydrogenase; MW 102.8-kDa protein; has been sequenced
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009687</DescriptorUI>
     <DescriptorName>
      <String>Nuclear Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029701</DescriptorUI>
     <DescriptorName>
      <String>Saccharomyces cerevisiae Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>FEBS Lett. 2000 Oct 20;483(2-3);87-92</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0372651</ConceptUI>
    <ConceptName>
     <String>SGD1 protein, S cerevisiae</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T493503</TermUI>
      <String>SGD1 protein, S cerevisiae</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>05</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
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     </Term>
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   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C112826</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>quillaic acid 3-O-xylopyranosyl-1-3-(galactopyranosyl-1-2)glucopyranosiduronic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>07</Month>
   <Day>03</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>08</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>isolated from Quillaja saponaria; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009828</DescriptorUI>
     <DescriptorName>
      <String>Oleanolic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012503</DescriptorUI>
     <DescriptorName>
      <String>Saponins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Phytochemistry 1998 May;48(1):175-80</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0291630</ConceptUI>
    <ConceptName>
     <String>quillaic acid 3-O-xylopyranosyl-1-3-(galactopyranosyl-1-2)glucopyranosiduronic acid</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T321635</TermUI>
      <String>quillaic acid 3-O-xylopyranosyl-1-3-(galactopyranosyl-1-2)glucopyranosiduronic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T321634</TermUI>
      <String>quillaic acid 3-O-XylGalGlcUA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007021</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-chloropropionanilide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PROPIONATES (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000813</DescriptorUI>
     <DescriptorName>
      <String>Anilides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Pharmacol 22(20):2565;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049931</ConceptUI>
    <ConceptName>
     <String>4-chloropropionanilide</String>
    </ConceptName>
    <RegistryNumber>2759-54-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079934</TermUI>
      <String>4-chloropropionanilide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007023</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-chloro-3-(2-propynyloxy)-2-propanol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1995</Year>
   <Month>08</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ALCOHOL, PROPYL (74-75)</PreviousIndexing>
   <PreviousIndexing>ALKYNES (74-82)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002728</DescriptorUI>
     <DescriptorName>
      <String>Chlorohydrins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 62(11):1894;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049936</ConceptUI>
    <ConceptName>
     <String>1-chloro-3-(2-propynyloxy)-2-propanol</String>
    </ConceptName>
    <CASN1Name>2-Propanol, 1-chloro-3-(2-propynyloxy)-</CASN1Name>
    <RegistryNumber>18180-29-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079939</TermUI>
      <String>1-chloro-3-(2-propynyloxy)-2-propanol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C412287</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cell-elongating factor, Vibrio cholerae</String>
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  <DateCreated>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>21</Day>
  </DateCreated>
  <Note>causes elongation of Chinese hamster ovary (CHO) cells; amino acid sequence in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001427</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Toxins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D014734</DescriptorUI>
     <DescriptorName>
      <String>Vibrio cholerae</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Microb Pathog 2000 Jul;29(1):1-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0368341</ConceptUI>
    <ConceptName>
     <String>cell-elongating factor, Vibrio cholerae</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T422255</TermUI>
      <String>cell-elongating factor, Vibrio cholerae</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>08</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T422258</TermUI>
      <String>85-kDa CEF</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>08</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T422256</TermUI>
      <String>cell-elongating toxin, Vibrio cholerae</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>08</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T422257</TermUI>
      <String>Vibrio cholerae CEF</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>08</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007019</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-(4-chlorophenyl)silatrane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>rodenticide against rats &amp; mice; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BICYCLO COMPOUNDS (94-95)</PreviousIndexing>
   <PreviousIndexing>*SILICON (75-93)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D017646</DescriptorUI>
     <DescriptorName>
      <String>Organosilicon Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D019086</DescriptorUI>
     <DescriptorName>
      <String>Bridged Bicyclo Compounds, Heterocyclic</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Hygiene 73(1):39;1974</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049918</ConceptUI>
    <ConceptName>
     <String>5-(4-chlorophenyl)silatrane</String>
    </ConceptName>
    <CASN1Name>1-(p-chlorophenyl)-2,8,9-trioxa-5-aza-1-silabicyclo(3.3.3)undecane</CASN1Name>
    <RegistryNumber>29025-67-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079921</TermUI>
      <String>5-(4-chlorophenyl)silatrane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T079920</TermUI>
      <String>5-(p-chlorophenyl)silatrane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C480142</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>calicheamicin thetaII</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>01</Month>
   <Day>06</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>is a member of the enediyne class of antitumor antibiotics that bind to DNA and induce apoptosis
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000617</DescriptorUI>
     <DescriptorName>
      <String>Aminoglycosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011743</DescriptorUI>
     <DescriptorName>
      <String>Pyrimidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D053281</DescriptorUI>
     <DescriptorName>
      <String>Enediynes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Oncogene. 2003 Dec 11;22(57):9107-20</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0458375</ConceptUI>
    <ConceptName>
     <String>calicheamicin thetaII</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T567312</TermUI>
      <String>calicheamicin thetaII</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>01</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T672651</TermUI>
      <String>calicheamicin theta-2</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>04</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T672650</TermUI>
      <String>calicheamicin theta-II</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>04</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007047</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>christofin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>24</Day>
  </DateRevised>
  <Note>isolated from Rubia tinctorum L.; structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ETHOXY COMPOUNDS (75-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000880</DescriptorUI>
     <DescriptorName>
      <String>Anthraquinones</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Pharmazie 29(7):478;1974</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049978</ConceptUI>
    <ConceptName>
     <String>christofin</String>
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    <CASN1Name>1,4-dihydroxy-2-ethoxymethylanthraquinone</CASN1Name>
    <RegistryNumber>53755-57-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079981</TermUI>
      <String>christofin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C091456</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,5-difluoroaniline</String>
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  <DateCreated>
   <Year>1995</Year>
   <Month>02</Month>
   <Day>10</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000814</DescriptorUI>
     <DescriptorName>
      <String>Aniline Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Biol Interact 1995 Jan;94(1):49-72</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0241524</ConceptUI>
    <ConceptName>
     <String>2,5-difluoroaniline</String>
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    <RegistryNumber>367-30-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T271529</TermUI>
      <String>2,5-difluoroaniline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T271528</TermUI>
      <String>2,5-difluorobenzenamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T271527</TermUI>
      <String>2,5-difluoroaminobenzene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
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   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007056</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>chrysophenine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1969</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>05</Month>
   <Day>14</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*STILBENES (69-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001391</DescriptorUI>
     <DescriptorName>
      <String>Azo Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049986</ConceptUI>
    <ConceptName>
     <String>chrysophenine</String>
    </ConceptName>
    <CASN1Name>4,4'-bis((p-ethoxyphenyl)azo)-2,2'-stilbenesulfonic acid disodium salt</CASN1Name>
    <RegistryNumber>2870-32-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079989</TermUI>
      <String>chrysophenine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1969)</ThesaurusID>
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   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C023423</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>AI 3-35765</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>04</Month>
   <Day>03</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>07</Month>
   <Day>31</Day>
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  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010880</DescriptorUI>
     <DescriptorName>
      <String>Piperidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Entomol 1979;16(6):524</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0080657</ConceptUI>
    <ConceptName>
     <String>AI 3-35765</String>
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    <CASN1Name>1-(3-cyclohexen-1-ylcarbonyl)piperidine</CASN1Name>
    <RegistryNumber>52736-58-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0080657</Concept1UI>
     <Concept2UI>M0351442</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T110660</TermUI>
      <String>AI 3-35765</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T110659</TermUI>
      <String>AI3-35765</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T110658</TermUI>
      <String>AI-3-35765</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0351442</ConceptUI>
    <ConceptName>
     <String>2 piperidines-1-(3-cyclohexen-1-ylcarbonyl)piperidine</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0080657</Concept1UI>
     <Concept2UI>M0351442</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T401159</TermUI>
      <String>2 piperidines-1-(3-cyclohexen-1-ylcarbonyl)piperidine</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>12</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C092367</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>NC 1005</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>04</Month>
   <Day>03</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000814</DescriptorUI>
     <DescriptorName>
      <String>Aniline Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011812</DescriptorUI>
     <DescriptorName>
      <String>Quinuclidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Gen Pharmacol 1994 Oct;25(6):1149-56</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0243818</ConceptUI>
    <ConceptName>
     <String>NC 1005</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0243818</Concept1UI>
     <Concept2UI>M0243816</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T273823</TermUI>
      <String>NC 1005</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T273822</TermUI>
      <String>NC-1005</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0243816</ConceptUI>
    <ConceptName>
     <String>N-(azabicyclo(2.2.2)octan-3-yl)methyl-N-(2-indanyl)aniline hydrochloride</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0243818</Concept1UI>
     <Concept2UI>M0243816</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T273821</TermUI>
      <String>N-(azabicyclo(2.2.2)octan-3-yl)methyl-N-(2-indanyl)aniline hydrochloride</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C092368</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>NC 1006</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>04</Month>
   <Day>03</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000814</DescriptorUI>
     <DescriptorName>
      <String>Aniline Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011812</DescriptorUI>
     <DescriptorName>
      <String>Quinuclidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Gen Pharmacol 1994 Oct;25(6):1149-56</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0243821</ConceptUI>
    <ConceptName>
     <String>NC 1006</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0243821</Concept1UI>
     <Concept2UI>M0243819</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T273826</TermUI>
      <String>NC 1006</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T273825</TermUI>
      <String>NC-1006</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0243819</ConceptUI>
    <ConceptName>
     <String>N-(azabicyclo(2.2.2)octan-2-yl)methyl-N-(2-indanyl)aniline hydrochloride</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0243821</Concept1UI>
     <Concept2UI>M0243819</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T273824</TermUI>
      <String>N-(azabicyclo(2.2.2)octan-2-yl)methyl-N-(2-indanyl)aniline hydrochloride</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C099233</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>FCE 27677</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>06</Month>
   <Day>10</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000814</DescriptorUI>
     <DescriptorName>
      <String>Aniline Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010671</DescriptorUI>
     <DescriptorName>
      <String>Phenylurea Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D002785</DescriptorUI>
     <DescriptorName>
      <String>Sterol O-Acyltransferase</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
     <QualifierName>
      <String>antagonists &amp; inhibitors</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Lipid Res 1996 Jan;37(1):1-14</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0260522</ConceptUI>
    <ConceptName>
     <String>FCE 27677</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0260522</Concept1UI>
     <Concept2UI>M0260521</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T290527</TermUI>
      <String>FCE 27677</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T290525</TermUI>
      <String>FCE-27677</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0260521</ConceptUI>
    <ConceptName>
     <String>N-(2,6-bis(1-methylethyl)phenyl)-N'-(2-(4-dimethylaminophenyl)-4,5-dimethyldioxolan-2-yl)methylurea hydrochloride</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0260522</Concept1UI>
     <Concept2UI>M0260521</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T290526</TermUI>
      <String>N-(2,6-bis(1-methylethyl)phenyl)-N'-(2-(4-dimethylaminophenyl)-4,5-dimethyldioxolan-2-yl)methylurea hydrochloride</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C085797</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>auxin regulated proteins, Vigna radiata</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>03</Month>
   <Day>14</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>01</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>from mung bean, Vigna radiata; ARG2 is 39% identical to LEA5-A protein from cotton; ARG1 is 69% identical to delta(15) fatty-acid desaturase; amino acid sequence given in first source amino acid sequence given in first source
  </Note>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*GROWTH SUBSTANCES (1994-2003)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010940</DescriptorUI>
     <DescriptorName>
      <String>Plant Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Planta 1994;192(3):359-64</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0227617</ConceptUI>
    <ConceptName>
     <String>auxin regulated proteins, Vigna radiata</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0227617</Concept1UI>
     <Concept2UI>M0430973</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0227617</Concept1UI>
     <Concept2UI>M0227614</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T504101</TermUI>
      <String>auxin regulated proteins, Vigna radiata</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>07</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0430973</ConceptUI>
    <ConceptName>
     <String>ARG2 protein, Vigna radiata</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0227617</Concept1UI>
     <Concept2UI>M0430973</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T504106</TermUI>
      <String>ARG2 protein, Vigna radiata</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>07</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0227614</ConceptUI>
    <ConceptName>
     <String>ARG1 protein, Vigna radiata</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0227617</Concept1UI>
     <Concept2UI>M0227614</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T504089</TermUI>
      <String>ARG1 protein, Vigna radiata</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>07</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007096</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cobalt-9-methyladenine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>10</Month>
   <Day>07</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ADENINE (74-75)</PreviousIndexing>
   <PreviousIndexing>*ORGANOMETALLIC COMPOUNDS (74-82)</PreviousIndexing>
   <PreviousIndexing>COBALT (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000225</DescriptorUI>
     <DescriptorName>
      <String>Adenine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 324(2):301;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050060</ConceptUI>
    <ConceptName>
     <String>cobalt-9-methyladenine</String>
    </ConceptName>
    <CASN1Name>Cobalt, dichloro(9-methyl-9H-purin-6-amine-N(1))-, homopolymer, stereoisomer</CASN1Name>
    <RegistryNumber>52639-70-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080063</TermUI>
      <String>cobalt-9-methyladenine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C085782</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>coat protein, Enterobacteria phage fr</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>03</Month>
   <Day>14</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>01</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>contains 129 amino acids; acts as a translational repressor of phage replicase; partial amino acid sequence given in first source
  </Note>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CAPSID (1994-2003)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D036022</DescriptorUI>
     <DescriptorName>
      <String>Capsid Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Protein Eng 1993 Nov;6(8):883-91</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0227576</ConceptUI>
    <ConceptName>
     <String>coat protein, Enterobacteria phage fr</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T566990</TermUI>
      <String>coat protein, Enterobacteria phage fr</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>01</Month>
       <Day>05</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T549955</TermUI>
      <String>coat protein, phage fr</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>09</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007099</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cobramine B</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PROTEINS (74-78)</PreviousIndexing>
   <PreviousIndexing>*SNAKE VENOMS (75-78)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004179</DescriptorUI>
     <DescriptorName>
      <String>Cobra Cardiotoxin Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Biochem Biophys 156(1):71;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050064</ConceptUI>
    <ConceptName>
     <String>cobramine B</String>
    </ConceptName>
    <RegistryNumber>12777-56-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080067</TermUI>
      <String>cobramine B</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007114</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>conopharyngine pseudoindoxyl</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>06</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>from Tabernamontana pachysiphon Stapf. var cumminsii (Staph.) H. Huber
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>INDOLES (74-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000470</DescriptorUI>
     <DescriptorName>
      <String>Alkaloids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Pharmacol 25(10):820;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050094</ConceptUI>
    <ConceptName>
     <String>conopharyngine pseudoindoxyl</String>
    </ConceptName>
    <RegistryNumber>52579-71-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080097</TermUI>
      <String>conopharyngine pseudoindoxyl</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007118</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>copper-bis-N,N,-dihydroxyethylglycine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>01</Month>
   <Day>06</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*COPPER (74-82)</PreviousIndexing>
   <PreviousIndexing>GLYCINE (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005998</DescriptorUI>
     <DescriptorName>
      <String>Glycine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Comp Gen Pharmacol 4(16):315;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050098</ConceptUI>
    <ConceptName>
     <String>copper-bis-N,N,-dihydroxyethylglycine</String>
    </ConceptName>
    <RegistryNumber>54873-37-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080101</TermUI>
      <String>copper-bis-N,N,-dihydroxyethylglycine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007126</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>coriolan</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>07</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>polysaccharide from Coriolus versicolor Composed of 1-2 or 1-6 linked glucopyranose residues
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*POLYSACCHARIDES (75-79)</PreviousIndexing>
   <PreviousIndexing>GLUCOSE (75-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005936</DescriptorUI>
     <DescriptorName>
      <String>Glucans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Folia Pharm Jpn 72(1):77;1976</Source>
   <Source>Jpn J Pharmacol 1979;29(6):953</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050113</ConceptUI>
    <ConceptName>
     <String>coriolan</String>
    </ConceptName>
    <RegistryNumber>54328-34-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080116</TermUI>
      <String>coriolan</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007128</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>coriose</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*KETOSES (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006539</DescriptorUI>
     <DescriptorName>
      <String>Heptoses</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Pharm Bull 22(7):1624;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050115</ConceptUI>
    <ConceptName>
     <String>coriose</String>
    </ConceptName>
    <CASN1Name>D-altro-3-heptulose</CASN1Name>
    <RegistryNumber>13059-96-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080118</TermUI>
      <String>coriose</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007187</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cyclo-CTP</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CYTOSINE NUCLEOTIDES (74-79)</PreviousIndexing>
   <PreviousIndexing>ANHYDRIDES (74-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003570</DescriptorUI>
     <DescriptorName>
      <String>Cytidine Triphosphate</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009712</DescriptorUI>
     <DescriptorName>
      <String>Nucleotides, Cyclic</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Pharmacol 22(22):2829;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050224</ConceptUI>
    <ConceptName>
     <String>cyclo-CTP</String>
    </ConceptName>
    <CASN1Name>Triphosphoric acid, P-((2,3,3a,9a-tetrahydro-3-hydroxy-6-imino-6H-furo(2',3':4,5)oxazolo(3,2-a)pyrimidin-2-yl)methyl) ester, monohydrochloride, (2R-(2alpha,3beta,3abeta,9abeta))-</CASN1Name>
    <RegistryNumber>76248-24-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080227</TermUI>
      <String>cyclo-CTP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T080226</TermUI>
      <String>cyclocytidine 5'-triphosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007151</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>S-crotonyl-N-acetylcysteamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>17</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CYSTEAMINE (74-75)</PreviousIndexing>
   <PreviousIndexing>CROTONATES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003543</DescriptorUI>
     <DescriptorName>
      <String>Cysteamine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemical J 135(3):385;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050160</ConceptUI>
    <ConceptName>
     <String>S-crotonyl-N-acetylcysteamine</String>
    </ConceptName>
    <RegistryNumber>23784-20-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080163</TermUI>
      <String>S-crotonyl-N-acetylcysteamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C050216</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>9-(1-hydroxy-4-phosphinyl-2-butoxymethyl)guanine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1986</Year>
   <Month>11</Month>
   <Day>19</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>07</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>GUANINE/*analogs and derivatives (86-97)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D015774</DescriptorUI>
     <DescriptorName>
      <String>Ganciclovir</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Antiviral Res 1986;6(5):299</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0143524</ConceptUI>
    <ConceptName>
     <String>9-(1-hydroxy-4-phosphinyl-2-butoxymethyl)guanine</String>
    </ConceptName>
    <RegistryNumber>104880-60-6</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0143524</Concept1UI>
     <Concept2UI>M0143521</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T173529</TermUI>
      <String>9-(1-hydroxy-4-phosphinyl-2-butoxymethyl)guanine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1986)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T173525</TermUI>
      <String>HPBMG</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1986)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0143521</ConceptUI>
    <ConceptName>
     <String>SR 3773</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0143524</Concept1UI>
     <Concept2UI>M0143521</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T173526</TermUI>
      <String>SR 3773</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1986)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T173528</TermUI>
      <String>SR3773</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1986)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T173527</TermUI>
      <String>SR-3773</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1986)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007154</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>crotyl phosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>07</Month>
   <Day>11</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ORGANOPHOSPHORUS COMPOUNDS (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000440</DescriptorUI>
     <DescriptorName>
      <String>Butanols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Xenobiotica 1(1):55;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050164</ConceptUI>
    <ConceptName>
     <String>crotyl phosphate</String>
    </ConceptName>
    <RegistryNumber>33170-77-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080167</TermUI>
      <String>crotyl phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C110878</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SA 6541</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>03</Month>
   <Day>17</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>inhibits leukotriene A4 hydrolase; structure in first source
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000814</DescriptorUI>
     <DescriptorName>
      <String>Aniline Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003545</DescriptorUI>
     <DescriptorName>
      <String>Cysteine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Pharmacol 1998 Feb 1;55(3):297-304</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0287324</ConceptUI>
    <ConceptName>
     <String>SA 6541</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0287324</Concept1UI>
     <Concept2UI>M0287322</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T317329</TermUI>
      <String>SA 6541</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T317328</TermUI>
      <String>SA-6541</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0287322</ConceptUI>
    <ConceptName>
     <String>S-(4-dimethylaminobenzyl)-N-(3-mercapto-2-methylpropionyl)cysteine</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0287324</Concept1UI>
     <Concept2UI>M0287322</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T317327</TermUI>
      <String>S-(4-dimethylaminobenzyl)-N-(3-mercapto-2-methylpropionyl)cysteine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C025080</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Peruvian balsam</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>07</Month>
   <Day>09</Day>
  </DateCreated>
  <DateRevised>
   <Year>2015</Year>
   <Month>11</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>used in treatment of radiation skin injuries in USSR; RN given refers to cpd with unknown MF; see also Peru balsam white: 8023-64-1
  </Note>
  <Frequency>161</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001453</DescriptorUI>
     <DescriptorName>
      <String>Balsams</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Farmakol Toksikol 1980;43(1):97</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0084028</ConceptUI>
    <ConceptName>
     <String>Peruvian balsam</String>
    </ConceptName>
    <CASN1Name>balsams, peru</CASN1Name>
    <RegistryNumber>8P5F881OCY</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>8007-00-9 (Peruvian balsam)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T114031</TermUI>
      <String>Peruvian balsam</String>
      <ThesaurusIDlist>
       <ThesaurusID>FDA SRS (2015)</ThesaurusID>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T114030</TermUI>
      <String>balsam of Peru</String>
      <ThesaurusIDlist>
       <ThesaurusID>FDA SRS (2015)</ThesaurusID>
       <ThesaurusID>INN (19XX)</ThesaurusID>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007890</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>guanidinoacetylglycine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>GLYCINE (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005998</DescriptorUI>
     <DescriptorName>
      <String>Glycine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006146</DescriptorUI>
     <DescriptorName>
      <String>Guanidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biochem (Tokyo): 75(4):825;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051346</ConceptUI>
    <ConceptName>
     <String>guanidinoacetylglycine</String>
    </ConceptName>
    <CASN1Name>Glycine, N-(N-(aminoiminomethyl)glycyl)-</CASN1Name>
    <RegistryNumber>2446-72-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081349</TermUI>
      <String>guanidinoacetylglycine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C511867</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>VHA-8 protein, C elegans</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>07</Month>
   <Day>19</Day>
  </DateCreated>
  <DateRevised>
   <Year>2007</Year>
   <Month>06</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>expressed in hypodermis, intestine, and H-shaped excretory cells
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D025262</DescriptorUI>
     <DescriptorName>
      <String>Vacuolar Proton-Translocating ATPases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029742</DescriptorUI>
     <DescriptorName>
      <String>Caenorhabditis elegans Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D021122</DescriptorUI>
     <DescriptorName>
      <String>Protein Subunits</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>FEBS Lett 2006 May 29;580(13):3161-6</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0500011</ConceptUI>
    <ConceptName>
     <String>VHA-8 protein, C elegans</String>
    </ConceptName>
    <RegistryNumber>EC 3.6.1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T678221</TermUI>
      <String>VHA-8 protein, C elegans</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>07</Month>
       <Day>19</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T678222</TermUI>
      <String>V-ATPase subunit E, C elegans</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>07</Month>
       <Day>19</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T678223</TermUI>
      <String>E subunit, V-ATPase, C elegans</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>07</Month>
       <Day>19</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C431426</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>thioplatin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>07</Month>
   <Day>26</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009944</DescriptorUI>
     <DescriptorName>
      <String>Organoplatinum Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013457</DescriptorUI>
     <DescriptorName>
      <String>Sulfur Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Chemother Pharmacol 2001 Jun;47(6):461-6</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0394212</ConceptUI>
    <ConceptName>
     <String>thioplatin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T455409</TermUI>
      <String>thioplatin</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>07</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007910</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>kamolol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>terpenoids from Ferula penninervis; structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>COUMARINS (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012717</DescriptorUI>
     <DescriptorName>
      <String>Sesquiterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Experientia 30(3):224;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051381</ConceptUI>
    <ConceptName>
     <String>kamolol</String>
    </ConceptName>
    <CASN1Name>7-((decahydro-7-hydroxy-1,4a,5,6-tetramethyl-1- naphthenyl)methoxy)-2H-1-benzopyran-2-one</CASN1Name>
    <RegistryNumber>58939-88-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081384</TermUI>
      <String>kamolol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007911</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>heliogen blue SBL</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>01</Month>
   <Day>05</Day>
  </DateRevised>
  <Frequency>6</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*INDOLES (74-77)</PreviousIndexing>
   <PreviousIndexing>COPPER (74-82)</PreviousIndexing>
   <PreviousIndexing>INDOLES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008665</DescriptorUI>
     <DescriptorName>
      <String>Metalloporphyrins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Tsitologiia 15(9):1103;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051382</ConceptUI>
    <ConceptName>
     <String>heliogen blue SBL</String>
    </ConceptName>
    <CASN1Name>copper(dihydrogen phthalocyaninedisulfonato(2)) disodium salt</CASN1Name>
    <RegistryNumber>1330-38-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081385</TermUI>
      <String>heliogen blue SBL</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007918</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hemodes</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Frequency>54</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>SALTS (74-78)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011205</DescriptorUI>
     <DescriptorName>
      <String>Povidone</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D010952</DescriptorUI>
     <DescriptorName>
      <String>Plasma Substitutes</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
    <PharmacologicalActionList>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D000276</DescriptorUI>
        <DescriptorName>
         <String>Adjuvants, Immunologic</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D000894</DescriptorUI>
        <DescriptorName>
         <String>Anti-Inflammatory Agents, Non-Steroidal</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
    </PharmacologicalActionList>
  <SourceList>
   <Source>Farmakol Toksikol 41(5):568;1978</Source>
   <Source>Sud Med Ekspert 1979;22(4):53</Source>
   <Source>Vestn Oftalmol 2:57;1973</Source>
   <Source>Z Nevropatol Psychiatr 76(2):278;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051393</ConceptUI>
    <ConceptName>
     <String>hemodes</String>
    </ConceptName>
    <RegistryNumber>53795-75-8</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0051393</Concept1UI>
     <Concept2UI>M0051391</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0051393</Concept1UI>
     <Concept2UI>M0051390</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0051393</Concept1UI>
     <Concept2UI>M0051392</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081396</TermUI>
      <String>hemodes</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0051391</ConceptUI>
    <ConceptName>
     <String>neocompensan</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0051393</Concept1UI>
     <Concept2UI>M0051391</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T081394</TermUI>
      <String>neocompensan</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0051390</ConceptUI>
    <ConceptName>
     <String>gemodes</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0051393</Concept1UI>
     <Concept2UI>M0051390</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T081393</TermUI>
      <String>gemodes</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0051392</ConceptUI>
    <ConceptName>
     <String>neohemodes</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0051393</Concept1UI>
     <Concept2UI>M0051392</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T081395</TermUI>
      <String>neohemodes</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007924</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>heptafluorobutyric anhydride</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>08</Month>
   <Day>15</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>60</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BUTYRATES (74-79)</PreviousIndexing>
   <PreviousIndexing>BUTYRATES (74-82)</PreviousIndexing>
   <PreviousIndexing>FLUORINE (74-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005466</DescriptorUI>
     <DescriptorName>
      <String>Fluorocarbons</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
    <PharmacologicalActionList>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D007202</DescriptorUI>
        <DescriptorName>
         <String>Indicators and Reagents</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
    </PharmacologicalActionList>
  <SourceList>
   <Source>Clin Chem 25(2):218;1979</Source>
   <Source>Infect Immun 9(4):1974</Source>
   <Source>J Chromatogr 123(2):287;1976</Source>
   <Source>J Lipid Res 20(1):78;1979</Source>
   <Source>J. Endocrinol 64:277;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051397</ConceptUI>
    <ConceptName>
     <String>heptafluorobutyric anhydride</String>
    </ConceptName>
    <RegistryNumber>336-59-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081400</TermUI>
      <String>heptafluorobutyric anhydride</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007925</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>heptamethyleneimine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001392</DescriptorUI>
     <DescriptorName>
      <String>Azocines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nature 244(412):176;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051398</ConceptUI>
    <ConceptName>
     <String>heptamethyleneimine</String>
    </ConceptName>
    <RegistryNumber>1121-92-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081401</TermUI>
      <String>heptamethyleneimine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007927</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,7-heptanediol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006018</DescriptorUI>
     <DescriptorName>
      <String>Glycols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nature 247(438):222;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051399</ConceptUI>
    <ConceptName>
     <String>1,7-heptanediol</String>
    </ConceptName>
    <RegistryNumber>629-30-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081402</TermUI>
      <String>1,7-heptanediol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C025096</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>titanium tetrachloride</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>07</Month>
   <Day>15</Day>
  </DateCreated>
  <DateRevised>
   <Year>2015</Year>
   <Month>11</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>RN given refers to TiCl4
  </Note>
  <Frequency>124</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014025</DescriptorUI>
     <DescriptorName>
      <String>Titanium</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biokhimiia 1980;45(4):683</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0084079</ConceptUI>
    <ConceptName>
     <String>titanium tetrachloride</String>
    </ConceptName>
    <CASN1Name>titanium chloride (TiCl4), (T-4)-</CASN1Name>
    <RegistryNumber>8O3PJE5T7Q</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>60027-92-1 (46Ti,35Cl4-labeled cpd)</RelatedRegistryNumber>
     <RelatedRegistryNumber>60027-93-2 (50Ti,35Cl4-labeled cpd)</RelatedRegistryNumber>
     <RelatedRegistryNumber>60027-94-3 (49Ti,35Cl4-labeled cpd)</RelatedRegistryNumber>
     <RelatedRegistryNumber>60027-95-4 (48Ti,35Cl4-labeled cpd)</RelatedRegistryNumber>
     <RelatedRegistryNumber>60027-96-5 (47Ti,35Cl4-labeled cpd)</RelatedRegistryNumber>
     <RelatedRegistryNumber>60027-97-6 (48Ti,37Cl4-labeled cpd)</RelatedRegistryNumber>
     <RelatedRegistryNumber>60027-98-7 (48Ti,35Cl3,37Cl-labeled cpd)</RelatedRegistryNumber>
     <RelatedRegistryNumber>7550-45-0 (titanium tetrachloride)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0084079</Concept1UI>
     <Concept2UI>M0316147</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0084079</Concept1UI>
     <Concept2UI>M0316144</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0084079</Concept1UI>
     <Concept2UI>M0316146</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0084079</Concept1UI>
     <Concept2UI>M0316148</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0084079</Concept1UI>
     <Concept2UI>M0316145</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0084079</Concept1UI>
     <Concept2UI>M0316143</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0084079</Concept1UI>
     <Concept2UI>M0316149</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T114082</TermUI>
      <String>titanium tetrachloride</String>
      <ThesaurusIDlist>
       <ThesaurusID>FDA SRS (2015)</ThesaurusID>
       <ThesaurusID>INN (19XX)</ThesaurusID>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T114081</TermUI>
      <String>TiCl4</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0316147</ConceptUI>
    <ConceptName>
     <String>titanium tetrachloride, 47Ti,35Cl4-labeled</String>
    </ConceptName>
    <RegistryNumber>60027-96-5</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0084079</Concept1UI>
     <Concept2UI>M0316147</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T346147</TermUI>
      <String>titanium tetrachloride, 47Ti,35Cl4-labeled</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0316144</ConceptUI>
    <ConceptName>
     <String>titanium tetrachloride, 50Ti,35Cl4-labeled</String>
    </ConceptName>
    <RegistryNumber>60027-93-2</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0084079</Concept1UI>
     <Concept2UI>M0316144</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T346144</TermUI>
      <String>titanium tetrachloride, 50Ti,35Cl4-labeled</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0316146</ConceptUI>
    <ConceptName>
     <String>titanium tetrachloride, 48Ti,35Cl4-labeled</String>
    </ConceptName>
    <RegistryNumber>60027-95-4</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0084079</Concept1UI>
     <Concept2UI>M0316146</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T346146</TermUI>
      <String>titanium tetrachloride, 48Ti,35Cl4-labeled</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0316148</ConceptUI>
    <ConceptName>
     <String>titanium tetrachloride, 48Ti,37Cl4-labeled</String>
    </ConceptName>
    <RegistryNumber>60027-97-6</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0084079</Concept1UI>
     <Concept2UI>M0316148</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T346148</TermUI>
      <String>titanium tetrachloride, 48Ti,37Cl4-labeled</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0316145</ConceptUI>
    <ConceptName>
     <String>titanium tetrachloride, 49Ti,35Cl4-labeled</String>
    </ConceptName>
    <RegistryNumber>60027-94-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0084079</Concept1UI>
     <Concept2UI>M0316145</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T346145</TermUI>
      <String>titanium tetrachloride, 49Ti,35Cl4-labeled</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0316143</ConceptUI>
    <ConceptName>
     <String>titanium tetrachloride, 46Ti,35Cl4-labeled</String>
    </ConceptName>
    <RegistryNumber>60027-92-1</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0084079</Concept1UI>
     <Concept2UI>M0316143</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T346143</TermUI>
      <String>titanium tetrachloride, 46Ti,35Cl4-labeled</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0316149</ConceptUI>
    <ConceptName>
     <String>titanium tetrachloride, 48Ti,35Cl3,37Cl-labeled</String>
    </ConceptName>
    <RegistryNumber>60027-98-7</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0084079</Concept1UI>
     <Concept2UI>M0316149</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T346149</TermUI>
      <String>titanium tetrachloride, 48Ti,35Cl3,37Cl-labeled</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007930</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hexacarbacholine bromide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1969</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CHOLINE (74-78)</PreviousIndexing>
   <PreviousIndexing>CARBAMATES (69-79)</PreviousIndexing>
   <PreviousIndexing>CHOLINE/*analogs (78-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002217</DescriptorUI>
     <DescriptorName>
      <String>Carbachol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Pharmacol Biochem Behav 8(4):357;1978</Source>
   <Source>Prakt Anaesth 13(5):398;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051402</ConceptUI>
    <ConceptName>
     <String>hexacarbacholine bromide</String>
    </ConceptName>
    <CASN1Name>choline bromide hexamethylenedicarbamate /OD/ imbretil /OD/ carbolonium bromide</CASN1Name>
    <RegistryNumber>306-41-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081405</TermUI>
      <String>hexacarbacholine bromide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1969)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007933</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>26,26,26,27,27,27-hexafluorodesmosterol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DESMOSTEROL (74-75)</PreviousIndexing>
   <PreviousIndexing>STEROIDS, FLUORINATED (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003897</DescriptorUI>
     <DescriptorName>
      <String>Desmosterol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Chem Soc (Perkin I):1233;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051409</ConceptUI>
    <ConceptName>
     <String>26,26,26,27,27,27-hexafluorodesmosterol</String>
    </ConceptName>
    <CASN1Name>26,26,26,27,27,27-hexafluorocholesta-5,24-dien- 3 beta-ol</CASN1Name>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081412</TermUI>
      <String>26,26,26,27,27,27-hexafluorodesmosterol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007938</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,5-hexanediol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1969</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>04</Month>
   <Day>18</Day>
  </DateRevised>
  <Frequency>29</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>HEXANES (79-80)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006018</DescriptorUI>
     <DescriptorName>
      <String>Glycols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ecotoxicol Environ Safety 1979;3(2):204</Source>
   <Source>Proc Royal Soc Med 70(1):37;1977</Source>
   <Source>Rinsho Shinkeigaku 18(11):697;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051414</ConceptUI>
    <ConceptName>
     <String>2,5-hexanediol</String>
    </ConceptName>
    <RegistryNumber>2935-44-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081417</TermUI>
      <String>2,5-hexanediol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1969)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C104074</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>RSS protein, rat</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1997</Year>
   <Month>02</Month>
   <Day>25</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>12</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>10-kDa protein related to serotonin receptors; role in serotonin receptor-mediated signal transduction unknown; isolated from rat; amino acid sequence in first source; GenBank D89965
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011506</DescriptorUI>
     <DescriptorName>
      <String>Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D015398</DescriptorUI>
     <DescriptorName>
      <String>Signal Transduction</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>FEBS Lett 1997 Jan 20;401(2-3):252-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0271948</ConceptUI>
    <ConceptName>
     <String>RSS protein, rat</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T301953</TermUI>
      <String>RSS protein, rat</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T561064</TermUI>
      <String>RSS protein</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T301952</TermUI>
      <String>rat stomach serotonin receptor-related protein</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007945</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hippuryl-L-lysine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>29</Day>
  </DateRevised>
  <Frequency>10</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*HIPPURATES (75-79)</PreviousIndexing>
   <PreviousIndexing>HIPPURATES (79-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008239</DescriptorUI>
     <DescriptorName>
      <String>Lysine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Zh Ushn Nos Gorl Bolezn 6:66;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051426</ConceptUI>
    <ConceptName>
     <String>hippuryl-L-lysine</String>
    </ConceptName>
    <CASN1Name>N-(N-benzoylglycyl)-L-lysine</CASN1Name>
    <RegistryNumber>740-63-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081429</TermUI>
      <String>hippuryl-L-lysine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007949</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hithiol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>L-cysteine &amp; glucose mixture used as radiation-protective agent
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003545</DescriptorUI>
     <DescriptorName>
      <String>Cysteine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005947</DescriptorUI>
     <DescriptorName>
      <String>Glucose</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Jpn J Clin Radiol 19(5):339;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051430</ConceptUI>
    <ConceptName>
     <String>hithiol</String>
    </ConceptName>
    <RegistryNumber>39322-47-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081433</TermUI>
      <String>hithiol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C018738</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>acetylspermidine deacetylase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>releases acetic acid from N-1-acetylspermidine, N-8-acetylspermidine and N-1-acetylspermine
  </Note>
  <Frequency>16</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>SPERMIDINE/*analogs (78-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000581</DescriptorUI>
     <DescriptorName>
      <String>Amidohydrolases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Biochem Biophys 199(2):360;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0070554</ConceptUI>
    <ConceptName>
     <String>acetylspermidine deacetylase</String>
    </ConceptName>
    <RegistryNumber>EC 3.5.1.48</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T100557</TermUI>
      <String>acetylspermidine deacetylase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T100554</TermUI>
      <String>N(1)-acetylspermidine deacetylase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T100556</TermUI>
      <String>acylpolyamine amidohydrolase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T100555</TermUI>
      <String>N(8)-acetylspermidine deacetylase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007958</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>18-homoestriol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ESTRIOL (74-75)</PreviousIndexing>
   <PreviousIndexing>HOMOSTEROIDS (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004964</DescriptorUI>
     <DescriptorName>
      <String>Estriol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Drug Metab Disp 1(2):537;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051449</ConceptUI>
    <ConceptName>
     <String>18-homoestriol</String>
    </ConceptName>
    <RegistryNumber>19882-03-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081452</TermUI>
      <String>18-homoestriol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007969</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hydrazinium</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>01</Month>
   <Day>26</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>8</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>AMMONIUM COMPOUNDS (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006834</DescriptorUI>
     <DescriptorName>
      <String>Hydrazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Life Sci 13(5):453;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051467</ConceptUI>
    <ConceptName>
     <String>hydrazinium</String>
    </ConceptName>
    <CASN1Name>Hydrazinium(1+)</CASN1Name>
    <RegistryNumber>18500-32-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081470</TermUI>
      <String>hydrazinium</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007976</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hydrodextran sulfate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>tried therapeutically in experimental arteriosclerosis; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DEXTRANS (74-90)</PreviousIndexing>
   <PreviousIndexing>SULFONIC ACIDS (74-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D016264</DescriptorUI>
     <DescriptorName>
      <String>Dextran Sulfate</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Folia Pharm Jap 69(6):931;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051479</ConceptUI>
    <ConceptName>
     <String>hydrodextran sulfate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081482</TermUI>
      <String>hydrodextran sulfate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007977</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hydrolapachol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>inhibits mitochondrial respiratory chain
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009285</DescriptorUI>
     <DescriptorName>
      <String>Naphthoquinones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 314(2):154;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051480</ConceptUI>
    <ConceptName>
     <String>hydrolapachol</String>
    </ConceptName>
    <CASN1Name>2-hydroxy-3-(3-methylbutyl)-1,4-naphthoquinone</CASN1Name>
    <RegistryNumber>3343-38-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081483</TermUI>
      <String>hydrolapachol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007995</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-hydroxychol-11-en-24-oic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>isolated from culture filtrate of Curvularia species (Deuteromycetes); structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*STEROLS (77-77)</PreviousIndexing>
   <PreviousIndexing>HYDROXYSTEROIDS (76-77)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002770</DescriptorUI>
     <DescriptorName>
      <String>Cholenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Chem Soc Perkin I 14(0):1597;1974</Source>
   <Source>J Steroid Biochem 8(1):69;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051502</ConceptUI>
    <ConceptName>
     <String>3-hydroxychol-11-en-24-oic acid</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081505</TermUI>
      <String>3-hydroxychol-11-en-24-oic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T081504</TermUI>
      <String>3 alpha-hydroxy-5 beta-chol-11-en-24-oic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007984</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>11-hydroxyaporphine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1994</Year>
   <Month>08</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>dopaminergic cpd; RN refers to HBr; structure
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001060</DescriptorUI>
     <DescriptorName>
      <String>Aporphines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 17(10):1090;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051490</ConceptUI>
    <ConceptName>
     <String>11-hydroxyaporphine</String>
    </ConceptName>
    <RegistryNumber>53055-01-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081493</TermUI>
      <String>11-hydroxyaporphine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007985</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N(5)-hydroxy-L-arginine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1996</Year>
   <Month>06</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>13</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ARGININE (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D001120</DescriptorUI>
     <DescriptorName>
      <String>Arginine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiotics 26(5):284;1973</Source>
   <Source>J Antibiotics 28(2):997;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051491</ConceptUI>
    <ConceptName>
     <String>N(5)-hydroxy-L-arginine</String>
    </ConceptName>
    <CASN1Name>N(5)-(aminoiminomethyl)-N(5)-hydroxy-L-ornithine</CASN1Name>
    <RegistryNumber>42599-90-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081494</TermUI>
      <String>N(5)-hydroxy-L-arginine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C064298</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>asialogalactochoriongonadotropin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1990</Year>
   <Month>06</Month>
   <Day>28</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>antagonist of the action of Graves' immunoglobulins in human thyroid membranes
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001212</DescriptorUI>
     <DescriptorName>
      <String>Asialoglycoproteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006063</DescriptorUI>
     <DescriptorName>
      <String>Chorionic Gonadotropin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Horm Metab Res 1990;22(3):196</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0177155</ConceptUI>
    <ConceptName>
     <String>asialogalactochoriongonadotropin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T207160</TermUI>
      <String>asialogalactochoriongonadotropin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T207159</TermUI>
      <String>choriongonadotropin, asialogalacto-</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T207158</TermUI>
      <String>asialogalacto-HCG</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007989</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-(alpha-hydroxybenzyl)imidazo(4,5-c)pyridine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>BENZYL COMPOUNDS (74-75)</PreviousIndexing>
   <PreviousIndexing>IMIDAZOLES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011725</DescriptorUI>
     <DescriptorName>
      <String>Pyridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 16(11):1296;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051495</ConceptUI>
    <ConceptName>
     <String>2-(alpha-hydroxybenzyl)imidazo(4,5-c)pyridine</String>
    </ConceptName>
    <RegistryNumber>2654-15-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081498</TermUI>
      <String>2-(alpha-hydroxybenzyl)imidazo(4,5-c)pyridine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007992</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>11-hydroxycephalotaxine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>alkaloid from Cephalotaxus harringtonia var. drupacea; structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ALKALOIDS (74-77)</PreviousIndexing>
   <PreviousIndexing>DIOXOLES (74-77)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006248</DescriptorUI>
     <DescriptorName>
      <String>Harringtonines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 39(5):676;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051498</ConceptUI>
    <ConceptName>
     <String>11-hydroxycephalotaxine</String>
    </ConceptName>
    <CASN1Name>Cephalotaxine, 11-hydroxy-, (11alpha)-</CASN1Name>
    <RegistryNumber>49686-55-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081501</TermUI>
      <String>11-hydroxycephalotaxine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C086457</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>asialoglycoprotein-polylysine conjugate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>04</Month>
   <Day>25</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>05</Day>
  </DateRevised>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001212</DescriptorUI>
     <DescriptorName>
      <String>Asialoglycoproteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011107</DescriptorUI>
     <DescriptorName>
      <String>Polylysine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Am J Med Sci 1994 Feb;307(2):138-43</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0229208</ConceptUI>
    <ConceptName>
     <String>asialoglycoprotein-polylysine conjugate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T259213</TermUI>
      <String>asialoglycoprotein-polylysine conjugate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T259212</TermUI>
      <String>AP-poly(L-lysine) conjugate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T259211</TermUI>
      <String>AP-PL</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007998</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-hydroxychromone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002867</DescriptorUI>
     <DescriptorName>
      <String>Chromones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Southern Med J 67(10):1191;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051508</ConceptUI>
    <ConceptName>
     <String>2-hydroxychromone</String>
    </ConceptName>
    <CASN1Name>4H-1-Benzopyran-4-one, 2-hydroxy-</CASN1Name>
    <RegistryNumber>22105-09-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081511</TermUI>
      <String>2-hydroxychromone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C103104</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>asialo-galactosyl-acetylgalactosamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1997</Year>
   <Month>01</Month>
   <Day>23</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>05</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000116</DescriptorUI>
     <DescriptorName>
      <String>Acetylgalactosamine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001212</DescriptorUI>
     <DescriptorName>
      <String>Asialoglycoproteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Am Soc Nephrol 1996 Jun;7(6):955-60</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0269675</ConceptUI>
    <ConceptName>
     <String>asialo-galactosyl-acetylgalactosamine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T299680</TermUI>
      <String>asialo-galactosyl-acetylgalactosamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T299679</TermUI>
      <String>asialo-galactosyl-beta(1-3)-3-N-acetylgalactosamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T299678</TermUI>
      <String>asialo-Gal-beta(1-3)-GalNAc</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008005</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hydroxydiiodophenylpyruvic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PYRUVATES (74-75)</PreviousIndexing>
   <PreviousIndexing>IODOBENZENES (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010667</DescriptorUI>
     <DescriptorName>
      <String>Phenylpyruvic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Fol Endocrinol Jap 49(9):1167;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051521</ConceptUI>
    <ConceptName>
     <String>hydroxydiiodophenylpyruvic acid</String>
    </ConceptName>
    <CASN1Name>Benzenepropanoic acid, 4-hydroxy-3,5-diiodo-alpha-oxo-</CASN1Name>
    <RegistryNumber>780-00-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081524</TermUI>
      <String>hydroxydiiodophenylpyruvic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008010</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>(8S)-8-hydroxyerythromycin-B</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ERYTHROMYCIN (74-78)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004917</DescriptorUI>
     <DescriptorName>
      <String>Erythromycin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Helv Chim Acta 56(5):1557;1973</Source>
   <Source>J Antibiot 31(1):55;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051524</ConceptUI>
    <ConceptName>
     <String>(8S)-8-hydroxyerythromycin-B</String>
    </ConceptName>
    <CASN1Name>Erythromycin, 12-deoxy-8-hydroxy-</CASN1Name>
    <RegistryNumber>36693-58-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081527</TermUI>
      <String>(8S)-8-hydroxyerythromycin-B</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008011</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-hydroxyestradiol 2,3-methylene ether</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1993</Year>
   <Month>06</Month>
   <Day>22</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ESTRADIOL (74-75)</PreviousIndexing>
   <PreviousIndexing>DIOXOLES (74-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004958</DescriptorUI>
     <DescriptorName>
      <String>Estradiol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D002393</DescriptorUI>
     <DescriptorName>
      <String>Estrogens, Catechol</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Steroids 23(6):869;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051525</ConceptUI>
    <ConceptName>
     <String>2-hydroxyestradiol 2,3-methylene ether</String>
    </ConceptName>
    <CASN1Name>Estra-1,3,5(10)-trien-17-ol, 2,3-(methylenebis(oxy))-, (17beta)-</CASN1Name>
    <RegistryNumber>53586-37-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081528</TermUI>
      <String>2-hydroxyestradiol 2,3-methylene ether</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008012</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-hydroxyestriol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1993</Year>
   <Month>06</Month>
   <Day>22</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>15</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ESTRIOL (74-75)</PreviousIndexing>
   <PreviousIndexing>HYDROXYSTEROIDS (75-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004964</DescriptorUI>
     <DescriptorName>
      <String>Estriol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D002393</DescriptorUI>
     <DescriptorName>
      <String>Estrogens, Catechol</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Chem Pharm Bull (Tokyo) 23(7):1613;1975</Source>
   <Source>J Endocrinol 1979;82(1):131</Source>
   <Source>J Steroid Biochem 5(1):1;1974</Source>
   <Source>J Steroid Biochem 6(7):1187;1975</Source>
   <Source>Steroids 28(5):733;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051526</ConceptUI>
    <ConceptName>
     <String>2-hydroxyestriol</String>
    </ConceptName>
    <CASN1Name>2,16 alpha-dihydroxyestradiol /OD/ estra-1,3,5(10)- triene-2,3,16 alpha,17 beta-tetrol</CASN1Name>
    <RegistryNumber>1232-80-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081529</TermUI>
      <String>2-hydroxyestriol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008016</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-hydroxyestrone 2,3-methylene ether</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1993</Year>
   <Month>06</Month>
   <Day>22</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ESTRONE (74-77)</PreviousIndexing>
   <PreviousIndexing>DIOXOLES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006894</DescriptorUI>
     <DescriptorName>
      <String>Hydroxyestrones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D002393</DescriptorUI>
     <DescriptorName>
      <String>Estrogens, Catechol</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Steroids 23(6):869;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051527</ConceptUI>
    <ConceptName>
     <String>2-hydroxyestrone 2,3-methylene ether</String>
    </ConceptName>
    <CASN1Name>Estra-1,3,5(10)-trien-17-one, 2,3-(methylenebis(oxy))-</CASN1Name>
    <RegistryNumber>53573-94-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081530</TermUI>
      <String>2-hydroxyestrone 2,3-methylene ether</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008027</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-(2-hydroxyethyl)-2-phenylethyl carbamate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>06</Month>
   <Day>15</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PHENYLPROPIONATES (76-77)</PreviousIndexing>
   <PreviousIndexing>ALCOHOL, ETHYL (75-76)</PreviousIndexing>
   <PreviousIndexing>ETHANOLAMINES (76-77)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002219</DescriptorUI>
     <DescriptorName>
      <String>Carbamates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Br J Pharmacol 51(1):55;1974</Source>
   <Source>West Afr J Pharmacol Drug Res 2(1):77P;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051549</ConceptUI>
    <ConceptName>
     <String>N-(2-hydroxyethyl)-2-phenylethyl carbamate</String>
    </ConceptName>
    <CASN1Name>(2-hydroxyethyl)carbamic acid 2-phenylethyl ester</CASN1Name>
    <RegistryNumber>30751-01-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081552</TermUI>
      <String>N-(2-hydroxyethyl)-2-phenylethyl carbamate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008028</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-hydroxy-2-ethyl-2-phenylglutarimide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>BENZENE DERIVATIVES (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010881</DescriptorUI>
     <DescriptorName>
      <String>Piperidones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Drug Metab Dispos 2(2):151;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051550</ConceptUI>
    <ConceptName>
     <String>4-hydroxy-2-ethyl-2-phenylglutarimide</String>
    </ConceptName>
    <CASN1Name>3-ethyl-5-hydroxy-3-phenyl-2,6-piperidinedione</CASN1Name>
    <RegistryNumber>50275-60-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081553</TermUI>
      <String>4-hydroxy-2-ethyl-2-phenylglutarimide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008030</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hydroxyethylthiamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Frequency>7</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*THIAMINE (74-76)</PreviousIndexing>
   <PreviousIndexing>ALCOHOL, ETHYL (74-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010119</DescriptorUI>
     <DescriptorName>
      <String>Oxythiamine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Am Chem Soc 98(3):808;1976</Source>
   <Source>J Nutr Sci Vitaminol 19:43;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051552</ConceptUI>
    <ConceptName>
     <String>hydroxyethylthiamine</String>
    </ConceptName>
    <CASN1Name>3-((4-amino-2-methyl-5-pyrimidinyl)methyl)-2,5- bis(2-hydroxyethyl)-4-methylthiazolium chloride</CASN1Name>
    <RegistryNumber>51230-37-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081555</TermUI>
      <String>hydroxyethylthiamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008035</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-hydroxy-4'-hydroxy-7,7'-diethyl-trans-N-4-stilbenylacetamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>analog of diethylstilbestrol; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DIETHYLSTILBESTROL (74-75)</PreviousIndexing>
   <PreviousIndexing>ACETAMIDES (74-82)</PreviousIndexing>
   <PreviousIndexing>HYDROXYLAMINES (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004054</DescriptorUI>
     <DescriptorName>
      <String>Diethylstilbestrol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 17(4):386;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051561</ConceptUI>
    <ConceptName>
     <String>N-hydroxy-4'-hydroxy-7,7'-diethyl-trans-N-4-stilbenylacetamide</String>
    </ConceptName>
    <CASN1Name>N-(4-(1-ethyl-2-(4-hydroxyphenyl)-1-butenyl)phenyl)-N-hydroxyacetamide</CASN1Name>
    <RegistryNumber>52498-24-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081564</TermUI>
      <String>N-hydroxy-4'-hydroxy-7,7'-diethyl-trans-N-4-stilbenylacetamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C519653</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-hydroxylup-12-en-28-oic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>05</Month>
   <Day>16</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014315</DescriptorUI>
     <DescriptorName>
      <String>Triterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Magn Reson Chem 2007 Mar;45(3):279-81</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0509718</ConceptUI>
    <ConceptName>
     <String>3-hydroxylup-12-en-28-oic acid</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T697791</TermUI>
      <String>3-hydroxylup-12-en-28-oic acid</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>05</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008042</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hydroxylamine-O-sulfonic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>SULFONIC ACIDS (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006898</DescriptorUI>
     <DescriptorName>
      <String>Hydroxylamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Soc Jpn 94(8):945;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051569</ConceptUI>
    <ConceptName>
     <String>hydroxylamine-O-sulfonic acid</String>
    </ConceptName>
    <RegistryNumber>2950-43-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081572</TermUI>
      <String>hydroxylamine-O-sulfonic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C431383</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>EAF1 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>07</Month>
   <Day>25</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>05</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>an ELL-associated factor that is delocalized by expression of the MLL-ELL fusion protein; RefSeq NM_033083
  </Note>
  <Frequency>15</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014157</DescriptorUI>
     <DescriptorName>
      <String>Transcription Factors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Blood 2001 Jul 1;98(1):201-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0394163</ConceptUI>
    <ConceptName>
     <String>EAF1 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T565602</TermUI>
      <String>EAF1 protein, human</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T565603</TermUI>
      <String>ELL associated factor 1 protein, human</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T566313</TermUI>
      <String>ELL-associated factor, human</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>31</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T565604</TermUI>
      <String>eleven nineteen lysine-rich leukemia gene-associated factor 1 protein, human</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C096454</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SmaPI protein, Serratia marcescens</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>12</Month>
   <Day>04</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>12</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>a metalloprotease inhibitor from Serratia marcescens; amino acid sequence given in first source; GenBank L09107
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Appl Environ Microbiol 1995 Aug;61(8):3035-41</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0253810</ConceptUI>
    <ConceptName>
     <String>SmaPI protein, Serratia marcescens</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T529279</TermUI>
      <String>SmaPI protein, Serratia marcescens</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>12</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008052</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>9-(3-C-hydroxymethyl-alpha-L-threofuranosyl)adenine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>10</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>branched-chain sugar nucleoside; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*NUCLEOSIDES (75-82)</PreviousIndexing>
   <PreviousIndexing>ADENINE/*analogs (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000241</DescriptorUI>
     <DescriptorName>
      <String>Adenosine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 17(10):1055;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051590</ConceptUI>
    <ConceptName>
     <String>9-(3-C-hydroxymethyl-alpha-L-threofuranosyl)adenine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081593</TermUI>
      <String>9-(3-C-hydroxymethyl-alpha-L-threofuranosyl)adenine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008053</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-hydroxymethyltubercidin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*RIBONUCLEOSIDES (74-75)</PreviousIndexing>
   <PreviousIndexing>PYRIMIDINES (74-75)</PreviousIndexing>
   <PreviousIndexing>PYRROLES (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014372</DescriptorUI>
     <DescriptorName>
      <String>Tubercidin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 16(12):1405;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051591</ConceptUI>
    <ConceptName>
     <String>5-hydroxymethyltubercidin</String>
    </ConceptName>
    <CASN1Name>4-amino-7-beta-D-ribofuranosyl-7H-pyrrolo(2,3-d)pyrimidine-5-methanol</CASN1Name>
    <RegistryNumber>49558-38-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081594</TermUI>
      <String>5-hydroxymethyltubercidin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008059</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>(4-hydroxy-3-nitro)benzylated polystyrene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>27</Day>
  </DateRevised>
  <Note>nitrophenol deriv for peptide synthesis
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>BENZYL COMPOUNDS (74-75)</PreviousIndexing>
   <PreviousIndexing>NITROPHENOLS (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011137</DescriptorUI>
     <DescriptorName>
      <String>Polystyrenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Biochem 42(1):151;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051599</ConceptUI>
    <ConceptName>
     <String>(4-hydroxy-3-nitro)benzylated polystyrene</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081602</TermUI>
      <String>(4-hydroxy-3-nitro)benzylated polystyrene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008065</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>14-hydroxy-3-oxo-1,4,20,22-bufatetraenolide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>11</Day>
  </DateRevised>
  <Note>RN given not in Chemline 8/83; structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>HYDROXYSTEROIDS (74-75)</PreviousIndexing>
   <PreviousIndexing>KETOSTEROIDS (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002018</DescriptorUI>
     <DescriptorName>
      <String>Bufanolides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Planta Med 24(3):201;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051612</ConceptUI>
    <ConceptName>
     <String>14-hydroxy-3-oxo-1,4,20,22-bufatetraenolide</String>
    </ConceptName>
    <RegistryNumber>41059-91-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081615</TermUI>
      <String>14-hydroxy-3-oxo-1,4,20,22-bufatetraenolide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008138</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-iodobenzylamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>substrate for monoamine oxidase
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>AMINES (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007462</DescriptorUI>
     <DescriptorName>
      <String>Iodobenzenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Anal Biochem 88(2):495;1978</Source>
   <Source>Res Commun Chem Pathol Pharmacol 7(2):419;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051722</ConceptUI>
    <ConceptName>
     <String>3-iodobenzylamine</String>
    </ConceptName>
    <CASN1Name>3-iodobenzenemethanamine</CASN1Name>
    <RegistryNumber>696-40-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081725</TermUI>
      <String>3-iodobenzylamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T081724</TermUI>
      <String>meta-iodobenzylamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008072</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>gamma-hydroxyphenylbutazone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1984</Year>
   <Month>06</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>metabolite of phenylbutazone; RN given refers to cpd with unspecified isomeric designation
  </Note>
  <Frequency>11</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>OXYPHENBUTAZONE/*analogs (75-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010653</DescriptorUI>
     <DescriptorName>
      <String>Phenylbutazone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Farmaco 31(9):665;1976</Source>
   <Source>J Pharm Sci 63(11):1751;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051625</ConceptUI>
    <ConceptName>
     <String>gamma-hydroxyphenylbutazone</String>
    </ConceptName>
    <CASN1Name>4-(3-hydroxybutyl)-1,2-diphenyl-3,5- pyrazolidinedione</CASN1Name>
    <RegistryNumber>568-76-3</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>36039-31-3 ((+-)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0051625</Concept1UI>
     <Concept2UI>M0310153</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0051625</Concept1UI>
     <Concept2UI>M0051624</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081628</TermUI>
      <String>gamma-hydroxyphenylbutazone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0310153</ConceptUI>
    <ConceptName>
     <String>(+-)-isomer of gamma-hydroxyphenylbutazone</String>
    </ConceptName>
    <RegistryNumber>36039-31-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0051625</Concept1UI>
     <Concept2UI>M0310153</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T340153</TermUI>
      <String>(+-)-isomer of gamma-hydroxyphenylbutazone</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0051624</ConceptUI>
    <ConceptName>
     <String>1,2-diphenyl-3,5-dioxo-4-(3-hydroxybutyl)pyrazolidine</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0051625</Concept1UI>
     <Concept2UI>M0051624</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T081627</TermUI>
      <String>1,2-diphenyl-3,5-dioxo-4-(3-hydroxybutyl)pyrazolidine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008074</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-hydroxy-5-phenyllevulinic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>metabolite of Tubercularia (Moniliales) with analgesic properties; structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*KETO ACIDS (74-75)</PreviousIndexing>
   <PreviousIndexing>*VALERATES (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007982</DescriptorUI>
     <DescriptorName>
      <String>Levulinic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 17(2):249;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051628</ConceptUI>
    <ConceptName>
     <String>5-hydroxy-5-phenyllevulinic acid</String>
    </ConceptName>
    <CASN1Name>delta-hydroxy-gamma-oxobenzenepentanoic acid</CASN1Name>
    <RegistryNumber>51366-15-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081631</TermUI>
      <String>5-hydroxy-5-phenyllevulinic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C519655</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>RDR2 protein, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>05</Month>
   <Day>16</Day>
  </DateCreated>
  <Note>RefSeq NM_117183
  </Note>
  <Frequency>27</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012324</DescriptorUI>
     <DescriptorName>
      <String>RNA-Dependent RNA Polymerase</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Plant Cell 2006 Jul;18(7):1559-74</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0509720</ConceptUI>
    <ConceptName>
     <String>RDR2 protein, Arabidopsis</String>
    </ConceptName>
    <RegistryNumber>EC 2.7.7.48</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T697794</TermUI>
      <String>RDR2 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>05</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008094</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hymenoflorin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>05</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>antileukemic agent isolated from Hymenoxygrandiflora; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>LACTONES (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012717</DescriptorUI>
     <DescriptorName>
      <String>Sesquiterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 39(14):2013;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051661</ConceptUI>
    <ConceptName>
     <String>hymenoflorin</String>
    </ConceptName>
    <RegistryNumber>51292-63-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081664</TermUI>
      <String>hymenoflorin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008104</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>IgO</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>postulated that hemolytic anemia is caused by IgO antibodies
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007136</DescriptorUI>
     <DescriptorName>
      <String>Immunoglobulins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Munch Med Wochenschr 115(39):1650;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051672</ConceptUI>
    <ConceptName>
     <String>IgO</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081675</TermUI>
      <String>IgO</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C519656</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SAR3 protein, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>05</Month>
   <Day>16</Day>
  </DateCreated>
  <Note>amino acid sequence in first source
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D028861</DescriptorUI>
     <DescriptorName>
      <String>Nuclear Pore Complex Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Plant Cell 2006 Jul;18(7):1590-603</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0509721</ConceptUI>
    <ConceptName>
     <String>SAR3 protein, Arabidopsis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T697795</TermUI>
      <String>SAR3 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>05</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T697796</TermUI>
      <String>SUPPRESSOR OF AUXIN RESISTANCE 3, Arabidopsis</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>05</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C510401</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>GKPV peptide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>05</Month>
   <Day>22</Day>
  </DateCreated>
  <Note>AA residues 10-13 (GKPV) of alpha-melanocyte stimulating hormone
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010446</DescriptorUI>
     <DescriptorName>
      <String>Peptide Fragments</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D009074</DescriptorUI>
     <DescriptorName>
      <String>Melanocyte-Stimulating Hormones</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Peptides 2006 Feb;27(2):431-7</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0498192</ConceptUI>
    <ConceptName>
     <String>GKPV peptide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0498192</Concept1UI>
     <Concept2UI>M0498193</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T674313</TermUI>
      <String>GKPV peptide</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>05</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T674314</TermUI>
      <String>Gly-Lys-Pro-Val</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>05</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0498193</ConceptUI>
    <ConceptName>
     <String>alpha-melanocyte stimulating hormone 10-13, human</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0498192</Concept1UI>
     <Concept2UI>M0498193</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T674315</TermUI>
      <String>alpha-melanocyte stimulating hormone 10-13, human</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>05</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C519660</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>STA1 protein, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>05</Month>
   <Day>16</Day>
  </DateCreated>
  <Note>required for pre-mRNA splicing; RefSeq NM_116581
  </Note>
  <Frequency>7</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009687</DescriptorUI>
     <DescriptorName>
      <String>Nuclear Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D012326</DescriptorUI>
     <DescriptorName>
      <String>RNA Splicing</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Plant Cell 2006 Jul;18(7):1736-49</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0509725</ConceptUI>
    <ConceptName>
     <String>STA1 protein, Arabidopsis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T697802</TermUI>
      <String>STA1 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>05</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T697803</TermUI>
      <String>STABILIZED1 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>05</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C519661</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Frem3 protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>05</Month>
   <Day>16</Day>
  </DateCreated>
  <Note>GenBank AB160989
  </Note>
  <Frequency>7</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D016326</DescriptorUI>
     <DescriptorName>
      <String>Extracellular Matrix Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Exp Cell Res 2005 May 15;306(1):9-23</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0509726</ConceptUI>
    <ConceptName>
     <String>Frem3 protein, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T697804</TermUI>
      <String>Frem3 protein, mouse</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>05</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C066466</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>myelin basic protein 1-14</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1990</Year>
   <Month>12</Month>
   <Day>27</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>05</Month>
   <Day>13</Day>
  </DateRevised>
  <Note>amino acid sequence given in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004676</DescriptorUI>
     <DescriptorName>
      <String>Myelin Basic Protein</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010446</DescriptorUI>
     <DescriptorName>
      <String>Peptide Fragments</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 1990;172(3):1167</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0182392</ConceptUI>
    <ConceptName>
     <String>myelin basic protein 1-14</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T640596</TermUI>
      <String>myelin basic protein 1-14</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>05</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T212395</TermUI>
      <String>pMPA14</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T212397</TermUI>
      <String>myelin basic protein peptide 1-14</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008121</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>indolylheptylamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>20</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007211</DescriptorUI>
     <DescriptorName>
      <String>Indoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D015306</DescriptorUI>
     <DescriptorName>
      <String>Biogenic Monoamines</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Sov J Dev Biol 2(1):1;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051697</ConceptUI>
    <ConceptName>
     <String>indolylheptylamine</String>
    </ConceptName>
    <CASN1Name>1H-indole-3-heptanamine</CASN1Name>
    <RegistryNumber>29852-47-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081700</TermUI>
      <String>indolylheptylamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C030911</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-nitro-7-methoxynaphtho(2-1b)furan</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>08</Month>
   <Day>14</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>29</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009581</DescriptorUI>
     <DescriptorName>
      <String>Nitrofurans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
    <PharmacologicalActionList>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D000970</DescriptorUI>
        <DescriptorName>
         <String>Antineoplastic Agents</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D002273</DescriptorUI>
        <DescriptorName>
         <String>Carcinogens</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D009153</DescriptorUI>
        <DescriptorName>
         <String>Mutagens</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
    </PharmacologicalActionList>
  <SourceList>
   <Source>Mutat Res 1981;88(4):355</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0097502</ConceptUI>
    <ConceptName>
     <String>2-nitro-7-methoxynaphtho(2-1b)furan</String>
    </ConceptName>
    <CASN1Name>Naphtho(2,1-b)furan, 7-methoxy-2-nitro-</CASN1Name>
    <RegistryNumber>75965-74-1</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0097502</Concept1UI>
     <Concept2UI>M0097505</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T127506</TermUI>
      <String>2-nitro-7-methoxynaphtho(2-1b)furan</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T127507</TermUI>
      <String>7-methoxy-2-nitronaphtho(2,1-b)furan</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0097505</ConceptUI>
    <ConceptName>
     <String>R 7000</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0097502</Concept1UI>
     <Concept2UI>M0097505</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T127509</TermUI>
      <String>R 7000</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T127508</TermUI>
      <String>R-7000</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C032572</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>furapyrimidone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1982</Year>
   <Month>01</Month>
   <Day>06</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>12</Day>
  </DateRevised>
  <Frequency>16</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009581</DescriptorUI>
     <DescriptorName>
      <String>Nitrofurans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chung-Kuo Yao Li Hseuh Pao 1980;1(1):60</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0101596</ConceptUI>
    <ConceptName>
     <String>furapyrimidone</String>
    </ConceptName>
    <RegistryNumber>75888-03-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T131600</TermUI>
      <String>furapyrimidone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008131</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>poly-O-acetylserine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1982</Year>
   <Month>01</Month>
   <Day>27</Day>
  </DateCreated>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010455</DescriptorUI>
     <DescriptorName>
      <String>Peptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Int J Pept Protein Res 1981;17(4):412</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051711</ConceptUI>
    <ConceptName>
     <String>poly-O-acetylserine</String>
    </ConceptName>
    <CASN1Name>L-Serine, acetate (ester), homopolymer</CASN1Name>
    <RegistryNumber>25248-96-8</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0051711</Concept1UI>
     <Concept2UI>M0051710</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081714</TermUI>
      <String>poly-O-acetylserine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0051710</ConceptUI>
    <ConceptName>
     <String>poly-O-acetyl-L-serine</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0051711</Concept1UI>
     <Concept2UI>M0051710</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T081713</TermUI>
      <String>poly-O-acetyl-L-serine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C044755</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-methyl-4-phenyl-2,3-dihydropyridinium</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1985</Year>
   <Month>04</Month>
   <Day>23</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>RN given from Toxline; RN not in Chemline 4/85
  </Note>
  <Frequency>46</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011726</DescriptorUI>
     <DescriptorName>
      <String>Pyridinium Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 1985;127(2):707</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0130518</ConceptUI>
    <ConceptName>
     <String>1-methyl-4-phenyl-2,3-dihydropyridinium</String>
    </ConceptName>
    <RegistryNumber>94613-45-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T160523</TermUI>
      <String>1-methyl-4-phenyl-2,3-dihydropyridinium</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T160522</TermUI>
      <String>MPDP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013502</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5,5-dimethyl-10-(4-(1-piperidine)butyryloxy)-8-(3-methyl-2- benzopyrano(3,4-d))pyridine.HCl</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001578</DescriptorUI>
     <DescriptorName>
      <String>Benzopyrans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 65(10):1543;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061304</ConceptUI>
    <ConceptName>
     <String>5,5-dimethyl-10-(4-(1-piperidine)butyryloxy)-8-(3-methyl-2- benzopyrano(3,4-d))pyridine.HCl</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091307</TermUI>
      <String>5,5-dimethyl-10-(4-(1-piperidine)butyryloxy)-8-(3-methyl-2- benzopyrano(3,4-d))pyridine.HCl</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013505</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5,5-dimethyl-delta(2)-thiazoline-4-carboxylic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>produced by cleavage of thiazolidine ring of Penicillin G.
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013844</DescriptorUI>
     <DescriptorName>
      <String>Thiazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>JBC 251(24):7947;1976</Source>
   <Source>JBC 253(10):3660;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061307</ConceptUI>
    <ConceptName>
     <String>5,5-dimethyl-delta(2)-thiazoline-4-carboxylic acid</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091310</TermUI>
      <String>5,5-dimethyl-delta(2)-thiazoline-4-carboxylic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013507</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,4-dinitrophenylmethacrylate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>11</Month>
   <Day>08</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008689</DescriptorUI>
     <DescriptorName>
      <String>Methacrylates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ann NY Acad Sci 277:412;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061309</ConceptUI>
    <ConceptName>
     <String>2,4-dinitrophenylmethacrylate</String>
    </ConceptName>
    <CASN1Name>2-Propenoic acid, 2-methyl-, 2,4-dinitrophenyl ester</CASN1Name>
    <RegistryNumber>54616-59-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091312</TermUI>
      <String>2,4-dinitrophenylmethacrylate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013509</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>diphloretin phosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>16</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011121</DescriptorUI>
     <DescriptorName>
      <String>Polyphloretin Phosphate</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Life Sci 19(11):1653;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061311</ConceptUI>
    <ConceptName>
     <String>diphloretin phosphate</String>
    </ConceptName>
    <RegistryNumber>39201-04-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091314</TermUI>
      <String>diphloretin phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013518</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>20,22-epoxycholesterol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>EPOXY COMPOUNDS (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002784</DescriptorUI>
     <DescriptorName>
      <String>Cholesterol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Chem Soc (Perkin Trans) 19:2116;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061319</ConceptUI>
    <ConceptName>
     <String>20,22-epoxycholesterol</String>
    </ConceptName>
    <CASN1Name>Cholest-5-en-3-ol, 20,22-epoxy-, (3beta,20xi)-</CASN1Name>
    <RegistryNumber>54993-23-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091322</TermUI>
      <String>20,22-epoxycholesterol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013527</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>etiocholenic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>RN given refers to (3 beta,17 beta)-isomer
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000737</DescriptorUI>
     <DescriptorName>
      <String>Androstenols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Jap J Exptl Med 46(4):213;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061334</ConceptUI>
    <ConceptName>
     <String>etiocholenic acid</String>
    </ConceptName>
    <CASN1Name>3-hydroxy-5-androstene-17-carboxylic acid</CASN1Name>
    <RegistryNumber>10325-79-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091337</TermUI>
      <String>etiocholenic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C436825</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,8-dihydroxyeudesman-3,7(11)-dien-8,12-olide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>10</Month>
   <Day>15</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>from Smyrnium olusatrum; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SESQUITERPENES (2001-2003)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007783</DescriptorUI>
     <DescriptorName>
      <String>Lactones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D045787</DescriptorUI>
     <DescriptorName>
      <String>Sesquiterpenes, Eudesmane</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Phytochemistry 2001 Aug;57(8):1197-200</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0401745</ConceptUI>
    <ConceptName>
     <String>1,8-dihydroxyeudesman-3,7(11)-dien-8,12-olide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T466138</TermUI>
      <String>1,8-dihydroxyeudesman-3,7(11)-dien-8,12-olide</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>10</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T543614</TermUI>
      <String>1,8-dihydroxy-eudesman-3,7(11)-dien-8,12-olide</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>06</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T466139</TermUI>
      <String>1beta,8beta-dihydroxyeudesman-3,7(11)-dien-8alpha,12-olide</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>10</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013535</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>fluorophene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012458</DescriptorUI>
     <DescriptorName>
      <String>Salicylanilides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Dental Res 55(6):1084;1976</Source>
   <Source>J Dental Res 55(6):1088;1976</Source>
   <Source>J Dental Res 56(4):443;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061358</ConceptUI>
    <ConceptName>
     <String>fluorophene</String>
    </ConceptName>
    <CASN1Name>3,5-dibromo-3'-trifluoromethylsalicylanilide</CASN1Name>
    <RegistryNumber>4776-06-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091361</TermUI>
      <String>fluorophene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013539</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>glucoolitoriside</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1995</Year>
   <Month>06</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>from Adonis mongolica Sim
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002298</DescriptorUI>
     <DescriptorName>
      <String>Cardenolides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D002301</DescriptorUI>
     <DescriptorName>
      <String>Cardiac Glycosides</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D006027</DescriptorUI>
     <DescriptorName>
      <String>Glycosides</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Pharmazie 31(8):565;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061362</ConceptUI>
    <ConceptName>
     <String>glucoolitoriside</String>
    </ConceptName>
    <CASN1Name>Card- 20(22)-enolide, 3-((O-beta-D-glucopyranosyl-(1-3)-O-beta-D-glucopyranosyl-(1-4)-2,6-dideoxy-beta-D-xylo-hexopyranosyl)oxy)-5,14-dihydroxy-19-oxo-, (3beta,5beta)-</CASN1Name>
    <RegistryNumber>39028-64-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091365</TermUI>
      <String>glucoolitoriside</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013541</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>gamma-glutamylhistamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>21</Day>
  </DateRevised>
  <Frequency>9</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>GLUTAMATES (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D006632</DescriptorUI>
     <DescriptorName>
      <String>Histamine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Neurochem 27:1461;1976</Source>
   <Source>J Neurochem 32(2):363;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061365</ConceptUI>
    <ConceptName>
     <String>gamma-glutamylhistamine</String>
    </ConceptName>
    <CASN1Name>L-Glutamine, N-(2-(1H-imidazol-4-yl)ethyl)-</CASN1Name>
    <RegistryNumber>46843-88-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091368</TermUI>
      <String>gamma-glutamylhistamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C443696</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,9-dihydroxyeudesm-3-en-5beta,6alpha,7alpha,11alphaH-12,6-olide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>01</Month>
   <Day>11</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>isolated from the fruit of Crataegus flava; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SESQUITERPENES (2002-2003)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007783</DescriptorUI>
     <DescriptorName>
      <String>Lactones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D045787</DescriptorUI>
     <DescriptorName>
      <String>Sesquiterpenes, Eudesmane</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Fitoterapia 2001 Nov;72(7):756-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0410507</ConceptUI>
    <ConceptName>
     <String>1,9-dihydroxyeudesm-3-en-5beta,6alpha,7alpha,11alphaH-12,6-olide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T477213</TermUI>
      <String>1,9-dihydroxyeudesm-3-en-5beta,6alpha,7alpha,11alphaH-12,6-olide</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>01</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T543615</TermUI>
      <String>1,9-dihydroxy-eudesm-3-en-5beta,6alpha,7alpha,11alphaH-12,6-olide</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>06</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013557</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>L-histidinyl-D-penicillaminatocobalt(III)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>05</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>model for binding of D-penicillamine to metal ions; RN given is for monohydrate
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009942</DescriptorUI>
     <DescriptorName>
      <String>Organometallic Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010396</DescriptorUI>
     <DescriptorName>
      <String>Penicillamine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Am Chem Soc 99(1):101;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061399</ConceptUI>
    <ConceptName>
     <String>L-histidinyl-D-penicillaminatocobalt(III)</String>
    </ConceptName>
    <RegistryNumber>60478-99-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091402</TermUI>
      <String>L-histidinyl-D-penicillaminatocobalt(III)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013560</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>homophthalaldehyde</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ALDEHYDES (77-78)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007189</DescriptorUI>
     <DescriptorName>
      <String>Indans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Soc Jpn 96(9):1114;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061404</ConceptUI>
    <ConceptName>
     <String>homophthalaldehyde</String>
    </ConceptName>
    <RegistryNumber>25705-34-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091407</TermUI>
      <String>homophthalaldehyde</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013562</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>20-hydroperoxy-20-isocholesterol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002784</DescriptorUI>
     <DescriptorName>
      <String>Cholesterol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>FEBS Lett 70(1):23;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061405</ConceptUI>
    <ConceptName>
     <String>20-hydroperoxy-20-isocholesterol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091408</TermUI>
      <String>20-hydroperoxy-20-isocholesterol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013564</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-(hydroxyethyl)benzimidazole</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001562</DescriptorUI>
     <DescriptorName>
      <String>Benzimidazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Polon Pharm 33(5):661;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061407</ConceptUI>
    <ConceptName>
     <String>2-(hydroxyethyl)benzimidazole</String>
    </ConceptName>
    <CASN1Name>1H-Benzimidazole-2-ethanol</CASN1Name>
    <RegistryNumber>4857-01-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091410</TermUI>
      <String>2-(hydroxyethyl)benzimidazole</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013573</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-iodo-5,6-dihydrouracil</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>11</Month>
   <Day>09</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>IODOURACIL/*analogs (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014498</DescriptorUI>
     <DescriptorName>
      <String>Uracil</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 251(22):6909;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061425</ConceptUI>
    <ConceptName>
     <String>5-iodo-5,6-dihydrouracil</String>
    </ConceptName>
    <CASN1Name>2,4(1H,3H)-Pyrimidinedione, dihydro-5-iodo-</CASN1Name>
    <RegistryNumber>60763-80-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091428</TermUI>
      <String>5-iodo-5,6-dihydrouracil</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C413029</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>11-hydroxy-3-oxo-6H,7H-10-methyl-eudesman-1,2-4,5-dien-6,12-olide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>09</Month>
   <Day>12</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>isolated from Melanoselinum decipiens; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SESQUITERPENES (2000-2003)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007783</DescriptorUI>
     <DescriptorName>
      <String>Lactones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D045787</DescriptorUI>
     <DescriptorName>
      <String>Sesquiterpenes, Eudesmane</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2000 Jul;63(7):934-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0369386</ConceptUI>
    <ConceptName>
     <String>11-hydroxy-3-oxo-6H,7H-10-methyl-eudesman-1,2-4,5-dien-6,12-olide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T423849</TermUI>
      <String>11-hydroxy-3-oxo-6H,7H-10-methyl-eudesman-1,2-4,5-dien-6,12-olide</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>09</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013578</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>isatin beta-thiosemicarbazone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>isatizon believed to be Russian synonym
  </Note>
  <Frequency>33</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>THIOSEMICARBAZONES (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007510</DescriptorUI>
     <DescriptorName>
      <String>Isatin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Microb Polon 27(2):111;1978</Source>
   <Source>J Gen Virol 40(3):695;1978</Source>
   <Source>Veterinariia 2:45;1977</Source>
   <Source>Virology 74(2):426;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061438</ConceptUI>
    <ConceptName>
     <String>isatin beta-thiosemicarbazone</String>
    </ConceptName>
    <CASN1Name>2-(1,2-dihydro-2-oxo-3H-indol-3-ylidene)hydrazinecarbothioamide</CASN1Name>
    <RegistryNumber>487-16-1</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061438</Concept1UI>
     <Concept2UI>M0061437</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091441</TermUI>
      <String>isatin beta-thiosemicarbazone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0061437</ConceptUI>
    <ConceptName>
     <String>isatizon</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061438</Concept1UI>
     <Concept2UI>M0061437</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T091440</TermUI>
      <String>isatizon</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013581</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>jacobine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>04</Month>
   <Day>17</Day>
  </DateRevised>
  <Note>RN given refers to (15alpha,20S)-isomer; structure
  </Note>
  <Frequency>13</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011763</DescriptorUI>
     <DescriptorName>
      <String>Pyrrolizidine Alkaloids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Int Agency Cancer Res 10:275;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061443</ConceptUI>
    <ConceptName>
     <String>jacobine</String>
    </ConceptName>
    <CASN1Name>(15 alpha,20R)15,20-epoxy-15,20-dihydro-12-hydroxy- senecionan-11,16-dione</CASN1Name>
    <RegistryNumber>6870-67-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091446</TermUI>
      <String>jacobine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C053369</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ascites microvillar protein p35</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1987</Year>
   <Month>09</Month>
   <Day>15</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateRevised>
  <Note>major calcium-sensitive protein from microvilli of mammary ascites tumor cells; binds phenothiazine in absence of calcium; MW 35kDa
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008840</DescriptorUI>
     <DescriptorName>
      <String>Microfilament Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009363</DescriptorUI>
     <DescriptorName>
      <String>Neoplasm Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>FASEB J 1987;1(1):46</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0151155</ConceptUI>
    <ConceptName>
     <String>ascites microvillar protein p35</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T181160</TermUI>
      <String>ascites microvillar protein p35</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T181159</TermUI>
      <String>AMV p35</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001472</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>iridine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>protamine from rainbow trout Salmo irideus
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011479</DescriptorUI>
     <DescriptorName>
      <String>Protamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Int J Pept Protein Res 1(3):221;1969</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041682</ConceptUI>
    <ConceptName>
     <String>iridine</String>
    </ConceptName>
    <CASN1Name>Iridine</CASN1Name>
    <RegistryNumber>67255-34-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071685</TermUI>
      <String>iridine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001477</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>isolichenin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011134</DescriptorUI>
     <DescriptorName>
      <String>Polysaccharides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 246(22):6722;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041691</ConceptUI>
    <ConceptName>
     <String>isolichenin</String>
    </ConceptName>
    <RegistryNumber>11014-35-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071694</TermUI>
      <String>isolichenin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C084806</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>GOS9 protein, Oryza sativa</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>01</Month>
   <Day>12</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>10</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>root-specific rice protein; has been sequenced
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010940</DescriptorUI>
     <DescriptorName>
      <String>Plant Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Plant Mol Biol 1993 Nov;23(4):889-94</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0225250</ConceptUI>
    <ConceptName>
     <String>GOS9 protein, Oryza sativa</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T509662</TermUI>
      <String>GOS9 protein, Oryza sativa</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>08</Month>
       <Day>05</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C478973</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Fem1c protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>11</Month>
   <Day>22</Day>
  </DateCreated>
  <DateRevised>
   <Year>2019</Year>
   <Month>12</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>a member of the Fem1 protein family; RefSeq NM_020177
  </Note>
  <Frequency>6</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*Proteins (2004-2020)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D043743</DescriptorUI>
     <DescriptorName>
      <String>Ubiquitin-Protein Ligase Complexes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 2003 Oct 17:310(2):133-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0456434</ConceptUI>
    <ConceptName>
     <String>Fem1c protein, human</String>
    </ConceptName>
    <RegistryNumber>EC 2.3.2.23</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T559567</TermUI>
      <String>Fem1c protein, human</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>11</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T587582</TermUI>
      <String>fem-1 homolog c (C.elegans) protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>05</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001492</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>juglomycin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>06</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>LACTONES (72-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009285</DescriptorUI>
     <DescriptorName>
      <String>Naphthoquinones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Jap J Antibiot 24(5):222;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041709</ConceptUI>
    <ConceptName>
     <String>juglomycin</String>
    </ConceptName>
    <CASN1Name>Juglomycin</CASN1Name>
    <RegistryNumber>77904-45-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071712</TermUI>
      <String>juglomycin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001497</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>kavaform</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>complex geriatric analeptic; each tablet contains (+-)-kavain 50mg, magnesium orotate 200mg, silicic acid 10mg, carriec 370mg &amp; extract of vitis viniferae rubr. 50mg
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PYRANS (71-81)</PreviousIndexing>
   <PreviousIndexing>*SILICA (71-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009963</DescriptorUI>
     <DescriptorName>
      <String>Orotic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011753</DescriptorUI>
     <DescriptorName>
      <String>Pyrones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012824</DescriptorUI>
     <DescriptorName>
      <String>Silicic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Z Alternsforsch 29(3):311;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041715</ConceptUI>
    <ConceptName>
     <String>kavaform</String>
    </ConceptName>
    <RegistryNumber>8074-25-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071718</TermUI>
      <String>kavaform</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C053630</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>serotonin-binding protein kinase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1987</Year>
   <Month>10</Month>
   <Day>16</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateRevised>
  <Note>an aspect of protein kinases EC 2.7.1.37
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011494</DescriptorUI>
     <DescriptorName>
      <String>Protein Kinases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Neurochem 1987;49(4):1105</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0151850</ConceptUI>
    <ConceptName>
     <String>serotonin-binding protein kinase</String>
    </ConceptName>
    <RegistryNumber>EC 2.7.1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T181855</TermUI>
      <String>serotonin-binding protein kinase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T181854</TermUI>
      <String>SBP kinase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C046709</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Scotchcast</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1985</Year>
   <Month>10</Month>
   <Day>25</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>07</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>polyurethane resin on fiberglass
  </Note>
  <Frequency>7</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005898</DescriptorUI>
     <DescriptorName>
      <String>Glass</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011140</DescriptorUI>
     <DescriptorName>
      <String>Polyurethanes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D002370</DescriptorUI>
     <DescriptorName>
      <String>Casts, Surgical</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Vet Rec 1985;117(3):55</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0135226</ConceptUI>
    <ConceptName>
     <String>Scotchcast</String>
    </ConceptName>
    <CASN1Name>Scotchcast</CASN1Name>
    <RegistryNumber>9085-80-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T165231</TermUI>
      <String>Scotchcast</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C053803</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hemeprotein b-559</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1987</Year>
   <Month>11</Month>
   <Day>04</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateRevised>
  <Note>MW 78kDa; from Bengal-gram seeds
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006420</DescriptorUI>
     <DescriptorName>
      <String>Hemeproteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem J 1987;243(3):723</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0152237</ConceptUI>
    <ConceptName>
     <String>hemeprotein b-559</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T182242</TermUI>
      <String>hemeprotein b-559</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T182241</TermUI>
      <String>haemoprotein b-559</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C044661</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Burinex K</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1985</Year>
   <Month>05</Month>
   <Day>23</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>07</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>combination of Potassium Chloride and Bumetanide; used in treatment of heart failure
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002034</DescriptorUI>
     <DescriptorName>
      <String>Bumetanide</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011189</DescriptorUI>
     <DescriptorName>
      <String>Potassium Chloride</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Prostgrad Med J 1985;61(711):29</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0130308</ConceptUI>
    <ConceptName>
     <String>Burinex K</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T160313</TermUI>
      <String>Burinex K</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001510</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>kromycin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>01</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>anhydro aglycone of antibiotic pikromycin
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007783</DescriptorUI>
     <DescriptorName>
      <String>Lactones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Am Chem Soc 92(26):7286;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041736</ConceptUI>
    <ConceptName>
     <String>kromycin</String>
    </ConceptName>
    <CASN1Name>((3R-(3R*,5E,7S*,9R*,11E,13S*,14R*))-14-ethyl-13-hydroxy-3,5,7,9,13-pentamethyloxacyclotetradeca-5,11-diene-2,4,10-trione)</CASN1Name>
    <RegistryNumber>20509-23-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071739</TermUI>
      <String>kromycin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001900</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,5-anhydro-D-mannitol-1,6-diphosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*HEXOSEDIPHOSPHATES (73-78)</PreviousIndexing>
   <PreviousIndexing>*MANNITOL (73-78)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008355</DescriptorUI>
     <DescriptorName>
      <String>Mannitol Phosphates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Biochem Biophys 152(10):272;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0042305</ConceptUI>
    <ConceptName>
     <String>2,5-anhydro-D-mannitol-1,6-diphosphate</String>
    </ConceptName>
    <RegistryNumber>671-08-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T072308</TermUI>
      <String>2,5-anhydro-D-mannitol-1,6-diphosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T072307</TermUI>
      <String>2,5-anhydro-D-mannitol-1,6-bisphosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C046806</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-nitrobenzyl mercaptan</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1985</Year>
   <Month>10</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>07</Month>
   <Day>16</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013438</DescriptorUI>
     <DescriptorName>
      <String>Sulfhydryl Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 1985;131(2):687</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0135444</ConceptUI>
    <ConceptName>
     <String>4-nitrobenzyl mercaptan</String>
    </ConceptName>
    <CASN1Name>Benzenemethanethiol, 4-nitro-</CASN1Name>
    <RegistryNumber>26798-33-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T165449</TermUI>
      <String>4-nitrobenzyl mercaptan</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C053834</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>insulin secretory granule membrane glycoprotein 110</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1987</Year>
   <Month>11</Month>
   <Day>10</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateRevised>
  <Note>MW 110kDa; from insulin secretory granule; used to study granule biogenesis
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008562</DescriptorUI>
     <DescriptorName>
      <String>Membrane Glycoproteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D007328</DescriptorUI>
     <DescriptorName>
      <String>Insulin</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Biochem J 1987;245(2):567</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0152327</ConceptUI>
    <ConceptName>
     <String>insulin secretory granule membrane glycoprotein 110</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T182332</TermUI>
      <String>insulin secretory granule membrane glycoprotein 110</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T182331</TermUI>
      <String>SGM 110</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C053835</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hemoglobin Hobart</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1987</Year>
   <Month>11</Month>
   <Day>10</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateRevised>
  <Note>His replaced by Arg in position 20(B1) on alpha chain
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006455</DescriptorUI>
     <DescriptorName>
      <String>Hemoglobins, Abnormal</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Hemoglobin 1987;11(3):211</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0152329</ConceptUI>
    <ConceptName>
     <String>hemoglobin Hobart</String>
    </ConceptName>
    <CASN1Name>Hemoglobin Hobart</CASN1Name>
    <RegistryNumber>111417-21-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T182334</TermUI>
      <String>hemoglobin Hobart</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T182333</TermUI>
      <String>Hb Hobart</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C091458</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-decenoyl-coenzyme A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>02</Month>
   <Day>10</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000214</DescriptorUI>
     <DescriptorName>
      <String>Acyl Coenzyme A</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 1995 Jan 17;34(2):442-50</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0241527</ConceptUI>
    <ConceptName>
     <String>5-decenoyl-coenzyme A</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0241527</Concept1UI>
     <Concept2UI>M0241525</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T271532</TermUI>
      <String>5-decenoyl-coenzyme A</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T271531</TermUI>
      <String>coenzyme A, 5-decenoyl-</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0241525</ConceptUI>
    <ConceptName>
     <String>cis-5-decenoyl-CoA</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0241527</Concept1UI>
     <Concept2UI>M0241525</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T271530</TermUI>
      <String>cis-5-decenoyl-CoA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C047269</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>polyphosphoric acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1986</Year>
   <Month>01</Month>
   <Day>07</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>07</Month>
   <Day>16</Day>
  </DateRevised>
  <Frequency>28</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010756</DescriptorUI>
     <DescriptorName>
      <String>Phosphoric Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011108</DescriptorUI>
     <DescriptorName>
      <String>Polymers</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Anal Biochem 1985;149(2):339</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0136613</ConceptUI>
    <ConceptName>
     <String>polyphosphoric acid</String>
    </ConceptName>
    <RegistryNumber>8017-16-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T166618</TermUI>
      <String>polyphosphoric acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1986)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001902</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cyclic 9 beta-D-arabinosyladenine 3',5'-monophosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CYCL AMP (73-79)</PreviousIndexing>
   <PreviousIndexing>*NUCLEOTIDES, CYCLIC (73-82)</PreviousIndexing>
   <PreviousIndexing>ARABINOSE (73-79)</PreviousIndexing>
   <PreviousIndexing>ARABINOSE/analogs (75-79)</PreviousIndexing>
   <PreviousIndexing>CYCL AMP/*analogs (75-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D001084</DescriptorUI>
     <DescriptorName>
      <String>Vidarabine Phosphate</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Res 32(9):1791;1972</Source>
   <Source>J Med Chem 17(3):259;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0042307</ConceptUI>
    <ConceptName>
     <String>cyclic 9 beta-D-arabinosyladenine 3',5'-monophosphate</String>
    </ConceptName>
    <RegistryNumber>32465-18-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T072310</TermUI>
      <String>cyclic 9 beta-D-arabinosyladenine 3',5'-monophosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T072309</TermUI>
      <String>9 beta-D-arabinofuranosyladenine cyclic 3',5'-phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001542</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>liatrin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>11</Month>
   <Day>18</Day>
  </DateRevised>
  <Note>antileukemic sesquiterpene lactone from Liatris chapmani
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ANTINEOPLASTIC AGENTS (74-79)</PreviousIndexing>
   <PreviousIndexing>LACTONES (74-81)</PreviousIndexing>
   <PreviousIndexing>PLANT EXTRACTS (74-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012717</DescriptorUI>
     <DescriptorName>
      <String>Sesquiterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Am Chem Soc 93(19):4916;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041776</ConceptUI>
    <ConceptName>
     <String>liatrin</String>
    </ConceptName>
    <RegistryNumber>34175-79-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071779</TermUI>
      <String>liatrin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C499046</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Ferd3l protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2019</Year>
   <Month>12</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>an evolutionarily conserved bHLH transcription factor expressed in the CNS; RefSeq NM_033522
  </Note>
  <Frequency>7</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*Nerve Tissue Proteins (2006-2020)</PreviousIndexing>
   <PreviousIndexing>*Transcription Factors (2006-2020)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012097</DescriptorUI>
     <DescriptorName>
      <String>Repressor Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0455257</ConceptUI>
    <ConceptName>
     <String>Ferd3l protein, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T554802</TermUI>
      <String>Ferd3l protein, mouse</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>10</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T635659</TermUI>
      <String>Nato3 protein, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>04</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T635660</TermUI>
      <String>nephew of atonal, fer3 protein, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>04</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T554803</TermUI>
      <String>Fer3-like (Drosophila) protein, mouse</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>10</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001560</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>lutean</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011134</DescriptorUI>
     <DescriptorName>
      <String>Polysaccharides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041791</ConceptUI>
    <ConceptName>
     <String>lutean</String>
    </ConceptName>
    <RegistryNumber>39409-41-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071794</TermUI>
      <String>lutean</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001563</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Lysoneuro</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009419</DescriptorUI>
     <DescriptorName>
      <String>Nerve Tissue Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Minerva Med 63(2):49-167;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041795</ConceptUI>
    <ConceptName>
     <String>Lysoneuro</String>
    </ConceptName>
    <RegistryNumber>11121-86-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071798</TermUI>
      <String>Lysoneuro</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001571</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>gamma-aminobutyrylcholine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>10</Month>
   <Day>27</Day>
  </DateRevised>
  <Frequency>7</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AMINOBUTYRIC ACIDS (72-76)</PreviousIndexing>
   <PreviousIndexing>*CHOLINE (72-75)</PreviousIndexing>
   <PreviousIndexing>GABA/analogs (76-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002794</DescriptorUI>
     <DescriptorName>
      <String>Choline</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Neurochem 30(6):1461;1978</Source>
   <Source>J Pharm Pharmacol 24(3):251;1972</Source>
   <Source>J Pharm Pharmacol 27:529;1975</Source>
   <Source>Trans Am Neurol Assn 99:50;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041802</ConceptUI>
    <ConceptName>
     <String>gamma-aminobutyrylcholine</String>
    </ConceptName>
    <RegistryNumber>541-18-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071805</TermUI>
      <String>gamma-aminobutyrylcholine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001586</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-benzyl salsolidine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>12</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ALKALOIDS (72-79)</PreviousIndexing>
   <PreviousIndexing>*ISOQUINOLINES (72-79)</PreviousIndexing>
   <PreviousIndexing>BENZYL COMPOUNDS (72-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012490</DescriptorUI>
     <DescriptorName>
      <String>Salsoline Alkaloids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Int Pharmacodyn Ther 196:106;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041828</ConceptUI>
    <ConceptName>
     <String>N-benzyl salsolidine</String>
    </ConceptName>
    <CASN1Name>1-methyl-2-benzyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline</CASN1Name>
    <RegistryNumber>19902-16-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071831</TermUI>
      <String>N-benzyl salsolidine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001587</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bimetopyrol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1986</Year>
   <Month>08</Month>
   <Day>05</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ANISOLES (72-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011758</DescriptorUI>
     <DescriptorName>
      <String>Pyrroles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Soc Jap 92(3):305;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041829</ConceptUI>
    <ConceptName>
     <String>bimetopyrol</String>
    </ConceptName>
    <CASN1Name>2-methyl-4,5-bis(p-methoxyphenyl)pyrrole</CASN1Name>
    <RegistryNumber>30011-11-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071832</TermUI>
      <String>bimetopyrol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001590</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,4-3,6-bis(thioanhydro)-D-iditol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1984</Year>
   <Month>10</Month>
   <Day>11</Day>
  </DateRevised>
  <Note>potential antineoplastic agents; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>SULFIDES (72-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013402</DescriptorUI>
     <DescriptorName>
      <String>Sugar Alcohols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Carbohyd Res 21(1):19;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041833</ConceptUI>
    <ConceptName>
     <String>1,4-3,6-bis(thioanhydro)-D-iditol</String>
    </ConceptName>
    <CASN1Name>D-Iditol, 1,3,4,6-tetradeoxy-1,4:3,6-diepithio-</CASN1Name>
    <RegistryNumber>35396-08-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071836</TermUI>
      <String>1,4-3,6-bis(thioanhydro)-D-iditol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001595</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>carbobiotin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BIOTIN (72-76)</PreviousIndexing>
   <PreviousIndexing>*CYCLOPENTANES (72-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D001710</DescriptorUI>
     <DescriptorName>
      <String>Biotin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041841</ConceptUI>
    <ConceptName>
     <String>carbobiotin</String>
    </ConceptName>
    <CASN1Name>cis-hexahydro-4-(4-carboxybutyl)-2-cyclopentimidazolone</CASN1Name>
    <RegistryNumber>37842-47-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071844</TermUI>
      <String>carbobiotin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C049420</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>MTP 1403</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1986</Year>
   <Month>07</Month>
   <Day>11</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>07</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011743</DescriptorUI>
     <DescriptorName>
      <String>Pyrimidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013438</DescriptorUI>
     <DescriptorName>
      <String>Sulfhydryl Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Int Pharmacodyn Ther 1986;280(2):302</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0141600</ConceptUI>
    <ConceptName>
     <String>MTP 1403</String>
    </ConceptName>
    <CASN1Name>6H-Thiopyrano(3,2-d)pyrimidin-2-amine, 7,8-dihydro-4-(1-piperazinyl)-</CASN1Name>
    <RegistryNumber>87466-13-5</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0141600</Concept1UI>
     <Concept2UI>M0141598</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T171605</TermUI>
      <String>MTP 1403</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1986)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T171604</TermUI>
      <String>MTP-1403</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1986)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0141598</ConceptUI>
    <ConceptName>
     <String>2-amino-7,8-dihydro-4-piperazinyl-6H-thiopyrano(3,2-d)pyrimidine</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0141600</Concept1UI>
     <Concept2UI>M0141598</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T171603</TermUI>
      <String>2-amino-7,8-dihydro-4-piperazinyl-6H-thiopyrano(3,2-d)pyrimidine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1986)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C054830</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>glycoprotein BCA 225</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1988</Year>
   <Month>03</Month>
   <Day>16</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateRevised>
  <Note>MW 225 kDa-250 kDa; found mainly in clone of 11T47D breast carcinoma cells; recognized by monoclonal antibodies CU18, CU26 &amp; CU46
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006023</DescriptorUI>
     <DescriptorName>
      <String>Glycoproteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D014408</DescriptorUI>
     <DescriptorName>
      <String>Biomarkers, Tumor</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Am J Pathol 1988;130(2):305</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0154638</ConceptUI>
    <ConceptName>
     <String>glycoprotein BCA 225</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T184643</TermUI>
      <String>glycoprotein BCA 225</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T184642</TermUI>
      <String>glycoprotein BCA-225</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C054836</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>protein C propeptide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1988</Year>
   <Month>03</Month>
   <Day>16</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateRevised>
  <Note>pro-portion of the leader sequence is 24-amino acids in length; do not confuse with pre-portion which is 18 amino acids in length
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011486</DescriptorUI>
     <DescriptorName>
      <String>Protein C</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011498</DescriptorUI>
     <DescriptorName>
      <String>Protein Precursors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 1987;26(22):7003</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0154665</ConceptUI>
    <ConceptName>
     <String>protein C propeptide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T184670</TermUI>
      <String>protein C propeptide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T184669</TermUI>
      <String>propeptide protein C</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C560820</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Fezf1 protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2011</Year>
   <Month>09</Month>
   <Day>06</Day>
  </DateCreated>
  <DateRevised>
   <Year>2019</Year>
   <Month>12</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>Fez - Forebrain Embryonic Zinc-finger; expressed in the forebrain of mouse embryos; RefSeq NM_028462
  </Note>
  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DNA-Binding Proteins (2011-2020)</PreviousIndexing>
   <PreviousIndexing>*Nerve Tissue Proteins (2011-2020)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012097</DescriptorUI>
     <DescriptorName>
      <String>Repressor Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D016335</DescriptorUI>
     <DescriptorName>
      <String>Zinc Fingers</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Comp Neurol. 2011 Jul 1;519(10):1829-46</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0560749</ConceptUI>
    <ConceptName>
     <String>Fezf1 protein, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T796460</TermUI>
      <String>Fezf1 protein, mouse</String>
      <DateCreated>
       <Year>2011</Year>
       <Month>09</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2011)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T796461</TermUI>
      <String>fez family zinc finger protein 1, mouse</String>
      <DateCreated>
       <Year>2011</Year>
       <Month>09</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2011)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001618</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dimethylquinazolone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>analog of METHAQUALONE
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*QUINAZOLINES (72-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008702</DescriptorUI>
     <DescriptorName>
      <String>Methaqualone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Brit J Pharmacol 44(4):805;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041878</ConceptUI>
    <ConceptName>
     <String>dimethylquinazolone</String>
    </ConceptName>
    <RegistryNumber>1769-25-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071881</TermUI>
      <String>dimethylquinazolone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C101347</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-hydroxybutyryl-coenzyme A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>10</Month>
   <Day>21</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000214</DescriptorUI>
     <DescriptorName>
      <String>Acyl Coenzyme A</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 1996 Sep 10;35(36):11710-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0265728</ConceptUI>
    <ConceptName>
     <String>4-hydroxybutyryl-coenzyme A</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T295733</TermUI>
      <String>4-hydroxybutyryl-coenzyme A</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T295732</TermUI>
      <String>coenzyme A, 4-hydroxybutyryl-</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T295731</TermUI>
      <String>4-hydroxybutyryl-CoA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C547153</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>spirastrellolide F methyl ester</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2010</Year>
   <Month>02</Month>
   <Day>18</Day>
  </DateCreated>
  <DateRevised>
   <Year>2014</Year>
   <Month>05</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013141</DescriptorUI>
     <DescriptorName>
      <String>Spiro Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D018942</DescriptorUI>
     <DescriptorName>
      <String>Macrolides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Angew Chem Int Ed Engl. 2009;48(52):9940-5</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0543665</ConceptUI>
    <ConceptName>
     <String>spirastrellolide F methyl ester</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T765910</TermUI>
      <String>spirastrellolide F methyl ester</String>
      <DateCreated>
       <Year>2010</Year>
       <Month>02</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2010)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T859316</TermUI>
      <String>spirastrellolide F</String>
      <DateCreated>
       <Year>2014</Year>
       <Month>05</Month>
       <Day>05</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2014)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C102828</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>methylsuccinyl-coenzyme A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1997</Year>
   <Month>01</Month>
   <Day>15</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateRevised>
  <Note>product of methylmalonyl-CoA mutase rearrangement of glutaryl-CoA; structure in first source
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000214</DescriptorUI>
     <DescriptorName>
      <String>Acyl Coenzyme A</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biofactors 1995-1996;5(2):83-6</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0269051</ConceptUI>
    <ConceptName>
     <String>methylsuccinyl-coenzyme A</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T299056</TermUI>
      <String>methylsuccinyl-coenzyme A</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T299055</TermUI>
      <String>methylsuccinyl-CoA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T299054</TermUI>
      <String>MeSuc-CoA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001629</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-ethyl-N-butylnitrosamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1985</Year>
   <Month>07</Month>
   <Day>19</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*NITROSAMINES (72-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004052</DescriptorUI>
     <DescriptorName>
      <String>Diethylnitrosamine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Z Krebsforsch 77(3):189;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041889</ConceptUI>
    <ConceptName>
     <String>N-ethyl-N-butylnitrosamine</String>
    </ConceptName>
    <RegistryNumber>4549-44-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071892</TermUI>
      <String>N-ethyl-N-butylnitrosamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001631</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N,N'-ethylenebis(5-(2-bromoethylthio)valeramide)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>AMIDES (72-76)</PreviousIndexing>
   <PreviousIndexing>VALERATES (72-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009150</DescriptorUI>
     <DescriptorName>
      <String>Mustard Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharmacol Exp Ther 182(1):77;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041890</ConceptUI>
    <ConceptName>
     <String>N,N'-ethylenebis(5-(2-bromoethylthio)valeramide)</String>
    </ConceptName>
    <RegistryNumber>870-03-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071893</TermUI>
      <String>N,N'-ethylenebis(5-(2-bromoethylthio)valeramide)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C070699</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>FGFBP1 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1991</Year>
   <Month>10</Month>
   <Day>02</Day>
  </DateCreated>
  <DateRevised>
   <Year>2019</Year>
   <Month>12</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>RefSeq NM_005130
  </Note>
  <Frequency>60</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*Carrier Proteins (2005-2020)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D036341</DescriptorUI>
     <DescriptorName>
      <String>Intercellular Signaling Peptides and Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 1991;266(25):16778</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0192384</ConceptUI>
    <ConceptName>
     <String>FGFBP1 protein, human</String>
    </ConceptName>
    <RegistryNumber>139946-12-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T605754</TermUI>
      <String>FGFBP1 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T605755</TermUI>
      <String>fibroblast growth factor binding protein 1, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T605760</TermUI>
      <String>heparin-binding protein 17, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T605761</TermUI>
      <String>HBGF-1-binding protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T605758</TermUI>
      <String>HBGF-2-binding protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T605756</TermUI>
      <String>HBP17 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T605757</TermUI>
      <String>FGFBP protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T605759</TermUI>
      <String>fibroblast growth factor-binding protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C102829</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ethylmalonyl-coenzyme A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1997</Year>
   <Month>01</Month>
   <Day>15</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateRevised>
  <Note>product of methylmalonyl-CoA mutase rearrangement of glutaryl-CoA, structure in first source
  </Note>
  <Frequency>50</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000214</DescriptorUI>
     <DescriptorName>
      <String>Acyl Coenzyme A</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biofactors 1995-1996;5(2):83-6</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0269054</ConceptUI>
    <ConceptName>
     <String>ethylmalonyl-coenzyme A</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T299059</TermUI>
      <String>ethylmalonyl-coenzyme A</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T299057</TermUI>
      <String>EtMal-CoA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T299058</TermUI>
      <String>ethylmalonyl-CoA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001651</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hippuryl-L-phenylacetate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>10</Month>
   <Day>06</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PHENYLACETATES (72-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006626</DescriptorUI>
     <DescriptorName>
      <String>Hippurates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Biochem 25(3):416;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041918</ConceptUI>
    <ConceptName>
     <String>hippuryl-L-phenylacetate</String>
    </ConceptName>
    <CASN1Name>Propanoic acid, 2-(((benzoylamino)acetyl)oxy)-, phenyl ester, (S)-</CASN1Name>
    <RegistryNumber>35935-30-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071921</TermUI>
      <String>hippuryl-L-phenylacetate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C055049</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>myeloma protein Rou</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1988</Year>
   <Month>04</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateRevised>
  <Note>human IgA2 myeloma protein; carries isoallotype marker A2m(2)
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009194</DescriptorUI>
     <DescriptorName>
      <String>Myeloma Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Immunol 1988;140(4):11236</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0155154</ConceptUI>
    <ConceptName>
     <String>myeloma protein Rou</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T185159</TermUI>
      <String>myeloma protein Rou</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T185158</TermUI>
      <String>IgA2 myeloma protein Rou</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001673</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>fluorescein mercuric acetate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>02</Month>
   <Day>25</Day>
  </DateRevised>
  <Note>important as a mercurial
  </Note>
  <Frequency>28</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*MERCURY (73-77)</PreviousIndexing>
   <PreviousIndexing>*ORGANOMETALLIC COMPOUNDS (73-77)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005452</DescriptorUI>
     <DescriptorName>
      <String>Fluoresceins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009941</DescriptorUI>
     <DescriptorName>
      <String>Organomercury Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 454(2):309;1976</Source>
   <Source>Biochim Biophys Acta 550(10):16;1979</Source>
   <Source>J Biochem (Tokyo) 85(2):359;1979</Source>
   <Source>J Biochem 81:971;1977</Source>
   <Source>J Biol Chem 1980;255(2):459</Source>
   <Source>J Biol Chem 248(10):3546;1973</Source>
   <Source>JBC 253(12):4279;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041944</ConceptUI>
    <ConceptName>
     <String>fluorescein mercuric acetate</String>
    </ConceptName>
    <RegistryNumber>3570-80-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071947</TermUI>
      <String>fluorescein mercuric acetate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001685</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>matchamycin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1970</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1987</Year>
   <Month>03</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>antibiotic produced by Streptomyces E-753
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009942</DescriptorUI>
     <DescriptorName>
      <String>Organometallic Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D003300</DescriptorUI>
     <DescriptorName>
      <String>Copper</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Antibiot 23(9):461;1970</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041957</ConceptUI>
    <ConceptName>
     <String>matchamycin</String>
    </ConceptName>
    <RegistryNumber>65454-21-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071960</TermUI>
      <String>matchamycin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C493366</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>berkeleydione</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>11</Month>
   <Day>29</Day>
  </DateCreated>
  <Note>polyketide-terpenoid metabolite, isolated from a Penicillium sp.; structure in first source
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013729</DescriptorUI>
     <DescriptorName>
      <String>Terpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D018942</DescriptorUI>
     <DescriptorName>
      <String>Macrolides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Org Lett. 2004 Mar 18;6(6):1049-52</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0476471</ConceptUI>
    <ConceptName>
     <String>berkeleydione</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T620355</TermUI>
      <String>berkeleydione</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>11</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C038028</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N(alpha)-benzoylarginineamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1983</Year>
   <Month>06</Month>
   <Day>03</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>11</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>RN given refers to parent cpd(S)-isomer
  </Note>
  <Frequency>10</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ARGININE (72-75)</PreviousIndexing>
   <PreviousIndexing>BENZAMIDES (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D001120</DescriptorUI>
     <DescriptorName>
      <String>Arginine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D014568</DescriptorUI>
     <DescriptorName>
      <String>Urokinase-Type Plasminogen Activator</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
     <QualifierName>
      <String>antagonists &amp; inhibitors</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 1983;112(2):754</Source>
   <Source>J Am Chem Soc 94(2):665;1972</Source>
   <Source>Lab Invest 75(32):86;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0114682</ConceptUI>
    <ConceptName>
     <String>N(alpha)-benzoylarginineamide</String>
    </ConceptName>
    <CASN1Name>Benzamide, N-(1-(aminocarbonyl)-4-((aminoiminomethyl)amino)butyl)-, (S)-</CASN1Name>
    <RegistryNumber>965-03-7</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>4299-03-0 (mono-HCl(s)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>4310-58-1 (mono-Na salt.mono-HCl(S)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0114682</Concept1UI>
     <Concept2UI>M0320883</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0114682</Concept1UI>
     <Concept2UI>M0320884</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T144686</TermUI>
      <String>N(alpha)-benzoylarginineamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T144683</TermUI>
      <String>N-BAA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T144685</TermUI>
      <String>N-benzoyl-L-argininamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T144684</TermUI>
      <String>N-alpha-benzoylarginineamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0320883</ConceptUI>
    <ConceptName>
     <String>N(alpha)-benzoylarginineamide monohydrochloride, (s)-isomer</String>
    </ConceptName>
    <RegistryNumber>4299-03-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0114682</Concept1UI>
     <Concept2UI>M0320883</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T350883</TermUI>
      <String>N(alpha)-benzoylarginineamide monohydrochloride, (s)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0320884</ConceptUI>
    <ConceptName>
     <String>N(alpha)-benzoylarginineamide monohydrochloride, monosodium salt., (S)-isomer</String>
    </ConceptName>
    <RegistryNumber>4310-58-1</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0114682</Concept1UI>
     <Concept2UI>M0320884</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T350884</TermUI>
      <String>N(alpha)-benzoylarginineamide monohydrochloride, monosodium salt., (S)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009992</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SC-28763</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>isolated from culture broth of Spicaria divaricata; structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009284</DescriptorUI>
     <DescriptorName>
      <String>Naphthols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiotics 27(10):760;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055185</ConceptUI>
    <ConceptName>
     <String>SC-28763</String>
    </ConceptName>
    <CASN1Name>3-(2-oxopropyl)-3'-methoxycarbonyl-methyl-3,3'4,4-tetrahydro-9,9',10,10'-tetrahydroxy-7,7'-dimeth oxy-1,1'-dioxo-8,8'-bi-1H-naphtho(2,3-c)pyran</CASN1Name>
    <RegistryNumber>55051-93-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T085188</TermUI>
      <String>SC-28763</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085187</TermUI>
      <String>SC 28763</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C049143</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-chloro-N-(4,6-dimethyl-2-pyridiny)benzamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1985</Year>
   <Month>12</Month>
   <Day>23</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001549</DescriptorUI>
     <DescriptorName>
      <String>Benzamides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Experientia 1985;41(11):1409</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0140952</ConceptUI>
    <ConceptName>
     <String>3-chloro-N-(4,6-dimethyl-2-pyridiny)benzamide</String>
    </ConceptName>
    <RegistryNumber>94843-57-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T170957</TermUI>
      <String>3-chloro-N-(4,6-dimethyl-2-pyridiny)benzamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T170956</TermUI>
      <String>N-PCB</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T170955</TermUI>
      <String>N-(4,6-dimethyl-2-pyridinyl)-3-chlorobenzamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C022312</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>acylglycerone-phosphate reductase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>07</Month>
   <Day>20</Day>
  </DateRevised>
  <Frequency>19</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>DIHYDROXYACETONE PHOSPHATE (78-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013401</DescriptorUI>
     <DescriptorName>
      <String>Sugar Alcohol Dehydrogenases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Neurochem 31:125;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0078143</ConceptUI>
    <ConceptName>
     <String>acylglycerone-phosphate reductase</String>
    </ConceptName>
    <RegistryNumber>EC 1.1.1.101</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0078143</Concept1UI>
     <Concept2UI>M0355804</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T108146</TermUI>
      <String>acylglycerone-phosphate reductase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T108143</TermUI>
      <String>acyl-alkyl DHAP reductase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T108142</TermUI>
      <String>acyl-DHAP oxidoreductase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T108140</TermUI>
      <String>acyl DHAP reductase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T108145</TermUI>
      <String>palmitoyldihydroxyacetone-phosphate reductase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T108141</TermUI>
      <String>acyl dihydroxyacetone phosphate NADPH oxidoreductase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T108144</TermUI>
      <String>acyl-dihydroxyacetone phosphate oxidoreductase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0355804</ConceptUI>
    <ConceptName>
     <String>Ayr1p</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0078143</Concept1UI>
     <Concept2UI>M0355804</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T405394</TermUI>
      <String>Ayr1p</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>01</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C489453</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Fgfbp1 protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>09</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2019</Year>
   <Month>12</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>binds to heparin-binding growth factors; RefSeq NM_008009
  </Note>
  <Frequency>27</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*Carrier Proteins (2005-2020)</PreviousIndexing>
   <PreviousIndexing>*Intracellular Signaling Peptides and Proteins (2005-2020)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D036341</DescriptorUI>
     <DescriptorName>
      <String>Intercellular Signaling Peptides and Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D006493</DescriptorUI>
     <DescriptorName>
      <String>Heparin</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0471422</ConceptUI>
    <ConceptName>
     <String>Fgfbp1 protein, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T605764</TermUI>
      <String>Fgfbp1 protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T605765</TermUI>
      <String>fibroblast growth factor binding protein 1, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T605766</TermUI>
      <String>FGF-BP protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C493367</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>berkeleytrione</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>11</Month>
   <Day>29</Day>
  </DateCreated>
  <Note>polyketide-terpenoid metabolite, isolated from a Penicillium sp.; structure in first source
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013729</DescriptorUI>
     <DescriptorName>
      <String>Terpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D018942</DescriptorUI>
     <DescriptorName>
      <String>Macrolides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Org Lett. 2004 Mar 18;6(6):1049-52</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0476472</ConceptUI>
    <ConceptName>
     <String>berkeleytrione</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T620356</TermUI>
      <String>berkeleytrione</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>11</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000592900</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>FJX1 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2014</Year>
   <Month>11</Month>
   <Day>08</Day>
  </DateCreated>
  <DateRevised>
   <Year>2019</Year>
   <Month>12</Month>
   <Day>12</Day>
  </DateRevised>
  <Frequency>6</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*Membrane Proteins (2014-2020)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D036341</DescriptorUI>
     <DescriptorName>
      <String>Intercellular Signaling Peptides and Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>FEBS Lett. 2014 Sep 17;588(18):3511-7.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M000599643</ConceptUI>
    <ConceptName>
     <String>FJX1 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T000870652</TermUI>
      <String>FJX1 protein, human</String>
      <DateCreated>
       <Year>2014</Year>
       <Month>11</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2014)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T000870653</TermUI>
      <String>Four-jointed box protein 1, human</String>
      <DateCreated>
       <Year>2014</Year>
       <Month>11</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2014)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C499093</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Fkrp protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2019</Year>
   <Month>12</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>mutated in one form of congenital muscular dystrophy; RefSeq NM_173430
  </Note>
  <Frequency>31</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*Proteins (2006-2020)</PreviousIndexing>
   <PreviousIndexing>*Transferases (2006-2020)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010430</DescriptorUI>
     <DescriptorName>
      <String>Pentosyltransferases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0467919</ConceptUI>
    <ConceptName>
     <String>Fkrp protein, mouse</String>
    </ConceptName>
    <RegistryNumber>EC 2.4.2.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T592674</TermUI>
      <String>Fkrp protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>06</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T592675</TermUI>
      <String>fukutin related protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>06</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C098179</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>FLII protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>03</Month>
   <Day>18</Day>
  </DateCreated>
  <DateRevised>
   <Year>2019</Year>
   <Month>12</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>RefSeq NM_002018
  </Note>
  <Frequency>104</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CALCIUM-BINDING PROTEINS (1996-2004)</PreviousIndexing>
   <PreviousIndexing>*GELSOLIN (2005-2006)</PreviousIndexing>
   <PreviousIndexing>*MICROFILAMENT PROTEINS (1996-2004)</PreviousIndexing>
   <PreviousIndexing>*Receptors, Cytoplasmic and Nuclear (1997-2020)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008840</DescriptorUI>
     <DescriptorName>
      <String>Microfilament Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015534</DescriptorUI>
     <DescriptorName>
      <String>Trans-Activators</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Am J Hum Genet 1995 Jan;56(1):175-82</Source>
   <Source>Mol Cell Biol. 2004 Mar;24(5):2103-7</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0257931</ConceptUI>
    <ConceptName>
     <String>FLII protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T589719</TermUI>
      <String>FLII protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>06</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T580201</TermUI>
      <String>flightless I protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>03</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T589720</TermUI>
      <String>flightless I homolog (Drosophila) protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>06</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T287936</TermUI>
      <String>FLI protein, human</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T580202</TermUI>
      <String>Fli-I protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>03</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000609263</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>FlII protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2016</Year>
   <Month>07</Month>
   <Day>24</Day>
  </DateCreated>
  <DateRevised>
   <Year>2019</Year>
   <Month>12</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>binds P-Rex1
  </Note>
  <Frequency>43</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*Carrier Proteins (2016-2020)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008840</DescriptorUI>
     <DescriptorName>
      <String>Microfilament Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015534</DescriptorUI>
     <DescriptorName>
      <String>Trans-Activators</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nat Commun. 2016;7:10664.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M000619858</ConceptUI>
    <ConceptName>
     <String>FlII protein, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T000904464</TermUI>
      <String>FlII protein, mouse</String>
      <DateCreated>
       <Year>2016</Year>
       <Month>07</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2016)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T831506</TermUI>
      <String>flil protein, mouse</String>
      <DateCreated>
       <Year>2012</Year>
       <Month>10</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T521827</TermUI>
      <String>flightless I homolog (Drosophila), mouse</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>10</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T521826</TermUI>
      <String>Fliih protein, mouse</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>10</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T648253</TermUI>
      <String>flightless I homolog (Drosophila) protein, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>08</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C024775</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>isoepoxydon dehydrogenase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>06</Month>
   <Day>17</Day>
  </DateCreated>
  <Note>interconversion between phyllostine (2-hydroxymethyl-5,6-epoxy-1,4-benzoquinone) and isoepoxydon (4-hydroxy-5,6-epoxycyclohex-2-en-1-one
  </Note>
  <Frequency>14</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>QUINONES (80-80)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010088</DescriptorUI>
     <DescriptorName>
      <String>Oxidoreductases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Can J Microbiol 1979;25(8):881</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0083344</ConceptUI>
    <ConceptName>
     <String>isoepoxydon dehydrogenase</String>
    </ConceptName>
    <RegistryNumber>EC 1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T113347</TermUI>
      <String>isoepoxydon dehydrogenase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C024831</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dTDP-L-dihydrostreptose-streptidine-6-phosphate dihydrostreptosyltransferase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>06</Month>
   <Day>20</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>enzyme involved in biosynthesis of streptomycin; from Streptomyces griseus
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010430</DescriptorUI>
     <DescriptorName>
      <String>Pentosyltransferases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Biochem 1980;105(1):139</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0083467</ConceptUI>
    <ConceptName>
     <String>dTDP-L-dihydrostreptose-streptidine-6-phosphate dihydrostreptosyltransferase</String>
    </ConceptName>
    <RegistryNumber>EC 2.4.2.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T113470</TermUI>
      <String>dTDP-L-dihydrostreptose-streptidine-6-phosphate dihydrostreptosyltransferase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T113469</TermUI>
      <String>DSSPDStransferase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C024794</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dihydrocytochalasin B</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>06</Month>
   <Day>30</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>inhibits cell motility in many eucaryotic cells
  </Note>
  <Frequency>82</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003571</DescriptorUI>
     <DescriptorName>
      <String>Cytochalasin B</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Anal Biochem 1980;103(2):316</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0083392</ConceptUI>
    <ConceptName>
     <String>dihydrocytochalasin B</String>
    </ConceptName>
    <RegistryNumber>39156-67-7</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>22263-93-0 (dihydrocytochalasin C)</RelatedRegistryNumber>
     <RelatedRegistryNumber>30276-81-4 (dihydrocytochalasin D)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0083392</Concept1UI>
     <Concept2UI>M0315938</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0083392</Concept1UI>
     <Concept2UI>M0315937</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T113395</TermUI>
      <String>dihydrocytochalasin B</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0315938</ConceptUI>
    <ConceptName>
     <String>dihydrocytochalasin D</String>
    </ConceptName>
    <RegistryNumber>30276-81-4</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0083392</Concept1UI>
     <Concept2UI>M0315938</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T345938</TermUI>
      <String>dihydrocytochalasin D</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0315937</ConceptUI>
    <ConceptName>
     <String>dihydrocytochalasin C</String>
    </ConceptName>
    <RegistryNumber>22263-93-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0083392</Concept1UI>
     <Concept2UI>M0315937</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T345937</TermUI>
      <String>dihydrocytochalasin C</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C024785</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-methylnicotinamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>06</Month>
   <Day>30</Day>
  </DateCreated>
  <DateRevised>
   <Year>1992</Year>
   <Month>06</Month>
   <Day>18</Day>
  </DateRevised>
  <Note>potentiates cytotoxicity of N-methyl-N-nitrosourea
  </Note>
  <Frequency>24</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009536</DescriptorUI>
     <DescriptorName>
      <String>Niacinamide</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Biochem 1980;105(3):525</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0083369</ConceptUI>
    <ConceptName>
     <String>5-methylnicotinamide</String>
    </ConceptName>
    <CASN1Name>5-methyl-3-pyridinecarboxamide</CASN1Name>
    <RegistryNumber>70-57-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T113372</TermUI>
      <String>5-methylnicotinamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C022275</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>pre-uteroglobin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>22</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011498</DescriptorUI>
     <DescriptorName>
      <String>Protein Precursors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014598</DescriptorUI>
     <DescriptorName>
      <String>Uteroglobin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Biochem 99(2):361;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0078063</ConceptUI>
    <ConceptName>
     <String>pre-uteroglobin</String>
    </ConceptName>
    <CASN1Name>Blastokinin, pre-</CASN1Name>
    <RegistryNumber>67512-09-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T108066</TermUI>
      <String>pre-uteroglobin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C447640</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>feralex</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>02</Month>
   <Day>24</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009005</DescriptorUI>
     <DescriptorName>
      <String>Monosaccharides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011728</DescriptorUI>
     <DescriptorName>
      <String>Pyridones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Inorg Biochem 2002 Jan 1;88(1):19-24</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0415530</ConceptUI>
    <ConceptName>
     <String>feralex</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T483322</TermUI>
      <String>feralex</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>02</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T483323</TermUI>
      <String>2-deoxy-2-(N-carbamoylmethyl-(N'-2'-methyl-3'-hydroxypyrid-4'-one))-D-glucopyranose</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>02</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C467714</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3,9-dicyano-5,6,6a,10a-tetrahydro-4a,7,7,10a-tetramethyl-2H-phenanthrene-2(4aH),8(7H)-dione</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>11</Month>
   <Day>11</Day>
  </DateCreated>
  <Note>inhibits nitric oxide production; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009570</DescriptorUI>
     <DescriptorName>
      <String>Nitriles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010616</DescriptorUI>
     <DescriptorName>
      <String>Phenanthrenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 2002 Oct 24;45(22):4801-5</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0441835</ConceptUI>
    <ConceptName>
     <String>3,9-dicyano-5,6,6a,10a-tetrahydro-4a,7,7,10a-tetramethyl-2H-phenanthrene-2(4aH),8(7H)-dione</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T525844</TermUI>
      <String>3,9-dicyano-5,6,6a,10a-tetrahydro-4a,7,7,10a-tetramethyl-2H-phenanthrene-2(4aH),8(7H)-dione</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>11</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T525845</TermUI>
      <String>ylgucpd40</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>11</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C561032</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>octaoxyethylene-laurate ester</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2011</Year>
   <Month>09</Month>
   <Day>15</Day>
  </DateCreated>
  <Note>a surfactant
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007848</DescriptorUI>
     <DescriptorName>
      <String>Laurates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011092</DescriptorUI>
     <DescriptorName>
      <String>Polyethylene Glycols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Int J Pharm 2011 Jun 30;412(1-2):142-7</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0561015</ConceptUI>
    <ConceptName>
     <String>octaoxyethylene-laurate ester</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T796923</TermUI>
      <String>octaoxyethylene-laurate ester</String>
      <DateCreated>
       <Year>2011</Year>
       <Month>09</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2011)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T796924</TermUI>
      <String>PEG-8-L</String>
      <DateCreated>
       <Year>2011</Year>
       <Month>09</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2011)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C530652</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SERPINB13 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2008</Year>
   <Month>08</Month>
   <Day>12</Day>
  </DateCreated>
  <DateRevised>
   <Year>2008</Year>
   <Month>08</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>RefSeq NM_012397
  </Note>
  <Frequency>19</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015843</DescriptorUI>
     <DescriptorName>
      <String>Serpins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0358479</ConceptUI>
    <ConceptName>
     <String>SERPINB13 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T408919</TermUI>
      <String>SERPINB13 protein, human</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>03</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T408920</TermUI>
      <String>headpin protein, human</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>03</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T581578</TermUI>
      <String>serine (or cysteine) proteinase inhibitor, clade B (ovalbumin), member 13 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>04</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C513365</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>brunsvicamide B</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>09</Month>
   <Day>11</Day>
  </DateCreated>
  <Note>isolated from Mycobacterium tuberculosis; structure in first source
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010456</DescriptorUI>
     <DescriptorName>
      <String>Peptides, Cyclic</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D017027</DescriptorUI>
     <DescriptorName>
      <String>Protein Tyrosine Phosphatases</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
     <QualifierName>
      <String>antagonists &amp; inhibitors</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Med Chem 2006 Aug 10;49(16):4871-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0501608</ConceptUI>
    <ConceptName>
     <String>brunsvicamide B</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T681223</TermUI>
      <String>brunsvicamide B</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C513366</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>brunsvicamide C</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>09</Month>
   <Day>11</Day>
  </DateCreated>
  <Note>isolated from Mycobacterium tuberculosis; structure in first source
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010456</DescriptorUI>
     <DescriptorName>
      <String>Peptides, Cyclic</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D017027</DescriptorUI>
     <DescriptorName>
      <String>Protein Tyrosine Phosphatases</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
     <QualifierName>
      <String>antagonists &amp; inhibitors</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Med Chem 2006 Aug 10;49(16):4871-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0501609</ConceptUI>
    <ConceptName>
     <String>brunsvicamide C</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T681224</TermUI>
      <String>brunsvicamide C</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C024803</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>pasresin B</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>05</Month>
   <Day>27</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>07</Month>
   <Day>15</Day>
  </DateRevised>
  <Note>RN given refers to cpd with unknown MF; see also pasresin A
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010895</DescriptorUI>
     <DescriptorName>
      <String>Pit and Fissure Sealants</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Wiad Lek 1980;33(1):19</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0083406</ConceptUI>
    <ConceptName>
     <String>pasresin B</String>
    </ConceptName>
    <CASN1Name>Pasresin B</CASN1Name>
    <RegistryNumber>78515-79-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T113409</TermUI>
      <String>pasresin B</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C024807</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>gumisol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>05</Month>
   <Day>27</Day>
  </DateCreated>
  <DateRevised>
   <Year>1999</Year>
   <Month>01</Month>
   <Day>06</Day>
  </DateRevised>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ANTIHYPERTENSIVE AGENTS (80-99)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006812</DescriptorUI>
     <DescriptorName>
      <String>Humic Substances</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Vrach Delo 1980;(1):103</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0083414</ConceptUI>
    <ConceptName>
     <String>gumisol</String>
    </ConceptName>
    <CASN1Name>Gumisol</CASN1Name>
    <RegistryNumber>77536-25-5</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0083414</Concept1UI>
     <Concept2UI>M0083413</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0083414</Concept1UI>
     <Concept2UI>M0083412</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T113417</TermUI>
      <String>gumisol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0083413</ConceptUI>
    <ConceptName>
     <String>humisol</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0083414</Concept1UI>
     <Concept2UI>M0083413</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T113416</TermUI>
      <String>humisol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0083412</ConceptUI>
    <ConceptName>
     <String>gumizol</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0083414</Concept1UI>
     <Concept2UI>M0083412</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T113415</TermUI>
      <String>gumizol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C513367</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6-cyanouridine 5'-O-monophosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>09</Month>
   <Day>11</Day>
  </DateCreated>
  <Note>inhibits orotidine monophosphate decarboxylase; structure in first source
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014542</DescriptorUI>
     <DescriptorName>
      <String>Uridine Monophosphate</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 2006 Aug 10;49(16):4937-45</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0501610</ConceptUI>
    <ConceptName>
     <String>6-cyanouridine 5'-O-monophosphate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T681225</TermUI>
      <String>6-cyanouridine 5'-O-monophosphate</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T681226</TermUI>
      <String>6-CN-UMP</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C491168</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Sorl1 protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>09</Month>
   <Day>29</Day>
  </DateCreated>
  <Note>sorLA -- sorting protein-related receptor containing LDLR class A repeats; binds alpha2-macroglobulin receptor-associated protein; RefSeq NM_011436
  </Note>
  <Frequency>47</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011973</DescriptorUI>
     <DescriptorName>
      <String>Receptors, LDL</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D026901</DescriptorUI>
     <DescriptorName>
      <String>Membrane Transport Proteins</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D009419</DescriptorUI>
     <DescriptorName>
      <String>Nerve Tissue Proteins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0468647</ConceptUI>
    <ConceptName>
     <String>Sorl1 protein, mouse</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T595040</TermUI>
      <String>Sorl1 protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T595043</TermUI>
      <String>SorLA protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T595041</TermUI>
      <String>sortilin-related receptor, LDLR class A repeats-containing protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T595042</TermUI>
      <String>LR11 protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C024815</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>9,10-dibromopalmitic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>06</Month>
   <Day>18</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>11</Month>
   <Day>26</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010169</DescriptorUI>
     <DescriptorName>
      <String>Palmitic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Lipids 1980;15(4):255</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0083432</ConceptUI>
    <ConceptName>
     <String>9,10-dibromopalmitic acid</String>
    </ConceptName>
    <RegistryNumber>77503-27-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T113435</TermUI>
      <String>9,10-dibromopalmitic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C513368</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6-aminouridine 5'-O-monophosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>09</Month>
   <Day>11</Day>
  </DateCreated>
  <Note>inhibits orotidine monophosphate decarboxylase; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014542</DescriptorUI>
     <DescriptorName>
      <String>Uridine Monophosphate</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 2006 Aug 10;49(16):4937-45</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0501611</ConceptUI>
    <ConceptName>
     <String>6-aminouridine 5'-O-monophosphate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T681227</TermUI>
      <String>6-aminouridine 5'-O-monophosphate</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T681228</TermUI>
      <String>6-NH2-UMP</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C024819</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>diethylstilbestrol pinacolone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>06</Month>
   <Day>18</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>07</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004054</DescriptorUI>
     <DescriptorName>
      <String>Diethylstilbestrol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem J 1980;185(1):129</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0083441</ConceptUI>
    <ConceptName>
     <String>diethylstilbestrol pinacolone</String>
    </ConceptName>
    <CASN1Name>3-hexanone, 4,4-bis(4-hydroxyphenyl)-</CASN1Name>
    <RegistryNumber>18922-13-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T113444</TermUI>
      <String>diethylstilbestrol pinacolone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C513369</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-(4-fluorophenyl)-2-methyl-3-(thiomorpholin-4-yl)methyl-5-(4-methylphenyl)-1H-pyrrole</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>09</Month>
   <Day>11</Day>
  </DateCreated>
  <Note>has antitubercular activity; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009025</DescriptorUI>
     <DescriptorName>
      <String>Morpholines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011758</DescriptorUI>
     <DescriptorName>
      <String>Pyrroles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 2006 Aug 10;49(16):4946-52</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0501612</ConceptUI>
    <ConceptName>
     <String>1-(4-fluorophenyl)-2-methyl-3-(thiomorpholin-4-yl)methyl-5-(4-methylphenyl)-1H-pyrrole</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T681229</TermUI>
      <String>1-(4-fluorophenyl)-2-methyl-3-(thiomorpholin-4-yl)methyl-5-(4-methylphenyl)-1H-pyrrole</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T681230</TermUI>
      <String>FMTMMP-pyrrole</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C513370</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>(2-tert-butoxy-1-(2-cyclohexyl-1-(1-formyl-2-(2-oxopyrrolidin-3-yl)ethylcarbamoyl)ethylcarbamoyl)propyl)carbamic acid benzyl ester</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>09</Month>
   <Day>11</Day>
  </DateCreated>
  <Note>inhibits SARS-CoV 3CL protease; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002219</DescriptorUI>
     <DescriptorName>
      <String>Carbamates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004151</DescriptorUI>
     <DescriptorName>
      <String>Dipeptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 2006 Aug 10;49(16):4971-80</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0501613</ConceptUI>
    <ConceptName>
     <String>(2-tert-butoxy-1-(2-cyclohexyl-1-(1-formyl-2-(2-oxopyrrolidin-3-yl)ethylcarbamoyl)ethylcarbamoyl)propyl)carbamic acid benzyl ester</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0501613</Concept1UI>
     <Concept2UI>M0501614</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T681231</TermUI>
      <String>(2-tert-butoxy-1-(2-cyclohexyl-1-(1-formyl-2-(2-oxopyrrolidin-3-yl)ethylcarbamoyl)ethylcarbamoyl)propyl)carbamic acid benzyl ester</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0501614</ConceptUI>
    <ConceptName>
     <String>TG 0205221</String>
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    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0501613</Concept1UI>
     <Concept2UI>M0501614</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T681232</TermUI>
      <String>TG 0205221</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T681234</TermUI>
      <String>TG0205221</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T681233</TermUI>
      <String>TG-0205221</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C513371</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,6-dimethylphenyl 2-((3,5-bis(methyloxy)-4-((3-(4-methyl-1-piperazinyl)propyl)oxy)phenyl)amino)-4-pyrimidinyl(2,4-bis(methyloxy)phenyl)carbamate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>09</Month>
   <Day>11</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002219</DescriptorUI>
     <DescriptorName>
      <String>Carbamates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011743</DescriptorUI>
     <DescriptorName>
      <String>Pyrimidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D019860</DescriptorUI>
     <DescriptorName>
      <String>Lymphocyte Specific Protein Tyrosine Kinase p56(lck)</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
     <QualifierName>
      <String>antagonists &amp; inhibitors</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Med Chem 2006 Aug 10;49(16):4981-91</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0501615</ConceptUI>
    <ConceptName>
     <String>2,6-dimethylphenyl 2-((3,5-bis(methyloxy)-4-((3-(4-methyl-1-piperazinyl)propyl)oxy)phenyl)amino)-4-pyrimidinyl(2,4-bis(methyloxy)phenyl)carbamate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T681235</TermUI>
      <String>2,6-dimethylphenyl 2-((3,5-bis(methyloxy)-4-((3-(4-methyl-1-piperazinyl)propyl)oxy)phenyl)amino)-4-pyrimidinyl(2,4-bis(methyloxy)phenyl)carbamate</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T681236</TermUI>
      <String>2,6-dimethylphenyl BMPPBC</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C024829</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>8-hydroxyguanine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>06</Month>
   <Day>20</Day>
  </DateCreated>
  <DateRevised>
   <Year>1993</Year>
   <Month>04</Month>
   <Day>15</Day>
  </DateRevised>
  <Frequency>1157</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D006147</DescriptorUI>
     <DescriptorName>
      <String>Guanine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Adv Exp Med Biol 1979;122B:395</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0083463</ConceptUI>
    <ConceptName>
     <String>8-hydroxyguanine</String>
    </ConceptName>
    <CASN1Name>1H-purine-6,8-dione, 2-amino-7,9-dihydro-</CASN1Name>
    <RegistryNumber>5614-64-2</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0083463</Concept1UI>
     <Concept2UI>M0083459</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0083463</Concept1UI>
     <Concept2UI>M0083462</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0083463</Concept1UI>
     <Concept2UI>M0083460</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0083463</Concept1UI>
     <Concept2UI>M0083461</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T113466</TermUI>
      <String>8-hydroxyguanine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0083459</ConceptUI>
    <ConceptName>
     <String>2-amino-6,8-dihydroxypurine</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0083463</Concept1UI>
     <Concept2UI>M0083459</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T113462</TermUI>
      <String>2-amino-6,8-dihydroxypurine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0083462</ConceptUI>
    <ConceptName>
     <String>oxo-8-Gua</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0083463</Concept1UI>
     <Concept2UI>M0083462</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T113465</TermUI>
      <String>oxo-8-Gua</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0083460</ConceptUI>
    <ConceptName>
     <String>8-oxo-7,8-dihydroguanine</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0083463</Concept1UI>
     <Concept2UI>M0083460</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T113463</TermUI>
      <String>8-oxo-7,8-dihydroguanine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0083461</ConceptUI>
    <ConceptName>
     <String>8-oxoguanine</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0083463</Concept1UI>
     <Concept2UI>M0083461</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T113464</TermUI>
      <String>8-oxoguanine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C530653</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Serpinb13 protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2008</Year>
   <Month>08</Month>
   <Day>12</Day>
  </DateCreated>
  <DateRevised>
   <Year>2008</Year>
   <Month>08</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>RefSeq NM_172852
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015843</DescriptorUI>
     <DescriptorName>
      <String>Serpins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0511311</ConceptUI>
    <ConceptName>
     <String>Serpinb13 protein, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T701550</TermUI>
      <String>Serpinb13 protein, mouse</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>07</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T701551</TermUI>
      <String>serine (or cysteine) peptidase inhibitor, clade B (ovalbumin), member 13, mouse</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>07</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C513372</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>P(1)-(adenosin-5'-yl)methylenephospho-P(2)-(7-hydroxy-6-(ethyl-2-yl)-5-methoxy-4-methylphthalan-1-one)phosphonate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>09</Month>
   <Day>11</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000249</DescriptorUI>
     <DescriptorName>
      <String>Adenosine Monophosphate</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D007168</DescriptorUI>
     <DescriptorName>
      <String>IMP Dehydrogenase</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
     <QualifierName>
      <String>antagonists &amp; inhibitors</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Med Chem 2006 Aug 10;49(16):5018-22</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0501616</ConceptUI>
    <ConceptName>
     <String>P(1)-(adenosin-5'-yl)methylenephospho-P(2)-(7-hydroxy-6-(ethyl-2-yl)-5-methoxy-4-methylphthalan-1-one)phosphonate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T681237</TermUI>
      <String>P(1)-(adenosin-5'-yl)methylenephospho-P(2)-(7-hydroxy-6-(ethyl-2-yl)-5-methoxy-4-methylphthalan-1-one)phosphonate</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T681238</TermUI>
      <String>P(1)-AMP-P(2)-HEMMP</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C417036</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>technetium Tc 99m annexin V</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>19</Day>
  </DateCreated>
  <Frequency>58</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015609</DescriptorUI>
     <DescriptorName>
      <String>Organotechnetium Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D017304</DescriptorUI>
     <DescriptorName>
      <String>Annexin A5</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Circulation 2000 Nov 7;102(19 Suppl 3):III228-32</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0374885</ConceptUI>
    <ConceptName>
     <String>technetium Tc 99m annexin V</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T431371</TermUI>
      <String>technetium Tc 99m annexin V</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>12</Month>
       <Day>19</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T431372</TermUI>
      <String>99m-Tc-annexin V</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>12</Month>
       <Day>19</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C108683</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>LCT1 protein, Triticum aestivum</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1997</Year>
   <Month>11</Month>
   <Day>07</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>low-affinity cation transporter; contains PEST sequences; isolated from Triticum aestivum; has been sequenced; GenBank AF015523
  </Note>
  <Frequency>7</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CARRIER PROTEINS (1997-2004)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010940</DescriptorUI>
     <DescriptorName>
      <String>Plant Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D027682</DescriptorUI>
     <DescriptorName>
      <String>Cation Transport Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Proc Natl Acad Sci U S A 1997 Sep 30;94(20):11079-84</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0282312</ConceptUI>
    <ConceptName>
     <String>LCT1 protein, Triticum aestivum</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T312317</TermUI>
      <String>LCT1 protein, Triticum aestivum</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C024847</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-nitro-2-aminopropionic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>06</Month>
   <Day>24</Day>
  </DateCreated>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000409</DescriptorUI>
     <DescriptorName>
      <String>Alanine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 1980;255(10):4772</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0083503</ConceptUI>
    <ConceptName>
     <String>3-nitro-2-aminopropionic acid</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0083503</Concept1UI>
     <Concept2UI>M0083502</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T113506</TermUI>
      <String>3-nitro-2-aminopropionic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0083502</ConceptUI>
    <ConceptName>
     <String>3-nitro-2-aminopropionate</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0083503</Concept1UI>
     <Concept2UI>M0083502</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T113505</TermUI>
      <String>3-nitro-2-aminopropionate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C101554</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ODV-E35 protein, Autographa californica nuclear polyhedrosis virus</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>10</Month>
   <Day>30</Day>
  </DateCreated>
  <DateRevised>
   <Year>2007</Year>
   <Month>10</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>ODV-E - Occlusion-Derived Virus Envelope protein; from Autographa californica nuclear polyhedrosis virus (AcMNPV);
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014759</DescriptorUI>
     <DescriptorName>
      <String>Viral Envelope Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Virology 1996 Aug 1;222(1):100-14</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0266194</ConceptUI>
    <ConceptName>
     <String>ODV-E35 protein, Autographa californica nuclear polyhedrosis virus</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T551222</TermUI>
      <String>ODV-E35 protein, Autographa californica nuclear polyhedrosis virus</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>09</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T551418</TermUI>
      <String>ODV-E35 protein, AcMNPV</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>09</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C024869</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-bromohexestrol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>07</Month>
   <Day>02</Day>
  </DateCreated>
  <Note>estrogen-receptor-based agent for imaging of human breast tumors
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D006589</DescriptorUI>
     <DescriptorName>
      <String>Hexestrol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nucl Med 1980;21(6):550</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0083566</ConceptUI>
    <ConceptName>
     <String>1-bromohexestrol</String>
    </ConceptName>
    <CASN1Name>Phenol, 4,4'-(1,2-diethyl-1,2-ethanediyl)bis(2-bromo-, (R*,S*)-</CASN1Name>
    <RegistryNumber>74536-64-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T113569</TermUI>
      <String>1-bromohexestrol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C024870</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-iodohexestrol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>07</Month>
   <Day>02</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>05</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>estrogen-receptor-based agent for imaging of human breast tumors; RN given refers to (R*,S*)-isomer
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D006589</DescriptorUI>
     <DescriptorName>
      <String>Hexestrol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nucl Med 1980;21(6):550</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0083567</ConceptUI>
    <ConceptName>
     <String>1-iodohexestrol</String>
    </ConceptName>
    <CASN1Name>Phenol, 4,4'-(1,2-diethyl-1,2-ethanediyl)bis(2-iodo-, (R*,S*)-</CASN1Name>
    <RegistryNumber>55508-15-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T113570</TermUI>
      <String>1-iodohexestrol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C024887</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N,N-dimethyldoxorubicin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>07</Month>
   <Day>07</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>11</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>RN given refers to parent cpd(8S-cis)-isomer
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004317</DescriptorUI>
     <DescriptorName>
      <String>Doxorubicin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Res 1980;40(6):1928</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0083602</ConceptUI>
    <ConceptName>
     <String>N,N-dimethyldoxorubicin</String>
    </ConceptName>
    <CASN1Name>5,12-naphthacenedione, 7,8,9,10-tetrahydro-6,8,11-trihydroxy-8-(hydroxyacetyl)-1-methoxy-10-((2,3,6-trideoxy-3-(dimethylamino)-alpha-L-lyxo-hexopyranosyl)oxy)-, (8S-cis)-</CASN1Name>
    <RegistryNumber>70222-95-6</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>67106-76-7 (HCl(8S-cis)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0083602</Concept1UI>
     <Concept2UI>M0316025</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T113605</TermUI>
      <String>N,N-dimethyldoxorubicin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T113604</TermUI>
      <String>N,N-dimethyladriamycin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0316025</ConceptUI>
    <ConceptName>
     <String>N,N-dimethyldoxorubicin hydrochloride, (8S-cis)-isomer</String>
    </ConceptName>
    <RegistryNumber>67106-76-7</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0083602</Concept1UI>
     <Concept2UI>M0316025</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T346025</TermUI>
      <String>N,N-dimethyldoxorubicin hydrochloride, (8S-cis)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T346026</TermUI>
      <String>N,N-dimethyldoxorubicin monohydrochloride</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C024878</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3',4'-dihydroxynomifensine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>07</Month>
   <Day>03</Day>
  </DateCreated>
  <DateRevised>
   <Year>1994</Year>
   <Month>07</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>partial dopamine vascular agonist
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009627</DescriptorUI>
     <DescriptorName>
      <String>Nomifensine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Pharmacol 1980;32(3):225</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0083587</ConceptUI>
    <ConceptName>
     <String>3',4'-dihydroxynomifensine</String>
    </ConceptName>
    <CASN1Name>1,2-benzenediol,4-(8-amino-1,2,3,4-tetrahydro-2-methyl-4-isoquinolinyl)-</CASN1Name>
    <RegistryNumber>69275-19-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T113590</TermUI>
      <String>3',4'-dihydroxynomifensine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C416354</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>aspergillamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>05</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004151</DescriptorUI>
     <DescriptorName>
      <String>Dipeptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007211</DescriptorUI>
     <DescriptorName>
      <String>Indoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Bioorg Med Chem Lett 2000 Aug 7;10(15):1701-5</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0373828</ConceptUI>
    <ConceptName>
     <String>aspergillamide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T430078</TermUI>
      <String>aspergillamide</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>12</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T430079</TermUI>
      <String>aspergillamide A</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>12</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C560998</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>BODIPY-PC</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2011</Year>
   <Month>09</Month>
   <Day>14</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>8</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001896</DescriptorUI>
     <DescriptorName>
      <String>Boron Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006575</DescriptorUI>
     <DescriptorName>
      <String>Heterocyclic Compounds, 3-Ring</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Phys Chem B. 2011 May 19;115(19):6157-65</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0560980</ConceptUI>
    <ConceptName>
     <String>BODIPY-PC</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T796859</TermUI>
      <String>BODIPY-PC</String>
      <DateCreated>
       <Year>2011</Year>
       <Month>09</Month>
       <Day>14</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2011)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C108667</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>TrwD protein, E coli</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1997</Year>
   <Month>11</Month>
   <Day>04</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>02</Month>
   <Day>24</Day>
  </DateRevised>
  <Note>required for bacterial conjugation; isolated from E. coli; amino acid sequence in first source; GenBank X81123
  </Note>
  <Frequency>7</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000251</DescriptorUI>
     <DescriptorName>
      <String>Adenosine Triphosphatases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029968</DescriptorUI>
     <DescriptorName>
      <String>Escherichia coli Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D001425</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Outer Membrane Proteins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D003227</DescriptorUI>
     <DescriptorName>
      <String>Conjugation, Genetic</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Biol Chem 1997 Oct 10;272(41):25583-90</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0282275</ConceptUI>
    <ConceptName>
     <String>TrwD protein, E coli</String>
    </ConceptName>
    <RegistryNumber>EC 3.6.1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T312280</TermUI>
      <String>TrwD protein, E coli</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C561033</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-O-demethylgrandisin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2011</Year>
   <Month>09</Month>
   <Day>15</Day>
  </DateCreated>
  <Note>a metabolite of grandisin; has antineoplastic activity; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005663</DescriptorUI>
     <DescriptorName>
      <String>Furans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D017705</DescriptorUI>
     <DescriptorName>
      <String>Lignans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Exp Toxicol Pathol 2011 Jul;63(5):505-10</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0561016</ConceptUI>
    <ConceptName>
     <String>4-O-demethylgrandisin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T796925</TermUI>
      <String>4-O-demethylgrandisin</String>
      <DateCreated>
       <Year>2011</Year>
       <Month>09</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2011)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C101540</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>DLL protein, Branchiostoma floridae</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>10</Month>
   <Day>28</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>09</Month>
   <Day>23</Day>
  </DateRevised>
  <Note>Distal-less homolog from amphioxus; amino acid sequence in first source; GenBank U47058
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004268</DescriptorUI>
     <DescriptorName>
      <String>DNA-Binding Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009419</DescriptorUI>
     <DescriptorName>
      <String>Nerve Tissue Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009687</DescriptorUI>
     <DescriptorName>
      <String>Nuclear Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Development 1996 Sep;122(9):2911-20</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0266161</ConceptUI>
    <ConceptName>
     <String>DLL protein, Branchiostoma floridae</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T551220</TermUI>
      <String>DLL protein, Branchiostoma floridae</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>09</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "2">
  <SupplementalRecordUI>C089158</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>PEN protocol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>a chemotherapy protocol consisting of the above compounds; used for the treatment of non-Hodgkin's lymphoma
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000971</DescriptorUI>
     <DescriptorName>
      <String>Antineoplastic Combined Chemotherapy Protocols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005047</DescriptorUI>
     <DescriptorName>
      <String>Etoposide</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008942</DescriptorUI>
     <DescriptorName>
      <String>Mitoxantrone</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011241</DescriptorUI>
     <DescriptorName>
      <String>Prednisone</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Semin Hematol 1994 Apr;31(2 Suppl 3):23-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0235757</ConceptUI>
    <ConceptName>
     <String>PEN protocol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T265762</TermUI>
      <String>PEN protocol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T430134</TermUI>
      <String>EMP regimen</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>12</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C024897</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dihydropteroylpolyglutamate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>07</Month>
   <Day>11</Day>
  </DateCreated>
  <Note>inhibits methylenetetrahydrofolate reductase
  </Note>
  <Frequency>7</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011624</DescriptorUI>
     <DescriptorName>
      <String>Pteroylpolyglutamic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 1980;19(10):2040</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0083632</ConceptUI>
    <ConceptName>
     <String>dihydropteroylpolyglutamate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T113635</TermUI>
      <String>dihydropteroylpolyglutamate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C084888</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-amino-(6-amidobiotinyl)pyridine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>01</Month>
   <Day>17</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>structure given in first source; used to tag oligosaccharides
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000631</DescriptorUI>
     <DescriptorName>
      <String>Aminopyridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D001710</DescriptorUI>
     <DescriptorName>
      <String>Biotin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Proc Natl Acad Sci U S A 1993 Dec 15;90(24):11939-43</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0225472</ConceptUI>
    <ConceptName>
     <String>2-amino-(6-amidobiotinyl)pyridine</String>
    </ConceptName>
    <RegistryNumber>153086-93-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T255477</TermUI>
      <String>2-amino-(6-amidobiotinyl)pyridine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C499392</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Ly6i protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2007</Year>
   <Month>10</Month>
   <Day>15</Day>
  </DateRevised>
  <Note>RefSeq NM_020498
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000950</DescriptorUI>
     <DescriptorName>
      <String>Antigens, Ly</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008565</DescriptorUI>
     <DescriptorName>
      <String>Membrane Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0473750</ConceptUI>
    <ConceptName>
     <String>Ly6i protein, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T612597</TermUI>
      <String>Ly6i protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>10</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T612598</TermUI>
      <String>lymphocyte antigen 6 complex, locus I protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>10</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T636480</TermUI>
      <String>Ly6I antigen, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>04</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T612600</TermUI>
      <String>Ly-6I protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>10</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T612599</TermUI>
      <String>Ly-6M protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>10</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T612601</TermUI>
      <String>Ly6m protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>10</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C481878</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-trans-caffeoyl-L-tyrosine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>02</Month>
   <Day>24</Day>
  </DateCreated>
  <Note>from Theobroma cacao; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002109</DescriptorUI>
     <DescriptorName>
      <String>Caffeic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014443</DescriptorUI>
     <DescriptorName>
      <String>Tyrosine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ann Bot (Lond) 2003 Oct;92(4);613-23</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0461303</ConceptUI>
    <ConceptName>
     <String>N-trans-caffeoyl-L-tyrosine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T574063</TermUI>
      <String>N-trans-caffeoyl-L-tyrosine</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>02</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C561001</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,6-dicyclopropane-2,4-hexyne</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2011</Year>
   <Month>09</Month>
   <Day>14</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000480</DescriptorUI>
     <DescriptorName>
      <String>Alkynes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003521</DescriptorUI>
     <DescriptorName>
      <String>Cyclopropanes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Phys Chem A. 2011 May 19;115(19):4941-50</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0560983</ConceptUI>
    <ConceptName>
     <String>1,6-dicyclopropane-2,4-hexyne</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T796862</TermUI>
      <String>1,6-dicyclopropane-2,4-hexyne</String>
      <DateCreated>
       <Year>2011</Year>
       <Month>09</Month>
       <Day>14</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2011)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C523488</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ErpA protein, E coli</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>10</Month>
   <Day>15</Day>
  </DateCreated>
  <Note>an iron sulfur (Fe S) protein of the A-type essential for respiratory metabolism; has been sequenced
  </Note>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007506</DescriptorUI>
     <DescriptorName>
      <String>Iron-Sulfur Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029968</DescriptorUI>
     <DescriptorName>
      <String>Escherichia coli Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Proc Natl Acad Sci U S A 2007 Aug 21;104(34):13626-31</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0514437</ConceptUI>
    <ConceptName>
     <String>ErpA protein, E coli</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T707703</TermUI>
      <String>ErpA protein, E coli</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>10</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C024922</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Ludox AM</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>06</Month>
   <Day>20</Day>
  </DateCreated>
  <DateRevised>
   <Year>1993</Year>
   <Month>09</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>silica sol from DuPont; generates density gradient when subjected to centrifugal force
  </Note>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012822</DescriptorUI>
     <DescriptorName>
      <String>Silicon Dioxide</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem J. 1980;186(2):507</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0083688</ConceptUI>
    <ConceptName>
     <String>Ludox AM</String>
    </ConceptName>
    <CASN1Name>Ludox AM</CASN1Name>
    <RegistryNumber>59112-39-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T113691</TermUI>
      <String>Ludox AM</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C523490</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4,4-difluoro-4-bora-3a,4a-diaza-s-indacene-geldanamycin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>10</Month>
   <Day>15</Day>
  </DateCreated>
  <Note>a fluorescently-labeled GA analog
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001896</DescriptorUI>
     <DescriptorName>
      <String>Boron Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D016227</DescriptorUI>
     <DescriptorName>
      <String>Benzoquinones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D047029</DescriptorUI>
     <DescriptorName>
      <String>Lactams, Macrocyclic</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Mol Biol 2007 Sep 14;372(2):287-97</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0514440</ConceptUI>
    <ConceptName>
     <String>4,4-difluoro-4-bora-3a,4a-diaza-s-indacene-geldanamycin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T707708</TermUI>
      <String>4,4-difluoro-4-bora-3a,4a-diaza-s-indacene-geldanamycin</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>10</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T707710</TermUI>
      <String>BODIPY-GA</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>10</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T707709</TermUI>
      <String>BODIPY-geldanamycin</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>10</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C074423</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bofA protein, Bacillus subtilis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1992</Year>
   <Month>06</Month>
   <Day>07</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>07</Month>
   <Day>11</Day>
  </DateRevised>
  <Note>isolated from Bacillus subtilis; involved in sporulation; may form heteromeric complex in mother cell membrane that surrounds forespore; amino acid sequence given in first source; do not confuse with the boron compound BOFA
  </Note>
  <Frequency>14</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008565</DescriptorUI>
     <DescriptorName>
      <String>Membrane Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Bacteriol 1992 May;174(10):3177-84</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0200942</ConceptUI>
    <ConceptName>
     <String>bofA protein, Bacillus subtilis</String>
    </ConceptName>
    <RegistryNumber>135844-35-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T540273</TermUI>
      <String>bofA protein, Bacillus subtilis</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>05</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T540275</TermUI>
      <String>sigma-K factor processing regulatory protein, Bacillus subtilis</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>05</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T540274</TermUI>
      <String>bypass-of-forespore protein A, Bacillus subtilis</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>05</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C024965</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bruceine B</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>07</Month>
   <Day>08</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>08</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>quassinoid which inhibits protein synthesis &amp; DNA synthesis in cells; structure in first source
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>GLAUCARUBIN/*AA (1980-2002)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D036702</DescriptorUI>
     <DescriptorName>
      <String>Quassins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D002472</DescriptorUI>
     <DescriptorName>
      <String>Cell Transformation, Viral</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000187</QualifierUI>
     <QualifierName>
      <String>drug effects</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D032269</DescriptorUI>
     <DescriptorName>
      <String>Brucea</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 1980;93(3):675</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0083780</ConceptUI>
    <ConceptName>
     <String>bruceine B</String>
    </ConceptName>
    <RegistryNumber>25514-29-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T113783</TermUI>
      <String>bruceine B</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C038408</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>CP 46665</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1983</Year>
   <Month>07</Month>
   <Day>11</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>immunomodulator; RN given refers to di-HCl
  </Note>
  <Frequency>17</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010880</DescriptorUI>
     <DescriptorName>
      <String>Piperidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ann Surg 1983;198(1):53</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0115627</ConceptUI>
    <ConceptName>
     <String>CP 46665</String>
    </ConceptName>
    <RegistryNumber>72618-10-1</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0115627</Concept1UI>
     <Concept2UI>M0115624</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T145631</TermUI>
      <String>CP 46665</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T145630</TermUI>
      <String>CP-46,665</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T145629</TermUI>
      <String>CP 46665-1</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0115624</ConceptUI>
    <ConceptName>
     <String>4-aminomethyl-1-(2,3-bis(decyloxy)propyl)-4-phenylpiperidine</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0115627</Concept1UI>
     <Concept2UI>M0115624</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T145628</TermUI>
      <String>4-aminomethyl-1-(2,3-bis(decyloxy)propyl)-4-phenylpiperidine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C492570</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>CCNO protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>10</Month>
   <Day>23</Day>
  </DateCreated>
  <DateRevised>
   <Year>2008</Year>
   <Month>09</Month>
   <Day>11</Day>
  </DateRevised>
  <Note>RefSeq NM_021147
  </Note>
  <Frequency>68</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D045647</DescriptorUI>
     <DescriptorName>
      <String>DNA Glycosylases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 1991 Feb 16;1088(2):197-207</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0474507</ConceptUI>
    <ConceptName>
     <String>CCNO protein, human</String>
    </ConceptName>
    <RegistryNumber>EC 3.2.2.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T725513</TermUI>
      <String>CCNO protein, human</String>
      <DateCreated>
       <Year>2008</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2008)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T725514</TermUI>
      <String>cyclin O protein, human</String>
      <DateCreated>
       <Year>2008</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2008)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T615207</TermUI>
      <String>UNG2 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>10</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T615206</TermUI>
      <String>uracil DNA glycosylase 2, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>10</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T702592</TermUI>
      <String>CCNU protein, human</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>07</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T702593</TermUI>
      <String>cyclin U protein, human</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>07</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C581244</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>BMP-PEI-pSLC-E7-Fc vaccine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>05</Month>
   <Day>26</Day>
  </DateCreated>
  <DateRevised>
   <Year>2013</Year>
   <Month>05</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>consists of pSLC-E7-Fc associated with a magnetosome-polyethylenimine gene delivery system for tumor immunotherapy
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D019444</DescriptorUI>
     <DescriptorName>
      <String>Vaccines, DNA</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Gene Ther. 2012 Dec;19(12):1187-95.</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0585034</ConceptUI>
    <ConceptName>
     <String>BMP-PEI-pSLC-E7-Fc vaccine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T844738</TermUI>
      <String>BMP-PEI-pSLC-E7-Fc vaccine</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>05</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T844821</TermUI>
      <String>BMP-V vaccine</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>05</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010691</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-bromo-N,N-dimethylaniline N-oxide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000814</DescriptorUI>
     <DescriptorName>
      <String>Aniline Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Naunyn Schmiedeberg's Arch Pharmacol 287 suppl R80;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056405</ConceptUI>
    <ConceptName>
     <String>4-bromo-N,N-dimethylaniline N-oxide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086408</TermUI>
      <String>4-bromo-N,N-dimethylaniline N-oxide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C424044</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>mbl protein, Bacillus subtilis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>20</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>08</Month>
   <Day>14</Day>
  </DateRevised>
  <Note>required for different aspects of cell morphogenesis; amino acid sequence in first source
  </Note>
  <Frequency>21</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ACTINS (2001-2002)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003598</DescriptorUI>
     <DescriptorName>
      <String>Cytoskeletal Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cell 2001 Mar 23;104(6):913-22</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0435071</ConceptUI>
    <ConceptName>
     <String>mbl protein, Bacillus subtilis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0435071</Concept1UI>
     <Concept2UI>M0384616</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T510843</TermUI>
      <String>mbl protein, Bacillus subtilis</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>08</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0384616</ConceptUI>
    <ConceptName>
     <String>mbl protein, bacterial</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0435071</Concept1UI>
     <Concept2UI>M0384616</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T443692</TermUI>
      <String>mbl protein, bacterial</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>04</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010702</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cyclohexylpuromycin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011691</DescriptorUI>
     <DescriptorName>
      <String>Puromycin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem J 145(2):169;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056417</ConceptUI>
    <ConceptName>
     <String>cyclohexylpuromycin</String>
    </ConceptName>
    <CASN1Name>Adenosine, 3'-((2-amino-3-cyclohexyl-1-oxopropyl)amino)-3'-deoxy-N,N-dimethyl-</CASN1Name>
    <RegistryNumber>55604-91-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086420</TermUI>
      <String>cyclohexylpuromycin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010706</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-deoxy-2-fluoroglycerol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>07</Month>
   <Day>31</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DEOXY SUGARS (81-82)</PreviousIndexing>
   <PreviousIndexing>DEOXY SUGARS (75-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005990</DescriptorUI>
     <DescriptorName>
      <String>Glycerol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem J 145(3):501;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056424</ConceptUI>
    <ConceptName>
     <String>2-deoxy-2-fluoroglycerol</String>
    </ConceptName>
    <CASN1Name>1,3-Propanediol, 2-fluoro-</CASN1Name>
    <RegistryNumber>453-09-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086427</TermUI>
      <String>2-deoxy-2-fluoroglycerol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010708</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-O-desosaminylerythronolide A oxime</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004917</DescriptorUI>
     <DescriptorName>
      <String>Erythromycin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 18(8):849;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056426</ConceptUI>
    <ConceptName>
     <String>5-O-desosaminylerythronolide A oxime</String>
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    <RegistryNumber>53066-45-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086429</TermUI>
      <String>5-O-desosaminylerythronolide A oxime</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C552098</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2'-fluoro-2'-methyl-3',5'-diisobutyryldeoxycytidine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2010</Year>
   <Month>09</Month>
   <Day>14</Day>
  </DateCreated>
  <DateRevised>
   <Year>2013</Year>
   <Month>05</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>inhibits HCV polymerase; structure in first source
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  <Frequency>32</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003841</DescriptorUI>
     <DescriptorName>
      <String>Deoxycytidine</String>
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    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Biomed Anal 2010 Nov 2;53(3):710-6</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0549872</ConceptUI>
    <ConceptName>
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    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
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     <Concept1UI>M0549872</Concept1UI>
     <Concept2UI>M0549873</Concept2UI>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0549872</Concept1UI>
     <Concept2UI>M0585085</Concept2UI>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0549872</Concept1UI>
     <Concept2UI>M0585084</Concept2UI>
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    <TermList>
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      <TermUI>T777299</TermUI>
      <String>2'-fluoro-2'-methyl-3',5'-diisobutyryldeoxycytidine</String>
      <DateCreated>
       <Year>2010</Year>
       <Month>09</Month>
       <Day>14</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2010)</ThesaurusID>
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   <Concept PreferredConceptYN="N">
    <ConceptUI>M0549873</ConceptUI>
    <ConceptName>
     <String>RG 7128</String>
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    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0549872</Concept1UI>
     <Concept2UI>M0549873</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T777300</TermUI>
      <String>RG 7128</String>
      <DateCreated>
       <Year>2010</Year>
       <Month>09</Month>
       <Day>14</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2010)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T777302</TermUI>
      <String>RG7128</String>
      <DateCreated>
       <Year>2010</Year>
       <Month>09</Month>
       <Day>14</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2010)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T777301</TermUI>
      <String>RG-7128</String>
      <DateCreated>
       <Year>2010</Year>
       <Month>09</Month>
       <Day>14</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2010)</ThesaurusID>
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   <Concept PreferredConceptYN="N">
    <ConceptUI>M0585085</ConceptUI>
    <ConceptName>
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    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0549872</Concept1UI>
     <Concept2UI>M0585085</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T844822</TermUI>
      <String>R7128</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>05</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
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   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0585084</ConceptUI>
    <ConceptName>
     <String>mericitabine</String>
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    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0549872</Concept1UI>
     <Concept2UI>M0585084</Concept2UI>
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      <DateCreated>
       <Year>2013</Year>
       <Month>05</Month>
       <Day>28</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C581592</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Q-1047H-A-A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>10</Day>
  </DateCreated>
  <Note>an ansamacrolactam from Pseudonocardia sp Q-1047; structure in first source
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007769</DescriptorUI>
     <DescriptorName>
      <String>Lactams</String>
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   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Org Lett. 2013 Feb 15;15(4):812-5</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0585474</ConceptUI>
    <ConceptName>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T845402</TermUI>
      <String>Q-1047H-A-A</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C510755</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>F protein, Nipah virus</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>06</Month>
   <Day>07</Day>
  </DateCreated>
  <Note>amino acid sequence in first source
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  <Frequency>28</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014759</DescriptorUI>
     <DescriptorName>
      <String>Viral Envelope Proteins</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>Virology 2000 Jun 5;271(2):334-49</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0498636</ConceptUI>
    <ConceptName>
     <String>F protein, Nipah virus</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T675423</TermUI>
      <String>F protein, Nipah virus</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>06</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T675425</TermUI>
      <String>fusion protein, Nipah virus</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>06</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T675424</TermUI>
      <String>Nipahn virus fusion protein</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>06</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010772</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>pterosin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>tumor producing 1-indanone derivatives from bracken fern (Pteridium aquilinum); there are 16 pterosins in Chemline
  </Note>
  <Frequency>20</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007189</DescriptorUI>
     <DescriptorName>
      <String>Indans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012717</DescriptorUI>
     <DescriptorName>
      <String>Sesquiterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D032498</DescriptorUI>
     <DescriptorName>
      <String>Pteridium</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Experientia 31(7):829;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056533</ConceptUI>
    <ConceptName>
     <String>pterosin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086536</TermUI>
      <String>pterosin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010736</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>alpha-hydrazino-alpha-methylornithine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>03</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>inhibitor of ornithine decarboxylase; structure; RN given refers to mono-HCl(+-)-isomer
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009952</DescriptorUI>
     <DescriptorName>
      <String>Ornithine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 18(9):945;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056480</ConceptUI>
    <ConceptName>
     <String>alpha-hydrazino-alpha-methylornithine</String>
    </ConceptName>
    <CASN1Name>Pentanoic acid, 5-amino-2-hydrazino-2-methyl-, monohydrochloride, (+-)-</CASN1Name>
    <RegistryNumber>56937-71-4</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0056480</Concept1UI>
     <Concept2UI>M0056479</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086483</TermUI>
      <String>alpha-hydrazino-alpha-methylornithine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0056479</ConceptUI>
    <ConceptName>
     <String>5-amino-2-hydrazino-2-methylpentanoic acid</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0056480</Concept1UI>
     <Concept2UI>M0056479</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T086482</TermUI>
      <String>5-amino-2-hydrazino-2-methylpentanoic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010743</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>lecithovitellin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>10</Month>
   <Day>07</Day>
  </DateRevised>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*EGG PROTEINS (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010713</DescriptorUI>
     <DescriptorName>
      <String>Phosphatidylcholines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mikrobiol Zh 36(4):522;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056493</ConceptUI>
    <ConceptName>
     <String>lecithovitellin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086496</TermUI>
      <String>lecithovitellin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C581593</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Q-1047H-R-A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>10</Day>
  </DateCreated>
  <Note>an ansamacrolactam from Pseudonocardia sp Q-1047; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007769</DescriptorUI>
     <DescriptorName>
      <String>Lactams</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Org Lett. 2013 Feb 15;15(4):812-5</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0585475</ConceptUI>
    <ConceptName>
     <String>Q-1047H-R-A</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T845403</TermUI>
      <String>Q-1047H-R-A</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C082808</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-benzyl-3,5-dichloro-6-(2-chlorophenyl)pyrazinone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1993</Year>
   <Month>09</Month>
   <Day>22</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>12</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001593</DescriptorUI>
     <DescriptorName>
      <String>Benzyl Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011719</DescriptorUI>
     <DescriptorName>
      <String>Pyrazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Pharmacol 1993 Aug;44(2):468-72</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0220508</ConceptUI>
    <ConceptName>
     <String>1-benzyl-3,5-dichloro-6-(2-chlorophenyl)pyrazinone</String>
    </ConceptName>
    <RegistryNumber>151936-24-2</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0220508</Concept1UI>
     <Concept2UI>M0220510</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T250513</TermUI>
      <String>1-benzyl-3,5-dichloro-6-(2-chlorophenyl)pyrazinone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0220510</ConceptUI>
    <ConceptName>
     <String>U 94863</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0220508</Concept1UI>
     <Concept2UI>M0220510</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T250515</TermUI>
      <String>U 94863</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T250514</TermUI>
      <String>U-94863</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010749</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>methyl N-acetylactinosaminide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>HEXOSAMINES (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008759</DescriptorUI>
     <DescriptorName>
      <String>Methylglycosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 18(7):768;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056500</ConceptUI>
    <ConceptName>
     <String>methyl N-acetylactinosaminide</String>
    </ConceptName>
    <RegistryNumber>40879-81-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086503</TermUI>
      <String>methyl N-acetylactinosaminide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010793</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tetraacetylglucosamine mustard</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ACETYLGLUCOSAMINE/*analogs (75-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009588</DescriptorUI>
     <DescriptorName>
      <String>Nitrogen Mustard Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Res 35(8):1903;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056569</ConceptUI>
    <ConceptName>
     <String>tetraacetylglucosamine mustard</String>
    </ConceptName>
    <RegistryNumber>56879-48-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086572</TermUI>
      <String>tetraacetylglucosamine mustard</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T086571</TermUI>
      <String>1,3,4,6-tetra-o-acetyl-2-(di-2-chloroethyl)amino-2- deoxy-D-glucopyranose</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010755</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>nucleoside 5'-phosphordiamidates</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009711</DescriptorUI>
     <DescriptorName>
      <String>Nucleotides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nucleic Acids Res 2(7):1223;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056505</ConceptUI>
    <ConceptName>
     <String>nucleoside 5'-phosphordiamidates</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086508</TermUI>
      <String>nucleoside 5'-phosphordiamidates</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010757</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>oxamicetin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>07</Month>
   <Day>14</Day>
  </DateRevised>
  <Note>closely related to amicetin with an additional hydroxyl group in the molecule; structure
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011741</DescriptorUI>
     <DescriptorName>
      <String>Pyrimidine Nucleosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiot 28(4):325;1975</Source>
   <Source>J Org Chem 41(4):600;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056508</ConceptUI>
    <ConceptName>
     <String>oxamicetin</String>
    </ConceptName>
    <RegistryNumber>52665-75-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086511</TermUI>
      <String>oxamicetin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C581744</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>TE-64562</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>18</Day>
  </DateCreated>
  <Note>consists of EGFR (645-662) conjugated to Tat
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011993</DescriptorUI>
     <DescriptorName>
      <String>Recombinant Fusion Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D000970</DescriptorUI>
     <DescriptorName>
      <String>Antineoplastic Agents</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>PLoS One. 2012;7(11):e49702.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0585666</ConceptUI>
    <ConceptName>
     <String>TE-64562</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T845848</TermUI>
      <String>TE-64562</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C581745</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cpLEPA protein, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>18</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D039642</DescriptorUI>
     <DescriptorName>
      <String>Eukaryotic Initiation Factors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D060365</DescriptorUI>
     <DescriptorName>
      <String>Chloroplast Proteins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>PLoS One. 2012;7(11):e49746.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0585667</ConceptUI>
    <ConceptName>
     <String>cpLEPA protein, Arabidopsis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T845849</TermUI>
      <String>cpLEPA protein, Arabidopsis</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010765</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>preparation P-1</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1986</Year>
   <Month>08</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>anti-inflammatory agent of pyrimidine series
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011743</DescriptorUI>
     <DescriptorName>
      <String>Pyrimidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mikrobiol Zh 36(4):520;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056520</ConceptUI>
    <ConceptName>
     <String>preparation P-1</String>
    </ConceptName>
    <CASN1Name>Preparation P 1</CASN1Name>
    <RegistryNumber>75718-63-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086523</TermUI>
      <String>preparation P-1</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C025768</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Persteril</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>11</Month>
   <Day>20</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>combination of peracetic acid, hydrogen peroxide &amp; sulfuric acid
  </Note>
  <Frequency>10</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006861</DescriptorUI>
     <DescriptorName>
      <String>Hydrogen Peroxide</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010463</DescriptorUI>
     <DescriptorName>
      <String>Peracetic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013464</DescriptorUI>
     <DescriptorName>
      <String>Sulfuric Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cesk Epidemiol Mikrobiol Imunol 1980;29(4):235</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0085541</ConceptUI>
    <ConceptName>
     <String>Persteril</String>
    </ConceptName>
    <RegistryNumber>8066-16-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="TRD"  RecordPreferredTermYN="Y">
      <TermUI>T115544</TermUI>
      <String>Persteril</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C067667</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-carbomethoxycarbonyl-prolyl-phenylalanyl-benzyl ester</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1991</Year>
   <Month>04</Month>
   <Day>05</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>CPF sticks to the gp120 molecules on the surface of HIV and blocks the site that enables the virus to stick to and penetrate healthy T cells
  </Note>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001593</DescriptorUI>
     <DescriptorName>
      <String>Benzyl Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004151</DescriptorUI>
     <DescriptorName>
      <String>Dipeptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>N Y State J Med 1990;90(9):480</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0185419</ConceptUI>
    <ConceptName>
     <String>N-carbomethoxycarbonyl-prolyl-phenylalanyl-benzyl ester</String>
    </ConceptName>
    <RegistryNumber>129987-97-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T215424</TermUI>
      <String>N-carbomethoxycarbonyl-prolyl-phenylalanyl-benzyl ester</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T215423</TermUI>
      <String>N-carbomethoxycarbonyl-Pro-Phe-benzyl ester</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T215422</TermUI>
      <String>CPF ester</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C075330</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3,3-dichloro-4-(alpha-chlorobenzyl)-1-methyl-5-phenyl-2-pyrrolidinone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1992</Year>
   <Month>07</Month>
   <Day>27</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>structure given in first source; RN refers to the (4alpha(R*),5beta)-(+)(-)-isomer
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001593</DescriptorUI>
     <DescriptorName>
      <String>Benzyl Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011760</DescriptorUI>
     <DescriptorName>
      <String>Pyrrolidinones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Crystallogr C 1992 Mar 15;48(Pt 3):568-70</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0203015</ConceptUI>
    <ConceptName>
     <String>3,3-dichloro-4-(alpha-chlorobenzyl)-1-methyl-5-phenyl-2-pyrrolidinone</String>
    </ConceptName>
    <RegistryNumber>141032-42-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0203015</Concept1UI>
     <Concept2UI>M0203014</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T233020</TermUI>
      <String>3,3-dichloro-4-(alpha-chlorobenzyl)-1-methyl-5-phenyl-2-pyrrolidinone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T233018</TermUI>
      <String>3,3-DCBMPP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0203014</ConceptUI>
    <ConceptName>
     <String>3,3-dichloro-4-(alpha-chlorobenzyl)-1-methyl-5-phenyl-2-pyrrolidinone, (4alpha(R*),5beta)-(+)(-)-isomer</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0203015</Concept1UI>
     <Concept2UI>M0203014</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T233019</TermUI>
      <String>3,3-dichloro-4-(alpha-chlorobenzyl)-1-methyl-5-phenyl-2-pyrrolidinone, (4alpha(R*),5beta)-(+)(-)-isomer</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C045076</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Fenton's reagent</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1985</Year>
   <Month>05</Month>
   <Day>21</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>used for oxidizing sugars &amp; alcohols
  </Note>
  <Frequency>1960</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006861</DescriptorUI>
     <DescriptorName>
      <String>Hydrogen Peroxide</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007501</DescriptorUI>
     <DescriptorName>
      <String>Iron</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem J 1985;226(2):455</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0131270</ConceptUI>
    <ConceptName>
     <String>Fenton's reagent</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T161275</TermUI>
      <String>Fenton's reagent</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T161274</TermUI>
      <String>Fenton reagent</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C091451</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>APO 10</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>12</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>a nonionic detergent; structure given in first source
  </Note>
  <Frequency>8</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010720</DescriptorUI>
     <DescriptorName>
      <String>Phosphines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biotechniques 1994 Sep;17(3):434-6</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0241507</ConceptUI>
    <ConceptName>
     <String>APO 10</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0241507</Concept1UI>
     <Concept2UI>M0241505</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T271512</TermUI>
      <String>APO 10</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T271509</TermUI>
      <String>APO-10</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0241505</ConceptUI>
    <ConceptName>
     <String>decyl(dimethyl)phosphine oxide</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0241507</Concept1UI>
     <Concept2UI>M0241505</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T271510</TermUI>
      <String>decyl(dimethyl)phosphine oxide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T271511</TermUI>
      <String>decyldimethylphosphine oxide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010784</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6-selenopurine arabinoside</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1992</Year>
   <Month>05</Month>
   <Day>14</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>SELENIUM (75-92)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011684</DescriptorUI>
     <DescriptorName>
      <String>Purine Nucleosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D016566</DescriptorUI>
     <DescriptorName>
      <String>Organoselenium Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 64(8):1343;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056555</ConceptUI>
    <ConceptName>
     <String>6-selenopurine arabinoside</String>
    </ConceptName>
    <CASN1Name>9-beta-D-arabinofuranosyl-1,9-dihydro-6H-purine-6-selone</CASN1Name>
    <RegistryNumber>56477-16-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086558</TermUI>
      <String>6-selenopurine arabinoside</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010797</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tolerin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1992</Year>
   <Month>09</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>endotoxin detoxified by irradiation
  </Note>
  <Frequency>13</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004731</DescriptorUI>
     <DescriptorName>
      <String>Endotoxins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Langenbecks Arch Chir (Suppl):293;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056578</ConceptUI>
    <ConceptName>
     <String>tolerin</String>
    </ConceptName>
    <RegistryNumber>57125-68-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086581</TermUI>
      <String>tolerin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010807</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>xylosides</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1987</Year>
   <Month>08</Month>
   <Day>03</Day>
  </DateRevised>
  <Frequency>302</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>XYLOSE/analogs (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006027</DescriptorUI>
     <DescriptorName>
      <String>Glycosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Biochem Biophys 192(1):148;1979</Source>
   <Source>Arch Int Physiol Biochim 84(3):576;1976</Source>
   <Source>Biochem Biophys Res Commun 67(3):1108;1975</Source>
   <Source>Biochem J 148(1):25;1975</Source>
   <Source>Connect Tissue Res 3:115;1975</Source>
   <Source>Eur J Biochem 1979;102(1):257</Source>
   <Source>J Biol Chem 254(8):2575;1979</Source>
   <Source>J Cell Physiol 100(1):33;1979</Source>
   <Source>Nature 273(5658):151;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056597</ConceptUI>
    <ConceptName>
     <String>xylosides</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0056597</Concept1UI>
     <Concept2UI>M0056596</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086600</TermUI>
      <String>xylosides</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0056596</ConceptUI>
    <ConceptName>
     <String>beta-D-xyloside</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0056597</Concept1UI>
     <Concept2UI>M0056596</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T086599</TermUI>
      <String>beta-D-xyloside</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C092422</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Prevention Mouthrinse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>04</Month>
   <Day>07</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>a prophylactic oral rinse; its active components are zinc chloride, hydrogen peroxide, sodium dodecyl sulfate, and sodium citrate
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002951</DescriptorUI>
     <DescriptorName>
      <String>Citrates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006861</DescriptorUI>
     <DescriptorName>
      <String>Hydrogen Peroxide</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013431</DescriptorUI>
     <DescriptorName>
      <String>Sulfates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D017967</DescriptorUI>
     <DescriptorName>
      <String>Zinc Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Am J Dent 1993 Oct;6(5):239-42</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0243957</ConceptUI>
    <ConceptName>
     <String>Prevention Mouthrinse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="TRD"  RecordPreferredTermYN="Y">
      <TermUI>T273962</TermUI>
      <String>Prevention Mouthrinse</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C030024</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>thyrotropin-daunomycin conjugate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>06</Month>
   <Day>22</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>13</Day>
  </DateRevised>
  <Note>covalently cross-linked for specific site-directed therapy of thyroid tumors
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003630</DescriptorUI>
     <DescriptorName>
      <String>Daunorubicin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013972</DescriptorUI>
     <DescriptorName>
      <String>Thyrotropin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Horm Metab Res 1981;13(2):110</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0095310</ConceptUI>
    <ConceptName>
     <String>thyrotropin-daunomycin conjugate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T125314</TermUI>
      <String>thyrotropin-daunomycin conjugate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T125313</TermUI>
      <String>TSH-DM</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C098761</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Mentadent Dentifrice</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>04</Month>
   <Day>27</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>dentifrice composed of above compounds
  </Note>
  <Frequency>10</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006861</DescriptorUI>
     <DescriptorName>
      <String>Hydrogen Peroxide</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D017693</DescriptorUI>
     <DescriptorName>
      <String>Sodium Bicarbonate</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Am J Dent 1995 Jun;8(3):125-7</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0259383</ConceptUI>
    <ConceptName>
     <String>Mentadent Dentifrice</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="TRD"  RecordPreferredTermYN="Y">
      <TermUI>T289388</TermUI>
      <String>Mentadent Dentifrice</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C581746</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>vertise flow</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>18</Day>
  </DateCreated>
  <Frequency>33</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003188</DescriptorUI>
     <DescriptorName>
      <String>Composite Resins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D017220</DescriptorUI>
     <DescriptorName>
      <String>Dentin-Bonding Agents</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Dent Mater. 2011 Dec;27(12):1221-8.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0585668</ConceptUI>
    <ConceptName>
     <String>vertise flow</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T845850</TermUI>
      <String>vertise flow</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C118625</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SUT1 protein, Pichia stipitis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1999</Year>
   <Month>05</Month>
   <Day>03</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>11</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>isolated from Pichia stipitis; amino acid sequence in first source
  </Note>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005656</DescriptorUI>
     <DescriptorName>
      <String>Fungal Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009004</DescriptorUI>
     <DescriptorName>
      <String>Monosaccharide Transport Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Microbiol 1999 Feb;31(3):871-83</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0303950</ConceptUI>
    <ConceptName>
     <String>SUT1 protein, Pichia stipitis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T522099</TermUI>
      <String>SUT1 protein, Pichia stipitis</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>10</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C581747</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>uromune</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>18</Day>
  </DateCreated>
  <Note>consists of a suspension of inactivated Escherichia coli, Klebsiella pneumoniae, Proteus vulgaris, and Enterococcus faecalis for the treatment of urinary tract infections
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001428</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Vaccines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Int Urogynecol J. 2013;24(1):127-34.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0585669</ConceptUI>
    <ConceptName>
     <String>uromune</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="TRD"  RecordPreferredTermYN="Y">
      <TermUI>T845851</TermUI>
      <String>uromune</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010853</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>angiokapsul</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>27</Day>
  </DateRevised>
  <Note>contains clofibrate &amp; insoitolnicotinate
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*NICOTINIC ACIDS (75-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002994</DescriptorUI>
     <DescriptorName>
      <String>Clofibrate</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007294</DescriptorUI>
     <DescriptorName>
      <String>Inositol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Med Welt 26(14):655;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056707</ConceptUI>
    <ConceptName>
     <String>angiokapsul</String>
    </ConceptName>
    <CASN1Name>myo-Inositol, hexa-3-pyridinecarboxylate, mixt. with ethyl 2-(4-chlorophenoxy)-2-methylpropanoate</CASN1Name>
    <RegistryNumber>76705-38-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086710</TermUI>
      <String>angiokapsul</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C581748</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hemoglobin Thailand</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>18</Day>
  </DateCreated>
  <Note>threonine replaces lysine at position 56(E5) of the alpha chain
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006455</DescriptorUI>
     <DescriptorName>
      <String>Hemoglobins, Abnormal</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Hemoglobin. 2013;37(1):37-47.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0585670</ConceptUI>
    <ConceptName>
     <String>hemoglobin Thailand</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T845852</TermUI>
      <String>hemoglobin Thailand</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T845853</TermUI>
      <String>Hb Thailand</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C581749</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>VK-II-36 compound</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>18</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002227</DescriptorUI>
     <DescriptorName>
      <String>Carbazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009025</DescriptorUI>
     <DescriptorName>
      <String>Morpholines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D000889</DescriptorUI>
     <DescriptorName>
      <String>Anti-Arrhythmia Agents</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Heat Rhythm. 2013 Jan;10(1):101-7.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0585671</ConceptUI>
    <ConceptName>
     <String>VK-II-36 compound</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T845854</TermUI>
      <String>VK-II-36 compound</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010864</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>benzoylthionocholine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002794</DescriptorUI>
     <DescriptorName>
      <String>Choline</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Febs Lett 57(1):19;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056723</ConceptUI>
    <ConceptName>
     <String>benzoylthionocholine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086726</TermUI>
      <String>benzoylthionocholine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010865</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-benzoyl-L-tyrosine thiobenzyl ester</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>12</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>protease substrate
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>BENZYL COMPOUNDS (75-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014443</DescriptorUI>
     <DescriptorName>
      <String>Tyrosine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 250(18):7366;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056724</ConceptUI>
    <ConceptName>
     <String>N-benzoyl-L-tyrosine thiobenzyl ester</String>
    </ConceptName>
    <CASN1Name>Benzenepropanethioic acid, alpha-(benzoylamino)-4-hydroxy-, S-(phenylmethyl) ester, (S)-</CASN1Name>
    <RegistryNumber>57282-60-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086727</TermUI>
      <String>N-benzoyl-L-tyrosine thiobenzyl ester</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010866</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bicyclo(2,2,2)octyloxyaniline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>12</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BICYCLO COMPOUNDS (76-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000814</DescriptorUI>
     <DescriptorName>
      <String>Aniline Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 18(11):1065;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056725</ConceptUI>
    <ConceptName>
     <String>bicyclo(2,2,2)octyloxyaniline</String>
    </ConceptName>
    <RegistryNumber>56714-25-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086728</TermUI>
      <String>bicyclo(2,2,2)octyloxyaniline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010870</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>16 alpha-bromoacetoxyestradiol-3-methyl ether</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>12</Month>
   <Day>10</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>STEROIDS, BROMINATED (76-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004958</DescriptorUI>
     <DescriptorName>
      <String>Estradiol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 250(19):7682;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056731</ConceptUI>
    <ConceptName>
     <String>16 alpha-bromoacetoxyestradiol-3-methyl ether</String>
    </ConceptName>
    <CASN1Name>Estra-1,3,5(10)-triene-16,17-diol, 3-methoxy-, 16-(bromoacetate), (16alpha,17beta)-</CASN1Name>
    <RegistryNumber>57456-71-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086734</TermUI>
      <String>16 alpha-bromoacetoxyestradiol-3-methyl ether</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010875</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>byssochlamic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>06</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>isolated from Byssochlamys nivea
  </Note>
  <Frequency>13</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005663</DescriptorUI>
     <DescriptorName>
      <String>Furans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D009183</DescriptorUI>
     <DescriptorName>
      <String>Mycotoxins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Ann Rech Vet 6(2):155-219;1975</Source>
   <Source>Ann Rech Vet 6(3):311;1975</Source>
   <Source>Ann Rech Vet 6(3):315;1975</Source>
   <Source>Nahrung 20(5):539;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056737</ConceptUI>
    <ConceptName>
     <String>byssochlamic acid</String>
    </ConceptName>
    <RegistryNumber>743-51-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086740</TermUI>
      <String>byssochlamic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010885</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>9-chloro-2,3-dihydro-5H-1,4-dioxepino(6,5-6)benzofuran</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>01</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>OXEPINS (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001572</DescriptorUI>
     <DescriptorName>
      <String>Benzofurans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 18(10):992;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056761</ConceptUI>
    <ConceptName>
     <String>9-chloro-2,3-dihydro-5H-1,4-dioxepino(6,5-6)benzofuran</String>
    </ConceptName>
    <RegistryNumber>5196-74-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086764</TermUI>
      <String>9-chloro-2,3-dihydro-5H-1,4-dioxepino(6,5-6)benzofuran</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010886</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6-chloro-2,4-dinitroaniline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>01</Month>
   <Day>22</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*NITROBENZENES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000814</DescriptorUI>
     <DescriptorName>
      <String>Aniline Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Gig Sanit 8:106;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056762</ConceptUI>
    <ConceptName>
     <String>6-chloro-2,4-dinitroaniline</String>
    </ConceptName>
    <RegistryNumber>3531-19-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086765</TermUI>
      <String>6-chloro-2,4-dinitroaniline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010887</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>chloromorphide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009022</DescriptorUI>
     <DescriptorName>
      <String>Morphine Derivatives</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biomed Mass Spectrom 1(5):350;1974</Source>
   <Source>J Pharm Sci 65(6):902;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056763</ConceptUI>
    <ConceptName>
     <String>chloromorphide</String>
    </ConceptName>
    <CASN1Name>8-chloro-6,7-didehydro-4,5-epoxy-17-methylmorphinan-3-ol</CASN1Name>
    <RegistryNumber>60048-95-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086766</TermUI>
      <String>chloromorphide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C031484</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>androstane-2,3,17-triol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>09</Month>
   <Day>25</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>27</Day>
  </DateRevised>
  <Note>RN given refers to (2alpha,3alpha,5alpha,17beta)-isomer
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D015113</DescriptorUI>
     <DescriptorName>
      <String>Androstane-3,17-diol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Steroid Biochem 1981;14(7):663</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0098890</ConceptUI>
    <ConceptName>
     <String>androstane-2,3,17-triol</String>
    </ConceptName>
    <RegistryNumber>56524-83-5</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>19316-57-5 ((2beta,3alpha,5alpha,17beta)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>19316-61-1 ((2beta,3beta,5alpha,17beta)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0098890</Concept1UI>
     <Concept2UI>M0319282</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0098890</Concept1UI>
     <Concept2UI>M0319281</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T128894</TermUI>
      <String>androstane-2,3,17-triol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T128893</TermUI>
      <String>5 alpha-androstane-2 alpha, 3 alpha,17 beta-triol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0319282</ConceptUI>
    <ConceptName>
     <String>androstane-2,3,17-triol, (2beta,3beta,5alpha,17beta)-isomer</String>
    </ConceptName>
    <RegistryNumber>19316-61-1</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0098890</Concept1UI>
     <Concept2UI>M0319282</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T349282</TermUI>
      <String>androstane-2,3,17-triol, (2beta,3beta,5alpha,17beta)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0319281</ConceptUI>
    <ConceptName>
     <String>androstane-2,3,17-triol, (2beta,3alpha,5alpha,17beta)-isomer</String>
    </ConceptName>
    <RegistryNumber>19316-57-5</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0098890</Concept1UI>
     <Concept2UI>M0319281</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T349281</TermUI>
      <String>androstane-2,3,17-triol, (2beta,3alpha,5alpha,17beta)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010895</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cobyrinic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>05</Month>
   <Day>14</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>23</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014805</DescriptorUI>
     <DescriptorName>
      <String>Vitamin B 12</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Anal Biochem 74(2):641;1976</Source>
   <Source>Experientia 34(1):1;1978</Source>
   <Source>Hoppe Seylers Z Physiol Chem 356(9):1353;1975</Source>
   <Source>Hoppe Seylers Z Physiol Chem 357(2):147;1976</Source>
   <Source>Hoppe Seylers Z Physiol Chem 358(10):1315;1977</Source>
   <Source>Hoppe Seylers Z Physiol Chem 358:339;1977</Source>
   <Source>J Chem Soc Perkin I 2:166;1977</Source>
   <Source>Methods Enzymol 1980;67:3</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056776</ConceptUI>
    <ConceptName>
     <String>cobyrinic acid</String>
    </ConceptName>
    <RegistryNumber>33593-50-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086779</TermUI>
      <String>cobyrinic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010899</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cuprocin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>combination of zinc &amp; copper dithiocarbamates
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013859</DescriptorUI>
     <DescriptorName>
      <String>Thiocarbamates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Gig Tr Prof Zabol 9:59;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056781</ConceptUI>
    <ConceptName>
     <String>cuprocin</String>
    </ConceptName>
    <CASN1Name>Zinc, ((1,2-ethanediylbis(carbamodithioato))(2-))-, mixt. with copper chloride oxide hydrate</CASN1Name>
    <RegistryNumber>8066-21-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086784</TermUI>
      <String>cuprocin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010904</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>degmin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>05</Month>
   <Day>27</Day>
  </DateRevised>
  <Note>hexamethyleneamine derivative antiseptic; used in surgical scrub; Russian drug
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008709</DescriptorUI>
     <DescriptorName>
      <String>Methenamine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Farmatsiia 24(2):91;1975</Source>
   <Source>Vestn Dermatol Venerol 1980;(3):55</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056788</ConceptUI>
    <ConceptName>
     <String>degmin</String>
    </ConceptName>
    <CASN1Name>1H-Azepinium, 1-(2-(decyloxy)-2-oxoethyl)-1-heptylhexahydro-, hydroxide</CASN1Name>
    <RegistryNumber>76391-82-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086791</TermUI>
      <String>degmin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010911</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dextran phosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>04</Day>
  </DateRevised>
  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SUGAR PHOSPHATES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003911</DescriptorUI>
     <DescriptorName>
      <String>Dextrans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Proc Soc Exptl Biol Med 149(4):1069;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056798</ConceptUI>
    <ConceptName>
     <String>dextran phosphate</String>
    </ConceptName>
    <RegistryNumber>9041-77-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086801</TermUI>
      <String>dextran phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010928</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-(3-dimethylamino-2-methylpropyl)dibenzo(a,d), (1,4)cyclooctadiene.HCl</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>has depressant effect
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*POLYCYCLIC COMPOUNDS (76-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003516</DescriptorUI>
     <DescriptorName>
      <String>Cycloparaffins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ind J Physiol Pharmacol 18(4):349;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056830</ConceptUI>
    <ConceptName>
     <String>5-(3-dimethylamino-2-methylpropyl)dibenzo(a,d), (1,4)cyclooctadiene.HCl</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086833</TermUI>
      <String>5-(3-dimethylamino-2-methylpropyl)dibenzo(a,d), (1,4)cyclooctadiene.HCl</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010930</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N,N-dimethyl-5H-dibenzo(a,d)cycloheptene-delta 5,alpha-propylamine N-oxide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>NITROGEN OXIDES (76-82)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003986</DescriptorUI>
     <DescriptorName>
      <String>Dibenzocycloheptenes</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biomed Mass Spectroml (5):329;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056832</ConceptUI>
    <ConceptName>
     <String>N,N-dimethyl-5H-dibenzo(a,d)cycloheptene-delta 5,alpha-propylamine N-oxide</String>
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    <RegistryNumber>6682-26-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086835</TermUI>
      <String>N,N-dimethyl-5H-dibenzo(a,d)cycloheptene-delta 5,alpha-propylamine N-oxide</String>
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       <ThesaurusID>NLM (1976)</ThesaurusID>
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   </Concept>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010931</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dimethyldiethanolammonium</String>
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  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
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  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AMMONIUM COMPOUNDS (76-79)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003642</DescriptorUI>
     <DescriptorName>
      <String>Deanol</String>
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    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Physiol Soc Jpn 36(8-9):337;1974</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056833</ConceptUI>
    <ConceptName>
     <String>dimethyldiethanolammonium</String>
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    <CASN1Name>Ethanaminium, 2-hydroxy-N-(2-hydroxyethyl)-N,N-dimethyl-</CASN1Name>
    <RegistryNumber>44798-79-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086836</TermUI>
      <String>dimethyldiethanolammonium</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C581750</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hemospray</String>
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  <DateCreated>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>19</Day>
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  <Note>a granular mineral blend nanopowder
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  <Frequency>80</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008903</DescriptorUI>
     <DescriptorName>
      <String>Minerals</String>
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   </HeadingMappedTo>
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  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D006490</DescriptorUI>
     <DescriptorName>
      <String>Hemostatics</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D011208</DescriptorUI>
     <DescriptorName>
      <String>Powders</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Endoscopy. 2011 Apr;43(4):296-9.</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0585672</ConceptUI>
    <ConceptName>
     <String>hemospray</String>
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    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0585672</Concept1UI>
     <Concept2UI>M0585673</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T845855</TermUI>
      <String>hemospray</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>19</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0585673</ConceptUI>
    <ConceptName>
     <String>TC-325</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0585672</Concept1UI>
     <Concept2UI>M0585673</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T845856</TermUI>
      <String>TC-325</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>19</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010946</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>polytetrafluoroethane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>07</Day>
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  <Frequency>59</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*POLYMERS (75-79)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005465</DescriptorUI>
     <DescriptorName>
      <String>Fluorocarbon Polymers</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D009779</DescriptorUI>
     <DescriptorName>
      <String>Occlusive Dressings</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Khirurgiia (Sofiia) 31(3):185;1978</Source>
   <Source>Praxis 64(19):592;1975</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056868</ConceptUI>
    <ConceptName>
     <String>polytetrafluoroethane</String>
    </ConceptName>
    <RegistryNumber>56093-67-5</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0056868</Concept1UI>
     <Concept2UI>M0056869</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086871</TermUI>
      <String>polytetrafluoroethane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0056869</ConceptUI>
    <ConceptName>
     <String>Epigard</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0056868</Concept1UI>
     <Concept2UI>M0056869</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="TRD"  RecordPreferredTermYN="N">
      <TermUI>T086872</TermUI>
      <String>Epigard</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C581751</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>7-((4-(4-(2-methoxyphenyl)piperazin-1-yl)butyl)thio)-4-methyl-2H-chromen-2-one</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>19</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003374</DescriptorUI>
     <DescriptorName>
      <String>Coumarins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010879</DescriptorUI>
     <DescriptorName>
      <String>Piperazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D058668</DescriptorUI>
     <DescriptorName>
      <String>Adrenergic alpha-1 Receptor Antagonists</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Chem Pharm Bull (Tokyo). 2013;61(1):16-24.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0585674</ConceptUI>
    <ConceptName>
     <String>7-((4-(4-(2-methoxyphenyl)piperazin-1-yl)butyl)thio)-4-methyl-2H-chromen-2-one</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T845857</TermUI>
      <String>7-((4-(4-(2-methoxyphenyl)piperazin-1-yl)butyl)thio)-4-methyl-2H-chromen-2-one</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>19</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C038128</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>coenzyme MF(430)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1983</Year>
   <Month>06</Month>
   <Day>16</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>coenzyme of methanogenesis in Methanobacterium thermoautotrophicum; structure given in first source
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  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003067</DescriptorUI>
     <DescriptorName>
      <String>Coenzymes</String>
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    </DescriptorReferredTo>
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  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Biohem Biophys 1983;223(1):235</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0114914</ConceptUI>
    <ConceptName>
     <String>coenzyme MF(430)</String>
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    <RegistryNumber>84012-70-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T144918</TermUI>
      <String>coenzyme MF(430)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T144916</TermUI>
      <String>CoMF(430)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T144917</TermUI>
      <String>coenzyme MF430</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C041221</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ITA 529</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1984</Year>
   <Month>05</Month>
   <Day>30</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001596</DescriptorUI>
     <DescriptorName>
      <String>Benzylamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Methods Find Exp Clin Pharmacol 1984;6(1):11</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0122345</ConceptUI>
    <ConceptName>
     <String>ITA 529</String>
    </ConceptName>
    <RegistryNumber>80626-07-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0122345</Concept1UI>
     <Concept2UI>M0122344</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T152350</TermUI>
      <String>ITA 529</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1984)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T152348</TermUI>
      <String>ITA-529</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1984)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0122344</ConceptUI>
    <ConceptName>
     <String>ethyl-beta((5-tert-butyl-3-chloro-2-hydroxy)benzylamino)crotonate</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0122345</Concept1UI>
     <Concept2UI>M0122344</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T152349</TermUI>
      <String>ethyl-beta((5-tert-butyl-3-chloro-2-hydroxy)benzylamino)crotonate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1984)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
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  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011678</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-(2-benzimidazolyl)-3-n-butylurea</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>06</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>metabolite of benomyl; structure
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  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>BENZIMIDAZOLES (76-81)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014508</DescriptorUI>
     <DescriptorName>
      <String>Urea</String>
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    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Agr Food Chem 24(2):314;1976</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058179</ConceptUI>
    <ConceptName>
     <String>1-(2-benzimidazolyl)-3-n-butylurea</String>
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    <RegistryNumber>24374-77-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088182</TermUI>
      <String>1-(2-benzimidazolyl)-3-n-butylurea</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
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   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011681</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N,N''-(5-(bis(2-chloroethyl)amino)-1,3-phenylene)bis-urea</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>01</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PHENYLUREA COMPOUNDS (76-82)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009588</DescriptorUI>
     <DescriptorName>
      <String>Nitrogen Mustard Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 19(3):426;1976</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058185</ConceptUI>
    <ConceptName>
     <String>N,N''-(5-(bis(2-chloroethyl)amino)-1,3-phenylene)bis-urea</String>
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    <RegistryNumber>58200-04-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088188</TermUI>
      <String>N,N''-(5-(bis(2-chloroethyl)amino)-1,3-phenylene)bis-urea</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
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     </Term>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011691</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>beta-(1-bromo-2-naphthyl)alanine</String>
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  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>11</Month>
   <Day>19</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>NAPHTHALENES (76-81)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000409</DescriptorUI>
     <DescriptorName>
      <String>Alanine</String>
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    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 19(3):429;1976</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058205</ConceptUI>
    <ConceptName>
     <String>beta-(1-bromo-2-naphthyl)alanine</String>
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    <RegistryNumber>58161-15-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088208</TermUI>
      <String>beta-(1-bromo-2-naphthyl)alanine</String>
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       <ThesaurusID>NLM (1976)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011722</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cholestane-3,7,26-triol</String>
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  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>07</Day>
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  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*STEROLS (76-78)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002777</DescriptorUI>
     <DescriptorName>
      <String>Cholestanols</String>
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  <SourceList>
   <Source>J Lipid Res 1980;21(1):130</Source>
   <Source>Lipids 11(2):148;1976</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058242</ConceptUI>
    <ConceptName>
     <String>cholestane-3,7,26-triol</String>
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    <RegistryNumber>15313-69-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088245</TermUI>
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       <ThesaurusID>NLM (1976)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T088244</TermUI>
      <String>5 beta-cholestane-3 alpha,7 alpha,26-triol</String>
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       <ThesaurusID>NLM (1976)</ThesaurusID>
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    </TermList>
   </Concept>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003059</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>pentaacetyldigitoxin</String>
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  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>05</Month>
   <Day>05</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DIGITOXIN (72-75)</PreviousIndexing>
   <PreviousIndexing>ACETIC ACIDS (72-75)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000112</DescriptorUI>
     <DescriptorName>
      <String>Acetyldigitoxins</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Clin Pharmacol 12:445;1977</Source>
   <Source>Eur J Clin Pharmacol 13(5):389;1978</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043993</ConceptUI>
    <ConceptName>
     <String>pentaacetyldigitoxin</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073996</TermUI>
      <String>pentaacetyldigitoxin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
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   </Concept>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C498038</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>angiotensin II, Val(5)-Ala(8)-</String>
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  <DateCreated>
   <Year>2005</Year>
   <Month>03</Month>
   <Day>23</Day>
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  <DateRevised>
   <Year>2005</Year>
   <Month>05</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>an apparent angiotensin antagonist
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000809</DescriptorUI>
     <DescriptorName>
      <String>Angiotensins</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>Hypertension 2004 Sep;44(3):360-4</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0482296</ConceptUI>
    <ConceptName>
     <String>angiotensin II, Val(5)-Ala(8)-</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T634188</TermUI>
      <String>angiotensin II, Val(5)-Ala(8)-</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>23</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T634189</TermUI>
      <String>angiotensin II, valyl(5)-alanyl(8)-</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T634191</TermUI>
      <String>Val(5)-Ala(8)-Ang II</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T634190</TermUI>
      <String>5-Val-8-Ala-angiotensin II</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
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   </Concept>
  </ConceptList>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C061390</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>7-(bromoethoxyphenyl)tetrahydropalmatine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1989</Year>
   <Month>11</Month>
   <Day>14</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>RN given from Toxlit 11/89
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  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ALKALOIDS (89-93)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001600</DescriptorUI>
     <DescriptorName>
      <String>Berberine Alkaloids</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Yao Hsueh Hsueh Pao 1989;24(2):81</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0170268</ConceptUI>
    <ConceptName>
     <String>7-(bromoethoxyphenyl)tetrahydropalmatine</String>
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    <RegistryNumber>121447-96-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T200273</TermUI>
      <String>7-(bromoethoxyphenyl)tetrahydropalmatine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T200272</TermUI>
      <String>7-bromoethoxybenzene-tetrahydropalmatine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T200271</TermUI>
      <String>7-BEBTP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011715</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hydroxychlormerodrin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002717</DescriptorUI>
     <DescriptorName>
      <String>Chlormerodrin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nuklearmedizin 14(4):374;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058231</ConceptUI>
    <ConceptName>
     <String>hydroxychlormerodrin</String>
    </ConceptName>
    <CASN1Name>3-chloromercuri-2-hydroxypropylurea</CASN1Name>
    <RegistryNumber>29620-52-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088234</TermUI>
      <String>hydroxychlormerodrin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011719</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>10-chloro-1,4,6,9-tetrahydro-4,6-dioxopyrido(3,2-g)quinoline-2,8-dicarboxylic acid</String>
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  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>inhibitor of allergic reactions; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PYRIDONES (76-82)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011804</DescriptorUI>
     <DescriptorName>
      <String>Quinolines</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Internat Arch Allergy Appl Immunol 50(4):446;1976</Source>
   <Source>Internat Arch Allergy Appl Immunol 50(4):454;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058238</ConceptUI>
    <ConceptName>
     <String>10-chloro-1,4,6,9-tetrahydro-4,6-dioxopyrido(3,2-g)quinoline-2,8-dicarboxylic acid</String>
    </ConceptName>
    <CASN1Name>Pyrido(3,2-g)quinoline-2,8-dicarboxylic acid, 10-chloro-1,4,6,9-tetrahydro-4,6-dioxo-</CASN1Name>
    <RegistryNumber>49635-52-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088241</TermUI>
      <String>10-chloro-1,4,6,9-tetrahydro-4,6-dioxopyrido(3,2-g)quinoline-2,8-dicarboxylic acid</String>
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       <ThesaurusID>NLM (1976)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C471568</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>11-Mrp-14-Nal-18-Cys-22-Asp-beta-MSH(11-22)NH2</String>
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  <DateCreated>
   <Year>2003</Year>
   <Month>03</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>2005</Year>
   <Month>05</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>a melanocortin 4 receptor antagonist
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  <Frequency>7</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010456</DescriptorUI>
     <DescriptorName>
      <String>Peptides, Cyclic</String>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D019824</DescriptorUI>
     <DescriptorName>
      <String>beta-MSH</String>
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  <SourceList>
   <Source>Peptides 2002 Jun;23(6):1069-76</Source>
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    <ConceptUI>M0446273</ConceptUI>
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    <TermList>
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      <TermUI>T534176</TermUI>
      <String>11-Mrp-14-Nal-18-Cys-22-Asp-beta-MSH(11-22)NH2</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>03</Month>
       <Day>01</Day>
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      <ThesaurusIDlist>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T534180</TermUI>
      <String>beta-MSH (11-12)-amide, mercaptopropionic acid(11)-naphthylalanyl(14)-cysteinyl(18)-aspartyl(22)-</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>03</Month>
       <Day>01</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T534179</TermUI>
      <String>beta-MSH (11-22)-amide, Mrp(11)-Nal(14)-Cys(18)-Asp(22)-</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>03</Month>
       <Day>01</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
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   <Concept PreferredConceptYN="N">
    <ConceptUI>M0450725</ConceptUI>
    <ConceptName>
     <String>JKC 363</String>
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     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T544096</TermUI>
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      <DateCreated>
       <Year>2003</Year>
       <Month>06</Month>
       <Day>23</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T544097</TermUI>
      <String>JKC363</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>06</Month>
       <Day>23</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T544098</TermUI>
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       <Year>2003</Year>
       <Month>06</Month>
       <Day>23</Day>
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      <ThesaurusIDlist>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C117843</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>13-demethylbacteriorhodopsin</String>
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  <DateCreated>
   <Year>1999</Year>
   <Month>03</Month>
   <Day>22</Day>
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  <DateRevised>
   <Year>2005</Year>
   <Month>05</Month>
   <Day>05</Day>
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
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    <DescriptorReferredTo>
     <DescriptorUI>D001436</DescriptorUI>
     <DescriptorName>
      <String>Bacteriorhodopsins</String>
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  <SourceList>
   <Source>Membr Cell Biol 1998;12(1):121-3</Source>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T332265</TermUI>
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   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
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   <Year>1993</Year>
   <Month>03</Month>
   <Day>29</Day>
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  <SourceList>
   <Source>J Chem Soc (Perk Trans) 22:2205;1975</Source>
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   <Concept PreferredConceptYN="Y">
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   <Concept PreferredConceptYN="N">
    <ConceptUI>M0058243</ConceptUI>
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     <String>5 alpha-cholestan-6 alpha-ol</String>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C514007</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>phyllanthusmin A</String>
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  <DateCreated>
   <Year>2006</Year>
   <Month>10</Month>
   <Day>08</Day>
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  <SourceList>
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  <DateCreated>
   <Year>1998</Year>
   <Month>10</Month>
   <Day>02</Day>
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  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>06</Day>
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    <DescriptorReferredTo>
     <DescriptorUI>*D001565</DescriptorUI>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009943</DescriptorUI>
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  <SourceList>
   <Source>Psychopharmacology (Berl) 1998 Jun;137(4):369-73</Source>
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      <TermUI>T325361</TermUI>
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       <ThesaurusID>NLM (1998)</ThesaurusID>
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   <Concept PreferredConceptYN="N">
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     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0295357</Concept1UI>
     <Concept2UI>M0295355</Concept2UI>
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      <TermUI>T325360</TermUI>
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       <ThesaurusID>NLM (1998)</ThesaurusID>
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  <SupplementalRecordUI>C113649</SupplementalRecordUI>
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  <DateCreated>
   <Year>1998</Year>
   <Month>08</Month>
   <Day>14</Day>
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  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>06</Day>
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  <Note>structure in first source
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001565</DescriptorUI>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003510</DescriptorUI>
     <DescriptorName>
      <String>Cyclohexanes</String>
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  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D012176</DescriptorUI>
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      <String>Retinoids</String>
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  <SourceList>
   <Source>J Med Chem 1998 Jul 30;41(16):3062-77</Source>
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   <Concept PreferredConceptYN="Y">
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     <String>4-(3-methyl-5-(2',6',6'-trimethyl-1'-cyclohex-1'-yl)pentadienamido)benzoic acid</String>
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    <RegistryNumber>0</RegistryNumber>
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     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T323429</TermUI>
      <String>4-(3-methyl-5-(2',6',6'-trimethyl-1'-cyclohex-1'-yl)pentadienamido)benzoic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T323428</TermUI>
      <String>4-M3MCP-benzoic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
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  <SupplementalRecordUI>C535263</SupplementalRecordUI>
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   <String>4,4'-biphenyldicarboxylic acid</String>
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  <DateCreated>
   <Year>2009</Year>
   <Month>02</Month>
   <Day>23</Day>
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  <DateRevised>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>20</Day>
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  <Note>structure in first source
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  <Frequency>8</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001713</DescriptorUI>
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      <String>Biphenyl Compounds</String>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003998</DescriptorUI>
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  <SourceList>
   <Source>Langmuir. 2009 Jan 20;25(2):968-72</Source>
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    <ConceptUI>M0529718</ConceptUI>
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     <Concept1UI>M0529718</Concept1UI>
     <Concept2UI>M0585721</Concept2UI>
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      <TermUI>T735505</TermUI>
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      <DateCreated>
       <Year>2009</Year>
       <Month>02</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2009)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T845944</TermUI>
      <String>4,4'-diphenyl dicarboxylic acid</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0585721</ConceptUI>
    <ConceptName>
     <String>IRMOF-10</String>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0529718</Concept1UI>
     <Concept2UI>M0585721</Concept2UI>
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     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T845945</TermUI>
      <String>IRMOF-10</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C113592</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>biphenyl-2-carboxylic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>08</Month>
   <Day>11</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001565</DescriptorUI>
     <DescriptorName>
      <String>Benzoates</String>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001713</DescriptorUI>
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  <SourceList>
   <Source>Acta Crystallogr C 1998 Jun 15;54 (Pt 6):795-8</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0293298</ConceptUI>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T323303</TermUI>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T323302</TermUI>
      <String>B-2-CA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
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     </Term>
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  <SupplementalRecordUI>C514008</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>phyllanthusmin B</String>
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  <DateCreated>
   <Year>2006</Year>
   <Month>10</Month>
   <Day>08</Day>
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  <Note>isolated from Phyllanthus oligospermus;structure in first source
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  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006027</DescriptorUI>
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      <String>Glycosides</String>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D052117</DescriptorUI>
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  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Pharm Bull (Tokyo) 2006 Aug;54(8):1223-5</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0502607</ConceptUI>
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    <RegistryNumber>0</RegistryNumber>
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     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T683188</TermUI>
      <String>phyllanthusmin B</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>10</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C096990</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-ketobacteriorhodopsin</String>
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  <DateCreated>
   <Year>1996</Year>
   <Month>01</Month>
   <Day>03</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>05</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>4-keto-bacteriorhodopsin polymer films are spectrally-selective photochromic and electrochromic materials
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  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D001436</DescriptorUI>
     <DescriptorName>
      <String>Bacteriorhodopsins</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biosystems 1995;35(2-3):129-32</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0255041</ConceptUI>
    <ConceptName>
     <String>4-ketobacteriorhodopsin</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T285046</TermUI>
      <String>4-ketobacteriorhodopsin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T285044</TermUI>
      <String>4-keto-BR</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T285045</TermUI>
      <String>4-keto-bacteriorhodopsin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
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  <SupplementalRecordName>
   <String>9-deoxy-4-dihydrospectinomycin</String>
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  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>1992</Year>
   <Month>09</Month>
   <Day>18</Day>
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  <Note>devoid of antibiotic activity
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  <Frequency>0</Frequency>
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     <DescriptorUI>D000198</DescriptorUI>
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   <Source>J Antibiotics 28(12):953;1975</Source>
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   <String>torulene</String>
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  <DateCreated>
   <Year>1993</Year>
   <Month>01</Month>
   <Day>28</Day>
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   <Year>2005</Year>
   <Month>05</Month>
   <Day>05</Day>
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   <Source>Prikl Biokhim Mikrobiol 1992 Sep-Oct;28(5):680-4</Source>
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     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T241428</TermUI>
      <String>torulin</String>
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       <ThesaurusID>NLM (1993)</ThesaurusID>
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  <SupplementalRecordName>
   <String>ZIP16 protein, Arabidopsis</String>
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  <DateCreated>
   <Year>2008</Year>
   <Month>05</Month>
   <Day>18</Day>
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  <DateRevised>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>amino acid sequence in first source
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  <Frequency>3</Frequency>
  <HeadingMappedToList>
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    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D050976</DescriptorUI>
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      <String>Basic-Leucine Zipper Transcription Factors</String>
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  <SourceList>
   <Source>BMB Rep 2008 Feb 29;41(2):132-8</Source>
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   <Year>1976</Year>
   <Month>01</Month>
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  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>08</Day>
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  <Note>from Streptococcus faecium UNH 564P; structure
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  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CAROTENOIDS (76-82)</PreviousIndexing>
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   <Month>01</Month>
   <Day>01</Day>
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  <HeadingMappedToList>
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    <DescriptorReferredTo>
     <DescriptorUI>D000404</DescriptorUI>
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     <QualifierUI>*Q000031</QualifierUI>
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   <Source>Boll Soc Ital Cardiol 17(11):1105;1972</Source>
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    <CASN1Name>Ajmalan-17,21-diol, bis(chloroacetate) (ester), (17R,21alpha)-</CASN1Name>
    <RegistryNumber>2800-66-0</RegistryNumber>
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   <String>methoxypropylcellulose</String>
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  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>2005</Year>
   <Month>05</Month>
   <Day>05</Day>
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  <Frequency>0</Frequency>
  <HeadingMappedToList>
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     <DescriptorUI>D002483</DescriptorUI>
     <DescriptorName>
      <String>Cellulose, Oxidized</String>
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  <SourceList>
   <Source>Probl Gematol Pereliv Krovi 21(9):30;1976</Source>
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    <ConceptUI>M0061481</ConceptUI>
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  <SupplementalRecordUI>C493044</SupplementalRecordUI>
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   <String>(22E)-3 alpha,6 beta,7 beta-trihydroxy-5 beta-chol-22-en-24-oic acid</String>
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  <DateCreated>
   <Year>2004</Year>
   <Month>11</Month>
   <Day>09</Day>
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  <DateRevised>
   <Year>2005</Year>
   <Month>05</Month>
   <Day>05</Day>
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  <Note>structure in first source
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D019826</DescriptorUI>
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      <String>Cholic Acid</String>
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  <SourceList>
   <Source>J Lipid Res. 2004 Mar;45(3):567-3</Source>
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  <ConceptList>
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      <DateCreated>
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       <Month>11</Month>
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      <String>22E-THCA</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>11</Month>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
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  <SupplementalRecordUI>C514010</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>IREG2 protein, Arabidopsis</String>
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  <DateCreated>
   <Year>2006</Year>
   <Month>10</Month>
   <Day>08</Day>
  </DateCreated>
  <Note>a nickel transporter expressed in roots during iron deficiency stress response; GenBank NM_120438
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D027682</DescriptorUI>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
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  <SourceList>
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       <Month>10</Month>
       <Day>08</Day>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
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       <Month>10</Month>
       <Day>08</Day>
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      <ThesaurusIDlist>
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       <Month>10</Month>
       <Day>08</Day>
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  <SupplementalRecordName>
   <String>2,4-diamino-6-(2-(3,4-dichlorophenyl)acetamido)quinazoline</String>
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  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011799</DescriptorUI>
     <DescriptorName>
      <String>Quinazolines</String>
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    </DescriptorReferredTo>
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  <SourceList>
   <Source>Proc Soc Exp Biol Med 151(1):173;1976</Source>
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  <ConceptList>
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    <RegistryNumber>0</RegistryNumber>
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      <TermUI>T088289</TermUI>
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     </Term>
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   </Concept>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011759</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dibenzoxanthenes</String>
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  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
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  <Frequency>13</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014966</DescriptorUI>
     <DescriptorName>
      <String>Xanthenes</String>
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  </HeadingMappedToList>
  <SourceList>
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  <ConceptList>
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      <TermUI>T088298</TermUI>
      <String>dibenzoxanthenes</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011760</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dibenzylcadaverine</String>
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  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>inhibits cross linkage of fibrin
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002103</DescriptorUI>
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  <SupplementalRecordUI>C529074</SupplementalRecordUI>
  <SupplementalRecordName>
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  <DateCreated>
   <Year>2008</Year>
   <Month>05</Month>
   <Day>22</Day>
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  <DateRevised>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>RefSeq NM_115206
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  <Frequency>11</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*LIGHT-HARVESTING PROTEIN COMPLEXES (2008-2011)</PreviousIndexing>
   <PreviousIndexing>*PHOTOSYSTEM II PROTEIN COMPLEX (2008-2011)</PreviousIndexing>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D060365</DescriptorUI>
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  <SourceList>
   <Source>Science 2008 May 9;320(5877):794-7</Source>
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      <DateCreated>
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       <Month>06</Month>
       <Day>28</Day>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
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       <Month>05</Month>
       <Day>22</Day>
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      <ThesaurusIDlist>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
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       <Month>06</Month>
       <Day>20</Day>
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      <DateCreated>
       <Year>2011</Year>
       <Month>06</Month>
       <Day>28</Day>
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      <DateCreated>
       <Year>2008</Year>
       <Month>05</Month>
       <Day>22</Day>
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      <ThesaurusIDlist>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C408425</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2'-desmethoxy spinosyn D</String>
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  <DateCreated>
   <Year>2000</Year>
   <Month>05</Month>
   <Day>30</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>family of macrolide natural products produced by the soil microorganism Saccharopolyspora spinosa; structure in first source
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D018942</DescriptorUI>
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  <SupplementalRecordUI>C011772</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-6-butyric acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>antisickling agent; structure
  </Note>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>BUTYRIC ACIDS (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001578</DescriptorUI>
     <DescriptorName>
      <String>Benzopyrans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>BBRC 75(3):636;1977</Source>
   <Source>Nature 258(5537):743;1975</Source>
   <Source>Nature 272(5656):833;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058329</ConceptUI>
    <ConceptName>
     <String>3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-6-butyric acid</String>
    </ConceptName>
    <RegistryNumber>58821-97-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088332</TermUI>
      <String>3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-6-butyric acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C030114</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Aplanin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>06</Month>
   <Day>30</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>04</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>oligosaccharide containing glucose as monomeric unit with an additional N-containing moiety
  </Note>
  <Frequency>7</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009844</DescriptorUI>
     <DescriptorName>
      <String>Oligosaccharides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Digestion 1981;21(2):74</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0465172</ConceptUI>
    <ConceptName>
     <String>Aplanin</String>
    </ConceptName>
    <RegistryNumber>65098-54-6</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0465172</Concept1UI>
     <Concept2UI>M0095559</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T585079</TermUI>
      <String>Aplanin</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>04</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0095559</ConceptUI>
    <ConceptName>
     <String>BAY-e 4609</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0465172</Concept1UI>
     <Concept2UI>M0095559</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T125563</TermUI>
      <String>BAY-e 4609</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T407337</TermUI>
      <String>BAYe4609</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>02</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T407336</TermUI>
      <String>BAY e4609</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>02</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T125561</TermUI>
      <String>BAY e 4609</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T125562</TermUI>
      <String>BAY-e-4609</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011790</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3,3-dimethylglutarate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>12</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005977</DescriptorUI>
     <DescriptorName>
      <String>Glutarates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D002021</DescriptorUI>
     <DescriptorName>
      <String>Buffers</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Am J Physiol 229(3):831;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058357</ConceptUI>
    <ConceptName>
     <String>3,3-dimethylglutarate</String>
    </ConceptName>
    <RegistryNumber>4839-46-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088360</TermUI>
      <String>3,3-dimethylglutarate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011796</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,3-dioxo-5-indolinesulfonic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>09</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>reagent for modification of tryptophan residues in peptides &amp; proteins
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007211</DescriptorUI>
     <DescriptorName>
      <String>Indoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 251(6):1653;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058367</ConceptUI>
    <ConceptName>
     <String>2,3-dioxo-5-indolinesulfonic acid</String>
    </ConceptName>
    <RegistryNumber>7313-70-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088370</TermUI>
      <String>2,3-dioxo-5-indolinesulfonic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011856</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>15 alpha-hydroxyestradiol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>11</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>RN given refers to (17beta)-isomer
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004958</DescriptorUI>
     <DescriptorName>
      <String>Estradiol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Can J Biochem 56(2):101;1978</Source>
   <Source>Chem Pharm Bull (Tokyo) 23(12):3141;1976</Source>
   <Source>Steroids 31(5):627;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058473</ConceptUI>
    <ConceptName>
     <String>15 alpha-hydroxyestradiol</String>
    </ConceptName>
    <CASN1Name>estra-1,3,5(10)-triene-3,15 alpha,17-triol</CASN1Name>
    <RegistryNumber>570-30-9</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>31002-81-0 ((17alpha)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0058473</Concept1UI>
     <Concept2UI>M0311621</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088476</TermUI>
      <String>15 alpha-hydroxyestradiol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0311621</ConceptUI>
    <ConceptName>
     <String>15 alpha-hydroxyestradiol, (17alpha)-isomer</String>
    </ConceptName>
    <RegistryNumber>31002-81-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0058473</Concept1UI>
     <Concept2UI>M0311621</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T341621</TermUI>
      <String>15 alpha-hydroxyestradiol, (17alpha)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011803</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>doxidan</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>14</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000880</DescriptorUI>
     <DescriptorName>
      <String>Anthraquinones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013386</DescriptorUI>
     <DescriptorName>
      <String>Succinates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ann Internal Med 84(3):290;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058383</ConceptUI>
    <ConceptName>
     <String>doxidan</String>
    </ConceptName>
    <CASN1Name>Butanedioic acid, sulfo-, 1,4-dioctyl ester, calcium salt, mixt. with 1,8-dihydroxy-9,10-anthracenedione</CASN1Name>
    <RegistryNumber>76404-07-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088386</TermUI>
      <String>doxidan</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011842</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-heptyl-2-nitrophenylmethylphosphonate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>09</Month>
   <Day>05</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009943</DescriptorUI>
     <DescriptorName>
      <String>Organophosphorus Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ukr Biokhim J 47(4):469;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058459</ConceptUI>
    <ConceptName>
     <String>2-heptyl-2-nitrophenylmethylphosphonate</String>
    </ConceptName>
    <RegistryNumber>56402-39-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088462</TermUI>
      <String>2-heptyl-2-nitrophenylmethylphosphonate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T088461</TermUI>
      <String>ortho-heptyl-ortho-nitrophenylmethylphosphonate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011811</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>alpha-ethyl alpha-aminopropylpenicillin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010406</DescriptorUI>
     <DescriptorName>
      <String>Penicillins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Med Dosw Mikrobiol 28(1):13;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058389</ConceptUI>
    <ConceptName>
     <String>alpha-ethyl alpha-aminopropylpenicillin</String>
    </ConceptName>
    <CASN1Name>4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid, 6-((2-amino-2-ethyl-1-oxobutyl)amino)-3,3-dimethyl-7-oxo-, (2S-(2alpha,5alpha,6beta))-</CASN1Name>
    <RegistryNumber>76741-90-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088392</TermUI>
      <String>alpha-ethyl alpha-aminopropylpenicillin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C408426</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>spinosyn K</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>05</Month>
   <Day>30</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>family of macrolide natural products produced by the soil microorganism Saccharopolyspora spinosa; structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D018942</DescriptorUI>
     <DescriptorName>
      <String>Macrolides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiot (Tokyo) 2000 Feb;53(2):171-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0363156</ConceptUI>
    <ConceptName>
     <String>spinosyn K</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T415494</TermUI>
      <String>spinosyn K</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>05</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T415495</TermUI>
      <String>spinosyn-K</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>05</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C094154</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>MFAP3 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>07</Month>
   <Day>17</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>06</Month>
   <Day>13</Day>
  </DateRevised>
  <Note>RefSeq NM_005927
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003285</DescriptorUI>
     <DescriptorName>
      <String>Contractile Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Genomics 1995 Mar 1;26(1):47-54</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0248104</ConceptUI>
    <ConceptName>
     <String>MFAP3 protein, human</String>
    </ConceptName>
    <RegistryNumber>165446-76-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T573397</TermUI>
      <String>MFAP3 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>02</Month>
       <Day>19</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T278107</TermUI>
      <String>MFAP3 microfibrillar protein, human</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T278109</TermUI>
      <String>microfibril-associated protein 3, human</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T278108</TermUI>
      <String>microfibril-associated protein-3, human</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C088792</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2'-O-(4-benzoylbenzoyl)guanosine cyclic 3',5'-monophosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>09</Month>
   <Day>09</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>04</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D006152</DescriptorUI>
     <DescriptorName>
      <String>Cyclic GMP</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D015106</DescriptorUI>
     <DescriptorName>
      <String>3',5'-Cyclic-GMP Phosphodiesterases</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
     <QualifierName>
      <String>antagonists &amp; inhibitors</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Med Chem 1994 Jul 22;37(15):2406-10</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0234928</ConceptUI>
    <ConceptName>
     <String>2'-O-(4-benzoylbenzoyl)guanosine cyclic 3',5'-monophosphate</String>
    </ConceptName>
    <RegistryNumber>137154-74-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T264933</TermUI>
      <String>2'-O-(4-benzoylbenzoyl)guanosine cyclic 3',5'-monophosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T261394</TermUI>
      <String>2'-O-(4-benzoyl)benzoylguanosine 3',5'-cyclic monophosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T261393</TermUI>
      <String>BB-cGMP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T264932</TermUI>
      <String>BBcGMP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C511155</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>kalihinol A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>06</Month>
   <Day>21</Day>
  </DateCreated>
  <Note>antifouling compound from the marine sponge Acanthella cavernosa; structure in first source
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004224</DescriptorUI>
     <DescriptorName>
      <String>Diterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biofouling 2006;22(1-2):23-32</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0499157</ConceptUI>
    <ConceptName>
     <String>kalihinol A</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T676409</TermUI>
      <String>kalihinol A</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>06</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C511153</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Rho1 protein, Drosophila</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateCreated>
  <Note>GenBank AE003808
  </Note>
  <Frequency>97</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D020741</DescriptorUI>
     <DescriptorName>
      <String>rho GTP-Binding Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029721</DescriptorUI>
     <DescriptorName>
      <String>Drosophila Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0491619</ConceptUI>
    <ConceptName>
     <String>Rho1 protein, Drosophila</String>
    </ConceptName>
    <RegistryNumber>EC 3.6.5.2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T658528</TermUI>
      <String>Rho1 protein, Drosophila</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>11</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T658529</TermUI>
      <String>RhoA protein, Drosophila</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>11</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C116777</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,25-dihydroxy-16,23-diene vitamin D3</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1999</Year>
   <Month>01</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>06</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>10</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002762</DescriptorUI>
     <DescriptorName>
      <String>Cholecalciferol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Bioorg Med Chem 1998 Nov;6(11):2051-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0300066</ConceptUI>
    <ConceptName>
     <String>1,25-dihydroxy-16,23-diene vitamin D3</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0300066</Concept1UI>
     <Concept2UI>M0498124</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0300066</Concept1UI>
     <Concept2UI>M0300065</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T330071</TermUI>
      <String>1,25-dihydroxy-16,23-diene vitamin D3</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T330069</TermUI>
      <String>1,25DHD Vit D3</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0498124</ConceptUI>
    <ConceptName>
     <String>Ro25-4020</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0300066</Concept1UI>
     <Concept2UI>M0498124</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T674195</TermUI>
      <String>Ro25-4020</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>05</Month>
       <Day>19</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T560895</TermUI>
      <String>Ro 25-4020</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0300065</ConceptUI>
    <ConceptName>
     <String>1alpha,25-dihydroxy-16,23E-diene vitamin D3</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0300066</Concept1UI>
     <Concept2UI>M0300065</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T330070</TermUI>
      <String>1alpha,25-dihydroxy-16,23E-diene vitamin D3</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011831</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>glyfluorine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>07</Month>
   <Day>15</Day>
  </DateRevised>
  <Note>contains difluorohydrin glycerin &amp; chlorofluorohydrin glycerin
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>FLUORINE (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002728</DescriptorUI>
     <DescriptorName>
      <String>Chlorohydrins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005990</DescriptorUI>
     <DescriptorName>
      <String>Glycerol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Hig Truda 12:53;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058445</ConceptUI>
    <ConceptName>
     <String>glyfluorine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088448</TermUI>
      <String>glyfluorine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C511156</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>rho1 protein, S pombe</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateCreated>
  <Frequency>44</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D020741</DescriptorUI>
     <DescriptorName>
      <String>rho GTP-Binding Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029702</DescriptorUI>
     <DescriptorName>
      <String>Schizosaccharomyces pombe Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0491620</ConceptUI>
    <ConceptName>
     <String>rho1 protein, S pombe</String>
    </ConceptName>
    <RegistryNumber>EC 3.6.5.2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T658530</TermUI>
      <String>rho1 protein, S pombe</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>11</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T658531</TermUI>
      <String>SPAC1F7.04 protein, S pombe</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>11</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C111754</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>endorphin (1-20)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>05</Month>
   <Day>08</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>a peptide fragment amino acid sequence given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001615</DescriptorUI>
     <DescriptorName>
      <String>beta-Endorphin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010446</DescriptorUI>
     <DescriptorName>
      <String>Peptide Fragments</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D004723</DescriptorUI>
     <DescriptorName>
      <String>Endorphins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Regul Pept 1998 Jan 2;73(1):67-72</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0289268</ConceptUI>
    <ConceptName>
     <String>endorphin (1-20)</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T319273</TermUI>
      <String>endorphin (1-20)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T319272</TermUI>
      <String>beta-endorphin-(1-20)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T319271</TermUI>
      <String>BEND (1-20)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011843</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>O-hexadecylethanediol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005026</DescriptorUI>
     <DescriptorName>
      <String>Ethylene Glycols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 409(3):311;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058460</ConceptUI>
    <ConceptName>
     <String>O-hexadecylethanediol</String>
    </ConceptName>
    <RegistryNumber>20294-76-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088463</TermUI>
      <String>O-hexadecylethanediol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011844</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hexahydro-1,4,5-oxadiazocine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010079</DescriptorUI>
     <DescriptorName>
      <String>Oxazocines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Pol Pharm 32(6):667;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058461</ConceptUI>
    <ConceptName>
     <String>hexahydro-1,4,5-oxadiazocine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088464</TermUI>
      <String>hexahydro-1,4,5-oxadiazocine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011851</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-hydroperoxymethyluracil</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013941</DescriptorUI>
     <DescriptorName>
      <String>Thymine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 41(3):567;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058468</ConceptUI>
    <ConceptName>
     <String>5-hydroperoxymethyluracil</String>
    </ConceptName>
    <CASN1Name>2,4(1H,3H)-Pyrimidinedione, 5-(hydroperoxymethyl)-</CASN1Name>
    <RegistryNumber>33499-50-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088471</TermUI>
      <String>5-hydroperoxymethyluracil</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011853</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>7-hydroxydiftalone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>diftalone metabolite
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010793</DescriptorUI>
     <DescriptorName>
      <String>Phthalazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Farmaco(Prat) 31(1):3;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058471</ConceptUI>
    <ConceptName>
     <String>7-hydroxydiftalone</String>
    </ConceptName>
    <RegistryNumber>54648-83-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088474</TermUI>
      <String>7-hydroxydiftalone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C111755</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>endorphin (20-31)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>05</Month>
   <Day>08</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>a peptide fragment amino acid sequence given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001615</DescriptorUI>
     <DescriptorName>
      <String>beta-Endorphin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010446</DescriptorUI>
     <DescriptorName>
      <String>Peptide Fragments</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D004723</DescriptorUI>
     <DescriptorName>
      <String>Endorphins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Regul Pept 1998 Jan 2;73(1):67-72</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0289271</ConceptUI>
    <ConceptName>
     <String>endorphin (20-31)</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T319276</TermUI>
      <String>endorphin (20-31)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T319275</TermUI>
      <String>beta-endorphin (20-31)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T319274</TermUI>
      <String>BEND (20-31)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C511157</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>GAHKNYLRFamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>06</Month>
   <Day>21</Day>
  </DateCreated>
  <Note>FMRFamide-like peptide from crabs of the genus Cancer
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D019835</DescriptorUI>
     <DescriptorName>
      <String>FMRFamide</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Neurochem 2006 May;97(3):784-99</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0499158</ConceptUI>
    <ConceptName>
     <String>GAHKNYLRFamide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T676410</TermUI>
      <String>GAHKNYLRFamide</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>06</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T676411</TermUI>
      <String>Gly-Ala-His-Lys-Asn-Tyrp-Lys-Arg-Phe amide</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>06</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011871</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-hydroxythiourea</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013890</DescriptorUI>
     <DescriptorName>
      <String>Thiourea</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 19(2):336;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058497</ConceptUI>
    <ConceptName>
     <String>N-hydroxythiourea</String>
    </ConceptName>
    <RegistryNumber>42008-54-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088500</TermUI>
      <String>N-hydroxythiourea</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011888</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>kauranoic acids</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004224</DescriptorUI>
     <DescriptorName>
      <String>Diterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 41(6):1021;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058517</ConceptUI>
    <ConceptName>
     <String>kauranoic acids</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088520</TermUI>
      <String>kauranoic acids</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011894</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>La Sota vaccine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Frequency>14</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014765</DescriptorUI>
     <DescriptorName>
      <String>Viral Vaccines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D009522</DescriptorUI>
     <DescriptorName>
      <String>Newcastle disease virus</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Vet Med Nauki 12(4):88;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058527</ConceptUI>
    <ConceptName>
     <String>La Sota vaccine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088530</TermUI>
      <String>La Sota vaccine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011904</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>lysoartrosi</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>lysate of amino acid &amp; low MW peptides from animal organs dry spleen, liver, thyroid, muscle
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010455</DescriptorUI>
     <DescriptorName>
      <String>Peptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D014020</DescriptorUI>
     <DescriptorName>
      <String>Tissue Extracts</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Boll Chim Farm 114(5):270;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058541</ConceptUI>
    <ConceptName>
     <String>lysoartrosi</String>
    </ConceptName>
    <RegistryNumber>39307-41-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088544</TermUI>
      <String>lysoartrosi</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C494558</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-(aminocarbonyl)-1-(3-(2-(aminocarbonyl)pyrrolidin-1-yl)-3-oxo-2-(((5-oxopyrrolidin-2-yl)carbonyl)amino)propyl)pyridinium</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>12</Month>
   <Day>29</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011726</DescriptorUI>
     <DescriptorName>
      <String>Pyridinium Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013973</DescriptorUI>
     <DescriptorName>
      <String>Thyrotropin-Releasing Hormone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 2004 Nov 18;47(24):6025-33</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0478743</ConceptUI>
    <ConceptName>
     <String>3-(aminocarbonyl)-1-(3-(2-(aminocarbonyl)pyrrolidin-1-yl)-3-oxo-2-(((5-oxopyrrolidin-2-yl)carbonyl)amino)propyl)pyridinium</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T626471</TermUI>
      <String>3-(aminocarbonyl)-1-(3-(2-(aminocarbonyl)pyrrolidin-1-yl)-3-oxo-2-(((5-oxopyrrolidin-2-yl)carbonyl)amino)propyl)pyridinium</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>12</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T626472</TermUI>
      <String>3-aminocarbonyl-APOOCAPP</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>12</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C099057</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>F0 protein, Sendai virus</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>05</Month>
   <Day>24</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>03</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>precursor of F1 and F2 proteins required for glycoprotein F activity; has been sequenced
  </Note>
  <Frequency>7</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011498</DescriptorUI>
     <DescriptorName>
      <String>Protein Precursors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014759</DescriptorUI>
     <DescriptorName>
      <String>Viral Envelope Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biochem (Tokyo) 1995 Dec;118(6):1248-54</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0260095</ConceptUI>
    <ConceptName>
     <String>F0 protein, Sendai virus</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T290098</TermUI>
      <String>F0 protein, Sendai virus</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T290100</TermUI>
      <String>F(0) protein, Sendai virus</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C467074</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-(N,N-bis(2-pyridyl)amino)stilbene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>10</Month>
   <Day>28</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013267</DescriptorUI>
     <DescriptorName>
      <String>Stilbenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Org Lett 2002 Mar 7;4(5):777-80</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0440847</ConceptUI>
    <ConceptName>
     <String>4-(N,N-bis(2-pyridyl)amino)stilbene</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0440847</Concept1UI>
     <Concept2UI>M0440848</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T524393</TermUI>
      <String>4-(N,N-bis(2-pyridyl)amino)stilbene</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>10</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0440848</ConceptUI>
    <ConceptName>
     <String>trans-4-(N,N-bis(2-pyridyl)amino)stilbene</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0440847</Concept1UI>
     <Concept2UI>M0440848</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T524394</TermUI>
      <String>trans-4-(N,N-bis(2-pyridyl)amino)stilbene</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>10</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011924</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>S-methylfenitrothion</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005278</DescriptorUI>
     <DescriptorName>
      <String>Fenitrothion</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Environ Res 10(3):407;1975</Source>
   <Source>Int Arch Occup Environ Health 36(1):67;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058567</ConceptUI>
    <ConceptName>
     <String>S-methylfenitrothion</String>
    </ConceptName>
    <CASN1Name>Phosphorothioic acid, O,S-dimethyl O-(3-methyl-4-nitrophenyl) ester</CASN1Name>
    <RegistryNumber>3344-14-7</RegistryNumber>
    <TermList>
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  <SourceList>
   <Source>Antimicrob Agents Chemother. 2000 Dec;44(12):3278-84</Source>
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       <Year>2001</Year>
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       <Day>09</Day>
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   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
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    <DescriptorReferredTo>
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  <SourceList>
   <Source>J Biochem (Tokyo):78(4):763;1975</Source>
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  <SupplementalRecordUI>C011927</SupplementalRecordUI>
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   <String>methylnitrosocyanamide</String>
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  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>29</Day>
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   <Source>Cancer Res 38(12):4630;1978</Source>
   <Source>Food Cosmet Toxicol 16:13;1978</Source>
   <Source>Gan 68(5):537;1977</Source>
   <Source>Gan 68(6):813;1977</Source>
   <Source>JNCI 55(6):1395;1975</Source>
   <Source>JNCI 62(1):71;1979</Source>
   <Source>Mutat Res 43(3):429;1977</Source>
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    <RegistryNumber>33868-17-6</RegistryNumber>
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  <SupplementalRecordUI>C011928</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-methylpethidine</String>
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  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>1998</Year>
   <Month>05</Month>
   <Day>29</Day>
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  <Note>RN given refers to iodide salt
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     <DescriptorUI>D008614</DescriptorUI>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0058576</Concept1UI>
     <Concept2UI>M0311657</Concept2UI>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0058576</Concept1UI>
     <Concept2UI>M0058575</Concept2UI>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0058576</Concept1UI>
     <Concept2UI>M0058573</Concept2UI>
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      <TermUI>T088579</TermUI>
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   <Concept PreferredConceptYN="N">
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     <String>N-methyldemerol</String>
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   <Concept PreferredConceptYN="N">
    <ConceptUI>M0311657</ConceptUI>
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       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
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   <Concept PreferredConceptYN="N">
    <ConceptUI>M0058575</ConceptUI>
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      <TermUI>T088578</TermUI>
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   <Concept PreferredConceptYN="N">
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0058576</Concept1UI>
     <Concept2UI>M0058573</Concept2UI>
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       <ThesaurusID>NLM (1975)</ThesaurusID>
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  <SupplementalRecordUI>C011929</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>10-(4-methylpiperazino)dibenzo(b,f)thiepin</String>
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  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1994</Year>
   <Month>06</Month>
   <Day>20</Day>
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  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PIPERAZINES (76-82)</PreviousIndexing>
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     <DescriptorUI>*D003988</DescriptorUI>
     <DescriptorName>
      <String>Dibenzothiepins</String>
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  <SourceList>
   <Source>Chem Pharm Bull 23(10):2223;1975</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058577</ConceptUI>
    <ConceptName>
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    <CASN1Name>Piperazine, 1-dibenzo(b,f)thiepin-10-yl-4-methyl-</CASN1Name>
    <RegistryNumber>22012-13-1</RegistryNumber>
    <TermList>
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      <TermUI>T088580</TermUI>
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  <SupplementalRecordUI>C011931</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>methyl alpha-vicianoside</String>
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  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <Note>From fusion of tetra-O-acetyl-alpha-L-arabinopyranoside and methyl 2,3,4-tri-O-acetyl-alpha-D-glucopyranoside.
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  <SourceList>
   <Source>Proc R Ir Acad 75(29):563;1975</Source>
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   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058579</ConceptUI>
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    <RegistryNumber>0</RegistryNumber>
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   <String>CGP 64213</String>
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  <DateCreated>
   <Year>1997</Year>
   <Month>04</Month>
   <Day>04</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>06</Day>
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  <Note>structure in first source
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  <Frequency>7</Frequency>
  <HeadingMappedToList>
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    <DescriptorReferredTo>
     <DescriptorUI>*D001565</DescriptorUI>
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      <String>Benzoates</String>
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     <DescriptorUI>*D009943</DescriptorUI>
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   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D007457</DescriptorUI>
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      <String>Iodine Radioisotopes</String>
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  <SourceList>
   <Source>Nature 1997 Mar 20;386(6622):239-46</Source>
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  <DateCreated>
   <Year>2004</Year>
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   <Source>J Med Chem 2004 Nov 18;47(24):6070-81</Source>
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      <String>aminopip-BFPBO</String>
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       <Year>2004</Year>
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   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
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   <Source>Ther Ggw 114(11):1912;1975</Source>
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   <Concept PreferredConceptYN="Y">
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  <DateCreated>
   <Year>2004</Year>
   <Month>11</Month>
   <Day>08</Day>
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  <DateRevised>
   <Year>2005</Year>
   <Month>09</Month>
   <Day>26</Day>
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  <Note>Improves permeability across blood-brain barrier; amino acid sequence in first source
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009479</DescriptorUI>
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      <String>Neuropeptides</String>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009842</DescriptorUI>
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  </HeadingMappedToList>
  <SourceList>
   <Source>J Neurosci Res. 2004 Oct 15;78(2):193-9</Source>
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       <Year>2004</Year>
       <Month>11</Month>
       <Day>08</Day>
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      <ThesaurusIDlist>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T653114</TermUI>
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       <Year>2005</Year>
       <Month>09</Month>
       <Day>26</Day>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C561037</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>PMI protein, Drosophila</String>
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  <DateCreated>
   <Year>2011</Year>
   <Month>09</Month>
   <Day>15</Day>
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  <Note>involved in mitochondrial morphogenesis
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  <Frequency>2</Frequency>
  <HeadingMappedToList>
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    <DescriptorReferredTo>
     <DescriptorUI>*D008565</DescriptorUI>
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      <String>Membrane Proteins</String>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029721</DescriptorUI>
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  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D024101</DescriptorUI>
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      <String>Mitochondrial Proteins</String>
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  <SourceList>
   <Source>EMBO Rep 2011 Mar;12(3):223-30</Source>
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  <ConceptList>
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    <ConceptUI>M0561021</ConceptUI>
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    <RegistryNumber>0</RegistryNumber>
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      <TermUI>T796931</TermUI>
      <String>PMI protein, Drosophila</String>
      <DateCreated>
       <Year>2011</Year>
       <Month>09</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2011)</ThesaurusID>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C561038</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ONCOFID-S</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2011</Year>
   <Month>09</Month>
   <Day>15</Day>
  </DateCreated>
  <Note>an antineoplastic agent; structure in first source
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  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002166</DescriptorUI>
     <DescriptorName>
      <String>Camptothecin</String>
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    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
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   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D006820</DescriptorUI>
     <DescriptorName>
      <String>Hyaluronic Acid</String>
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    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
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  <SourceList>
   <Source>Curr Cancer Drug Targets 2011 Jun;11(5):572-85</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0561022</ConceptUI>
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    <RegistryNumber>0</RegistryNumber>
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      <TermUI>T796932</TermUI>
      <String>ONCOFID-S</String>
      <DateCreated>
       <Year>2011</Year>
       <Month>09</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2011)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C561039</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>NIR-mbc94</String>
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  <DateCreated>
   <Year>2011</Year>
   <Month>09</Month>
   <Day>15</Day>
  </DateCreated>
  <Note>a fluorescent ligand of CB2 receptors; structure in first source
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  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009636</DescriptorUI>
     <DescriptorName>
      <String>Norbornanes</String>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011720</DescriptorUI>
     <DescriptorName>
      <String>Pyrazoles</String>
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  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D008024</DescriptorUI>
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  <SourceList>
   <Source>Chem Biol 2011 May 27;18(5):563-8</Source>
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  <ConceptList>
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    <ConceptUI>M0561023</ConceptUI>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T796933</TermUI>
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      <DateCreated>
       <Year>2011</Year>
       <Month>09</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2011)</ThesaurusID>
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  <SupplementalRecordUI>C561040</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bisdionin F</String>
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  <DateCreated>
   <Year>2011</Year>
   <Month>09</Month>
   <Day>15</Day>
  </DateCreated>
  <Note>inhibitor of acidic mammalian chitinase; structure in first source
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014970</DescriptorUI>
     <DescriptorName>
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  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D002688</DescriptorUI>
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    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
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      <DateCreated>
       <Year>2011</Year>
       <Month>09</Month>
       <Day>15</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2011)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C561041</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>(2,6-bis(dimethylamino)-10-(4-((4,7,10-tris(carboxymethyl)-1,4,7,10-tetraazacyclododecan-1-yl)methyl)benzyl)acridin-10-ium)copper(II)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2011</Year>
   <Month>09</Month>
   <Day>15</Day>
  </DateCreated>
  <Note>a PET radiotracer that targets the mitochondria of tumors; structure in first source
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D056831</DescriptorUI>
     <DescriptorName>
      <String>Coordination Complexes</String>
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  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D003301</DescriptorUI>
     <DescriptorName>
      <String>Copper Radioisotopes</String>
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     </DescriptorReferredTo>
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  </IndexingInformationList>
  <SourceList>
   <Source>Bioconjug Chem 2011 Apr 20;22(4):700-8</Source>
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  <ConceptList>
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    <ConceptName>
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    <RegistryNumber>0</RegistryNumber>
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     <Concept1UI>M0561025</Concept1UI>
     <Concept2UI>M0561026</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T796935</TermUI>
      <String>(2,6-bis(dimethylamino)-10-(4-((4,7,10-tris(carboxymethyl)-1,4,7,10-tetraazacyclododecan-1-yl)methyl)benzyl)acridin-10-ium)copper(II)</String>
      <DateCreated>
       <Year>2011</Year>
       <Month>09</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2011)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T796936</TermUI>
      <String>Cu(DO3A-xy-ACR)</String>
      <DateCreated>
       <Year>2011</Year>
       <Month>09</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2011)</ThesaurusID>
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   <Concept PreferredConceptYN="N">
    <ConceptUI>M0561026</ConceptUI>
    <ConceptName>
     <String>64Cu(DO3A-xy-ACR)</String>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0561025</Concept1UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
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      <String>64Cu(DO3A-xy-ACR)</String>
      <DateCreated>
       <Year>2011</Year>
       <Month>09</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2011)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C028476</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Zami 1327</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>03</Month>
   <Day>24</Day>
  </DateCreated>
  <DateRevised>
   <Year>1994</Year>
   <Month>09</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>structure given in first source
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  <Frequency>7</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011412</DescriptorUI>
     <DescriptorName>
      <String>Propanolamines</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>Toxicol Lett 1980;5(2):109</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0091615</ConceptUI>
    <ConceptName>
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    <RegistryNumber>67971-73-7</RegistryNumber>
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      <String>Zami 1327</String>
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  <SupplementalRecordUI>C028478</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-tert-butyl-2,6-diisopropylphenol</String>
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  <DateCreated>
   <Year>1981</Year>
   <Month>03</Month>
   <Day>24</Day>
  </DateCreated>
  <Note>induces hemorrhage in rats
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  <Frequency>2</Frequency>
  <HeadingMappedToList>
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  <SourceList>
   <Source>Toxicol Lett 1980;5(2):147</Source>
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  <ConceptList>
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   <String>hookeroside A</String>
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  <DateCreated>
   <Year>2004</Year>
   <Month>05</Month>
   <Day>18</Day>
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  <Note>biologically active (inhibits pancreatic lipase) triterpenoid saponin from Scabiosa tschiliensis; structure in first source
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   <HeadingMappedTo>
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   <Source>J Nat Prod 2004 Apr;67(4):604-13</Source>
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       <Month>05</Month>
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   <Month>07</Month>
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       <Month>07</Month>
       <Day>18</Day>
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   <Concept PreferredConceptYN="N">
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       <Month>07</Month>
       <Day>18</Day>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C028489</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-nitroso-4-benzoyl-3,5-dimethylpiperazine</String>
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  <DateCreated>
   <Year>1981</Year>
   <Month>03</Month>
   <Day>25</Day>
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  <Note>structure given in first source
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009602</DescriptorUI>
     <DescriptorName>
      <String>Nitrosamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Res 1981;41(3):1034</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0091644</ConceptUI>
    <ConceptName>
     <String>1-nitroso-4-benzoyl-3,5-dimethylpiperazine</String>
    </ConceptName>
    <RegistryNumber>61034-40-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T121647</TermUI>
      <String>1-nitroso-4-benzoyl-3,5-dimethylpiperazine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C485170</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hookeroside B</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>05</Month>
   <Day>18</Day>
  </DateCreated>
  <Note>biologically active (inhibits pancreatic lipase) triterpenoid saponin from Scabiosa tschiliensis; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012503</DescriptorUI>
     <DescriptorName>
      <String>Saponins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014315</DescriptorUI>
     <DescriptorName>
      <String>Triterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2004 Apr;67(4):604-13</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0465986</ConceptUI>
    <ConceptName>
     <String>hookeroside B</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T587072</TermUI>
      <String>hookeroside B</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>05</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C028501</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>galactosylumbelliferone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>03</Month>
   <Day>13</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>05</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>fluorescent substrate
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014468</DescriptorUI>
     <DescriptorName>
      <String>Umbelliferones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ther Drug Monitor 1980;2(3):2611</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0091682</ConceptUI>
    <ConceptName>
     <String>galactosylumbelliferone</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T121685</TermUI>
      <String>galactosylumbelliferone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C417114</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>feigrisolide A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>21</Day>
  </DateCreated>
  <Note>a lactone with antibacterial activities from Streptomyces; structure in first source
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007783</DescriptorUI>
     <DescriptorName>
      <String>Lactones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiot (Tokyo) 2000 Sep;53(9):934-43</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0375003</ConceptUI>
    <ConceptName>
     <String>feigrisolide A</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T431527</TermUI>
      <String>feigrisolide A</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>12</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C417115</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>feigrisolide B</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>21</Day>
  </DateCreated>
  <Note>a lactone with antibacterial activities from Streptomyces; structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007783</DescriptorUI>
     <DescriptorName>
      <String>Lactones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiot (Tokyo) 2000 Sep;53(9):934-43</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0375004</ConceptUI>
    <ConceptName>
     <String>feigrisolide B</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T431528</TermUI>
      <String>feigrisolide B</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>12</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C028518</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1',2'-epoxyvinylbital</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>03</Month>
   <Day>19</Day>
  </DateCreated>
  <DateRevised>
   <Year>1994</Year>
   <Month>07</Month>
   <Day>28</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>BUTABARBITAL/*analogs (81-94)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001463</DescriptorUI>
     <DescriptorName>
      <String>Barbiturates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Xenobiotica 1980;10(3):159</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0091714</ConceptUI>
    <ConceptName>
     <String>1',2'-epoxyvinylbital</String>
    </ConceptName>
    <CASN1Name>2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-(1-methylbutyl)-5-oxiranyl-</CASN1Name>
    <RegistryNumber>75319-56-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T121717</TermUI>
      <String>1',2'-epoxyvinylbital</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C028524</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3,4-dimethylhippuric acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>03</Month>
   <Day>19</Day>
  </DateCreated>
  <Note>metabolite of pseudocumene in urine
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006626</DescriptorUI>
     <DescriptorName>
      <String>Hippurates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Toxicol 1980;45(2):93</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0091722</ConceptUI>
    <ConceptName>
     <String>3,4-dimethylhippuric acid</String>
    </ConceptName>
    <RegistryNumber>23082-12-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T121725</TermUI>
      <String>3,4-dimethylhippuric acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C028527</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>guaiacol glycerol ether O-demethylase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>03</Month>
   <Day>24</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010090</DescriptorUI>
     <DescriptorName>
      <String>Oxidoreductases, O-Demethylating</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Toxicol 1980;45(2):149</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0091729</ConceptUI>
    <ConceptName>
     <String>guaiacol glycerol ether O-demethylase</String>
    </ConceptName>
    <RegistryNumber>EC 1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T121732</TermUI>
      <String>guaiacol glycerol ether O-demethylase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C028534</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>thymone A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>03</Month>
   <Day>24</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>10</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>peptide isolated from bovine thymus
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010455</DescriptorUI>
     <DescriptorName>
      <String>Peptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D013951</DescriptorUI>
     <DescriptorName>
      <String>Thymus Hormones</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 1980;97(2):595</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0091743</ConceptUI>
    <ConceptName>
     <String>thymone A</String>
    </ConceptName>
    <RegistryNumber>76775-49-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T121746</TermUI>
      <String>thymone A</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C028535</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>thymone B</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>03</Month>
   <Day>24</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>10</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>peptide isolated from bovine thymus
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010455</DescriptorUI>
     <DescriptorName>
      <String>Peptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D013951</DescriptorUI>
     <DescriptorName>
      <String>Thymus Hormones</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 1980;97(2):601</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0091744</ConceptUI>
    <ConceptName>
     <String>thymone B</String>
    </ConceptName>
    <RegistryNumber>76775-55-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T121747</TermUI>
      <String>thymone B</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C028542</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>pre-beta-lactoglobulin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>03</Month>
   <Day>24</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007782</DescriptorUI>
     <DescriptorName>
      <String>Lactoglobulins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011498</DescriptorUI>
     <DescriptorName>
      <String>Protein Precursors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 1980;97(2):802</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0091758</ConceptUI>
    <ConceptName>
     <String>pre-beta-lactoglobulin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T121761</TermUI>
      <String>pre-beta-lactoglobulin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C028543</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>glucosamine-trans-parinarate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>03</Month>
   <Day>24</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>05</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>fluorescent probe
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006017</DescriptorUI>
     <DescriptorName>
      <String>Glycolipids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Biochem 1980;112(2):293</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0091759</ConceptUI>
    <ConceptName>
     <String>glucosamine-trans-parinarate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T121762</TermUI>
      <String>glucosamine-trans-parinarate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C028579</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-(guanosin-8-yl)-4-aminobiphenyl-5'-monophosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>03</Month>
   <Day>30</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AMINOBIPHENYL COMPOUNDS (81-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D006157</DescriptorUI>
     <DescriptorName>
      <String>Guanosine Monophosphate</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Biol Interact 1981;34(2):239</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0091825</ConceptUI>
    <ConceptName>
     <String>N-(guanosin-8-yl)-4-aminobiphenyl-5'-monophosphate</String>
    </ConceptName>
    <CASN1Name>5'-Guanylic acid, 8-((1,1'-biphenyl)-4-ylamino)-</CASN1Name>
    <RegistryNumber>78281-08-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T121828</TermUI>
      <String>N-(guanosin-8-yl)-4-aminobiphenyl-5'-monophosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T121827</TermUI>
      <String>GMP-ABP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C028550</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>peptide CN1</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>03</Month>
   <Day>24</Day>
  </DateCreated>
  <Note>neuritogenic peptide from P2 protein
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009185</DescriptorUI>
     <DescriptorName>
      <String>Myelin Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010446</DescriptorUI>
     <DescriptorName>
      <String>Peptide Fragments</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Immunol 1981;126(3):1203</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0091769</ConceptUI>
    <ConceptName>
     <String>peptide CN1</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T121772</TermUI>
      <String>peptide CN1</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C028559</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bathocuproine sulfonate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>03</Month>
   <Day>25</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>reagent for copper; RN given refers to parent cpd
  </Note>
  <Frequency>102</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010618</DescriptorUI>
     <DescriptorName>
      <String>Phenanthrolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
    <PharmacologicalActionList>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D002614</DescriptorUI>
        <DescriptorName>
         <String>Chelating Agents</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D007202</DescriptorUI>
        <DescriptorName>
         <String>Indicators and Reagents</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
    </PharmacologicalActionList>
  <SourceList>
   <Source>J Biol Chem 1981;256(4):1669</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0091789</ConceptUI>
    <ConceptName>
     <String>bathocuproine sulfonate</String>
    </ConceptName>
    <RegistryNumber>73348-75-1</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>52698-84-7 (di-Na salt)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0091789</Concept1UI>
     <Concept2UI>M0091788</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0091789</Concept1UI>
     <Concept2UI>M0317814</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0091789</Concept1UI>
     <Concept2UI>M0091787</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T121792</TermUI>
      <String>bathocuproine sulfonate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0091788</ConceptUI>
    <ConceptName>
     <String>bathocuproine disulfonic acid, disodium salt</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0091789</Concept1UI>
     <Concept2UI>M0091788</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T121791</TermUI>
      <String>bathocuproine disulfonic acid, disodium salt</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0317814</ConceptUI>
    <ConceptName>
     <String>bathocuproine sulfonate, disodium salt</String>
    </ConceptName>
    <RegistryNumber>52698-84-7</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0091789</Concept1UI>
     <Concept2UI>M0317814</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T347814</TermUI>
      <String>bathocuproine sulfonate, disodium salt</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0091787</ConceptUI>
    <ConceptName>
     <String>bathocuproine disulfonate</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0091789</Concept1UI>
     <Concept2UI>M0091787</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T121790</TermUI>
      <String>bathocuproine disulfonate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C028562</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>lac alpha peptide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>03</Month>
   <Day>26</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>03</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010455</DescriptorUI>
     <DescriptorName>
      <String>Peptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D007763</DescriptorUI>
     <DescriptorName>
      <String>Lac Operon</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Biol Chem 1981;256(4):1896</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0091795</ConceptUI>
    <ConceptName>
     <String>lac alpha peptide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T121798</TermUI>
      <String>lac alpha peptide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C112935</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>PLYTW protein, Staphylococcus phage Twort</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>07</Month>
   <Day>08</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>01</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>amino acid sequence in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009238</DescriptorUI>
     <DescriptorName>
      <String>N-Acetylmuramoyl-L-alanine Amidase</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014764</DescriptorUI>
     <DescriptorName>
      <String>Viral Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>FEMS Microbiol Lett 1998 May 15;162(2):256-74</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0291865</ConceptUI>
    <ConceptName>
     <String>PLYTW protein, Staphylococcus phage Twort</String>
    </ConceptName>
    <RegistryNumber>EC 3.5.1.28</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T520393</TermUI>
      <String>PLYTW protein, Staphylococcus phage Twort</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>09</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C028565</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>porphyrin pi cation radical</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>03</Month>
   <Day>26</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>formed in Zn-substituted horseradish peroxidase
  </Note>
  <Frequency>18</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011166</DescriptorUI>
     <DescriptorName>
      <String>Porphyrins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D002412</DescriptorUI>
     <DescriptorName>
      <String>Cations</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Biochemistry 1980;19(25):5795</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0091801</ConceptUI>
    <ConceptName>
     <String>porphyrin pi cation radical</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T121804</TermUI>
      <String>porphyrin pi cation radical</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C076748</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>lacto-N-biosidase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1992</Year>
   <Month>10</Month>
   <Day>17</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>hydrolyzes oligosaccharides containing a type 1 structure at the nonreducing terminus &amp; produces lacto-N-biose (Gal beta1-3GlcNAc)
  </Note>
  <Frequency>10</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006026</DescriptorUI>
     <DescriptorName>
      <String>Glycoside Hydrolases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Proc Natl Acad Sci U S A 1992 Sep 15;89(18):8512-6</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0206310</ConceptUI>
    <ConceptName>
     <String>lacto-N-biosidase</String>
    </ConceptName>
    <RegistryNumber>EC 3.2.1.140</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T236315</TermUI>
      <String>lacto-N-biosidase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C028570</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Ringer's acetate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>03</Month>
   <Day>27</Day>
  </DateCreated>
  <Frequency>171</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007552</DescriptorUI>
     <DescriptorName>
      <String>Isotonic Solutions</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Crit Care Med 1981;9(1):42</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0091813</ConceptUI>
    <ConceptName>
     <String>Ringer's acetate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T121816</TermUI>
      <String>Ringer's acetate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C445419</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tris(hydroxymethyl)-acrylamidomethane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>01</Month>
   <Day>30</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>8</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000178</DescriptorUI>
     <DescriptorName>
      <String>Acrylamides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biopolymers 2000-2001;56(2):77-84</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0412889</ConceptUI>
    <ConceptName>
     <String>tris(hydroxymethyl)-acrylamidomethane</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T480080</TermUI>
      <String>tris(hydroxymethyl)-acrylamidomethane</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>01</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T480081</TermUI>
      <String>THAM cpd</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>01</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C584454</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-hydroxy-6-(3-methylhexa-3,5-dienyl)tetrahydropyran-2-one</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>11</Month>
   <Day>17</Day>
  </DateCreated>
  <Note>isolated from marine Bacillus; structure in first source
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007783</DescriptorUI>
     <DescriptorName>
      <String>Lactones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011753</DescriptorUI>
     <DescriptorName>
      <String>Pyrones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D000900</DescriptorUI>
     <DescriptorName>
      <String>Anti-Bacterial Agents</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Nat Prod. 2011 Jul 22;74(7):1606-12.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0589030</ConceptUI>
    <ConceptName>
     <String>4-hydroxy-6-(3-methylhexa-3,5-dienyl)tetrahydropyran-2-one</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0589030</Concept1UI>
     <Concept2UI>M0589031</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T851122</TermUI>
      <String>4-hydroxy-6-(3-methylhexa-3,5-dienyl)tetrahydropyran-2-one</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>11</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2014)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0589031</ConceptUI>
    <ConceptName>
     <String>ieodomycin B</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0589030</Concept1UI>
     <Concept2UI>M0589031</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T851123</TermUI>
      <String>ieodomycin B</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>11</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2014)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C502167</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ASL1-LBD36 protein, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>20</Day>
  </DateCreated>
  <Note>ASL1 - ASYMMETRIC LEAVES2-LIKE1; LBD36 - LATERAL ORGAN BOUNDARIES domain gene 36; a member of the AS2 (ASYMMETRIC LEAVES2)/LOB (LATERAL ORGAN BOUNDARIES) family that controls proximal-distal patterning in Arabidopsis petals; has been sequenced
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Plant Mol Biol 2005 Mar;57(4):559-75</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0487147</ConceptUI>
    <ConceptName>
     <String>ASL1-LBD36 protein, Arabidopsis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T646348</TermUI>
      <String>ASL1-LBD36 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>07</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C028545</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-(2,4-dinitrophenyl)alanine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>03</Month>
   <Day>24</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>15</Day>
  </DateRevised>
  <Note>RN given refers to (L)-isomer
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010649</DescriptorUI>
     <DescriptorName>
      <String>Phenylalanine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Biochem 1980;112(2):403</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0091764</ConceptUI>
    <ConceptName>
     <String>N-(2,4-dinitrophenyl)alanine</String>
    </ConceptName>
    <RegistryNumber>1655-52-3</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>10250-67-6 ((DL)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>6367-22-2 ((D)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0091764</Concept1UI>
     <Concept2UI>M0317812</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0091764</Concept1UI>
     <Concept2UI>M0317811</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T121767</TermUI>
      <String>N-(2,4-dinitrophenyl)alanine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T121765</TermUI>
      <String>2,4-dinitrobenzene alanine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T121766</TermUI>
      <String>DNP-alanine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0317812</ConceptUI>
    <ConceptName>
     <String>N-(2,4-dinitrophenyl)alanine, (D)-isomer</String>
    </ConceptName>
    <RegistryNumber>6367-22-2</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0091764</Concept1UI>
     <Concept2UI>M0317812</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T347812</TermUI>
      <String>N-(2,4-dinitrophenyl)alanine, (D)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0317811</ConceptUI>
    <ConceptName>
     <String>N-(2,4-dinitrophenyl)alanine, (DL)-isomer</String>
    </ConceptName>
    <RegistryNumber>10250-67-6</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0091764</Concept1UI>
     <Concept2UI>M0317811</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T347811</TermUI>
      <String>N-(2,4-dinitrophenyl)alanine, (DL)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C095848</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Kn1 protein, plant</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>10</Month>
   <Day>27</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>01</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>members of KNOX class homeobox gene products; amino acid sequence in first source
  </Note>
  <Frequency>79</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010940</DescriptorUI>
     <DescriptorName>
      <String>Plant Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D018398</DescriptorUI>
     <DescriptorName>
      <String>Homeodomain Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Genes Dev 1995 Sep 15;9(18):2292-304</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0252334</ConceptUI>
    <ConceptName>
     <String>Kn1 protein, plant</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0252334</Concept1UI>
     <Concept2UI>M0252331</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0252334</Concept1UI>
     <Concept2UI>M0252330</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T517632</TermUI>
      <String>Kn1 protein, plant</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>08</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T282338</TermUI>
      <String>knotted1 protein, plant</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T282334</TermUI>
      <String>KNOTTED-1 protein, plant</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0252331</ConceptUI>
    <ConceptName>
     <String>Oskn3 protein, Oryza sativa</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0252334</Concept1UI>
     <Concept2UI>M0252331</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T517629</TermUI>
      <String>Oskn3 protein, Oryza sativa</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>08</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0252330</ConceptUI>
    <ConceptName>
     <String>Oskn2 protein, Oryza sativa</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0252334</Concept1UI>
     <Concept2UI>M0252330</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T517628</TermUI>
      <String>Oskn2 protein, Oryza sativa</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>08</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C028588</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>spiralin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>04</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>10</Month>
   <Day>25</Day>
  </DateRevised>
  <Note>amphilhilic protein from Spiroplasma citri cell membrane
  </Note>
  <Frequency>42</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BACTERIAL PROTEINS (81-84)</PreviousIndexing>
   <PreviousIndexing>*MEMBRANE PROTEINS (81-84)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001425</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Outer Membrane Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D008074</DescriptorUI>
     <DescriptorName>
      <String>Lipoproteins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Bacteriol 1981;145(1):61</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0091839</ConceptUI>
    <ConceptName>
     <String>spiralin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T121842</TermUI>
      <String>spiralin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C028596</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>S-carboxymethyl-papain</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>04</Month>
   <Day>02</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>04</Month>
   <Day>17</Day>
  </DateRevised>
  <Note>derivative of papain EC 3.4.22.2
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010206</DescriptorUI>
     <DescriptorName>
      <String>Papain</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Biochem 1980;113(1):189</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0091864</ConceptUI>
    <ConceptName>
     <String>S-carboxymethyl-papain</String>
    </ConceptName>
    <RegistryNumber>EC 3.4.22.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T121867</TermUI>
      <String>S-carboxymethyl-papain</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C028597</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>S-carboxamido-papain</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>04</Month>
   <Day>02</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>04</Month>
   <Day>17</Day>
  </DateRevised>
  <Note>derivative of papain EC 3.4.22.2
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010206</DescriptorUI>
     <DescriptorName>
      <String>Papain</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Biochem 1980;113(1):189</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0091865</ConceptUI>
    <ConceptName>
     <String>S-carboxamido-papain</String>
    </ConceptName>
    <RegistryNumber>EC 3.4.22.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T121868</TermUI>
      <String>S-carboxamido-papain</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C031795</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-amino-5,8-dimethoxy-6-methyl-1,2-dihydronaphthalene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>10</Month>
   <Day>15</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>06</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>has serotonin-like activity; RN given refers to parent cpd; structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D015081</DescriptorUI>
     <DescriptorName>
      <String>2-Naphthylamine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 1981;24(7):882</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0099659</ConceptUI>
    <ConceptName>
     <String>2-amino-5,8-dimethoxy-6-methyl-1,2-dihydronaphthalene</String>
    </ConceptName>
    <CASN1Name>2-Naphthalenamine, 1,2-dihydro-5,8-dimethoxy-6-methyl-</CASN1Name>
    <RegistryNumber>80387-95-7</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>77886-58-9 (HCl(+-)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0099659</Concept1UI>
     <Concept2UI>M0319394</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T129663</TermUI>
      <String>2-amino-5,8-dimethoxy-6-methyl-1,2-dihydronaphthalene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T129662</TermUI>
      <String>2-ADMDN</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0319394</ConceptUI>
    <ConceptName>
     <String>2-amino-5,8-dimethoxy-6-methyl-1,2-dihydronaphthalene hydrochloride, (+-)-isomer</String>
    </ConceptName>
    <RegistryNumber>77886-58-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0099659</Concept1UI>
     <Concept2UI>M0319394</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T349394</TermUI>
      <String>2-amino-5,8-dimethoxy-6-methyl-1,2-dihydronaphthalene hydrochloride, (+-)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C480727</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>PBP1a protein, Streptococcus pneumoniae</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>01</Month>
   <Day>21</Day>
  </DateCreated>
  <Note>catalyzes the last, crucial steps in peptidoglycan biosynthesis and several of them are essential for bacterial survival
  </Note>
  <Frequency>26</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010458</DescriptorUI>
     <DescriptorName>
      <String>Peptidyl Transferases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Crystallogr D Biol Crystallogr. 2003 Jun;59(Pt 6):1067-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0459475</ConceptUI>
    <ConceptName>
     <String>PBP1a protein, Streptococcus pneumoniae</String>
    </ConceptName>
    <RegistryNumber>EC 2.3.2.12</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T569665</TermUI>
      <String>PBP1a protein, Streptococcus pneumoniae</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>01</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C028516</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-(p-sulfophenyldiazo)-4-hydroxyphenylacetic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>03</Month>
   <Day>17</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>21</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001557</DescriptorUI>
     <DescriptorName>
      <String>Benzenesulfonates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D006241</DescriptorUI>
     <DescriptorName>
      <String>Haptens</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Eur J Immunol 1980;10(11):828</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0091708</ConceptUI>
    <ConceptName>
     <String>3-(p-sulfophenyldiazo)-4-hydroxyphenylacetic acid</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T121711</TermUI>
      <String>3-(p-sulfophenyldiazo)-4-hydroxyphenylacetic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T121710</TermUI>
      <String>SPDHPAA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C113000</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>srw1 protein, S pombe</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>07</Month>
   <Day>13</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>01</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>a negative regulator of cell cycle progression during G1 phase; homolog of Hct1/Cdh1 and related to Fizzy; amino acid sequence in first source
  </Note>
  <Frequency>13</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D018797</DescriptorUI>
     <DescriptorName>
      <String>Cell Cycle Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029702</DescriptorUI>
     <DescriptorName>
      <String>Schizosaccharomyces pombe Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Biol Cell 1998 May;9(5):1065-80</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0292000</ConceptUI>
    <ConceptName>
     <String>srw1 protein, S pombe</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T400887</TermUI>
      <String>srw1 protein, S pombe</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>11</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T497161</TermUI>
      <String>Ste9 protein, S pombe</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>06</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T569666</TermUI>
      <String>SPAC144.13c protein, S pombe</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>01</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C028637</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-hydroxytriazolam</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>03</Month>
   <Day>19</Day>
  </DateCreated>
  <DateRevised>
   <Year>1985</Year>
   <Month>07</Month>
   <Day>24</Day>
  </DateRevised>
  <Note>triazolam metabolite; structure in first source
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014229</DescriptorUI>
     <DescriptorName>
      <String>Triazolam</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Clin Pharmacol Ther 1981;29(1):81</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0091952</ConceptUI>
    <ConceptName>
     <String>4-hydroxytriazolam</String>
    </ConceptName>
    <RegistryNumber>65686-11-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T121955</TermUI>
      <String>4-hydroxytriazolam</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C584455</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>carboxyformin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>11</Month>
   <Day>17</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001645</DescriptorUI>
     <DescriptorName>
      <String>Biguanides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D007004</DescriptorUI>
     <DescriptorName>
      <String>Hypoglycemic Agents</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Diabetes Sci Technol. 2013;7(2):308-12.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0589032</ConceptUI>
    <ConceptName>
     <String>carboxyformin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T851124</TermUI>
      <String>carboxyformin</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>11</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2014)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C028693</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-fluorouracil 5S ribonucleic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>04</Month>
   <Day>16</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>5S RNA from E. coli with uracil residues about 80% replaced by fluorouracil
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012329</DescriptorUI>
     <DescriptorName>
      <String>RNA, Bacterial</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 1980;19(26):5955</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0092086</ConceptUI>
    <ConceptName>
     <String>5-fluorouracil 5S ribonucleic acid</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T122089</TermUI>
      <String>5-fluorouracil 5S ribonucleic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T122087</TermUI>
      <String>E. coli 5-fluorouracil 5S RNA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T122088</TermUI>
      <String>FU-5S RNA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T122086</TermUI>
      <String>5-FU 5S RNA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C028650</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-chlorotubercidin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>03</Month>
   <Day>24</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014372</DescriptorUI>
     <DescriptorName>
      <String>Tubercidin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nucleic Acids Res 1980;8(24):6213</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0091983</ConceptUI>
    <ConceptName>
     <String>5-chlorotubercidin</String>
    </ConceptName>
    <RegistryNumber>24386-95-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T121986</TermUI>
      <String>5-chlorotubercidin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C584456</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Rv1681 protein, Mycobacterium tuberculosis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>11</Month>
   <Day>17</Day>
  </DateCreated>
  <Note>marker for active tuberculosis
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D015415</DescriptorUI>
     <DescriptorName>
      <String>Biomarkers</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Clin Microbiol. 2013 May;51(5):1367-73.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0589033</ConceptUI>
    <ConceptName>
     <String>Rv1681 protein, Mycobacterium tuberculosis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T851125</TermUI>
      <String>Rv1681 protein, Mycobacterium tuberculosis</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>11</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2014)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C028655</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>black mamba protein A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>03</Month>
   <Day>26</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>from Dendroaspis polylepis polylepis venom; 81 amino acids; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PEPTIDES (81-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004546</DescriptorUI>
     <DescriptorName>
      <String>Elapid Venoms</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Hoppe Seylers Z Physiol Chem 1980;361(12):1787</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0091994</ConceptUI>
    <ConceptName>
     <String>black mamba protein A</String>
    </ConceptName>
    <RegistryNumber>76723-44-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T121997</TermUI>
      <String>black mamba protein A</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C518172</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>OZ78 compound</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>03</Month>
   <Day>21</Day>
  </DateCreated>
  <Note>trematocidal; effective against Echinostoma caproni and Fasciola hepatica; structure in first source
  </Note>
  <Frequency>16</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000218</DescriptorUI>
     <DescriptorName>
      <String>Adamantane</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antimicrob Chemother 2006 Dec;58(6):1193-7</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0507929</ConceptUI>
    <ConceptName>
     <String>OZ78 compound</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T694070</TermUI>
      <String>OZ78 compound</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>03</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C584457</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-butyl-4-nitromethyl-3-quinolin-2-yl-4H-quinoline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>11</Month>
   <Day>17</Day>
  </DateCreated>
  <Note>inhibits the transcriptional activator activities of both RhaS and RhaR; structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011804</DescriptorUI>
     <DescriptorName>
      <String>Quinolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biomol Screen. 2013 Jun;18(5):588-98.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0589034</ConceptUI>
    <ConceptName>
     <String>1-butyl-4-nitromethyl-3-quinolin-2-yl-4H-quinoline</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0589034</Concept1UI>
     <Concept2UI>M0589035</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T851126</TermUI>
      <String>1-butyl-4-nitromethyl-3-quinolin-2-yl-4H-quinoline</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>11</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2014)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0589035</ConceptUI>
    <ConceptName>
     <String>OSSL-051168</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0589034</Concept1UI>
     <Concept2UI>M0589035</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T851127</TermUI>
      <String>OSSL-051168</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>11</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2014)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C584458</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>caffeic acid phenethyl amide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>11</Month>
   <Day>17</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002109</DescriptorUI>
     <DescriptorName>
      <String>Caffeic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D007004</DescriptorUI>
     <DescriptorName>
      <String>Hypoglycemic Agents</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Cardiovasc Diabetol. 2013;12:99.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0589036</ConceptUI>
    <ConceptName>
     <String>caffeic acid phenethyl amide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T851128</TermUI>
      <String>caffeic acid phenethyl amide</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>11</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2014)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C518173</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>piperazinyl-cross-linked ciprofloxacin dimer</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>03</Month>
   <Day>21</Day>
  </DateCreated>
  <Note>antibacterial, effective on Staphylococcus aureus; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002939</DescriptorUI>
     <DescriptorName>
      <String>Ciprofloxacin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010879</DescriptorUI>
     <DescriptorName>
      <String>Piperazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antimicrob Chemother 2006 Dec;58(6):1283-6</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0507930</ConceptUI>
    <ConceptName>
     <String>piperazinyl-cross-linked ciprofloxacin dimer</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T694071</TermUI>
      <String>piperazinyl-cross-linked ciprofloxacin dimer</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>03</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T694072</TermUI>
      <String>piperazinyl-ciprofloxacin dimer</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>03</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C089252</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>DNA modification methylase XorII, Xanthomonas oryzae</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>10</Month>
   <Day>04</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>02</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>recognizes CGATCG; amino acid sequence given in first source; GenBank U06424
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015254</DescriptorUI>
     <DescriptorName>
      <String>DNA Modification Methylases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Gen Genet 1994 Aug 15;244(4):383-90</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0236006</ConceptUI>
    <ConceptName>
     <String>DNA modification methylase XorII, Xanthomonas oryzae</String>
    </ConceptName>
    <RegistryNumber>EC 2.1.1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T266011</TermUI>
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      <DateCreated>
       <Year>2001</Year>
       <Month>06</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T452434</TermUI>
      <String>XP-280</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>06</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015516</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>succinyl-trialanine-4-nitroanilide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>06</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>synthetic substrate of porcine pancreatic elastase
  </Note>
  <Frequency>49</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ANILIDES (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009842</DescriptorUI>
     <DescriptorName>
      <String>Oligopeptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
    <PharmacologicalActionList>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D002863</DescriptorUI>
        <DescriptorName>
         <String>Chromogenic Compounds</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
    </PharmacologicalActionList>
  <SourceList>
   <Source>Ann Clin Biochem 1979;16(6):320</Source>
   <Source>Clin Chim Acta 1979;95(2):401</Source>
   <Source>Clin Chim Acta 96(3):215;1979</Source>
   <Source>FEBS Lett 80(1):182;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064846</ConceptUI>
    <ConceptName>
     <String>succinyl-trialanine-4-nitroanilide</String>
    </ConceptName>
    <CASN1Name>L-Alaninamide, N-(3-carboxy-1-oxopropyl)-L-alanyl-L-alanyl-N-(4-nitrophenyl)-</CASN1Name>
    <RegistryNumber>52299-14-6</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0064846</Concept1UI>
     <Concept2UI>M0064845</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094849</TermUI>
      <String>succinyl-trialanine-4-nitroanilide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T094847</TermUI>
      <String>succinyltrialanine-p-nitroanilide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T674933</TermUI>
      <String>succinyl(Ala)3-p-nitroanilide</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>06</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T674934</TermUI>
      <String>suc(Ala)3-p-NA</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>06</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T094837</TermUI>
      <String>3-carboxypropionyl-alanyl-alanyl-alanyl-4-nitroanilide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T094845</TermUI>
      <String>succinyl-alanyl-alanyl-alanine-p-nitroanilide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T094839</TermUI>
      <String>N-succinyl-L-trialanine p-nitroanilide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T094840</TermUI>
      <String>SANA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T094841</TermUI>
      <String>SLAPN</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T094842</TermUI>
      <String>Suc-Ala(3)-NA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T094843</TermUI>
      <String>Suc-Ala(3)-Nan</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T094844</TermUI>
      <String>Suc-Ala-Ala-Ala-p-nitroanilide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T094846</TermUI>
      <String>succinyl-trialanine-p-nitroanilide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T094838</TermUI>
      <String>3-carboxypropionyl-trialanine-p-nitroanilide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0064845</ConceptUI>
    <ConceptName>
     <String>trianiline-4-nitroanilide</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0064846</Concept1UI>
     <Concept2UI>M0064845</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T094848</TermUI>
      <String>trianiline-4-nitroanilide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C496469</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>MAGI3 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>06</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>RefSeq NM_152900
  </Note>
  <Frequency>23</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008565</DescriptorUI>
     <DescriptorName>
      <String>Membrane Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0465078</ConceptUI>
    <ConceptName>
     <String>MAGI3 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T641103</TermUI>
      <String>MAGI3 protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>05</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T584843</TermUI>
      <String>membrane-associated guanylate kinase-related (MAGI-3), human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>04</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T584842</TermUI>
      <String>MAGI-3 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>04</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C510837</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>trisilanolisobutyl-POSS</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>06</Month>
   <Day>09</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D017646</DescriptorUI>
     <DescriptorName>
      <String>Organosilicon Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Langmuir. 2005 Mar 1;21(5):1908-16</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0498741</ConceptUI>
    <ConceptName>
     <String>trisilanolisobutyl-POSS</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T675608</TermUI>
      <String>trisilanolisobutyl-POSS</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>06</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T675609</TermUI>
      <String>trisilanolisobutyl-polyhedral oligomeric silsesquioxane</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>06</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C101505</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>PRP protein, Brassica napus</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>10</Month>
   <Day>28</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>09</Month>
   <Day>23</Day>
  </DateRevised>
  <Note>a cold-induced, proline-rich, cell wall-plasma membrane linker protein isolated from Brassica napus; amino acid sequence in first source; GenBank X94976
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006360</DescriptorUI>
     <DescriptorName>
      <String>Heat-Shock Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008565</DescriptorUI>
     <DescriptorName>
      <String>Membrane Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010940</DescriptorUI>
     <DescriptorName>
      <String>Plant Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Plant Mol Biol 1996 Jul;31(4):771-81</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0266075</ConceptUI>
    <ConceptName>
     <String>PRP protein, Brassica napus</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T551217</TermUI>
      <String>PRP protein, Brassica napus</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>09</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006230</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ORF 8511</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CYCLOHEXANOLS (74-80)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003506</DescriptorUI>
     <DescriptorName>
      <String>Cyclofenil</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Contraception 9(4):393;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0048558</ConceptUI>
    <ConceptName>
     <String>ORF 8511</String>
    </ConceptName>
    <CASN1Name>cyclohexanol, 4-(diphenylmethylene)-2-ethyl-3-methyl-, acetate</CASN1Name>
    <RegistryNumber>52236-34-7</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0048558</Concept1UI>
     <Concept2UI>M0048557</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T078561</TermUI>
      <String>ORF 8511</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0048557</ConceptUI>
    <ConceptName>
     <String>1-(diphenylmethylenyl)-2-methyl-3-ethyl-4-acetoxycyclohexane</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0048558</Concept1UI>
     <Concept2UI>M0048557</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T078560</TermUI>
      <String>1-(diphenylmethylenyl)-2-methyl-3-ethyl-4-acetoxycyclohexane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006151</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>R 1342</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1996</Year>
   <Month>09</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>appetite stimulant; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>OXIMES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010627</DescriptorUI>
     <DescriptorName>
      <String>Phenethylamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Naturwissenschaften 60(9):432;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0048332</ConceptUI>
    <ConceptName>
     <String>R 1342</String>
    </ConceptName>
    <CASN1Name>N,alpha,4-trihydroxybenzeneethanimidamide</CASN1Name>
    <RegistryNumber>50602-45-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T078335</TermUI>
      <String>R 1342</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006226</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-bromotetramisole</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>available in levo &amp; dextro form; L-form potent inhibitor of non specific alkaline phosphatase; RN given refers to cpd without isomeric designation
  </Note>
  <Frequency>39</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*THIAZOLES (74-76)</PreviousIndexing>
   <PreviousIndexing>IMIDAZOLES (74-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013773</DescriptorUI>
     <DescriptorName>
      <String>Tetramisole</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D007978</DescriptorUI>
     <DescriptorName>
      <String>Levamisole</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
    <PharmacologicalActionList>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D000871</DescriptorUI>
        <DescriptorName>
         <String>Anthelmintics</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
    </PharmacologicalActionList>
  <SourceList>
   <Source>Acta Odontol Scand 33(3):143;1976</Source>
   <Source>Biochem Pharmacol 24:1175;1975</Source>
   <Source>Clin Chem 23(3):454;1977</Source>
   <Source>Experientia 33(2):154;1977</Source>
   <Source>Histochemistry 44(3):277;1975</Source>
   <Source>Infect Immun 23(1):94;1979</Source>
   <Source>J Clin Chem Clin Biochem 1979;17(9):605</Source>
   <Source>J Histochem Cytochem 21(9):812;1973</Source>
   <Source>J Histochem Cytochem 26(5):359;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0048547</ConceptUI>
    <ConceptName>
     <String>4-bromotetramisole</String>
    </ConceptName>
    <RegistryNumber>6646-46-4</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>56943-06-7 ((S)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>62284-79-1 (oxalate[1:1] salt(S)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0048547</Concept1UI>
     <Concept2UI>M0309502</Concept2UI>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0048547</Concept1UI>
     <Concept2UI>M0309501</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T078550</TermUI>
      <String>4-bromotetramisole</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T078548</TermUI>
      <String>L-4-bromotetramisole</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T078546</TermUI>
      <String>6-bromolevamisole</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T078547</TermUI>
      <String>D-4-bromotetramisole</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T078549</TermUI>
      <String>p-bromotetramisole</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T078545</TermUI>
      <String>1-(para-bromotetramisole)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0309502</ConceptUI>
    <ConceptName>
     <String>4-bromotetramisole, oxalate (1:1), salt(S)-isomer</String>
    </ConceptName>
    <RegistryNumber>62284-79-1</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0048547</Concept1UI>
     <Concept2UI>M0309502</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T339502</TermUI>
      <String>4-bromotetramisole, oxalate (1:1), salt(S)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0309501</ConceptUI>
    <ConceptName>
     <String>4-bromotetramisole, (S)-isomer</String>
    </ConceptName>
    <RegistryNumber>56943-06-7</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0048547</Concept1UI>
     <Concept2UI>M0309501</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T339501</TermUI>
      <String>4-bromotetramisole, (S)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C431783</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>RPR 200765A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>02</Day>
  </DateCreated>
  <Note>a p38 MAP kinase inhibitor; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007093</DescriptorUI>
     <DescriptorName>
      <String>Imidazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Bioorg Med Chem 2001 Feb;9(2):537-54</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0394659</ConceptUI>
    <ConceptName>
     <String>RPR 200765A</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T456110</TermUI>
      <String>RPR 200765A</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>08</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T456111</TermUI>
      <String>RPR-200765 A</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>08</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C066241</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>gamma1-purothionin, Triticum aestivum</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1990</Year>
   <Month>11</Month>
   <Day>28</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>06</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>from wheat endosperm; amino acid sequence given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010940</DescriptorUI>
     <DescriptorName>
      <String>Plant Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D023181</DescriptorUI>
     <DescriptorName>
      <String>Antimicrobial Cationic Peptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>FEBS Lett 1990;270(1-2):191</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0181830</ConceptUI>
    <ConceptName>
     <String>gamma1-purothionin, Triticum aestivum</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T508561</TermUI>
      <String>gamma1-purothionin, Triticum aestivum</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>07</Month>
       <Day>31</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T211835</TermUI>
      <String>gamma1-purothionin protein, Triticum aestivum</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T211834</TermUI>
      <String>gamma(1)-purothionin protein, Triticum aestivum</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006170</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dactylarin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>03</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>isolated from Dactylaria lutea (Deuteromycetes); structure
  </Note>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ANISOLES (74-78)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001572</DescriptorUI>
     <DescriptorName>
      <String>Benzofurans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Res 1979;39(10):4242</Source>
   <Source>J Antibiotics 26(11):692;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0048383</ConceptUI>
    <ConceptName>
     <String>dactylarin</String>
    </ConceptName>
    <CASN1Name>3,7-dihydroxy-2',5-dimethoxy-6'-methylspiro(benzofuran-2(3H),1'-(2,5)CYCLOHEXADIEN)-4'-ONE</CASN1Name>
    <RegistryNumber>52212-96-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T078386</TermUI>
      <String>dactylarin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C101508</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hsp17.7 protein, Helianthus annuus</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>10</Month>
   <Day>28</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>09</Month>
   <Day>23</Day>
  </DateRevised>
  <Note>a small heat-shock protein isolated from sunflow Helianthus annuus; amino acid sequence in first source; GenBank U46545
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006360</DescriptorUI>
     <DescriptorName>
      <String>Heat-Shock Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010940</DescriptorUI>
     <DescriptorName>
      <String>Plant Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Plant Mol Biol 1996 Jul;31(4):863-76</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0266081</ConceptUI>
    <ConceptName>
     <String>hsp17.7 protein, Helianthus annuus</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T551218</TermUI>
      <String>hsp17.7 protein, Helianthus annuus</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>09</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C036092</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hordothionin protein, Hordeum vulgare</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1982</Year>
   <Month>11</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>06</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>barley proteins
  </Note>
  <Frequency>23</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010940</DescriptorUI>
     <DescriptorName>
      <String>Plant Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D023181</DescriptorUI>
     <DescriptorName>
      <String>Antimicrobial Cationic Peptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 1982;21(20):4843</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0110177</ConceptUI>
    <ConceptName>
     <String>hordothionin protein, Hordeum vulgare</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0110177</Concept1UI>
     <Concept2UI>M0110174</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0110177</Concept1UI>
     <Concept2UI>M0110176</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0110177</Concept1UI>
     <Concept2UI>M0110175</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0110177</Concept1UI>
     <Concept2UI>M0110173</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T510061</TermUI>
      <String>hordothionin protein, Hordeum vulgare</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>08</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T140181</TermUI>
      <String>hordothionin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0110174</ConceptUI>
    <ConceptName>
     <String>THI1.2 protein, Hordeum vulgare</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0110177</Concept1UI>
     <Concept2UI>M0110174</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T510063</TermUI>
      <String>THI1.2 protein, Hordeum vulgare</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>08</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T140178</TermUI>
      <String>beta-hordothionin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0110176</ConceptUI>
    <ConceptName>
     <String>omega-hordothionin protein, Hordeum vulgare</String>
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    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0110177</Concept1UI>
     <Concept2UI>M0110176</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T510065</TermUI>
      <String>omega-hordothionin protein, Hordeum vulgare</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>08</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T140180</TermUI>
      <String>omega-hordothionin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0110175</ConceptUI>
    <ConceptName>
     <String>gamma-hordithionin protein, Hordeum vulgare</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0110177</Concept1UI>
     <Concept2UI>M0110175</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T510064</TermUI>
      <String>gamma-hordithionin protein, Hordeum vulgare</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>08</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T140179</TermUI>
      <String>gamma-hordithionin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0110173</ConceptUI>
    <ConceptName>
     <String>Hth-1 protein, Hordeum vulgare</String>
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    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0110177</Concept1UI>
     <Concept2UI>M0110173</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T510062</TermUI>
      <String>Hth-1 protein, Hordeum vulgare</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>08</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T140177</TermUI>
      <String>alpha-hordothionin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C101509</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hsp18.6 protein, Helianthus annuus</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>10</Month>
   <Day>28</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>09</Month>
   <Day>23</Day>
  </DateRevised>
  <Note>small heat-shock protein isolated from sunflower Helianthus annuus; GenBank U46544
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006360</DescriptorUI>
     <DescriptorName>
      <String>Heat-Shock Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010940</DescriptorUI>
     <DescriptorName>
      <String>Plant Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Plant Mol Biol 1996 Jul;31(4):863-76</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0266083</ConceptUI>
    <ConceptName>
     <String>hsp18.6 protein, Helianthus annuus</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T551219</TermUI>
      <String>hsp18.6 protein, Helianthus annuus</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>09</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C095395</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>CVD 112</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>10</Month>
   <Day>02</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>07</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>a vaccine for Vibrio cholera O139
  </Note>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BACTERIAL VACCINES (1996-2000)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D022121</DescriptorUI>
     <DescriptorName>
      <String>Cholera Vaccines</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Infect Dis 1995 Sep;172(3):883-6</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0251219</ConceptUI>
    <ConceptName>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T281224</TermUI>
      <String>CVD 112</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T281223</TermUI>
      <String>CVD-112</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C050745</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-hydroxyaminopropiophenone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1986</Year>
   <Month>12</Month>
   <Day>16</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>02</Day>
  </DateRevised>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011427</DescriptorUI>
     <DescriptorName>
      <String>Propiophenones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Hum Toxicol 1986;5(5):295</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0144732</ConceptUI>
    <ConceptName>
     <String>4-hydroxyaminopropiophenone</String>
    </ConceptName>
    <RegistryNumber>55-34-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T174737</TermUI>
      <String>4-hydroxyaminopropiophenone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1986)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T174736</TermUI>
      <String>p-hydroxylaminopropiophenone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1986)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T174735</TermUI>
      <String>PHAPP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1986)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T174734</TermUI>
      <String>4-hydroxylaminopropiophenone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1986)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C411197</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-oxo-4,9-dihydroxy-8-methoxy-6-hydroxymethyl-1,2,3,4-tetrahydroanthracene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>07</Month>
   <Day>26</Day>
  </DateCreated>
  <Note>from Eremurus chinensis; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000873</DescriptorUI>
     <DescriptorName>
      <String>Anthracenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2000 May;63(5):653-6</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0366649</ConceptUI>
    <ConceptName>
     <String>1-oxo-4,9-dihydroxy-8-methoxy-6-hydroxymethyl-1,2,3,4-tetrahydroanthracene</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T419997</TermUI>
      <String>1-oxo-4,9-dihydroxy-8-methoxy-6-hydroxymethyl-1,2,3,4-tetrahydroanthracene</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>07</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T419998</TermUI>
      <String>1-ODMHTA</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>07</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C044942</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>THI1 protein, Pyrularia pubera</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1985</Year>
   <Month>05</Month>
   <Day>15</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>06</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>47 amino acid sequence given in first source; from Pyrularia (Santalaceae)
  </Note>
  <Frequency>24</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010940</DescriptorUI>
     <DescriptorName>
      <String>Plant Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D023181</DescriptorUI>
     <DescriptorName>
      <String>Antimicrobial Cationic Peptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D003603</DescriptorUI>
     <DescriptorName>
      <String>Cytotoxins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Arch Biochem Biophys 1985;238(1):18</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0130964</ConceptUI>
    <ConceptName>
     <String>THI1 protein, Pyrularia pubera</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T517983</TermUI>
      <String>THI1 protein, Pyrularia pubera</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>08</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T160968</TermUI>
      <String>Pyrularia pubera thionin toxin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T160969</TermUI>
      <String>thionin toxin, Pyrularia</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009563</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,3,5-trihydroxyphenethylamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>isomeric amine (with 6-hydroxydopamine) that causes destruction of adrenergic terminals; structure
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010627</DescriptorUI>
     <DescriptorName>
      <String>Phenethylamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Pharmacol 9(6):711;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054377</ConceptUI>
    <ConceptName>
     <String>2,3,5-trihydroxyphenethylamine</String>
    </ConceptName>
    <CASN1Name>6-(2-aminoethyl)-1,2,4-benzenetriol</CASN1Name>
    <RegistryNumber>41241-46-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084380</TermUI>
      <String>2,3,5-trihydroxyphenethylamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C475806</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Sop-2 protein, C elegans</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>07</Month>
   <Day>23</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>11</Month>
   <Day>23</Day>
  </DateRevised>
  <Note>a SAM domain protein that affects Hox gene expression; amino acid sequence in first source
  </Note>
  <Frequency>8</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012097</DescriptorUI>
     <DescriptorName>
      <String>Repressor Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029742</DescriptorUI>
     <DescriptorName>
      <String>Caenorhabditis elegans Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Dev Cell 2003 Jun;4(6):903-15</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0451966</ConceptUI>
    <ConceptName>
     <String>Sop-2 protein, C elegans</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T546725</TermUI>
      <String>Sop-2 protein, C elegans</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>07</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009574</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,1'-trimethylenebisnicotinamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1992</Year>
   <Month>06</Month>
   <Day>18</Day>
  </DateRevised>
  <Note>analog of NAD; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*NICOTINAMIDE (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009536</DescriptorUI>
     <DescriptorName>
      <String>Niacinamide</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Am Chem Soc 95(16):5886;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054402</ConceptUI>
    <ConceptName>
     <String>1,1'-trimethylenebisnicotinamide</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084405</TermUI>
      <String>1,1'-trimethylenebisnicotinamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009582</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4,8,12-trimethyltridecanoic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005227</DescriptorUI>
     <DescriptorName>
      <String>Fatty Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 360(2):166;1974</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054414</ConceptUI>
    <ConceptName>
     <String>4,8,12-trimethyltridecanoic acid</String>
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    <RegistryNumber>10339-73-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084417</TermUI>
      <String>4,8,12-trimethyltridecanoic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009588</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>triolandren</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>05</Day>
  </DateRevised>
  <Frequency>10</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*TESTOSTERONE (74-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013739</DescriptorUI>
     <DescriptorName>
      <String>Testosterone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer 33(5):1226;1974</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054423</ConceptUI>
    <ConceptName>
     <String>triolandren</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084426</TermUI>
      <String>triolandren</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C418002</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>albutensin A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>11</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>01</Month>
   <Day>24</Day>
  </DateRevised>
  <Note>angiotensin-I-converting enzyme inhibitory peptide isolated from a tryptic hydrolysate of human serum albumin
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009842</DescriptorUI>
     <DescriptorName>
      <String>Oligopeptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biol Pharm Bull 2000 Jul;23(7):879-83</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0376211</ConceptUI>
    <ConceptName>
     <String>albutensin A</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T432947</TermUI>
      <String>albutensin A</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>01</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T432949</TermUI>
      <String>alanyl-phenylalany-lysyl-alanyl-tryptophyl-alanyl-valanyl-alanyl-arginine</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>01</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T432948</TermUI>
      <String>Ala-Phe-Lys-Ala-Trp-Ala-Val-Ala-Arg</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>01</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
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   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C493699</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>polyneuridine-N-oxide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>12</Month>
   <Day>06</Day>
  </DateCreated>
  <Note>from the roots of Ochrosia acuminata collected in Savu, Indonesia; structure in first source
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D026121</DescriptorUI>
     <DescriptorName>
      <String>Indole Alkaloids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2004 Oct;67(10):1719-21</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0477099</ConceptUI>
    <ConceptName>
     <String>polyneuridine-N-oxide</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T622111</TermUI>
      <String>polyneuridine-N-oxide</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>12</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009593</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tripotassium hexathiocyanatochromate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>08</Month>
   <Day>29</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CHROMATES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013861</DescriptorUI>
     <DescriptorName>
      <String>Thiocyanates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Pol Pharm 30(5):505;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054433</ConceptUI>
    <ConceptName>
     <String>tripotassium hexathiocyanatochromate</String>
    </ConceptName>
    <CASN1Name>(OC-6-11)-tripotassium hexakis(thiocyanato-N)chromate(3-)</CASN1Name>
    <RegistryNumber>14282-33-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084436</TermUI>
      <String>tripotassium hexathiocyanatochromate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C437905</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>DEFB118 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>10</Month>
   <Day>25</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>05</Month>
   <Day>15</Day>
  </DateRevised>
  <Note>RefSeq NM_054112
  </Note>
  <Frequency>4</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*Proteins (2001-2004)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D023082</DescriptorUI>
     <DescriptorName>
      <String>Defensins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D004822</DescriptorUI>
     <DescriptorName>
      <String>Epididymis</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Endocrinology 2001 Oct;142(10):4529-39</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0403150</ConceptUI>
    <ConceptName>
     <String>DEFB118 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T521609</TermUI>
      <String>DEFB118 protein, human</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>10</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T467882</TermUI>
      <String>epididymis-specific clone 42 protein, human</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>10</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T467884</TermUI>
      <String>ESC42 protein, human</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>10</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T583539</TermUI>
      <String>defensin, beta 118 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>04</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009604</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N,N'-diallyltartardiamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>04</Month>
   <Day>22</Day>
  </DateRevised>
  <Note>cross linking reagent; RN given refers to (R-(R*,R*))-isomer
  </Note>
  <Frequency>11</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AMIDES (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013644</DescriptorUI>
     <DescriptorName>
      <String>Tartrates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Anal Biochem 93(2):275;1979</Source>
   <Source>Eur J Immunol 7(10):690;1977</Source>
   <Source>Mol Cell Biochem 1980;29(1):23</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054445</ConceptUI>
    <ConceptName>
     <String>N,N'-diallyltartardiamide</String>
    </ConceptName>
    <CASN1Name>Butanediamide, 2,3-dihydroxy-N,N'-di-2-propenyl-, (R-(R*,R*))-</CASN1Name>
    <RegistryNumber>58477-85-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084448</TermUI>
      <String>N,N'-diallyltartardiamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C057298</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>FR 65814</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1988</Year>
   <Month>11</Month>
   <Day>07</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>analog of fumagillol; from Penicillium jensenii F-2883; structure given in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003510</DescriptorUI>
     <DescriptorName>
      <String>Cyclohexanes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012717</DescriptorUI>
     <DescriptorName>
      <String>Sesquiterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiot (Tokyo) 1988;41(8):999</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0160393</ConceptUI>
    <ConceptName>
     <String>FR 65814</String>
    </ConceptName>
    <CASN1Name>1-Oxaspiro(2.5)octane-5,6-diol, 4-(2-methyl-3-(3-methyl-2-butenyl)oxiranyl)-</CASN1Name>
    <RegistryNumber>103470-60-6</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0160393</Concept1UI>
     <Concept2UI>M0160390</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T190398</TermUI>
      <String>FR 65814</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T190397</TermUI>
      <String>Fr65814</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T190396</TermUI>
      <String>FR-65814</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0160390</ConceptUI>
    <ConceptName>
     <String>5,6-dihydroxy-4-(1,2-epoxy-1,5-dimethyl-4-hexenyl)-1-oxaspiro(2,5)octane</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0160393</Concept1UI>
     <Concept2UI>M0160390</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T190395</TermUI>
      <String>5,6-dihydroxy-4-(1,2-epoxy-1,5-dimethyl-4-hexenyl)-1-oxaspiro(2,5)octane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009609</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tubercidin 5'-triphosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*RIBONUCLEOTIDES (74-82)</PreviousIndexing>
   <PreviousIndexing>PYRROLES (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000227</DescriptorUI>
     <DescriptorName>
      <String>Adenine Nucleotides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014372</DescriptorUI>
     <DescriptorName>
      <String>Tubercidin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 57(2):434;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054452</ConceptUI>
    <ConceptName>
     <String>tubercidin 5'-triphosphate</String>
    </ConceptName>
    <CASN1Name>5-(5-O-(hydroxy((hydroxy(phosphonooxy)phosphinyl)oxy)phosphinyl)-beta-D-ribofuranosyl)-7H- pyrrolo(2,3-d)pyrimidin-4-amine</CASN1Name>
    <RegistryNumber>10058-66-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084455</TermUI>
      <String>tubercidin 5'-triphosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C095574</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>G deamidase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>10</Month>
   <Day>11</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>MW 81 kDa; a chymotrypsin-like serine carboxypeptidase; responsible for the degradation of antagonist G
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002268</DescriptorUI>
     <DescriptorName>
      <String>Carboxypeptidases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Pharmacol 1995 Aug 25;50(5):585-90</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0251665</ConceptUI>
    <ConceptName>
     <String>G deamidase</String>
    </ConceptName>
    <RegistryNumber>EC 3.4.16.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T281670</TermUI>
      <String>G deamidase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T281669</TermUI>
      <String>G-deamidase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C057299</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>fumagillol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1988</Year>
   <Month>11</Month>
   <Day>07</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>from Penicillium jensenii; FR 65814 is an analog; structure given in first source
  </Note>
  <Frequency>10</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003510</DescriptorUI>
     <DescriptorName>
      <String>Cyclohexanes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012717</DescriptorUI>
     <DescriptorName>
      <String>Sesquiterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiot (Tokyo) 1988;41(8):999</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0160394</ConceptUI>
    <ConceptName>
     <String>fumagillol</String>
    </ConceptName>
    <CASN1Name>1-Oxaspiro(2.5)octan-6-ol, 5-methoxy-4-(2-methyl-3-(3-methyl-2-butenyl)oxiranyl)-, (3R-(3alpha,4alpha(2R*,3R*),5beta,6beta))-</CASN1Name>
    <RegistryNumber>108102-51-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T190399</TermUI>
      <String>fumagillol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C493697</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dictyoceratin-C</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>12</Month>
   <Day>06</Day>
  </DateCreated>
  <Note>from the marine species Spongia sp.; structure in first source
  </Note>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012717</DescriptorUI>
     <DescriptorName>
      <String>Sesquiterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2004 Oct;67(10);1716-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0477097</ConceptUI>
    <ConceptName>
     <String>dictyoceratin-C</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T622109</TermUI>
      <String>dictyoceratin-C</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>12</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C026134</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>glutamate carboxypeptidase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Frequency>30</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>GLUTAMATES (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002268</DescriptorUI>
     <DescriptorName>
      <String>Carboxypeptidases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 381(1):28;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0086160</ConceptUI>
    <ConceptName>
     <String>glutamate carboxypeptidase</String>
    </ConceptName>
    <RegistryNumber>EC 3.4.17.11</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T116163</TermUI>
      <String>glutamate carboxypeptidase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009619</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>uridylyl-(3'-5')-N(6)-(N-threonylcarbonyl)adenosine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1995</Year>
   <Month>06</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*URIDINE MONOPHOSPHATE/analogs (78-88)</PreviousIndexing>
   <PreviousIndexing>ADENOSINE/*analogs (78-88)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015226</DescriptorUI>
     <DescriptorName>
      <String>Dinucleoside Phosphates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 524(2):491;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054473</ConceptUI>
    <ConceptName>
     <String>uridylyl-(3'-5')-N(6)-(N-threonylcarbonyl)adenosine</String>
    </ConceptName>
    <CASN1Name>Adenosine, uridylyl-(3'-5')-N-(((1-carboxy-2-hydroxypropyl)amino)carbonyl)-, (S)-</CASN1Name>
    <RegistryNumber>66004-53-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084476</TermUI>
      <String>uridylyl-(3'-5')-N(6)-(N-threonylcarbonyl)adenosine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009621</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>undecaprenyl phosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>RN's in Chemline for diphosphate esters: 31589-58-9, 31867-59-1
  </Note>
  <Frequency>39</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PHOSPHOLIPIDS (75-78)</PreviousIndexing>
   <PreviousIndexing>TERPENES (75-78)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011106</DescriptorUI>
     <DescriptorName>
      <String>Polyisoprenyl Phosphates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 250(1):156;1975</Source>
   <Source>J Biol Chem 250(1):164;1975</Source>
   <Source>J Biol Chem 252(12):4118;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054475</ConceptUI>
    <ConceptName>
     <String>undecaprenyl phosphate</String>
    </ConceptName>
    <CASN1Name>3,7,11,15,19,23,27,31,35,39,43-undecamethyl-2,6,10,14,18,22,26,30,34,38,42-tetratetracontaun decaen-1-ol, dihydrogen phosphate</CASN1Name>
    <RegistryNumber>25126-51-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084478</TermUI>
      <String>undecaprenyl phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009627</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>uridylyl-(2'-5')-adenosine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*URACIL NUCLEOTIDES (75-79)</PreviousIndexing>
   <PreviousIndexing>*URIDINE MONOPHOSPHATE/analogs (80-88)</PreviousIndexing>
   <PreviousIndexing>ADENOSINE/*analogs (75-88)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015226</DescriptorUI>
     <DescriptorName>
      <String>Dinucleoside Phosphates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 60(1):456;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054484</ConceptUI>
    <ConceptName>
     <String>uridylyl-(2'-5')-adenosine</String>
    </ConceptName>
    <RegistryNumber>10453-52-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084487</TermUI>
      <String>uridylyl-(2'-5')-adenosine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C112641</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>DENR protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>06</Month>
   <Day>24</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>05</Month>
   <Day>15</Day>
  </DateRevised>
  <Note>expressed at high cell density but not during growth arrest, isolated from human teratocarcinoma cells; RefSeq NM_003677
  </Note>
  <Frequency>12</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*NEOPLASM PROTEINS (1998-2006)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D039642</DescriptorUI>
     <DescriptorName>
      <String>Eukaryotic Initiation Factors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>DNA Cell Biol 1998 May;17(5):437-47</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0291221</ConceptUI>
    <ConceptName>
     <String>DENR protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T523059</TermUI>
      <String>DENR protein, human</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>10</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T523061</TermUI>
      <String>smooth muscle cell associated protein-3, human</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>10</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T523062</TermUI>
      <String>SMAP-3 protein, human</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>10</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T523513</TermUI>
      <String>density-regulated protein, human</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>10</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T523060</TermUI>
      <String>DRP protein, human</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>10</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009629</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>uridylyl-(3'-5')-adenosine phosphonate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ADENINE NUCLEOTIDES (76-88)</PreviousIndexing>
   <PreviousIndexing>*URACIL NUCLEOTIDES (75-79)</PreviousIndexing>
   <PreviousIndexing>*URIDINE MONOPHOSPHATE/analogs (80-88)</PreviousIndexing>
   <PreviousIndexing>ADENOSINE (74-75)</PreviousIndexing>
   <PreviousIndexing>PHOSPHONIC ACIDS (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015226</DescriptorUI>
     <DescriptorName>
      <String>Dinucleoside Phosphates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 13(5):981;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054490</ConceptUI>
    <ConceptName>
     <String>uridylyl-(3'-5')-adenosine phosphonate</String>
    </ConceptName>
    <CASN1Name>Adenosine, 5'-(hydrogen 3'-uridylylmethyl)phosphonate)</CASN1Name>
    <RegistryNumber>52077-33-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084493</TermUI>
      <String>uridylyl-(3'-5')-adenosine phosphonate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009632</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-urocanylhistamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*HISTAMINE (74-75)</PreviousIndexing>
   <PreviousIndexing>*IMIDAZOLES (74-75)</PreviousIndexing>
   <PreviousIndexing>ACRYLATES (74-75)</PreviousIndexing>
   <PreviousIndexing>UROCANIC ACID/analogs (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D006632</DescriptorUI>
     <DescriptorName>
      <String>Histamine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Pharmacol 23(9):1431;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054492</ConceptUI>
    <ConceptName>
     <String>N-urocanylhistamine</String>
    </ConceptName>
    <CASN1Name>2-Propenamide, 3-(1H-imidazol-4-yl)-N-(2-(1H-imidazol-4-yl)ethyl)-</CASN1Name>
    <RegistryNumber>53215-86-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084495</TermUI>
      <String>N-urocanylhistamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009634</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-acetylmannosamine 2-epimerase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>07</Month>
   <Day>16</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>HEXOSAMINES (79-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002238</DescriptorUI>
     <DescriptorName>
      <String>Carbohydrate Epimerases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 585(4):535;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054503</ConceptUI>
    <ConceptName>
     <String>N-acetylmannosamine 2-epimerase</String>
    </ConceptName>
    <RegistryNumber>EC 5.1.3.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084506</TermUI>
      <String>N-acetylmannosamine 2-epimerase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009641</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>vagotonin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>10</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>pancreatic extract of hormonal nature from horses
  </Note>
  <Frequency>15</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010184</DescriptorUI>
     <DescriptorName>
      <String>Pancreatic Extracts</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D010187</DescriptorUI>
     <DescriptorName>
      <String>Pancreatic Hormones</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Ann Pharm Fr 30(11):745;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054506</ConceptUI>
    <ConceptName>
     <String>vagotonin</String>
    </ConceptName>
    <RegistryNumber>37349-92-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084509</TermUI>
      <String>vagotonin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009655</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ROM 205</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>06</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>RN given refers to di-HCl; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ETHYLENEDIAMINES (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011412</DescriptorUI>
     <DescriptorName>
      <String>Propanolamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Physiol Pol 25(6):565;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054531</ConceptUI>
    <ConceptName>
     <String>ROM 205</String>
    </ConceptName>
    <CASN1Name>1,1'-(1,2-ethanediylbis(methylimino))bis(3-phenoxy-2-propanol, dihydrochloride</CASN1Name>
    <RegistryNumber>55053-79-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084534</TermUI>
      <String>ROM 205</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C493698</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>17-O-isoprenyldictyoceratin-C</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>12</Month>
   <Day>06</Day>
  </DateCreated>
  <Note>from the marine species Spongia sp.; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012717</DescriptorUI>
     <DescriptorName>
      <String>Sesquiterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2004 Oct;67(10):1716-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0477098</ConceptUI>
    <ConceptName>
     <String>17-O-isoprenyldictyoceratin-C</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T622110</TermUI>
      <String>17-O-isoprenyldictyoceratin-C</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>12</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009665</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>vincarodine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>minor alkaloid from leaves of Vinca rosea L.; structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*VINCA ALKALOIDS (74-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014749</DescriptorUI>
     <DescriptorName>
      <String>Vincamine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Helv Chim Acta 56(7):2660;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054547</ConceptUI>
    <ConceptName>
     <String>vincarodine</String>
    </ConceptName>
    <CASN1Name>(14 alpha,17 alpha,18 beta)-14,17-epoxy-14,15- dihydro-18-hydroxy-11-methoxyeburnamenine-14- carboxylic acid, methyl ester</CASN1Name>
    <RegistryNumber>1362-08-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084550</TermUI>
      <String>vincarodine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009670</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>vinylglycolic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>potent, irreversible inactivator of vectorial phosphorylation; structure
  </Note>
  <Frequency>4</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*GLYCOLATES (74-75)</PreviousIndexing>
   <PreviousIndexing>VINYL CPDS (74-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006880</DescriptorUI>
     <DescriptorName>
      <String>Hydroxy Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Bacteriol 127(1):671;1976</Source>
   <Source>J Biol Chem 248(15):5456;1973</Source>
   <Source>Proc Natl Acad Sci USA 71(12):5032;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054554</ConceptUI>
    <ConceptName>
     <String>vinylglycolic acid</String>
    </ConceptName>
    <CASN1Name>2-hydroxy-3-butenoic acid</CASN1Name>
    <RegistryNumber>600-17-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084557</TermUI>
      <String>vinylglycolic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009676</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>butyrylethyleneimine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AZIRINES (72-75)</PreviousIndexing>
   <PreviousIndexing>BUTYRATES (72-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001388</DescriptorUI>
     <DescriptorName>
      <String>Aziridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054572</ConceptUI>
    <ConceptName>
     <String>butyrylethyleneimine</String>
    </ConceptName>
    <RegistryNumber>10431-86-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084575</TermUI>
      <String>butyrylethyleneimine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C467206</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>luteolin-7-glucuronide ethyl ester</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>10</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>08</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*FLAVONOIDS (2002-2004)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D020719</DescriptorUI>
     <DescriptorName>
      <String>Glucuronides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D047311</DescriptorUI>
     <DescriptorName>
      <String>Luteolin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Clin Chim Acta 2002 Feb;316(1-2):95-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0441001</ConceptUI>
    <ConceptName>
     <String>luteolin-7-glucuronide ethyl ester</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T524727</TermUI>
      <String>luteolin-7-glucuronide ethyl ester</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>10</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009692</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>xykos</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>06</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>combination of ziram and zineb; russian drug
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*FUNGICIDES, INDUSTRIAL (74-75)</PreviousIndexing>
   <PreviousIndexing>*THIOCARBAMATES (74-75)</PreviousIndexing>
   <PreviousIndexing>DRUG COMBINATIONS (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015038</DescriptorUI>
     <DescriptorName>
      <String>Zineb</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015039</DescriptorUI>
     <DescriptorName>
      <String>Ziram</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Gig Sanit 38(12):55;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054600</ConceptUI>
    <ConceptName>
     <String>xykos</String>
    </ConceptName>
    <RegistryNumber>8004-24-8</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0054600</Concept1UI>
     <Concept2UI>M0054599</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0054600</Concept1UI>
     <Concept2UI>M0054597</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0054600</Concept1UI>
     <Concept2UI>M0054598</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084603</TermUI>
      <String>xykos</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0054599</ConceptUI>
    <ConceptName>
     <String>zikos</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0054600</Concept1UI>
     <Concept2UI>M0054599</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T084602</TermUI>
      <String>zikos</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0054597</ConceptUI>
    <ConceptName>
     <String>cikos</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0054600</Concept1UI>
     <Concept2UI>M0054597</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T084600</TermUI>
      <String>cikos</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0054598</ConceptUI>
    <ConceptName>
     <String>tsikos</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0054600</Concept1UI>
     <Concept2UI>M0054598</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T084601</TermUI>
      <String>tsikos</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C113736</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>BA14K protein, Brucella</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>08</Month>
   <Day>19</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>04</Month>
   <Day>25</Day>
  </DateRevised>
  <Note>isolated from Brucella abortus, MW 14-kDa, amino acid sequence in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001425</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Outer Membrane Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011994</DescriptorUI>
     <DescriptorName>
      <String>Recombinant Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D000942</DescriptorUI>
     <DescriptorName>
      <String>Antigens, Bacterial</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Infect Immun 1998 Aug;66(8):4000-3</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0293597</ConceptUI>
    <ConceptName>
     <String>BA14K protein, Brucella</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T323602</TermUI>
      <String>BA14K protein, Brucella</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T637803</TermUI>
      <String>BA 14kDa protein, Brucella</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>04</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C096015</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Sn-2 protein, Capsicum annuum</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>11</Month>
   <Day>08</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>10</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>a fruit-specific wound-stimulated protein; from bell pepper Capsicum annuum; homologous to Sn-1; amino acid sequence given in first source; GenBank X79231
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010940</DescriptorUI>
     <DescriptorName>
      <String>Plant Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Plant Mol Biol 1995 Sep;28(6):1011-25</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0252740</ConceptUI>
    <ConceptName>
     <String>Sn-2 protein, Capsicum annuum</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T517773</TermUI>
      <String>Sn-2 protein, Capsicum annuum</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>08</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C496942</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6-O-demethylancistrobenomine A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>03</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>5,1'-coupled naphthylisoquinoline alkaloid from the stem bark of highland liana Ancistrocladus sp.; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007546</DescriptorUI>
     <DescriptorName>
      <String>Isoquinolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009281</DescriptorUI>
     <DescriptorName>
      <String>Naphthalenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2004 Dec;67(12):2058-62</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0481346</ConceptUI>
    <ConceptName>
     <String>6-O-demethylancistrobenomine A</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T632004</TermUI>
      <String>6-O-demethylancistrobenomine A</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C484615</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-deoxyadenophorine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>05</Month>
   <Day>03</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005944</DescriptorUI>
     <DescriptorName>
      <String>Glucosamine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem. 2004 Mar 5;69(5):1497-503</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0465358</ConceptUI>
    <ConceptName>
     <String>5-deoxyadenophorine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T585540</TermUI>
      <String>5-deoxyadenophorine</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>05</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014348</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>azadieldrin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004026</DescriptorUI>
     <DescriptorName>
      <String>Dieldrin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Agr Food Chem 25(3):489;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062825</ConceptUI>
    <ConceptName>
     <String>azadieldrin</String>
    </ConceptName>
    <CASN1Name>6H-2,7:3,6-Dimethanooxireno(g)quinoline, 4,5,6,9,9-pentachloro-1a,2,2a,6a,7,7a-hexahydro-, (1aalpha,2beta,2aalpha,3alpha,6beta,6aalpha,7beta,7aalpha)-</CASN1Name>
    <RegistryNumber>61473-90-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092828</TermUI>
      <String>azadieldrin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014351</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>benulin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>pentacyclic triterpene hemiketal from Bursa arida
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014315</DescriptorUI>
     <DescriptorName>
      <String>Triterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 42(9):1627;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062830</ConceptUI>
    <ConceptName>
     <String>benulin</String>
    </ConceptName>
    <CASN1Name>3 alpha-hydroxy-3,25-epoxylup-20(29)-en-28-oic acid</CASN1Name>
    <RegistryNumber>59157-84-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092833</TermUI>
      <String>benulin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014354</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>benzofuroxan</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>13</Day>
  </DateRevised>
  <Frequency>42</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CYCLIC N-OXIDES (76-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001583</DescriptorUI>
     <DescriptorName>
      <String>Benzoxazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D013439</DescriptorUI>
     <DescriptorName>
      <String>Sulfhydryl Reagents</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Biochem J 161(3):627;1977</Source>
   <Source>Biochem J 167:799;1977</Source>
   <Source>Cancer Res 35(12):3735;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062834</ConceptUI>
    <ConceptName>
     <String>benzofuroxan</String>
    </ConceptName>
    <CASN1Name>benzofurazan 1-oxide</CASN1Name>
    <RegistryNumber>480-96-6</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062834</Concept1UI>
     <Concept2UI>M0062833</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092837</TermUI>
      <String>benzofuroxan</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0062833</ConceptUI>
    <ConceptName>
     <String>benzo-2-oxa-1,3-diazole-N-oxide</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062834</Concept1UI>
     <Concept2UI>M0062833</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T092836</TermUI>
      <String>benzo-2-oxa-1,3-diazole-N-oxide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C518810</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2',3'-O-isopropylideneadenosine-5'-carboxylic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>04</Month>
   <Day>15</Day>
  </DateCreated>
  <DateRevised>
   <Year>2007</Year>
   <Month>04</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000241</DescriptorUI>
     <DescriptorName>
      <String>Adenosine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nucleosides Nucleotides Nucleic Acids 2007;26(1):121-7</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0508757</ConceptUI>
    <ConceptName>
     <String>2',3'-O-isopropylideneadenosine-5'-carboxylic acid</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T695545</TermUI>
      <String>2',3'-O-isopropylideneadenosine-5'-carboxylic acid</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>04</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T695628</TermUI>
      <String>2',3'-O-iPrACA</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>04</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014362</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-(N,N-bis(2-chloroethyl)amino)phenyl-O-beta-D-glucopyranosiduronic acid methyl ester</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*GLUCURONATES (77-81)</PreviousIndexing>
   <PreviousIndexing>*NITROGEN MUSTARD CPDS (77-80)</PreviousIndexing>
   <PreviousIndexing>GLUCOSIDES (77-80)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000816</DescriptorUI>
     <DescriptorName>
      <String>Aniline Mustard</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Pharmazie 32(3):183;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062839</ConceptUI>
    <ConceptName>
     <String>4-(N,N-bis(2-chloroethyl)amino)phenyl-O-beta-D-glucopyranosiduronic acid methyl ester</String>
    </ConceptName>
    <RegistryNumber>38099-66-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092842</TermUI>
      <String>4-(N,N-bis(2-chloroethyl)amino)phenyl-O-beta-D-glucopyranosiduronic acid methyl ester</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014371</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6 beta-bromoethyl-19-norcholest-5(10)-en-3 beta-ol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>11</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>STEROIDS, BROMINATED (77-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002784</DescriptorUI>
     <DescriptorName>
      <String>Cholesterol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Steroids 29(4):443;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062856</ConceptUI>
    <ConceptName>
     <String>6 beta-bromoethyl-19-norcholest-5(10)-en-3 beta-ol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092859</TermUI>
      <String>6 beta-bromoethyl-19-norcholest-5(10)-en-3 beta-ol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014383</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>carbacefamandole</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>Cephem S replaced by CH(2); structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CEFAMANDOLE/analogs (78-83)</PreviousIndexing>
   <PreviousIndexing>*CEPHALOSPORINS (77-78)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002435</DescriptorUI>
     <DescriptorName>
      <String>Cefamandole</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 20(4):551;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062871</ConceptUI>
    <ConceptName>
     <String>carbacefamandole</String>
    </ConceptName>
    <RegistryNumber>62284-44-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092874</TermUI>
      <String>carbacefamandole</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C518798</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Fgfrl1a protein, zebrafish</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>04</Month>
   <Day>15</Day>
  </DateCreated>
  <DateRevised>
   <Year>2007</Year>
   <Month>04</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>involved in gill cartilage development; GenBank AJ574916
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D017468</DescriptorUI>
     <DescriptorName>
      <String>Receptors, Fibroblast Growth Factor</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029961</DescriptorUI>
     <DescriptorName>
      <String>Zebrafish Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 2003 Sep 5;278(36):33857-65</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0508745</ConceptUI>
    <ConceptName>
     <String>Fgfrl1a protein, zebrafish</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T695522</TermUI>
      <String>Fgfrl1a protein, zebrafish</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>04</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014391</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>gamma-carboxyglutamylleucine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>12</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>1-CARBOXYGLUTAMIC ACID/analogs (77-82)</PreviousIndexing>
   <PreviousIndexing>GLUTAMATES (77-79)</PreviousIndexing>
   <PreviousIndexing>LEUCINE/analogs (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004151</DescriptorUI>
     <DescriptorName>
      <String>Dipeptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Helv Chim Acta 60(3):807;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062889</ConceptUI>
    <ConceptName>
     <String>gamma-carboxyglutamylleucine</String>
    </ConceptName>
    <CASN1Name>Propanedioic acid, (2-amino-3-((1-carboxy-3-methylbutyl)amino)-3-oxopropyl)-, (R-(R*,S*))-</CASN1Name>
    <RegistryNumber>64153-44-2</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062889</Concept1UI>
     <Concept2UI>M0062888</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092892</TermUI>
      <String>gamma-carboxyglutamylleucine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0062888</ConceptUI>
    <ConceptName>
     <String>D-gamma-carboxyglutamyl-L-leucine</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062889</Concept1UI>
     <Concept2UI>M0062888</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T092891</TermUI>
      <String>D-gamma-carboxyglutamyl-L-leucine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C063439</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ETH 5282</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1990</Year>
   <Month>04</Month>
   <Day>23</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>10</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000577</DescriptorUI>
     <DescriptorName>
      <String>Amides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008314</DescriptorUI>
     <DescriptorName>
      <String>Malonates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D007476</DescriptorUI>
     <DescriptorName>
      <String>Ionophores</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Clin Chem 1990;36(3):466</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0175120</ConceptUI>
    <ConceptName>
     <String>ETH 5282</String>
    </ConceptName>
    <RegistryNumber>127192-89-6</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0175120</Concept1UI>
     <Concept2UI>M0175118</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T205125</TermUI>
      <String>ETH 5282</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T205124</TermUI>
      <String>ETH-5282</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0175118</ConceptUI>
    <ConceptName>
     <String>(N',N'',N'''-imino-di-6,1-hexanediyl)tris(N-heptyl-N-methylmalonamide)</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0175120</Concept1UI>
     <Concept2UI>M0175118</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T205123</TermUI>
      <String>(N',N'',N'''-imino-di-6,1-hexanediyl)tris(N-heptyl-N-methylmalonamide)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014405</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-chloro-7-iodo-8-quinolinol sulfonate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1992</Year>
   <Month>06</Month>
   <Day>18</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CHLOROQUINOLINOLS (77-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007464</DescriptorUI>
     <DescriptorName>
      <String>Clioquinol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 66(3):440;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062914</ConceptUI>
    <ConceptName>
     <String>5-chloro-7-iodo-8-quinolinol sulfonate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092917</TermUI>
      <String>5-chloro-7-iodo-8-quinolinol sulfonate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014406</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6-chloro-9-(2-(6-methyl-3-pyridyl)ethyl)-1,2,3,4- tetrahydrocarbazole-2-carboxylic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>RN given refers to HCl; RN for parent cpd not in Chemline 8/4/83; structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002227</DescriptorUI>
     <DescriptorName>
      <String>Carbazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 66(3):348;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062915</ConceptUI>
    <ConceptName>
     <String>6-chloro-9-(2-(6-methyl-3-pyridyl)ethyl)-1,2,3,4- tetrahydrocarbazole-2-carboxylic acid</String>
    </ConceptName>
    <RegistryNumber>58479-48-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092918</TermUI>
      <String>6-chloro-9-(2-(6-methyl-3-pyridyl)ethyl)-1,2,3,4- tetrahydrocarbazole-2-carboxylic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014407</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cholestane-3,5,6,7-tetrol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1993</Year>
   <Month>03</Month>
   <Day>29</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*STEROLS (77-78)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002777</DescriptorUI>
     <DescriptorName>
      <String>Cholestanols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Pharm Bull 24(12):3109;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062917</ConceptUI>
    <ConceptName>
     <String>cholestane-3,5,6,7-tetrol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062917</Concept1UI>
     <Concept2UI>M0062916</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092920</TermUI>
      <String>cholestane-3,5,6,7-tetrol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0062916</ConceptUI>
    <ConceptName>
     <String>5 alpha-cholestane-3 beta,5,6 beta,7 alpha-tetrol</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062917</Concept1UI>
     <Concept2UI>M0062916</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T092919</TermUI>
      <String>5 alpha-cholestane-3 beta,5,6 beta,7 alpha-tetrol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014408</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cholest-5,7-diene-1 alpha,3 beta-diol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002775</DescriptorUI>
     <DescriptorName>
      <String>Cholestadienols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Chem Soc (Perkin Trans) 8:720;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062918</ConceptUI>
    <ConceptName>
     <String>cholest-5,7-diene-1 alpha,3 beta-diol</String>
    </ConceptName>
    <RegistryNumber>41461-10-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092921</TermUI>
      <String>cholest-5,7-diene-1 alpha,3 beta-diol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014412</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>7-chromanol-3-methyltaxifoline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011794</DescriptorUI>
     <DescriptorName>
      <String>Quercetin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Sci Med 134(2):103;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062921</ConceptUI>
    <ConceptName>
     <String>7-chromanol-3-methyltaxifoline</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092924</TermUI>
      <String>7-chromanol-3-methyltaxifoline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014414</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>chuangxinmycin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>produced by Actinoplanes tsinanensis; structure
  </Note>
  <Frequency>19</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007211</DescriptorUI>
     <DescriptorName>
      <String>Indoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Sci Sin 20(1):106;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062927</ConceptUI>
    <ConceptName>
     <String>chuangxinmycin</String>
    </ConceptName>
    <CASN1Name>2H-Thiopyrano(4,3,2-cd)indole-2-carboxylic acid, 3,5-dihydro-3-methyl-, cis-(-)-</CASN1Name>
    <RegistryNumber>63339-68-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092930</TermUI>
      <String>chuangxinmycin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014418</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>colchiceineamide-L-ephedrine phosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>04</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>RN given refers to 2-Na salt(7S-(7R*(1R*,2S*)))-isomer
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ORGANOPHOSPHORUS COMPOUNDS (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003078</DescriptorUI>
     <DescriptorName>
      <String>Colchicine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004809</DescriptorUI>
     <DescriptorName>
      <String>Ephedrine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Treat Rep 61(2):259;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062934</ConceptUI>
    <ConceptName>
     <String>colchiceineamide-L-ephedrine phosphate</String>
    </ConceptName>
    <CASN1Name>Benzo(a)heptalen-9(5H)-one, 6,7-dihydro-1,2,3,10-tetramethoxy-7-(methyl(1-methyl-2-phenyl-2-(phosphonooxy)ethyl)amino)-, disodium salt, (7S-(7R*(1R*,2S*)))-</CASN1Name>
    <RegistryNumber>76109-92-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092937</TermUI>
      <String>colchiceineamide-L-ephedrine phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014422</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>combutec</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>Russian drug; no other information available 1977; "collagen base" of trophic ulcers (venous)
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003094</DescriptorUI>
     <DescriptorName>
      <String>Collagen</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Sov Med 3:97;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062938</ConceptUI>
    <ConceptName>
     <String>combutec</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092941</TermUI>
      <String>combutec</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014428</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cudranone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>potential antimicrobial agent isolated from stems &amp; roots of Chineses plant Cudrania chochinchinensis; structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001577</DescriptorUI>
     <DescriptorName>
      <String>Benzophenones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 66(6):908;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062944</ConceptUI>
    <ConceptName>
     <String>cudranone</String>
    </ConceptName>
    <CASN1Name>2,6,3'-trihydroxy-4-methoxy-2'-(3-methyl-2-butenyl)benzophenone</CASN1Name>
    <RegistryNumber>63596-94-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092947</TermUI>
      <String>cudranone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C514750</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,3,5,7-tetrakis(4-(ditrifluoroacetoxyiodo)phenyl)adamantane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateCreated>
  <Note>contains hypervalent iodine(III); may prove useful as an environmentally benign oxidizing agent; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000218</DescriptorUI>
     <DescriptorName>
      <String>Adamantane</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Yakugaku Zasshi 2006 Sep;126(9):757-66</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0503841</ConceptUI>
    <ConceptName>
     <String>1,3,5,7-tetrakis(4-(ditrifluoroacetoxyiodo)phenyl)adamantane</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T685856</TermUI>
      <String>1,3,5,7-tetrakis(4-(ditrifluoroacetoxyiodo)phenyl)adamantane</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>11</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T685857</TermUI>
      <String>1,3,5,7-tetrakisDTAIPA</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>11</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014454</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-desmethylephedrine phosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>11</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ORGANOPHOSPHORUS COMPOUNDS (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004809</DescriptorUI>
     <DescriptorName>
      <String>Ephedrine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Treat Rep 61(2):259;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062975</ConceptUI>
    <ConceptName>
     <String>N-desmethylephedrine phosphate</String>
    </ConceptName>
    <CASN1Name>Benzenemethanol, alpha-(1-aminoethyl)-, dihydrogen phosphate (ester)</CASN1Name>
    <RegistryNumber>63620-43-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092978</TermUI>
      <String>N-desmethylephedrine phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T092977</TermUI>
      <String>phosphoryldesmethylephedrine phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014433</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>18,20-cyclo-20,21-dihydroxy-4-pregnen-3-one</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>07</Month>
   <Day>15</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>EPOXY COMPOUNDS (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D015070</DescriptorUI>
     <DescriptorName>
      <String>18-Hydroxydesoxycorticosterone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Steroid Biochem 7(11/12):949;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062951</ConceptUI>
    <ConceptName>
     <String>18,20-cyclo-20,21-dihydroxy-4-pregnen-3-one</String>
    </ConceptName>
    <CASN1Name>18,20-epoxy-20,21-dihydroxypregn-4-en-3-one</CASN1Name>
    <RegistryNumber>10385-97-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092954</TermUI>
      <String>18,20-cyclo-20,21-dihydroxy-4-pregnen-3-one</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C514749</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,3,5,7-tetrakis(4-((hydroxy)(tosyloxy)iodo)phenyl)adamantane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>contains hypervalent iodine(III); may prove useful as an environmentally benign oxidizing agent; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000218</DescriptorUI>
     <DescriptorName>
      <String>Adamantane</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Yakugaku Zasshi 2006 Sep;126(9):757-66</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0503840</ConceptUI>
    <ConceptName>
     <String>1,3,5,7-tetrakis(4-((hydroxy)(tosyloxy)iodo)phenyl)adamantane</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T685854</TermUI>
      <String>1,3,5,7-tetrakis(4-((hydroxy)(tosyloxy)iodo)phenyl)adamantane</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>11</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T685855</TermUI>
      <String>1,3,5,7-tetrakisHTIPA</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>11</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014441</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cytenamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003986</DescriptorUI>
     <DescriptorName>
      <String>Dibenzocycloheptenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Chromatog 134(2):299;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062960</ConceptUI>
    <ConceptName>
     <String>cytenamide</String>
    </ConceptName>
    <CASN1Name>5H-dibenzo(a,d)cycloheptatriene-5-carboxamide</CASN1Name>
    <RegistryNumber>10423-37-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092963</TermUI>
      <String>cytenamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014446</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>7-demethylfarnesyl pyrophosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1986</Year>
   <Month>01</Month>
   <Day>06</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ORGANOPHOSPHORUS COMPOUNDS (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005204</DescriptorUI>
     <DescriptorName>
      <String>Farnesol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Comm 76(2):520;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062963</ConceptUI>
    <ConceptName>
     <String>7-demethylfarnesyl pyrophosphate</String>
    </ConceptName>
    <CASN1Name>Diphosphoric acid, mono(3,11-dimethyl-2,6,10-dodecatrienyl) ester, (E,E)-</CASN1Name>
    <RegistryNumber>63408-39-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092966</TermUI>
      <String>7-demethylfarnesyl pyrophosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014447</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>deneosaminyllividomycins</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*LIVIDOMYCINS (77-87)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010303</DescriptorUI>
     <DescriptorName>
      <String>Paromomycin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiotics 30(4):332;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062964</ConceptUI>
    <ConceptName>
     <String>deneosaminyllividomycins</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092967</TermUI>
      <String>deneosaminyllividomycins</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C514751</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>PRR9 protein, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateCreated>
  <Note>RefSeq NM_130245
  </Note>
  <Frequency>28</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014157</DescriptorUI>
     <DescriptorName>
      <String>Transcription Factors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Plant Cell 2006 Sep;18(9):2157-71</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0503842</ConceptUI>
    <ConceptName>
     <String>PRR9 protein, Arabidopsis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T685858</TermUI>
      <String>PRR9 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>11</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T685859</TermUI>
      <String>PSEUDO-RESPONSE REGULATOR9 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>11</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014449</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-deoxy-D-lyxose</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003837</DescriptorUI>
     <DescriptorName>
      <String>Deoxy Sugars</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Carbohydrate Res 53(2):177;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062966</ConceptUI>
    <ConceptName>
     <String>5-deoxy-D-lyxose</String>
    </ConceptName>
    <CASN1Name>D-Lyxose, 5-deoxy-</CASN1Name>
    <RegistryNumber>49694-62-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092969</TermUI>
      <String>5-deoxy-D-lyxose</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014450</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>9-(5-deoxy-beta-erythro-pent-4-enofuranosyl)adenine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1989</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003839</DescriptorUI>
     <DescriptorName>
      <String>Deoxyadenosines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Carbohyd Res 53(2):177;1977</Source>
   <Source>J Med Chem 22(1):24;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062967</ConceptUI>
    <ConceptName>
     <String>9-(5-deoxy-beta-erythro-pent-4-enofuranosyl)adenine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092970</TermUI>
      <String>9-(5-deoxy-beta-erythro-pent-4-enofuranosyl)adenine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014452</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>desferritriacetylfusigen</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>01</Month>
   <Day>06</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009952</DescriptorUI>
     <DescriptorName>
      <String>Ornithine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiotics 30(2):125;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062972</ConceptUI>
    <ConceptName>
     <String>desferritriacetylfusigen</String>
    </ConceptName>
    <CASN1Name>Acetamide, N,N',N''-(7,19,31-trihydroxy-10,22,34-trimethyl-2,8,14,20,26,32-hexaoxo-1,13,25-trioxa-7,19,31-triazacyclohexatriaconta-9,21,33-triene-3,15,27-triyl)tris-, (3S-(3R*,9Z,15R*,21Z,27R*,33Z))-</CASN1Name>
    <RegistryNumber>20186-12-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092975</TermUI>
      <String>desferritriacetylfusigen</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014453</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5'-desmethyldeoxypodophyllotoxin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011034</DescriptorUI>
     <DescriptorName>
      <String>Podophyllotoxin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 66(6):892;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062973</ConceptUI>
    <ConceptName>
     <String>5'-desmethyldeoxypodophyllotoxin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092976</TermUI>
      <String>5'-desmethyldeoxypodophyllotoxin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C028593</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>colicin receptor, E coli</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>04</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>02</Month>
   <Day>04</Day>
  </DateRevised>
  <Frequency>61</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*RECEPTORS, IMMUNOLOGIC (81-93)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011956</DescriptorUI>
     <DescriptorName>
      <String>Receptors, Cell Surface</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029968</DescriptorUI>
     <DescriptorName>
      <String>Escherichia coli Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D003087</DescriptorUI>
     <DescriptorName>
      <String>Colicins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Bacteriol 1981;145(1):647</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0091861</ConceptUI>
    <ConceptName>
     <String>colicin receptor, E coli</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0091861</Concept1UI>
     <Concept2UI>M0091854</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0091861</Concept1UI>
     <Concept2UI>M0091853</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0091861</Concept1UI>
     <Concept2UI>M0377950</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T545188</TermUI>
      <String>colicin receptor, E coli</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>07</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0091854</ConceptUI>
    <ConceptName>
     <String>colicin E3 receptor, E coli</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0091861</Concept1UI>
     <Concept2UI>M0091854</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T571399</TermUI>
      <String>colicin E3 receptor, E coli</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>02</Month>
       <Day>04</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0091853</ConceptUI>
    <ConceptName>
     <String>colicin A receptor, E coli</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0091861</Concept1UI>
     <Concept2UI>M0091853</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T545182</TermUI>
      <String>colicin A receptor, E coli</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>07</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T545184</TermUI>
      <String>FEUA protein, E coli</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>07</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T545183</TermUI>
      <String>CIRA protein, E coli</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>07</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0377950</ConceptUI>
    <ConceptName>
     <String>colicin Ia receptor, E coli</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0091861</Concept1UI>
     <Concept2UI>M0377950</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T571400</TermUI>
      <String>colicin Ia receptor, E coli</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>02</Month>
       <Day>04</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014456</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dexphenmetrazine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1996</Year>
   <Month>08</Month>
   <Day>16</Day>
  </DateRevised>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010633</DescriptorUI>
     <DescriptorName>
      <String>Phenmetrazine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D013237</DescriptorUI>
     <DescriptorName>
      <String>Stereoisomerism</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Physiolog Bohemos 2:139;1977</Source>
   <Source>Physiolog Bohemos 2:143;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062976</ConceptUI>
    <ConceptName>
     <String>dexphenmetrazine</String>
    </ConceptName>
    <RegistryNumber>21288-73-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092979</TermUI>
      <String>dexphenmetrazine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C029553</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>nucleotide peptide, Anabaena variabilis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>06</Month>
   <Day>02</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>02</Month>
   <Day>04</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009711</DescriptorUI>
     <DescriptorName>
      <String>Nucleotides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mikrobiologiia 1981;50(1):5</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0094229</ConceptUI>
    <ConceptName>
     <String>nucleotide peptide, Anabaena variabilis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T124232</TermUI>
      <String>nucleotide peptide, Anabaena variabilis</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014461</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,4-dibromodeuteroheme</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D006418</DescriptorUI>
     <DescriptorName>
      <String>Heme</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>JBC 252(12):4225;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062982</ConceptUI>
    <ConceptName>
     <String>2,4-dibromodeuteroheme</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T092985</TermUI>
      <String>2,4-dibromodeuteroheme</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014480</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5,6-dihydro-5-azathymidine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013936</DescriptorUI>
     <DescriptorName>
      <String>Thymidine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Antimicrob Ag Chemother 11(4):765;1977</Source>
   <Source>Antimicrob Ag Chemother 13(4):613;1978</Source>
   <Source>Antimicrob Ag Chemother 15(2):213;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063001</ConceptUI>
    <ConceptName>
     <String>5,6-dihydro-5-azathymidine</String>
    </ConceptName>
    <CASN1Name>1,3,5-Triazine-2,4(1H,3H)-dione, 1-(2-deoxy-beta-D-erythro-pentofuranosyl)dihydro-5-methyl-</CASN1Name>
    <RegistryNumber>57350-36-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093004</TermUI>
      <String>5,6-dihydro-5-azathymidine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014483</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dihydrofuranocaulesone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012717</DescriptorUI>
     <DescriptorName>
      <String>Sesquiterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Soc Jap 97(4):393;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063010</ConceptUI>
    <ConceptName>
     <String>dihydrofuranocaulesone</String>
    </ConceptName>
    <CASN1Name>Cyclodeca(b)furan-11(4H)-one, 7,8,9,10-tetrahydro-3,6,10-trimethyl-, (E)-(+-)-</CASN1Name>
    <RegistryNumber>76465-76-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093013</TermUI>
      <String>dihydrofuranocaulesone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013799</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>agrocin 84</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>14</Day>
  </DateRevised>
  <Note>contains glucose, deoxy arabinose &amp; other yet unidentified sugars
  </Note>
  <Frequency>31</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000227</DescriptorUI>
     <DescriptorName>
      <String>Adenine Nucleotides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D001430</DescriptorUI>
     <DescriptorName>
      <String>Bacteriocins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Antimicrob Agents Chemother 10(3):498;1976</Source>
   <Source>Antimicrob Agents Chemother 1979;16(3):293</Source>
   <Source>J Antibiot (Tokyo) 31(5):490;1978</Source>
   <Source>Mol Gen Genet 138(4):345;1975</Source>
   <Source>Nature 265(5592):379;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061871</ConceptUI>
    <ConceptName>
     <String>agrocin 84</String>
    </ConceptName>
    <RegistryNumber>59111-78-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061871</Concept1UI>
     <Concept2UI>M0061870</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091874</TermUI>
      <String>agrocin 84</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0061870</ConceptUI>
    <ConceptName>
     <String>agrocin</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061871</Concept1UI>
     <Concept2UI>M0061870</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T091873</TermUI>
      <String>agrocin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014488</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dihydroaminopterin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1986</Year>
   <Month>01</Month>
   <Day>08</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000630</DescriptorUI>
     <DescriptorName>
      <String>Aminopterin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Matl Cancer Inst 59(1):245;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063020</ConceptUI>
    <ConceptName>
     <String>dihydroaminopterin</String>
    </ConceptName>
    <CASN1Name>L-Glutamic acid, N-(4-(((2,4-diamino-1,4-dihydro-6-pteridinyl)methyl)amino)benzoyl)-</CASN1Name>
    <RegistryNumber>36093-88-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093023</TermUI>
      <String>dihydroaminopterin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014490</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dihydromethotrexate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1985</Year>
   <Month>12</Month>
   <Day>24</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008727</DescriptorUI>
     <DescriptorName>
      <String>Methotrexate</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Cancer Inst 59(1):245;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063022</ConceptUI>
    <ConceptName>
     <String>dihydromethotrexate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093025</TermUI>
      <String>dihydromethotrexate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014491</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,3-dihydroxy-3-methylpentanoic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*HYDROXY ACIDS (77-79)</PreviousIndexing>
   <PreviousIndexing>HYDROXY ACIDS (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010421</DescriptorUI>
     <DescriptorName>
      <String>Pentanoic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Chem Soc (Perkin Trans) 5:544;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063023</ConceptUI>
    <ConceptName>
     <String>2,3-dihydroxy-3-methylpentanoic acid</String>
    </ConceptName>
    <RegistryNumber>562-43-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093026</TermUI>
      <String>2,3-dihydroxy-3-methylpentanoic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014492</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,2-dihydroxyphenyl-4-pyridinium bromide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>sympathomimetic action may be due to catechol substructure in molecule
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CATECHOLS (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011726</DescriptorUI>
     <DescriptorName>
      <String>Pyridinium Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ind J Exp Biol 14(6):672;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063024</ConceptUI>
    <ConceptName>
     <String>1,2-dihydroxyphenyl-4-pyridinium bromide</String>
    </ConceptName>
    <RegistryNumber>61799-01-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093027</TermUI>
      <String>1,2-dihydroxyphenyl-4-pyridinium bromide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014493</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dihydroxyphysalin B</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012991</DescriptorUI>
     <DescriptorName>
      <String>Solanaceous Alkaloids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Lloydia 39(6):405;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063025</ConceptUI>
    <ConceptName>
     <String>dihydroxyphysalin B</String>
    </ConceptName>
    <CASN1Name>16,24-Cyclo-13,14-secoergost-2-ene-18,26-dioic acid, 14,17:14,27-diepoxy-?,?,13,20,22-pentahydroxy-1,15-dioxo-, gamma-lactone delta-lactone, (14alpha,16beta,22alpha,25S)-</CASN1Name>
    <RegistryNumber>62857-87-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093028</TermUI>
      <String>dihydroxyphysalin B</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C514752</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>E2FC protein, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateCreated>
  <Note>GenBank AJ417834
  </Note>
  <Frequency>7</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D050684</DescriptorUI>
     <DescriptorName>
      <String>E2F Transcription Factors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 2002 Mar 22;277(12):9911-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0503843</ConceptUI>
    <ConceptName>
     <String>E2FC protein, Arabidopsis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T685860</TermUI>
      <String>E2FC protein, Arabidopsis</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>11</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014501</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>9,9-dimethylacridane-10-carboxylic acid S-(2-dimethylamino)thiolethyl ester</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000166</DescriptorUI>
     <DescriptorName>
      <String>Acridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arzneim Forsch 27(3):575;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063038</ConceptUI>
    <ConceptName>
     <String>9,9-dimethylacridane-10-carboxylic acid S-(2-dimethylamino)thiolethyl ester</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093041</TermUI>
      <String>9,9-dimethylacridane-10-carboxylic acid S-(2-dimethylamino)thiolethyl ester</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C514753</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>EPSIN1 protein, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>GenBank AY074304
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D033942</DescriptorUI>
     <DescriptorName>
      <String>Adaptor Proteins, Vesicular Transport</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Plant Cell 2006 Sep;18(9):2258-74</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0503844</ConceptUI>
    <ConceptName>
     <String>EPSIN1 protein, Arabidopsis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T685861</TermUI>
      <String>EPSIN1 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>11</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T685862</TermUI>
      <String>At5g11710 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>11</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C106706</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>chromium(IV)-glutathione complex</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1997</Year>
   <Month>07</Month>
   <Day>18</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>14</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002840</DescriptorUI>
     <DescriptorName>
      <String>Chromates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005978</DescriptorUI>
     <DescriptorName>
      <String>Glutathione</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 1997 Jun 9;235(1):54-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0277925</ConceptUI>
    <ConceptName>
     <String>chromium(IV)-glutathione complex</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T307930</TermUI>
      <String>chromium(IV)-glutathione complex</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T307929</TermUI>
      <String>Cr(IV)-GSH</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000144</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Avcothane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2007</Year>
   <Month>11</Month>
   <Day>26</Day>
  </DateRevised>
  <Note>blood compatible elastomer consisting of polyurethane &amp; poly(dialkylsiloxane)
  </Note>
  <Frequency>14</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011140</DescriptorUI>
     <DescriptorName>
      <String>Polyurethanes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012826</DescriptorUI>
     <DescriptorName>
      <String>Silicone Elastomers</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biomed Mater 11(1):69;1977</Source>
   <Source>J Thorac Cardiovasc Surg 62(6):851;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040159</ConceptUI>
    <ConceptName>
     <String>Avcothane</String>
    </ConceptName>
    <RegistryNumber>37226-50-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0040159</Concept1UI>
     <Concept2UI>M0515867</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0040159</Concept1UI>
     <Concept2UI>M0040156</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070160</TermUI>
      <String>Avcothane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T070159</TermUI>
      <String>cardiothane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0515867</ConceptUI>
    <ConceptName>
     <String>Cardiothane 51</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0040159</Concept1UI>
     <Concept2UI>M0515867</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T709979</TermUI>
      <String>Cardiothane 51</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>11</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0040156</ConceptUI>
    <ConceptName>
     <String>Avcothane 51</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0040159</Concept1UI>
     <Concept2UI>M0040156</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="TRD"  RecordPreferredTermYN="N">
      <TermUI>T070157</TermUI>
      <String>Avcothane 51</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T070158</TermUI>
      <String>Avcothane-51</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014508</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,4-dimethyldeuteroheme</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D006418</DescriptorUI>
     <DescriptorName>
      <String>Heme</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>JBC 252(12):4225;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063045</ConceptUI>
    <ConceptName>
     <String>2,4-dimethyldeuteroheme</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093048</TermUI>
      <String>2,4-dimethyldeuteroheme</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014510</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,3-dioxabicyclo(2.2.1)heptane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1995</Year>
   <Month>08</Month>
   <Day>18</Day>
  </DateRevised>
  <Note>possible precursor to chem syn of prostaglandin endoperoxides
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BICYCLO COMPOUNDS (77-95)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D019086</DescriptorUI>
     <DescriptorName>
      <String>Bridged Bicyclo Compounds, Heterocyclic</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Am Chem Soc 99(10):3503;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063048</ConceptUI>
    <ConceptName>
     <String>2,3-dioxabicyclo(2.2.1)heptane</String>
    </ConceptName>
    <CASN1Name>2,3-Dioxabicyclo(2.2.1)heptane</CASN1Name>
    <RegistryNumber>279-35-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093051</TermUI>
      <String>2,3-dioxabicyclo(2.2.1)heptane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014511</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,4-diphenylbutane-2,3-diol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>03</Month>
   <Day>25</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ALCOHOLS, BUTYL</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006018</DescriptorUI>
     <DescriptorName>
      <String>Glycols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Experientia 33(3):396;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063049</ConceptUI>
    <ConceptName>
     <String>1,4-diphenylbutane-2,3-diol</String>
    </ConceptName>
    <RegistryNumber>18069-22-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093052</TermUI>
      <String>1,4-diphenylbutane-2,3-diol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014572</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>glucuronosyl-N-acetylglucosaminyl pyrophosphoryldolichol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>11</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*GLUCOSEPHOSPHATES (77-78)</PreviousIndexing>
   <PreviousIndexing>DOLICHOL/analogs (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011104</DescriptorUI>
     <DescriptorName>
      <String>Polyisoprenyl Phosphate Oligosaccharides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 252(9):2918;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063188</ConceptUI>
    <ConceptName>
     <String>glucuronosyl-N-acetylglucosaminyl pyrophosphoryldolichol</String>
    </ConceptName>
    <CASN1Name>D-Glucopyranose, 2-(acetylamino)-2-deoxy-4-O-D-glucopyranuronosyl-, 1-ester with dolichol (trihydrogen diphosphate)</CASN1Name>
    <RegistryNumber>63194-44-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093191</TermUI>
      <String>glucuronosyl-N-acetylglucosaminyl pyrophosphoryldolichol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T093190</TermUI>
      <String>D-Glucopyranose, 2-(acetylamino)-2-deoxy-4-O-D-glucopyranuronosyl-, 1-monoester with dolichol trihydrogen diphosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014528</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>17 alpha-estradiol-3-galacturonide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004958</DescriptorUI>
     <DescriptorName>
      <String>Estradiol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem J 161(2):279;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063080</ConceptUI>
    <ConceptName>
     <String>17 alpha-estradiol-3-galacturonide</String>
    </ConceptName>
    <CASN1Name>beta-D-Galactopyranosiduronic acid, (17alpha)-17-hydroxyestra-1,3,5(10)-trien-3-yl</CASN1Name>
    <RegistryNumber>63307-54-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093083</TermUI>
      <String>17 alpha-estradiol-3-galacturonide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C525105</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4,5-dimethoxy-2-nitrobenzylserine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>12</Month>
   <Day>20</Day>
  </DateCreated>
  <Note>a photocaged amino acid; structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009578</DescriptorUI>
     <DescriptorName>
      <String>Nitrobenzenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D012694</DescriptorUI>
     <DescriptorName>
      <String>Serine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nat Chem Biol 2007 Dec;3(12):769-72</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0516694</ConceptUI>
    <ConceptName>
     <String>4,5-dimethoxy-2-nitrobenzylserine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T711502</TermUI>
      <String>4,5-dimethoxy-2-nitrobenzylserine</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>12</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T711503</TermUI>
      <String>DMNB-Ser</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>12</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014538</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ethpenal</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>DIETHYLAMINES (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001561</DescriptorUI>
     <DescriptorName>
      <String>Benzilates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Z Eksp Klin Med 161(1):54;1976</Source>
   <Source>Z Eksp Klin Med 18(1):24;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063103</ConceptUI>
    <ConceptName>
     <String>ethpenal</String>
    </ConceptName>
    <RegistryNumber>3626-03-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093106</TermUI>
      <String>ethpenal</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T093105</TermUI>
      <String>etpenal-3</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T093104</TermUI>
      <String>etpenal-14</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T093103</TermUI>
      <String>etpenal</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T093102</TermUI>
      <String>3-diethylaminopropyl-o-ethylbenzilate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C097834</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>B2 protease, Dichelobacter nodosus</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>02</Month>
   <Day>26</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>02</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>isolated from benign strain of Dichelobacter nodosus; amino acid sequence given in first source; differs from V2 protease by a single amino acid at position 219
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012697</DescriptorUI>
     <DescriptorName>
      <String>Serine Endopeptidases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Gene 1995 Dec 29;167(1-2):279-83</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0257126</ConceptUI>
    <ConceptName>
     <String>B2 protease, Dichelobacter nodosus</String>
    </ConceptName>
    <RegistryNumber>EC 3.4.21.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T287131</TermUI>
      <String>B2 protease, Dichelobacter nodosus</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T287130</TermUI>
      <String>aprB2 protein, Dichelobacter nodosus</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C020895</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N,N-di-n-propyldopamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>RN given refers to parent cpd
  </Note>
  <Frequency>27</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004298</DescriptorUI>
     <DescriptorName>
      <String>Dopamine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
    <PharmacologicalActionList>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D000959</DescriptorUI>
        <DescriptorName>
         <String>Antihypertensive Agents</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
    </PharmacologicalActionList>
  <SourceList>
   <Source>Eur J Pharmacol 56(3):207;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0075170</ConceptUI>
    <ConceptName>
     <String>N,N-di-n-propyldopamine</String>
    </ConceptName>
    <CASN1Name>4-(2-(dipropylamino)ethyl)-1,2-benzenediol</CASN1Name>
    <RegistryNumber>66185-61-3</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>65273-66-7 (HBr)</RelatedRegistryNumber>
     <RelatedRegistryNumber>67482-66-0 (HI)</RelatedRegistryNumber>
     <RelatedRegistryNumber>67482-71-7 (HCl)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0075170</Concept1UI>
     <Concept2UI>M0314366</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0075170</Concept1UI>
     <Concept2UI>M0314365</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0075170</Concept1UI>
     <Concept2UI>M0314364</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T105173</TermUI>
      <String>N,N-di-n-propyldopamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T105172</TermUI>
      <String>DPDA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0314366</ConceptUI>
    <ConceptName>
     <String>N,N-di-n-propyldopamine hydrochloride</String>
    </ConceptName>
    <RegistryNumber>67482-71-7</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0075170</Concept1UI>
     <Concept2UI>M0314366</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T344366</TermUI>
      <String>N,N-di-n-propyldopamine hydrochloride</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0314365</ConceptUI>
    <ConceptName>
     <String>N,N-di-n-propyldopamine hydroiodide</String>
    </ConceptName>
    <RegistryNumber>67482-66-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0075170</Concept1UI>
     <Concept2UI>M0314365</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T344365</TermUI>
      <String>N,N-di-n-propyldopamine hydroiodide</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0314364</ConceptUI>
    <ConceptName>
     <String>N,N-di-n-propyldopamine hydrobromide</String>
    </ConceptName>
    <RegistryNumber>65273-66-7</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0075170</Concept1UI>
     <Concept2UI>M0314364</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T344364</TermUI>
      <String>N,N-di-n-propyldopamine hydrobromide</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C097905</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>vnfDGK protein, Azotobacter</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>03</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>02</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>amino acid sequence has been determined
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009591</DescriptorUI>
     <DescriptorName>
      <String>Nitrogenase</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Met Ions Biol Syst 1995;31:363-405</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0257271</ConceptUI>
    <ConceptName>
     <String>vnfDGK protein, Azotobacter</String>
    </ConceptName>
    <RegistryNumber>EC 1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T287276</TermUI>
      <String>vnfDGK protein, Azotobacter</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T287275</TermUI>
      <String>V-nitrogenase, Azotobacter</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C078175</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>extra sheep E antigen, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1992</Year>
   <Month>12</Month>
   <Day>18</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>08</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>partial amino acid sequence given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000954</DescriptorUI>
     <DescriptorName>
      <String>Antigens, Surface</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Immunol 1992 Dec 1;149(11):3574-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0209631</ConceptUI>
    <ConceptName>
     <String>extra sheep E antigen, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T498156</TermUI>
      <String>extra sheep E antigen, mouse</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>06</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T239634</TermUI>
      <String>ese determinant</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T239635</TermUI>
      <String>ese epitope</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T239636</TermUI>
      <String>extra sheep E antigen</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014542</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>9-ethylguanine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>11</Month>
   <Day>28</Day>
  </DateRevised>
  <Frequency>36</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D006147</DescriptorUI>
     <DescriptorName>
      <String>Guanine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 1979;564(2):182</Source>
   <Source>J Am Chem Soc 99(12):3934;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063110</ConceptUI>
    <ConceptName>
     <String>9-ethylguanine</String>
    </ConceptName>
    <RegistryNumber>879-08-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093113</TermUI>
      <String>9-ethylguanine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014543</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ethyl methylaminosulfonate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>03</Month>
   <Day>24</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ETHYL METHANESULFONATE/analogs (77-80)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005020</DescriptorUI>
     <DescriptorName>
      <String>Ethyl Methanesulfonate</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Z Naturforsch 13(1-2):140;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063111</ConceptUI>
    <ConceptName>
     <String>ethyl methylaminosulfonate</String>
    </ConceptName>
    <RegistryNumber>26118-70-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093114</TermUI>
      <String>ethyl methylaminosulfonate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C494208</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SNAP25 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2008</Year>
   <Month>09</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>RefSeq NM_130811
  </Note>
  <Frequency>370</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D050825</DescriptorUI>
     <DescriptorName>
      <String>Synaptosomal-Associated Protein 25</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0466492</ConceptUI>
    <ConceptName>
     <String>SNAP25 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0466492</Concept1UI>
     <Concept2UI>M0478970</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T588482</TermUI>
      <String>SNAP25 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>05</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T627004</TermUI>
      <String>SNAP25A protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>01</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T588484</TermUI>
      <String>synaptosomal-associated protein, 25kDa, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>05</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T588483</TermUI>
      <String>SNAP-25 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>05</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0478970</ConceptUI>
    <ConceptName>
     <String>SNAP25B protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0466492</Concept1UI>
     <Concept2UI>M0478970</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T627005</TermUI>
      <String>SNAP25B protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>01</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C494482</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>TRPV1 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>12</Month>
   <Day>27</Day>
  </DateCreated>
  <DateRevised>
   <Year>2008</Year>
   <Month>09</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>RefSeq NM_018727
  </Note>
  <Frequency>1165</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*Ion Channels (2004-2005)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D050916</DescriptorUI>
     <DescriptorName>
      <String>TRPV Cation Channels</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0452222</ConceptUI>
    <ConceptName>
     <String>TRPV1 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T547276</TermUI>
      <String>TRPV1 protein, human</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>07</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T693989</TermUI>
      <String>vanilloid receptor 1, human</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>03</Month>
       <Day>19</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T646811</TermUI>
      <String>transient receptor potential cation channel, subfamily V, member 1 protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>07</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C088780</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>O-methyl-methionine-dichloroplatinum(II)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>09</Month>
   <Day>08</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>22</Day>
  </DateRevised>
  <Note>RN refers to stereoisomer; structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009944</DescriptorUI>
     <DescriptorName>
      <String>Organoplatinum Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Inorg Biochem 1994 Aug 15;55(3):175-81</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0234900</ConceptUI>
    <ConceptName>
     <String>O-methyl-methionine-dichloroplatinum(II)</String>
    </ConceptName>
    <RegistryNumber>139014-07-6</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>139066-04-9 (stereoisomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0234900</Concept1UI>
     <Concept2UI>M0326642</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T264905</TermUI>
      <String>O-methyl-methionine-dichloroplatinum(II)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T264903</TermUI>
      <String>Pt(O-Me-Met)Cl2</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T264904</TermUI>
      <String>Pt(O-methyl-methionine)Cl2</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0326642</ConceptUI>
    <ConceptName>
     <String>O-methyl-methionine-dichloroplatinum(II), stereoisomer</String>
    </ConceptName>
    <RegistryNumber>139066-04-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0234900</Concept1UI>
     <Concept2UI>M0326642</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T356642</TermUI>
      <String>O-methyl-methionine-dichloroplatinum(II), stereoisomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002850</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4,7-diphenylphenanthroline sulfonate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>01</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>color reagent for serum iron
  </Note>
  <Frequency>11</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ARYL SULFONATES (74-76)</PreviousIndexing>
   <PreviousIndexing>LIGANDS (73-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010618</DescriptorUI>
     <DescriptorName>
      <String>Phenanthrolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ann Clin Lab Sci 1(1):14;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043638</ConceptUI>
    <ConceptName>
     <String>4,7-diphenylphenanthroline sulfonate</String>
    </ConceptName>
    <CASN1Name>4,7-diphenyl-1,10-phenanthrolinesulfonic acid</CASN1Name>
    <RegistryNumber>40795-59-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0043638</Concept1UI>
     <Concept2UI>M0043637</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073641</TermUI>
      <String>4,7-diphenylphenanthroline sulfonate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0043637</ConceptUI>
    <ConceptName>
     <String>bathophenanthroline sulfonate</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0043638</Concept1UI>
     <Concept2UI>M0043637</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073640</TermUI>
      <String>bathophenanthroline sulfonate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002903</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>formohydroxamic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>26</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006877</DescriptorUI>
     <DescriptorName>
      <String>Hydroxamic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Experientia 29(2):228;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043722</ConceptUI>
    <ConceptName>
     <String>formohydroxamic acid</String>
    </ConceptName>
    <RegistryNumber>4312-87-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073725</TermUI>
      <String>formohydroxamic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073724</TermUI>
      <String>formhydroxamic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002884</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ophiobolins</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>tricyclic sesterterpenes, include ophiobolins A,B,C,D,F; RN in Chemline for ophiobolin A: 4611-05-6; RN for ophiobolin B: 5601-74-1; RN for ophiobolin C: 19022-51-6; structure
  </Note>
  <Frequency>33</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D054830</DescriptorUI>
     <DescriptorName>
      <String>Sesterterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 296(3):615;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043685</ConceptUI>
    <ConceptName>
     <String>ophiobolins</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073688</TermUI>
      <String>ophiobolins</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C551955</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4'-(pyridin-4-ylmethyl)biphenyl-3-amine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2010</Year>
   <Month>09</Month>
   <Day>07</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001713</DescriptorUI>
     <DescriptorName>
      <String>Biphenyl Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011725</DescriptorUI>
     <DescriptorName>
      <String>Pyridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D013252</DescriptorUI>
     <DescriptorName>
      <String>Steroid 11-beta-Hydroxylase</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
     <QualifierName>
      <String>antagonists &amp; inhibitors</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D013254</DescriptorUI>
     <DescriptorName>
      <String>Steroid 17-alpha-Hydroxylase</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
     <QualifierName>
      <String>antagonists &amp; inhibitors</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Med Chem 2010 Aug 12;53(15):5749-58</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0549673</ConceptUI>
    <ConceptName>
     <String>4'-(pyridin-4-ylmethyl)biphenyl-3-amine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T776917</TermUI>
      <String>4'-(pyridin-4-ylmethyl)biphenyl-3-amine</String>
      <DateCreated>
       <Year>2010</Year>
       <Month>09</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2010)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002862</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>homothiotaurine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*TAURINE (73-75)</PreviousIndexing>
   <PreviousIndexing>SULFHYDRYL COMPOUNDS (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013654</DescriptorUI>
     <DescriptorName>
      <String>Taurine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Analyt Biochem 51(1);1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043656</ConceptUI>
    <ConceptName>
     <String>homothiotaurine</String>
    </ConceptName>
    <CASN1Name>3-aminopropanethiosulfonic acid</CASN1Name>
    <RegistryNumber>40957-87-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073659</TermUI>
      <String>homothiotaurine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002863</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>homohypotaurine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*TAURINE (73-75)</PreviousIndexing>
   <PreviousIndexing>SULFINIC ACIDS (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013654</DescriptorUI>
     <DescriptorName>
      <String>Taurine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Anal Biochem 51(1):265;1973</Source>
   <Source>Physiol Chem Phys 10(5):435;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043657</ConceptUI>
    <ConceptName>
     <String>homohypotaurine</String>
    </ConceptName>
    <CASN1Name>3-aminopropansulfinic acid</CASN1Name>
    <RegistryNumber>25346-09-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073660</TermUI>
      <String>homohypotaurine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002886</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Bax 439</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>17</Day>
  </DateRevised>
  <Note>decreases concentrating ability of kidney; RN given refers to parent cpd
  </Note>
  <Frequency>17</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013844</DescriptorUI>
     <DescriptorName>
      <String>Thiazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Lab Invest 31(6):658;1974</Source>
   <Source>Proc Soc Exp Biol Med 142(2):720;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043689</ConceptUI>
    <ConceptName>
     <String>Bax 439</String>
    </ConceptName>
    <CASN1Name>4,5-diphenyl-2-thiazolamine, monohydrochloride</CASN1Name>
    <RegistryNumber>6318-74-7</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>36761-88-3 (HCl)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0043689</Concept1UI>
     <Concept2UI>M0308103</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0043689</Concept1UI>
     <Concept2UI>M0043687</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T073692</TermUI>
      <String>Bax 439</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073691</TermUI>
      <String>Bax-439</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0308103</ConceptUI>
    <ConceptName>
     <String>Bax 439 hydrochloride</String>
    </ConceptName>
    <RegistryNumber>36761-88-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0043689</Concept1UI>
     <Concept2UI>M0308103</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T338103</TermUI>
      <String>Bax 439 hydrochloride</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0043687</ConceptUI>
    <ConceptName>
     <String>2-amino-4,5-diphenylthiazole</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0043689</Concept1UI>
     <Concept2UI>M0043687</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073690</TermUI>
      <String>2-amino-4,5-diphenylthiazole</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002867</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>beta-hydroxyethyl-2,4-dinitrophenyl disulfide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>13</Day>
  </DateRevised>
  <Note>used for characterizing protein thiol groups
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*NITROBENZENES (73-77)</PreviousIndexing>
   <PreviousIndexing>DISULFIDES (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004136</DescriptorUI>
     <DescriptorName>
      <String>Dinitrobenzenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D013439</DescriptorUI>
     <DescriptorName>
      <String>Sulfhydryl Reagents</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Acta Pol Pharm 29(4):439;1972</Source>
   <Source>Ann Univ Mariae Curie Sklodowska Med 30(17):131;1976</Source>
   <Source>Pol J Pharmacol Pharm 27:493;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043665</ConceptUI>
    <ConceptName>
     <String>beta-hydroxyethyl-2,4-dinitrophenyl disulfide</String>
    </ConceptName>
    <CASN1Name>HEDD /OD/ 2-((2,4-dinitrophenyl)dithio)ethanol</CASN1Name>
    <RegistryNumber>955-59-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073668</TermUI>
      <String>beta-hydroxyethyl-2,4-dinitrophenyl disulfide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015036</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bis-2,5-(4-hydroxyiminomethylpyridinium)dihydrofuran dibromide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1994</Year>
   <Month>05</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>reactivator of phosphonylated acetylcholinesterase
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*OXIMES (78-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011726</DescriptorUI>
     <DescriptorName>
      <String>Pyridinium Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Sbor Ved Pr Lek Fak Karlovy Univ 19(5):581;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064020</ConceptUI>
    <ConceptName>
     <String>bis-2,5-(4-hydroxyiminomethylpyridinium)dihydrofuran dibromide</String>
    </ConceptName>
    <CASN1Name>Pyridinium, 1,1'-(2,5-dihydro-2,5-furandiyl)bis(4-((hydroxyimino)methyl)-, dibromide</CASN1Name>
    <RegistryNumber>58921-39-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094023</TermUI>
      <String>bis-2,5-(4-hydroxyiminomethylpyridinium)dihydrofuran dibromide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C482093</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-azido-1,2-4,5-diepoxypentane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>03</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001386</DescriptorUI>
     <DescriptorName>
      <String>Azides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004852</DescriptorUI>
     <DescriptorName>
      <String>Epoxy Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem. 2003 Oct 17;68(21):8252-5</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0461580</ConceptUI>
    <ConceptName>
     <String>3-azido-1,2-4,5-diepoxypentane</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T574803</TermUI>
      <String>3-azido-1,2-4,5-diepoxypentane</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>03</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C495270</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>CTNNB1 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2008</Year>
   <Month>09</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>RefSeq NM_001098210
  </Note>
  <Frequency>5974</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D051176</DescriptorUI>
     <DescriptorName>
      <String>beta Catenin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0479525</ConceptUI>
    <ConceptName>
     <String>CTNNB1 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T628143</TermUI>
      <String>CTNNB1 protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>01</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T628145</TermUI>
      <String>catenin (cadherin-associated protein), beta 1, 88kDa, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>01</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T628144</TermUI>
      <String>beta-catenin protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>01</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015057</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>celacinnine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>spermidine alkaloid from Maytenus
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000470</DescriptorUI>
     <DescriptorName>
      <String>Alkaloids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Planta Med 32A(1):9;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064050</ConceptUI>
    <ConceptName>
     <String>celacinnine</String>
    </ConceptName>
    <RegistryNumber>53938-05-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094053</TermUI>
      <String>celacinnine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015063</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>(beta'-chloroethyl)phosphonylethyl-DL-phenylalanine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>01</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ORGANOPHOSPHORUS COMPOUNDS (78-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010649</DescriptorUI>
     <DescriptorName>
      <String>Phenylalanine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Adv Exptl Med Biol 86A:727;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064060</ConceptUI>
    <ConceptName>
     <String>(beta'-chloroethyl)phosphonylethyl-DL-phenylalanine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094063</TermUI>
      <String>(beta'-chloroethyl)phosphonylethyl-DL-phenylalanine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015066</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-chloropentylphosphonate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009943</DescriptorUI>
     <DescriptorName>
      <String>Organophosphorus Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>BBA 499:212;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064064</ConceptUI>
    <ConceptName>
     <String>5-chloropentylphosphonate</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094067</TermUI>
      <String>5-chloropentylphosphonate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C479234</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-(4-dimethylaminomethylphenyl)-8,9-dihydro-7H-2,7,9a-benzo(cd)azulen-6-one</String>
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  <DateCreated>
   <Year>2003</Year>
   <Month>12</Month>
   <Day>02</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>a radiosensitizing agent that inhibits poly(ADP-ribose) polymerase-1; structure in first source
  </Note>
  <Frequency>15</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001569</DescriptorUI>
     <DescriptorName>
      <String>Benzodiazepines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D052176</DescriptorUI>
     <DescriptorName>
      <String>Azulenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D011065</DescriptorUI>
     <DescriptorName>
      <String>Poly(ADP-ribose) Polymerases</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
     <QualifierName>
      <String>antagonists &amp; inhibitors</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Cancer Res 2003 Sep 15;63(18):6008-15</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0456815</ConceptUI>
    <ConceptName>
     <String>1-(4-dimethylaminomethylphenyl)-8,9-dihydro-7H-2,7,9a-benzo(cd)azulen-6-one</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0456815</Concept1UI>
     <Concept2UI>M0456816</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T561097</TermUI>
      <String>1-(4-dimethylaminomethylphenyl)-8,9-dihydro-7H-2,7,9a-benzo(cd)azulen-6-one</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0456816</ConceptUI>
    <ConceptName>
     <String>AG 14361</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0456815</Concept1UI>
     <Concept2UI>M0456816</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T561098</TermUI>
      <String>AG 14361</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T561100</TermUI>
      <String>AG14361</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T561099</TermUI>
      <String>AG-14361</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015072</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-cholestanyl phosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>07</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ORGANOPHOSPHORUS COMPOUNDS (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002776</DescriptorUI>
     <DescriptorName>
      <String>Cholestanes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Soc Jpn 97(5):528;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064079</ConceptUI>
    <ConceptName>
     <String>3-cholestanyl phosphate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094082</TermUI>
      <String>3-cholestanyl phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C090162</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>PSO2 protein, S cerevisiae</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>11</Month>
   <Day>25</Day>
  </DateCreated>
  <DateRevised>
   <Year>2012</Year>
   <Month>05</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>SNM - sensitive to nitrogen mustard; from Saccharomyces cerevisiae; found in other organisms; has been sequenced; GenBank X64004
  </Note>
  <Frequency>38</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DNA-BINDING PROTEINS (1994-2012)</PreviousIndexing>
   <PreviousIndexing>*FUNGAL PROTEINS (1994-2002)</PreviousIndexing>
   <PreviousIndexing>*NUCLEAR PROTEINS (1994-2012)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004706</DescriptorUI>
     <DescriptorName>
      <String>Endodeoxyribonucleases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029701</DescriptorUI>
     <DescriptorName>
      <String>Saccharomyces cerevisiae Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D004260</DescriptorUI>
     <DescriptorName>
      <String>DNA Repair</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Mutat Res 1994 Nov;315(3):275-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0238271</ConceptUI>
    <ConceptName>
     <String>PSO2 protein, S cerevisiae</String>
    </ConceptName>
    <RegistryNumber>EC 3.1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T569197</TermUI>
      <String>PSO2 protein, S cerevisiae</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>01</Month>
       <Day>19</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T268276</TermUI>
      <String>YMR137C protein, S cerevisiae</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T522302</TermUI>
      <String>SNM1protein, S cerevisiae</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>10</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002434</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>debestran</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ESTROGENS (73-76)</PreviousIndexing>
   <PreviousIndexing>CYCLOHEXANES (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013267</DescriptorUI>
     <DescriptorName>
      <String>Stilbenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043019</ConceptUI>
    <ConceptName>
     <String>debestran</String>
    </ConceptName>
    <CASN1Name>1-(p-ethoxycyclohexyl)-1-(p-ethoxyphenyl)-2- bromo-1-phenylethylene</CASN1Name>
    <RegistryNumber>60883-77-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073022</TermUI>
      <String>debestran</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C036745</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2',3'-(O-(2,4,6-trinitrocyclohexadienylidine))adenosine 5'-diphosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1983</Year>
   <Month>01</Month>
   <Day>21</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>15</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>40</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000244</DescriptorUI>
     <DescriptorName>
      <String>Adenosine Diphosphate</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
    <PharmacologicalActionList>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D005456</DescriptorUI>
        <DescriptorName>
         <String>Fluorescent Dyes</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
    </PharmacologicalActionList>
  <SourceList>
   <Source>Biochim Biophys Acta 1982;719(3):509</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0111642</ConceptUI>
    <ConceptName>
     <String>2',3'-(O-(2,4,6-trinitrocyclohexadienylidine))adenosine 5'-diphosphate</String>
    </ConceptName>
    <CASN1Name>Adenosine 5'-(trihydrogen diphosphate), 2',3'-O-(2,4,6-trinitro-2,4-cyclohexadienylidene)-, ion(1-), sodium</CASN1Name>
    <RegistryNumber>84430-17-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T141646</TermUI>
      <String>2',3'-(O-(2,4,6-trinitrocyclohexadienylidine))adenosine 5'-diphosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T141645</TermUI>
      <String>TNP-ADP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015093</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>8-cyano-10-methyl-5-deazaisoalloxazine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>01</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>NITRILES (78-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005415</DescriptorUI>
     <DescriptorName>
      <String>Flavins</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Am Chem Soc 99(20):6721;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064114</ConceptUI>
    <ConceptName>
     <String>8-cyano-10-methyl-5-deazaisoalloxazine</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094117</TermUI>
      <String>8-cyano-10-methyl-5-deazaisoalloxazine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
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   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C022775</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>delta (2,16)-5 alpha-androstadiene-3,17-diol-3,17-diacetate</String>
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  <DateCreated>
   <Year>1970</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>synthetic steroid with androgenic activity
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  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ANDROGENS (70-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000734</DescriptorUI>
     <DescriptorName>
      <String>Androstenediols</String>
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   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D045165</DescriptorUI>
     <DescriptorName>
      <String>Testosterone Congeners</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Steroid Biochem 1979;11(5-6):1513</Source>
   <Source>Steroidologia 1(2):94;1970</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0079349</ConceptUI>
    <ConceptName>
     <String>delta (2,16)-5 alpha-androstadiene-3,17-diol-3,17-diacetate</String>
    </ConceptName>
    <CASN1Name>Androsta-2,16-diene-3,17-diol, diacetate, (5alpha)-</CASN1Name>
    <RegistryNumber>28312-74-5</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0079349</Concept1UI>
     <Concept2UI>M0079347</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T109352</TermUI>
      <String>delta (2,16)-5 alpha-androstadiene-3,17-diol-3,17-diacetate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T109351</TermUI>
      <String>delta (2,16)-androstadiene-3,17-diol-3,17-diacetate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0079347</ConceptUI>
    <ConceptName>
     <String>NB 06</String>
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    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0079349</Concept1UI>
     <Concept2UI>M0079347</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T109350</TermUI>
      <String>NB 06</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C024110</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>11-deoxy-16,16-trimethyleneprostaglandin E1</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>10</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>inhibitor of prostaglandin E-induced contractions of the gerbil colon; RN given refers to (1alpha,2beta(1E,3S*))-(+-)-isomer
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000527</DescriptorUI>
     <DescriptorName>
      <String>Alprostadil</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D011459</DescriptorUI>
     <DescriptorName>
      <String>Prostaglandins E, Synthetic</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Prostaglandins 18(3):349;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0082049</ConceptUI>
    <ConceptName>
     <String>11-deoxy-16,16-trimethyleneprostaglandin E1</String>
    </ConceptName>
    <CASN1Name>Cyclopentaneheptanoic acid, 2-(3-(1-butylcyclobutyl)-3-hydroxy-1-propenyl)-5-oxo-, (1alpha,2beta(1E,3S*))-(+-)-</CASN1Name>
    <RegistryNumber>62407-92-5</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>62446-41-7 ((1alpha,2beta(1E,3R*))-(+-)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0082049</Concept1UI>
     <Concept2UI>M0315599</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T112052</TermUI>
      <String>11-deoxy-16,16-trimethyleneprostaglandin E1</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0315599</ConceptUI>
    <ConceptName>
     <String>11-deoxy-16,16-trimethyleneprostaglandin E1, (1alpha,2beta(1E,3R*))-(+-)-isomer</String>
    </ConceptName>
    <RegistryNumber>62446-41-7</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0082049</Concept1UI>
     <Concept2UI>M0315599</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T345599</TermUI>
      <String>11-deoxy-16,16-trimethyleneprostaglandin E1, (1alpha,2beta(1E,3R*))-(+-)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C475158</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>RO 10-5824</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>07</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011725</DescriptorUI>
     <DescriptorName>
      <String>Pyridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011743</DescriptorUI>
     <DescriptorName>
      <String>Pyrimidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Neuropharmacology. 2003 Mar;44(4):473-81</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0451161</ConceptUI>
    <ConceptName>
     <String>RO 10-5824</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T544954</TermUI>
      <String>RO 10-5824</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>07</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T544955</TermUI>
      <String>RO-10-5824</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>07</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015110</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>deoxyadenylyl-(5'-3')-deoxyadenylyl-(5'-N)-L-phenylalanine methyl ester</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1995</Year>
   <Month>06</Month>
   <Day>19</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*OLIGODEOXYRIBONUCLEOTIDES (78-79)</PreviousIndexing>
   <PreviousIndexing>PHENYLALANINE/*analogs (78-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003838</DescriptorUI>
     <DescriptorName>
      <String>Deoxyadenine Nucleotides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nucleic Acid Res 4(8):2609;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064141</ConceptUI>
    <ConceptName>
     <String>deoxyadenylyl-(5'-3')-deoxyadenylyl-(5'-N)-L-phenylalanine methyl ester</String>
    </ConceptName>
    <CASN1Name>Adenosine, 2'-deoxyadenylyl-(5'-3')-2'-deoxy-, 5'-P-ester with N-phosphono-L-phenylalanine 1-methyl ester</CASN1Name>
    <RegistryNumber>33019-68-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094144</TermUI>
      <String>deoxyadenylyl-(5'-3')-deoxyadenylyl-(5'-N)-L-phenylalanine methyl ester</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015112</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2'-deoxycytidine-diphosphate-diglyceride</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>03</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>DEOXYCYTIDINE/analogs (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003567</DescriptorUI>
     <DescriptorName>
      <String>Cytidine Diphosphate Diglycerides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Neurochem 29(2):383;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064143</ConceptUI>
    <ConceptName>
     <String>2'-deoxycytidine-diphosphate-diglyceride</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094146</TermUI>
      <String>2'-deoxycytidine-diphosphate-diglyceride</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015113</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-deoxy-2-fluoro-D-glucitol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>08</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DEOXY SUGARS (81-82)</PreviousIndexing>
   <PreviousIndexing>DEOXY SUGARS (77-81)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013012</DescriptorUI>
     <DescriptorName>
      <String>Sorbitol</String>
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    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Folia Microbiol 22(4):295;1977</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064144</ConceptUI>
    <ConceptName>
     <String>2-deoxy-2-fluoro-D-glucitol</String>
    </ConceptName>
    <CASN1Name>D-Glucitol, 2-deoxy-2-fluoro-</CASN1Name>
    <RegistryNumber>34339-80-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094147</TermUI>
      <String>2-deoxy-2-fluoro-D-glucitol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015116</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-deoxy-5-fluoro-L-sorbose</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>03</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DEOXY SUGARS (81-82)</PreviousIndexing>
   <PreviousIndexing>DEOXY SUGARS (77-81)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013013</DescriptorUI>
     <DescriptorName>
      <String>Sorbose</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
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   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Folia Microbiol 22(4):295;1977</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064146</ConceptUI>
    <ConceptName>
     <String>5-deoxy-5-fluoro-L-sorbose</String>
    </ConceptName>
    <CASN1Name>L-Sorbose, 5-deoxy-5-fluoro-</CASN1Name>
    <RegistryNumber>66558-67-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094149</TermUI>
      <String>5-deoxy-5-fluoro-L-sorbose</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015118</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>desaminoactinomycin C</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1995</Year>
   <Month>07</Month>
   <Day>26</Day>
  </DateRevised>
  <Note>RN given is for the actinomycin C(3) derivative
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003609</DescriptorUI>
     <DescriptorName>
      <String>Dactinomycin</String>
     </DescriptorName>
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    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
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    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Riv Biol 69(3-4):169;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064148</ConceptUI>
    <ConceptName>
     <String>desaminoactinomycin C</String>
    </ConceptName>
    <RegistryNumber>23067-37-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094151</TermUI>
      <String>desaminoactinomycin C</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
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   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015120</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dexamyl</String>
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  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000654</DescriptorUI>
     <DescriptorName>
      <String>Amobarbital</String>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003913</DescriptorUI>
     <DescriptorName>
      <String>Dextroamphetamine</String>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>Ann Intern Med 87(2):246;1977</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064160</ConceptUI>
    <ConceptName>
     <String>dexamyl</String>
    </ConceptName>
    <RegistryNumber>8065-31-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094163</TermUI>
      <String>dexamyl</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C025013</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-oxa-4,5,6-nor-3,7-inter-3-phenyleneprostaglandin E1</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>06</Month>
   <Day>26</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>10</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000527</DescriptorUI>
     <DescriptorName>
      <String>Alprostadil</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D011459</DescriptorUI>
     <DescriptorName>
      <String>Prostaglandins E, Synthetic</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Steroids 1980;19(1):123</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0083887</ConceptUI>
    <ConceptName>
     <String>3-oxa-4,5,6-nor-3,7-inter-3-phenyleneprostaglandin E1</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T113890</TermUI>
      <String>3-oxa-4,5,6-nor-3,7-inter-3-phenyleneprostaglandin E1</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T113889</TermUI>
      <String>OI-PGE1</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T113888</TermUI>
      <String>3-oxa-4,5,6-nor-3,7-inter-3-phenylene-PGE1</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015122</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>diacetylcymarol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1986</Year>
   <Month>08</Month>
   <Day>11</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002934</DescriptorUI>
     <DescriptorName>
      <String>Cinnamates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Xenobiotica 7(5):267;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064164</ConceptUI>
    <ConceptName>
     <String>diacetylcymarol</String>
    </ConceptName>
    <RegistryNumber>6473-40-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094167</TermUI>
      <String>diacetylcymarol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015123</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,2-bi(adenosine-N(6)-yl)ethane-2'(3')-O-L-phenylalanyl derivative</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>11</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PHENYLALANINE/analogs (78-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000241</DescriptorUI>
     <DescriptorName>
      <String>Adenosine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Comm 77(4):1237;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064165</ConceptUI>
    <ConceptName>
     <String>1,2-bi(adenosine-N(6)-yl)ethane-2'(3')-O-L-phenylalanyl derivative</String>
    </ConceptName>
    <CASN1Name>L-Phenylalanine, 2'(or 3')-ester with N,N'-1,2-ethanediylbis(adenosine)</CASN1Name>
    <RegistryNumber>64542-52-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094168</TermUI>
      <String>1,2-bi(adenosine-N(6)-yl)ethane-2'(3')-O-L-phenylalanyl derivative</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015124</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,2-di(adenosine-N(6)-yl)ethane-2'(3')-O-L-leucyl derivative</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>04</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>LEUCINE/analogs (79-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000241</DescriptorUI>
     <DescriptorName>
      <String>Adenosine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Comm 77(4):1237;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064166</ConceptUI>
    <ConceptName>
     <String>1,2-di(adenosine-N(6)-yl)ethane-2'(3')-O-L-leucyl derivative</String>
    </ConceptName>
    <CASN1Name>L-Leucine, 2'(or 3')-ester with N,N'-1,2-ethanediylbis(adenosine)</CASN1Name>
    <RegistryNumber>64542-53-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094169</TermUI>
      <String>1,2-di(adenosine-N(6)-yl)ethane-2'(3')-O-L-leucyl derivative</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015128</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,3-4,5-dianhydroallitol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>04</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>EPOXY COMPOUNDS (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013402</DescriptorUI>
     <DescriptorName>
      <String>Sugar Alcohols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Carbohydrate Res 56:43;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064174</ConceptUI>
    <ConceptName>
     <String>2,3-4,5-dianhydroallitol</String>
    </ConceptName>
    <CASN1Name>Allitol, 2,3:4,5-dianhydro-</CASN1Name>
    <RegistryNumber>63699-93-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094177</TermUI>
      <String>2,3-4,5-dianhydroallitol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015131</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dichloralurea</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1985</Year>
   <Month>04</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CHLORAL HYDRATE (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014508</DescriptorUI>
     <DescriptorName>
      <String>Urea</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Tsitolog Genetika 11(4):357;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064179</ConceptUI>
    <ConceptName>
     <String>dichloralurea</String>
    </ConceptName>
    <RegistryNumber>116-52-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094182</TermUI>
      <String>dichloralurea</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015134</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>diethylglyoxime</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>10</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*GLYOXAL/analogs (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010091</DescriptorUI>
     <DescriptorName>
      <String>Oximes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Vutr Bolesti 16(1):93;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064187</ConceptUI>
    <ConceptName>
     <String>diethylglyoxime</String>
    </ConceptName>
    <CASN1Name>3,4-Hexanedione, dioxime</CASN1Name>
    <RegistryNumber>4437-52-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094190</TermUI>
      <String>diethylglyoxime</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015135</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>diethylphenylphosphine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009943</DescriptorUI>
     <DescriptorName>
      <String>Organophosphorus Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Hoppe-Seyler Z Physiol Chem 358:689;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064188</ConceptUI>
    <ConceptName>
     <String>diethylphenylphosphine</String>
    </ConceptName>
    <CASN1Name>Phosphine, diethylphenyl-</CASN1Name>
    <RegistryNumber>1605-53-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094191</TermUI>
      <String>diethylphenylphosphine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015139</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>diguanosine triphosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1988</Year>
   <Month>08</Month>
   <Day>19</Day>
  </DateRevised>
  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>GUANOSINE TRIPHOSPHATE/*analogs (77-88)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015226</DescriptorUI>
     <DescriptorName>
      <String>Dinucleoside Phosphates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Can J Biochem 55(8):841;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064196</ConceptUI>
    <ConceptName>
     <String>diguanosine triphosphate</String>
    </ConceptName>
    <RegistryNumber>6674-45-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094199</TermUI>
      <String>diguanosine triphosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C105377</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>aflastatin A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1997</Year>
   <Month>05</Month>
   <Day>02</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>inhibitor of aflatoxin production by aflatoxigenic fungi; from Streptomyces sp.; structure given in first source
  </Note>
  <Frequency>12</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*Antibiotics (1997-2001)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011760</DescriptorUI>
     <DescriptorName>
      <String>Pyrrolidinones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiot (Tokyo) 1997 Feb;50(2):111-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0274928</ConceptUI>
    <ConceptName>
     <String>aflastatin A</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T304933</TermUI>
      <String>aflastatin A</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015141</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dihydroazapetine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1994</Year>
   <Month>06</Month>
   <Day>13</Day>
  </DateRevised>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003984</DescriptorUI>
     <DescriptorName>
      <String>Dibenzazepines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Pharmacol 30(8):498;1978</Source>
   <Source>J Pharmacol Exp Ther 202(2):278;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064198</ConceptUI>
    <ConceptName>
     <String>dihydroazapetine</String>
    </ConceptName>
    <RegistryNumber>58335-95-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094201</TermUI>
      <String>dihydroazapetine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015143</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3a,8a-dihydrofuro(2,3-b)benzofuran</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001572</DescriptorUI>
     <DescriptorName>
      <String>Benzofurans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>BBRC 76(3):888;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064200</ConceptUI>
    <ConceptName>
     <String>3a,8a-dihydrofuro(2,3-b)benzofuran</String>
    </ConceptName>
    <RegistryNumber>53737-95-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094203</TermUI>
      <String>3a,8a-dihydrofuro(2,3-b)benzofuran</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015146</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3,4-dihydro-1H-1,4-oxazino(4,3a)indole</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*OXAZINES (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007211</DescriptorUI>
     <DescriptorName>
      <String>Indoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Int Pharmacodyn 227:324;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064205</ConceptUI>
    <ConceptName>
     <String>3,4-dihydro-1H-1,4-oxazino(4,3a)indole</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094208</TermUI>
      <String>3,4-dihydro-1H-1,4-oxazino(4,3a)indole</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015159</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>7,10-dimethylbenzo(a)pyrene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1985</Year>
   <Month>09</Month>
   <Day>18</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001580</DescriptorUI>
     <DescriptorName>
      <String>Benzopyrenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 42(20):3284;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064228</ConceptUI>
    <ConceptName>
     <String>7,10-dimethylbenzo(a)pyrene</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094231</TermUI>
      <String>7,10-dimethylbenzo(a)pyrene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C097248</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>gdcsPB protein, Flaveria pringlei</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>01</Month>
   <Day>24</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>10</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>a P-isoprotein of the glycine-cleavage system from Flaveria pringlei; amino acid sequence given in first source; GenBank Z54239
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010940</DescriptorUI>
     <DescriptorName>
      <String>Plant Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Biochem 1995 Nov 15;234(1):116-24</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0255658</ConceptUI>
    <ConceptName>
     <String>gdcsPB protein, Flaveria pringlei</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T508683</TermUI>
      <String>gdcsPB protein, Flaveria pringlei</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>07</Month>
       <Day>31</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015169</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>n-dioctyl ether</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004987</DescriptorUI>
     <DescriptorName>
      <String>Ethers</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Bacteriol 131(1):92;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064256</ConceptUI>
    <ConceptName>
     <String>n-dioctyl ether</String>
    </ConceptName>
    <RegistryNumber>629-82-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094259</TermUI>
      <String>n-dioctyl ether</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C111793</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>AATP2 protein, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>05</Month>
   <Day>11</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>11</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>an ATP/ADP translocator from the plastid envelope of Arabidopsis thaliana; amino acid sequence in first source; GenBank X94626
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000226</DescriptorUI>
     <DescriptorName>
      <String>Mitochondrial ADP, ATP Translocases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Biochem 1998 Mar 15;252(3):353-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0289347</ConceptUI>
    <ConceptName>
     <String>AATP2 protein, Arabidopsis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T497341</TermUI>
      <String>AATP2 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>06</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C111803</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>din1 protein, Raphanus sativus</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>05</Month>
   <Day>11</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>11</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>amino acid sequence in first source
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010940</DescriptorUI>
     <DescriptorName>
      <String>Plant Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D002736</DescriptorUI>
     <DescriptorName>
      <String>Chloroplasts</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Plant Cell Physiol 1998 Feb;39(2):139-43</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0289369</ConceptUI>
    <ConceptName>
     <String>din1 protein, Raphanus sativus</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T507561</TermUI>
      <String>din1 protein, Raphanus sativus</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>07</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015176</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3,9-di-3-pyridyl-2,4,8,10-tetraoxaspiro-5,5-undecane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>10</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>SPIRO COMPOUNDS (78-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011725</DescriptorUI>
     <DescriptorName>
      <String>Pyridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Exp Pathol 13(2-3):180;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064274</ConceptUI>
    <ConceptName>
     <String>3,9-di-3-pyridyl-2,4,8,10-tetraoxaspiro-5,5-undecane</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094277</TermUI>
      <String>3,9-di-3-pyridyl-2,4,8,10-tetraoxaspiro-5,5-undecane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015181</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Dolo-Buscopan Suppository</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>14</Day>
  </DateRevised>
  <Note>contaons buscopan, codeine phosphate, amobarbital, novaminsulfone
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000654</DescriptorUI>
     <DescriptorName>
      <String>Amobarbital</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002086</DescriptorUI>
     <DescriptorName>
      <String>Butylscopolammonium Bromide</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003061</DescriptorUI>
     <DescriptorName>
      <String>Codeine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004177</DescriptorUI>
     <DescriptorName>
      <String>Dipyrone</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Med Monatschr 31(7):325;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064275</ConceptUI>
    <ConceptName>
     <String>Dolo-Buscopan Suppository</String>
    </ConceptName>
    <CASN1Name>Morphinan-6-ol, 7,8-didehydro-4,5-epoxy-3-methoxy-17-methyl-, (5alpha,6alpha)-, phosphate (1-1) (salt), mixt. with (7(S)-(1alpha,2beta,4beta,5alpha,7beta))-9-butyl-7-(3-hydroxy-1-oxo-2-phenylpropoxy)-9-methyl-3-oxa-9-azoniatricyclo(3.3.1.0(2,4))nonane bromide, 5-ethyl-5-(3-methylbutyl)-2,4,6(1H,3H,5H)-pyrimidinetrione and sodium ((2,3-dihydro-1,5-dimethyl-3-oxo-2-phenyl-1H-pyrazol-4-yl)methylamino)methanesulfonate</CASN1Name>
    <RegistryNumber>76422-10-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094278</TermUI>
      <String>Dolo-Buscopan Suppository</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015182</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>DPH-L</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>phosphorylated brain proteins
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PHOSPHOPROTEINS (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009419</DescriptorUI>
     <DescriptorName>
      <String>Nerve Tissue Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Epilepsia 18(3):357;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064276</ConceptUI>
    <ConceptName>
     <String>DPH-L</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094279</TermUI>
      <String>DPH-L</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015183</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>DPH-M</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>phosphorylated brain proteins
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PHOSPHOPROTEINS (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009419</DescriptorUI>
     <DescriptorName>
      <String>Nerve Tissue Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Epilepsia 18(3):357;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064277</ConceptUI>
    <ConceptName>
     <String>DPH-M</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094280</TermUI>
      <String>DPH-M</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015184</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>durylglyoxal</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D006037</DescriptorUI>
     <DescriptorName>
      <String>Glyoxal</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Boll Chim Farm 165(5):277;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064278</ConceptUI>
    <ConceptName>
     <String>durylglyoxal</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094281</TermUI>
      <String>durylglyoxal</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015192</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>estriol-3-methyl ether</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004964</DescriptorUI>
     <DescriptorName>
      <String>Estriol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ind J Exptl Biol 15:16;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064283</ConceptUI>
    <ConceptName>
     <String>estriol-3-methyl ether</String>
    </ConceptName>
    <RegistryNumber>1474-53-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094286</TermUI>
      <String>estriol-3-methyl ether</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015193</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4,6 beta-ethanoestradiol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004958</DescriptorUI>
     <DescriptorName>
      <String>Estradiol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 42(18):3091;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064284</ConceptUI>
    <ConceptName>
     <String>4,6 beta-ethanoestradiol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094287</TermUI>
      <String>4,6 beta-ethanoestradiol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015194</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4,6 beta-ethanoestrone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004970</DescriptorUI>
     <DescriptorName>
      <String>Estrone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 42(18):3091;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064285</ConceptUI>
    <ConceptName>
     <String>4,6 beta-ethanoestrone</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094288</TermUI>
      <String>4,6 beta-ethanoestrone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015196</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N(2),3-ethenoguanine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1994</Year>
   <Month>02</Month>
   <Day>26</Day>
  </DateRevised>
  <Note>formed from 2-halooxiranes
  </Note>
  <Frequency>25</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D006147</DescriptorUI>
     <DescriptorName>
      <String>Guanine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 42(20):3292;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064291</ConceptUI>
    <ConceptName>
     <String>N(2),3-ethenoguanine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094294</TermUI>
      <String>N(2),3-ethenoguanine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015197</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ethidium-5-iodocytidylyl(3'-5')guanosine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1995</Year>
   <Month>06</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>complex of above two cpds
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*OLIGONUCLEOTIDES (78-88)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004996</DescriptorUI>
     <DescriptorName>
      <String>Ethidium</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015226</DescriptorUI>
     <DescriptorName>
      <String>Dinucleoside Phosphates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Mol Biol 114:317;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064292</ConceptUI>
    <ConceptName>
     <String>ethidium-5-iodocytidylyl(3'-5')guanosine</String>
    </ConceptName>
    <CASN1Name>Guanosine, 5-iodocytidylyl-(3'-5')-, ion(1-), 3,8-diamino-5-ethyl-6-phenylphenanthridinium</CASN1Name>
    <RegistryNumber>64822-98-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094295</TermUI>
      <String>ethidium-5-iodocytidylyl(3'-5')guanosine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015206</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>17 alpha-ethynyl-4,6 beta-ethanoestradiol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004997</DescriptorUI>
     <DescriptorName>
      <String>Ethinyl Estradiol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 42(18):3091;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064301</ConceptUI>
    <ConceptName>
     <String>17 alpha-ethynyl-4,6 beta-ethanoestradiol</String>
    </ConceptName>
    <CASN1Name>5'H-Cyclopenta(4,5,6)-19-norpregna-1(10),2,4-trien-20-yne-3,17-diol, 4',6-dihydro-, (6alpha,17alpha)-</CASN1Name>
    <RegistryNumber>62842-09-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094304</TermUI>
      <String>17 alpha-ethynyl-4,6 beta-ethanoestradiol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015218</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>flastipiol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>extract of parsley seeds flamine, stachyrene &amp; pectin
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>SEEDS (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010936</DescriptorUI>
     <DescriptorName>
      <String>Plant Extracts</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Farm Zh 3:76;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064334</ConceptUI>
    <ConceptName>
     <String>flastipiol</String>
    </ConceptName>
    <CASN1Name>Flamin, mixt. with stachyrene</CASN1Name>
    <RegistryNumber>77257-31-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094337</TermUI>
      <String>flastipiol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015269</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hydroxyacetone phosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>17</Day>
  </DateRevised>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000096</DescriptorUI>
     <DescriptorName>
      <String>Acetone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 16(18):3988;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064417</ConceptUI>
    <ConceptName>
     <String>hydroxyacetone phosphate</String>
    </ConceptName>
    <RegistryNumber>926-43-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094420</TermUI>
      <String>hydroxyacetone phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015224</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>formaldehydeaminal</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>condensation product of formaldehyde &amp; 2 moles of a secondary amine; structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003959</DescriptorUI>
     <DescriptorName>
      <String>Diamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Zbl Bakt. Parasit Infect Hyg 238(3):402;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064345</ConceptUI>
    <ConceptName>
     <String>formaldehydeaminal</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094348</TermUI>
      <String>formaldehydeaminal</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015226</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-formyl-1,4-benzodioxane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DIOXANES (77-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010883</DescriptorUI>
     <DescriptorName>
      <String>Piperoxan</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Farmaco (Ed Sci) 32(7):512;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064347</ConceptUI>
    <ConceptName>
     <String>2-formyl-1,4-benzodioxane</String>
    </ConceptName>
    <CASN1Name>1,4-Benzodioxin-2-carboxaldehyde, 2,3-dihydro-</CASN1Name>
    <RegistryNumber>64179-67-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094350</TermUI>
      <String>2-formyl-1,4-benzodioxane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015227</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>formylmethylcobalamin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014805</DescriptorUI>
     <DescriptorName>
      <String>Vitamin B 12</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>JBC 252(14):5004;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064348</ConceptUI>
    <ConceptName>
     <String>formylmethylcobalamin</String>
    </ConceptName>
    <CASN1Name>Cobinamide, Co-(2-oxoethyl) deriv., hydroxide, dihydrogen phosphate (ester), inner salt, 3'-ester with 5,6-dimethyl-1-alpha-D-ribofuranosyl-1H-benzimidazole</CASN1Name>
    <RegistryNumber>41871-63-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094351</TermUI>
      <String>formylmethylcobalamin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C016325</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cyclo(glycylprolyl)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>17</Day>
  </DateRevised>
  <Note>RN given refers to cpd without isomeric designation
  </Note>
  <Frequency>8</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DIPEPTIDES (78-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010456</DescriptorUI>
     <DescriptorName>
      <String>Peptides, Cyclic</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Experientia 34(5):579;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0066261</ConceptUI>
    <ConceptName>
     <String>cyclo(glycylprolyl)</String>
    </ConceptName>
    <CASN1Name>Pyrrolo(1,2-a)pyrazine-1,4-dione, hexahydro-, (S)-</CASN1Name>
    <RegistryNumber>19179-12-5</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>3705-27-9 ((L)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0066261</Concept1UI>
     <Concept2UI>M0313158</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T096264</TermUI>
      <String>cyclo(glycylprolyl)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T096261</TermUI>
      <String>cyclo(Gly-O-Pro)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T096262</TermUI>
      <String>cyclo(Gly-Pro)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0313158</ConceptUI>
    <ConceptName>
     <String>cyclo(glycylprolyl), (L)-isomer</String>
    </ConceptName>
    <RegistryNumber>3705-27-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0066261</Concept1UI>
     <Concept2UI>M0313158</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T343158</TermUI>
      <String>cyclo(glycylprolyl), (L)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T096263</TermUI>
      <String>cyclo(glycyl-L-prolyl)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C495815</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>CFL2 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2008</Year>
   <Month>09</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>RefSeq NM_138638
  </Note>
  <Frequency>24</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D051340</DescriptorUI>
     <DescriptorName>
      <String>Cofilin 2</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0480174</ConceptUI>
    <ConceptName>
     <String>CFL2 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T629421</TermUI>
      <String>CFL2 protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>02</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T629422</TermUI>
      <String>cofilin 2 (muscle) protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>02</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C551950</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>fluorastrol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2010</Year>
   <Month>09</Month>
   <Day>07</Day>
  </DateCreated>
  <Note>inhibits kinesin Eg5; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011743</DescriptorUI>
     <DescriptorName>
      <String>Pyrimidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013871</DescriptorUI>
     <DescriptorName>
      <String>Thiones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D016547</DescriptorUI>
     <DescriptorName>
      <String>Kinesin</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
     <QualifierName>
      <String>antagonists &amp; inhibitors</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Med Chem 2010 Aug 12;53(15):5676-83</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0549667</ConceptUI>
    <ConceptName>
     <String>fluorastrol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T776906</TermUI>
      <String>fluorastrol</String>
      <DateCreated>
       <Year>2010</Year>
       <Month>09</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2010)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015251</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>guanylyl 2'-5' guanosine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1995</Year>
   <Month>06</Month>
   <Day>20</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*GUANOSINE MONOPHOSPHATE/analogs (77-88)</PreviousIndexing>
   <PreviousIndexing>GUANOSINE/*analogs (77-88)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015226</DescriptorUI>
     <DescriptorName>
      <String>Dinucleoside Phosphates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>BBRC 77(3):1084;1977</Source>
   <Source>J Biochem (Tokyo) 83(3):783;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064397</ConceptUI>
    <ConceptName>
     <String>guanylyl 2'-5' guanosine</String>
    </ConceptName>
    <CASN1Name>Guanosine, guanylyl-(2'-5')-</CASN1Name>
    <RegistryNumber>22886-44-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094400</TermUI>
      <String>guanylyl 2'-5' guanosine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015259</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hepalotoxin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008978</DescriptorUI>
     <DescriptorName>
      <String>Mollusk Venoms</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Toxicon 15(5):463;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064403</ConceptUI>
    <ConceptName>
     <String>hepalotoxin</String>
    </ConceptName>
    <CASN1Name>Hepalotoxin</CASN1Name>
    <RegistryNumber>77536-28-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094406</TermUI>
      <String>hepalotoxin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015271</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-(2-hydroxybenzoyl)xanthone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*XANTHENES (1983-2003)</PreviousIndexing>
   <PreviousIndexing>HYDROXYBENZOIC ACIDS (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D044004</DescriptorUI>
     <DescriptorName>
      <String>Xanthones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Pharm 310(6):506;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064419</ConceptUI>
    <ConceptName>
     <String>2-(2-hydroxybenzoyl)xanthone</String>
    </ConceptName>
    <CASN1Name>9H-Xanthen-9-one, 2-(2-hydroxybenzoyl)-</CASN1Name>
    <RegistryNumber>31964-91-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094422</TermUI>
      <String>2-(2-hydroxybenzoyl)xanthone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015264</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>histopine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D006639</DescriptorUI>
     <DescriptorName>
      <String>Histidine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 78(2):785;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064413</ConceptUI>
    <ConceptName>
     <String>histopine</String>
    </ConceptName>
    <CASN1Name>N(2)-(1-carboxyethyl)-L-histidine</CASN1Name>
    <RegistryNumber>25303-09-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094416</TermUI>
      <String>histopine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C038378</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>prodiame</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>17</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D045166</DescriptorUI>
     <DescriptorName>
      <String>Estradiol Congeners</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Proc West Pharmacol Soc 1983;26:111</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0115584</ConceptUI>
    <ConceptName>
     <String>prodiame</String>
    </ConceptName>
    <CASN1Name>Estra-1,3,5(10)-trien-3-ol, 17-((3-aminopropyl)amino)-, (17beta)-</CASN1Name>
    <RegistryNumber>87189-13-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T145588</TermUI>
      <String>prodiame</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T145587</TermUI>
      <String>N-(3-hydroxyestra-1,3,5(10)-triene-1,3-17beta)-1,3-propylenediamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C497121</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SP3 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2008</Year>
   <Month>09</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>RefSeq NM_003111
  </Note>
  <Frequency>397</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D051705</DescriptorUI>
     <DescriptorName>
      <String>Sp3 Transcription Factor</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0475869</ConceptUI>
    <ConceptName>
     <String>SP3 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T618816</TermUI>
      <String>SP3 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>11</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T618818</TermUI>
      <String>SPR-2 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>11</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T618817</TermUI>
      <String>Sp3 transcription factor, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>11</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C497139</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>DGKD protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>03</Month>
   <Day>06</Day>
  </DateCreated>
  <DateRevised>
   <Year>2008</Year>
   <Month>09</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>RefSeq NM_003648
  </Note>
  <Frequency>15</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D019852</DescriptorUI>
     <DescriptorName>
      <String>Diacylglycerol Kinase</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem J 2004 Sep 15;382(Pt 3):957-66</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0481572</ConceptUI>
    <ConceptName>
     <String>DGKD protein, human</String>
    </ConceptName>
    <RegistryNumber>EC 2.7.1.107</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T650814</TermUI>
      <String>DGKD protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>09</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T632483</TermUI>
      <String>diacylglycerol kinase delta1, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T650815</TermUI>
      <String>diacylglycerol kinase, delta 130kDa, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>09</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T632484</TermUI>
      <String>DGKdelta1, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C497894</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>CD47 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2008</Year>
   <Month>09</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>RefSeq NM_001777
  </Note>
  <Frequency>478</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D051928</DescriptorUI>
     <DescriptorName>
      <String>CD47 Antigen</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0473048</ConceptUI>
    <ConceptName>
     <String>CD47 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T610689</TermUI>
      <String>CD47 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T633903</TermUI>
      <String>IAP-50 antigen, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T616704</TermUI>
      <String>OVTL3 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>11</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T610691</TermUI>
      <String>leukocyte surface antigen CD47, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T633904</TermUI>
      <String>OA3 antigen, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>03</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T610690</TermUI>
      <String>CD47 antigen (Rh-related antigen, integrin-associated signal transducer), human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T616705</TermUI>
      <String>integrin-associated protein IAP, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>11</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003849</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3,3',5-triiodothyroacetic acid N,N-diethanolamine (1:1) complex</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>thyromimetic agent; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*TRIIODOTHYRONINE (73-75)</PreviousIndexing>
   <PreviousIndexing>ACETIC ACIDS (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014284</DescriptorUI>
     <DescriptorName>
      <String>Triiodothyronine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 52(2):430;1973</Source>
   <Source>Lancet 2(8031):221;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044958</ConceptUI>
    <ConceptName>
     <String>3,3',5-triiodothyroacetic acid N,N-diethanolamine (1:1) complex</String>
    </ConceptName>
    <CASN1Name>4-(4-hydroxy-3-iodophenoxy)-3,5-diiodobenzeneacetic acid, compd. with 2,2'-iminobis(ethanol) (1:1)</CASN1Name>
    <RegistryNumber>1052-92-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074961</TermUI>
      <String>3,3',5-triiodothyroacetic acid N,N-diethanolamine (1:1) complex</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C091671</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>XCR1 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1999</Year>
   <Month>11</Month>
   <Day>04</Day>
  </DateCreated>
  <DateRevised>
   <Year>2008</Year>
   <Month>05</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>RefSeq NM_005283
  </Note>
  <Frequency>57</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*RECEPTORS, CELL SURFACE (1999-2003)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D043562</DescriptorUI>
     <DescriptorName>
      <String>Receptors, G-Protein-Coupled</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>DNA Cell Biol 1995 Jan;14(1):25-35</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0242131</ConceptUI>
    <ConceptName>
     <String>XCR1 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T545086</TermUI>
      <String>XCR1 protein, human</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>07</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T500382</TermUI>
      <String>CCXCR1 protein, human</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>06</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T545087</TermUI>
      <String>chemokine (C motif) receptor 1, human</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>07</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T545089</TermUI>
      <String>G-protein-coupled receptor 5, human</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>07</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T545088</TermUI>
      <String>XCR1 receptor, human</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>07</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T545090</TermUI>
      <String>CCXCR1 receptor, human</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>07</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C467228</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>homoazanicotine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>10</Month>
   <Day>30</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>10</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>a nicotinic aceytlcholine receptor ligand; structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009538</DescriptorUI>
     <DescriptorName>
      <String>Nicotine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D008024</DescriptorUI>
     <DescriptorName>
      <String>Ligands</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Med Chem 2002 Oct 10;45(21):4724-31</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0441033</ConceptUI>
    <ConceptName>
     <String>homoazanicotine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T524771</TermUI>
      <String>homoazanicotine</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>10</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009720</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-aminobenzenesulfonamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>11</Month>
   <Day>07</Day>
  </DateRevised>
  <Frequency>4</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ANILINE COMPOUNDS (75-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013449</DescriptorUI>
     <DescriptorName>
      <String>Sulfonamides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Il Farm 30(1):47;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054659</ConceptUI>
    <ConceptName>
     <String>2-aminobenzenesulfonamide</String>
    </ConceptName>
    <RegistryNumber>3306-62-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084662</TermUI>
      <String>2-aminobenzenesulfonamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C096315</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>COR19 protein, Poncirus trifoliata</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>11</Month>
   <Day>28</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>10</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>a cold-induced protein; from the hardy citrus relative Poncirus trifoliata; MW 19.8 kDa; amino acid sequence given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010940</DescriptorUI>
     <DescriptorName>
      <String>Plant Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Plant Mol Biol 1995 Oct;29(1):11-23</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0253421</ConceptUI>
    <ConceptName>
     <String>COR19 protein, Poncirus trifoliata</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T283425</TermUI>
      <String>COR19 protein, Poncirus trifoliata</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009730</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bromomalonitrile</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>11</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>oxidizing agent; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>MALONATES (75-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009570</DescriptorUI>
     <DescriptorName>
      <String>Nitriles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem 14(3):498;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054679</ConceptUI>
    <ConceptName>
     <String>bromomalonitrile</String>
    </ConceptName>
    <CASN1Name>Propanedinitrile, bromo-</CASN1Name>
    <RegistryNumber>1885-22-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084682</TermUI>
      <String>bromomalonitrile</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C064701</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-methoxy-3-indolylmethylglucosinolate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1990</Year>
   <Month>07</Month>
   <Day>31</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>09</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>isolated from Moricandia arvensis (Cruciferae); structure given in first source
  </Note>
  <Frequency>8</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005961</DescriptorUI>
     <DescriptorName>
      <String>Glucosinolates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007211</DescriptorUI>
     <DescriptorName>
      <String>Indoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D019607</DescriptorUI>
     <DescriptorName>
      <String>Brassicaceae</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Phytochemistry 1990;29(4):1315</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0178158</ConceptUI>
    <ConceptName>
     <String>1-methoxy-3-indolylmethylglucosinolate</String>
    </ConceptName>
    <RegistryNumber>5187-84-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T208163</TermUI>
      <String>1-methoxy-3-indolylmethylglucosinolate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T208162</TermUI>
      <String>MIMG</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C437803</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>EvxA protein, amphioxus</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>10</Month>
   <Day>24</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>05</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>involved in evolution of the amphioxus (Branchiostoma floridae) midbrain-hindbrain boundary and the chordate tailbud; amino acid sequence in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D018398</DescriptorUI>
     <DescriptorName>
      <String>Homeodomain Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D002816</DescriptorUI>
     <DescriptorName>
      <String>Chordata, Nonvertebrate</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Dev Biol 2001 Sep 15;237(2):270-81</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0403003</ConceptUI>
    <ConceptName>
     <String>EvxA protein, amphioxus</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T467672</TermUI>
      <String>EvxA protein, amphioxus</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>10</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009736</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-(3-carboxy-4-hydroxyphenyl)alanine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>01</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>HYDROXYBENZOIC ACIDS (75-82)</PreviousIndexing>
   <PreviousIndexing>PHENYLALANINE/*analogs (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014443</DescriptorUI>
     <DescriptorName>
      <String>Tyrosine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 381(2):397;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054688</ConceptUI>
    <ConceptName>
     <String>3-(3-carboxy-4-hydroxyphenyl)alanine</String>
    </ConceptName>
    <RegistryNumber>4303-95-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084691</TermUI>
      <String>3-(3-carboxy-4-hydroxyphenyl)alanine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009738</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-(3-carboxyphenyl)alanine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010649</DescriptorUI>
     <DescriptorName>
      <String>Phenylalanine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 381(2):397;1975</Source>
   <Source>Biochim Biophys Acta 542(2):253;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054690</ConceptUI>
    <ConceptName>
     <String>3-(3-carboxyphenyl)alanine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084693</TermUI>
      <String>3-(3-carboxyphenyl)alanine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C095085</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>CXCR5 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1999</Year>
   <Month>11</Month>
   <Day>04</Day>
  </DateCreated>
  <DateRevised>
   <Year>2008</Year>
   <Month>05</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>RefSeq NM_001716
  </Note>
  <Frequency>429</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*GTP-BINDING PROTEINS (1995-1999)</PreviousIndexing>
   <PreviousIndexing>*RECEPTORS, CHEMOKINE (2007)</PreviousIndexing>
   <PreviousIndexing>*RECEPTORS, CYTOKINE (2000-2006)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D054380</DescriptorUI>
     <DescriptorName>
      <String>Receptors, CXCR5</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem J 1995 Aug 1;309( Pt 3):773-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0250433</ConceptUI>
    <ConceptName>
     <String>CXCR5 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T661253</TermUI>
      <String>CXCR5 protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>12</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T661254</TermUI>
      <String>B-lymphocyte chemoattractant receptor, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>12</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T661255</TermUI>
      <String>BCA-1 protein receptor, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>12</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T567332</TermUI>
      <String>monocyte-derived receptor 15 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>01</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T567334</TermUI>
      <String>Burkitt lymphoma receptor 1, GTP binding protein (chemokine (C-X-C motif) receptor 5) protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>01</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T661257</TermUI>
      <String>Burkitt lymphoma receptor 1, GTP binding protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>12</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T661256</TermUI>
      <String>C-X-C chemokine receptor type 5, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>12</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T280438</TermUI>
      <String>MDR15 protein, human</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T567330</TermUI>
      <String>BLR1 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>01</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T567333</TermUI>
      <String>Burkitt lymphoma receptor 1 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>01</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C434938</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>exo-alpha-L-arabinanase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>09</Month>
   <Day>18</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>05</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>catalyzes hydrolysis at the nonreducing terminus of alpha-1,5-L-arabinan to release arabinobiose
  </Note>
  <Frequency>13</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006026</DescriptorUI>
     <DescriptorName>
      <String>Glycoside Hydrolases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Appl Environ Microbiol 2001 Jul;67(7):3319-21</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0398740</ConceptUI>
    <ConceptName>
     <String>exo-alpha-L-arabinanase</String>
    </ConceptName>
    <RegistryNumber>EC 3.2.1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T462183</TermUI>
      <String>exo-alpha-L-arabinanase</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>09</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T639091</TermUI>
      <String>exo-1,5-alpha-L-arabinanase</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>05</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T462456</TermUI>
      <String>exo-arabinanase</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>09</Month>
       <Day>19</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009752</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>epidian</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>7</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004853</DescriptorUI>
     <DescriptorName>
      <String>Epoxy Resins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Immunol Ther Exp 23(1):155;1975</Source>
   <Source>Przegl Dermatol 63(6):775;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054714</ConceptUI>
    <ConceptName>
     <String>epidian</String>
    </ConceptName>
    <RegistryNumber>9087-76-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084717</TermUI>
      <String>epidian</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C531295</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>aplysinoplide B</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2008</Year>
   <Month>09</Month>
   <Day>11</Day>
  </DateCreated>
  <Note>isolated from the marine sponge Aplysinopsis digitata; exhibited cytotoxic activity against P388 mouse leukemia cells; structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D054830</DescriptorUI>
     <DescriptorName>
      <String>Sesterterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2008 Jun;71(6):1089-91</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0524688</ConceptUI>
    <ConceptName>
     <String>aplysinoplide B</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T725533</TermUI>
      <String>aplysinoplide B</String>
      <DateCreated>
       <Year>2008</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2008)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009773</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-methyl-4-(5-amino-2-furyl)thiazole</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>07</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>FURANS (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013844</DescriptorUI>
     <DescriptorName>
      <String>Thiazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Pharmacol 24(2):291;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054765</ConceptUI>
    <ConceptName>
     <String>2-methyl-4-(5-amino-2-furyl)thiazole</String>
    </ConceptName>
    <RegistryNumber>55582-77-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084768</TermUI>
      <String>2-methyl-4-(5-amino-2-furyl)thiazole</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009774</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>10-methylisoalloxazine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>05</Month>
   <Day>29</Day>
  </DateRevised>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*FLAVINS (75-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D012256</DescriptorUI>
     <DescriptorName>
      <String>Riboflavin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 1980;255(8):3472</Source>
   <Source>J Biol Chem 250(3):946;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054766</ConceptUI>
    <ConceptName>
     <String>10-methylisoalloxazine</String>
    </ConceptName>
    <RegistryNumber>4074-58-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084769</TermUI>
      <String>10-methylisoalloxazine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C099100</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SDF4 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>05</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2008</Year>
   <Month>05</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>RefSeq NM_016176
  </Note>
  <Frequency>14</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002135</DescriptorUI>
     <DescriptorName>
      <String>Calcium-Binding Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006023</DescriptorUI>
     <DescriptorName>
      <String>Glycoproteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Cell Biol 1996 Apr;133(2):257-68</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0260204</ConceptUI>
    <ConceptName>
     <String>SDF4 protein, human</String>
    </ConceptName>
    <RegistryNumber>176592-21-5</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0260204</Concept1UI>
     <Concept2UI>M0456734</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0260204</Concept1UI>
     <Concept2UI>M0456733</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T677514</TermUI>
      <String>SDF4 protein, human</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>07</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T560711</TermUI>
      <String>calcium binding protein Cab45 precursor, human</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T677515</TermUI>
      <String>stromal cell derived factor 4 protein, human</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>07</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T290209</TermUI>
      <String>Cab45 protein, human</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0456734</ConceptUI>
    <ConceptName>
     <String>Cab45b protein, human</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0260204</Concept1UI>
     <Concept2UI>M0456734</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T560710</TermUI>
      <String>Cab45b protein, human</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0456733</ConceptUI>
    <ConceptName>
     <String>Cab45a protein, human</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0260204</Concept1UI>
     <Concept2UI>M0456733</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T560709</TermUI>
      <String>Cab45a protein, human</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009870</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>meso-1,2-diphenylethylenediamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>07</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PHENETHYLAMINES (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005029</DescriptorUI>
     <DescriptorName>
      <String>Ethylenediamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Pol Pharm 32(1):1;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054940</ConceptUI>
    <ConceptName>
     <String>meso-1,2-diphenylethylenediamine</String>
    </ConceptName>
    <CASN1Name>1,2-Ethanediamine, 1,2-diphenyl-, (R*,S*)-</CASN1Name>
    <RegistryNumber>5700-60-7</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>16635-95-3 (((R*,R*)-(+-))-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>29841-69-8 ((S-(R*,R*))-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>35132-20-8 ((R-(R*,S*))-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>951-87-1 ((R*,S*)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0054940</Concept1UI>
     <Concept2UI>M0310954</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0054940</Concept1UI>
     <Concept2UI>M0310955</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0054940</Concept1UI>
     <Concept2UI>M0310953</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0054940</Concept1UI>
     <Concept2UI>M0310956</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084943</TermUI>
      <String>meso-1,2-diphenylethylenediamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T084942</TermUI>
      <String>1,2-diamino-1,2-diphenylethane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0310954</ConceptUI>
    <ConceptName>
     <String>meso-1,2-diphenylethylenediamine, (S-(R*,R*))-isomer</String>
    </ConceptName>
    <RegistryNumber>29841-69-8</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0054940</Concept1UI>
     <Concept2UI>M0310954</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T340954</TermUI>
      <String>meso-1,2-diphenylethylenediamine, (S-(R*,R*))-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0310955</ConceptUI>
    <ConceptName>
     <String>meso-1,2-diphenylethylenediamine, (R-(R*,S*))-isomer</String>
    </ConceptName>
    <RegistryNumber>35132-20-8</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0054940</Concept1UI>
     <Concept2UI>M0310955</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T340955</TermUI>
      <String>meso-1,2-diphenylethylenediamine, (R-(R*,S*))-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0310953</ConceptUI>
    <ConceptName>
     <String>meso-1,2-diphenylethylenediamine, ((R*,R*)-(+-))-isomer</String>
    </ConceptName>
    <RegistryNumber>16635-95-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0054940</Concept1UI>
     <Concept2UI>M0310953</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T340953</TermUI>
      <String>meso-1,2-diphenylethylenediamine, ((R*,R*)-(+-))-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0310956</ConceptUI>
    <ConceptName>
     <String>meso-1,2-diphenylethylenediamine, (R*,S*)-isomer</String>
    </ConceptName>
    <RegistryNumber>951-87-1</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0054940</Concept1UI>
     <Concept2UI>M0310956</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T340956</TermUI>
      <String>meso-1,2-diphenylethylenediamine, (R*,S*)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009780</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6,8-dichloro-alpha-((dibutylamino)methyl)naphtho(2,1-b)thiophene-4-methanol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*THIOPHENES (75-79)</PreviousIndexing>
   <PreviousIndexing>ETHANOLAMINES (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009281</DescriptorUI>
     <DescriptorName>
      <String>Naphthalenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 14(3):521;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054776</ConceptUI>
    <ConceptName>
     <String>6,8-dichloro-alpha-((dibutylamino)methyl)naphtho(2,1-b)thiophene-4-methanol</String>
    </ConceptName>
    <RegistryNumber>34861-51-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084779</TermUI>
      <String>6,8-dichloro-alpha-((dibutylamino)methyl)naphtho(2,1-b)thiophene-4-methanol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009781</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>neominophagen C</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>contains above 3 cpds
  </Note>
  <Frequency>13</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003545</DescriptorUI>
     <DescriptorName>
      <String>Cysteine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005998</DescriptorUI>
     <DescriptorName>
      <String>Glycine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009828</DescriptorUI>
     <DescriptorName>
      <String>Oleanolic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D006035</DescriptorUI>
     <DescriptorName>
      <String>Glycyrrhiza</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Jpn J Clin Pathol 22(10):52;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054777</ConceptUI>
    <ConceptName>
     <String>neominophagen C</String>
    </ConceptName>
    <CASN1Name>Olean-12-en-29-oic acid, 3-hydroxy-11-oxo-, (3beta,20beta)-, mixt. with L-cysteine and glycine</CASN1Name>
    <RegistryNumber>70242-82-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084780</TermUI>
      <String>neominophagen C</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009788</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-phenyl-3-methyl-5-sulfanilamidopyrazole</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>06</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SULFANILAMIDES (75-79)</PreviousIndexing>
   <PreviousIndexing>PYRAZOLES (75-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013426</DescriptorUI>
     <DescriptorName>
      <String>Sulfaphenazole</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Il Farmaco 30(1):20;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054790</ConceptUI>
    <ConceptName>
     <String>1-phenyl-3-methyl-5-sulfanilamidopyrazole</String>
    </ConceptName>
    <RegistryNumber>852-19-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084793</TermUI>
      <String>1-phenyl-3-methyl-5-sulfanilamidopyrazole</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T084792</TermUI>
      <String>sulfamethylphenazole</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C113190</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>nucleocapsid protein, Ebola virus</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>07</Month>
   <Day>24</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>12</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>protects mice from lethal challenge; has been sequenced; GenBank AF054908
  </Note>
  <Frequency>16</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D019590</DescriptorUI>
     <DescriptorName>
      <String>Nucleocapsid Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D014765</DescriptorUI>
     <DescriptorName>
      <String>Viral Vaccines</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Virology 1998 Jun 20;246(1):134-44</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0292437</ConceptUI>
    <ConceptName>
     <String>nucleocapsid protein, Ebola virus</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T322442</TermUI>
      <String>nucleocapsid protein, Ebola virus</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C503028</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>aspernigrin A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>08</Month>
   <Day>23</Day>
  </DateCreated>
  <Note>from Cladosporium herbarum IFB-E002; structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004095</DescriptorUI>
     <DescriptorName>
      <String>Dihydropyridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2005 Jul;68(7):1106-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0488273</ConceptUI>
    <ConceptName>
     <String>aspernigrin A</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0488273</Concept1UI>
     <Concept2UI>M0488274</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T649235</TermUI>
      <String>aspernigrin A</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>08</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0488274</ConceptUI>
    <ConceptName>
     <String>6-benzyl-4-oxo-1,4-dihydropyridine-3-carboxamide</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0488273</Concept1UI>
     <Concept2UI>M0488274</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T649236</TermUI>
      <String>6-benzyl-4-oxo-1,4-dihydropyridine-3-carboxamide</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>08</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C493889</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-(2-ethylthio-6-benzthiazolyl)-2-hydroxy-3-bromobenzamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>12</Month>
   <Day>10</Day>
  </DateCreated>
  <Note>an anthelmintic; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001549</DescriptorUI>
     <DescriptorName>
      <String>Benzamides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013844</DescriptorUI>
     <DescriptorName>
      <String>Thiazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Med Parazitol (Mosk). 2004 Jul-Sep;(3):38-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0477477</ConceptUI>
    <ConceptName>
     <String>N-(2-ethylthio-6-benzthiazolyl)-2-hydroxy-3-bromobenzamide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0477477</Concept1UI>
     <Concept2UI>M0477478</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T623256</TermUI>
      <String>N-(2-ethylthio-6-benzthiazolyl)-2-hydroxy-3-bromobenzamide</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>12</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0477478</ConceptUI>
    <ConceptName>
     <String>VIG-01</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0477477</Concept1UI>
     <Concept2UI>M0477478</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T623257</TermUI>
      <String>VIG-01</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>12</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C484327</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2'-benzoyloxycinnamaldehyde</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>04</Month>
   <Day>28</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>04</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>induces apoptosis in cancer cells; possible antineoplastic agent
  </Note>
  <Frequency>21</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000171</DescriptorUI>
     <DescriptorName>
      <String>Acrolein</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001565</DescriptorUI>
     <DescriptorName>
      <String>Benzoates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D017209</DescriptorUI>
     <DescriptorName>
      <String>Apoptosis</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Biol Chem 2004 Feb 20;279(8):6911-20</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0465205</ConceptUI>
    <ConceptName>
     <String>2'-benzoyloxycinnamaldehyde</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T585174</TermUI>
      <String>2'-benzoyloxycinnamaldehyde</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>04</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C419725</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>nardostachysin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateCreated>
  <Note>from the rhizomes of Nardostachys jatamansi; structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013729</DescriptorUI>
     <DescriptorName>
      <String>Terpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Antimicrob Agents Chemother. 2000 Dec;44(12):3381-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0378335</ConceptUI>
    <ConceptName>
     <String>nardostachysin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T435733</TermUI>
      <String>nardostachysin</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>02</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T435734</TermUI>
      <String>7',8'-dihydroxy-4'-methylene hexahydrocyclopenta(c)pyran-1'-one-8'-methyl ester of 7,9-guaiadien-14-oic acid</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>02</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C484325</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-nitrophenyl hexanoate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>04</Month>
   <Day>28</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>04</Month>
   <Day>28</Day>
  </DateRevised>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002208</DescriptorUI>
     <DescriptorName>
      <String>Caproates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009578</DescriptorUI>
     <DescriptorName>
      <String>Nitrobenzenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 2004 Feb 20;279(8):6815-23</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0465203</ConceptUI>
    <ConceptName>
     <String>4-nitrophenyl hexanoate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T585171</TermUI>
      <String>4-nitrophenyl hexanoate</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>04</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T585188</TermUI>
      <String>p-nitrophenyl hexanoate</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>04</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C493890</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-(2-ethylthio-6-benzoxazolyl)-2-hydroxy-3,5-dibromobenzamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>12</Month>
   <Day>10</Day>
  </DateCreated>
  <Note>an anthelmintic; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001549</DescriptorUI>
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      <String>Benzamides</String>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001583</DescriptorUI>
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      <String>Benzoxazoles</String>
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  <SourceList>
   <Source>Med Parazitol (Mosk). 2004 Jul-Sep;(3):38-9</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0477479</ConceptUI>
    <ConceptName>
     <String>N-(2-ethylthio-6-benzoxazolyl)-2-hydroxy-3,5-dibromobenzamide</String>
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    <RegistryNumber>0</RegistryNumber>
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      <TermUI>T623258</TermUI>
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       <Year>2004</Year>
       <Month>12</Month>
       <Day>10</Day>
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       <ThesaurusID>NLM (2004)</ThesaurusID>
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   <Concept PreferredConceptYN="N">
    <ConceptUI>M0477480</ConceptUI>
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     <Concept1UI>M0477479</Concept1UI>
     <Concept2UI>M0477480</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T623259</TermUI>
      <String>VIG-02</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>12</Month>
       <Day>10</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C400536</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>silaffin 1B</String>
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  <DateCreated>
   <Year>1999</Year>
   <Month>11</Month>
   <Day>30</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>08</Month>
   <Day>23</Day>
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  <Note>involved in silica nanosphere formation in diatoms; derived from Sil1 protein
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  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PROTEINS (1999-2005)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010455</DescriptorUI>
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  <SourceList>
   <Source>Science 1999 Nov 5;286(5442):1129-32</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0351324</ConceptUI>
    <ConceptName>
     <String>silaffin 1B</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T401077</TermUI>
      <String>silaffin 1B</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>11</Month>
       <Day>30</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T401078</TermUI>
      <String>silaffin-1B</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>11</Month>
       <Day>30</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C503029</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>gesashidine A</String>
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  <DateCreated>
   <Year>2005</Year>
   <Month>08</Month>
   <Day>23</Day>
  </DateCreated>
  <Note>beta-carboline alkaloid with an imidazole ring from a Thorectidae sponge; structure in first source
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002243</DescriptorUI>
     <DescriptorName>
      <String>Carbolines</String>
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   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007093</DescriptorUI>
     <DescriptorName>
      <String>Imidazoles</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2005 Jul;68(7):1109-10</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0488275</ConceptUI>
    <ConceptName>
     <String>gesashidine A</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T649237</TermUI>
      <String>gesashidine A</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>08</Month>
       <Day>23</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
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   </Concept>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013388</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>acetylpyrrolidinecholine</String>
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  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>10</Month>
   <Day>31</Day>
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  <Note>structure
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  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ACETYLCHOLINE/*analogs (77-81)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011759</DescriptorUI>
     <DescriptorName>
      <String>Pyrrolidines</String>
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    </DescriptorReferredTo>
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  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Pharmacol 296:153;1977</Source>
   <Source>Naunyn Schmiedeberg Arch Pharm 295(1):81;1976</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061126</ConceptUI>
    <ConceptName>
     <String>acetylpyrrolidinecholine</String>
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    <RegistryNumber>54377-96-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091129</TermUI>
      <String>acetylpyrrolidinecholine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C400709</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Tifacogin</String>
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  <DateCreated>
   <Year>1999</Year>
   <Month>12</Month>
   <Day>03</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>08</Month>
   <Day>23</Day>
  </DateRevised>
  <Note>a recombinant form of tissue factor pathway inhibitor, RN &amp; amino acid sequence in first source; MW about 32 kDa
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  <Frequency>13</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011506</DescriptorUI>
     <DescriptorName>
      <String>Proteins</String>
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    </DescriptorReferredTo>
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  </HeadingMappedToList>
  <SourceList>
   <Source>Clin Pharmacol Ther 1999 Nov;66(5):543</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0352035</ConceptUI>
    <ConceptName>
     <String>Tifacogin</String>
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    <RegistryNumber>148883-56-1</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0352035</Concept1UI>
     <Concept2UI>M0488276</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="TRD"  RecordPreferredTermYN="Y">
      <TermUI>T401460</TermUI>
      <String>Tifacogin</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>12</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0488276</ConceptUI>
    <ConceptName>
     <String>SC-59735</String>
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    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0352035</Concept1UI>
     <Concept2UI>M0488276</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T401461</TermUI>
      <String>SC-59735</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>12</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C581182</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-dodecyl-6-methoxycyclohexa-2,5-diene-1,4-dione</String>
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  <DateCreated>
   <Year>2013</Year>
   <Month>05</Month>
   <Day>21</Day>
  </DateCreated>
  <Note>isolated from Averrhoa carambola L. (Oxalidaceae) roots; structure in first source
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  <Frequency>11</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D053138</DescriptorUI>
     <DescriptorName>
      <String>Cyclohexenes</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D017127</DescriptorUI>
     <DescriptorName>
      <String>Glycation End Products, Advanced</String>
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     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
     <QualifierName>
      <String>antagonists &amp; inhibitors</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Toxicol Lett. 2013 May 10;219(1):77-84</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0584915</ConceptUI>
    <ConceptName>
     <String>2-dodecyl-6-methoxycyclohexa-2,5-diene-1,4-dione</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T844456</TermUI>
      <String>2-dodecyl-6-methoxycyclohexa-2,5-diene-1,4-dione</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>05</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T844457</TermUI>
      <String>DMDD compound</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>05</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013400</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6-aminouracil</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>24</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014498</DescriptorUI>
     <DescriptorName>
      <String>Uracil</String>
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    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Chem Soc(Perkin Trans) 22:2398;1976</Source>
   <Source>J Pharm Soc Jap 97(8):906;1977</Source>
   <Source>J Pharm Soc Jpn 97(2):202;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061155</ConceptUI>
    <ConceptName>
     <String>6-aminouracil</String>
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    <RegistryNumber>873-83-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091158</TermUI>
      <String>6-aminouracil</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013402</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>aplysistatin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>04</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>from sea hare (Mollusca, Aplysiidae); structure
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  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012717</DescriptorUI>
     <DescriptorName>
      <String>Sesquiterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Am Chem Soc 99(1):262;1976</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061158</ConceptUI>
    <ConceptName>
     <String>aplysistatin</String>
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    <RegistryNumber>62003-89-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091161</TermUI>
      <String>aplysistatin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013408</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>benziloyltropine methyliodide</String>
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  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>11</Month>
   <Day>28</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BENZILATES (77-81)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014326</DescriptorUI>
     <DescriptorName>
      <String>Tropanes</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Brit J Pharmacol 58(1):57;1976</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061166</ConceptUI>
    <ConceptName>
     <String>benziloyltropine methyliodide</String>
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    <CASN1Name>8-Azoniabicyclo(3.2.1)octane, 3-((hydroxydiphenylacetyl)oxy)-8,8-dimethyl-, iodide, endo-</CASN1Name>
    <RegistryNumber>21735-94-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091169</TermUI>
      <String>benziloyltropine methyliodide</String>
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       <ThesaurusID>NLM (1977)</ThesaurusID>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C581187</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>MIRN276 microRNA, Drosophila</String>
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  <DateCreated>
   <Year>2013</Year>
   <Month>05</Month>
   <Day>21</Day>
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  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D035683</DescriptorUI>
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      <String>MicroRNAs</String>
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  <SourceList>
   <Source>J Neurosci. 2013 Mar 27;33(13):5821-33</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0584920</ConceptUI>
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     <String>MIRN276 microRNA, Drosophila</String>
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    <RegistryNumber>0</RegistryNumber>
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      <DateCreated>
       <Year>2013</Year>
       <Month>05</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
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      <String>miR-276, Drosophila</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>05</Month>
       <Day>21</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T844467</TermUI>
      <String>miRNA276, Drosophila</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>05</Month>
       <Day>21</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T844465</TermUI>
      <String>dme-mir-276</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>05</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
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      <String>microRNA-276, Drosophila</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>05</Month>
       <Day>21</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
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   <Concept PreferredConceptYN="N">
    <ConceptUI>M0584921</ConceptUI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T844469</TermUI>
      <String>microRNA-276a, Drosophila</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>05</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013410</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-benzoyl-D-glucosamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005944</DescriptorUI>
     <DescriptorName>
      <String>Glucosamine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Antimicrob Ag Chemother 10(5):786;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061168</ConceptUI>
    <ConceptName>
     <String>N-benzoyl-D-glucosamine</String>
    </ConceptName>
    <RegistryNumber>655-42-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091171</TermUI>
      <String>N-benzoyl-D-glucosamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013413</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,3-bis(acetylmercaptomethyl)quinoxaline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011810</DescriptorUI>
     <DescriptorName>
      <String>Quinoxalines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Intervirol 6:285;1975-76</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061172</ConceptUI>
    <ConceptName>
     <String>2,3-bis(acetylmercaptomethyl)quinoxaline</String>
    </ConceptName>
    <CASN1Name>Ethanethioic acid, S,S'-(2,3-quinoxalinediylbis(methylene)) ester</CASN1Name>
    <RegistryNumber>36014-40-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091175</TermUI>
      <String>2,3-bis(acetylmercaptomethyl)quinoxaline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013414</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bis(bis(2-pyridyl)disulfide)copper(I)perchlorate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>12</Month>
   <Day>30</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ORGANOMETALLIC COMPOUNDS (77-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011725</DescriptorUI>
     <DescriptorName>
      <String>Pyridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Am Chem Soc 98(24):7569;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061173</ConceptUI>
    <ConceptName>
     <String>bis(bis(2-pyridyl)disulfide)copper(I)perchlorate</String>
    </ConceptName>
    <CASN1Name>Copper(1+), (2,2'-dithiobis(pyridine))(2,2'-dithiobis(pyridine)-N,N')-, (T-4)-, perchlorate</CASN1Name>
    <RegistryNumber>58659-46-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091176</TermUI>
      <String>bis(bis(2-pyridyl)disulfide)copper(I)perchlorate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013416</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,1-bis(diazoacetyl)-2-phenylethane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>11</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AZO CPDS (77-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003979</DescriptorUI>
     <DescriptorName>
      <String>Diazonium Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Molec Basis Malignancy QZ 202 M718:97;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061176</ConceptUI>
    <ConceptName>
     <String>1,1-bis(diazoacetyl)-2-phenylethane</String>
    </ConceptName>
    <RegistryNumber>35807-86-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091179</TermUI>
      <String>1,1-bis(diazoacetyl)-2-phenylethane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013419</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bromoacetylaminoisophthalic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>13</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010795</DescriptorUI>
     <DescriptorName>
      <String>Phthalic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D013439</DescriptorUI>
     <DescriptorName>
      <String>Sulfhydryl Reagents</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>FEBS Lett 70(1):76;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061187</ConceptUI>
    <ConceptName>
     <String>bromoacetylaminoisophthalic acid</String>
    </ConceptName>
    <RegistryNumber>61389-10-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091190</TermUI>
      <String>bromoacetylaminoisophthalic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013420</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bromoacetylsulfanilic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BENZENESULFONATES/analogs (77-82)</PreviousIndexing>
   <PreviousIndexing>*SULFANILIC ACID/analogs (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013425</DescriptorUI>
     <DescriptorName>
      <String>Sulfanilic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D013439</DescriptorUI>
     <DescriptorName>
      <String>Sulfhydryl Reagents</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>FEBS Lett 70(1):76;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061188</ConceptUI>
    <ConceptName>
     <String>bromoacetylsulfanilic acid</String>
    </ConceptName>
    <RegistryNumber>61389-09-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091191</TermUI>
      <String>bromoacetylsulfanilic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C581188</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>(S)-chloro-1-(2-thienyl)-1-propanol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>05</Month>
   <Day>21</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013876</DescriptorUI>
     <DescriptorName>
      <String>Thiophenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D020005</DescriptorUI>
     <DescriptorName>
      <String>Propanols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Appl Biochem Biotechnol. 2012 Dec;168(8):2297-308</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0584922</ConceptUI>
    <ConceptName>
     <String>(S)-chloro-1-(2-thienyl)-1-propanol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T844470</TermUI>
      <String>(S)-chloro-1-(2-thienyl)-1-propanol</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>05</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013423</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-(2-bromo-1,2-diphenylvinyl)anisole</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013267</DescriptorUI>
     <DescriptorName>
      <String>Stilbenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 65(10):1545;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061191</ConceptUI>
    <ConceptName>
     <String>4-(2-bromo-1,2-diphenylvinyl)anisole</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091194</TermUI>
      <String>4-(2-bromo-1,2-diphenylvinyl)anisole</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013424</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-(2-bromo-1,2-diphenylvinyl)phenol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013267</DescriptorUI>
     <DescriptorName>
      <String>Stilbenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 65(10):1545;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061192</ConceptUI>
    <ConceptName>
     <String>4-(2-bromo-1,2-diphenylvinyl)phenol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091195</TermUI>
      <String>4-(2-bromo-1,2-diphenylvinyl)phenol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013432</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>catalponol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009284</DescriptorUI>
     <DescriptorName>
      <String>Naphthols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Pharm 309(10):829;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061205</ConceptUI>
    <ConceptName>
     <String>catalponol</String>
    </ConceptName>
    <CASN1Name>(3R,4S)-4-hydroxy-3-(2'-isopentenyl)-1,2,3,4-tetrahydronaphthalen-1-one</CASN1Name>
    <RegistryNumber>34168-56-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091208</TermUI>
      <String>catalponol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013435</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-chloro-4-cyclohexylphenylglycolic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006016</DescriptorUI>
     <DescriptorName>
      <String>Glycolates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 65(11):1686;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061211</ConceptUI>
    <ConceptName>
     <String>3-chloro-4-cyclohexylphenylglycolic acid</String>
    </ConceptName>
    <RegistryNumber>57992-89-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091214</TermUI>
      <String>3-chloro-4-cyclohexylphenylglycolic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013443</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>C.I. acid black 107</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>01</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>azo dye-metal complex used in hair colorants
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001391</DescriptorUI>
     <DescriptorName>
      <String>Azo Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Inserm Symp Ser 52; IARC 13 Environ Poll Carcin Risk: 263;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061220</ConceptUI>
    <ConceptName>
     <String>C.I. acid black 107</String>
    </ConceptName>
    <RegistryNumber>12218-96-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091223</TermUI>
      <String>C.I. acid black 107</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013450</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>corchoroside A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>from Adonis mongolica Sim.
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*GLYCOSIDES (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002298</DescriptorUI>
     <DescriptorName>
      <String>Cardenolides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D002301</DescriptorUI>
     <DescriptorName>
      <String>Cardiac Glycosides</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Acta Pharm Sinica 1979;14(3):267</Source>
   <Source>Farmatsiia 27(3):28;1978</Source>
   <Source>Pharmazie 31(8):565;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061228</ConceptUI>
    <ConceptName>
     <String>corchoroside A</String>
    </ConceptName>
    <RegistryNumber>508-76-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091231</TermUI>
      <String>corchoroside A</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013454</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>crotocin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>10</Month>
   <Day>14</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*MYCOTOXINS (77-78)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014255</DescriptorUI>
     <DescriptorName>
      <String>Trichothecenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 454(2):273;1976</Source>
   <Source>Poultry Sci 57(3):807;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061237</ConceptUI>
    <ConceptName>
     <String>crotocin</String>
    </ConceptName>
    <CASN1Name>NSC 145,414</CASN1Name>
    <RegistryNumber>21284-11-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091240</TermUI>
      <String>crotocin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013456</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-cyanomethylpyridinium iodide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>NAD model compound; structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011726</DescriptorUI>
     <DescriptorName>
      <String>Pyridinium Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 41(25):3967;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061239</ConceptUI>
    <ConceptName>
     <String>3-cyanomethylpyridinium iodide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091242</TermUI>
      <String>3-cyanomethylpyridinium iodide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013458</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cyclohexanone phenylhydrazone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003512</DescriptorUI>
     <DescriptorName>
      <String>Cyclohexanones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 65(11):1639;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061243</ConceptUI>
    <ConceptName>
     <String>cyclohexanone phenylhydrazone</String>
    </ConceptName>
    <RegistryNumber>946-82-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091246</TermUI>
      <String>cyclohexanone phenylhydrazone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014265</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>EG 467</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>phthalazinol cpd
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PHOSPHODIESTERASE/*antag (77-78)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010793</DescriptorUI>
     <DescriptorName>
      <String>Phthalazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Jpn J Pharmacol 27:97;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062665</ConceptUI>
    <ConceptName>
     <String>EG 467</String>
    </ConceptName>
    <RegistryNumber>56748-21-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T092668</TermUI>
      <String>EG 467</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T092667</TermUI>
      <String>EG-467</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C082348</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>des(Glu(84))-calmodulin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1993</Year>
   <Month>08</Month>
   <Day>25</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>06</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>a calmodulin mutant lacking Glu-84
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002147</DescriptorUI>
     <DescriptorName>
      <String>Calmodulin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Proc Natl Acad Sci U S A 1993 Jul 15;90(14):6869-73</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0219446</ConceptUI>
    <ConceptName>
     <String>des(Glu(84))-calmodulin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T249451</TermUI>
      <String>des(Glu(84))-calmodulin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T249449</TermUI>
      <String>calmodulin des(Glu(84))</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T249450</TermUI>
      <String>des(glutamyl(84))calmodulin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013467</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-deaza-6-thioguanine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013866</DescriptorUI>
     <DescriptorName>
      <String>Thioguanine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 41(24):3784;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061256</ConceptUI>
    <ConceptName>
     <String>1-deaza-6-thioguanine</String>
    </ConceptName>
    <RegistryNumber>60282-76-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091259</TermUI>
      <String>1-deaza-6-thioguanine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013468</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>deisovalerylblastmycin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000968</DescriptorUI>
     <DescriptorName>
      <String>Antimycin A</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiot 29(8):804;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061257</ConceptUI>
    <ConceptName>
     <String>deisovalerylblastmycin</String>
    </ConceptName>
    <CASN1Name>Benzamide, N-(7-butyl-8-hydroxy-4,9-dimethyl-2,6-dioxo-1,5-dioxonan-3-yl)-3-(formylamino)-2-hydroxy-, (3S-(3R*,4S*,7S*,8S*,9R*))-</CASN1Name>
    <RegistryNumber>60504-95-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091260</TermUI>
      <String>deisovalerylblastmycin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013519</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>9,10-epoxystearic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>RN given refers to parent cpd with unspecified isomeric designation; structure
  </Note>
  <Frequency>30</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>EPOXY COMPOUNDS (77-84)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013229</DescriptorUI>
     <DescriptorName>
      <String>Stearic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Bull Environ Contam Toxicol 1979;22(4-5):462</Source>
   <Source>IARC Monogr Eval Carcinog Risk Chem Man 11:153;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061322</ConceptUI>
    <ConceptName>
     <String>9,10-epoxystearic acid</String>
    </ConceptName>
    <CASN1Name>cis-3-octyloxiraneoctanoic acid</CASN1Name>
    <RegistryNumber>2443-39-2</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>13980-07-9 ((trans)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>2060-05-1 (Na salt)</RelatedRegistryNumber>
     <RelatedRegistryNumber>24560-98-3 ((cis)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>57384-08-4 (K salt)</RelatedRegistryNumber>
     <RelatedRegistryNumber>61792-39-0 (NH4 salt)</RelatedRegistryNumber>
     <RelatedRegistryNumber>71567-96-9 (14C-acid)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061322</Concept1UI>
     <Concept2UI>M0312204</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061322</Concept1UI>
     <Concept2UI>M0312208</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061322</Concept1UI>
     <Concept2UI>M0312207</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061322</Concept1UI>
     <Concept2UI>M0312205</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061322</Concept1UI>
     <Concept2UI>M0312206</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061322</Concept1UI>
     <Concept2UI>M0312209</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091325</TermUI>
      <String>9,10-epoxystearic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T091323</TermUI>
      <String>9,10-epoxyoctadecanoic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312204</ConceptUI>
    <ConceptName>
     <String>9,10-epoxystearic acid, (trans)-isomer</String>
    </ConceptName>
    <RegistryNumber>13980-07-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061322</Concept1UI>
     <Concept2UI>M0312204</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342204</TermUI>
      <String>9,10-epoxystearic acid, (trans)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312208</ConceptUI>
    <ConceptName>
     <String>9,10-epoxystearic acid, ammonium salt</String>
    </ConceptName>
    <RegistryNumber>61792-39-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061322</Concept1UI>
     <Concept2UI>M0312208</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342208</TermUI>
      <String>9,10-epoxystearic acid, ammonium salt</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312207</ConceptUI>
    <ConceptName>
     <String>9,10-epoxystearic acid, potassium salt</String>
    </ConceptName>
    <RegistryNumber>57384-08-4</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061322</Concept1UI>
     <Concept2UI>M0312207</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342207</TermUI>
      <String>9,10-epoxystearic acid, potassium salt</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312205</ConceptUI>
    <ConceptName>
     <String>9,10-epoxystearic acid, sodium salt</String>
    </ConceptName>
    <RegistryNumber>2060-05-1</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061322</Concept1UI>
     <Concept2UI>M0312205</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342205</TermUI>
      <String>9,10-epoxystearic acid, sodium salt</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312206</ConceptUI>
    <ConceptName>
     <String>9,10-epoxystearic acid, (cis)-isomer</String>
    </ConceptName>
    <RegistryNumber>24560-98-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061322</Concept1UI>
     <Concept2UI>M0312206</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342206</TermUI>
      <String>9,10-epoxystearic acid, (cis)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T091324</TermUI>
      <String>cis-9,10-epoxystearic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312209</ConceptUI>
    <ConceptName>
     <String>9,10-epoxystearic acid, 14C-acid</String>
    </ConceptName>
    <RegistryNumber>71567-96-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061322</Concept1UI>
     <Concept2UI>M0312209</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342209</TermUI>
      <String>9,10-epoxystearic acid, 14C-acid</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C103776</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>trabecular meshwork-induced glucocorticoid response protein</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1997</Year>
   <Month>02</Month>
   <Day>12</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>06</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>encodes a trabecular meshwork protein; causes primary open angle glaucoma; amino acid sequence known; GenBank R95491; RefSeq NM_000261 (human), NM_010865 (mouse), NM_030865 (rat)
  </Note>
  <Frequency>596</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003598</DescriptorUI>
     <DescriptorName>
      <String>Cytoskeletal Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005136</DescriptorUI>
     <DescriptorName>
      <String>Eye Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006023</DescriptorUI>
     <DescriptorName>
      <String>Glycoproteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D005901</DescriptorUI>
     <DescriptorName>
      <String>Glaucoma</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D014129</DescriptorUI>
     <DescriptorName>
      <String>Trabecular Meshwork</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D016350</DescriptorUI>
     <DescriptorName>
      <String>Leucine Zippers</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Science 1996 Jan 31;275(5300):668-70</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0271248</ConceptUI>
    <ConceptName>
     <String>trabecular meshwork-induced glucocorticoid response protein</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0271248</Concept1UI>
     <Concept2UI>M0486102</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0271248</Concept1UI>
     <Concept2UI>M0486100</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0271248</Concept1UI>
     <Concept2UI>M0486101</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T301253</TermUI>
      <String>trabecular meshwork-induced glucocorticoid response protein</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T643778</TermUI>
      <String>MYOC protein</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>06</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T643777</TermUI>
      <String>GLC1A protein</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>06</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T301250</TermUI>
      <String>TIGR protein</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T301251</TermUI>
      <String>myocilin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0486102</ConceptUI>
    <ConceptName>
     <String>Myoc protein, rat</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0271248</Concept1UI>
     <Concept2UI>M0486102</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T643787</TermUI>
      <String>Myoc protein, rat</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>06</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T643788</TermUI>
      <String>myocilin protein, rat</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>06</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0486100</ConceptUI>
    <ConceptName>
     <String>MYOC protein, human</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0271248</Concept1UI>
     <Concept2UI>M0486100</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T643779</TermUI>
      <String>MYOC protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>06</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T643781</TermUI>
      <String>GLC1A protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>06</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T643782</TermUI>
      <String>TIGR protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>06</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T643780</TermUI>
      <String>myocilin, trabecular meshwork inducible glucocorticoid response protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>06</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0486101</ConceptUI>
    <ConceptName>
     <String>Myoc protein, mouse</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0271248</Concept1UI>
     <Concept2UI>M0486101</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T643783</TermUI>
      <String>Myoc protein, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>06</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T643784</TermUI>
      <String>myocilin protein, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>06</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T643785</TermUI>
      <String>GLC1A protein, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>06</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T643786</TermUI>
      <String>TIGR protein, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>06</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C073879</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>calmodulin-diazopyruvamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1992</Year>
   <Month>05</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>12</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002147</DescriptorUI>
     <DescriptorName>
      <String>Calmodulin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011773</DescriptorUI>
     <DescriptorName>
      <String>Pyruvates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 1992 Mar 25;267(9):5847-54</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0199605</ConceptUI>
    <ConceptName>
     <String>calmodulin-diazopyruvamide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0199605</Concept1UI>
     <Concept2UI>M0199603</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T229610</TermUI>
      <String>calmodulin-diazopyruvamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T229609</TermUI>
      <String>CaM-DAP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0199603</ConceptUI>
    <ConceptName>
     <String>125I-CaM-DAP</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0199605</Concept1UI>
     <Concept2UI>M0199603</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T229608</TermUI>
      <String>125I-CaM-DAP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013476</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-diazoacetyl-L-phenylalanine-3-phenylpropylamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>09</Month>
   <Day>16</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>AZO COMPOUNDS (77-80)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010649</DescriptorUI>
     <DescriptorName>
      <String>Phenylalanine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem J 1979;183(2):389</Source>
   <Source>Biochem Soc Trans 4(4):643;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061278</ConceptUI>
    <ConceptName>
     <String>N-diazoacetyl-L-phenylalanine-3-phenylpropylamide</String>
    </ConceptName>
    <CASN1Name>Benzenepropanamide, alpha-((diazoacetyl)amino)-N-(3-phenylpropyl)-, (S)-</CASN1Name>
    <RegistryNumber>61715-45-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091281</TermUI>
      <String>N-diazoacetyl-L-phenylalanine-3-phenylpropylamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C033443</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>EDTAC</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>24</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>used for enlargement of narrow root canals &amp; cleansing of instrumental dentinal walls
  </Note>
  <Frequency>23</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004492</DescriptorUI>
     <DescriptorName>
      <String>Edetic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Oral Surg 1982;53(1):74</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0103729</ConceptUI>
    <ConceptName>
     <String>EDTAC</String>
    </ConceptName>
    <RegistryNumber>66458-09-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T133733</TermUI>
      <String>EDTAC</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013482</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dichlorobutadiene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002070</DescriptorUI>
     <DescriptorName>
      <String>Butadienes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Gig Sanit 8:96;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061282</ConceptUI>
    <ConceptName>
     <String>dichlorobutadiene</String>
    </ConceptName>
    <RegistryNumber>28577-62-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091285</TermUI>
      <String>dichlorobutadiene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C419842</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bradykinin (2-9)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>12</Day>
  </DateCreated>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001920</DescriptorUI>
     <DescriptorName>
      <String>Bradykinin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010446</DescriptorUI>
     <DescriptorName>
      <String>Peptide Fragments</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Brain Res. 2000 Dec 15;886(1-2):67-72</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0378490</ConceptUI>
    <ConceptName>
     <String>bradykinin (2-9)</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T435971</TermUI>
      <String>bradykinin (2-9)</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>02</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C486998</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ancistrotanzanine C</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>06</Month>
   <Day>16</Day>
  </DateCreated>
  <Note>naphthylisoquinoline alkaloid from Ancistrocladus tanzaniensis; structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007546</DescriptorUI>
     <DescriptorName>
      <String>Isoquinolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2004 May;67(5):743-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0467546</ConceptUI>
    <ConceptName>
     <String>ancistrotanzanine C</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T591598</TermUI>
      <String>ancistrotanzanine C</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>06</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013492</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dihydrothobainone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*THEBAINE DERIVATIVES (77-78)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013797</DescriptorUI>
     <DescriptorName>
      <String>Thebaine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 19(10):1171;1976</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061296</ConceptUI>
    <ConceptName>
     <String>dihydrothobainone</String>
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    <RegistryNumber>847-86-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091299</TermUI>
      <String>dihydrothobainone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
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     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013496</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>7,7'-dihydroxypelentanic acid</String>
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  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <Frequency>0</Frequency>
  <HeadingMappedToList>
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    <DescriptorReferredTo>
     <DescriptorUI>*D014468</DescriptorUI>
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      <String>Umbelliferones</String>
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    </DescriptorReferredTo>
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  </HeadingMappedToList>
  <SourceList>
   <Source>Cesk Farm 25(7):236;1976</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061298</ConceptUI>
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    <RegistryNumber>50966-80-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091301</TermUI>
      <String>7,7'-dihydroxypelentanic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013498</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dimethylbenzacridines</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1987</Year>
   <Month>08</Month>
   <Day>07</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BENZACRIDINE/analogs</PreviousIndexing>
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  <HeadingMappedToList>
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    <DescriptorReferredTo>
     <DescriptorUI>*D000166</DescriptorUI>
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      <String>Acridines</String>
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  <SourceList>
   <Source>J Chem Soc(Perkin I); 2277</Source>
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      <TermUI>T091302</TermUI>
      <String>dimethylbenzacridines</String>
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       <ThesaurusID>NLM (1977)</ThesaurusID>
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     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013996</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-formylpyridine thiosemicarbazone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>structure; RN given refers to parent cpd without isomeric designation
  </Note>
  <Frequency>16</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PYRIDINES</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013882</DescriptorUI>
     <DescriptorName>
      <String>Thiosemicarbazones</String>
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   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 20(3):447;1977</Source>
   <Source>Mol Pharmacol 13(1):89;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062207</ConceptUI>
    <ConceptName>
     <String>2-formylpyridine thiosemicarbazone</String>
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    <RegistryNumber>3608-75-1</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>2260-14-2 (mono-HCl)</RelatedRegistryNumber>
     <RelatedRegistryNumber>61043-10-5 ((E)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>61043-11-6 ((Z)-isomer)</RelatedRegistryNumber>
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    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062207</Concept1UI>
     <Concept2UI>M0312373</Concept2UI>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062207</Concept1UI>
     <Concept2UI>M0312371</Concept2UI>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062207</Concept1UI>
     <Concept2UI>M0312372</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
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      <TermUI>T092210</TermUI>
      <String>2-formylpyridine thiosemicarbazone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T092209</TermUI>
      <String>pyridine-2-carboxaldehyde thiosemicarbazone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T092208</TermUI>
      <String>Pyr-2-CTS</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312373</ConceptUI>
    <ConceptName>
     <String>2-formylpyridine thiosemicarbazone, (Z)-isomer</String>
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    <RegistryNumber>61043-11-6</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062207</Concept1UI>
     <Concept2UI>M0312373</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342373</TermUI>
      <String>2-formylpyridine thiosemicarbazone, (Z)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312371</ConceptUI>
    <ConceptName>
     <String>2-formylpyridine thiosemicarbazone, monohydrochloride</String>
    </ConceptName>
    <RegistryNumber>2260-14-2</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062207</Concept1UI>
     <Concept2UI>M0312371</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342371</TermUI>
      <String>2-formylpyridine thiosemicarbazone, monohydrochloride</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312372</ConceptUI>
    <ConceptName>
     <String>2-formylpyridine thiosemicarbazone, (E)-isomer</String>
    </ConceptName>
    <RegistryNumber>61043-10-5</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062207</Concept1UI>
     <Concept2UI>M0312372</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342372</TermUI>
      <String>2-formylpyridine thiosemicarbazone, (E)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013500</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,2-dimethyl-2,3-dihydrobenzofuranyl-7-N-dimethoxyphosphinothioyl-N-methylcarbamate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009946</DescriptorUI>
     <DescriptorName>
      <String>Organothiophosphorus Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Environ Contam Toxicol 4(4):483;1976</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061302</ConceptUI>
    <ConceptName>
     <String>2,2-dimethyl-2,3-dihydrobenzofuranyl-7-N-dimethoxyphosphinothioyl-N-methylcarbamate</String>
    </ConceptName>
    <CASN1Name>(dimethoxyphosphinothioyl)methylcarbamic acid 2,3-dihydro-2,2-dimethyl-7-benzofuranyl ester</CASN1Name>
    <RegistryNumber>28789-80-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091305</TermUI>
      <String>2,2-dimethyl-2,3-dihydrobenzofuranyl-7-N-dimethoxyphosphinothioyl-N-methylcarbamate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C046470</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>MDL 19744A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1985</Year>
   <Month>10</Month>
   <Day>15</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>RN &amp; structure given in first source; RN given refers to (+-)-free base
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013876</DescriptorUI>
     <DescriptorName>
      <String>Thiophenes</String>
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    </DescriptorReferredTo>
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  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 1985;28(9):1142</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0134619</ConceptUI>
    <ConceptName>
     <String>MDL 19744A</String>
    </ConceptName>
    <RegistryNumber>97233-26-6</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>97275-04-2 ((+-)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0134619</Concept1UI>
     <Concept2UI>M0134617</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0134619</Concept1UI>
     <Concept2UI>M0322455</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T164624</TermUI>
      <String>MDL 19744A</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T164623</TermUI>
      <String>MDL-19,744A</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0134617</ConceptUI>
    <ConceptName>
     <String>6,7-dihydro-5-(((2-hydroxy-3-phenoxycyclopentyl)amino)methyl)-2-methylbenzo(b)thiophen-4(5H)-one</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0134619</Concept1UI>
     <Concept2UI>M0134617</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T164622</TermUI>
      <String>6,7-dihydro-5-(((2-hydroxy-3-phenoxycyclopentyl)amino)methyl)-2-methylbenzo(b)thiophen-4(5H)-one</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0322455</ConceptUI>
    <ConceptName>
     <String>MDL 19744A, (+-)-isomer</String>
    </ConceptName>
    <RegistryNumber>97275-04-2</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0134619</Concept1UI>
     <Concept2UI>M0322455</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T352455</TermUI>
      <String>MDL 19744A, (+-)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C094435</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>GEA 5016</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>20</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014230</DescriptorUI>
     <DescriptorName>
      <String>Triazoles</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>J Physiol Pharmacol 1995 Mar;46(1):37-44</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0248818</ConceptUI>
    <ConceptName>
     <String>GEA 5016</String>
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    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0248818</Concept1UI>
     <Concept2UI>M0248815</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T278823</TermUI>
      <String>GEA 5016</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T278822</TermUI>
      <String>GEA5016</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T278821</TermUI>
      <String>GEA-5016</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0248815</ConceptUI>
    <ConceptName>
     <String>1,2,3,4-oxatriazolum, 5-amino-3-(4-chloro-3-(trifluoromethyl)phenyl)chloride</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0248818</Concept1UI>
     <Concept2UI>M0248815</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T278820</TermUI>
      <String>1,2,3,4-oxatriazolum, 5-amino-3-(4-chloro-3-(trifluoromethyl)phenyl)chloride</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C096807</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>LmrP protein, Lactococcus lactis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>12</Month>
   <Day>20</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>10</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>a proton motive force-dependent drug transporter; from Lactococcus lactis; has 408 amino acid residues; amino acid sequence given in first source; GenBank X89779
  </Note>
  <Frequency>31</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D026901</DescriptorUI>
     <DescriptorName>
      <String>Membrane Transport Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 1995 Nov 3;270(44):26092-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0254577</ConceptUI>
    <ConceptName>
     <String>LmrP protein, Lactococcus lactis</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T463693</TermUI>
      <String>LmrP protein, Lactococcus lactis</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>09</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C094434</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>GEA 3198</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>20</Day>
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014230</DescriptorUI>
     <DescriptorName>
      <String>Triazoles</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>J Physiol Pharmacol 1995 Mar;46(1):37-44</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0248814</ConceptUI>
    <ConceptName>
     <String>GEA 3198</String>
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    <RegistryNumber>0</RegistryNumber>
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     <Concept1UI>M0248814</Concept1UI>
     <Concept2UI>M0248811</Concept2UI>
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       <ThesaurusID>NLM (1995)</ThesaurusID>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
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   <Concept PreferredConceptYN="N">
    <ConceptUI>M0248811</ConceptUI>
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      <TermUI>T278816</TermUI>
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       <ThesaurusID>NLM (1995)</ThesaurusID>
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 </SupplementalRecord>
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  <SupplementalRecordUI>C049483</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3,4-dihydroxysulfolane</String>
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  <DateCreated>
   <Year>1986</Year>
   <Month>08</Month>
   <Day>12</Day>
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  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>20</Day>
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  <SourceList>
   <Source>Eksp Onkol 1986;8(3):75</Source>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T171754</TermUI>
      <String>doxilane-diolane</String>
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       <ThesaurusID>NLM (1986)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
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      <TermUI>T352837</TermUI>
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      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (1986)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001740</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6-methoxy-2-nonaprenylphenol</String>
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  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>03</Day>
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  <Note>structure
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  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>METHYL ETHERS (72-76)</PreviousIndexing>
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    <DescriptorReferredTo>
     <DescriptorUI>*D010636</DescriptorUI>
     <DescriptorName>
      <String>Phenols</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 11(5):896;1972</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0042041</ConceptUI>
    <ConceptName>
     <String>6-methoxy-2-nonaprenylphenol</String>
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    <RegistryNumber>10232-06-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T072044</TermUI>
      <String>6-methoxy-2-nonaprenylphenol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
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   </Concept>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001742</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SC 3123</String>
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  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>1994</Year>
   <Month>06</Month>
   <Day>14</Day>
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  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AMIDINES (72-82)</PreviousIndexing>
   <PreviousIndexing>METHYL ETHERS (72-76)</PreviousIndexing>
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    <DescriptorReferredTo>
     <DescriptorUI>*D007546</DescriptorUI>
     <DescriptorName>
      <String>Isoquinolines</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>Boll Chim Farm 111(6):353;1972</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0042045</ConceptUI>
    <ConceptName>
     <String>SC 3123</String>
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    <CASN1Name>N-(2-o-methoxyphenoxyethyl)-6,7-dimethoxy- 3,4-dihydro-2-(1H)-isoquinoline carboxamidine</CASN1Name>
    <RegistryNumber>36576-29-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T072048</TermUI>
      <String>SC 3123</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
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  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C065325</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>MDL 19660</String>
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  <DateCreated>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>13</Day>
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  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>20</Day>
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  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014230</DescriptorUI>
     <DescriptorName>
      <String>Triazoles</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>Neuropharmacology 1990;29(6):555</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0179663</ConceptUI>
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    <TermList>
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      <TermUI>T209668</TermUI>
      <String>MDL 19660</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T209667</TermUI>
      <String>MDL-19660</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T209666</TermUI>
      <String>MDL 19,660</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
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     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0179660</ConceptUI>
    <ConceptName>
     <String>5-(4-chlorophenyl)-2,4-dihydro-2,4-dimethyl-3H-1,2,4-triazole-3-thione</String>
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    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0179663</Concept1UI>
     <Concept2UI>M0179660</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T209665</TermUI>
      <String>5-(4-chlorophenyl)-2,4-dihydro-2,4-dimethyl-3H-1,2,4-triazole-3-thione</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
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  <SupplementalRecordName>
   <String>7-oxa-13-prostynoic acid</String>
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  <DateCreated>
   <Year>1981</Year>
   <Month>08</Month>
   <Day>19</Day>
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  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>22</Day>
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  <Note>potentiates prostaglandin E(2)-induced release of LH; RN given refers to cpd without isomeric designation
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     <DescriptorUI>*D005231</DescriptorUI>
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  <SourceList>
   <Source>Acta Endocrinol 1981;97(3):297</Source>
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  <ConceptList>
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    <RegistryNumber>22707-29-5</RegistryNumber>
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     <RelatedRegistryNumber>22662-17-5 ((trans)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>27166-04-7 ((1S-trans)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>32567-98-9 ((trans-(+))-isomer)</RelatedRegistryNumber>
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    <ConceptRelationList>
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     <Concept2UI>M0319112</Concept2UI>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0098027</Concept1UI>
     <Concept2UI>M0319111</Concept2UI>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0098027</Concept1UI>
     <Concept2UI>M0319110</Concept2UI>
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      <TermUI>T128031</TermUI>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
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   <Concept PreferredConceptYN="N">
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    <TermList>
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      <TermUI>T349112</TermUI>
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      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
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   <Concept PreferredConceptYN="N">
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      <TermUI>T349111</TermUI>
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      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
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   <Concept PreferredConceptYN="N">
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    <RegistryNumber>22662-17-5</RegistryNumber>
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    <TermList>
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      <TermUI>T349110</TermUI>
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      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
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 </SupplementalRecord>
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  <SupplementalRecordUI>C001755</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>methyl-4,5-benzindan-2-carboxylate</String>
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  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <Note>structure
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  <Frequency>0</Frequency>
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   <PreviousIndexing>*INDENES (72-75)</PreviousIndexing>
   <PreviousIndexing>CARBOXYLIC ACIDS (72-76)</PreviousIndexing>
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    <DescriptorReferredTo>
     <DescriptorUI>*D007189</DescriptorUI>
     <DescriptorName>
      <String>Indans</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 247(10):3029;1972</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0042073</ConceptUI>
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     <String>methyl-4,5-benzindan-2-carboxylate</String>
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    <CASN1Name>1H-Benz(e)indene-2-carboxylic acid, 2,3-dihydro-, methyl ester</CASN1Name>
    <RegistryNumber>78150-03-5</RegistryNumber>
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     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T072076</TermUI>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C064553</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>VPS1 protein, S cerevisiae</String>
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  <DateCreated>
   <Year>1999</Year>
   <Month>11</Month>
   <Day>04</Day>
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  <DateRevised>
   <Year>2009</Year>
   <Month>07</Month>
   <Day>23</Day>
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  <Frequency>54</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*Carrier Proteins (1999-2002)</PreviousIndexing>
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    <DescriptorReferredTo>
     <DescriptorUI>*D019204</DescriptorUI>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D033921</DescriptorUI>
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      <String>Vesicular Transport Proteins</String>
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  <SourceList>
   <Source>Cell 1990;61(6):1063</Source>
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  <ConceptList>
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    <ConceptUI>M0177789</ConceptUI>
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    <RegistryNumber>EC 3.6.1.-</RegistryNumber>
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      <TermUI>T497463</TermUI>
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      <DateCreated>
       <Year>2002</Year>
       <Month>06</Month>
       <Day>07</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T755254</TermUI>
      <String>YKR001C protein, S cerevisiae</String>
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       <Year>2009</Year>
       <Month>07</Month>
       <Day>23</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2009)</ThesaurusID>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T557376</TermUI>
      <String>SPO15 protein, S cerevisiae</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>11</Month>
       <Day>06</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006209</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>DWP 7055</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>chlorinated homologs of oxybenzol
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002722</DescriptorUI>
     <DescriptorName>
      <String>Chlorobenzenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Czas Stomatol 27(11):1173;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0048503</ConceptUI>
    <ConceptName>
     <String>DWP 7055</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T078506</TermUI>
      <String>DWP 7055</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C076157</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>high-iron diamine-thiocarbohydrazide-silver proteinate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1992</Year>
   <Month>09</Month>
   <Day>17</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>combination of high-iron diamine, thiocarbohydrazide and silver proteinate; used in microscopy
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006834</DescriptorUI>
     <DescriptorName>
      <String>Hydrazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012836</DescriptorUI>
     <DescriptorName>
      <String>Silver Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Histochem Cytochem 1992 Sep;40(9):1257-67</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0204918</ConceptUI>
    <ConceptName>
     <String>high-iron diamine-thiocarbohydrazide-silver proteinate</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T234923</TermUI>
      <String>high-iron diamine-thiocarbohydrazide-silver proteinate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T234922</TermUI>
      <String>HID-TCH-SP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006248</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Wy 12157</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>RN &amp; N1 refer to mono-HCl
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>INDOLIZINES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007211</DescriptorUI>
     <DescriptorName>
      <String>Indoles</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
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  <SourceList>
   <Source>J Pharm Sci 63(5):787;1974</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0048621</ConceptUI>
    <ConceptName>
     <String>Wy 12157</String>
    </ConceptName>
    <CASN1Name>1H-indolizino(8,7-b)indole, 2,3,5,6,11,11b-hexahydro-11,11b-dimethyl-, monohydrochloride</CASN1Name>
    <RegistryNumber>33621-13-5</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0048621</Concept1UI>
     <Concept2UI>M0048618</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T078624</TermUI>
      <String>Wy 12157</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T078622</TermUI>
      <String>Wy-12,157</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T078623</TermUI>
      <String>Wy-12157</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0048618</ConceptUI>
    <ConceptName>
     <String>2,3,5,6,11,11b-hexahydro-11,11b-dimethyl-14-indolizino(8,7-b)indole hydrochloride</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0048621</Concept1UI>
     <Concept2UI>M0048618</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T078621</TermUI>
      <String>2,3,5,6,11,11b-hexahydro-11,11b-dimethyl-14-indolizino(8,7-b)indole hydrochloride</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C433928</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>EUK-134</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>09</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>antioxidant; structure in first source
  </Note>
  <Frequency>86</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009942</DescriptorUI>
     <DescriptorName>
      <String>Organometallic Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012459</DescriptorUI>
     <DescriptorName>
      <String>Salicylates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D000975</DescriptorUI>
     <DescriptorName>
      <String>Antioxidants</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D017895</DescriptorUI>
     <DescriptorName>
      <String>Manganese Compounds</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Bioorg Med Chem Lett 2001 Jun 4;11(11):1367-79</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0397232</ConceptUI>
    <ConceptName>
     <String>EUK-134</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0397232</Concept1UI>
     <Concept2UI>M0456140</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T459997</TermUI>
      <String>EUK-134</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>09</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T558500</TermUI>
      <String>EUK134</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>11</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0456140</ConceptUI>
    <ConceptName>
     <String>((N,N'-bis(3-methoxysalicylidene)ethylenediamine)Mn(III))(+) Cl(-)</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0397232</Concept1UI>
     <Concept2UI>M0456140</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T558501</TermUI>
      <String>((N,N'-bis(3-methoxysalicylidene)ethylenediamine)Mn(III))(+) Cl(-)</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>11</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T845391</TermUI>
      <String>Mn(III) 3-methoxy N,N-bis(salicylidene)ethylenediamine chloride</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T558502</TermUI>
      <String>MeO-salenMn(III)</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>11</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C029491</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>insulin, 3-iodo-Tyr(A14)-</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>05</Month>
   <Day>28</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>23</Day>
  </DateRevised>
  <Note>used with (125)I for receptor assay
  </Note>
  <Frequency>23</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007328</DescriptorUI>
     <DescriptorName>
      <String>Insulin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D007457</DescriptorUI>
     <DescriptorName>
      <String>Iodine Radioisotopes</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Biol Chem 1981;256(8):4042</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0094051</ConceptUI>
    <ConceptName>
     <String>insulin, 3-iodo-Tyr(A14)-</String>
    </ConceptName>
    <RegistryNumber>51798-73-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T124054</TermUI>
      <String>insulin, 3-iodo-Tyr(A14)-</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T124052</TermUI>
      <String>A14-3-iodotyrosine-insulin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T124053</TermUI>
      <String>insulin, 3-iodotyrosine(A14)-</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T124051</TermUI>
      <String>A14-3-iodo-Tyr-insulin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C029788</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>insulin, Trp(B1)-</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>06</Month>
   <Day>12</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>23</Day>
  </DateRevised>
  <Note>Trp replacement of B1 Phe in bovine &amp; porcine insulins
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007328</DescriptorUI>
     <DescriptorName>
      <String>Insulin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Sci Sin 1980:23(11):1443</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0094786</ConceptUI>
    <ConceptName>
     <String>insulin, Trp(B1)-</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T124789</TermUI>
      <String>insulin, Trp(B1)-</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T124787</TermUI>
      <String>B1-tryptophan-insulin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T124786</TermUI>
      <String>B1-Trp-insulin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T124788</TermUI>
      <String>insulin, tryptophan(B1)-</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C030057</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>insulin, Asn(B12)-</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>06</Month>
   <Day>26</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>23</Day>
  </DateRevised>
  <Note>human insulin; valine is replaced by asparagine at position B12; RN given refers to ion(2-)
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007328</DescriptorUI>
     <DescriptorName>
      <String>Insulin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Int J Pept Protein Res 1981;17(2):243</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0095397</ConceptUI>
    <ConceptName>
     <String>insulin, Asn(B12)-</String>
    </ConceptName>
    <CASN1Name>Insulin, 12-L-asparagine-30-L-threonine-, 7,19-bis(hydrogen sulfate), ion(2-)</CASN1Name>
    <RegistryNumber>78212-36-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T125401</TermUI>
      <String>insulin, Asn(B12)-</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T125399</TermUI>
      <String>B12-asparagine-insulin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T125400</TermUI>
      <String>insulin, asparagine(B12)-</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T125398</TermUI>
      <String>B12-Asn-insulin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C030314</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>insulin, Leu(B30)-</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>07</Month>
   <Day>10</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>23</Day>
  </DateRevised>
  <Note>semisynthetic insulin with Leu in the B30 position; has less immunoreactivity than other B30 position insulin analogs; has full activity in receptor binding &amp; biological effects
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007328</DescriptorUI>
     <DescriptorName>
      <String>Insulin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Diabetes 1981;30(6):519</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0095970</ConceptUI>
    <ConceptName>
     <String>insulin, Leu(B30)-</String>
    </ConceptName>
    <RegistryNumber>92679-50-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T125974</TermUI>
      <String>insulin, Leu(B30)-</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T125972</TermUI>
      <String>B30-leucine-insulin</String>
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       <ThesaurusID>NLM (1981)</ThesaurusID>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T125973</TermUI>
      <String>insulin, leucine(B30)-</String>
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       <ThesaurusID>NLM (1981)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T125971</TermUI>
      <String>B30-Leu-insulin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C031207</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>insulin, Leu(B24,B25)-</String>
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  <DateCreated>
   <Year>1981</Year>
   <Month>08</Month>
   <Day>19</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>23</Day>
  </DateRevised>
  <Note>leucine was substituted at position B24 &amp; B25 in insulin chain
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007328</DescriptorUI>
     <DescriptorName>
      <String>Insulin</String>
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    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
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  <SourceList>
   <Source>Hoppe Seylers Z Physiol Chem 1981;362(5):557</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0098247</ConceptUI>
    <ConceptName>
     <String>insulin, Leu(B24,B25)-</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
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      <TermUI>T128251</TermUI>
      <String>insulin, Leu(B24,B25)-</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T128250</TermUI>
      <String>insulin, leucine (B24,B25)-</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T128248</TermUI>
      <String>B24,B25-Leu-insulin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T128249</TermUI>
      <String>B24,B25-leucine-insulin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C070672</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>DAC 5945</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1991</Year>
   <Month>10</Month>
   <Day>02</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>30</Day>
  </DateRevised>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010879</DescriptorUI>
     <DescriptorName>
      <String>Piperazines</String>
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  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0192318</ConceptUI>
    <ConceptName>
     <String>DAC 5945</String>
    </ConceptName>
    <CASN1Name>1-Piperazineethanol, alpha-cyclohexyl-4-(iminomethyl)-alpha-phenyl-, monohydrochloride</CASN1Name>
    <RegistryNumber>124065-13-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0192318</Concept1UI>
     <Concept2UI>M0192317</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T222323</TermUI>
      <String>DAC 5945</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T222321</TermUI>
      <String>DAC-5945</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0192317</ConceptUI>
    <ConceptName>
     <String>N-iminomethyl-N'-((2-hydroxy-2-phenyl-2-cyclohexyl)ethyl)piperazine hydrochloride</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0192318</Concept1UI>
     <Concept2UI>M0192317</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T222322</TermUI>
      <String>N-iminomethyl-N'-((2-hydroxy-2-phenyl-2-cyclohexyl)ethyl)piperazine hydrochloride</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C489153</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>AhpD protein, Mycobacterium tuberculosis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>09</Month>
   <Day>04</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>11</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>reduces peroxiredoxin AhpC; has alkylhydroperoxidase activity; GenBank U44840
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010544</DescriptorUI>
     <DescriptorName>
      <String>Peroxidases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Antimicrob Agents Chemother 2004 Jul;48(7):2424-30</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0472095</ConceptUI>
    <ConceptName>
     <String>AhpD protein, Mycobacterium tuberculosis</String>
    </ConceptName>
    <RegistryNumber>EC 1.11.1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T608106</TermUI>
      <String>AhpD protein, Mycobacterium tuberculosis</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>04</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C523557</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>(trifluoromethyl)-trimethylsilane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>10</Month>
   <Day>16</Day>
  </DateCreated>
  <DateRevised>
   <Year>2014</Year>
   <Month>05</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>9</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006845</DescriptorUI>
     <DescriptorName>
      <String>Hydrocarbons, Fluorinated</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014297</DescriptorUI>
     <DescriptorName>
      <String>Trimethylsilyl Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Phys Chem A 2005 Sep 22;109(37):8438-42</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0514528</ConceptUI>
    <ConceptName>
     <String>(trifluoromethyl)-trimethylsilane</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T707850</TermUI>
      <String>(trifluoromethyl)-trimethylsilane</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>10</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T859317</TermUI>
      <String>(trifluoromethyl)trimethylsilane</String>
      <DateCreated>
       <Year>2014</Year>
       <Month>05</Month>
       <Day>05</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2014)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T707851</TermUI>
      <String>CF3SiMe3</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>10</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C489156</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>CcrC protein, Staphylococcus aureus</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>09</Month>
   <Day>04</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>11</Month>
   <Day>04</Day>
  </DateRevised>
  <Frequency>15</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D045522</DescriptorUI>
     <DescriptorName>
      <String>Recombinases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Antimicrob Agents Chemother 2004 Jul;48(7):2637-51</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0472098</ConceptUI>
    <ConceptName>
     <String>CcrC protein, Staphylococcus aureus</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T617281</TermUI>
      <String>CcrC protein, Staphylococcus aureus</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>11</Month>
       <Day>04</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T608110</TermUI>
      <String>cassette chromosome recombinase C, Staphylococcus aureus</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>04</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T608111</TermUI>
      <String>CcrC protein, S aureus</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>04</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
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   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C072978</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>R 73335</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1992</Year>
   <Month>03</Month>
   <Day>20</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>inhibitor of adenosine flux
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010879</DescriptorUI>
     <DescriptorName>
      <String>Piperazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Adv Exp Med Biol 1991;309A:415-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0197450</ConceptUI>
    <ConceptName>
     <String>R 73335</String>
    </ConceptName>
    <CASN1Name>1-Piperazineacetamide, 2-(aminocarbonyl)-4-(5,5-bis(4-fluorophenyl)pentyl)-N-(3-chloro-2,5,6,7-tetrahydro-2-oxo-1H-1-pyrindin-4-yl)-</CASN1Name>
    <RegistryNumber>120785-90-2</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0197450</Concept1UI>
     <Concept2UI>M0197448</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T227455</TermUI>
      <String>R 73335</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T227454</TermUI>
      <String>R-73335</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0197448</ConceptUI>
    <ConceptName>
     <String>2-(aminocarbonyl)-4-(5,5-bis(4-fluorophenyl)pentyl)-N-(3-chloro-2,5,6,7-tetrahydro-2-oxo-1H-pyridin-4-yl)-1-piperazine acetamide</String>
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    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T227453</TermUI>
      <String>2-(aminocarbonyl)-4-(5,5-bis(4-fluorophenyl)pentyl)-N-(3-chloro-2,5,6,7-tetrahydro-2-oxo-1H-pyridin-4-yl)-1-piperazine acetamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
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     </Term>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C046114</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>CLS 2210</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1985</Year>
   <Month>08</Month>
   <Day>30</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>benzenesulfonate derivative which cleans cardiac lymph vessels better tha hyaluronidase; thereby reduces the size of myocardial infarcts after coronary occlusion
  </Note>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001557</DescriptorUI>
     <DescriptorName>
      <String>Benzenesulfonates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Angiology 1985;36(7):452</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0133774</ConceptUI>
    <ConceptName>
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    <CASN1Name>CLS 2210</CASN1Name>
    <RegistryNumber>99270-13-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T163779</TermUI>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T163778</TermUI>
      <String>CLS-2210</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C046065</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4,4'-(carbonylbis(benzene-4,1-diyl)bis(imino))bis(benzene sulfonate) sodium salt</String>
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  <DateCreated>
   <Year>1985</Year>
   <Month>08</Month>
   <Day>22</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>fluorochrome from aniline blue
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001557</DescriptorUI>
     <DescriptorName>
      <String>Benzenesulfonates</String>
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  <SourceList>
   <Source>Stain Technol 1985;60(3):155</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0133633</ConceptUI>
    <ConceptName>
     <String>4,4'-(carbonylbis(benzene-4,1-diyl)bis(imino))bis(benzene sulfonate) sodium salt</String>
    </ConceptName>
    <CASN1Name>Benzenesulfonic acid, 4,4'-(carbonylbis(4,1-phenyleneimino))bis-</CASN1Name>
    <RegistryNumber>85137-47-9</RegistryNumber>
    <ConceptRelationList>
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     <Concept1UI>M0133633</Concept1UI>
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      <TermUI>T163638</TermUI>
      <String>4,4'-(carbonylbis(benzene-4,1-diyl)bis(imino))bis(benzene sulfonate) sodium salt</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
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   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0133634</ConceptUI>
    <ConceptName>
     <String>Sirofluor</String>
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     <Concept1UI>M0133633</Concept1UI>
     <Concept2UI>M0133634</Concept2UI>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006293</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>F 30385</String>
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  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009581</DescriptorUI>
     <DescriptorName>
      <String>Nitrofurans</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chinese Med J 1:40;1974</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0048759</ConceptUI>
    <ConceptName>
     <String>F 30385</String>
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    <RegistryNumber>3830-11-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T078762</TermUI>
      <String>F 30385</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T078761</TermUI>
      <String>F-30385</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002114</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Histaglobin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>drug combination of histamine &amp; gamma globulin; see also histaglobulin
  </Note>
  <Frequency>26</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005719</DescriptorUI>
     <DescriptorName>
      <String>gamma-Globulins</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006632</DescriptorUI>
     <DescriptorName>
      <String>Histamine</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D001249</DescriptorUI>
     <DescriptorName>
      <String>Asthma</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000188</QualifierUI>
     <QualifierName>
      <String>drug therapy</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Fiziol Ah 22(3):357;1976</Source>
   <Source>Pediatr Akush Ginekol 1:18;1977</Source>
   <Source>Probl Tuberk 2:47;1976</Source>
   <Source>Srp Arh Celok Lek 1979;107(5):477</Source>
   <Source>Vestn Otorinolaringol 3:26;1979</Source>
   <Source>Z Erkr Atmungsorgane 136(3):337;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0042592</ConceptUI>
    <ConceptName>
     <String>Histaglobin</String>
    </ConceptName>
    <CASN1Name>1H-Imidazole-4-ethanamine, dihydrochloride, mixt. with gamma-globulins</CASN1Name>
    <RegistryNumber>37317-09-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="TRD"  RecordPreferredTermYN="Y">
      <TermUI>T072595</TermUI>
      <String>Histaglobin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C073650</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>S 14671</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1992</Year>
   <Month>04</Month>
   <Day>20</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>serotonin receptor agonist; RN from toxlit
  </Note>
  <Frequency>7</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010879</DescriptorUI>
     <DescriptorName>
      <String>Piperazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013876</DescriptorUI>
     <DescriptorName>
      <String>Thiophenes</String>
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  <SourceList>
   <Source>Eur J Pharmacol 1991 Oct 15;203(2):319-22</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0199038</ConceptUI>
    <ConceptName>
     <String>S 14671</String>
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    <RegistryNumber>135722-27-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0199038</Concept1UI>
     <Concept2UI>M0199036</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T229043</TermUI>
      <String>S 14671</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T229042</TermUI>
      <String>S-14671</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0199036</ConceptUI>
    <ConceptName>
     <String>4-((thenoyl)-2-aminoethyl)-1-(7-methoxynaphthylpiperazine)</String>
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    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0199038</Concept1UI>
     <Concept2UI>M0199036</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T229041</TermUI>
      <String>4-((thenoyl)-2-aminoethyl)-1-(7-methoxynaphthylpiperazine)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C489242</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Prdm2 protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>09</Month>
   <Day>07</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>11</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>an estrogen receptor coactivator with histone lysine methyltransferase activity; RefSeq XM_204027
  </Note>
  <Frequency>7</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011495</DescriptorUI>
     <DescriptorName>
      <String>Histone-Lysine N-Methyltransferase</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014157</DescriptorUI>
     <DescriptorName>
      <String>Transcription Factors</String>
     </DescriptorName>
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   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Cell Biol 2004 Aug;24(16):7032-42</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0472177</ConceptUI>
    <ConceptName>
     <String>Prdm2 protein, mouse</String>
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    <RegistryNumber>EC 2.1.1.43</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T617282</TermUI>
      <String>Prdm2 protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>11</Month>
       <Day>04</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T617283</TermUI>
      <String>PR domain containing 2, with ZNF domain protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>11</Month>
       <Day>04</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T608381</TermUI>
      <String>RIZ1 protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C076312</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dithiobis(N,N-dimethyl-4-acetylpiperazinium)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1992</Year>
   <Month>09</Month>
   <Day>24</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>structure given in first source; stimulates nicotinic receptors in the chick retina; blocks binding to neuronal bungarotoxin to retinal homogenates; RN refers to the diiodide cpd
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010879</DescriptorUI>
     <DescriptorName>
      <String>Piperazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D011978</DescriptorUI>
     <DescriptorName>
      <String>Receptors, Nicotinic</String>
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     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Mol Pharmacol 1992 Aug;42(2):356-63</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0205305</ConceptUI>
    <ConceptName>
     <String>dithiobis(N,N-dimethyl-4-acetylpiperazinium)</String>
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    <RegistryNumber>145707-16-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0205305</Concept1UI>
     <Concept2UI>M0205304</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T235310</TermUI>
      <String>dithiobis(N,N-dimethyl-4-acetylpiperazinium)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T235308</TermUI>
      <String>DT-DMAP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0205304</ConceptUI>
    <ConceptName>
     <String>dithiobis(N,N-dimethyl-4-acetylpiperazinium), diiodide</String>
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    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0205305</Concept1UI>
     <Concept2UI>M0205304</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T235309</TermUI>
      <String>dithiobis(N,N-dimethyl-4-acetylpiperazinium), diiodide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C476332</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>EPs 7630</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>13</Day>
  </DateCreated>
  <DateRevised>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>potentially useful in treating bronchitis; isolated from Pelargonium sidoides
  </Note>
  <Frequency>45</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010936</DescriptorUI>
     <DescriptorName>
      <String>Plant Extracts</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D000998</DescriptorUI>
     <DescriptorName>
      <String>Antiviral Agents</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D018927</DescriptorUI>
     <DescriptorName>
      <String>Anti-Asthmatic Agents</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Phytomedicine 2003;10 Suppl 4:7-17</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0452703</ConceptUI>
    <ConceptName>
     <String>EPs 7630</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T548123</TermUI>
      <String>EPs 7630</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>08</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T548125</TermUI>
      <String>EPs7630</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>08</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T548124</TermUI>
      <String>EPs-7630</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>08</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C077079</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-methylpiperazine-2,6-dione</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1992</Year>
   <Month>11</Month>
   <Day>02</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010879</DescriptorUI>
     <DescriptorName>
      <String>Piperazines</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Pharm Res 1992 Sep;9(9):1209-14</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0207130</ConceptUI>
    <ConceptName>
     <String>4-methylpiperazine-2,6-dione</String>
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    <CASN1Name>2,6-Piperazinedione, 4-methyl-</CASN1Name>
    <RegistryNumber>60725-35-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T237135</TermUI>
      <String>4-methylpiperazine-2,6-dione</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T237133</TermUI>
      <String>4-MP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T237134</TermUI>
      <String>4-methyl-2,6-piperazinedione</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006309</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>BRL 51242</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*IMIDAZOLES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014226</DescriptorUI>
     <DescriptorName>
      <String>Triazenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Chemother Rep 57(3):263;1973</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0048812</ConceptUI>
    <ConceptName>
     <String>BRL 51242</String>
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    <RegistryNumber>37126-45-7</RegistryNumber>
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     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0048812</Concept1UI>
     <Concept2UI>M0048809</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T078815</TermUI>
      <String>BRL 51242</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T078813</TermUI>
      <String>BRL-51242</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0048811</ConceptUI>
    <ConceptName>
     <String>NSC 166721</String>
    </ConceptName>
    <ConceptRelationList>
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     <Concept1UI>M0048812</Concept1UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T078814</TermUI>
      <String>NSC 166721</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
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   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0048809</ConceptUI>
    <ConceptName>
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    <TermList>
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      <TermUI>T078812</TermUI>
      <String>4-carbethoxy-5-(3,3-dimethyl-1-triazeno)-2-phenylimidazole</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006294</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Abbott 31699</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013844</DescriptorUI>
     <DescriptorName>
      <String>Thiazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 16(10):1157;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0048760</ConceptUI>
    <ConceptName>
     <String>Abbott 31699</String>
    </ConceptName>
    <CASN1Name>5-(p-hydroxyanilino)-1,2,3,4-thiatriazole</CASN1Name>
    <RegistryNumber>23567-67-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T078763</TermUI>
      <String>Abbott 31699</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C528424</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>huangbai</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2008</Year>
   <Month>04</Month>
   <Day>28</Day>
  </DateCreated>
  <DateRevised>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>used to treat recurrent genital herpes
  </Note>
  <Frequency>17</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004365</DescriptorUI>
     <DescriptorName>
      <String>Drugs, Chinese Herbal</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D018696</DescriptorUI>
     <DescriptorName>
      <String>Neuroprotective Agents</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Zhongguo Zhong Xi Yi Hie He Za Zhi 2006 Dec;26(12):1119-21</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0520841</ConceptUI>
    <ConceptName>
     <String>huangbai</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T718850</TermUI>
      <String>huangbai</String>
      <DateCreated>
       <Year>2008</Year>
       <Month>04</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2008)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T845394</TermUI>
      <String>huang bai</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006375</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>acetylgitoxin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>05</Month>
   <Day>05</Day>
  </DateRevised>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DIGITALIS GLYCOSIDES (74-78)</PreviousIndexing>
   <PreviousIndexing>ACETIC ACIDS (74-78)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000112</DescriptorUI>
     <DescriptorName>
      <String>Acetyldigitoxins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biull Eksp Biol Med 75(10):61;1973</Source>
   <Source>Europ J Clin Pharmacol 12:445;1977</Source>
   <Source>Europ J Clin Pharmacol 13(5):389;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0048886</ConceptUI>
    <ConceptName>
     <String>acetylgitoxin</String>
    </ConceptName>
    <RegistryNumber>7242-40-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T078889</TermUI>
      <String>acetylgitoxin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C581546</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N1,N12-bis(retinoyl)spermine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>07</Day>
  </DateCreated>
  <DateRevised>
   <Year>2013</Year>
   <Month>06</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>also has antineoplastic activity; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013096</DescriptorUI>
     <DescriptorName>
      <String>Spermine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014212</DescriptorUI>
     <DescriptorName>
      <String>Tretinoin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D020533</DescriptorUI>
     <DescriptorName>
      <String>Angiogenesis Inhibitors</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Eur J Pharmacol. 2013 Jan 5;698(1-3):122-30.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0585391</ConceptUI>
    <ConceptName>
     <String>N1,N12-bis(retinoyl)spermine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0585391</Concept1UI>
     <Concept2UI>M0585392</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T845288</TermUI>
      <String>N1,N12-bis(retinoyl)spermine</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T845396</TermUI>
      <String>RASP compound</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0585392</ConceptUI>
    <ConceptName>
     <String>N1,N12-bis(all-trans-retinoyl)spermine</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0585391</Concept1UI>
     <Concept2UI>M0585392</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T845289</TermUI>
      <String>N1,N12-bis(all-trans-retinoyl)spermine</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>06</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C452442</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Mac Bond II</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>04</Month>
   <Day>24</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>11</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>a dentin bonding system composed of Primer (MAC-10, acetone, ethanol, methacryloyloxyalkylacid phosphate, water); Bonding resin (MAC-10, hydroxyethyl methacrylate (HEMA), Bis-GMA, TEGDMA and photoinitiator) &amp; Resin composite (Bis-GMA, TEGMA &amp; filler)
  </Note>
  <Frequency>22</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D019279</DescriptorUI>
     <DescriptorName>
      <String>Resin Cements</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Am J Dent 2001 Dec;14(6):355-60</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0421273</ConceptUI>
    <ConceptName>
     <String>Mac Bond II</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="TRD"  RecordPreferredTermYN="Y">
      <TermUI>T490681</TermUI>
      <String>Mac Bond II</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>04</Month>
       <Day>24</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="TRD"  RecordPreferredTermYN="N">
      <TermUI>T526261</TermUI>
      <String>Mac-Bond II</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>11</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C036461</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>J 2644</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1982</Year>
   <Month>12</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>20</Day>
  </DateRevised>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010636</DescriptorUI>
     <DescriptorName>
      <String>Phenols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Econ Entomol 1982;75(5):877</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0111057</ConceptUI>
    <ConceptName>
     <String>J 2644</String>
    </ConceptName>
    <RegistryNumber>71712-03-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0111057</Concept1UI>
     <Concept2UI>M0111054</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T141061</TermUI>
      <String>J 2644</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T141060</TermUI>
      <String>J2644</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T141059</TermUI>
      <String>J-2644</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0111054</ConceptUI>
    <ConceptName>
     <String>2,4-bis(1,1-dimethylethyl)-6-(4-methoxyphenylmethyl)phenol</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0111057</Concept1UI>
     <Concept2UI>M0111054</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T141058</TermUI>
      <String>2,4-bis(1,1-dimethylethyl)-6-(4-methoxyphenylmethyl)phenol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006322</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>compound 70-352</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001567</DescriptorUI>
     <DescriptorName>
      <String>Benzocycloheptenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Jap J Pharmacol 24(1):5;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0048838</ConceptUI>
    <ConceptName>
     <String>compound 70-352</String>
    </ConceptName>
    <CASN1Name>cis-2,3-dihydroxy-6 amino-6,7,8,9-tetrahydro-5-H- benzocyclohepten-5-ol HCl</CASN1Name>
    <RegistryNumber>52079-42-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T078841</TermUI>
      <String>compound 70-352</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006324</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Ro 7-4632</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1986</Year>
   <Month>07</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CYCLOHEXANECARBOXYLIC ACIDS (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007211</DescriptorUI>
     <DescriptorName>
      <String>Indoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Clin Pharm Ther 16(1)(part 2):176;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0048841</ConceptUI>
    <ConceptName>
     <String>Ro 7-4632</String>
    </ConceptName>
    <RegistryNumber>56573-69-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T078844</TermUI>
      <String>Ro 7-4632</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C501202</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Hop2 protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>06</Month>
   <Day>15</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>06</Month>
   <Day>15</Day>
  </DateRevised>
  <Note>the Hop2 and Mnd1 proteins act in concert with Rad51 and Dmc1 in meiotic recombination; disruption of meiosis-specific HOP2 or MND1 genes leads to severe defects in homologous synapsis and an early-stage recombination failure resulting in sterility; RefSeq: mRNA sequence NM_008949; Source Sequence BC030169; Product NP_032975
  </Note>
  <Frequency>11</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D018797</DescriptorUI>
     <DescriptorName>
      <String>Cell Cycle Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nat Struct Mol Biol 2005 May;12(5):449-53</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0485876</ConceptUI>
    <ConceptName>
     <String>Hop2 protein, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T643226</TermUI>
      <String>Hop2 protein, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>06</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006329</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>MJ 9465-2</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>08</Month>
   <Day>14</Day>
  </DateRevised>
  <Note>antidiuretic; structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007093</DescriptorUI>
     <DescriptorName>
      <String>Imidazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D004231</DescriptorUI>
     <DescriptorName>
      <String>Diuresis</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000187</QualifierUI>
     <QualifierName>
      <String>drug effects</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Proc Soc Exptl Biol Med 144(1):203;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0048849</ConceptUI>
    <ConceptName>
     <String>MJ 9465-2</String>
    </ConceptName>
    <CASN1Name>2-amino-4-(4-chlorophenyl)-2-imidazoline.HBr</CASN1Name>
    <RegistryNumber>40658-97-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T078852</TermUI>
      <String>MJ 9465-2</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006377</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>(N)1-acetylisoniazid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>biologically inactive metabolite of isoniazid
  </Note>
  <Frequency>40</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ISONIAZID (74-76)</PreviousIndexing>
   <PreviousIndexing>ACETIC ACIDS (74-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007538</DescriptorUI>
     <DescriptorName>
      <String>Isoniazid</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Annals Internal Med 84(2):181;1976</Source>
   <Source>Can Med Assoc J 109(6):483;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0048887</ConceptUI>
    <ConceptName>
     <String>(N)1-acetylisoniazid</String>
    </ConceptName>
    <RegistryNumber>1078-38-2</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>77280-85-4 (mono-HCl)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0048887</Concept1UI>
     <Concept2UI>M0309540</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T078890</TermUI>
      <String>(N)1-acetylisoniazid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0309540</ConceptUI>
    <ConceptName>
     <String>(N)1-acetylisoniazid monohydrochloride</String>
    </ConceptName>
    <RegistryNumber>77280-85-4</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0048887</Concept1UI>
     <Concept2UI>M0309540</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T339540</TermUI>
      <String>(N)1-acetylisoniazid monohydrochloride</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006367</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-beta-acetoxy-27-nor-5-cholesten-25-one</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1987</Year>
   <Month>09</Month>
   <Day>22</Day>
  </DateRevised>
  <Note>starting material for synthesizing 24,25-dihydroxy-vitamin D(3)
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CHOLESTENES (74-75)</PreviousIndexing>
   <PreviousIndexing>*STEROLS (74-87)</PreviousIndexing>
   <PreviousIndexing>NORSTEROIDS (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002783</DescriptorUI>
     <DescriptorName>
      <String>Cholestenones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 12(24):4852;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0048874</ConceptUI>
    <ConceptName>
     <String>3-beta-acetoxy-27-nor-5-cholesten-25-one</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T078877</TermUI>
      <String>3-beta-acetoxy-27-nor-5-cholesten-25-one</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002869</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>8-azainosine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*INOSINE (73-75)</PreviousIndexing>
   <PreviousIndexing>AZA COMPOUNDS (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007288</DescriptorUI>
     <DescriptorName>
      <String>Inosine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Res 33(3):465;1973</Source>
   <Source>J Med Chem 20(1):116;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043666</ConceptUI>
    <ConceptName>
     <String>8-azainosine</String>
    </ConceptName>
    <RegistryNumber>4968-68-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073669</TermUI>
      <String>8-azainosine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002881</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-hydroxy-2-ketoheptadecane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>KETONES (73-74)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005233</DescriptorUI>
     <DescriptorName>
      <String>Fatty Alcohols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 296(2):265;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043677</ConceptUI>
    <ConceptName>
     <String>1-hydroxy-2-ketoheptadecane</String>
    </ConceptName>
    <CASN1Name>1-hydroxy-2-heptadecanone</CASN1Name>
    <RegistryNumber>41265-63-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073680</TermUI>
      <String>1-hydroxy-2-ketoheptadecane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006212</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>BS 7564</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*TROPANES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003986</DescriptorUI>
     <DescriptorName>
      <String>Dibenzocycloheptenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Int Pharmacodyn Ther 205(1):61;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0048507</ConceptUI>
    <ConceptName>
     <String>BS 7564</String>
    </ConceptName>
    <CASN1Name>8-azoniabicyclo(3.2.1)octane, 3-(((10,11-dihydro-5H-dibenzo(a,d)cyclohepten-5-yl)carbonyl)oxy)-8,8-dimethyl-, bromide, endo-</CASN1Name>
    <RegistryNumber>7530-51-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0048507</Concept1UI>
     <Concept2UI>M0048506</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T078510</TermUI>
      <String>BS 7564</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0048506</ConceptUI>
    <ConceptName>
     <String>10,11-dihydro-5H-dibenzo(a,d)cycloheptene-5-carboxylic acid tropine ester methobromide</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0048507</Concept1UI>
     <Concept2UI>M0048506</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T078509</TermUI>
      <String>10,11-dihydro-5H-dibenzo(a,d)cycloheptene-5-carboxylic acid tropine ester methobromide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006223</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Abbott 40060</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ISOQUINOLINES (75-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014230</DescriptorUI>
     <DescriptorName>
      <String>Triazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Int Pharmacodyn 212(2):205;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0048537</ConceptUI>
    <ConceptName>
     <String>Abbott 40060</String>
    </ConceptName>
    <CASN1Name>3-trifluoromethyl-s-triazolo(3,4-a)-isoquinoline</CASN1Name>
    <RegistryNumber>27022-50-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0048537</Concept1UI>
     <Concept2UI>M0048536</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T078540</TermUI>
      <String>Abbott 40060</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0048536</ConceptUI>
    <ConceptName>
     <String>NC 1140</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0048537</Concept1UI>
     <Concept2UI>M0048536</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T078539</TermUI>
      <String>NC 1140</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C432948</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>11-tetradecenoic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>17</Day>
  </DateCreated>
  <Note>metabolite formed during the biosynthesis of the Spodoptera littoralis sex pheromone; structure in first source
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005229</DescriptorUI>
     <DescriptorName>
      <String>Fatty Acids, Monounsaturated</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Insect Biochem Mol Biol 2001 Jun 22;31(8):799-803</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0395876</ConceptUI>
    <ConceptName>
     <String>11-tetradecenoic acid</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T457920</TermUI>
      <String>11-tetradecenoic acid</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>08</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C432949</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>9,11-tetradecadienoic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>17</Day>
  </DateCreated>
  <Note>formed during the biosynthesis of the Spodoptera littoralis sex pheromone; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005231</DescriptorUI>
     <DescriptorName>
      <String>Fatty Acids, Unsaturated</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Insect Biochem Mol Biol 2001 Jun 22;31(8):799-803</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0395877</ConceptUI>
    <ConceptName>
     <String>9,11-tetradecadienoic acid</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T457921</TermUI>
      <String>9,11-tetradecadienoic acid</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>08</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002891</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-methoxyxanthine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>METHYL ETHERS (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014970</DescriptorUI>
     <DescriptorName>
      <String>Xanthines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 11(25):4844;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043702</ConceptUI>
    <ConceptName>
     <String>3-methoxyxanthine</String>
    </ConceptName>
    <CASN1Name>1H-Purine-2,6-dione, 3,7-dihydro-3-methoxy-</CASN1Name>
    <RegistryNumber>30345-91-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073705</TermUI>
      <String>3-methoxyxanthine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002898</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ceramide aminoethylphosphonate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Frequency>12</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ETHYLAMINES (73-75)</PreviousIndexing>
   <PreviousIndexing>ORGANOPHOSPHORUS CPDS (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000615</DescriptorUI>
     <DescriptorName>
      <String>Aminoethylphosphonic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002518</DescriptorUI>
     <DescriptorName>
      <String>Ceramides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 296(1):171;1973</Source>
   <Source>Biochim Biophys Acta 486(1):172;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043713</ConceptUI>
    <ConceptName>
     <String>ceramide aminoethylphosphonate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073716</TermUI>
      <String>ceramide aminoethylphosphonate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002900</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3 beta-(beta-dimethylaminoethoxy)androst-5-en-17-one</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>12</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>17-KETOSTEROIDS (73-81)</PreviousIndexing>
   <PreviousIndexing>ETHYL ETHERS (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000736</DescriptorUI>
     <DescriptorName>
      <String>Androstenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Biochem Biophys 180:465;1977</Source>
   <Source>Biochem Pharm 25(11):1249;1976</Source>
   <Source>Biochim Biophys Acta 296(1):221;1973</Source>
   <Source>Lipids 1979;14(8):741</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043717</ConceptUI>
    <ConceptName>
     <String>3 beta-(beta-dimethylaminoethoxy)androst-5-en-17-one</String>
    </ConceptName>
    <RegistryNumber>7635-03-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073720</TermUI>
      <String>3 beta-(beta-dimethylaminoethoxy)androst-5-en-17-one</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002908</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-thiocytidine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>07</Month>
   <Day>13</Day>
  </DateRevised>
  <Frequency>14</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CYTIDINE (73-75)</PreviousIndexing>
   <PreviousIndexing>THIONES (74-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003562</DescriptorUI>
     <DescriptorName>
      <String>Cytidine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 18(1):91;1979</Source>
   <Source>Eur J Biochem 33(3):545;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043727</ConceptUI>
    <ConceptName>
     <String>2-thiocytidine</String>
    </ConceptName>
    <RegistryNumber>13239-97-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073730</TermUI>
      <String>2-thiocytidine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002911</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>8-azaethynylestradiol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ETHINYL ESTRADIOL (73-75)</PreviousIndexing>
   <PreviousIndexing>AZA COMPOUNDS (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004997</DescriptorUI>
     <DescriptorName>
      <String>Ethinyl Estradiol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Steroid Lip Res 3(2):185;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043735</ConceptUI>
    <ConceptName>
     <String>8-azaethynylestradiol</String>
    </ConceptName>
    <RegistryNumber>39650-18-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073738</TermUI>
      <String>8-azaethynylestradiol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002918</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>methylthioinosine dicarboxaldehyde</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*INOSINE (73-75)</PreviousIndexing>
   <PreviousIndexing>ALDEHYDES (73-76)</PreviousIndexing>
   <PreviousIndexing>SULFIDES (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008778</DescriptorUI>
     <DescriptorName>
      <String>Methylthioinosine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Res 33(4):856;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043747</ConceptUI>
    <ConceptName>
     <String>methylthioinosine dicarboxaldehyde</String>
    </ConceptName>
    <RegistryNumber>31654-43-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073750</TermUI>
      <String>methylthioinosine dicarboxaldehyde</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002920</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>retamycin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1995</Year>
   <Month>07</Month>
   <Day>28</Day>
  </DateRevised>
  <Frequency>4</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>POLYCYCLIC COMPOUNDS (73-95)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D018943</DescriptorUI>
     <DescriptorName>
      <String>Anthracyclines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Rev Inst Antibiot (Recife) 11(1):3;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043748</ConceptUI>
    <ConceptName>
     <String>retamycin</String>
    </ConceptName>
    <RegistryNumber>11130-68-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073751</TermUI>
      <String>retamycin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C479481</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tributylphenyltetraethoxylate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>12</Month>
   <Day>09</Day>
  </DateCreated>
  <Note>a nonionic surfactant
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011092</DescriptorUI>
     <DescriptorName>
      <String>Polyethylene Glycols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Appl Biochem Biotechnol. 2003 Jul;110(1):33-44</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0457160</ConceptUI>
    <ConceptName>
     <String>tributylphenyltetraethoxylate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T562276</TermUI>
      <String>tributylphenyltetraethoxylate</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002924</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-bromoacetyl-beta-D-galactosylamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1984</Year>
   <Month>01</Month>
   <Day>04</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*GALACTOSAMINE (73-76)</PreviousIndexing>
   <PreviousIndexing>ACETIC ACIDS (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000116</DescriptorUI>
     <DescriptorName>
      <String>Acetylgalactosamine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 410(2):347;1975</Source>
   <Source>Nature (New Biol) 242(115):52;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043759</ConceptUI>
    <ConceptName>
     <String>N-bromoacetyl-beta-D-galactosylamine</String>
    </ConceptName>
    <CASN1Name>Acetamide, 2-bromo-N-beta-D-galactopyranosyl-</CASN1Name>
    <RegistryNumber>29086-04-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073762</TermUI>
      <String>N-bromoacetyl-beta-D-galactosylamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002930</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>L-fuconate dehydratase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>11</Day>
  </DateRevised>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>FUCOSE/analogs (75-82)</PreviousIndexing>
   <PreviousIndexing>SUGAR ACIDS (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006836</DescriptorUI>
     <DescriptorName>
      <String>Hydro-Lyases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 254(15):7060;1979</Source>
   <Source>Methods Enzymol 42(C):305;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043764</ConceptUI>
    <ConceptName>
     <String>L-fuconate dehydratase</String>
    </ConceptName>
    <RegistryNumber>EC 4.2.1.68</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073767</TermUI>
      <String>L-fuconate dehydratase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002990</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>butyl isocyanide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>11</Day>
  </DateRevised>
  <Frequency>21</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>BUTANES (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009570</DescriptorUI>
     <DescriptorName>
      <String>Nitriles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 248(5):1616;1973</Source>
   <Source>J Biol Chem 252(12):4102;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043882</ConceptUI>
    <ConceptName>
     <String>butyl isocyanide</String>
    </ConceptName>
    <RegistryNumber>2769-64-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073885</TermUI>
      <String>butyl isocyanide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073884</TermUI>
      <String>n-butylisocyanide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073883</TermUI>
      <String>1-isocyanobutane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002938</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>polyfructosan</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1984</Year>
   <Month>05</Month>
   <Day>15</Day>
  </DateRevised>
  <Frequency>43</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*POLYSACCHARIDES (73-75)</PreviousIndexing>
   <PreviousIndexing>FRUCTOSE (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005630</DescriptorUI>
     <DescriptorName>
      <String>Fructans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Pharmacol 30(2):182;1975</Source>
   <Source>Lab Pract 22(4):256;1973</Source>
   <Source>Pfluegers Arch 369:281;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043780</ConceptUI>
    <ConceptName>
     <String>polyfructosan</String>
    </ConceptName>
    <RegistryNumber>39421-73-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0043780</Concept1UI>
     <Concept2UI>M0043779</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0043780</Concept1UI>
     <Concept2UI>M0043778</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0043780</Concept1UI>
     <Concept2UI>M0043777</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073783</TermUI>
      <String>polyfructosan</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0043779</ConceptUI>
    <ConceptName>
     <String>polyfructosan-S</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0043780</Concept1UI>
     <Concept2UI>M0043779</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073782</TermUI>
      <String>polyfructosan-S</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0043778</ConceptUI>
    <ConceptName>
     <String>polyfructan-A48</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0043780</Concept1UI>
     <Concept2UI>M0043778</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073781</TermUI>
      <String>polyfructan-A48</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0043777</ConceptUI>
    <ConceptName>
     <String>Fructan S</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0043780</Concept1UI>
     <Concept2UI>M0043777</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073780</TermUI>
      <String>Fructan S</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002949</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>16 beta-21-methyl-D-nor-5-pregnen-3 beta-ol-20,21-dione 21-ethylene ketal</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>08</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PREGNENES (73-76)</PreviousIndexing>
   <PreviousIndexing>HYDROXYSTEROIDS (74-76)</PreviousIndexing>
   <PreviousIndexing>PREGNENEDIONES (73-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009652</DescriptorUI>
     <DescriptorName>
      <String>Norpregnenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Steroids Lipids Res 3(4):201;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043797</ConceptUI>
    <ConceptName>
     <String>16 beta-21-methyl-D-nor-5-pregnen-3 beta-ol-20,21-dione 21-ethylene ketal</String>
    </ConceptName>
    <CASN1Name>Methanone, ((3beta,16beta)-3-hydroxy-D-norandrost-5-en-16-yl)(2-methyl-1,3-dioxolan-2-yl)-</CASN1Name>
    <RegistryNumber>39932-40-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073800</TermUI>
      <String>16 beta-21-methyl-D-nor-5-pregnen-3 beta-ol-20,21-dione 21-ethylene ketal</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C409628</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>17-dimethylaminolobohedleolide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>06</Month>
   <Day>20</Day>
  </DateCreated>
  <Note>isolated from the soft coral Lobophytum; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001643</DescriptorUI>
     <DescriptorName>
      <String>Bridged Bicyclo Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005663</DescriptorUI>
     <DescriptorName>
      <String>Furans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2000 Apr;63(4):531-3</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0364577</ConceptUI>
    <ConceptName>
     <String>17-dimethylaminolobohedleolide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T417256</TermUI>
      <String>17-dimethylaminolobohedleolide</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>06</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C579003</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Prph2 protein, rat</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>10</Month>
   <Day>24</Day>
  </DateCreated>
  <Note>RefSeq:NP_037153.1. NM_013021.1.
  </Note>
  <Frequency>13</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D064531</DescriptorUI>
     <DescriptorName>
      <String>Peripherins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0466151</ConceptUI>
    <ConceptName>
     <String>Prph2 protein, rat</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T587639</TermUI>
      <String>Prph2 protein, rat</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>05</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T587641</TermUI>
      <String>Rds protein, rat</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>05</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T587640</TermUI>
      <String>peripherin 2, rat</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>05</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C509109</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>haiweeite</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>03</Month>
   <Day>30</Day>
  </DateCreated>
  <Note>an uranyl silicate  mineral compound
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D017640</DescriptorUI>
     <DescriptorName>
      <String>Silicates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D017974</DescriptorUI>
     <DescriptorName>
      <String>Uranium Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Spectrochim Acta A Mol Biomol Spectrosc. 2006 Feb;63(2):305-12</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0496539</ConceptUI>
    <ConceptName>
     <String>haiweeite</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T670130</TermUI>
      <String>haiweeite</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>03</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C409627</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>lobohedleolide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>06</Month>
   <Day>20</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>06</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>RN given for (3aS-(3aR*,6E,10E,14E,15aR*))-isomer; isolated from the soft coral Lobophytum; structure in first source
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001643</DescriptorUI>
     <DescriptorName>
      <String>Bridged Bicyclo Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005663</DescriptorUI>
     <DescriptorName>
      <String>Furans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2000 Apr;63(4):531-3</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0364576</ConceptUI>
    <ConceptName>
     <String>lobohedleolide</String>
    </ConceptName>
    <RegistryNumber>81026-38-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T417255</TermUI>
      <String>lobohedleolide</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>06</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C409629</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tylopiol A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>06</Month>
   <Day>20</Day>
  </DateCreated>
  <Note>isolated from the fungus Tylopilus plumbeoviolaceus; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004875</DescriptorUI>
     <DescriptorName>
      <String>Ergosterol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012632</DescriptorUI>
     <DescriptorName>
      <String>Secosteroids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2000 Apr;63(4):534-6</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0364578</ConceptUI>
    <ConceptName>
     <String>tylopiol A</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T417257</TermUI>
      <String>tylopiol A</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>06</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T417258</TermUI>
      <String>3-hydroxy-8,9-oxido-8,9-secoergosta-7,9(11),22-triene</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>06</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C509111</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hydrazinethiocarbamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>03</Month>
   <Day>30</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014508</DescriptorUI>
     <DescriptorName>
      <String>Urea</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Spectrochim Acta A Mol Biomol Spectrosc. 2006 Feb;63(2):416-22</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0496541</ConceptUI>
    <ConceptName>
     <String>hydrazinethiocarbamide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T670133</TermUI>
      <String>hydrazinethiocarbamide</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>03</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011801</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,2'-dithiobis(5-nitropyridine)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>11</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>17</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>DISULFIDES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011725</DescriptorUI>
     <DescriptorName>
      <String>Pyridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D013439</DescriptorUI>
     <DescriptorName>
      <String>Sulfhydryl Reagents</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Biochim Biophys Acta 423(3):590;1976</Source>
   <Source>Biochim Biophys Acta 459(1):20;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058381</ConceptUI>
    <ConceptName>
     <String>2,2'-dithiobis(5-nitropyridine)</String>
    </ConceptName>
    <RegistryNumber>2127-10-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088384</TermUI>
      <String>2,2'-dithiobis(5-nitropyridine)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T088381</TermUI>
      <String>2,2'-dithio-bis(5-nitropyridine)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T088383</TermUI>
      <String>DTBNP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T088382</TermUI>
      <String>2,2-DNP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002987</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4,5-dihydro-1,3-dimethyl-1,H-pyrazolo-(3,4-b)(1,4)- benzoxazepine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1989</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>RN given refers to HCl; RN for parent cpd not in Chemline 8/4/83; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BENZAZEPINES (73-75)</PreviousIndexing>
   <PreviousIndexing>PYRAZOLES (73-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010077</DescriptorUI>
     <DescriptorName>
      <String>Oxazepines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Int Pharmacodyn 202(1):119;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043871</ConceptUI>
    <ConceptName>
     <String>4,5-dihydro-1,3-dimethyl-1,H-pyrazolo-(3,4-b)(1,4)- benzoxazepine</String>
    </ConceptName>
    <RegistryNumber>34375-78-5</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0043871</Concept1UI>
     <Concept2UI>M0043870</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073874</TermUI>
      <String>4,5-dihydro-1,3-dimethyl-1,H-pyrazolo-(3,4-b)(1,4)- benzoxazepine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0043870</ConceptUI>
    <ConceptName>
     <String>4,5-dihydro-1,3-dimethyl-1,H-pyrazolo-(3,4-b)(1,4)-benzoxazepine, monohydrochloride</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0043871</Concept1UI>
     <Concept2UI>M0043870</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073873</TermUI>
      <String>4,5-dihydro-1,3-dimethyl-1,H-pyrazolo-(3,4-b)(1,4)-benzoxazepine, monohydrochloride</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C409630</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tylopiol B</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>06</Month>
   <Day>20</Day>
  </DateCreated>
  <Note>isolated from the fungus Tylopilus plumbeoviolaceus; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004875</DescriptorUI>
     <DescriptorName>
      <String>Ergosterol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012632</DescriptorUI>
     <DescriptorName>
      <String>Secosteroids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2000 Apr;63(4):534-6</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0364579</ConceptUI>
    <ConceptName>
     <String>tylopiol B</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T417259</TermUI>
      <String>tylopiol B</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>06</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T417260</TermUI>
      <String>3-hydroxy-8,9-oxido-8,9-secoergosta-7,22-dien-12-one</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>06</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013109</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>metapyrone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>11</Day>
  </DateRevised>
  <Note>inhibits adrenal 11 beta-hydroxylase
  </Note>
  <Frequency>116</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011725</DescriptorUI>
     <DescriptorName>
      <String>Pyridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mater Med Pol 8(2):108;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060621</ConceptUI>
    <ConceptName>
     <String>metapyrone</String>
    </ConceptName>
    <RegistryNumber>17286-92-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090624</TermUI>
      <String>metapyrone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T090623</TermUI>
      <String>2-methyl-1,2(bispyridyl)-1-propanone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002991</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>beta-methyl-asparagine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>03</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>RN given refers to (DL-threo)-isomer; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ASPARAGINE (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D001216</DescriptorUI>
     <DescriptorName>
      <String>Asparagine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 248(5):1741;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043883</ConceptUI>
    <ConceptName>
     <String>beta-methyl-asparagine</String>
    </ConceptName>
    <RegistryNumber>50817-24-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073886</TermUI>
      <String>beta-methyl-asparagine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003000</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>histocon</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>tissue transport medium used in lipid histochemical analysis of biopsies
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012996</DescriptorUI>
     <DescriptorName>
      <String>Solutions</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D014021</DescriptorUI>
     <DescriptorName>
      <String>Tissue Preservation</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Histochemie 34(3):249;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043904</ConceptUI>
    <ConceptName>
     <String>histocon</String>
    </ConceptName>
    <RegistryNumber>39346-80-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073907</TermUI>
      <String>histocon</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C443127</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>PPO 464</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>01</Month>
   <Day>08</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001381</DescriptorUI>
     <DescriptorName>
      <String>Azepines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011725</DescriptorUI>
     <DescriptorName>
      <String>Pyridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Microbiology 2001 Nov;147(Pt 11):44653-62</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0409884</ConceptUI>
    <ConceptName>
     <String>PPO 464</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T476528</TermUI>
      <String>PPO 464</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>01</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T476530</TermUI>
      <String>PPO464</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>01</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T476529</TermUI>
      <String>PPO-464</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>01</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003037</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>palmitoyl dihydroxyacetone phosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>27</Day>
  </DateRevised>
  <Frequency>10</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PALMITIC ACIDS (75-82)</PreviousIndexing>
   <PreviousIndexing>*TRIOSES (72-75)</PreviousIndexing>
   <PreviousIndexing>ORGANOPHOSPHORUS CPDS (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004099</DescriptorUI>
     <DescriptorName>
      <String>Dihydroxyacetone Phosphate</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 247(9):2944;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043968</ConceptUI>
    <ConceptName>
     <String>palmitoyl dihydroxyacetone phosphate</String>
    </ConceptName>
    <CASN1Name>hexadecanoic acid 2-oxo-3-(phosphonooxy)propyl ester</CASN1Name>
    <RegistryNumber>17378-38-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073971</TermUI>
      <String>palmitoyl dihydroxyacetone phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073970</TermUI>
      <String>palmitoyl glycerone phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073969</TermUI>
      <String>hexadecanoyl dihydroxyacetone phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C029597</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Concise-Cap-C-Rynge</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>06</Month>
   <Day>08</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>03</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>photoactivated composite dental restorative material
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003188</DescriptorUI>
     <DescriptorName>
      <String>Composite Resins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Dent 1981;9(1):36</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0094322</ConceptUI>
    <ConceptName>
     <String>Concise-Cap-C-Rynge</String>
    </ConceptName>
    <CASN1Name>Concise-Cap-C-Rynge</CASN1Name>
    <RegistryNumber>78590-47-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T124325</TermUI>
      <String>Concise-Cap-C-Rynge</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T124324</TermUI>
      <String>CCCR</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C087654</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3'-O-galactopyranosyl-1-4-O-galactopyranosylcytarabine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>07</Month>
   <Day>08</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>03</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003561</DescriptorUI>
     <DescriptorName>
      <String>Cytarabine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004187</DescriptorUI>
     <DescriptorName>
      <String>Disaccharides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biosci Biotechnol Biochem 1994 Apr;58(4):639-43</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0232113</ConceptUI>
    <ConceptName>
     <String>3'-O-galactopyranosyl-1-4-O-galactopyranosylcytarabine</String>
    </ConceptName>
    <RegistryNumber>155603-73-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T262118</TermUI>
      <String>3'-O-galactopyranosyl-1-4-O-galactopyranosylcytarabine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T262117</TermUI>
      <String>3'-O-galactopyranosyl-1-4-O-galactopyranosyl-ara-C</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T262116</TermUI>
      <String>3'-Gal-1-4-Gal-ara-C</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003033</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>pachymaran</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>derived from a natural glucan, pachyman
  </Note>
  <Frequency>8</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*POLYSACCHARIDES (72-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005936</DescriptorUI>
     <DescriptorName>
      <String>Glucans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cell Immunol 38(2):328;1978</Source>
   <Source>Chem Biol Interact 3(1):69;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043963</ConceptUI>
    <ConceptName>
     <String>pachymaran</String>
    </ConceptName>
    <RegistryNumber>65637-98-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073966</TermUI>
      <String>pachymaran</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C029606</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hemoglobin Genova</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>06</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>03</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>Leu replaced by Pro at position 28 on beta chain
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006455</DescriptorUI>
     <DescriptorName>
      <String>Hemoglobins, Abnormal</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 1981;667(2):233</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0094345</ConceptUI>
    <ConceptName>
     <String>hemoglobin Genova</String>
    </ConceptName>
    <RegistryNumber>9034-78-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T124348</TermUI>
      <String>hemoglobin Genova</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T124347</TermUI>
      <String>Hb Genova</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C061823</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-propylpentanal diisopropyl acetal</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1989</Year>
   <Month>12</Month>
   <Day>27</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>structure given in first source; precursor to valproic acid
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000080</DescriptorUI>
     <DescriptorName>
      <String>Acetals</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Drug Metab Dispos 1989;17(5):233</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0171319</ConceptUI>
    <ConceptName>
     <String>2-propylpentanal diisopropyl acetal</String>
    </ConceptName>
    <RegistryNumber>124345-19-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T201324</TermUI>
      <String>2-propylpentanal diisopropyl acetal</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T201323</TermUI>
      <String>PPDIIA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C087758</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>difructose anhydride III</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>07</Month>
   <Day>14</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>03</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>a non-reducing derivative of inulobiose
  </Note>
  <Frequency>56</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004187</DescriptorUI>
     <DescriptorName>
      <String>Disaccharides</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Appl Biochem Biotechnol 1994 Spring;45-46:269-82</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0232384</ConceptUI>
    <ConceptName>
     <String>difructose anhydride III</String>
    </ConceptName>
    <CASN1Name>alpha-D-Fructofuranose beta-D-fructofuranose 1,2':2,3'-dianhydride</CASN1Name>
    <RegistryNumber>81129-73-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T262389</TermUI>
      <String>difructose anhydride III</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T262388</TermUI>
      <String>beta-2,1'-alpha-2',3-difructofuranose anhydride</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T262387</TermUI>
      <String>DFA III</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C509114</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,4-diamino-6-hydroxy-5-nitroso pyrimidine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>03</Month>
   <Day>30</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009603</DescriptorUI>
     <DescriptorName>
      <String>Nitroso Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011743</DescriptorUI>
     <DescriptorName>
      <String>Pyrimidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Spectrochim Acta A Mol Biomol Spectrosc. 2006 Feb;63(2):454-63</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0496545</ConceptUI>
    <ConceptName>
     <String>2,4-diamino-6-hydroxy-5-nitroso pyrimidine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
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       <Year>2006</Year>
       <Month>03</Month>
       <Day>30</Day>
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       <ThesaurusID>NLM (2006)</ThesaurusID>
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  <DateCreated>
   <Year>1994</Year>
   <Month>07</Month>
   <Day>18</Day>
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  <DateRevised>
   <Year>2001</Year>
   <Month>03</Month>
   <Day>01</Day>
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  <Frequency>1</Frequency>
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  <SourceList>
   <Source>Carbohydr Res 1994 Apr 16;257(1):25-33</Source>
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       <ThesaurusID>NLM (1994)</ThesaurusID>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T262522</TermUI>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T262521</TermUI>
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   <String>4-chloromethyl-2-(2-hydroxybenzilidenehydrazino) thiazole</String>
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  <DateCreated>
   <Year>2006</Year>
   <Month>03</Month>
   <Day>30</Day>
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  <Note>structure in first source
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  <Frequency>1</Frequency>
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     <DescriptorUI>*D006834</DescriptorUI>
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   <HeadingMappedTo>
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  <SourceList>
   <Source>Spectrochim Acta A Mol Biomol Spectrosc. 2006 Feb;63(2):506-10</Source>
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      <DateCreated>
       <Year>2006</Year>
       <Month>03</Month>
       <Day>30</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T670143</TermUI>
      <String>4-CM-HBH-T</String>
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       <Year>2006</Year>
       <Month>03</Month>
       <Day>30</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
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  <SupplementalRecordName>
   <String>2-hydroxy-3-methoxy-5-nitrobenzaldehyde</String>
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  <DateCreated>
   <Year>2006</Year>
   <Month>03</Month>
   <Day>30</Day>
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  <DateRevised>
   <Year>2006</Year>
   <Month>03</Month>
   <Day>30</Day>
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  <Note>structure in first source
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  <Frequency>1</Frequency>
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     <DescriptorUI>*D001547</DescriptorUI>
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  <SourceList>
   <Source>Spectrochim Acta A Mol Biomol Spectrosc. 2006 Feb;63(2):464-76</Source>
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   <Concept PreferredConceptYN="Y">
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     <String>2-hydroxy-3-methoxy-5-nitrobenzaldehyde</String>
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    <RegistryNumber>0</RegistryNumber>
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      <TermUI>T670139</TermUI>
      <String>2-hydroxy-3-methoxy-5-nitrobenzaldehyde</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>03</Month>
       <Day>30</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T670140</TermUI>
      <String>HMN cpd</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>03</Month>
       <Day>30</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
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  <SupplementalRecordUI>C003028</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-(1-oxyl-2,2,6,6-tetramethyl-4-piperidinyl)iodoacetamide</String>
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  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>11</Day>
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  <Note>structure
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  <Frequency>23</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PIPERIDINES (71-81)</PreviousIndexing>
   <PreviousIndexing>ACETAMIDES (71-75)</PreviousIndexing>
   <PreviousIndexing>IODOACETAMIDE/analogs (75-76)</PreviousIndexing>
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    <DescriptorReferredTo>
     <DescriptorUI>*D003497</DescriptorUI>
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      <String>Cyclic N-Oxides</String>
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  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D013113</DescriptorUI>
     <DescriptorName>
      <String>Spin Labels</String>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043958</ConceptUI>
    <ConceptName>
     <String>N-(1-oxyl-2,2,6,6-tetramethyl-4-piperidinyl)iodoacetamide</String>
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    <RegistryNumber>25713-24-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073961</TermUI>
      <String>N-(1-oxyl-2,2,6,6-tetramethyl-4-piperidinyl)iodoacetamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073955</TermUI>
      <String>4-(2-iodoacetamido)-2,2,6,6-tetramethylpiperidine-1-oxyl</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073960</TermUI>
      <String>TMPIA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073958</TermUI>
      <String>N-(1-oxy-2,2,6,6-tetramethyl-4-piperidinyl)iodoacetamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073959</TermUI>
      <String>N-(oxyl-2,2,6,6-tetramethylpiperid-4-yl)iodoacetamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073957</TermUI>
      <String>IASL</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073954</TermUI>
      <String>2,2,6,6-tetramethylpiperdin-N-1-oxyiodoacetamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073956</TermUI>
      <String>4-(N-iodoacetamide)-2,2,6,6-tetramethylpiperidine-1-oxyl</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
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   </Concept>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C443129</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>BF9 chymotrypsin inhibitor</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>01</Month>
   <Day>08</Day>
  </DateCreated>
  <Note>isolated from Bungarus fasciatus; amino acid sequence in first source
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  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002038</DescriptorUI>
     <DescriptorName>
      <String>Bungarotoxins</String>
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    </DescriptorReferredTo>
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  </HeadingMappedToList>
  <SourceList>
   <Source>Int J Pept Protein Res 1983 Feb;21(2):209-15</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0409886</ConceptUI>
    <ConceptName>
     <String>BF9 chymotrypsin inhibitor</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T476532</TermUI>
      <String>BF9 chymotrypsin inhibitor</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>01</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
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     </Term>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003071</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>perfluorohexylbromide</String>
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  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>05</Month>
   <Day>28</Day>
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  <Note>6-carbon perfluorocarbon radiopaque compound
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  <Frequency>6</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*HYDROCARBONS, FLUORINATED (74-77)</PreviousIndexing>
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     <DescriptorUI>*D005466</DescriptorUI>
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  <SourceList>
   <Source>Chest 61(2):64S;1972</Source>
   <Source>J Comput Assist Tomogr 1979;3(5):622</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043999</ConceptUI>
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    <RegistryNumber>335-56-8</RegistryNumber>
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     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
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  <DateCreated>
   <Year>1994</Year>
   <Month>07</Month>
   <Day>18</Day>
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  <DateRevised>
   <Year>2001</Year>
   <Month>03</Month>
   <Day>01</Day>
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
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    <DescriptorReferredTo>
     <DescriptorUI>*D004187</DescriptorUI>
     <DescriptorName>
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  <SourceList>
   <Source>Carbohydr Res 1994 Apr 16;257(1):25-33</Source>
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    <RegistryNumber>0</RegistryNumber>
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     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
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      <String>6-C-(benzyl 5-deoxy-2,3-O-isopropylidene-ribofuranosid-5-yl)-1,2-3,4-di-O-isopropylidene-glycero-galacto-hexopyranose</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T262529</TermUI>
      <String>BDIRIG</String>
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       <ThesaurusID>NLM (1994)</ThesaurusID>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T262528</TermUI>
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   <String>2-chloro-6-(3-methoxyphenyl)aminopurine</String>
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  <DateCreated>
   <Year>2013</Year>
   <Month>04</Month>
   <Day>30</Day>
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  <Note>inhibits cytokine degradation; inhibits AtCKX2 protein
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    <DescriptorReferredTo>
     <DescriptorUI>D000225</DescriptorUI>
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      <String>analogs &amp; derivatives</String>
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  <SourceList>
   <Source>Bioorg Med Chem. 2008 Oct 15;16(20):9268-75.</Source>
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      <TermUI>T843399</TermUI>
      <String>2-chloro-6-(3-methoxyphenyl)aminopurine</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>04</Month>
       <Day>30</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T843400</TermUI>
      <String>INCYDE</String>
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       <Year>2013</Year>
       <Month>04</Month>
       <Day>30</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C509116</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-methoxy-1-naphthaldehyde</String>
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  <DateCreated>
   <Year>2006</Year>
   <Month>03</Month>
   <Day>30</Day>
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  <Note>structure in first source
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  <Frequency>1</Frequency>
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    <DescriptorReferredTo>
     <DescriptorUI>*D000447</DescriptorUI>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009281</DescriptorUI>
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   <Source>Spectrochim Acta A Mol Biomol Spectrosc. 2006 Feb;63(2):464-76</Source>
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     <String>2-methoxy-1-naphthaldehyde</String>
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    <RegistryNumber>0</RegistryNumber>
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     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T670141</TermUI>
      <String>2-methoxy-1-naphthaldehyde</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>03</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003092</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-phenyl-1-(2',5'-dimethoxyphenyl)-3-piperidinobutanol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>06</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>RN given refers to HCl
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ALCOHOLS, BUTYL (72-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010880</DescriptorUI>
     <DescriptorName>
      <String>Piperidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Int Pharmacodyn 193(2):372;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044038</ConceptUI>
    <ConceptName>
     <String>1-phenyl-1-(2',5'-dimethoxyphenyl)-3-piperidinobutanol</String>
    </ConceptName>
    <RegistryNumber>858-68-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074041</TermUI>
      <String>1-phenyl-1-(2',5'-dimethoxyphenyl)-3-piperidinobutanol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003096</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>alpha-phenylglutarimide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>27</Day>
  </DateRevised>
  <Note>metabolite of glutethimide; structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PIPERIDIONES (73-79)</PreviousIndexing>
   <PreviousIndexing>BENZENE DERIVATIVES (75-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005984</DescriptorUI>
     <DescriptorName>
      <String>Glutethimide</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Med 6(2):127;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044039</ConceptUI>
    <ConceptName>
     <String>alpha-phenylglutarimide</String>
    </ConceptName>
    <RegistryNumber>14149-34-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074042</TermUI>
      <String>alpha-phenylglutarimide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003104</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-(4-phenyl-1-piperazinylmethyl)cyclohexanone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>08</Month>
   <Day>14</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CYCLOHEXANE (72-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003512</DescriptorUI>
     <DescriptorName>
      <String>Cyclohexanones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010879</DescriptorUI>
     <DescriptorName>
      <String>Piperazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D003665</DescriptorUI>
     <DescriptorName>
      <String>Decompression Sickness</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000188</QualifierUI>
     <QualifierName>
      <String>drug therapy</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Aerosp Med 42(8):837;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044045</ConceptUI>
    <ConceptName>
     <String>2-(4-phenyl-1-piperazinylmethyl)cyclohexanone</String>
    </ConceptName>
    <RegistryNumber>735-78-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074048</TermUI>
      <String>2-(4-phenyl-1-piperazinylmethyl)cyclohexanone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C580808</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,4-bis(p-hydroxyphenyl)-2-butenal</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>04</Month>
   <Day>30</Day>
  </DateCreated>
  <Note>has antineoplastic activity
  </Note>
  <Frequency>8</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000447</DescriptorUI>
     <DescriptorName>
      <String>Aldehydes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010636</DescriptorUI>
     <DescriptorName>
      <String>Phenols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nutr Cancer. 2012;64(8):1236-44.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0584354</ConceptUI>
    <ConceptName>
     <String>2,4-bis(p-hydroxyphenyl)-2-butenal</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0584354</Concept1UI>
     <Concept2UI>M0584355</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T843402</TermUI>
      <String>2,4-bis(p-hydroxyphenyl)-2-butenal</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>04</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0584355</ConceptUI>
    <ConceptName>
     <String>HPB242</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0584354</Concept1UI>
     <Concept2UI>M0584355</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T843403</TermUI>
      <String>HPB242</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>04</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C043278</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>indolizomycin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1985</Year>
   <Month>02</Month>
   <Day>05</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>17</Day>
  </DateRevised>
  <Note>isolated from Streptomyces griseus and S. tenjimarienis; structure given in first source
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007212</DescriptorUI>
     <DescriptorName>
      <String>Indolizines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiot (Tokyo) 1984;37(11):1491</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0127435</ConceptUI>
    <ConceptName>
     <String>indolizomycin</String>
    </ConceptName>
    <CASN1Name>6bH-Cycloprop(a)oxireno(g)indolizin-6b-ol, octahydro-5-(5-methyl-1,3,5-heptatrienyl)-</CASN1Name>
    <RegistryNumber>94935-24-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T157440</TermUI>
      <String>indolizomycin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T157439</TermUI>
      <String>(1S,2R,3S,7R,8R)-7,8-epoxy-8a-hydroxy-1,2-dimethylene-3-(1E,3E,5E)-(5-methyl-1,3,5-heptatrienyl)octahydroindolizine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C580810</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>echinohalimane A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>04</Month>
   <Day>30</Day>
  </DateCreated>
  <Note>has antineoplastic activtiy; isolated from the gorgonian Echinomuricea
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004224</DescriptorUI>
     <DescriptorName>
      <String>Diterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D015107</DescriptorUI>
     <DescriptorName>
      <String>4-Butyrolactone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mar Drugs. 2012 Oct;10(10):2246-53.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0584357</ConceptUI>
    <ConceptName>
     <String>echinohalimane A</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T843406</TermUI>
      <String>echinohalimane A</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>04</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C104848</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>FruA protein, Myxococcus xanthus</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1997</Year>
   <Month>03</Month>
   <Day>28</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>11</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>required for development; isolated from Myxococcus xanthus; amino acid sequence in first source; GenBank D50555
  </Note>
  <Frequency>37</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DNA-BINDING PROTEINS (1997-2002)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014157</DescriptorUI>
     <DescriptorName>
      <String>Transcription Factors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Microbiol 1996 Nov;22(4):757-67</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0273719</ConceptUI>
    <ConceptName>
     <String>FruA protein, Myxococcus xanthus</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T520905</TermUI>
      <String>FruA protein, Myxococcus xanthus</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>09</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007172</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-cyano-2-furaldehyde</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*FURALDEHYDE (74-75)</PreviousIndexing>
   <PreviousIndexing>NITRILES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005662</DescriptorUI>
     <DescriptorName>
      <String>Furaldehyde</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Soc Jpn 93(11):1526;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050198</ConceptUI>
    <ConceptName>
     <String>5-cyano-2-furaldehyde</String>
    </ConceptName>
    <RegistryNumber>42061-89-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080201</TermUI>
      <String>5-cyano-2-furaldehyde</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007184</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cyclo-CDP</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CYTOSINE NUCLEOTIDES (74-78)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003565</DescriptorUI>
     <DescriptorName>
      <String>Cytidine Diphosphate</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009712</DescriptorUI>
     <DescriptorName>
      <String>Nucleotides, Cyclic</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Pharmacol 22(22):2829;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050220</ConceptUI>
    <ConceptName>
     <String>cyclo-CDP</String>
    </ConceptName>
    <CASN1Name>cyclocytidine 5'-diphosphate</CASN1Name>
    <RegistryNumber>5511-94-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080223</TermUI>
      <String>cyclo-CDP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007185</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cyclo-CMP</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CYTOSINE NUCLEOTIDES (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003568</DescriptorUI>
     <DescriptorName>
      <String>Cytidine Monophosphate</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009712</DescriptorUI>
     <DescriptorName>
      <String>Nucleotides, Cyclic</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Pharmacol 22(22):2829;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050221</ConceptUI>
    <ConceptName>
     <String>cyclo-CMP</String>
    </ConceptName>
    <CASN1Name>cyclocytidine 5'-monophosphate</CASN1Name>
    <RegistryNumber>39679-56-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080224</TermUI>
      <String>cyclo-CMP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007197</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5',2-O-cyclo,2'3'-O-isopropylidene uridine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*URIDINE (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014529</DescriptorUI>
     <DescriptorName>
      <String>Uridine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 340(4):472;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050231</ConceptUI>
    <ConceptName>
     <String>5',2-O-cyclo,2'3'-O-isopropylidene uridine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080234</TermUI>
      <String>5',2-O-cyclo,2'3'-O-isopropylidene uridine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007200</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cyclopenin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1984</Year>
   <Month>02</Month>
   <Day>24</Day>
  </DateRevised>
  <Note>Penicillium metabolite; structure
  </Note>
  <Frequency>12</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>EPOXY COMPOUNDS (75-78)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D001570</DescriptorUI>
     <DescriptorName>
      <String>Benzodiazepinones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 42(23):3650;1977</Source>
   <Source>Pharmazie 29(8):506;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050236</ConceptUI>
    <ConceptName>
     <String>cyclopenin</String>
    </ConceptName>
    <CASN1Name>4-methyl-3'-phenylspiro(3H-1,4-benzodiazepine- 3,2'-oxirane)-2,5(1H,4H)-dione</CASN1Name>
    <RegistryNumber>20007-87-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080239</TermUI>
      <String>cyclopenin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007207</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cyclotrichosantol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>24</Day>
  </DateRevised>
  <Note>isolated from leaves of Trichosantes palmata L., Cucurbitaceae; also characterized as a C(31) 31- nortriterpene; structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CYCLOSTEROIDS (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013261</DescriptorUI>
     <DescriptorName>
      <String>Sterols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 38(21):3688;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050251</ConceptUI>
    <ConceptName>
     <String>cyclotrichosantol</String>
    </ConceptName>
    <CASN1Name>4 alpha,14 alpha-dimethyl-24-ethyl-9,19-cyclocholest-25-ene-3 beta-ol</CASN1Name>
    <RegistryNumber>41507-26-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080254</TermUI>
      <String>cyclotrichosantol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C105035</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>IAP34 protein, Pisum sativum</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1997</Year>
   <Month>04</Month>
   <Day>09</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>11</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>a 34 kDa component of the outer membrane complex involved in chloroplast protein import; amino acid sequence known
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*GTP-BINDING PROTEINS (1997-2002)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010940</DescriptorUI>
     <DescriptorName>
      <String>Plant Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D020559</DescriptorUI>
     <DescriptorName>
      <String>Monomeric GTP-Binding Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D002736</DescriptorUI>
     <DescriptorName>
      <String>Chloroplasts</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Biol Chem 1997 Mar 7;272(10):6614-20</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0274158</ConceptUI>
    <ConceptName>
     <String>IAP34 protein, Pisum sativum</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T519665</TermUI>
      <String>IAP34 protein, Pisum sativum</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>09</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C465816</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>8-methoxy-5'-deoxyadenosylcobalamin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>09</Month>
   <Day>30</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003038</DescriptorUI>
     <DescriptorName>
      <String>Cobamides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Inorg Biochem 2002 Aug 15;91(2):388-99</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0439178</ConceptUI>
    <ConceptName>
     <String>8-methoxy-5'-deoxyadenosylcobalamin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T520845</TermUI>
      <String>8-methoxy-5'-deoxyadenosylcobalamin</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>09</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T520846</TermUI>
      <String>8-M-5'-DAC</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>09</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007213</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cytidine diphosphate-4-keto-3,6-dideoxyglucose</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>02</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*NUCLEOSIDE DIPHOSPHATE SUGARS (74-78)</PreviousIndexing>
   <PreviousIndexing>CDP/analogs (78-78)</PreviousIndexing>
   <PreviousIndexing>CYTOSINE NUCLEOTIDES (74-78)</PreviousIndexing>
   <PreviousIndexing>DEOXY SUGARS (74-78)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009702</DescriptorUI>
     <DescriptorName>
      <String>Nucleoside Diphosphate Sugars</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 249(12):3776;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050263</ConceptUI>
    <ConceptName>
     <String>cytidine diphosphate-4-keto-3,6-dideoxyglucose</String>
    </ConceptName>
    <CASN1Name>Cytidine 5'-(trihydrogen diphosphate), mono(3,6-dideoxy-alpha-D-erythro-hexopyranos-4-ulosyl) ester</CASN1Name>
    <RegistryNumber>21870-27-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080266</TermUI>
      <String>cytidine diphosphate-4-keto-3,6-dideoxyglucose</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007264</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6-seleno-2'-deoxyguanosine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DEOXYTRIBONUCLEOSIDES (74-79)</PreviousIndexing>
   <PreviousIndexing>*GUANOSINE (74-79)</PreviousIndexing>
   <PreviousIndexing>SELENIUM (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003849</DescriptorUI>
     <DescriptorName>
      <String>Deoxyguanosine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 17(3):263;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050344</ConceptUI>
    <ConceptName>
     <String>6-seleno-2'-deoxyguanosine</String>
    </ConceptName>
    <RegistryNumber>37025-79-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080347</TermUI>
      <String>6-seleno-2'-deoxyguanosine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T080346</TermUI>
      <String>2'-deoxy-6-selenoguanosine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003850</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>benzyl-2-hydroxyethyl-trisulfide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>07</Month>
   <Day>11</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BENZYL COMPOUNDS (73-76)</PreviousIndexing>
   <PreviousIndexing>ALCOHOL, ETHYL (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000431</DescriptorUI>
     <DescriptorName>
      <String>Ethanol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013440</DescriptorUI>
     <DescriptorName>
      <String>Sulfides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arzneim Forsch 22(11):1975;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044959</ConceptUI>
    <ConceptName>
     <String>benzyl-2-hydroxyethyl-trisulfide</String>
    </ConceptName>
    <RegistryNumber>40096-00-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074962</TermUI>
      <String>benzyl-2-hydroxyethyl-trisulfide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003858</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,2,6,6-tetramethyl-4-chloromercuricarbobenzoxypiperidine-1-oxyl</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>07</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ORGANOMETALLIC COMPOUNDS (73-76)</PreviousIndexing>
   <PreviousIndexing>PIPERIDINES (73-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003497</DescriptorUI>
     <DescriptorName>
      <String>Cyclic N-Oxides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D013113</DescriptorUI>
     <DescriptorName>
      <String>Spin Labels</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Mol Biol 6(4):455;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044969</ConceptUI>
    <ConceptName>
     <String>2,2,6,6-tetramethyl-4-chloromercuricarbobenzoxypiperidine-1-oxyl</String>
    </ConceptName>
    <CASN1Name>1-Pyrrolidinyloxy, 4-((4-(chloromercurio)phenoxy)carbonyl)-2,2,6,6-tetramethyl-</CASN1Name>
    <RegistryNumber>78717-58-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074972</TermUI>
      <String>2,2,6,6-tetramethyl-4-chloromercuricarbobenzoxypiperidine-1-oxyl</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003859</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>methylthioethanol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*MERCAPTOETHANOL (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008623</DescriptorUI>
     <DescriptorName>
      <String>Mercaptoethanol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 286(1):84;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044970</ConceptUI>
    <ConceptName>
     <String>methylthioethanol</String>
    </ConceptName>
    <CASN1Name>Ethanol, 2-(methylthio)-</CASN1Name>
    <RegistryNumber>5271-38-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074973</TermUI>
      <String>methylthioethanol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003862</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>homoadenosine 6'-phosphonic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PHOSPHONIC ACIDS (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000227</DescriptorUI>
     <DescriptorName>
      <String>Adenine Nucleotides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 12(9):1730;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044973</ConceptUI>
    <ConceptName>
     <String>homoadenosine 6'-phosphonic acid</String>
    </ConceptName>
    <CASN1Name>9H-Purin-6-amine, 9-(5-deoxy-6-C-phosphono-beta-D-ribo-hexofuranosyl)-</CASN1Name>
    <RegistryNumber>42155-80-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074976</TermUI>
      <String>homoadenosine 6'-phosphonic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003876</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6,7-dihydroxytetrahydroisoquinoline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007546</DescriptorUI>
     <DescriptorName>
      <String>Isoquinolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Brain Res 51(0):161;1973</Source>
   <Source>J Chromatogr 114(2):476;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044990</ConceptUI>
    <ConceptName>
     <String>6,7-dihydroxytetrahydroisoquinoline</String>
    </ConceptName>
    <RegistryNumber>40704-74-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074993</TermUI>
      <String>6,7-dihydroxytetrahydroisoquinoline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003879</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-pentynoic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>9</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ALKYNES (73-75)</PreviousIndexing>
   <PreviousIndexing>PENTANOIC ACIDS (75-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005231</DescriptorUI>
     <DescriptorName>
      <String>Fatty Acids, Unsaturated</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Experientia 29(3):277;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044991</ConceptUI>
    <ConceptName>
     <String>4-pentynoic acid</String>
    </ConceptName>
    <RegistryNumber>6089-09-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074994</TermUI>
      <String>4-pentynoic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003881</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cannabivarichromene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>24</Day>
  </DateRevised>
  <Note>cannabinoid with a propyl side chain
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CANNABIS (73-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002186</DescriptorUI>
     <DescriptorName>
      <String>Cannabinoids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Experentia 29(3):260;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044992</ConceptUI>
    <ConceptName>
     <String>cannabivarichromene</String>
    </ConceptName>
    <RegistryNumber>41408-19-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T074995</TermUI>
      <String>cannabivarichromene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003886</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dihydroxythiobinupharidine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>06</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>7</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*QUINOLIZINES (73-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000470</DescriptorUI>
     <DescriptorName>
      <String>Alkaloids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 62(5):826;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0044997</ConceptUI>
    <ConceptName>
     <String>dihydroxythiobinupharidine</String>
    </ConceptName>
    <RegistryNumber>30343-70-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T075000</TermUI>
      <String>dihydroxythiobinupharidine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003895</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>10-(2',6'-dimethylphenyl)-3-methylisoalloxazine-6,8- disulfonate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>09</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ARYL SULFONATES (73-82)</PreviousIndexing>
   <PreviousIndexing>SULFONIC ACIDS (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005415</DescriptorUI>
     <DescriptorName>
      <String>Flavins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 12(11):2083;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0045005</ConceptUI>
    <ConceptName>
     <String>10-(2',6'-dimethylphenyl)-3-methylisoalloxazine-6,8- disulfonate</String>
    </ConceptName>
    <CASN1Name>Benzo(g)pteridine-6,8-disulfonic acid, 10-(2,6-dimethylphenyl)-2,3,4,10-tetrahydro-3-methyl-2,4-dioxo-</CASN1Name>
    <RegistryNumber>40155-15-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T075008</TermUI>
      <String>10-(2',6'-dimethylphenyl)-3-methylisoalloxazine-6,8- disulfonate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003948</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>amenorone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>08</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>oral contraceptive used in pregnancy test; contains above 2 cpds
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CONTRACEPTIVES, ORAL (73-76)</PreviousIndexing>
   <PreviousIndexing>DRUG COMBINATIONS (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004997</DescriptorUI>
     <DescriptorName>
      <String>Ethinyl Estradiol</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005003</DescriptorUI>
     <DescriptorName>
      <String>Ethisterone</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D003277</DescriptorUI>
     <DescriptorName>
      <String>Contraceptives, Oral, Combined</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Nature 242(397):410;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0045089</ConceptUI>
    <ConceptName>
     <String>amenorone</String>
    </ConceptName>
    <RegistryNumber>53568-84-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T075092</TermUI>
      <String>amenorone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C004934</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>eleostearic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>12</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>RN given refers to cpd with unspecified isomeric designation
  </Note>
  <Frequency>74</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*FATTY ACIDS, UNSATURATED (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008042</DescriptorUI>
     <DescriptorName>
      <String>Linolenic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0046163</ConceptUI>
    <ConceptName>
     <String>eleostearic acid</String>
    </ConceptName>
    <CASN1Name>9,11,13-octadecatrienoic acid</CASN1Name>
    <RegistryNumber>13296-76-9</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>4337-71-7 ((Z,E,E)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>506-23-0 ((E,Z,E)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>544-72-9 ((Z,Z,E)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>544-73-0 ((E,E,E)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0046163</Concept1UI>
     <Concept2UI>M0492408</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0046163</Concept1UI>
     <Concept2UI>M0308803</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0046163</Concept1UI>
     <Concept2UI>M0308805</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0046163</Concept1UI>
     <Concept2UI>M0308806</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0046163</Concept1UI>
     <Concept2UI>M0308804</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T076166</TermUI>
      <String>eleostearic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T661015</TermUI>
      <String>9,11,13-CLN</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>12</Month>
       <Day>04</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T661014</TermUI>
      <String>9,11,13-conjugated linolenic acid</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>12</Month>
       <Day>04</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T076165</TermUI>
      <String>trichosanic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T661013</TermUI>
      <String>9,11,13-octadecatrienoic acid</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>12</Month>
       <Day>04</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0492408</ConceptUI>
    <ConceptName>
     <String>9cis,11trans,13trans-conjugated linolenic acid</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0046163</Concept1UI>
     <Concept2UI>M0492408</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T661016</TermUI>
      <String>9cis,11trans,13trans-conjugated linolenic acid</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>12</Month>
       <Day>04</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T661017</TermUI>
      <String>9c,11t,13t-CLN</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>12</Month>
       <Day>04</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0308803</ConceptUI>
    <ConceptName>
     <String>eleostearic acid, (Z,E,E)-isomer</String>
    </ConceptName>
    <RegistryNumber>4337-71-7</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0046163</Concept1UI>
     <Concept2UI>M0308803</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T338803</TermUI>
      <String>eleostearic acid, (Z,E,E)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0308805</ConceptUI>
    <ConceptName>
     <String>eleostearic acid, (Z,Z,E)-isomer</String>
    </ConceptName>
    <RegistryNumber>544-72-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0046163</Concept1UI>
     <Concept2UI>M0308805</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T338805</TermUI>
      <String>eleostearic acid, (Z,Z,E)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0308806</ConceptUI>
    <ConceptName>
     <String>eleostearic acid, (E,E,E)-isomer</String>
    </ConceptName>
    <RegistryNumber>544-73-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0046163</Concept1UI>
     <Concept2UI>M0308806</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T338806</TermUI>
      <String>eleostearic acid, (E,E,E)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0308804</ConceptUI>
    <ConceptName>
     <String>eleostearic acid, (E,Z,E)-isomer</String>
    </ConceptName>
    <RegistryNumber>506-23-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0046163</Concept1UI>
     <Concept2UI>M0308804</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T338804</TermUI>
      <String>eleostearic acid, (E,Z,E)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C074773</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hydantoin racemase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1992</Year>
   <Month>06</Month>
   <Day>28</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>10</Month>
   <Day>24</Day>
  </DateRevised>
  <Note>amino acid sequence given in first source; catalyzes the racemization of 5-substituted hydantoins in Pseudomonas to their corresponding N-carbamoyl amino acids and ultimately to the corresponding L-amino acid; expressed in Acrobacter aurescens
  </Note>
  <Frequency>14</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D019998</DescriptorUI>
     <DescriptorName>
      <String>Racemases and Epimerases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D011549</DescriptorUI>
     <DescriptorName>
      <String>Pseudomonas</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Bacteriol 1992 Jun;174(11):3461-6</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0201762</ConceptUI>
    <ConceptName>
     <String>hydantoin racemase</String>
    </ConceptName>
    <RegistryNumber>EC 5.1.99.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T231767</TermUI>
      <String>hydantoin racemase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C071931</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bombinin-like peptide-3, Bombina orientalis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1992</Year>
   <Month>01</Month>
   <Day>10</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>07</Month>
   <Day>14</Day>
  </DateRevised>
  <Note>amino acid sequence given in first source
  </Note>
  <Frequency>4</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PEPTIDES (1992-2000)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D023181</DescriptorUI>
     <DescriptorName>
      <String>Antimicrobial Cationic Peptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029845</DescriptorUI>
     <DescriptorName>
      <String>Amphibian Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 1991;266(34):23103</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0195108</ConceptUI>
    <ConceptName>
     <String>bombinin-like peptide-3, Bombina orientalis</String>
    </ConceptName>
    <RegistryNumber>138220-02-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T596584</TermUI>
      <String>bombinin-like peptide-3, Bombina orientalis</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>14</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T596585</TermUI>
      <String>BLP-3 protein, Bombina orientalis</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>14</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C049646</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N,N-dimethylformamidase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1986</Year>
   <Month>09</Month>
   <Day>24</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>hydrolyzes N,N-dimethylformamide into dimethylamine &amp; formate; enzyme isolated from Pseudomonas DMF 3/3
  </Note>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000581</DescriptorUI>
     <DescriptorName>
      <String>Amidohydrolases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Biochem 1986;158(3):469</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0142145</ConceptUI>
    <ConceptName>
     <String>N,N-dimethylformamidase</String>
    </ConceptName>
    <RegistryNumber>EC 3.5.1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T172150</TermUI>
      <String>N,N-dimethylformamidase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1986)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T172148</TermUI>
      <String>DMFase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1986)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T172149</TermUI>
      <String>N,N-dimethylformamide-hydrolyzing enzyme</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1986)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003909</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-methylaminomethyl-2-thiouridylate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>METHYLAMINES (73-75)</PreviousIndexing>
   <PreviousIndexing>THIOURACIL (73-77)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013873</DescriptorUI>
     <DescriptorName>
      <String>Thionucleotides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014500</DescriptorUI>
     <DescriptorName>
      <String>Uracil Nucleotides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 51(4):1062;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0045030</ConceptUI>
    <ConceptName>
     <String>5-methylaminomethyl-2-thiouridylate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T075033</TermUI>
      <String>5-methylaminomethyl-2-thiouridylate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C502723</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>MER3 protein, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>08</Month>
   <Day>10</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>12</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>required for generating crossover events during recombination; GenBank AY822649
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004265</DescriptorUI>
     <DescriptorName>
      <String>DNA Helicases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Curr Biol 2005 Apr 26;15(8):692-701</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0487845</ConceptUI>
    <ConceptName>
     <String>MER3 protein, Arabidopsis</String>
    </ConceptName>
    <RegistryNumber>EC 5.99.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T648279</TermUI>
      <String>MER3 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>08</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T661011</TermUI>
      <String>ROCK-N-ROLLERS, Arabidopsis</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>12</Month>
       <Day>04</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T648280</TermUI>
      <String>meiotic recombination protein, Arabidopsis</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>08</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T661012</TermUI>
      <String>RCK protein, Arabidopsis</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>12</Month>
       <Day>04</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012210</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>BES</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>buffer for physiological pH range; structure
  </Note>
  <Frequency>20</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ALKANESULFONATES (76-93)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D017738</DescriptorUI>
     <DescriptorName>
      <String>Alkanesulfonic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D002021</DescriptorUI>
     <DescriptorName>
      <String>Buffers</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Anal Chem 48(9):1293;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059105</ConceptUI>
    <ConceptName>
     <String>BES</String>
    </ConceptName>
    <CASN1Name>N,N-bis(2-hydroxyethyl)aminoethanesulfonic acid</CASN1Name>
    <RegistryNumber>10191-18-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089108</TermUI>
      <String>BES</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C580818</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ROCK2 protein, rat</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>04</Month>
   <Day>30</Day>
  </DateCreated>
  <Note>RefSeq NM_013022
  </Note>
  <Frequency>93</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D054460</DescriptorUI>
     <DescriptorName>
      <String>rho-Associated Kinases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Cancer Ther. 2006 Sep;5(9):2158-64.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0584366</ConceptUI>
    <ConceptName>
     <String>ROCK2 protein, rat</String>
    </ConceptName>
    <RegistryNumber>EC 2.7.11.1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T843421</TermUI>
      <String>ROCK2 protein, rat</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>04</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C580819</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>calsequestrin 2, rat</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>04</Month>
   <Day>30</Day>
  </DateCreated>
  <Note>GenBank BC072547
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002155</DescriptorUI>
     <DescriptorName>
      <String>Calsequestrin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Physiol. 2004 Dec 1;561(Pt 2):515-24.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0584367</ConceptUI>
    <ConceptName>
     <String>calsequestrin 2, rat</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T843422</TermUI>
      <String>calsequestrin 2, rat</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>04</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003962</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-ethyl-2-aminopentanoic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AMINO ACIDS (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007930</DescriptorUI>
     <DescriptorName>
      <String>Leucine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Can J Biochem 51(5):673;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0045113</ConceptUI>
    <ConceptName>
     <String>2-ethyl-2-aminopentanoic acid</String>
    </ConceptName>
    <CASN1Name>L-Norvaline, 2-ethyl-</CASN1Name>
    <RegistryNumber>78737-63-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T075116</TermUI>
      <String>2-ethyl-2-aminopentanoic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C003963</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cytidine-2'(3')-P-5'-puromycin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PUROMYCIN (73-75)</PreviousIndexing>
   <PreviousIndexing>NUCLEOTIDES, CYCLIC (74-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003597</DescriptorUI>
     <DescriptorName>
      <String>Cytosine Nucleotides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011691</DescriptorUI>
     <DescriptorName>
      <String>Puromycin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0045114</ConceptUI>
    <ConceptName>
     <String>cytidine-2'(3')-P-5'-puromycin</String>
    </ConceptName>
    <RegistryNumber>40951-29-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T075117</TermUI>
      <String>cytidine-2'(3')-P-5'-puromycin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C004155</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-methylhomopavine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1988</Year>
   <Month>11</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>poppy alkaloid of the pavine group; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>BICYCLO COMPOUNDS (73-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000470</DescriptorUI>
     <DescriptorName>
      <String>Alkaloids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 38(11):2099;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0045125</ConceptUI>
    <ConceptName>
     <String>N-methylhomopavine</String>
    </ConceptName>
    <RegistryNumber>39013-26-8</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0045125</Concept1UI>
     <Concept2UI>M0045124</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T075128</TermUI>
      <String>N-methylhomopavine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0045124</ConceptUI>
    <ConceptName>
     <String>6,11,12,13-tetrahydro-2,3,8,9-tetramethoxy-14-methyl-5H-dibenzo(a,e)cyclononen-5,11-imine</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0045125</Concept1UI>
     <Concept2UI>M0045124</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T075127</TermUI>
      <String>6,11,12,13-tetrahydro-2,3,8,9-tetramethoxy-14-methyl-5H-dibenzo(a,e)cyclononen-5,11-imine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C004163</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>lacticolorin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>01</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>phenolic glucoside ester; metabolite of Protea lacticolor Salisb.; structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*GLYCOSIDES (73-75)</PreviousIndexing>
   <PreviousIndexing>BENZOATES (73-76)</PreviousIndexing>
   <PreviousIndexing>CATECHOLS (79-81)</PreviousIndexing>
   <PreviousIndexing>GLUCOSE (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005960</DescriptorUI>
     <DescriptorName>
      <String>Glucosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Chem Soc (Perkin I) 6:638;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0045138</ConceptUI>
    <ConceptName>
     <String>lacticolorin</String>
    </ConceptName>
    <CASN1Name>2-hydroxy-4-hydroxymethylphenyl-6-O-benzoyl- beta-D-glucopyranoside</CASN1Name>
    <RegistryNumber>41942-94-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T075141</TermUI>
      <String>lacticolorin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C004229</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>16 beta-hydroxynorgestrel</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>urinary metabolite of norgestrel; RN given refers to (16beta,17alpha)-isomer; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*NORGESTREL (73-75)</PreviousIndexing>
   <PreviousIndexing>HYDROXYSTEROIDS (73-76)</PreviousIndexing>
   <PreviousIndexing>KETOSTEROIDS (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009644</DescriptorUI>
     <DescriptorName>
      <String>Norgestrel</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Endocrinol 73(1):91;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0045228</ConceptUI>
    <ConceptName>
     <String>16 beta-hydroxynorgestrel</String>
    </ConceptName>
    <CASN1Name>13-ethyl-16 beta,17-dihydroxy-18,19-dinor- 17 alpha-pregn-4-en-20-yn-3-one</CASN1Name>
    <RegistryNumber>40915-03-5</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>40915-07-9 ((16alpha,17alpha)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>56298-27-2 ((8alpha,9beta,10alpha,13alpha,14beta,16beta)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>56324-27-7 ((8alpha,9beta,10alpha,13alpha,14beta,16alpha)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0045228</Concept1UI>
     <Concept2UI>M0308489</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0045228</Concept1UI>
     <Concept2UI>M0308488</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0045228</Concept1UI>
     <Concept2UI>M0308487</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T075231</TermUI>
      <String>16 beta-hydroxynorgestrel</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0308489</ConceptUI>
    <ConceptName>
     <String>16 beta-hydroxynorgestrel, (8alpha,9beta,10alpha,13alpha,14beta,16alpha)-isomer</String>
    </ConceptName>
    <RegistryNumber>56324-27-7</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0045228</Concept1UI>
     <Concept2UI>M0308489</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T338489</TermUI>
      <String>16 beta-hydroxynorgestrel, (8alpha,9beta,10alpha,13alpha,14beta,16alpha)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0308488</ConceptUI>
    <ConceptName>
     <String>16 beta-hydroxynorgestrel, (8alpha,9beta,10alpha,13alpha,14beta,16beta)-isomer</String>
    </ConceptName>
    <RegistryNumber>56298-27-2</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0045228</Concept1UI>
     <Concept2UI>M0308488</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T338488</TermUI>
      <String>16 beta-hydroxynorgestrel, (8alpha,9beta,10alpha,13alpha,14beta,16beta)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0308487</ConceptUI>
    <ConceptName>
     <String>16 beta-hydroxynorgestrel, (16alpha,17alpha)-isomer</String>
    </ConceptName>
    <RegistryNumber>40915-07-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0045228</Concept1UI>
     <Concept2UI>M0308487</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T338487</TermUI>
      <String>16 beta-hydroxynorgestrel, (16alpha,17alpha)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C004175</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hydroxymethylflavin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ALCOHOL, METHYL (73-75)</PreviousIndexing>
   <PreviousIndexing>ALCOHOL, METHYL/analogs (75-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005415</DescriptorUI>
     <DescriptorName>
      <String>Flavins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Chromatogr 78(1):105;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0045149</ConceptUI>
    <ConceptName>
     <String>hydroxymethylflavin</String>
    </ConceptName>
    <CASN1Name>Benzo(g)pteridine-2,4(3H,10H)-dione, 10-((acetyloxy)methyl)-7,8-dimethyl-</CASN1Name>
    <RegistryNumber>35847-78-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T075152</TermUI>
      <String>hydroxymethylflavin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C074576</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>V protein, Porcine rubulavirus</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1992</Year>
   <Month>06</Month>
   <Day>16</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>02</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>encoded by the P gene of the porcine paramyxovirus La-Piedad-Michoacan-Mexico virus; has a conserved cysteine-rich C-terminal region; amino acid sequence given in first source
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014764</DescriptorUI>
     <DescriptorName>
      <String>Viral Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Gen Virol 1992 May;73(Pt 5):1195-1200</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0201315</ConceptUI>
    <ConceptName>
     <String>V protein, Porcine rubulavirus</String>
    </ConceptName>
    <RegistryNumber>147652-41-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T462598</TermUI>
      <String>V protein, Porcine rubulavirus</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>09</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T231319</TermUI>
      <String>VPPPV protein, Porcine rubulavirus</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T231320</TermUI>
      <String>V protein, porcine paramyxovirus</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C092807</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>deformin protein, Bartonella bacilliformis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>05</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>02</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>an extracellular protein synthesized by Bartonella bacilliformis; a dimer of a 67-kDa polypeptide; native MW 130 kDa; causes deformation of erythrocyte membranes
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D001473</DescriptorUI>
     <DescriptorName>
      <String>Bartonella</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Biochim Biophys Acta 1995 Mar 22;1234(2):173-83</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0244915</ConceptUI>
    <ConceptName>
     <String>deformin protein, Bartonella bacilliformis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T274920</TermUI>
      <String>deformin protein, Bartonella bacilliformis</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T274919</TermUI>
      <String>deformation factor, Bartonella bacilliformis</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C004186</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>carolenin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>11</Month>
   <Day>18</Day>
  </DateRevised>
  <Note>guaianolide--sesquiterpene lactone from Helenium autumnale L.; structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>LACTONES (74-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012717</DescriptorUI>
     <DescriptorName>
      <String>Sesquiterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 38(9):1722;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0045168</ConceptUI>
    <ConceptName>
     <String>carolenin</String>
    </ConceptName>
    <RegistryNumber>38769-36-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T075171</TermUI>
      <String>carolenin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000631504</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>AT1G42430 protein, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2019</Year>
   <Month>06</Month>
   <Day>10</Day>
  </DateCreated>
  <DateRevised>
   <Year>2019</Year>
   <Month>06</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>RefSeq NM_103431.7
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Plant J. 2018 Jul;95(1):126-137.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M000650817</ConceptUI>
    <ConceptName>
     <String>AT1G42430 protein, Arabidopsis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T000960036</TermUI>
      <String>AT1G42430 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2019</Year>
       <Month>06</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2019)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T000960038</TermUI>
      <String>EARLY STARVATION 1 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2019</Year>
       <Month>06</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2019)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T000960039</TermUI>
      <String>inactive purple acid phosphatase-like protein, Arabidopsis</String>
      <DateCreated>
       <Year>2019</Year>
       <Month>06</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2019)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T000960037</TermUI>
      <String>ESV1 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2019</Year>
       <Month>06</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2019)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C004193</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,1'-trimethylenebis(thymine)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*THYMINE (73-75)</PreviousIndexing>
   <PreviousIndexing>PROPANE (73-75)</PreviousIndexing>
   <PreviousIndexing>PROPANE/analogs (75-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013941</DescriptorUI>
     <DescriptorName>
      <String>Thymine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Am Chem Soc 95(7):2320;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0045177</ConceptUI>
    <ConceptName>
     <String>1,1'-trimethylenebis(thymine)</String>
    </ConceptName>
    <CASN1Name>2,4(1H,3H)-Pyrimidinedione, 1,1'-(1,3-propanediyl)bis(5-methyl-</CASN1Name>
    <RegistryNumber>22917-75-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T075180</TermUI>
      <String>1,1'-trimethylenebis(thymine)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C074550</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>protein p12, African swine fever virus</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1992</Year>
   <Month>06</Month>
   <Day>14</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>amino acid sequence given in first source; involved in virus attachment to the host cell; expressed by the African swine fever virus
  </Note>
  <Frequency>8</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014764</DescriptorUI>
     <DescriptorName>
      <String>Viral Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D000358</DescriptorUI>
     <DescriptorName>
      <String>African Swine Fever Virus</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Virol 1992 Jun;66(6):3860-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0201246</ConceptUI>
    <ConceptName>
     <String>protein p12, African swine fever virus</String>
    </ConceptName>
    <RegistryNumber>147994-32-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T231251</TermUI>
      <String>protein p12, African swine fever virus</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T231250</TermUI>
      <String>ASF protein p12</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000631506</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Rbfox2 protein, rat</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2019</Year>
   <Month>06</Month>
   <Day>10</Day>
  </DateCreated>
  <DateRevised>
   <Year>2019</Year>
   <Month>06</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>RefSeq  NM_001079895
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000072260</DescriptorUI>
     <DescriptorName>
      <String>RNA Splicing Factors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Sci Rep. 2017 Aug 30;7(1):9929.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M000650819</ConceptUI>
    <ConceptName>
     <String>Rbfox2 protein, rat</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T000960041</TermUI>
      <String>Rbfox2 protein, rat</String>
      <DateCreated>
       <Year>2019</Year>
       <Month>06</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2019)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T000960042</TermUI>
      <String>RNA binding fox-1 homolog 2 protein, rat</String>
      <DateCreated>
       <Year>2019</Year>
       <Month>06</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2019)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C580821</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>RPB2 protein, S cerevisiae</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>04</Month>
   <Day>30</Day>
  </DateCreated>
  <Note>RefSeq NM_001183570
  </Note>
  <Frequency>13</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012319</DescriptorUI>
     <DescriptorName>
      <String>RNA Polymerase II</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029701</DescriptorUI>
     <DescriptorName>
      <String>Saccharomyces cerevisiae Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D021122</DescriptorUI>
     <DescriptorName>
      <String>Protein Subunits</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Proc Natl Acad Sci U S A. 1987 Mar;84(5):1192-6.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0584369</ConceptUI>
    <ConceptName>
     <String>RPB2 protein, S cerevisiae</String>
    </ConceptName>
    <RegistryNumber>EC 2.7.7.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T843425</TermUI>
      <String>RPB2 protein, S cerevisiae</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>04</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C580822</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>iab-4 microRNA, Drosophila</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>04</Month>
   <Day>30</Day>
  </DateCreated>
  <Note>RefSeq NR_002037
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D035683</DescriptorUI>
     <DescriptorName>
      <String>MicroRNAs</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Genes Dev. 2005 Dec 15;19(24):2947-52.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0584370</ConceptUI>
    <ConceptName>
     <String>iab-4 microRNA, Drosophila</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T843426</TermUI>
      <String>iab-4 microRNA, Drosophila</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>04</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C435188</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,2-dihydro-10-methoxy-2,2,4-trimethyl-5-(3-methylthiomethoxyphenyl)-5H-chromeno(3,4-f)quinoline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>09</Month>
   <Day>21</Day>
  </DateCreated>
  <Note>a glucocorticoid receptor ligand; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001578</DescriptorUI>
     <DescriptorName>
      <String>Benzopyrans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011804</DescriptorUI>
     <DescriptorName>
      <String>Quinolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D008024</DescriptorUI>
     <DescriptorName>
      <String>Ligands</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Med Chem 2001 Aug 30;44(18):2879-85</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0399117</ConceptUI>
    <ConceptName>
     <String>1,2-dihydro-10-methoxy-2,2,4-trimethyl-5-(3-methylthiomethoxyphenyl)-5H-chromeno(3,4-f)quinoline</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T462717</TermUI>
      <String>1,2-dihydro-10-methoxy-2,2,4-trimethyl-5-(3-methylthiomethoxyphenyl)-5H-chromeno(3,4-f)quinoline</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>09</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T462718</TermUI>
      <String>1,2-dihydro-MTMCQ</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>09</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C435189</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-(3-benzoyl-4-(2-(4-methylphenyl)acetylamino)phenyl)cysteinamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>09</Month>
   <Day>21</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>a farnesyltransferase inhibitor; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003545</DescriptorUI>
     <DescriptorName>
      <String>Cysteine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 2001 Aug 30;44(18):2886-99</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0399118</ConceptUI>
    <ConceptName>
     <String>N-(3-benzoyl-4-(2-(4-methylphenyl)acetylamino)phenyl)cysteinamide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T462719</TermUI>
      <String>N-(3-benzoyl-4-(2-(4-methylphenyl)acetylamino)phenyl)cysteinamide</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>09</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T462720</TermUI>
      <String>3-benzoyl-MPAAPCysNH2</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>09</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C004225</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>oxypurinol ribosyl phosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PURINONES (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010117</DescriptorUI>
     <DescriptorName>
      <String>Oxypurinol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012265</DescriptorUI>
     <DescriptorName>
      <String>Ribonucleotides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 248(11):3801;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0045223</ConceptUI>
    <ConceptName>
     <String>oxypurinol ribosyl phosphate</String>
    </ConceptName>
    <RegistryNumber>31883-21-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T075226</TermUI>
      <String>oxypurinol ribosyl phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000631508</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Apl protein, Drosophila</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2019</Year>
   <Month>06</Month>
   <Day>10</Day>
  </DateCreated>
  <DateRevised>
   <Year>2019</Year>
   <Month>06</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>RefSeq NM_168676
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D028961</DescriptorUI>
     <DescriptorName>
      <String>beta Karyopherins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029721</DescriptorUI>
     <DescriptorName>
      <String>Drosophila Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nat Ecol Evol. 2018 Apr;2(4):705-712.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M000650821</ConceptUI>
    <ConceptName>
     <String>Apl protein, Drosophila</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T000960047</TermUI>
      <String>Apl protein, Drosophila</String>
      <DateCreated>
       <Year>2019</Year>
       <Month>06</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2019)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T000960048</TermUI>
      <String>Apollo protein, Drosophila</String>
      <DateCreated>
       <Year>2019</Year>
       <Month>06</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2019)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C051282</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>13-hydroxy-14,15-epoxyeicosa-5,8,11-trienoic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1987</Year>
   <Month>02</Month>
   <Day>27</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>02</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D015126</DescriptorUI>
     <DescriptorName>
      <String>8,11,14-Eicosatrienoic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Biochem Biophys 1987;252(1):334</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0145998</ConceptUI>
    <ConceptName>
     <String>13-hydroxy-14,15-epoxyeicosa-5,8,11-trienoic acid</String>
    </ConceptName>
    <RegistryNumber>79595-80-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T176003</TermUI>
      <String>13-hydroxy-14,15-epoxyeicosa-5,8,11-trienoic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T176002</TermUI>
      <String>13H-14,15-EET</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C435190</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-((1-(4-chlorobenzyl)-4-methoxy-1H-indol-2-yl)methyl)propanamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>09</Month>
   <Day>21</Day>
  </DateCreated>
  <Note>an MT(2)-selective melatonin antagonist; structure in first soiurce
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007211</DescriptorUI>
     <DescriptorName>
      <String>Indoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D008550</DescriptorUI>
     <DescriptorName>
      <String>Melatonin</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
     <QualifierName>
      <String>antagonists &amp; inhibitors</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Med Chem 2001 Aug 30;44(18):2900-12</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0399119</ConceptUI>
    <ConceptName>
     <String>N-((1-(4-chlorobenzyl)-4-methoxy-1H-indol-2-yl)methyl)propanamide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T462721</TermUI>
      <String>N-((1-(4-chlorobenzyl)-4-methoxy-1H-indol-2-yl)methyl)propanamide</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>09</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T462722</TermUI>
      <String>chlorobenzyl-MIMP</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>09</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C004232</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>mercaptodextran</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>01</Month>
   <Day>07</Day>
  </DateRevised>
  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SULFHYDRYL COMPOUNDS (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003911</DescriptorUI>
     <DescriptorName>
      <String>Dextrans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Pharmacol 22(10):1179;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0045233</ConceptUI>
    <ConceptName>
     <String>mercaptodextran</String>
    </ConceptName>
    <RegistryNumber>42612-66-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T075236</TermUI>
      <String>mercaptodextran</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C580823</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>iab-8 microRNA, Drosophila</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>04</Month>
   <Day>30</Day>
  </DateCreated>
  <Note>RefSeq NR_048415
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D035683</DescriptorUI>
     <DescriptorName>
      <String>MicroRNAs</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Genes Dev. 2008 Jan 1;22(1):14-9.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0584371</ConceptUI>
    <ConceptName>
     <String>iab-8 microRNA, Drosophila</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T843427</TermUI>
      <String>iab-8 microRNA, Drosophila</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>04</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C004255</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,1-diphenylcyclopentanetetrone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*KETONES (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003517</DescriptorUI>
     <DescriptorName>
      <String>Cyclopentanes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Yakugaku Zasshi 93(1):1;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0045242</ConceptUI>
    <ConceptName>
     <String>1,1-diphenylcyclopentanetetrone</String>
    </ConceptName>
    <RegistryNumber>41998-32-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T075245</TermUI>
      <String>1,1-diphenylcyclopentanetetrone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C004256</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>amphodyn</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>horse chestnut extract &amp; hydroxyphenylethylamino-ethanol; improves venous circulation
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PLANT EXTRACTS (73-83)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004983</DescriptorUI>
     <DescriptorName>
      <String>Ethanolamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Z Allgemein Med 48(34):1608;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0045243</ConceptUI>
    <ConceptName>
     <String>amphodyn</String>
    </ConceptName>
    <RegistryNumber>1336-78-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T075246</TermUI>
      <String>amphodyn</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C004264</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bromamphenicol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ANTIBIOTICS (73-75)</PreviousIndexing>
   <PreviousIndexing>BROMINE (75-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002701</DescriptorUI>
     <DescriptorName>
      <String>Chloramphenicol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Proc Nat Acad Sci 70(5):1423;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0045252</ConceptUI>
    <ConceptName>
     <String>bromamphenicol</String>
    </ConceptName>
    <CASN1Name>threo-N-(beta hydroxy-alpha hydroxymethyl-p-nitrophenethyl)dibromoacetamide</CASN1Name>
    <RegistryNumber>40027-72-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T075255</TermUI>
      <String>bromamphenicol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C004265</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-bromoacetylphenylalanine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PHENYLALANINE (73-76)</PreviousIndexing>
   <PreviousIndexing>ACETIC ACIDS (75-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010649</DescriptorUI>
     <DescriptorName>
      <String>Phenylalanine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Proc Nat Acad Sci 70(5):1423;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0045253</ConceptUI>
    <ConceptName>
     <String>N-bromoacetylphenylalanine</String>
    </ConceptName>
    <CASN1Name>L-Phenylalanine, N-(bromoacetyl)-</CASN1Name>
    <RegistryNumber>36753-68-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T075256</TermUI>
      <String>N-bromoacetylphenylalanine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C051283</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>11,14,15-trihydroxyeicosa-5,8,12-trienoic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1987</Year>
   <Month>02</Month>
   <Day>27</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>02</Day>
  </DateRevised>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D015126</DescriptorUI>
     <DescriptorName>
      <String>8,11,14-Eicosatrienoic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Biochem Biophys 1987;252(1):334</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0146002</ConceptUI>
    <ConceptName>
     <String>11,14,15-trihydroxyeicosa-5,8,12-trienoic acid</String>
    </ConceptName>
    <RegistryNumber>79595-81-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T176007</TermUI>
      <String>11,14,15-trihydroxyeicosa-5,8,12-trienoic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T176005</TermUI>
      <String>11,14,15-THETA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T176006</TermUI>
      <String>11,14,15-trihydroxyeicosatetraenoic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T176004</TermUI>
      <String>11,14,15-THET</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C435191</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>(benzodioxan-6-yl)(2-trifluoromethyl-4-((3-carboxypyrrolidin-1-yl)carbonyl)ethenyl)phenyl sulfide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>09</Month>
   <Day>21</Day>
  </DateCreated>
  <Note>a leukocyte function-associated antigen-1 (LFA-1)/ICAM-1 antagonist; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009557</DescriptorUI>
     <DescriptorName>
      <String>Nipecotic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013440</DescriptorUI>
     <DescriptorName>
      <String>Sulfides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 2001 Aug 30;44(18):2913-20</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0399120</ConceptUI>
    <ConceptName>
     <String>(benzodioxan-6-yl)(2-trifluoromethyl-4-((3-carboxypyrrolidin-1-yl)carbonyl)ethenyl)phenyl sulfide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T462723</TermUI>
      <String>(benzodioxan-6-yl)(2-trifluoromethyl-4-((3-carboxypyrrolidin-1-yl)carbonyl)ethenyl)phenyl sulfide</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>09</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T462724</TermUI>
      <String>benzodioxan-6-yl TCCEP sulfide</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>09</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C004270</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>phenyl N-methylacetimidate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*IMINES (73-80)</PreviousIndexing>
   <PreviousIndexing>PHENYL ETHERS (74-80)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007096</DescriptorUI>
     <DescriptorName>
      <String>Imidoesters</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 12(13):2483;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0045262</ConceptUI>
    <ConceptName>
     <String>phenyl N-methylacetimidate</String>
    </ConceptName>
    <CASN1Name>Ethanimidic acid, N-methyl-, phenyl ester</CASN1Name>
    <RegistryNumber>22084-79-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T075265</TermUI>
      <String>phenyl N-methylacetimidate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C004271</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-acetoxy-2,6-dinitropyridine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011725</DescriptorUI>
     <DescriptorName>
      <String>Pyridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 12(13):2475;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0045263</ConceptUI>
    <ConceptName>
     <String>3-acetoxy-2,6-dinitropyridine</String>
    </ConceptName>
    <RegistryNumber>35666-27-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T075266</TermUI>
      <String>3-acetoxy-2,6-dinitropyridine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C004276</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>glutamylalanine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>29</Day>
  </DateRevised>
  <Frequency>8</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ALANINE (73-75)</PreviousIndexing>
   <PreviousIndexing>GLUTAMATES (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004151</DescriptorUI>
     <DescriptorName>
      <String>Dipeptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Acta 304(2):363;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0045271</ConceptUI>
    <ConceptName>
     <String>glutamylalanine</String>
    </ConceptName>
    <RegistryNumber>21064-18-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T075274</TermUI>
      <String>glutamylalanine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T075273</TermUI>
      <String>Glu-Ala</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C074703</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>outer membrane protein P2, Haemophilus influenzae type b</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1992</Year>
   <Month>06</Month>
   <Day>24</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>amino acid sequence has been determined
  </Note>
  <Frequency>14</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001425</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Outer Membrane Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D000942</DescriptorUI>
     <DescriptorName>
      <String>Antigens, Bacterial</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Infect Dis 1992 Jun;165 Suppl 1:S86-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0201615</ConceptUI>
    <ConceptName>
     <String>outer membrane protein P2, Haemophilus influenzae type b</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T231620</TermUI>
      <String>outer membrane protein P2, Haemophilus influenzae type b</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T231619</TermUI>
      <String>OMP P2-HI type b</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C004380</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>H 35-25</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>RN given refers to parent cpd; structure
  </Note>
  <Frequency>16</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PROPANOLAMINES (76-80)</PreviousIndexing>
   <PreviousIndexing>PROPYLAMINES (72-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004809</DescriptorUI>
     <DescriptorName>
      <String>Ephedrine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Physiol Scand 102:459;1978</Source>
   <Source>Acta Physiol Scand 97(1):88;1976</Source>
   <Source>Br J Pharmacol 59(1):135;1977</Source>
   <Source>Clin Sci Mol Med 48(Suppl 2):89;1975</Source>
   <Source>Eur J Pharmacol 37(1):91;1976</Source>
   <Source>J Pharm Pharmacol 29(3):184;1977</Source>
   <Source>Res Vet Sci 1979;27(3):372</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0045444</ConceptUI>
    <ConceptName>
     <String>H 35-25</String>
    </ConceptName>
    <CASN1Name>benzenemethanol, 4-methyl-alpha-(1-((1-methylethyl)amino)ethyl)-</CASN1Name>
    <RegistryNumber>13549-60-5</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>13549-69-4 (HCl)</RelatedRegistryNumber>
     <RelatedRegistryNumber>41599-59-1 (HCl(+-)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0045444</Concept1UI>
     <Concept2UI>M0308565</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0045444</Concept1UI>
     <Concept2UI>M0045443</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0045444</Concept1UI>
     <Concept2UI>M0308566</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T075447</TermUI>
      <String>H 35-25</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T075445</TermUI>
      <String>H35-25</String>
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   <Month>03</Month>
   <Day>27</Day>
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   <Month>07</Month>
   <Day>20</Day>
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   <Month>06</Month>
   <Day>10</Day>
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       <Month>07</Month>
       <Day>20</Day>
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  <DateCreated>
   <Year>2013</Year>
   <Month>04</Month>
   <Day>30</Day>
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   <Year>1985</Year>
   <Month>10</Month>
   <Day>11</Day>
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  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>12</Day>
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   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>28</Day>
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   <Source>FEBS Lett 35(1):137;1973</Source>
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   <String>EM5744</String>
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  <DateCreated>
   <Year>2007</Year>
   <Month>12</Month>
   <Day>06</Day>
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  <Frequency>1</Frequency>
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  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>1994</Year>
   <Month>02</Month>
   <Day>03</Day>
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   <Source>J Am Chem Soc 98(8):2295;1976</Source>
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   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0048912</ConceptUI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T078915</TermUI>
      <String>jatrophone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C430887</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>signal recognition particle RNA 3'-adenylating enzyme</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>07</Month>
   <Day>17</Day>
  </DateCreated>
  <Note>GenBank AY029162
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009713</DescriptorUI>
     <DescriptorName>
      <String>Nucleotidyltransferases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 2001 Jun 15;276(24):21791-6</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0393554</ConceptUI>
    <ConceptName>
     <String>signal recognition particle RNA 3'-adenylating enzyme</String>
    </ConceptName>
    <RegistryNumber>EC 2.7.7.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T454505</TermUI>
      <String>signal recognition particle RNA 3'-adenylating enzyme</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>07</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T454506</TermUI>
      <String>SRP RNA adenylating enzyme</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>07</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000631509</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>methoxyvinylglycine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2019</Year>
   <Month>06</Month>
   <Day>10</Day>
  </DateCreated>
  <DateRevised>
   <Year>2019</Year>
   <Month>06</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>a member of a family of nonproteinogenic amino acids featuring an essential vinyl ether conferring mechanism-based inhibition of pyridoxal phosphate enzymes
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004987</DescriptorUI>
     <DescriptorName>
      <String>Ethers</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005998</DescriptorUI>
     <DescriptorName>
      <String>Glycine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Angew Chem Int Ed Engl. 2018 Jun 4;57(23):6780-6785.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M000650822</ConceptUI>
    <ConceptName>
     <String>methoxyvinylglycine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T000960049</TermUI>
      <String>methoxyvinylglycine</String>
      <DateCreated>
       <Year>2019</Year>
       <Month>06</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2019)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006396</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>acofriose</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>10</Month>
   <Day>07</Day>
  </DateRevised>
  <Frequency>6</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DEOXY SUGARS (75-82)</PreviousIndexing>
   <PreviousIndexing>MANNOSE/analogs</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008358</DescriptorUI>
     <DescriptorName>
      <String>Mannose</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Bact 120(2):672;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0048934</ConceptUI>
    <ConceptName>
     <String>acofriose</String>
    </ConceptName>
    <CASN1Name>6-deoxy-3-O-methylmannose</CASN1Name>
    <RegistryNumber>4598-54-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T078937</TermUI>
      <String>acofriose</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006398</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>21-acryloxyprogesterone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PROGESTERONE (74-75)</PreviousIndexing>
   <PreviousIndexing>ACRYLATES (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011374</DescriptorUI>
     <DescriptorName>
      <String>Progesterone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Gynec Investig 4(3):165;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0048937</ConceptUI>
    <ConceptName>
     <String>21-acryloxyprogesterone</String>
    </ConceptName>
    <RegistryNumber>27953-65-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T078940</TermUI>
      <String>21-acryloxyprogesterone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006406</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-acylglycerophosphorylinositol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PHOSPHIDYLINOSITOLS (75-87)</PreviousIndexing>
   <PreviousIndexing>*PHOSPHOINOSITIDES (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008246</DescriptorUI>
     <DescriptorName>
      <String>Lysophospholipids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 248(20):7060;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0048950</ConceptUI>
    <ConceptName>
     <String>1-acylglycerophosphorylinositol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T078953</TermUI>
      <String>1-acylglycerophosphorylinositol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C055019</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-diethylaminoethylphenobarbital</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1988</Year>
   <Month>03</Month>
   <Day>31</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>structure given in first source; RN given refers to parent compound
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010634</DescriptorUI>
     <DescriptorName>
      <String>Phenobarbital</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Pharm (Weinheim) 1987;320(11):1103</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0155094</ConceptUI>
    <ConceptName>
     <String>1-diethylaminoethylphenobarbital</String>
    </ConceptName>
    <RegistryNumber>1164-33-6</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>110927-31-6 ((R)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>110947-87-0 ((S)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0155094</Concept1UI>
     <Concept2UI>M0323576</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0155094</Concept1UI>
     <Concept2UI>M0323575</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T185099</TermUI>
      <String>1-diethylaminoethylphenobarbital</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T185098</TermUI>
      <String>DEAE-phenobarbital</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0323576</ConceptUI>
    <ConceptName>
     <String>1-diethylaminoethylphenobarbital, (S)-isomer</String>
    </ConceptName>
    <RegistryNumber>110947-87-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0155094</Concept1UI>
     <Concept2UI>M0323576</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T353576</TermUI>
      <String>1-diethylaminoethylphenobarbital, (S)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0323575</ConceptUI>
    <ConceptName>
     <String>1-diethylaminoethylphenobarbital, (R)-isomer</String>
    </ConceptName>
    <RegistryNumber>110927-31-6</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0155094</Concept1UI>
     <Concept2UI>M0323575</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T353575</TermUI>
      <String>1-diethylaminoethylphenobarbital, (R)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006412</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>adenylyl-(3'-5')-adenosine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1988</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>20</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ADENINE NUCLEOTIDES (74-79)</PreviousIndexing>
   <PreviousIndexing>ADENOSINE MONOPHOSPHATE/*analogs (74-88)</PreviousIndexing>
   <PreviousIndexing>ADENOSINE/analogs (79-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015226</DescriptorUI>
     <DescriptorName>
      <String>Dinucleoside Phosphates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 13(5):981;1974</Source>
   <Source>Biochemistry 15(4):756;1976</Source>
   <Source>Nucleic Acids Res 5(11):4417;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0048961</ConceptUI>
    <ConceptName>
     <String>adenylyl-(3'-5')-adenosine</String>
    </ConceptName>
    <RegistryNumber>2391-46-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T078964</TermUI>
      <String>adenylyl-(3'-5')-adenosine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006413</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>adenylyl-(3'-5')-uridine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1988</Year>
   <Month>08</Month>
   <Day>10</Day>
  </DateRevised>
  <Frequency>4</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ADENINE NUCLEOTIDES (74-79)</PreviousIndexing>
   <PreviousIndexing>ADENOSINE MONOPHOSPHATE/*analogs (74-88)</PreviousIndexing>
   <PreviousIndexing>URIDINE (74-75)</PreviousIndexing>
   <PreviousIndexing>URIDINE/*analogs (75-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015226</DescriptorUI>
     <DescriptorName>
      <String>Dinucleoside Phosphates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 13(5):981;1974</Source>
   <Source>Biochemistry 16(15):3322;1977</Source>
   <Source>Nature 253(5490):324;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0048962</ConceptUI>
    <ConceptName>
     <String>adenylyl-(3'-5')-uridine</String>
    </ConceptName>
    <RegistryNumber>3051-84-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T078965</TermUI>
      <String>adenylyl-(3'-5')-uridine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C075326</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,4,5,8-naphthalene tetracarboxylic acid 4,5-anhydride</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1992</Year>
   <Month>07</Month>
   <Day>27</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>23</Day>
  </DateRevised>
  <Note>structure given in first source; RN refers to the monosodium salt, monohydrate
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009281</DescriptorUI>
     <DescriptorName>
      <String>Naphthalenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011753</DescriptorUI>
     <DescriptorName>
      <String>Pyrones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Crystallogr C 1992 Mar 15;48(Pt 3):460-5</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0203003</ConceptUI>
    <ConceptName>
     <String>1,4,5,8-naphthalene tetracarboxylic acid 4,5-anhydride</String>
    </ConceptName>
    <RegistryNumber>141193-56-8</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0203003</Concept1UI>
     <Concept2UI>M0203002</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T233008</TermUI>
      <String>1,4,5,8-naphthalene tetracarboxylic acid 4,5-anhydride</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T233006</TermUI>
      <String>1,4,5,8-NTCAA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T233005</TermUI>
      <String>1,3-dioxo-1H,3H-naphtho(1,8-cd)pyran-6,7-dicarboxylate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0203002</ConceptUI>
    <ConceptName>
     <String>1,4,5,8-naphthalene tetracarboxylic acid 4,5-anhydride, monosodium salt, monohydrate</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0203003</Concept1UI>
     <Concept2UI>M0203002</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T233007</TermUI>
      <String>1,4,5,8-naphthalene tetracarboxylic acid 4,5-anhydride, monosodium salt, monohydrate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006427</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>afrodex</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>combination of above for treatment of male impotence
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008777</DescriptorUI>
     <DescriptorName>
      <String>Methyltestosterone</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013331</DescriptorUI>
     <DescriptorName>
      <String>Strychnine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015016</DescriptorUI>
     <DescriptorName>
      <String>Yohimbine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Curr Therap Res 16(1):96;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0048994</ConceptUI>
    <ConceptName>
     <String>afrodex</String>
    </ConceptName>
    <CASN1Name>Afrodex</CASN1Name>
    <RegistryNumber>8054-03-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T078997</TermUI>
      <String>afrodex</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C485102</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>C,C,C-trifluoro-N-(5-(2-pyridin-2-ylvinyl)naphthalen-2-yl)methanesulfonamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>05</Month>
   <Day>15</Day>
  </DateCreated>
  <Note>an HCMV protease inhibitor; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013449</DescriptorUI>
     <DescriptorName>
      <String>Sulfonamides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D015081</DescriptorUI>
     <DescriptorName>
      <String>2-Naphthylamine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 2004 Apr 8;47(8):1893-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0465900</ConceptUI>
    <ConceptName>
     <String>C,C,C-trifluoro-N-(5-(2-pyridin-2-ylvinyl)naphthalen-2-yl)methanesulfonamide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T586806</TermUI>
      <String>C,C,C-trifluoro-N-(5-(2-pyridin-2-ylvinyl)naphthalen-2-yl)methanesulfonamide</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>05</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T586807</TermUI>
      <String>C,C,C-trifluoro-PVNMSA</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>05</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C025079</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>diazoline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>07</Month>
   <Day>09</Day>
  </DateCreated>
  <DateRevised>
   <Year>2015</Year>
   <Month>11</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>see also record for mebhydroline, RN: 524-81-2
  </Note>
  <Frequency>28</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*NAPHTHALENESULFONATES (80-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002243</DescriptorUI>
     <DescriptorName>
      <String>Carbolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Farmakol Toksikol 1980;43(1):62</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0084026</ConceptUI>
    <ConceptName>
     <String>diazoline</String>
    </ConceptName>
    <CASN1Name>1,5-naphthalenedisulfonic acid, compd. with 2,3,4,5-tetrahydro-2-methyl-5-(phenylmethyl)-1H-pyrido(4,3-b)indole (1:2)</CASN1Name>
    <RegistryNumber>O5G04RB25M</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>6153-33-9 (diazoline)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0084026</Concept1UI>
     <Concept2UI>M0084020</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0084026</Concept1UI>
     <Concept2UI>M0084021</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0084026</Concept1UI>
     <Concept2UI>M0084023</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T114029</TermUI>
      <String>diazoline</String>
      <ThesaurusIDlist>
       <ThesaurusID>FDA SRS (2015)</ThesaurusID>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T114028</TermUI>
      <String>mebhydroline 1,5-naphthalenedisulfonate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T114025</TermUI>
      <String>diazolin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T114027</TermUI>
      <String>mebhydrolin napadisylate</String>
      <ThesaurusIDlist>
       <ThesaurusID>FDA SRS (2015)</ThesaurusID>
       <ThesaurusID>INN (19XX)</ThesaurusID>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0084020</ConceptUI>
    <ConceptName>
     <String>Incidal</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0084026</Concept1UI>
     <Concept2UI>M0084020</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="TRD"  RecordPreferredTermYN="N">
      <TermUI>T114023</TermUI>
      <String>Incidal</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0084021</ConceptUI>
    <ConceptName>
     <String>Omeril</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0084026</Concept1UI>
     <Concept2UI>M0084021</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T114024</TermUI>
      <String>Omeril</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0084023</ConceptUI>
    <ConceptName>
     <String>Fabahistin</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0084026</Concept1UI>
     <Concept2UI>M0084023</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="TRD"  RecordPreferredTermYN="N">
      <TermUI>T114026</TermUI>
      <String>Fabahistin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009794</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>procion yellow</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>07</Month>
   <Day>23</Day>
  </DateRevised>
  <Frequency>34</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AZO COMPOUNDS (75-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014227</DescriptorUI>
     <DescriptorName>
      <String>Triazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
    <PharmacologicalActionList>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D004396</DescriptorUI>
        <DescriptorName>
         <String>Coloring Agents</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D005456</DescriptorUI>
        <DescriptorName>
         <String>Fluorescent Dyes</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
    </PharmacologicalActionList>
  <SourceList>
   <Source>Clin Chim Acta 1980;100(1):7</Source>
   <Source>Exp Brain Res 20(5):527;1974</Source>
   <Source>Exp Eye Res 28(1):1;1979</Source>
   <Source>Fed Proc 34(7):1616;1975</Source>
   <Source>J Physiol (Lond) 275:495;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054796</ConceptUI>
    <ConceptName>
     <String>procion yellow</String>
    </ConceptName>
    <CASN1Name>C.I. Reactive Yellow 86</CASN1Name>
    <RegistryNumber>61951-86-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084799</TermUI>
      <String>procion yellow</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C512489</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>MM1 compound</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>08</Month>
   <Day>16</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007093</DescriptorUI>
     <DescriptorName>
      <String>Imidazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011759</DescriptorUI>
     <DescriptorName>
      <String>Pyrrolidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Bioorg Med Chem. 2006 Jul 1;14(13):4353-60</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0500830</ConceptUI>
    <ConceptName>
     <String>MM1 compound</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T679739</TermUI>
      <String>MM1 compound</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>08</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002980</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>streptamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>07</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>RN given refers to parent cpd; structure
  </Note>
  <Frequency>12</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CYCLOHEXYLAMINES (73-76)</PreviousIndexing>
   <PreviousIndexing>CYCLOHEXANOLS (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D006595</DescriptorUI>
     <DescriptorName>
      <String>Hexosamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiot (Tokyo) 29(5):532;1976</Source>
   <Source>J Biol Chem 248(7):2441;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043860</ConceptUI>
    <ConceptName>
     <String>streptamine</String>
    </ConceptName>
    <RegistryNumber>488-52-8</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>16647-43-1 ((myo)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>5469-74-9 (sulfate[1:1])</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0043860</Concept1UI>
     <Concept2UI>M0308140</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0043860</Concept1UI>
     <Concept2UI>M0308139</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073863</TermUI>
      <String>streptamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0308140</ConceptUI>
    <ConceptName>
     <String>streptamine sulfate (1:1)</String>
    </ConceptName>
    <RegistryNumber>5469-74-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0043860</Concept1UI>
     <Concept2UI>M0308140</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T338140</TermUI>
      <String>streptamine sulfate (1:1)</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0308139</ConceptUI>
    <ConceptName>
     <String>streptamine, (myo)-isomer</String>
    </ConceptName>
    <RegistryNumber>16647-43-1</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0043860</Concept1UI>
     <Concept2UI>M0308139</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T338139</TermUI>
      <String>streptamine, (myo)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C067830</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-(phenylthio)-2-aminopropane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1991</Year>
   <Month>04</Month>
   <Day>15</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>12</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>racemic &amp; S-isomer have hypertensive actions; R-isomer is inactive; structure given in first source; RN given refers to cpd without isomeric designation
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011437</DescriptorUI>
     <DescriptorName>
      <String>Propylamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013440</DescriptorUI>
     <DescriptorName>
      <String>Sulfides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 1991;34(3):1082</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0185812</ConceptUI>
    <ConceptName>
     <String>1-(phenylthio)-2-aminopropane</String>
    </ConceptName>
    <RegistryNumber>2014-77-9</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>122673-69-2 ((R)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>122673-70-5 ((S)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>91281-30-0 (HCl(+-)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>91281-31-1 ((+-)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0185812</Concept1UI>
     <Concept2UI>M0325157</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0185812</Concept1UI>
     <Concept2UI>M0325156</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0185812</Concept1UI>
     <Concept2UI>M0325158</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0185812</Concept1UI>
     <Concept2UI>M0325159</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T215817</TermUI>
      <String>1-(phenylthio)-2-aminopropane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T215815</TermUI>
      <String>MePAES</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T215816</TermUI>
      <String>alpha-methylphenyl-2-aminoethylsulfide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0325157</ConceptUI>
    <ConceptName>
     <String>1-(phenylthio)-2-aminopropane, (S)-isomer</String>
    </ConceptName>
    <RegistryNumber>122673-70-5</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T355157</TermUI>
      <String>1-(phenylthio)-2-aminopropane, (S)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0325156</ConceptUI>
    <ConceptName>
     <String>1-(phenylthio)-2-aminopropane, (R)-isomer</String>
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    <RegistryNumber>122673-69-2</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0185812</Concept1UI>
     <Concept2UI>M0325156</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T355156</TermUI>
      <String>1-(phenylthio)-2-aminopropane, (R)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0325158</ConceptUI>
    <ConceptName>
     <String>1-(phenylthio)-2-aminopropane hydrochloride, (+-)-isomer</String>
    </ConceptName>
    <RegistryNumber>91281-30-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0185812</Concept1UI>
     <Concept2UI>M0325158</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T355158</TermUI>
      <String>1-(phenylthio)-2-aminopropane hydrochloride, (+-)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0325159</ConceptUI>
    <ConceptName>
     <String>1-(phenylthio)-2-aminopropane, (+-)-isomer</String>
    </ConceptName>
    <RegistryNumber>91281-31-1</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0185812</Concept1UI>
     <Concept2UI>M0325159</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T355159</TermUI>
      <String>1-(phenylthio)-2-aminopropane, (+-)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C118811</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Su(var)2-10 protein, Drosophila</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1999</Year>
   <Month>05</Month>
   <Day>14</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>homologous to Miz1 and PIAS3 proteins; amino acid sequence in first source
  </Note>
  <Frequency>7</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*Carrier Proteins (1999-2004)</PreviousIndexing>
   <PreviousIndexing>*Intracellular Signaling Peptides and Proteins (2005)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029721</DescriptorUI>
     <DescriptorName>
      <String>Drosophila Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D050828</DescriptorUI>
     <DescriptorName>
      <String>Protein Inhibitors of Activated STAT</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D016335</DescriptorUI>
     <DescriptorName>
      <String>Zinc Fingers</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Gene 1999 Mar 18;229(1-2):109-18</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0304356</ConceptUI>
    <ConceptName>
     <String>Su(var)2-10 protein, Drosophila</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T562516</TermUI>
      <String>Su(var)2-10 protein, Drosophila</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T334361</TermUI>
      <String>Zimp protein, Drosophila</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T562517</TermUI>
      <String>Suppressor of variegation 2-10 protein, Drosophila</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T603668</TermUI>
      <String>Pias3 protein, Drosophila</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T603669</TermUI>
      <String>protein inhibitor of activated STAT 3, Drosophila</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>08</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009807</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>uridylyl-(3'-5')-cytidine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*URIDYLIC ACID (75-88)</PreviousIndexing>
   <PreviousIndexing>CYTIDINE/*analogs (75-88)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015226</DescriptorUI>
     <DescriptorName>
      <String>Dinucleoside Phosphates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biokhimiia 39(4):839;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054835</ConceptUI>
    <ConceptName>
     <String>uridylyl-(3'-5')-cytidine</String>
    </ConceptName>
    <CASN1Name>cytidylyl-(5'-3')-uridine</CASN1Name>
    <RegistryNumber>3013-97-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084838</TermUI>
      <String>uridylyl-(3'-5')-cytidine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C069742</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-palmitoyl-2-(16-doxystearoyl)phosphatidylcholine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1991</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>12</Month>
   <Day>10</Day>
  </DateRevised>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003497</DescriptorUI>
     <DescriptorName>
      <String>Cyclic N-Oxides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010713</DescriptorUI>
     <DescriptorName>
      <String>Phosphatidylcholines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D013113</DescriptorUI>
     <DescriptorName>
      <String>Spin Labels</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Biophys J 1991;59(4):950</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0190240</ConceptUI>
    <ConceptName>
     <String>1-palmitoyl-2-(16-doxystearoyl)phosphatidylcholine</String>
    </ConceptName>
    <RegistryNumber>63321-67-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T220245</TermUI>
      <String>1-palmitoyl-2-(16-doxystearoyl)phosphatidylcholine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T220244</TermUI>
      <String>16-PC</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C531296</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>aplysinoplide C</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2008</Year>
   <Month>09</Month>
   <Day>11</Day>
  </DateCreated>
  <Note>isolated from the marine sponge Aplysinopsis digitata; exhibited cytotoxic activity against P388 mouse leukemia cells; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D054830</DescriptorUI>
     <DescriptorName>
      <String>Sesterterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2008 Jun;71(6):1089-91</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0524689</ConceptUI>
    <ConceptName>
     <String>aplysinoplide C</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T725534</TermUI>
      <String>aplysinoplide C</String>
      <DateCreated>
       <Year>2008</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2008)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009831</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-pyridinealdehyde-NAD</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ALDEHYDES (75-79)</PreviousIndexing>
   <PreviousIndexing>PYRIDINES (75-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009243</DescriptorUI>
     <DescriptorName>
      <String>NAD</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 250(5):1734;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054890</ConceptUI>
    <ConceptName>
     <String>3-pyridinealdehyde-NAD</String>
    </ConceptName>
    <RegistryNumber>86-07-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084893</TermUI>
      <String>3-pyridinealdehyde-NAD</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009858</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bradykininogen</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>29</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*KININOGENS (75-77)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001920</DescriptorUI>
     <DescriptorName>
      <String>Bradykinin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011498</DescriptorUI>
     <DescriptorName>
      <String>Protein Precursors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Can J Zool 54(6):941;1976</Source>
   <Source>Fiziol Zh 23(3):318;1977</Source>
   <Source>J Reprod Fertil 42(2):229;1975</Source>
   <Source>Khirurgiia 11:74;1977</Source>
   <Source>Med Interne 14(2):87;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054918</ConceptUI>
    <ConceptName>
     <String>bradykininogen</String>
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    <RegistryNumber>12642-94-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084921</TermUI>
      <String>bradykininogen</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009867</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>diazodiphenoquinone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>07</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AZO COMPOUNDS (75-79)</PreviousIndexing>
   <PreviousIndexing>*QUINONES (75-82)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003979</DescriptorUI>
     <DescriptorName>
      <String>Diazonium Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D010860</DescriptorUI>
     <DescriptorName>
      <String>Pigments, Biological</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Biochem J 141(2):577;1974</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054938</ConceptUI>
    <ConceptName>
     <String>diazodiphenoquinone</String>
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    <CASN1Name>2,6(1H,3H)-Pyridinedione, 3-(1,6-dihydro-5-hydroxy-2,6-dioxo-3(2H)-pyridinylidene)-5-hydroxy-</CASN1Name>
    <RegistryNumber>2435-60-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084941</TermUI>
      <String>diazodiphenoquinone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C512491</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>MMK2 compound</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>08</Month>
   <Day>16</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007093</DescriptorUI>
     <DescriptorName>
      <String>Imidazoles</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011759</DescriptorUI>
     <DescriptorName>
      <String>Pyrrolidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Bioorg Med Chem. 2006 Jul 1;14(13):4353-60</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0500832</ConceptUI>
    <ConceptName>
     <String>MMK2 compound</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T679742</TermUI>
      <String>MMK2 compound</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>08</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C512492</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>MMK3 compound</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>08</Month>
   <Day>16</Day>
  </DateCreated>
  <Note>structure in first source
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  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007093</DescriptorUI>
     <DescriptorName>
      <String>Imidazoles</String>
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   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011759</DescriptorUI>
     <DescriptorName>
      <String>Pyrrolidines</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>Bioorg Med Chem. 2006 Jul 1;14(13):4353-60</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0500833</ConceptUI>
    <ConceptName>
     <String>MMK3 compound</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T679743</TermUI>
      <String>MMK3 compound</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>08</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009977</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Z 2004</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>24</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ANILIDES (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000111</DescriptorUI>
     <DescriptorName>
      <String>Acetylcysteine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Minerva Pediatr 27(19):1126;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055140</ConceptUI>
    <ConceptName>
     <String>Z 2004</String>
    </ConceptName>
    <CASN1Name>Ethanethioic acid, S-(2-(acetylamino)-3-((4-hydroxyphenyl)amino)-3-oxopropyl) ester, (R)-</CASN1Name>
    <RegistryNumber>35143-94-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0055140</Concept1UI>
     <Concept2UI>M0055138</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T085143</TermUI>
      <String>Z 2004</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085142</TermUI>
      <String>Z-2004</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0055138</ConceptUI>
    <ConceptName>
     <String>N,S-diacetylcysteine-p-hydroxyanilide</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0055140</Concept1UI>
     <Concept2UI>M0055138</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085141</TermUI>
      <String>N,S-diacetylcysteine-p-hydroxyanilide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009889</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hexsyn</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>04</Month>
   <Day>14</Day>
  </DateRevised>
  <Note>an alpha-olefin rubber produced by solution polymerization suitable for artificial hearts in chem and phys properties.
  </Note>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ALKENES (75-83)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011108</DescriptorUI>
     <DescriptorName>
      <String>Polymers</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Trans Amer Soc Artif Int Organs 20(B):660;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054960</ConceptUI>
    <ConceptName>
     <String>hexsyn</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084963</TermUI>
      <String>hexsyn</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C512496</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>7-amino-3a,4-dihydro-3H-(1)benzopyrano(4,3-c)isoxazole</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>08</Month>
   <Day>16</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007555</DescriptorUI>
     <DescriptorName>
      <String>Isoxazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011714</DescriptorUI>
     <DescriptorName>
      <String>Pyrans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Bioorg Med Chem. 2006 Jul 1;14(13):4361-72</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0500837</ConceptUI>
    <ConceptName>
     <String>7-amino-3a,4-dihydro-3H-(1)benzopyrano(4,3-c)isoxazole</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T679749</TermUI>
      <String>7-amino-3a,4-dihydro-3H-(1)benzopyrano(4,3-c)isoxazole</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>08</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T679750</TermUI>
      <String>7-ADH-BP-I cpd</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>08</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000323</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bromotubercidin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateRevised>
  <Frequency>4</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*NUCLEOSIDES (71-74)</PreviousIndexing>
   <PreviousIndexing>*PYRIMIDINE NUCLEOSIDES (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014372</DescriptorUI>
     <DescriptorName>
      <String>Tubercidin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Exp Med 134(4):955;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040419</ConceptUI>
    <ConceptName>
     <String>bromotubercidin</String>
    </ConceptName>
    <RegistryNumber>21193-80-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070421</TermUI>
      <String>bromotubercidin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T070420</TermUI>
      <String>5-bromotubericidin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C518378</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Galbulimima alkaloid 13</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>03</Month>
   <Day>28</Day>
  </DateCreated>
  <Note>complex polycyclic alkaloid from Galbulimima belgraveana, a rain forest tree native to Papua New Guinea and northern Australia; structure in first source
  </Note>
  <Frequency>7</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006571</DescriptorUI>
     <DescriptorName>
      <String>Heterocyclic Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Am Chem Soc 2007 Feb 7;129(5):1048-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0508161</ConceptUI>
    <ConceptName>
     <String>Galbulimima alkaloid 13</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T694504</TermUI>
      <String>Galbulimima alkaloid 13</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>03</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009993</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>U-30,964</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>07</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>diabetogenic nitrosourea cpd identical to streptozotocin except for prescence of an ethyl end group
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013311</DescriptorUI>
     <DescriptorName>
      <String>Streptozocin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Pharmacol 24(6):746;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055191</ConceptUI>
    <ConceptName>
     <String>U-30,964</String>
    </ConceptName>
    <CASN1Name>deoxy-2-(((ethylnitrosoamino)carbonyl)amino)-D-glucopyranose</CASN1Name>
    <RegistryNumber>41135-12-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0055191</Concept1UI>
     <Concept2UI>M0055187</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0055191</Concept1UI>
     <Concept2UI>M0055186</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T085194</TermUI>
      <String>U-30,964</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085192</TermUI>
      <String>U 30964</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085193</TermUI>
      <String>U-30964</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085191</TermUI>
      <String>U 30,964</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0055187</ConceptUI>
    <ConceptName>
     <String>NSC-174793</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0055191</Concept1UI>
     <Concept2UI>M0055187</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T085190</TermUI>
      <String>NSC-174793</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0055186</ConceptUI>
    <ConceptName>
     <String>DENU</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0055191</Concept1UI>
     <Concept2UI>M0055186</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085189</TermUI>
      <String>DENU</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C531297</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>monocarpinine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2008</Year>
   <Month>09</Month>
   <Day>11</Day>
  </DateCreated>
  <Note>isolated from a stem bark extract of the Malayan species Monocarpia marginalis; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014315</DescriptorUI>
     <DescriptorName>
      <String>Triterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2008 Jun;71(6):1104-6</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0524690</ConceptUI>
    <ConceptName>
     <String>monocarpinine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T725535</TermUI>
      <String>monocarpinine</String>
      <DateCreated>
       <Year>2008</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2008)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C041254</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>flustramine B</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1984</Year>
   <Month>06</Month>
   <Day>12</Day>
  </DateCreated>
  <DateRevised>
   <Year>2007</Year>
   <Month>03</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>from Flustra foliacea L.; exhibits muscle relaxant activity both in vivo &amp; in vitro; structure given in first source
  </Note>
  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ALKALOIDS (1984-2008)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D026121</DescriptorUI>
     <DescriptorName>
      <String>Indole Alkaloids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D010946</DescriptorUI>
     <DescriptorName>
      <String>Plants, Medicinal</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Acta Pharm Suec 1983;20(6):415</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0122424</ConceptUI>
    <ConceptName>
     <String>flustramine B</String>
    </ConceptName>
    <RegistryNumber>71239-65-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T152429</TermUI>
      <String>flustramine B</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1984)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C511648</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>flustramine C</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>07</Month>
   <Day>10</Day>
  </DateCreated>
  <DateRevised>
   <Year>2007</Year>
   <Month>03</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>4</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*HETEROCYCLIC COMPOUNDS, 3-RING (2005-2008)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D026121</DescriptorUI>
     <DescriptorName>
      <String>Indole Alkaloids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Org Lett 2005 Feb 17;7(4):677-80</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0499735</ConceptUI>
    <ConceptName>
     <String>flustramine C</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T677655</TermUI>
      <String>flustramine C</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>07</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009912</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>narcotic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009665</DescriptorUI>
     <DescriptorName>
      <String>Noscapine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Pol J Pharmacol Pharm 27(1):69;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054997</ConceptUI>
    <ConceptName>
     <String>narcotic acid</String>
    </ConceptName>
    <RegistryNumber>55836-07-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085000</TermUI>
      <String>narcotic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009913</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>nifosept</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009582</DescriptorUI>
     <DescriptorName>
      <String>Nitrofurantoin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mater Med Pol 6(4):303;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054999</ConceptUI>
    <ConceptName>
     <String>nifosept</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0054999</Concept1UI>
     <Concept2UI>M0054998</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085002</TermUI>
      <String>nifosept</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0054998</ConceptUI>
    <ConceptName>
     <String>N-(5-dinitro-2-furfurylidene)aminohydantoin</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0054999</Concept1UI>
     <Concept2UI>M0054998</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085001</TermUI>
      <String>N-(5-dinitro-2-furfurylidene)aminohydantoin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009918</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-imino-4-oxoselenazolidine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>08</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>IMINES (75-76)</PreviousIndexing>
   <PreviousIndexing>SELENIUM (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001393</DescriptorUI>
     <DescriptorName>
      <String>Azoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Pol J Pharmacol Pharm 27(1):57;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055017</ConceptUI>
    <ConceptName>
     <String>2-imino-4-oxoselenazolidine</String>
    </ConceptName>
    <CASN1Name>4(5H)-Selenazolone, 2-amino-</CASN1Name>
    <RegistryNumber>40675-18-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085020</TermUI>
      <String>2-imino-4-oxoselenazolidine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011024</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>24-methylcholestane-3,5,6,25-pentol-25-monoacetate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>isolated from Alcyonarian Sarcophyton elegans; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*STEROLS (76-78)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002777</DescriptorUI>
     <DescriptorName>
      <String>Cholestanols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Steroids 26(1):107;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057021</ConceptUI>
    <ConceptName>
     <String>24-methylcholestane-3,5,6,25-pentol-25-monoacetate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087024</TermUI>
      <String>24-methylcholestane-3,5,6,25-pentol-25-monoacetate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T087023</TermUI>
      <String>24-methylcholestane-3 beta,5 alpha,6 beta,25-pentol-25- monoacetate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012614</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-nitrohydroxyphenyl-N-benzoylalanine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>15</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001549</DescriptorUI>
     <DescriptorName>
      <String>Benzamides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014443</DescriptorUI>
     <DescriptorName>
      <String>Tyrosine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Agressologie 17(1):43;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059751</ConceptUI>
    <ConceptName>
     <String>1-nitrohydroxyphenyl-N-benzoylalanine</String>
    </ConceptName>
    <CASN1Name>N-benzoyl-3-nitro-L-tyrosine</CASN1Name>
    <RegistryNumber>59921-69-6</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0059751</Concept1UI>
     <Concept2UI>M0059753</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089754</TermUI>
      <String>1-nitrohydroxyphenyl-N-benzoylalanine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0059753</ConceptUI>
    <ConceptName>
     <String>GAL-1</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0059751</Concept1UI>
     <Concept2UI>M0059753</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T089756</TermUI>
      <String>GAL-1</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T089755</TermUI>
      <String>GAL 1</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C107354</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-acetyl-S-(3,4-dichlorophenyl)cysteine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1997</Year>
   <Month>08</Month>
   <Day>22</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateRevised>
  <Note>biomarker for monitoring exposure to 1,2-dichlorobenzene
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000111</DescriptorUI>
     <DescriptorName>
      <String>Acetylcysteine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Int Arch Occup Environ Health 1997;69(4):252-4</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0279329</ConceptUI>
    <ConceptName>
     <String>N-acetyl-S-(3,4-dichlorophenyl)cysteine</String>
    </ConceptName>
    <RegistryNumber>13443-69-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T309334</TermUI>
      <String>N-acetyl-S-(3,4-dichlorophenyl)cysteine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T309333</TermUI>
      <String>3,4-DCPMA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T309332</TermUI>
      <String>(3,4-dichlorophenyl)mercapturic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009929</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>podolide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>13</Day>
  </DateRevised>
  <Note>antileukemic norditerpene lactone from Podocarpus gracilior; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ANTINEOPLASTIC AGENTS (75-76)</PreviousIndexing>
   <PreviousIndexing>LACTONES (75-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013729</DescriptorUI>
     <DescriptorName>
      <String>Terpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Experentia 31(2):1;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055029</ConceptUI>
    <ConceptName>
     <String>podolide</String>
    </ConceptName>
    <RegistryNumber>55786-36-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085032</TermUI>
      <String>podolide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000324</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Brown FK</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateRevised>
  <Note>mixture of 2,4-diamino-5-(p-sulfophenylazo)toluene and 1,3-diamino-4,6-bis(p-sulfophenylazo)benzene
  </Note>
  <Frequency>6</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*FOOD ADDITIVES (74-75)</PreviousIndexing>
   <PreviousIndexing>*PHENYLENEDIAMINES (74-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001391</DescriptorUI>
     <DescriptorName>
      <String>Azo Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D005505</DescriptorUI>
     <DescriptorName>
      <String>Food Coloring Agents</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Mutation Res 40:309;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040421</ConceptUI>
    <ConceptName>
     <String>Brown FK</String>
    </ConceptName>
    <RegistryNumber>8062-14-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070423</TermUI>
      <String>Brown FK</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T070422</TermUI>
      <String>Brown-FK</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011035</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N(beta)-naphthylaminomethyl-L-alanine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*2-NAPHTHYLAMINE/analogs (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000409</DescriptorUI>
     <DescriptorName>
      <String>Alanine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Soc Jpn 95(4):397;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057037</ConceptUI>
    <ConceptName>
     <String>N(beta)-naphthylaminomethyl-L-alanine</String>
    </ConceptName>
    <RegistryNumber>32945-07-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087040</TermUI>
      <String>N(beta)-naphthylaminomethyl-L-alanine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T087039</TermUI>
      <String>N-beta-naphthylaminomethyl-L-alanine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C022913</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>YM-08050</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001549</DescriptorUI>
     <DescriptorName>
      <String>Benzamides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Int Pharmacodyn Ther 241(1):68;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0079582</ConceptUI>
    <ConceptName>
     <String>YM-08050</String>
    </ConceptName>
    <CASN1Name>Benzamide, 5-chloro-2-methoxy-4-(methylamino)-N-(1-(phenylmethyl)-3-pyrrolidinyl)-</CASN1Name>
    <RegistryNumber>73328-60-6</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0079582</Concept1UI>
     <Concept2UI>M0079580</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T109585</TermUI>
      <String>YM-08050</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T109584</TermUI>
      <String>YM 08050</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0079580</ConceptUI>
    <ConceptName>
     <String>N-(1-benzyl-3-pyrrolidinyl)-5-chloro-2-methoxy-4-methylaminobenzamide</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0079582</Concept1UI>
     <Concept2UI>M0079580</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T109583</TermUI>
      <String>N-(1-benzyl-3-pyrrolidinyl)-5-chloro-2-methoxy-4-methylaminobenzamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011039</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>nifuron</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009581</DescriptorUI>
     <DescriptorName>
      <String>Nitrofurans</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009588</DescriptorUI>
     <DescriptorName>
      <String>Nitrogen Mustard Compounds</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eksp Med Morfol 13(4):237;1974</Source>
   <Source>Mikrobiol Zh 40(1):73;1978</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057044</ConceptUI>
    <ConceptName>
     <String>nifuron</String>
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    <RegistryNumber>19819-47-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087047</TermUI>
      <String>nifuron</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T087046</TermUI>
      <String>(5'-nitro-2'-furyl)acrylidene bis(2- chloroethyl)hydrazone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009949</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tri-methacycline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>complex of methacycline with 3 mols of organic base
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008690</DescriptorUI>
     <DescriptorName>
      <String>Methacycline</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arzneim Forsch 25(2):234;1975</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055070</ConceptUI>
    <ConceptName>
     <String>tri-methacycline</String>
    </ConceptName>
    <CASN1Name>(4S-(4 alpha,4a alpha,5 alpha,5a alpha,12a alpha))-4-(dimethylamino)-1,4,4a,5,5a,6,11,12a- octahydro-3,5,10,12,12a-pentahydroxy-6-methylene- 1,11-dioxo-2-naphthacenecarboxamide, compd. with 2-amino-2-(hydroxymethyl)-1,3-propanediol (1:3)</CASN1Name>
    <RegistryNumber>53101-42-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085073</TermUI>
      <String>tri-methacycline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
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   </Concept>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C045012</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>fibrinogen Bbeta (30-43)</String>
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  <DateCreated>
   <Year>1985</Year>
   <Month>05</Month>
   <Day>13</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>07</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>corresponds to amino acid residues 30-43 of the human fibrinogen Bbeta-chain
  </Note>
  <Frequency>4</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*FIBRIN FIBRINOGEN DEGRADATION PRODUCTS (85-88)</PreviousIndexing>
   <PreviousIndexing>*FIBRINOPEPTIDES B (89-95)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005338</DescriptorUI>
     <DescriptorName>
      <String>Fibrin Fibrinogen Degradation Products</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010446</DescriptorUI>
     <DescriptorName>
      <String>Peptide Fragments</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Thomb Res 1985;37(1):85</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0131116</ConceptUI>
    <ConceptName>
     <String>fibrinogen Bbeta (30-43)</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T161121</TermUI>
      <String>fibrinogen Bbeta (30-43)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T161116</TermUI>
      <String>Bbeta 30-43 peptide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T161120</TermUI>
      <String>vasoactive Bbeta peptide 30-43</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T161119</TermUI>
      <String>peptide Bbeta (30-43)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T161117</TermUI>
      <String>fibrinogen-derived vasoactive peptide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T161115</TermUI>
      <String>Bbeta (30-43)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T161118</TermUI>
      <String>fibrinopeptide Bbeta (30-43)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C034511</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>LHRH, pGlu(1)-Phe(2)-Trp(3,6)-</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1982</Year>
   <Month>06</Month>
   <Day>08</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>11</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>gonadorelin antagonist; RN given refers to (D)-isomer
  </Note>
  <Frequency>21</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007987</DescriptorUI>
     <DescriptorName>
      <String>Gonadotropin-Releasing Hormone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011761</DescriptorUI>
     <DescriptorName>
      <String>Pyrrolidonecarboxylic Acid</String>
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    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Endocrinology 1982;110(5):1663</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0106343</ConceptUI>
    <ConceptName>
     <String>LHRH, pGlu(1)-Phe(2)-Trp(3,6)-</String>
    </ConceptName>
    <CASN1Name>Luteinizing hormone-releasing factor, 1-(5-oxo-D-proline)-2-D-phenylalanine-3-D-tryptophan-6-D-tryptophan-</CASN1Name>
    <RegistryNumber>68059-94-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0106343</Concept1UI>
     <Concept2UI>M0106341</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T136347</TermUI>
      <String>LHRH, pGlu(1)-Phe(2)-Trp(3,6)-</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T136346</TermUI>
      <String>LHRH,-pyroglutamyl(1)-phenylalanyl(2)-tryptophyl(3,6)-</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T136343</TermUI>
      <String>GPT-LHRH</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T136342</TermUI>
      <String>1-Pyr-2-Phe-3,6-Trp-LHRH</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T136344</TermUI>
      <String>GnRH, pGlu(1)-Phe(2)-Trp(3,6)-</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0106341</ConceptUI>
    <ConceptName>
     <String>LHRH, D-pGlu(1)-D-Phe(2)-D-Trp(3,6)-</String>
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    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0106343</Concept1UI>
     <Concept2UI>M0106341</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T136345</TermUI>
      <String>LHRH, D-pGlu(1)-D-Phe(2)-D-Trp(3,6)-</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C578034</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>MEF2 protein, Xenopus</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>10</Month>
   <Day>24</Day>
  </DateCreated>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D029867</DescriptorUI>
     <DescriptorName>
      <String>Xenopus Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D064326</DescriptorUI>
     <DescriptorName>
      <String>MEF2 Transcription Factors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0579456</ConceptUI>
    <ConceptName>
     <String>MEF2 protein, Xenopus</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T833991</TermUI>
      <String>MEF2 protein, Xenopus</String>
      <DateCreated>
       <Year>2012</Year>
       <Month>12</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T833992</TermUI>
      <String>myocyte enhancer factor 2D, Xenopus</String>
      <DateCreated>
       <Year>2012</Year>
       <Month>12</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C578036</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Mef2a protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>10</Month>
   <Day>24</Day>
  </DateCreated>
  <Frequency>123</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D064326</DescriptorUI>
     <DescriptorName>
      <String>MEF2 Transcription Factors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0483267</ConceptUI>
    <ConceptName>
     <String>Mef2a protein, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T636507</TermUI>
      <String>Mef2a protein, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>04</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T636508</TermUI>
      <String>myocyte enhancer factor 2A, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>04</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C578037</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>MEF2A protein, rat</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>10</Month>
   <Day>24</Day>
  </DateCreated>
  <Frequency>33</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D064326</DescriptorUI>
     <DescriptorName>
      <String>MEF2 Transcription Factors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0525553</ConceptUI>
    <ConceptName>
     <String>MEF2A protein, rat</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T728064</TermUI>
      <String>MEF2A protein, rat</String>
      <DateCreated>
       <Year>2008</Year>
       <Month>10</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2008)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T728065</TermUI>
      <String>myocyte enhancer factor 2A, rat</String>
      <DateCreated>
       <Year>2008</Year>
       <Month>10</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2008)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T728066</TermUI>
      <String>MADS box transcription enhancer factor 2, polypeptide A, rat</String>
      <DateCreated>
       <Year>2008</Year>
       <Month>10</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2008)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C578038</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>MEF2B protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>10</Month>
   <Day>24</Day>
  </DateCreated>
  <Frequency>40</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D064326</DescriptorUI>
     <DescriptorName>
      <String>MEF2 Transcription Factors</String>
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  <ConceptList>
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    <ConceptUI>M0483264</ConceptUI>
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     <String>MEF2B protein, human</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T636496</TermUI>
      <String>MEF2B protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>04</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T636497</TermUI>
      <String>myocyte enhancer factor 2B, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>04</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T661060</TermUI>
      <String>RSRFR2 protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>12</Month>
       <Day>05</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T636498</TermUI>
      <String>MADS box transcription enhancer factor 2, polypeptide B, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>04</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C578039</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Mef2b protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>10</Month>
   <Day>24</Day>
  </DateCreated>
  <Frequency>13</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D064326</DescriptorUI>
     <DescriptorName>
      <String>MEF2 Transcription Factors</String>
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   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0483268</ConceptUI>
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     <String>Mef2b protein, mouse</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T636509</TermUI>
      <String>Mef2b protein, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>04</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T636510</TermUI>
      <String>myocyte enhancer factor 2B, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>04</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C472849</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>8-prenylmucronulatol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>04</Month>
   <Day>08</Day>
  </DateCreated>
  <Note>from Smirnowia iranica (Leguminosae-Papilionoideae); structure In first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007529</DescriptorUI>
     <DescriptorName>
      <String>Isoflavones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2002 Dec;65(12):1754-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0447919</ConceptUI>
    <ConceptName>
     <String>8-prenylmucronulatol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T537658</TermUI>
      <String>8-prenylmucronulatol</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>04</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017620</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>phenylalanyl-5'-AMP</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>04</Month>
   <Day>22</Day>
  </DateRevised>
  <Note>RN given refers to (S)-isomer
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000249</DescriptorUI>
     <DescriptorName>
      <String>Adenosine Monophosphate</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 17(12):2443;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068545</ConceptUI>
    <ConceptName>
     <String>phenylalanyl-5'-AMP</String>
    </ConceptName>
    <RegistryNumber>6372-09-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098548</TermUI>
      <String>phenylalanyl-5'-AMP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C408445</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Cha o 1 protein, Chamaecyparis obtusa</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>05</Month>
   <Day>30</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>02</Month>
   <Day>13</Day>
  </DateRevised>
  <Note>one of the major allergen of  the Japanese cypress pollen
  </Note>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010940</DescriptorUI>
     <DescriptorName>
      <String>Plant Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D000485</DescriptorUI>
     <DescriptorName>
      <String>Allergens</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D011058</DescriptorUI>
     <DescriptorName>
      <String>Pollen</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Immunology 2000 Apr;99(4):625-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0363193</ConceptUI>
    <ConceptName>
     <String>Cha o 1 protein, Chamaecyparis obtusa</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T503785</TermUI>
      <String>Cha o 1 protein, Chamaecyparis obtusa</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>07</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T415534</TermUI>
      <String>allergen Cha o1, Chamaecyparis obtusa</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>05</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017624</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-phenylpyrrolidone-2</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>07</Month>
   <Day>18</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011760</DescriptorUI>
     <DescriptorName>
      <String>Pyrrolidinones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biul Eksp Biol Med 85(3):304;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068551</ConceptUI>
    <ConceptName>
     <String>4-phenylpyrrolidone-2</String>
    </ConceptName>
    <RegistryNumber>1198-97-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098554</TermUI>
      <String>4-phenylpyrrolidone-2</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017626</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-phenylthiazolone-(2)-hydrazone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>07</Month>
   <Day>18</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*HYDRAZONES (78-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013844</DescriptorUI>
     <DescriptorName>
      <String>Thiazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ann Univ Mariae Curie Sklodowska (Med) 32:221;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068554</ConceptUI>
    <ConceptName>
     <String>4-phenylthiazolone-(2)-hydrazone</String>
    </ConceptName>
    <RegistryNumber>34176-52-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098557</TermUI>
      <String>4-phenylthiazolone-(2)-hydrazone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017627</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>phleic acids</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005231</DescriptorUI>
     <DescriptorName>
      <String>Fatty Acids, Unsaturated</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Prog Chem Fats Other Lipids 16:59;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068555</ConceptUI>
    <ConceptName>
     <String>phleic acids</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098558</TermUI>
      <String>phleic acids</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017628</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>phosphatidyl-N-methyl-N-isopropylethanolamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010714</DescriptorUI>
     <DescriptorName>
      <String>Phosphatidylethanolamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Phys Lipids 21(3):175;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068556</ConceptUI>
    <ConceptName>
     <String>phosphatidyl-N-methyl-N-isopropylethanolamine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098559</TermUI>
      <String>phosphatidyl-N-methyl-N-isopropylethanolamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C408483</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Tp92 antigen, Treponema pallidum</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>05</Month>
   <Day>31</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>02</Month>
   <Day>13</Day>
  </DateRevised>
  <Note>a 92 kDa antigen from Treponema pallidum; amino acid sequence in first source
  </Note>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000954</DescriptorUI>
     <DescriptorName>
      <String>Antigens, Surface</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Infect Dis 2000 Apr;181(4):1401-13</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0363250</ConceptUI>
    <ConceptName>
     <String>Tp92 antigen, Treponema pallidum</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T498139</TermUI>
      <String>Tp92 antigen, Treponema pallidum</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>06</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T415607</TermUI>
      <String>Tp92 protein, Treponema pallidum</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>05</Month>
       <Day>31</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T415608</TermUI>
      <String>antigen, Tp92, Treponema pallidum</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>05</Month>
       <Day>31</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017639</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-pivaloylglycine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>12</Month>
   <Day>21</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PENTANOIC ACIDS (78-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005998</DescriptorUI>
     <DescriptorName>
      <String>Glycine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 524(2):393;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068577</ConceptUI>
    <ConceptName>
     <String>N-pivaloylglycine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098580</TermUI>
      <String>N-pivaloylglycine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C118946</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-fluoroacetanilide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1999</Year>
   <Month>05</Month>
   <Day>24</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000083</DescriptorUI>
     <DescriptorName>
      <String>Acetanilides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Xenobiotica 1999 Feb;29(2):205-16</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0304673</ConceptUI>
    <ConceptName>
     <String>4-fluoroacetanilide</String>
    </ConceptName>
    <RegistryNumber>351-83-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T334678</TermUI>
      <String>4-fluoroacetanilide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T334677</TermUI>
      <String>N-p-fluorophenylacetamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T334676</TermUI>
      <String>N-(4-fluorophenyl)acetamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017647</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>polycarbon monofluoride</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005465</DescriptorUI>
     <DescriptorName>
      <String>Fluorocarbon Polymers</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Bull Osaka Med Sch 23(1):14;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068586</ConceptUI>
    <ConceptName>
     <String>polycarbon monofluoride</String>
    </ConceptName>
    <RegistryNumber>51311-17-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098589</TermUI>
      <String>polycarbon monofluoride</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017653</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>polyethyleneglycol diflufenamate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>POLYETHYLENE GLYCOLS (78-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005439</DescriptorUI>
     <DescriptorName>
      <String>Flufenamic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Thromb Res 12(4):707;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068595</ConceptUI>
    <ConceptName>
     <String>polyethyleneglycol diflufenamate</String>
    </ConceptName>
    <RegistryNumber>67186-14-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098598</TermUI>
      <String>polyethyleneglycol diflufenamate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017655</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>polymethacryloyloxybenzoic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>20</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>HYDROXYBENZOIC ACIDS (78-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011109</DescriptorUI>
     <DescriptorName>
      <String>Polymethacrylic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biomed Mater Res 12(4):525;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068598</ConceptUI>
    <ConceptName>
     <String>polymethacryloyloxybenzoic acid</String>
    </ConceptName>
    <RegistryNumber>39276-30-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098601</TermUI>
      <String>polymethacryloyloxybenzoic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017657</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>poly(2-methyl-5-vinyl-N-ethylpyridinium bromide)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>20</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PYRIDINIUM COMPOUNDS (78-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011145</DescriptorUI>
     <DescriptorName>
      <String>Polyvinyls</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Polim Med 7(4):255;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068600</ConceptUI>
    <ConceptName>
     <String>poly(2-methyl-5-vinyl-N-ethylpyridinium bromide)</String>
    </ConceptName>
    <RegistryNumber>42936-61-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098603</TermUI>
      <String>poly(2-methyl-5-vinyl-N-ethylpyridinium bromide)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017671</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>preprolactin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>01</Month>
   <Day>03</Day>
  </DateRevised>
  <Frequency>88</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011388</DescriptorUI>
     <DescriptorName>
      <String>Prolactin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011498</DescriptorUI>
     <DescriptorName>
      <String>Protein Precursors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D002148</DescriptorUI>
     <DescriptorName>
      <String>Calmodulin-Binding Proteins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Biol Chem 253(11):3753;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068616</ConceptUI>
    <ConceptName>
     <String>preprolactin</String>
    </ConceptName>
    <CASN1Name>Prolactin, pre-</CASN1Name>
    <RegistryNumber>65637-74-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098619</TermUI>
      <String>preprolactin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C445321</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>trophinin, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>01</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>01</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>the magphinins are melanoma-associated antigen superfamily members that are alternatively spliced forms of trophinin
  </Note>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015815</DescriptorUI>
     <DescriptorName>
      <String>Cell Adhesion Molecules</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 2001 Dec 28;276(52):49378-89</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0412780</ConceptUI>
    <ConceptName>
     <String>trophinin, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0412780</Concept1UI>
     <Concept2UI>M0479101</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0412780</Concept1UI>
     <Concept2UI>M0412783</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0412780</Concept1UI>
     <Concept2UI>M0412781</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0412780</Concept1UI>
     <Concept2UI>M0412782</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T479949</TermUI>
      <String>trophinin, mouse</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>01</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0479101</ConceptUI>
    <ConceptName>
     <String>Maged3 protein, mouse</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0412780</Concept1UI>
     <Concept2UI>M0479101</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T627271</TermUI>
      <String>Maged3 protein, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>01</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0412783</ConceptUI>
    <ConceptName>
     <String>magphinin-gamma</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0412780</Concept1UI>
     <Concept2UI>M0412783</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T479952</TermUI>
      <String>magphinin-gamma</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>01</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0412781</ConceptUI>
    <ConceptName>
     <String>magphinin-alpha</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0412780</Concept1UI>
     <Concept2UI>M0412781</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T479950</TermUI>
      <String>magphinin-alpha</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>01</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0412782</ConceptUI>
    <ConceptName>
     <String>magphinin-beta</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0412780</Concept1UI>
     <Concept2UI>M0412782</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T479951</TermUI>
      <String>magphinin-beta</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>01</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017693</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-pyrenyloxirane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>EPOXY COMPOUNDS (79-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011721</DescriptorUI>
     <DescriptorName>
      <String>Pyrenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 82(3):929;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068665</ConceptUI>
    <ConceptName>
     <String>1-pyrenyloxirane</String>
    </ConceptName>
    <RegistryNumber>61695-74-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098668</TermUI>
      <String>1-pyrenyloxirane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017695</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>pyridoxylidenevaline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>used in conjunction with technetium for radionuclide imaging
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PYRIDOXAL/*analogs (78-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014633</DescriptorUI>
     <DescriptorName>
      <String>Valine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Jap J Nucl Med 14(6):927;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068666</ConceptUI>
    <ConceptName>
     <String>pyridoxylidenevaline</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098669</TermUI>
      <String>pyridoxylidenevaline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C495668</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bZIP63 protein, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>01</Month>
   <Day>28</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>a basic leucine zipper (bZIP) transcription factor &amp; lesion simulating disease 1 (LSD1) protein from Arabidopsis; has been sequenced
  </Note>
  <Frequency>11</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*Transcription Factors (2005)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D050976</DescriptorUI>
     <DescriptorName>
      <String>Basic-Leucine Zipper Transcription Factors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Plant J 2004 Nov;40(3):428-38</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0480006</ConceptUI>
    <ConceptName>
     <String>bZIP63 protein, Arabidopsis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T629065</TermUI>
      <String>bZIP63 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>01</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017711</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>selenohomolysine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>03</Month>
   <Day>14</Day>
  </DateRevised>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SELENIUM (78-91)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008239</DescriptorUI>
     <DescriptorName>
      <String>Lysine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D016566</DescriptorUI>
     <DescriptorName>
      <String>Organoselenium Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ital J Biochem 27(1):29;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068691</ConceptUI>
    <ConceptName>
     <String>selenohomolysine</String>
    </ConceptName>
    <CASN1Name>Alanine, 3-((3-aminopropyl)seleno)-</CASN1Name>
    <RegistryNumber>67392-14-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098694</TermUI>
      <String>selenohomolysine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T098692</TermUI>
      <String>Se-(3-aminopropyl)selenocysteine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T098693</TermUI>
      <String>selenahomolysine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T098691</TermUI>
      <String>APSeC</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017672</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>presqualene pyrophosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>13</Day>
  </DateRevised>
  <Frequency>21</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*TERPENES (78-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011106</DescriptorUI>
     <DescriptorName>
      <String>Polyisoprenyl Phosphates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 253(13):4566;1978</Source>
   <Source>Mol Cell Biochem 1979;27(2):97</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068618</ConceptUI>
    <ConceptName>
     <String>presqualene pyrophosphate</String>
    </ConceptName>
    <RegistryNumber>29849-75-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098621</TermUI>
      <String>presqualene pyrophosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T098620</TermUI>
      <String>presqualene diphosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C495667</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>MCP1 protein, rabbit</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>01</Month>
   <Day>28</Day>
  </DateCreated>
  <Note>This protein is synthesized in vivo by cells of the vascular wall and its expression is largely controlled by NF-kB nuclear transcription factor
  </Note>
  <Frequency>9</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D018932</DescriptorUI>
     <DescriptorName>
      <String>Chemokine CCL2</String>
     </DescriptorName>
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  <SourceList>
   <Source>Ann Acad Med Stetin. 2003;49():79-90</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0480005</ConceptUI>
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    <RegistryNumber>0</RegistryNumber>
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       <Month>01</Month>
       <Day>28</Day>
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      <ThesaurusIDlist>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
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       <Month>01</Month>
       <Day>28</Day>
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<SupplementalRecord SCRClass = "1">
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   <String>silver carbonate-Celite</String>
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  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1993</Year>
   <Month>09</Month>
   <Day>14</Day>
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  <Note>used to oxidize bile acid methyl esters to 3-keto bile acids
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  <Frequency>1</Frequency>
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   <PreviousIndexing>*SILVER (78-93)</PreviousIndexing>
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   <HeadingMappedTo>
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  <SourceList>
   <Source>J Lipid Res 19:501;1978</Source>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
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  <SupplementalRecordName>
   <String>vhtD protein, Methanosarcina mazei</String>
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  <DateCreated>
   <Year>1996</Year>
   <Month>03</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>2003</Year>
   <Month>09</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>part of the vht operon which encodes an F420-nonreducing hydrogenase from Methanosarcina mazei Go1; amino acid sequence in first source
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
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    <DescriptorReferredTo>
     <DescriptorUI>*D010088</DescriptorUI>
     <DescriptorName>
      <String>Oxidoreductases</String>
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   <HeadingMappedTo>
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     <DescriptorUI>*D019843</DescriptorUI>
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  <SourceList>
   <Source>Arch Microbiol 1995 Nov;164(5):370-6</Source>
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  <ConceptList>
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    <RegistryNumber>EC 1.12.2.-</RegistryNumber>
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      <DateCreated>
       <Year>2003</Year>
       <Month>09</Month>
       <Day>11</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
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  <SupplementalRecordName>
   <String>S37731 protein, Vibrio cholerae</String>
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  <DateCreated>
   <Year>1996</Year>
   <Month>03</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>2003</Year>
   <Month>09</Month>
   <Day>12</Day>
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  <Note>lipocalin isolated from Vibrio cholerae; amino acid sequence in first source
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  <Frequency>1</Frequency>
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    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
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      <String>Bacterial Proteins</String>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002352</DescriptorUI>
     <DescriptorName>
      <String>Carrier Proteins</String>
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  <SourceList>
   <Source>Trends Biochem Sci 1995 Dec;20(12):498-9</Source>
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    <RegistryNumber>0</RegistryNumber>
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      <TermUI>T550597</TermUI>
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      <DateCreated>
       <Year>2003</Year>
       <Month>09</Month>
       <Day>11</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
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  <SupplementalRecordName>
   <String>stigmast-4-ene-3,6-dione</String>
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  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <Frequency>8</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002783</DescriptorUI>
     <DescriptorName>
      <String>Cholestenones</String>
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  <SourceList>
   <Source>Pharmazie 33(1):82;1978</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068725</ConceptUI>
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     <String>stigmast-4-ene-3,6-dione</String>
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    <RegistryNumber>23670-94-2</RegistryNumber>
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      <TermUI>T098728</TermUI>
      <String>stigmast-4-ene-3,6-dione</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
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  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017728</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>streptovarone</String>
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  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1994</Year>
   <Month>09</Month>
   <Day>30</Day>
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  <Note>structure
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013310</DescriptorUI>
     <DescriptorName>
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    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
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  <SourceList>
   <Source>Mol Pharmacol 14:442;1978</Source>
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  <ConceptList>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017742</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>technetium Tc 99m stannous pyrophosphate</String>
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  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>1991</Year>
   <Month>11</Month>
   <Day>29</Day>
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  <Frequency>107</Frequency>
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  <HeadingMappedToList>
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    <DescriptorReferredTo>
     <DescriptorUI>*D014003</DescriptorUI>
     <DescriptorName>
      <String>Tin Polyphosphates</String>
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   <HeadingMappedTo>
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     <DescriptorUI>*D016698</DescriptorUI>
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  <SourceList>
   <Source>Eur J Nucl Med 3(4):219;1978</Source>
   <Source>J Nucl Med 19(10):1111;1978</Source>
   <Source>J Nucl Med 19(8):895;1978</Source>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0068746</Concept1UI>
     <Concept2UI>M0068744</Concept2UI>
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    <TermList>
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      <TermUI>T098749</TermUI>
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     </Term>
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   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0068745</ConceptUI>
    <ConceptName>
     <String>technetium tin pyrophosphate</String>
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     <Concept2UI>M0068745</Concept2UI>
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      <TermUI>T098748</TermUI>
      <String>technetium tin pyrophosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0068743</ConceptUI>
    <ConceptName>
     <String>Tc-99m-Sn pyrophosphate</String>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0068746</Concept1UI>
     <Concept2UI>M0068743</Concept2UI>
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      <TermUI>T098746</TermUI>
      <String>Tc-99m-Sn pyrophosphate</String>
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       <ThesaurusID>NLM (1978)</ThesaurusID>
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   <Concept PreferredConceptYN="N">
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 </SupplementalRecord>
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  <SupplementalRecordName>
   <String>testosterone 3-(O-dimethylaminopropyl)oxime</String>
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  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <Note>structure
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
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    <DescriptorReferredTo>
     <DescriptorUI>D013739</DescriptorUI>
     <DescriptorName>
      <String>Testosterone</String>
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     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
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  <SourceList>
   <Source>J Med Chem 21(7):712;1978</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
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    <ConceptName>
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    <RegistryNumber>66818-35-7</RegistryNumber>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017746</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,2,3,4-tetrabromobutane</String>
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  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
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     <DescriptorUI>*D006842</DescriptorUI>
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  <SourceList>
   <Source>Toxicol Appl Pharmacol 44(3):661;1978</Source>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
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  <SupplementalRecordName>
   <String>thiamine monophosphate bis(glucosamine)</String>
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  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>1990</Year>
   <Month>11</Month>
   <Day>14</Day>
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  <Frequency>0</Frequency>
  <HeadingMappedToList>
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     <QualifierUI>*Q000031</QualifierUI>
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  <SourceList>
   <Source>Int J Vitam Nutr Res 48(2):136;1978</Source>
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    <CASN1Name>D-Glucose, 2-amino-2-deoxy-, compd. with 3-((4-amino-2-methyl-5-pyrimidinyl)methyl)-4-methyl-5-(2-(phosphonooxy)ethyl)thiazolium chloride (2:1)</CASN1Name>
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     <ConceptRelation RelationName="NRW">
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   <Concept PreferredConceptYN="N">
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     <String>Thiazolium, 3-(4-amino-2-methyl-5-pyrimidinyl)methyl-4-methyl-5-(2-(phosphonooxy)ethyl)-, chloride, compd. with 2-amino-2-deoxy-D-glucose (1:2)</String>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0068759</Concept1UI>
     <Concept2UI>M0068757</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T098760</TermUI>
      <String>Thiazolium, 3-(4-amino-2-methyl-5-pyrimidinyl)methyl-4-methyl-5-(2-(phosphonooxy)ethyl)-, chloride, compd. with 2-amino-2-deoxy-D-glucose (1:2)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C064686</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>eriotriochin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1990</Year>
   <Month>07</Month>
   <Day>31</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>09</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>isolated from Erythriina eriotriocha; structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007529</DescriptorUI>
     <DescriptorName>
      <String>Isoflavones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D004895</DescriptorUI>
     <DescriptorName>
      <String>Erythrina</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Nat Prod 1990;53(2):509</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0178131</ConceptUI>
    <ConceptName>
     <String>eriotriochin</String>
    </ConceptName>
    <CASN1Name>5H-Furo(3,2-g)(1)benzopyran-5-one, 2,3-dihydro-4-hydroxy-2-(1-(2-hydroxyethoxy)-1-methylethyl)-6-(4-hydroxyphenyl)-9-(3-methyl-2-butenyl)-</CASN1Name>
    <RegistryNumber>128585-07-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T208136</TermUI>
      <String>eriotriochin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017764</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N(10)-tosylisohomoaminopterin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000630</DescriptorUI>
     <DescriptorName>
      <String>Aminopterin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 21(7):673;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068784</ConceptUI>
    <ConceptName>
     <String>N(10)-tosylisohomoaminopterin</String>
    </ConceptName>
    <CASN1Name>N-(4-((((2,4-diamino-6-pteridinyl)methylphenyl)sulfonyl)amino)methyl)benzoyl)-L-glutamic acid</CASN1Name>
    <RegistryNumber>66801-30-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098787</TermUI>
      <String>N(10)-tosylisohomoaminopterin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017772</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>methyl hydroxyurea</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>07</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>RN given refers to cpd with unspecified locants
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D006918</DescriptorUI>
     <DescriptorName>
      <String>Hydroxyurea</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Aust NZ J Surg 49(3):335;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068793</ConceptUI>
    <ConceptName>
     <String>methyl hydroxyurea</String>
    </ConceptName>
    <CASN1Name>Urea, hydroxymethyl-</CASN1Name>
    <RegistryNumber>78200-36-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098796</TermUI>
      <String>methyl hydroxyurea</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017775</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,3,5-trimethoxytoluene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014050</DescriptorUI>
     <DescriptorName>
      <String>Toluene</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Yakugaku Zasshi 98(6):789;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068797</ConceptUI>
    <ConceptName>
     <String>2,3,5-trimethoxytoluene</String>
    </ConceptName>
    <CASN1Name>1,2,5-trimethoxy-3-methylbenzene</CASN1Name>
    <RegistryNumber>38790-14-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098800</TermUI>
      <String>2,3,5-trimethoxytoluene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017776</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3,4,5-trimethoxytoluene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014050</DescriptorUI>
     <DescriptorName>
      <String>Toluene</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Yakugaku Zasshi 98(6):789;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068798</ConceptUI>
    <ConceptName>
     <String>3,4,5-trimethoxytoluene</String>
    </ConceptName>
    <CASN1Name>1,2,3-trimethoxy-5-methylbenzene</CASN1Name>
    <RegistryNumber>6443-69-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098801</TermUI>
      <String>3,4,5-trimethoxytoluene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017779</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tris(2,3-dichloropropyl)phosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>06</Month>
   <Day>14</Day>
  </DateRevised>
  <Frequency>4</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>HYDROCARBONS, CHLORINATED (79-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009943</DescriptorUI>
     <DescriptorName>
      <String>Organophosphorus Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D005411</DescriptorUI>
     <DescriptorName>
      <String>Flame Retardants</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Am Ind Hyg Assoc J 39(8):633;1978</Source>
   <Source>Bull Environ Contam Toxicol 21(3):409;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068801</ConceptUI>
    <ConceptName>
     <String>tris(2,3-dichloropropyl)phosphate</String>
    </ConceptName>
    <CASN1Name>2,3-dichloro-1-propanol phosphate (3:1)</CASN1Name>
    <RegistryNumber>78-43-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098804</TermUI>
      <String>tris(2,3-dichloropropyl)phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017811</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ICI 73602</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>13</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PHENYLUREA COMPOUNDS (79-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006146</DescriptorUI>
     <DescriptorName>
      <String>Guanidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ann NY Acad Sci 284:305;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068866</ConceptUI>
    <ConceptName>
     <String>ICI 73602</String>
    </ConceptName>
    <CASN1Name>1-(p-chlorophenyl)-3-(m-3-isobutylguanidinophenyl)urea.HCl</CASN1Name>
    <RegistryNumber>38787-32-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098869</TermUI>
      <String>ICI 73602</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T098868</TermUI>
      <String>ICI-73602</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017784</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tuberactinomycin-O</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004776</DescriptorUI>
     <DescriptorName>
      <String>Enviomycin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 82(3):972;1978</Source>
   <Source>J Antibiot (Tokyo) 31(8):792;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068819</ConceptUI>
    <ConceptName>
     <String>tuberactinomycin-O</String>
    </ConceptName>
    <CASN1Name>(R)-6-(L-2-(2-amino-1,4,5,6-tetrahydro-4-pyrimidinyl)glycine)viomycin</CASN1Name>
    <RegistryNumber>33137-73-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098822</TermUI>
      <String>tuberactinomycin-O</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017789</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>uridine diphosphate adenosine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1995</Year>
   <Month>06</Month>
   <Day>21</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*URIDINE DIPHOSPHATE/analogs (78-88)</PreviousIndexing>
   <PreviousIndexing>ADENOSINE/*analogs (78-88)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015226</DescriptorUI>
     <DescriptorName>
      <String>Dinucleoside Phosphates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Mol Evol 11:17;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068825</ConceptUI>
    <ConceptName>
     <String>uridine diphosphate adenosine</String>
    </ConceptName>
    <CASN1Name>Adenosine--5'-(trihydrogen diphosphate), 5'-5'-ester with uridine</CASN1Name>
    <RegistryNumber>65331-79-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098828</TermUI>
      <String>uridine diphosphate adenosine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017793</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>vitamycin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>carotenoid produced by acrinomycetes used as vitamin A substitute in fowl
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002338</DescriptorUI>
     <DescriptorName>
      <String>Carotenoids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D006133</DescriptorUI>
     <DescriptorName>
      <String>Growth Substances</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Vopr Pitan 78(3):84;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068829</ConceptUI>
    <ConceptName>
     <String>vitamycin</String>
    </ConceptName>
    <RegistryNumber>12778-25-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098832</TermUI>
      <String>vitamycin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017796</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>7 xi-hydroxytetrahydrocortisol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>found in urine from newborn baboons
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013760</DescriptorUI>
     <DescriptorName>
      <String>Tetrahydrocortisol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Steroids 31(4):501;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068835</ConceptUI>
    <ConceptName>
     <String>7 xi-hydroxytetrahydrocortisol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098838</TermUI>
      <String>7 xi-hydroxytetrahydrocortisol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017797</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>7 xi-hydroxytetrahydrocortisone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>found in urine of newborn baboons
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013761</DescriptorUI>
     <DescriptorName>
      <String>Tetrahydrocortisone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Steroids 31(4):501;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068836</ConceptUI>
    <ConceptName>
     <String>7 xi-hydroxytetrahydrocortisone</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098839</TermUI>
      <String>7 xi-hydroxytetrahydrocortisone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C440668</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>isaindigotone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>12</Month>
   <Day>10</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>01</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>3-arylidenepyrrolo(2,1-b)quinazoline-9-one from Isatis indigotica; structure in first source
  </Note>
  <Frequency>11</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000470</DescriptorUI>
     <DescriptorName>
      <String>Alkaloids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011799</DescriptorUI>
     <DescriptorName>
      <String>Quinazolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2001 Oct;64(10):1297-300</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0406891</ConceptUI>
    <ConceptName>
     <String>isaindigotone</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T472905</TermUI>
      <String>isaindigotone</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>12</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C490371</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>FabZ protein, Enterococcus faecalis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>09</Month>
   <Day>21</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>11</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>a beta-hydroxyacyl-ACP dehydatase that also catalyzes isomerization of trans-2-decenoyl-ACP to cis-3-decenoyl-ACP
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009097</DescriptorUI>
     <DescriptorName>
      <String>Multienzyme Complexes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D006836</DescriptorUI>
     <DescriptorName>
      <String>Hydro-Lyases</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D019745</DescriptorUI>
     <DescriptorName>
      <String>cis-trans-Isomerases</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Biol Chem 2004 Aug 13;279(33):34489-95</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0472950</ConceptUI>
    <ConceptName>
     <String>FabZ protein, Enterococcus faecalis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0472950</Concept1UI>
     <Concept2UI>M0472952</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0472950</Concept1UI>
     <Concept2UI>M0472951</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T610400</TermUI>
      <String>FabZ protein, Enterococcus faecalis</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0472952</ConceptUI>
    <ConceptName>
     <String>FabZ2 protein, E faecalis</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0472950</Concept1UI>
     <Concept2UI>M0472952</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T610402</TermUI>
      <String>FabZ2 protein, E faecalis</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0472951</ConceptUI>
    <ConceptName>
     <String>FabZ1 protein, E faecalis</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0472950</Concept1UI>
     <Concept2UI>M0472951</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T610401</TermUI>
      <String>FabZ1 protein, E faecalis</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C029518</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hemoglobin F Iwata</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>05</Month>
   <Day>28</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>11</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>Gly replaced by Arg at position 72(E16) on gamma chain; found in Japan
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005319</DescriptorUI>
     <DescriptorName>
      <String>Fetal Hemoglobin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006455</DescriptorUI>
     <DescriptorName>
      <String>Hemoglobins, Abnormal</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Hemoglobin 1981;5(2):139</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0094139</ConceptUI>
    <ConceptName>
     <String>hemoglobin F Iwata</String>
    </ConceptName>
    <RegistryNumber>77907-57-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T124142</TermUI>
      <String>hemoglobin F Iwata</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T590335</TermUI>
      <String>HBGA g.339G&gt;C</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>06</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T124141</TermUI>
      <String>Hb F-Iwata</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C089732</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>P2-C protein, Coxsackievirus</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>11</Month>
   <Day>02</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>01</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>from coxsackie virus B4; has striking similarity in certain amino acid sequences with human glutamic acid decarboxylase (GAD); antibodies to GAD &amp; P2C are found in sera of virus infected mice &amp; in isulin-depedendent diabetes mellitus (IDDM) patients; partial AA sequence given in first source
  </Note>
  <Frequency>8</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014764</DescriptorUI>
     <DescriptorName>
      <String>Viral Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D000956</DescriptorUI>
     <DescriptorName>
      <String>Antigens, Viral</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Diabetes 1994 Oct;43(10):1260-6</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0237204</ConceptUI>
    <ConceptName>
     <String>P2-C protein, Coxsackievirus</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T267209</TermUI>
      <String>P2-C protein, Coxsackievirus</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T267208</TermUI>
      <String>P2-C peptide, Coxsackievirus</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017812</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Ro 7-9749</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>11</Month>
   <Day>17</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001570</DescriptorUI>
     <DescriptorName>
      <String>Benzodiazepinones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Clin Chem 24(10):1838;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068867</ConceptUI>
    <ConceptName>
     <String>Ro 7-9749</String>
    </ConceptName>
    <CASN1Name>2H-1,4-Benzodiazepin-2-one, 5-(2-fluorophenyl)-1,3-dihydro-7-iodo-</CASN1Name>
    <RegistryNumber>30843-56-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098870</TermUI>
      <String>Ro 7-9749</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017820</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-((4-aminomethylphenyl)aza)-2-naphthol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>09</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>used in assay for monoamine oxidase in serum
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>BENZYLAMINES (79-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009284</DescriptorUI>
     <DescriptorName>
      <String>Naphthols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Clin Chim Acta 88(2):315;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068882</ConceptUI>
    <ConceptName>
     <String>1-((4-aminomethylphenyl)aza)-2-naphthol</String>
    </ConceptName>
    <CASN1Name>2-Naphthalenol, 1-((4-(aminomethyl)phenyl)azo)-, monohydrochloride</CASN1Name>
    <RegistryNumber>51389-61-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098885</TermUI>
      <String>1-((4-aminomethylphenyl)aza)-2-naphthol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017830</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bis(2-chloroisopropyl)ether</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004987</DescriptorUI>
     <DescriptorName>
      <String>Ethers</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ann NY Acad Sci 298:111;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068897</ConceptUI>
    <ConceptName>
     <String>bis(2-chloroisopropyl)ether</String>
    </ConceptName>
    <RegistryNumber>39638-32-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098900</TermUI>
      <String>bis(2-chloroisopropyl)ether</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017833</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>calendulozide B</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>triglycoside of oleanolic acid; structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>GLYCOSIDES (79-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009828</DescriptorUI>
     <DescriptorName>
      <String>Oleanolic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D012503</DescriptorUI>
     <DescriptorName>
      <String>Saponins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Farmakol Toksikol 41(5):556;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068900</ConceptUI>
    <ConceptName>
     <String>calendulozide B</String>
    </ConceptName>
    <CASN1Name>Olean-12-en-28-oic acid, 3-((4-O-beta-D-galactopyranosyl-beta-D-glucopyranosyl)oxy)-, alpha-D-glucopyranosyl ester, (3beta)-</CASN1Name>
    <RegistryNumber>34381-98-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098903</TermUI>
      <String>calendulozide B</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017838</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-chloroacetophenone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002721</DescriptorUI>
     <DescriptorName>
      <String>omega-Chloroacetophenone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068904</ConceptUI>
    <ConceptName>
     <String>4-chloroacetophenone</String>
    </ConceptName>
    <CASN1Name>1-(4-chlorophenyl)-ethanone</CASN1Name>
    <RegistryNumber>99-91-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098907</TermUI>
      <String>4-chloroacetophenone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C029521</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hemoglobin G Copenhagen</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>05</Month>
   <Day>28</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>11</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>Asp replaced by Asn at position 47(CD6) on beta chain
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006455</DescriptorUI>
     <DescriptorName>
      <String>Hemoglobins, Abnormal</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Hemoglobin 1981;5(2):195</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0094145</ConceptUI>
    <ConceptName>
     <String>hemoglobin G Copenhagen</String>
    </ConceptName>
    <RegistryNumber>9034-69-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T124148</TermUI>
      <String>hemoglobin G Copenhagen</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T124147</TermUI>
      <String>Hb G-Copenhagen</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T590373</TermUI>
      <String>HBB g.272G&gt;A</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>06</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C029522</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hemoglobin J Bangkok</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>05</Month>
   <Day>28</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>11</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>glycine replaced by aspartic acid at position 56(D7) on beta chain
  </Note>
  <Frequency>14</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006448</DescriptorUI>
     <DescriptorName>
      <String>Hemoglobin J</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Hemoglobin 1981;5(2):199</Source>
   <Source>Hemoglobin 2002 Aug;26(3):325-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0094147</ConceptUI>
    <ConceptName>
     <String>hemoglobin J Bangkok</String>
    </ConceptName>
    <RegistryNumber>71396-39-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T124150</TermUI>
      <String>hemoglobin J Bangkok</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T544644</TermUI>
      <String>hemoglobin J-Meinung</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>06</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T124149</TermUI>
      <String>Hb J Bangkok</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T544645</TermUI>
      <String>Hb J-Meinung</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>06</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017934</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>platinum-6-mercaptopurine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>13</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>MERCAPTOPURINE/*analogs (79-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009944</DescriptorUI>
     <DescriptorName>
      <String>Organoplatinum Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Br J Cancer 38(2):325;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0069083</ConceptUI>
    <ConceptName>
     <String>platinum-6-mercaptopurine</String>
    </ConceptName>
    <CASN1Name>Platinum, bis(1,7-dihydro-6H-purine-6-thionato-N7,S6)-</CASN1Name>
    <RegistryNumber>20146-85-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T099086</TermUI>
      <String>platinum-6-mercaptopurine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T099085</TermUI>
      <String>6-mercaptopurine platinum</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017865</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>elasnin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1995</Year>
   <Month>11</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>elastase inhibitor isolated from Streptomyces noboritoensis
  </Note>
  <Frequency>4</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PROTEASE INHIBITORS (79-89)</PreviousIndexing>
   <PreviousIndexing>*SERINE PROTEINASE INHIBITORS (90-95)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011753</DescriptorUI>
     <DescriptorName>
      <String>Pyrones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 83(2):704;1978</Source>
   <Source>J Antibiotics 31(11):1116;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068957</ConceptUI>
    <ConceptName>
     <String>elasnin</String>
    </ConceptName>
    <CASN1Name>2H-Pyran-2-one, 3,5-dibutyl-6-(1-butyl-2-oxoheptyl)-4-hydroxy-</CASN1Name>
    <RegistryNumber>68112-21-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098960</TermUI>
      <String>elasnin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C031679</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hemoglobin G Philadelphia</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>10</Month>
   <Day>13</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>11</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>Asn replaced by Lys in position 68 on alpha chain
  </Note>
  <Frequency>33</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006455</DescriptorUI>
     <DescriptorName>
      <String>Hemoglobins, Abnormal</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Sangre 1981;26(2):224</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0099344</ConceptUI>
    <ConceptName>
     <String>hemoglobin G Philadelphia</String>
    </ConceptName>
    <RegistryNumber>9034-74-6</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0099344</Concept1UI>
     <Concept2UI>M0467147</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0099344</Concept1UI>
     <Concept2UI>M0467148</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T129348</TermUI>
      <String>hemoglobin G Philadelphia</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T129345</TermUI>
      <String>Hb G Phila</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T129346</TermUI>
      <String>Hb G-Philadelphia</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T129347</TermUI>
      <String>Hb alpha-G Philadelphia</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0467147</ConceptUI>
    <ConceptName>
     <String>HBA2 g.324C&gt;G</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0099344</Concept1UI>
     <Concept2UI>M0467147</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T590386</TermUI>
      <String>HBA2 g.324C&gt;G</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>06</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0467148</ConceptUI>
    <ConceptName>
     <String>HBA2 g.324C&gt;A</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0099344</Concept1UI>
     <Concept2UI>M0467148</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T590387</TermUI>
      <String>HBA2 g.324C&gt;A</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>06</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017869</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-(beta,gamma-epoxypropyl)-8-bromotheobromine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>12</Month>
   <Day>28</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>EPOXY COMPOUNDS (79-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013805</DescriptorUI>
     <DescriptorName>
      <String>Theobromine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Pol Pharm 35(4):417;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068963</ConceptUI>
    <ConceptName>
     <String>1-(beta,gamma-epoxypropyl)-8-bromotheobromine</String>
    </ConceptName>
    <CASN1Name>1H-Purine-2,6-dione, 8-bromo-3,7-dihydro-3,7-dimethyl-1-(oxiranylmethyl)-</CASN1Name>
    <RegistryNumber>16877-94-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098966</TermUI>
      <String>1-(beta,gamma-epoxypropyl)-8-bromotheobromine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C479258</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3'-deoxy-3'-C-methyleneuridine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>12</Month>
   <Day>03</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014529</DescriptorUI>
     <DescriptorName>
      <String>Uridine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nucleosides Nucleotides Nucleic Acids. 2003 May-Aug;22(5-8):1159-61</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0456877</ConceptUI>
    <ConceptName>
     <String>3'-deoxy-3'-C-methyleneuridine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T561184</TermUI>
      <String>3'-deoxy-3'-C-methyleneuridine</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C030901</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hemoglobin Brisbane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>08</Month>
   <Day>12</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>11</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>produces mild erythrocytosis; high oxygen affinity; Leu replaced by His at position 68(E12) on beta chain
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006455</DescriptorUI>
     <DescriptorName>
      <String>Hemoglobins, Abnormal</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Blood 1981;58(4):813</Source>
   <Source>Hemoglobin 1981;5(4):325</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0097473</ConceptUI>
    <ConceptName>
     <String>hemoglobin Brisbane</String>
    </ConceptName>
    <RegistryNumber>78922-38-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T127477</TermUI>
      <String>hemoglobin Brisbane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T129864</TermUI>
      <String>hemoglobin Great Lakes</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T129863</TermUI>
      <String>HbGL</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T127476</TermUI>
      <String>Hb Brisbane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T129862</TermUI>
      <String>Hb Great Lakes</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017877</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-fluorogeranyl pyrophosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*TERPENES (79-79)</PreviousIndexing>
   <PreviousIndexing>ORGANOPHOSPHORUS COMPOUNDS (79-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011106</DescriptorUI>
     <DescriptorName>
      <String>Polyisoprenyl Phosphates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 253(20):7227;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068973</ConceptUI>
    <ConceptName>
     <String>2-fluorogeranyl pyrophosphate</String>
    </ConceptName>
    <CASN1Name>Diphosphoric acid, mono(2-fluoro-3,7-dimethyl-2,6-octadienyl) ester, (Z)-</CASN1Name>
    <RegistryNumber>62163-14-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098976</TermUI>
      <String>2-fluorogeranyl pyrophosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008290</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>lipophosphonoglycan</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>macromolecule accounting for approx 31% of mass of plasma membrane of Acanthamoeba castellanii; consists of neutral sugars, amino sugars, aminophosphonates and long chain fatty acids; present also in Entamoeba histolytica and Leishmania major
  </Note>
  <Frequency>361</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*LIPOPOLYSACCHARIDES (74-76)</PreviousIndexing>
   <PreviousIndexing>FATTY ACIDS (74-76)</PreviousIndexing>
   <PreviousIndexing>FATTY ACIDS, UNSATURATED (74-76)</PreviousIndexing>
   <PreviousIndexing>PHOSPHOLIPIDS (74-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006028</DescriptorUI>
     <DescriptorName>
      <String>Glycosphingolipids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 249(11):3335-42;1974</Source>
   <Source>J Biol Chem 251(10):2976;1976</Source>
   <Source>J Cell Biol 62(2):533;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0052013</ConceptUI>
    <ConceptName>
     <String>lipophosphonoglycan</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T082016</TermUI>
      <String>lipophosphonoglycan</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T082015</TermUI>
      <String>lipophosphoglycan</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007224</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>8-deazafolic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>03</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*FOLIC ACID (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005492</DescriptorUI>
     <DescriptorName>
      <String>Folic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 17(4):470;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050281</ConceptUI>
    <ConceptName>
     <String>8-deazafolic acid</String>
    </ConceptName>
    <RegistryNumber>51989-25-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080284</TermUI>
      <String>8-deazafolic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007227</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>8-deazapteroic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011622</DescriptorUI>
     <DescriptorName>
      <String>Pterins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 17(4):470;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050285</ConceptUI>
    <ConceptName>
     <String>8-deazapteroic acid</String>
    </ConceptName>
    <RegistryNumber>51989-24-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080288</TermUI>
      <String>8-deazapteroic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007228</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-deazariboflavin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>04</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>deaza analog of riboflavin used to elucidate chemical role of the flavin coenzyme; structure
  </Note>
  <Frequency>24</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*RIBOFLAVIN (74-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D012256</DescriptorUI>
     <DescriptorName>
      <String>Riboflavin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 15(5):1043;1976</Source>
   <Source>Biochemistry 16(6):3586;1977</Source>
   <Source>Biochim Biophys Acta 1980;590(1):97</Source>
   <Source>J Am Chem Soc 96(13):4345;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050286</ConceptUI>
    <ConceptName>
     <String>5-deazariboflavin</String>
    </ConceptName>
    <RegistryNumber>19342-73-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080289</TermUI>
      <String>5-deazariboflavin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007233</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dehydrocorydalmine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>06</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>4</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*QUINOLIZINES (74-81)</PreviousIndexing>
   <PreviousIndexing>METHYL ETHERS (74-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000470</DescriptorUI>
     <DescriptorName>
      <String>Alkaloids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 63(4):618;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050293</ConceptUI>
    <ConceptName>
     <String>dehydrocorydalmine</String>
    </ConceptName>
    <RegistryNumber>2007-07-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080296</TermUI>
      <String>dehydrocorydalmine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007234</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>9-dehydro-18-dihydroleuconolide-A(3)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>deriv of leucomycin-A(3); structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ANTIBIOTICS (74-76)</PreviousIndexing>
   <PreviousIndexing>AMINOGLYCOSIDES (74-76)</PreviousIndexing>
   <PreviousIndexing>LACTONES (74-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007933</DescriptorUI>
     <DescriptorName>
      <String>Leucomycins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiot (Tokyo) 27(2):147;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050294</ConceptUI>
    <ConceptName>
     <String>9-dehydro-18-dihydroleuconolide-A(3)</String>
    </ConceptName>
    <RegistryNumber>52442-94-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080297</TermUI>
      <String>9-dehydro-18-dihydroleuconolide-A(3)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007239</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dehydromerodesmosine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AMINO ACIDS (75-76)</PreviousIndexing>
   <PreviousIndexing>*PYRIDINIUM COMPOUNDS (75-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003895</DescriptorUI>
     <DescriptorName>
      <String>Desmosine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Connect Tissue Res 2(3):231;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050304</ConceptUI>
    <ConceptName>
     <String>dehydromerodesmosine</String>
    </ConceptName>
    <CASN1Name>5-Undecenedioic acid, 2,10-diamino-5-(((5-amino-5-carboxypentyl)imino)methyl)-, (2S-(2R*,5(R*),10R*))-</CASN1Name>
    <RegistryNumber>51299-87-7</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0050304</Concept1UI>
     <Concept2UI>M0050303</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080307</TermUI>
      <String>dehydromerodesmosine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0050303</ConceptUI>
    <ConceptName>
     <String>5-Undecenedioic acid, 2,10-diamino-5-(((5-amino-5-carboxypentyl)imino)methyl)-, (2S-(2S*,5(S*),10S*))-</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0050304</Concept1UI>
     <Concept2UI>M0050303</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T080306</TermUI>
      <String>5-Undecenedioic acid, 2,10-diamino-5-(((5-amino-5-carboxypentyl)imino)methyl)-, (2S-(2S*,5(S*),10S*))-</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007243</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-demethylcelesticetin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>11</Month>
   <Day>05</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ANTIBIOTICS (74-75)</PreviousIndexing>
   <PreviousIndexing>*CELESTICETIN/analogs (75-79)</PreviousIndexing>
   <PreviousIndexing>*THIOGLYCOSIDES (74-75)</PreviousIndexing>
   <PreviousIndexing>PYRROLIDINES (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013862</DescriptorUI>
     <DescriptorName>
      <String>Thiogalactosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiotics 26(1):7;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050310</ConceptUI>
    <ConceptName>
     <String>N-demethylcelesticetin</String>
    </ConceptName>
    <CASN1Name>D-erythro-alpha-D-galacto-Octopyranoside, 2-((2-hydroxybenzoyl)oxy)ethyl 6,8-dideoxy-7-O-methyl-6-((2-pyrrolidinylcarbonyl)amino)-1-thio-, (S)-</CASN1Name>
    <RegistryNumber>40736-31-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080313</TermUI>
      <String>N-demethylcelesticetin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007245</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-demethyl-7-O-demethylcelesticetin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>16</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ANTIBIOTICS (74-75)</PreviousIndexing>
   <PreviousIndexing>*CELESTICETIN/analogs (75-79)</PreviousIndexing>
   <PreviousIndexing>*THIOGLYCOSIDES (74-75)</PreviousIndexing>
   <PreviousIndexing>PYRROLIDINES (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013862</DescriptorUI>
     <DescriptorName>
      <String>Thiogalactosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiot 26(1):7;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050313</ConceptUI>
    <ConceptName>
     <String>N-demethyl-7-O-demethylcelesticetin</String>
    </ConceptName>
    <CASN1Name>D-erythro-alpha-D-galacto-Octopyranoside, 2-((2-hydroxybenzoyl)oxy)ethyl 6,8-dideoxy-6-((2-pyrrolidinylcarbonyl)amino)-1-thio-, (S)-</CASN1Name>
    <RegistryNumber>40736-32-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080316</TermUI>
      <String>N-demethyl-7-O-demethylcelesticetin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007252</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>L-1-deoxyfluoroglycerol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>07</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DEOXY SUGARS (81-82)</PreviousIndexing>
   <PreviousIndexing>*GLYCERIN (74-75)</PreviousIndexing>
   <PreviousIndexing>DEOXY SUGARS (74-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005990</DescriptorUI>
     <DescriptorName>
      <String>Glycerol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 17(7):697;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050325</ConceptUI>
    <ConceptName>
     <String>L-1-deoxyfluoroglycerol</String>
    </ConceptName>
    <CASN1Name>1,2-Propanediol, 3-fluoro-, 1-(dihydrogen phosphate), (S)-, cpd with cyclohexanamine (1:2)</CASN1Name>
    <RegistryNumber>40147-95-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080328</TermUI>
      <String>L-1-deoxyfluoroglycerol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C059997</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Hin recombinase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1989</Year>
   <Month>07</Month>
   <Day>12</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>from Salmonella typhimurium; mediates site-specific recombination between two inverted repeat sequences(hixL &amp; hixR) resulting in inversion of the DNA segment between these two sequences
  </Note>
  <Frequency>66</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004254</DescriptorUI>
     <DescriptorName>
      <String>DNA Nucleotidyltransferases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 1989;264(17):10072</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0166767</ConceptUI>
    <ConceptName>
     <String>Hin recombinase</String>
    </ConceptName>
    <RegistryNumber>EC 2.7.7.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T196772</TermUI>
      <String>Hin recombinase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007254</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>L-1-deoxyfluoroglycerol 3-phosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>10</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DEOXY SUGARS (81-82)</PreviousIndexing>
   <PreviousIndexing>*GLYCERIN (74-79)</PreviousIndexing>
   <PreviousIndexing>DEOXY SUGARS (74-81)</PreviousIndexing>
   <PreviousIndexing>ORGANOPHOSPHORUS CPDS (74-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005994</DescriptorUI>
     <DescriptorName>
      <String>Glycerophosphates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 17(7):697;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050328</ConceptUI>
    <ConceptName>
     <String>L-1-deoxyfluoroglycerol 3-phosphate</String>
    </ConceptName>
    <CASN1Name>1,2-Propanediol, 3-fluoro-, 1-(dihydrogen phosphate), (S)-</CASN1Name>
    <RegistryNumber>44925-02-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080331</TermUI>
      <String>L-1-deoxyfluoroglycerol 3-phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007259</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>9-(6-deoxy-alpha-L-mannofuranosyl)adenine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ADENINE (74-79)</PreviousIndexing>
   <PreviousIndexing>*NUCLEOSIDES (74-79)</PreviousIndexing>
   <PreviousIndexing>MANNOSE (74-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000241</DescriptorUI>
     <DescriptorName>
      <String>Adenosine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 38(21):3704;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050335</ConceptUI>
    <ConceptName>
     <String>9-(6-deoxy-alpha-L-mannofuranosyl)adenine</String>
    </ConceptName>
    <RegistryNumber>29847-43-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080338</TermUI>
      <String>9-(6-deoxy-alpha-L-mannofuranosyl)adenine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008330</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>marthasterone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>principal aglycone from saponins of starfish, Marthasterias glacialis; structure
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CHOLESTADIENOLS (74-82)</PreviousIndexing>
   <PreviousIndexing>KETOSTEROIDS (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013261</DescriptorUI>
     <DescriptorName>
      <String>Sterols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Chem Soc (Perkin I) 12:1357;1976</Source>
   <Source>J Chem Soc (Perkin I) 16:1745;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0052063</ConceptUI>
    <ConceptName>
     <String>marthasterone</String>
    </ConceptName>
    <CASN1Name>(3 beta,5 alpha,6 alpha)-3,6- dihydroxy-cholesta-9(11),24-dien-23-one</CASN1Name>
    <RegistryNumber>36564-29-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T082066</TermUI>
      <String>marthasterone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T082065</TermUI>
      <String>3-beta,6 alpha-dihydroxy-5 alpha-cholesta-9(11),24-dien-23-one</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007263</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-(2-deoxy-D-ribofuranosyl)-4-pyridone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PYRIDONES (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003853</DescriptorUI>
     <DescriptorName>
      <String>Deoxyribonucleosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 17(9):1027;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050342</ConceptUI>
    <ConceptName>
     <String>1-(2-deoxy-D-ribofuranosyl)-4-pyridone</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080345</TermUI>
      <String>1-(2-deoxy-D-ribofuranosyl)-4-pyridone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008344</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>alpha-melanotropin hydrazide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>05</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>HYDRAZINES (75-81)</PreviousIndexing>
   <PreviousIndexing>MSH/*analogs (75-87)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000521</DescriptorUI>
     <DescriptorName>
      <String>alpha-MSH</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Int J Pept Protein Res 6(5):303;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0052086</ConceptUI>
    <ConceptName>
     <String>alpha-melanotropin hydrazide</String>
    </ConceptName>
    <CASN1Name>alpha-Melanotropin, 13-L-valine-, 13-hydrazide</CASN1Name>
    <RegistryNumber>55325-41-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T082089</TermUI>
      <String>alpha-melanotropin hydrazide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T082088</TermUI>
      <String>MSH hydrazide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007275</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>descarboxylysergic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ERGOLINES (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008237</DescriptorUI>
     <DescriptorName>
      <String>Lysergic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 17(3):312;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050364</ConceptUI>
    <ConceptName>
     <String>descarboxylysergic acid</String>
    </ConceptName>
    <CASN1Name>9,10-didehydro-6-methylergoline</CASN1Name>
    <RegistryNumber>51867-17-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080367</TermUI>
      <String>descarboxylysergic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C531287</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>artemisinic aldehyde delta11(13) reductase, Artemisia annua</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2008</Year>
   <Month>09</Month>
   <Day>11</Day>
  </DateCreated>
  <Note>involved in the glandular trichome-dependent biosynthesis of artemisinin; has been sequenced
  </Note>
  <Frequency>12</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010088</DescriptorUI>
     <DescriptorName>
      <String>Oxidoreductases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010940</DescriptorUI>
     <DescriptorName>
      <String>Plant Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 2008 Aug 1;283(31):21501-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0524677</ConceptUI>
    <ConceptName>
     <String>artemisinic aldehyde delta11(13) reductase, Artemisia annua</String>
    </ConceptName>
    <RegistryNumber>EC 1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T725515</TermUI>
      <String>artemisinic aldehyde delta11(13) reductase, Artemisia annua</String>
      <DateCreated>
       <Year>2008</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2008)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T725516</TermUI>
      <String>Dbr2 protein, Artemisia annua</String>
      <DateCreated>
       <Year>2008</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2008)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C414423</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>arenosclerin A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>10</Month>
   <Day>18</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>08</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>tetracyclic (two piperidines and two macrocyclic alkyl) alkylpiperidine alkaloid from a Brazilian endemic Haplosclerid sponge, Arenosclera brasiliensis; structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000470</DescriptorUI>
     <DescriptorName>
      <String>Alkaloids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010880</DescriptorUI>
     <DescriptorName>
      <String>Piperidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D047028</DescriptorUI>
     <DescriptorName>
      <String>Macrocyclic Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2000 Aug;63(8):1098-105</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0371252</ConceptUI>
    <ConceptName>
     <String>arenosclerin A</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T426769</TermUI>
      <String>arenosclerin A</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>10</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007295</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4,4'-diaminodicyclohexylmethane carbonate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1994</Year>
   <Month>05</Month>
   <Day>26</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>AMINES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003510</DescriptorUI>
     <DescriptorName>
      <String>Cyclohexanes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Gig Sanit 38(11):31;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050405</ConceptUI>
    <ConceptName>
     <String>4,4'-diaminodicyclohexylmethane carbonate</String>
    </ConceptName>
    <RegistryNumber>37872-62-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080408</TermUI>
      <String>4,4'-diaminodicyclohexylmethane carbonate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007298</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4,5-diaminohypoxanthine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007042</DescriptorUI>
     <DescriptorName>
      <String>Hypoxanthines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 63(4):622;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050412</ConceptUI>
    <ConceptName>
     <String>4,5-diaminohypoxanthine</String>
    </ConceptName>
    <CASN1Name>4,5-diamino-6-hydroxypyrimidine</CASN1Name>
    <RegistryNumber>1672-50-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080415</TermUI>
      <String>4,5-diaminohypoxanthine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007299</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,3-diaminoisocarbostyril 3,4 dihydro</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>07</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>DIAMINES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007546</DescriptorUI>
     <DescriptorName>
      <String>Isoquinolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Soc Jap 93(12):1581;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050413</ConceptUI>
    <ConceptName>
     <String>2,3-diaminoisocarbostyril 3,4 dihydro</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080416</TermUI>
      <String>2,3-diaminoisocarbostyril 3,4 dihydro</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007302</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4,5-diamino-2-thiouracil</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>03</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*THIOURACIL (74-75)</PreviousIndexing>
   <PreviousIndexing>DIAMINES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013889</DescriptorUI>
     <DescriptorName>
      <String>Thiouracil</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 63(4):622;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050417</ConceptUI>
    <ConceptName>
     <String>4,5-diamino-2-thiouracil</String>
    </ConceptName>
    <CASN1Name>4,5-diamino-6-hydroxy-2-thiopyrimidine</CASN1Name>
    <RegistryNumber>1004-76-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080420</TermUI>
      <String>4,5-diamino-2-thiouracil</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007309</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-diazo-3,5-dimethylpyrazole</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>AZO CPDS (74-79)</PreviousIndexing>
   <PreviousIndexing>DIAZONIUM COMPOUNDS (79-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011720</DescriptorUI>
     <DescriptorName>
      <String>Pyrazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Soc Jpn 94(1):17;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050431</ConceptUI>
    <ConceptName>
     <String>4-diazo-3,5-dimethylpyrazole</String>
    </ConceptName>
    <CASN1Name>4H-Pyrazole, 4-diazo-3,5-dimethyl-</CASN1Name>
    <RegistryNumber>51463-90-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080434</TermUI>
      <String>4-diazo-3,5-dimethylpyrazole</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007312</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-diazoquinoline tetrafluoroborate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>reagent for specific modification of lysyl residues
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>AZO CPDS (74-79)</PreviousIndexing>
   <PreviousIndexing>DIAZONIUM COMPOUNDS (74-82)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011804</DescriptorUI>
     <DescriptorName>
      <String>Quinolines</String>
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   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050435</ConceptUI>
    <ConceptName>
     <String>3-diazoquinoline tetrafluoroborate</String>
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    <CASN1Name>3-Quinolinediazonium, tetrafluoroborate(1-)</CASN1Name>
    <RegistryNumber>398-41-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080438</TermUI>
      <String>3-diazoquinoline tetrafluoroborate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
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   </Concept>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007315</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dibenzothioazocines</String>
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  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <Note>structure
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  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001392</DescriptorUI>
     <DescriptorName>
      <String>Azocines</String>
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    </DescriptorReferredTo>
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  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Soc Jpn 93(8):991;1973</Source>
   <Source>J Pharm Soc Jpn 97(1):24-31;1977</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050438</ConceptUI>
    <ConceptName>
     <String>dibenzothioazocines</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080441</TermUI>
      <String>dibenzothioazocines</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
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   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C412102</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>(4,5-bis(aminomethyl)-2,2-dimethyl-1,3-dioxolane-N,N')-(malonato-O,O')platinum(II)</String>
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  <DateCreated>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>17</Day>
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  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>17</Day>
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  <Note>structure in first source
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009944</DescriptorUI>
     <DescriptorName>
      <String>Organoplatinum Compounds</String>
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  <SourceList>
   <Source>Acta Crystallogr C 2000 Jun;56 ( Pt 6):653-4</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0368130</ConceptUI>
    <ConceptName>
     <String>(4,5-bis(aminomethyl)-2,2-dimethyl-1,3-dioxolane-N,N')-(malonato-O,O')platinum(II)</String>
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    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0368130</Concept1UI>
     <Concept2UI>M0368131</Concept2UI>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0368130</Concept1UI>
     <Concept2UI>M0368132</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T421967</TermUI>
      <String>(4,5-bis(aminomethyl)-2,2-dimethyl-1,3-dioxolane-N,N')-(malonato-O,O')platinum(II)</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>08</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0368131</ConceptUI>
    <ConceptName>
     <String>cis-((4R,5R)-4,5-bis(aminomethyl)-2,2-dimethyl-1,3-dioxolane-N,N')-(malonato-O,O')platinum(II)</String>
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    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0368130</Concept1UI>
     <Concept2UI>M0368131</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T421968</TermUI>
      <String>cis-((4R,5R)-4,5-bis(aminomethyl)-2,2-dimethyl-1,3-dioxolane-N,N')-(malonato-O,O')platinum(II)</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>08</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0368132</ConceptUI>
    <ConceptName>
     <String>B(AMe)-D-D-M-platinum(II)</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0368130</Concept1UI>
     <Concept2UI>M0368132</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T421969</TermUI>
      <String>B(AMe)-D-D-M-platinum(II)</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>08</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007319</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,1-dibromoethylene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ETHYLENES (75-82)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006842</DescriptorUI>
     <DescriptorName>
      <String>Hydrocarbons, Brominated</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Environ Health 30(1):26;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050446</ConceptUI>
    <ConceptName>
     <String>1,1-dibromoethylene</String>
    </ConceptName>
    <RegistryNumber>593-92-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080449</TermUI>
      <String>1,1-dibromoethylene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "2">
  <SupplementalRecordUI>C044144</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>T7 protocol</String>
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  <DateCreated>
   <Year>1985</Year>
   <Month>02</Month>
   <Day>25</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>chemotherapy protocol consisting of above 7 cpds; used in treatment of osteosarcoma
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  <Frequency>7</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000971</DescriptorUI>
     <DescriptorName>
      <String>Antineoplastic Combined Chemotherapy Protocols</String>
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   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D001761</DescriptorUI>
     <DescriptorName>
      <String>Bleomycin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002955</DescriptorUI>
     <DescriptorName>
      <String>Leucovorin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003520</DescriptorUI>
     <DescriptorName>
      <String>Cyclophosphamide</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003609</DescriptorUI>
     <DescriptorName>
      <String>Dactinomycin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004317</DescriptorUI>
     <DescriptorName>
      <String>Doxorubicin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008727</DescriptorUI>
     <DescriptorName>
      <String>Methotrexate</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014750</DescriptorUI>
     <DescriptorName>
      <String>Vincristine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ann Pediatr (Paris) 1984;31(9):773</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0129133</ConceptUI>
    <ConceptName>
     <String>T7 protocol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0129133</Concept1UI>
     <Concept2UI>M0129131</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T159138</TermUI>
      <String>T7 protocol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0129131</ConceptUI>
    <ConceptName>
     <String>T-10 protocol</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0129133</Concept1UI>
     <Concept2UI>M0129131</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T159136</TermUI>
      <String>T-10 protocol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T159137</TermUI>
      <String>T10 protocol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C016180</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>argipressin, Val(4)-</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>17</Day>
  </DateRevised>
  <Note>RN given refers to (L-Val-D-Arg)-isomer
  </Note>
  <Frequency>13</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D001127</DescriptorUI>
     <DescriptorName>
      <String>Arginine Vasopressin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 20(9):1173;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0065999</ConceptUI>
    <ConceptName>
     <String>argipressin, Val(4)-</String>
    </ConceptName>
    <RegistryNumber>52049-52-2</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>51980-15-5 ((L-Val-L-Arg)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0065999</Concept1UI>
     <Concept2UI>M0313113</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T096002</TermUI>
      <String>argipressin, Val(4)-</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T095999</TermUI>
      <String>VDAVP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T096001</TermUI>
      <String>argipressin, valine(4)-</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T095998</TermUI>
      <String>4-Val-argipressin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T096000</TermUI>
      <String>arginine vasopressin, Val(4)-</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0313113</ConceptUI>
    <ConceptName>
     <String>argipressin, Val(4)-, (L-Val-L-Arg)-isomer</String>
    </ConceptName>
    <RegistryNumber>51980-15-5</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0065999</Concept1UI>
     <Concept2UI>M0313113</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T343113</TermUI>
      <String>argipressin, Val(4)-, (L-Val-L-Arg)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007328</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N(6)-2'-O-dibutyryl-8-thiocyclic AMP</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1993</Year>
   <Month>08</Month>
   <Day>19</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CYCL AMP (74-75)</PreviousIndexing>
   <PreviousIndexing>BUTYRATES (74-75)</PreviousIndexing>
   <PreviousIndexing>SULFIDES (74-75)</PreviousIndexing>
   <PreviousIndexing>THIONUCLEOTIDES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003994</DescriptorUI>
     <DescriptorName>
      <String>Bucladesine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>C R Acad Sci Paris 277(19):2057;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050462</ConceptUI>
    <ConceptName>
     <String>N(6)-2'-O-dibutyryl-8-thiocyclic AMP</String>
    </ConceptName>
    <RegistryNumber>34409-10-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080465</TermUI>
      <String>N(6)-2'-O-dibutyryl-8-thiocyclic AMP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "2">
  <SupplementalRecordUI>C044922</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>MACOP-B protocol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1985</Year>
   <Month>05</Month>
   <Day>09</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>chemotherapy protocol consisting of above cpds; used in treatment of large cell and immunoblastic lymphomas
  </Note>
  <Frequency>165</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000971</DescriptorUI>
     <DescriptorName>
      <String>Antineoplastic Combined Chemotherapy Protocols</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D001761</DescriptorUI>
     <DescriptorName>
      <String>Bleomycin</String>
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   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002955</DescriptorUI>
     <DescriptorName>
      <String>Leucovorin</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003520</DescriptorUI>
     <DescriptorName>
      <String>Cyclophosphamide</String>
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   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004317</DescriptorUI>
     <DescriptorName>
      <String>Doxorubicin</String>
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   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008727</DescriptorUI>
     <DescriptorName>
      <String>Methotrexate</String>
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   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011241</DescriptorUI>
     <DescriptorName>
      <String>Prednisone</String>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014750</DescriptorUI>
     <DescriptorName>
      <String>Vincristine</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>Ann Intern Med 1985;102(5):596</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0130915</ConceptUI>
    <ConceptName>
     <String>MACOP-B protocol</String>
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    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0130915</Concept1UI>
     <Concept2UI>M0130914</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T160920</TermUI>
      <String>MACOP-B protocol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T160918</TermUI>
      <String>MECOP-B PROTOCOL</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0130914</ConceptUI>
    <ConceptName>
     <String>TTL-I protocol</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0130915</Concept1UI>
     <Concept2UI>M0130914</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T160919</TermUI>
      <String>TTL-I protocol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007344</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,6-dichloromercuri-4-nitrophenol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>13</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*MERCURY (74-77)</PreviousIndexing>
   <PreviousIndexing>*ORGANOMETALLIC COMPOUNDS (74-77)</PreviousIndexing>
   <PreviousIndexing>NITROPHENOLS (74-77)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002730</DescriptorUI>
     <DescriptorName>
      <String>Chloromercurinitrophenols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D013439</DescriptorUI>
     <DescriptorName>
      <String>Sulfhydryl Reagents</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Arch Int Physiol Biochem 81(2):366;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050487</ConceptUI>
    <ConceptName>
     <String>2,6-dichloromercuri-4-nitrophenol</String>
    </ConceptName>
    <RegistryNumber>24579-93-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080490</TermUI>
      <String>2,6-dichloromercuri-4-nitrophenol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007345</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,5-dichloro-4-methoxyphenol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PHENOLS (74-77)</PreviousIndexing>
   <PreviousIndexing>CHLOROBENZENES (74-77)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002733</DescriptorUI>
     <DescriptorName>
      <String>Chlorophenols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Agric Food Chem 19(4):750;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050488</ConceptUI>
    <ConceptName>
     <String>2,5-dichloro-4-methoxyphenol</String>
    </ConceptName>
    <RegistryNumber>18113-14-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080491</TermUI>
      <String>2,5-dichloro-4-methoxyphenol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C412103</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>trichodion</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>17</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011753</DescriptorUI>
     <DescriptorName>
      <String>Pyrones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>FEBS Lett 2000 Jul 21;477(3):219-23</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0368134</ConceptUI>
    <ConceptName>
     <String>trichodion</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T421971</TermUI>
      <String>trichodion</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>08</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007360</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,3-dicyclohexyl-5,5-diallylbarbituric acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1994</Year>
   <Month>07</Month>
   <Day>28</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BARBITURATES (74-76)</PreviousIndexing>
   <PreviousIndexing>ALLOBARBITAL/*analogs (77-94)</PreviousIndexing>
   <PreviousIndexing>ALLYL COMPOUNDS (74-76)</PreviousIndexing>
   <PreviousIndexing>CYCLOHEXANES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001463</DescriptorUI>
     <DescriptorName>
      <String>Barbiturates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Pol J Pharmacol Pharm 25(4):379;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050512</ConceptUI>
    <ConceptName>
     <String>1,3-dicyclohexyl-5,5-diallylbarbituric acid</String>
    </ConceptName>
    <RegistryNumber>34374-12-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080515</TermUI>
      <String>1,3-dicyclohexyl-5,5-diallylbarbituric acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C033890</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>phenoxyacetone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1982</Year>
   <Month>04</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>17</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000096</DescriptorUI>
     <DescriptorName>
      <String>Acetone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 1982;104(2):597</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0104851</ConceptUI>
    <ConceptName>
     <String>phenoxyacetone</String>
    </ConceptName>
    <RegistryNumber>621-87-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T134855</TermUI>
      <String>phenoxyacetone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007364</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>didodecylphthalate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>FATTY ALCOHOLS (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010795</DescriptorUI>
     <DescriptorName>
      <String>Phthalic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Gig Tr Prof Zabol 17(11):51;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050515</ConceptUI>
    <ConceptName>
     <String>didodecylphthalate</String>
    </ConceptName>
    <RegistryNumber>2432-90-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080518</TermUI>
      <String>didodecylphthalate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C507731</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-(4-(1,3,4,6-tetra-O-acetyl-2-amido-2-desoxy-beta-D-glucopyranose phenyl))-10,15,20-triphenyl porphyrin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>a photosensititizing agent; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009005</DescriptorUI>
     <DescriptorName>
      <String>Monosaccharides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011166</DescriptorUI>
     <DescriptorName>
      <String>Porphyrins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Med Chem. 2005 Nov;40(11):1111-22</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0494821</ConceptUI>
    <ConceptName>
     <String>5-(4-(1,3,4,6-tetra-O-acetyl-2-amido-2-desoxy-beta-D-glucopyranose phenyl))-10,15,20-triphenyl porphyrin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T666067</TermUI>
      <String>5-(4-(1,3,4,6-tetra-O-acetyl-2-amido-2-desoxy-beta-D-glucopyranose phenyl))-10,15,20-triphenyl porphyrin</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>02</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T666068</TermUI>
      <String>5-(4-AA-GP)-TPP</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>02</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007371</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6-((3-(N,N-diethylamino)methyl-4-hydroxy)anilino)-5,8-dimethoxy-2,4-dimethylquinoline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>analog of amodiaquine; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ANILINE COMPOUNDS (75-82)</PreviousIndexing>
   <PreviousIndexing>DIETHYLAMINES (75-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011804</DescriptorUI>
     <DescriptorName>
      <String>Quinolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 17(9):972;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050534</ConceptUI>
    <ConceptName>
     <String>6-((3-(N,N-diethylamino)methyl-4-hydroxy)anilino)-5,8-dimethoxy-2,4-dimethylquinoline</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080537</TermUI>
      <String>6-((3-(N,N-diethylamino)methyl-4-hydroxy)anilino)-5,8-dimethoxy-2,4-dimethylquinoline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C507734</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5,15-bis(4-(1,3,4,6-tetra-O-acetyl-2-amido-2-desoxy-beta-D-glucopyranose phenyl))-10,20-biphenyl porphyrin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateCreated>
  <Note>a photosensititizing agent; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009005</DescriptorUI>
     <DescriptorName>
      <String>Monosaccharides</String>
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   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011166</DescriptorUI>
     <DescriptorName>
      <String>Porphyrins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Med Chem. 2005 Nov;40(11):1111-22</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0494825</ConceptUI>
    <ConceptName>
     <String>5,15-bis(4-(1,3,4,6-tetra-O-acetyl-2-amido-2-desoxy-beta-D-glucopyranose phenyl))-10,20-biphenyl porphyrin</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T666075</TermUI>
      <String>5,15-bis(4-(1,3,4,6-tetra-O-acetyl-2-amido-2-desoxy-beta-D-glucopyranose phenyl))-10,20-biphenyl porphyrin</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>02</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T666076</TermUI>
      <String>5,15-B(TAAGP)-BP</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>02</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007376</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5,5-diethyl-2-ethoxytetrahydro-4,6-pyrimidinedione</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ETHOXY COMPOUNDS (75-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011744</DescriptorUI>
     <DescriptorName>
      <String>Pyrimidinones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 63(10):1633;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050538</ConceptUI>
    <ConceptName>
     <String>5,5-diethyl-2-ethoxytetrahydro-4,6-pyrimidinedione</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080541</TermUI>
      <String>5,5-diethyl-2-ethoxytetrahydro-4,6-pyrimidinedione</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C507733</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-(4-(1,3,4,6-tetra-O-acetyl-2-amido-2-desoxy-beta-D-glucopyranose phenyl))-10,15,20-triphenyl chlorin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>a photosensititizing agent; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009005</DescriptorUI>
     <DescriptorName>
      <String>Monosaccharides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Med Chem. 2005 Nov;40(11):1111-22</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0494824</ConceptUI>
    <ConceptName>
     <String>5-(4-(1,3,4,6-tetra-O-acetyl-2-amido-2-desoxy-beta-D-glucopyranose phenyl))-10,15,20-triphenyl chlorin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T666072</TermUI>
      <String>5-(4-(1,3,4,6-tetra-O-acetyl-2-amido-2-desoxy-beta-D-glucopyranose phenyl))-10,15,20-triphenyl chlorin</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>02</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T666073</TermUI>
      <String>5-(4-AA-GP)-TPCl</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>02</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007380</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>diethyl S-n-propyl phosphorothiolate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009946</DescriptorUI>
     <DescriptorName>
      <String>Organothiophosphorus Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Pharmacol 23(3):751;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050545</ConceptUI>
    <ConceptName>
     <String>diethyl S-n-propyl phosphorothiolate</String>
    </ConceptName>
    <RegistryNumber>20195-06-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080548</TermUI>
      <String>diethyl S-n-propyl phosphorothiolate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007398</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dihydrocorynantheol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>06</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>alkaloid from Mitragyna species; isomer of corynantheidol;
  </Note>
  <Frequency>10</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>INDOLES (74-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000470</DescriptorUI>
     <DescriptorName>
      <String>Alkaloids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Planta Med (24(1):13;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050579</ConceptUI>
    <ConceptName>
     <String>dihydrocorynantheol</String>
    </ConceptName>
    <CASN1Name>Corynan-17-ol</CASN1Name>
    <RegistryNumber>2270-72-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080582</TermUI>
      <String>dihydrocorynantheol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007400</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3,12-dihydro-6,11-dihydroxy-3,3,12-trimethyl-5-(3- methylbut-2-enyl)pyrano(3,2-c)acrid-7-one</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>analog of acronycine from wood of Atlantia ceylanica; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ACRIDINES (74-75)</PreviousIndexing>
   <PreviousIndexing>*ALKALOIDS (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000175</DescriptorUI>
     <DescriptorName>
      <String>Acronine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050584</ConceptUI>
    <ConceptName>
     <String>3,12-dihydro-6,11-dihydroxy-3,3,12-trimethyl-5-(3- methylbut-2-enyl)pyrano(3,2-c)acrid-7-one</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080587</TermUI>
      <String>3,12-dihydro-6,11-dihydroxy-3,3,12-trimethyl-5-(3- methylbut-2-enyl)pyrano(3,2-c)acrid-7-one</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010947</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>erythromycin 2'-dodecyl glutaramide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>11</Month>
   <Day>27</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004917</DescriptorUI>
     <DescriptorName>
      <String>Erythromycin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Vet Pathol 12(1):72;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056870</ConceptUI>
    <ConceptName>
     <String>erythromycin 2'-dodecyl glutaramide</String>
    </ConceptName>
    <RegistryNumber>32452-91-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086873</TermUI>
      <String>erythromycin 2'-dodecyl glutaramide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013141</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>mustelan</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>malodorous substance from anal gland of mink; structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006571</DescriptorUI>
     <DescriptorName>
      <String>Heterocyclic Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013440</DescriptorUI>
     <DescriptorName>
      <String>Sulfides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Agnew Chem (Engl) 15(4):242;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060676</ConceptUI>
    <ConceptName>
     <String>mustelan</String>
    </ConceptName>
    <CASN1Name>Thietane, 2,2-dimethyl-</CASN1Name>
    <RegistryNumber>55022-72-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090679</TermUI>
      <String>mustelan</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T090678</TermUI>
      <String>2,2-dimethylthietane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010949</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,N(6)-ethenoadenosylcobalamin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>03</Month>
   <Day>05</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ADENOSINE/*analogs</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014805</DescriptorUI>
     <DescriptorName>
      <String>Vitamin B 12</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Z Naturforsch C 30(4):460;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056872</ConceptUI>
    <ConceptName>
     <String>1,N(6)-ethenoadenosylcobalamin</String>
    </ConceptName>
    <CASN1Name>Cobinamide, Co-(3-(5-deoxy-beta-D-ribofuranosyl)-3H-imidazo(2,1-i)purine-5') deriv., hydroxide, dihydrogen phosphate (ester), inner salt, 3'-ester with 5,6-dimethyl-1-alpha-D-ribofuranosyl-1H-benzimidazole</CASN1Name>
    <RegistryNumber>54635-00-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086875</TermUI>
      <String>1,N(6)-ethenoadenosylcobalamin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010951</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-ethyl-N-methylaniline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>10</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000814</DescriptorUI>
     <DescriptorName>
      <String>Aniline Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Xenobiotica 5(8):453;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056873</ConceptUI>
    <ConceptName>
     <String>N-ethyl-N-methylaniline</String>
    </ConceptName>
    <RegistryNumber>613-97-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086876</TermUI>
      <String>N-ethyl-N-methylaniline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C515096</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>penifulvin A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>11</Month>
   <Day>28</Day>
  </DateCreated>
  <Note>a sesquiterpenoid-derived metabolite containing a dioxa(5,5,5,6)fenestrane ring system from a fungicolous isolate of Penicillium griseofulvum; structure in first source
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012717</DescriptorUI>
     <DescriptorName>
      <String>Sesquiterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Org Lett 2006 Mar 16;8(6):1225-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0504271</ConceptUI>
    <ConceptName>
     <String>penifulvin A</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T686785</TermUI>
      <String>penifulvin A</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>11</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010953</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>exochelins</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>07</Month>
   <Day>14</Day>
  </DateRevised>
  <Note>functional extracellular iron-binding agent; water-soluble iron-binding cpds from Mycobacteria; major component a cyclic hexapeptide containing 3 mol of epsilon N-acetyl-epsilon-N-hydroxylysine; structure
  </Note>
  <Frequency>36</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010456</DescriptorUI>
     <DescriptorName>
      <String>Peptides, Cyclic</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
    <PharmacologicalActionList>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D007502</DescriptorUI>
        <DescriptorName>
         <String>Iron Chelating Agents</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
    </PharmacologicalActionList>
  <SourceList>
   <Source>Infect Immunity 12(6):1242;1975</Source>
   <Source>J Gen Microbiol 89:379;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056876</ConceptUI>
    <ConceptName>
     <String>exochelins</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086879</TermUI>
      <String>exochelins</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010957</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-2-fluorenesulfonyl-beta-alanine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>03</Month>
   <Day>11</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>3-AMINOPROPIONIC ACID/*analogs</PreviousIndexing>
   <PreviousIndexing>ALANINE/*analogs (76-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005449</DescriptorUI>
     <DescriptorName>
      <String>Fluorenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Soc Jap 95(4):397;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056877</ConceptUI>
    <ConceptName>
     <String>N-2-fluorenesulfonyl-beta-alanine</String>
    </ConceptName>
    <RegistryNumber>32869-90-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086880</TermUI>
      <String>N-2-fluorenesulfonyl-beta-alanine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013151</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>nioben</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>RN given refers to HCl salt
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PROPIOPHENONES (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010880</DescriptorUI>
     <DescriptorName>
      <String>Piperidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ther Hung 24(1):17;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060692</ConceptUI>
    <ConceptName>
     <String>nioben</String>
    </ConceptName>
    <RegistryNumber>18787-40-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090695</TermUI>
      <String>nioben</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T090694</TermUI>
      <String>1-piperidino-3-(4-n-octylphenyl)propan-3-one</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010961</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Fluress</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1991</Year>
   <Month>10</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>a fluorescent-anesthetic solution containing sodium fluorescein, benoxinate, povidone, chlorbutanol, EDTA &amp; boric acid for buffering
  </Note>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002724</DescriptorUI>
     <DescriptorName>
      <String>Chlorobutanol</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004492</DescriptorUI>
     <DescriptorName>
      <String>Edetic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005452</DescriptorUI>
     <DescriptorName>
      <String>Fluoresceins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011205</DescriptorUI>
     <DescriptorName>
      <String>Povidone</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011343</DescriptorUI>
     <DescriptorName>
      <String>Procaine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Annals Ophthalmol 7(8):1101;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056887</ConceptUI>
    <ConceptName>
     <String>Fluress</String>
    </ConceptName>
    <RegistryNumber>37209-61-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086890</TermUI>
      <String>Fluress</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010963</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>formose sugars</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>complex mixture of sugars which arises from self-condensation of formaldehyde
  </Note>
  <Frequency>23</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002241</DescriptorUI>
     <DescriptorName>
      <String>Carbohydrates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Environ Biol Med 1(4):243;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056891</ConceptUI>
    <ConceptName>
     <String>formose sugars</String>
    </ConceptName>
    <CASN1Name>Formose</CASN1Name>
    <RegistryNumber>8069-42-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086894</TermUI>
      <String>formose sugars</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C118414</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>OMP26 protein, Haemophilus influenzae</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1999</Year>
   <Month>04</Month>
   <Day>21</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>02</Month>
   <Day>11</Day>
  </DateRevised>
  <Note>a 26-kDa protein (OMP26) isolated and purified from nontypealbe Haemophilus influenzae (NTHI) strain 289 has been shown to enhance clearance of infection following pulmonary challenge with NTHI in rats; amino acid sequence in first source
  </Note>
  <Frequency>8</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001425</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Outer Membrane Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D006193</DescriptorUI>
     <DescriptorName>
      <String>Haemophilus influenzae</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Infect Immun 1999 Apr;67(4):1935-42</Source>
   <Source>Infect Immun. 1998 May;66(5):2272-8.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0303493</ConceptUI>
    <ConceptName>
     <String>OMP26 protein, Haemophilus influenzae</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T333498</TermUI>
      <String>OMP26 protein, Haemophilus influenzae</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010970</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>glucose-N-acetylaminomannuronic acid polymer</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>23</Day>
  </DateRevised>
  <Note>polymer found in Micrococcus lysodeikticus
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>URONIC ACIDS (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011135</DescriptorUI>
     <DescriptorName>
      <String>Polysaccharides, Bacterial</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Z Immunitaetsforsch 149(2-4):193;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056904</ConceptUI>
    <ConceptName>
     <String>glucose-N-acetylaminomannuronic acid polymer</String>
    </ConceptName>
    <CASN1Name>D-Mannuronic acid, 2-(acetylamino)-2-deoxy-, polymer with D-glucose</CASN1Name>
    <RegistryNumber>56727-45-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086907</TermUI>
      <String>glucose-N-acetylaminomannuronic acid polymer</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010977</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hexacaine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>local anesthetic of beta-aminoketone group.; structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011427</DescriptorUI>
     <DescriptorName>
      <String>Propiophenones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cor Vasa 17(2):133;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056914</ConceptUI>
    <ConceptName>
     <String>hexacaine</String>
    </ConceptName>
    <CASN1Name>beta-N-hexamethylenimino-p-propoxypropiophenone. HCl /OD/ TG-16</CASN1Name>
    <RegistryNumber>16689-12-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086917</TermUI>
      <String>hexacaine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013167</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>octopinic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>08</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009952</DescriptorUI>
     <DescriptorName>
      <String>Ornithine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 78(2):785;1977</Source>
   <Source>J Gen Microbiol 96(1):155;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060726</ConceptUI>
    <ConceptName>
     <String>octopinic acid</String>
    </ConceptName>
    <RegistryNumber>20197-09-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T090729</TermUI>
      <String>octopinic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T090728</TermUI>
      <String>B(2)-(D-1-carboxyethyl)-L-ornithine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010986</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-hydroxybutylphthalate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010795</DescriptorUI>
     <DescriptorName>
      <String>Phthalic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Agr Food Chem 23(5):854;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056940</ConceptUI>
    <ConceptName>
     <String>4-hydroxybutylphthalate</String>
    </ConceptName>
    <RegistryNumber>17498-34-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086943</TermUI>
      <String>4-hydroxybutylphthalate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010990</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-hydroxyimino-4-methyl-2-pentanone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010091</DescriptorUI>
     <DescriptorName>
      <String>Oximes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Toxicol 8(4):220;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056944</ConceptUI>
    <ConceptName>
     <String>1-hydroxyimino-4-methyl-2-pentanone</String>
    </ConceptName>
    <CASN1Name>4-methyl-2-oxopentanal 1-oxime</CASN1Name>
    <RegistryNumber>50627-09-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086947</TermUI>
      <String>1-hydroxyimino-4-methyl-2-pentanone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C479338</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>TRUSS protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>12</Month>
   <Day>04</Day>
  </DateCreated>
  <Note>TRUSS - tumor necrosis factor receptor (TNF-R)-associated ubiquitous scaffolding and signaling protein; mediates activation of the transcription factor NF-kappaB; MW 90.7 kDa; amino acid sequence in first source
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015534</DescriptorUI>
     <DescriptorName>
      <String>Trans-Activators</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Cell Biol. 2003 Nov;23(22); 8334-44</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0456965</ConceptUI>
    <ConceptName>
     <String>TRUSS protein, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T561528</TermUI>
      <String>TRUSS protein, mouse</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>04</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008148</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>iodomelphalan</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*MELPHALAN (74-75)</PreviousIndexing>
   <PreviousIndexing>IODINE (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008558</DescriptorUI>
     <DescriptorName>
      <String>Melphalan</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 17(2):194;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051740</ConceptUI>
    <ConceptName>
     <String>iodomelphalan</String>
    </ConceptName>
    <CASN1Name>4-(bis(2-chloroethyl)amino)-2-iodo-L- phenylalanine</CASN1Name>
    <RegistryNumber>51554-04-2</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0051740</Concept1UI>
     <Concept2UI>M0051739</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081743</TermUI>
      <String>iodomelphalan</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0051739</ConceptUI>
    <ConceptName>
     <String>3-(4-(bis(2-chloroethyl)amino)-2-iodophenyl)-L- alanine</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0051740</Concept1UI>
     <Concept2UI>M0051739</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T081742</TermUI>
      <String>3-(4-(bis(2-chloroethyl)amino)-2-iodophenyl)-L- alanine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008150</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-iodophthalimide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>IMIDES (75-75)</PreviousIndexing>
   <PreviousIndexing>IODINE (75-75)</PreviousIndexing>
   <PreviousIndexing>PHTHALIC ACID/*analogs (75-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010797</DescriptorUI>
     <DescriptorName>
      <String>Phthalimides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharmacol Exp Ther 191(2):341;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051744</ConceptUI>
    <ConceptName>
     <String>N-iodophthalimide</String>
    </ConceptName>
    <CASN1Name>2-iodo-1H-isoindole-1,3(2H)-dione</CASN1Name>
    <RegistryNumber>20919-42-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081747</TermUI>
      <String>N-iodophthalimide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008152</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-iodosalicylic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>06</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>SALICYLIC ACIDS (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007463</DescriptorUI>
     <DescriptorName>
      <String>Iodobenzoates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Pharmacol 23(9):1367;1974</Source>
   <Source>Vestn Dermatol Venerol 1:72;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051748</ConceptUI>
    <ConceptName>
     <String>4-iodosalicylic acid</String>
    </ConceptName>
    <CASN1Name>2-hydroxy-4-iodobenzoic acid</CASN1Name>
    <RegistryNumber>16870-28-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081751</TermUI>
      <String>4-iodosalicylic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008120</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>indolyl-3-acetic acid (1-phenyl-2,3-dimethyl-5-oxo-4- pyrazolyl) amide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>05</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*INDOLEACETIC ACID (74-75)</PreviousIndexing>
   <PreviousIndexing>AMIDES (74-75)</PreviousIndexing>
   <PreviousIndexing>PYRAZOLES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007210</DescriptorUI>
     <DescriptorName>
      <String>Indoleacetic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Pol Pharm 31(2):151;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051696</ConceptUI>
    <ConceptName>
     <String>indolyl-3-acetic acid (1-phenyl-2,3-dimethyl-5-oxo-4- pyrazolyl) amide</String>
    </ConceptName>
    <CASN1Name>1H-Indole-3-acetamide, N-(2,3-dihydro-1,5-dimethyl-3-oxo-2-phenyl-1H-pyrazol-4-yl)-</CASN1Name>
    <RegistryNumber>53995-76-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081699</TermUI>
      <String>indolyl-3-acetic acid (1-phenyl-2,3-dimethyl-5-oxo-4- pyrazolyl) amide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C425925</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>myelin basic protein 121-150</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>05</Month>
   <Day>18</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>05</Month>
   <Day>13</Day>
  </DateRevised>
  <Note>has been sequenced
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004676</DescriptorUI>
     <DescriptorName>
      <String>Myelin Basic Protein</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010446</DescriptorUI>
     <DescriptorName>
      <String>Peptide Fragments</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Immunity 2001 Apr;14(4):471-81</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0387264</ConceptUI>
    <ConceptName>
     <String>myelin basic protein 121-150</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T640598</TermUI>
      <String>myelin basic protein 121-150</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>05</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T457757</TermUI>
      <String>myelin basic protein peptide 121-150</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>08</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T446978</TermUI>
      <String>myelin basic protein (121-150)</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>05</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T446979</TermUI>
      <String>MBP peptide 121-150</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>05</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T446980</TermUI>
      <String>MBP121-150</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>05</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C050978</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>myelin basic protein 114-122</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1987</Year>
   <Month>03</Month>
   <Day>19</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>05</Month>
   <Day>13</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004676</DescriptorUI>
     <DescriptorName>
      <String>Myelin Basic Protein</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010446</DescriptorUI>
     <DescriptorName>
      <String>Peptide Fragments</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biull Eksp Biol Med 1987;103(1):92</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0145304</ConceptUI>
    <ConceptName>
     <String>myelin basic protein 114-122</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T640597</TermUI>
      <String>myelin basic protein 114-122</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>05</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T175309</TermUI>
      <String>myelin basic protein peptide 114-122</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T175308</TermUI>
      <String>Phe-Ser-Trp-Gly-Ala-Glu-Gly-Gln-Arg-OH</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T175307</TermUI>
      <String>MBPP 114-122</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C022917</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-acetoxy-N-2-acetylamino-7-iodofluorene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>23</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000099</DescriptorUI>
     <DescriptorName>
      <String>Acetoxyacetylaminofluorene</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>FEBS Lett 180(1):66;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0079594</ConceptUI>
    <ConceptName>
     <String>N-acetoxy-N-2-acetylamino-7-iodofluorene</String>
    </ConceptName>
    <CASN1Name>N-(acetyloxy)-N-(7-iodo-9H-fluoren-2-yl)acetamide</CASN1Name>
    <RegistryNumber>43146-76-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T109597</TermUI>
      <String>N-acetoxy-N-2-acetylamino-7-iodofluorene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C456846</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>GPRI2 protein, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>06</Month>
   <Day>19</Day>
  </DateCreated>
  <Note>GenBank AB062490
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015534</DescriptorUI>
     <DescriptorName>
      <String>Trans-Activators</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D004268</DescriptorUI>
     <DescriptorName>
      <String>DNA-Binding Proteins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Plant Cell Physiol 2002 Jan;43(1):99-107</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0427456</ConceptUI>
    <ConceptName>
     <String>GPRI2 protein, Arabidopsis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T499155</TermUI>
      <String>GPRI2 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>06</Month>
       <Day>19</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C456848</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>diplodiatoxin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>06</Month>
   <Day>19</Day>
  </DateCreated>
  <Note>a bicyclic beta-gamma unsaturated carboxylic acid with keto side chain
  </Note>
  <Frequency>7</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002867</DescriptorUI>
     <DescriptorName>
      <String>Chromones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Indian J Exp Biol 2001 Dec;39(12):1243-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0427458</ConceptUI>
    <ConceptName>
     <String>diplodiatoxin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T499157</TermUI>
      <String>diplodiatoxin</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>06</Month>
       <Day>19</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C037147</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>myelin basic protein 43-88</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1983</Year>
   <Month>03</Month>
   <Day>04</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>05</Month>
   <Day>13</Day>
  </DateRevised>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004676</DescriptorUI>
     <DescriptorName>
      <String>Myelin Basic Protein</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010446</DescriptorUI>
     <DescriptorName>
      <String>Peptide Fragments</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Chromatogr 1983;254:211</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0112598</ConceptUI>
    <ConceptName>
     <String>myelin basic protein 43-88</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T640599</TermUI>
      <String>myelin basic protein 43-88</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>05</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T142601</TermUI>
      <String>MBPP 43-88</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T142602</TermUI>
      <String>myelin basic protein peptide 43-88</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C110235</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>myelin basic protein 68-86</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>02</Month>
   <Day>13</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>05</Month>
   <Day>13</Day>
  </DateRevised>
  <Frequency>20</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004676</DescriptorUI>
     <DescriptorName>
      <String>Myelin Basic Protein</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010446</DescriptorUI>
     <DescriptorName>
      <String>Peptide Fragments</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Neuroreport 1997 Dec 1;8(17):3727-30</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0285843</ConceptUI>
    <ConceptName>
     <String>myelin basic protein 68-86</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T315848</TermUI>
      <String>myelin basic protein 68-86</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T457767</TermUI>
      <String>myelin basic protein peptide 68-86</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>08</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T315847</TermUI>
      <String>encephalitogenic peptide (68-86)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C041031</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>myelin basic protein 45-89</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1984</Year>
   <Month>05</Month>
   <Day>24</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>05</Month>
   <Day>13</Day>
  </DateRevised>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004676</DescriptorUI>
     <DescriptorName>
      <String>Myelin Basic Protein</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010446</DescriptorUI>
     <DescriptorName>
      <String>Peptide Fragments</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 1984;259(8):5028</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0121864</ConceptUI>
    <ConceptName>
     <String>myelin basic protein 45-89</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T640600</TermUI>
      <String>myelin basic protein 45-89</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>05</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T151869</TermUI>
      <String>myelin basic protein peptide 45-89</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1984)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008190</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>isomannide dinitrate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*MANNITOL (74-75)</PreviousIndexing>
   <PreviousIndexing>ETHERS, CYCLIC (74-75)</PreviousIndexing>
   <PreviousIndexing>NITRATES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008353</DescriptorUI>
     <DescriptorName>
      <String>Mannitol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Pharmacol 22(1):67;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051829</ConceptUI>
    <ConceptName>
     <String>isomannide dinitrate</String>
    </ConceptName>
    <CASN1Name>1,4,3,6-dianhydro-D-mannitol dinitrate</CASN1Name>
    <RegistryNumber>551-43-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081832</TermUI>
      <String>isomannide dinitrate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C050951</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tetrakis(N-methyl-4-pyridinium)yl-porphine iron(III) complex</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1987</Year>
   <Month>02</Month>
   <Day>26</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>23</Day>
  </DateRevised>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005290</DescriptorUI>
     <DescriptorName>
      <String>Ferric Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008665</DescriptorUI>
     <DescriptorName>
      <String>Metalloporphyrins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 1986;25(22):6875</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0145253</ConceptUI>
    <ConceptName>
     <String>tetrakis(N-methyl-4-pyridinium)yl-porphine iron(III) complex</String>
    </ConceptName>
    <RegistryNumber>60489-13-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T175258</TermUI>
      <String>tetrakis(N-methyl-4-pyridinium)yl-porphine iron(III) complex</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T175257</TermUI>
      <String>meso tetrakis(N-methyl-4-pyridiniumyl)porphine Fe(III) complex</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T175256</TermUI>
      <String>FeT4MPyP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008201</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>isopropoxyphosphine oxide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1995</Year>
   <Month>12</Month>
   <Day>12</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PHOSPHINES (74-78)</PreviousIndexing>
   <PreviousIndexing>ALCOHOL, PROPYL (74-78)</PreviousIndexing>
   <PreviousIndexing>OXIDES (74-78)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009943</DescriptorUI>
     <DescriptorName>
      <String>Organophosphorus Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cytologia 42:621;1977</Source>
   <Source>Folia Biol (Krakow) 21(4):439;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051843</ConceptUI>
    <ConceptName>
     <String>isopropoxyphosphine oxide</String>
    </ConceptName>
    <CASN1Name>phosphinic acid 1-methylethyl ester</CASN1Name>
    <RegistryNumber>51963-59-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081846</TermUI>
      <String>isopropoxyphosphine oxide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C500408</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>FAUC 88</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>05</Month>
   <Day>13</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000480</DescriptorUI>
     <DescriptorName>
      <String>Alkynes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003514</DescriptorUI>
     <DescriptorName>
      <String>Cyclohexylamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Bioorg Med Chem. 2005 Jan 3;13(1):185-91</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0484674</ConceptUI>
    <ConceptName>
     <String>FAUC 88</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T640603</TermUI>
      <String>FAUC 88</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>05</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008209</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-isoquinolinecarbonitrile</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>NITRILES (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007546</DescriptorUI>
     <DescriptorName>
      <String>Isoquinolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Yakugaku Zasshi 94(4):510;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051867</ConceptUI>
    <ConceptName>
     <String>4-isoquinolinecarbonitrile</String>
    </ConceptName>
    <RegistryNumber>34846-65-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081870</TermUI>
      <String>4-isoquinolinecarbonitrile</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C118872</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>myelin basic protein 72-85</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1999</Year>
   <Month>05</Month>
   <Day>18</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>05</Month>
   <Day>13</Day>
  </DateRevised>
  <Frequency>7</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004676</DescriptorUI>
     <DescriptorName>
      <String>Myelin Basic Protein</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010446</DescriptorUI>
     <DescriptorName>
      <String>Peptide Fragments</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 1999 Apr 8;42(7):1170-7</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0304499</ConceptUI>
    <ConceptName>
     <String>myelin basic protein 72-85</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T640604</TermUI>
      <String>myelin basic protein 72-85</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>05</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T334504</TermUI>
      <String>myelin basic protein (72-85)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T457759</TermUI>
      <String>myelin basic protein peptide 72-85</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>08</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C113782</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>myelin basic protein 70-88</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>08</Month>
   <Day>21</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>05</Month>
   <Day>13</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004676</DescriptorUI>
     <DescriptorName>
      <String>Myelin Basic Protein</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010446</DescriptorUI>
     <DescriptorName>
      <String>Peptide Fragments</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Neuroimmunol 1998 Aug 1;88(1-2):21-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0293695</ConceptUI>
    <ConceptName>
     <String>myelin basic protein 70-88</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T323700</TermUI>
      <String>myelin basic protein 70-88</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T457768</TermUI>
      <String>myelin basic protein peptide 70-88</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>08</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T323699</TermUI>
      <String>MBP peptide 70-88</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008217</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>isoxanthopterin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>43</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PTERIDINES (74-75)</PreviousIndexing>
   <PreviousIndexing>AMINES (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014976</DescriptorUI>
     <DescriptorName>
      <String>Xanthopterin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Berichte 106(6):1952;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051880</ConceptUI>
    <ConceptName>
     <String>isoxanthopterin</String>
    </ConceptName>
    <CASN1Name>2-amino-4,7(1H,8H)-pteridinedione</CASN1Name>
    <RegistryNumber>529-69-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081883</TermUI>
      <String>isoxanthopterin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008222</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>itridal</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>contains cyclobarbital &amp; dominal
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001463</DescriptorUI>
     <DescriptorName>
      <String>Barbiturates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004290</DescriptorUI>
     <DescriptorName>
      <String>2,5-Dimethoxy-4-Methylamphetamine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Munch Med Wochenschr 116(48):2119;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051887</ConceptUI>
    <ConceptName>
     <String>itridal</String>
    </ConceptName>
    <CASN1Name>5-(1-cyclohexen-1-yl)-5-ethyl-2,4,6(1H,3H,5H)- pyrimidinetrione mixt. with N,N-dimethyl-10H- pyrido(3,2-B)(1,4)benzothiazine-10-propanamine</CASN1Name>
    <RegistryNumber>8058-55-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081890</TermUI>
      <String>itridal</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C093411</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tetrakis(pentafluorophenyl)porphyrinato iron(III) chloride</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>06</Month>
   <Day>05</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>23</Day>
  </DateRevised>
  <Frequency>9</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005290</DescriptorUI>
     <DescriptorName>
      <String>Ferric Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008665</DescriptorUI>
     <DescriptorName>
      <String>Metalloporphyrins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biol Pharm Bull 1995 Jan;18(1):49-52</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0246365</ConceptUI>
    <ConceptName>
     <String>tetrakis(pentafluorophenyl)porphyrinato iron(III) chloride</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T276370</TermUI>
      <String>tetrakis(pentafluorophenyl)porphyrinato iron(III) chloride</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T276368</TermUI>
      <String>Fe(TPFPP)Cl</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T276367</TermUI>
      <String>Fe(F5P)Cl</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T276369</TermUI>
      <String>meso-tetrakis(pentafluorophenyl)porphyrin iron chloride</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008231</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ketomycin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1984</Year>
   <Month>02</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>3-cyclohexeneglyoxylic acid
  </Note>
  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CYCLOHEXANES (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D006038</DescriptorUI>
     <DescriptorName>
      <String>Glyoxylates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Antimicrob Agents Chemother 3(4):510;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051910</ConceptUI>
    <ConceptName>
     <String>ketomycin</String>
    </ConceptName>
    <RegistryNumber>23364-22-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081913</TermUI>
      <String>ketomycin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C406463</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tetrakis-N,N,N',N'-(2-pyridylmethyl)ethylenediamineiron(III)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>04</Month>
   <Day>14</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>23</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005029</DescriptorUI>
     <DescriptorName>
      <String>Ethylenediamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005290</DescriptorUI>
     <DescriptorName>
      <String>Ferric Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Pharm Bull (Tokyo) 2000 Feb;48(2):223-30</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0360568</ConceptUI>
    <ConceptName>
     <String>tetrakis-N,N,N',N'-(2-pyridylmethyl)ethylenediamineiron(III)</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T411942</TermUI>
      <String>tetrakis-N,N,N',N'-(2-pyridylmethyl)ethylenediamineiron(III)</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>04</Month>
       <Day>14</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T411943</TermUI>
      <String>iron(III) tetrakis-N,N,N',N'(2-pyridylmethyl)ethylenediamine</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>04</Month>
       <Day>14</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T411944</TermUI>
      <String>Fe(III)-TPEN</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>04</Month>
       <Day>14</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008238</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>kreysiginone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>homoproaporohine alkaloid; RN given refers to (7r-trans)-isomer
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001060</DescriptorUI>
     <DescriptorName>
      <String>Aporphines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Pharm Bull (Tokyo) 22(8):1835;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051926</ConceptUI>
    <ConceptName>
     <String>kreysiginone</String>
    </ConceptName>
    <CASN1Name>1,2,3,8,9,9a-hexahydro-6-hydroxy-3',5-dimethoxy-1-methylspiro(7H-benzo(de)quinoline-7,1'-(2,5)cyclohexadien)-4'-one</CASN1Name>
    <RegistryNumber>17441-87-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081929</TermUI>
      <String>kreysiginone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008242</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>lactacyd</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1996</Year>
   <Month>09</Month>
   <Day>11</Day>
  </DateRevised>
  <Note>lactoserum-lactic acid compound soap which changes pH of skin surface
  </Note>
  <Frequency>7</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*LACTATES (74-96)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007106</DescriptorUI>
     <DescriptorName>
      <String>Immune Sera</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D019344</DescriptorUI>
     <DescriptorName>
      <String>Lactic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D012915</DescriptorUI>
     <DescriptorName>
      <String>Soaps</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Can Med Assoc J 110(11):1248;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051930</ConceptUI>
    <ConceptName>
     <String>lactacyd</String>
    </ConceptName>
    <RegistryNumber>39468-19-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081933</TermUI>
      <String>lactacyd</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008245</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>lactosides</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1987</Year>
   <Month>08</Month>
   <Day>03</Day>
  </DateRevised>
  <Frequency>89</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>LACTOSE (75-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006027</DescriptorUI>
     <DescriptorName>
      <String>Glycosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Immunol 113(3):769;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051933</ConceptUI>
    <ConceptName>
     <String>lactosides</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081936</TermUI>
      <String>lactosides</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008248</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>laminitol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007294</DescriptorUI>
     <DescriptorName>
      <String>Inositol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Hoppe Seyler Z Physiol Chem 355(6):633;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051936</ConceptUI>
    <ConceptName>
     <String>laminitol</String>
    </ConceptName>
    <CASN1Name>4-C-methyl-myo-inositol</CASN1Name>
    <RegistryNumber>472-95-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081939</TermUI>
      <String>laminitol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C062026</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-acetoxy-N-trifluoroacetyl-2-aminofluorene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1990</Year>
   <Month>01</Month>
   <Day>19</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>23</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000099</DescriptorUI>
     <DescriptorName>
      <String>Acetoxyacetylaminofluorene</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Carcinogenesis 1989;10(12):2321</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0171849</ConceptUI>
    <ConceptName>
     <String>N-acetoxy-N-trifluoroacetyl-2-aminofluorene</String>
    </ConceptName>
    <RegistryNumber>99475-95-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T201854</TermUI>
      <String>N-acetoxy-N-trifluoroacetyl-2-aminofluorene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T201853</TermUI>
      <String>N-AcO-TFA-AF</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C083494</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cwlC protein, Bacillus subtilis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1993</Year>
   <Month>10</Month>
   <Day>30</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>02</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>from Bacillus subtilis; 255-amino acid protein MW 27.146 kDa; hydrolyzes both vegetative cell walls &amp; spore peptidoglycan; aa sequence given in first source; Genbank D14666
  </Note>
  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*HYDROLASES (93-95)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009238</DescriptorUI>
     <DescriptorName>
      <String>N-Acetylmuramoyl-L-alanine Amidase</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Bacteriol 1993 Oct;175(19):6260-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0222134</ConceptUI>
    <ConceptName>
     <String>cwlC protein, Bacillus subtilis</String>
    </ConceptName>
    <RegistryNumber>EC 3.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T571159</TermUI>
      <String>cwlC protein, Bacillus subtilis</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>02</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T252139</TermUI>
      <String>sporulation-specific cell wall hydrolase, Bacillus subtilis</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008251</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>(23S)-lanosta-8,24-diene-3 beta,23-diol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*LANOSTEROL (74-75)</PreviousIndexing>
   <PreviousIndexing>HYDROXYSTEROIDS (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007810</DescriptorUI>
     <DescriptorName>
      <String>Lanosterol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Chem Soc (Perkin I):1235;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051939</ConceptUI>
    <ConceptName>
     <String>(23S)-lanosta-8,24-diene-3 beta,23-diol</String>
    </ConceptName>
    <CASN1Name>Lanosta-8,24-diene-3,23-diol, (3beta,23S)-</CASN1Name>
    <RegistryNumber>22611-41-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081942</TermUI>
      <String>(23S)-lanosta-8,24-diene-3 beta,23-diol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C091329</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Tox1 protein, Cochliobolus heterostrophus</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>02</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>02</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>controls the production of T toxin, a linear polyketide involved in the virulence of the fungus to its host plant; from Cochliobolus heterostrophus
  </Note>
  <Frequency>8</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005656</DescriptorUI>
     <DescriptorName>
      <String>Fungal Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009183</DescriptorUI>
     <DescriptorName>
      <String>Mycotoxins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Proc Natl Acad Sci USA 1994 Dec 20;91(26):12649-53</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0241186</ConceptUI>
    <ConceptName>
     <String>Tox1 protein, Cochliobolus heterostrophus</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T271191</TermUI>
      <String>Tox1 protein, Cochliobolus heterostrophus</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C088411</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>L 684248</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>08</Month>
   <Day>15</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001384</DescriptorUI>
     <DescriptorName>
      <String>Azetidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 1994 Jul 12;33(27):8347-54</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0234017</ConceptUI>
    <ConceptName>
     <String>L 684248</String>
    </ConceptName>
    <RegistryNumber>156728-18-6</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0234017</Concept1UI>
     <Concept2UI>M0234015</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T264022</TermUI>
      <String>L 684248</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T264021</TermUI>
      <String>L-684248</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0234015</ConceptUI>
    <ConceptName>
     <String>4-((1-(((1-(5-toluoyl)butyl)amino)carbonyl)-3,3-dimethyl-4-oxo-2-azetidinyl)oxy)benzoic acid</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0234017</Concept1UI>
     <Concept2UI>M0234015</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T264020</TermUI>
      <String>4-((1-(((1-(5-toluoyl)butyl)amino)carbonyl)-3,3-dimethyl-4-oxo-2-azetidinyl)oxy)benzoic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008255</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>laurifoline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>01</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>AMMMONIUM COMPOUNDS (74-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001060</DescriptorUI>
     <DescriptorName>
      <String>Aporphines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 63(4):618;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051946</ConceptUI>
    <ConceptName>
     <String>laurifoline</String>
    </ConceptName>
    <RegistryNumber>7224-61-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081949</TermUI>
      <String>laurifoline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008258</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>S-lauroylmercaptoethanol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>01</Month>
   <Day>09</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*MERCAPTOETHANOL (74-75)</PreviousIndexing>
   <PreviousIndexing>FATTY ACIDS (74-75)</PreviousIndexing>
   <PreviousIndexing>LAURATES (75-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008623</DescriptorUI>
     <DescriptorName>
      <String>Mercaptoethanol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biochem 74(4):785;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051951</ConceptUI>
    <ConceptName>
     <String>S-lauroylmercaptoethanol</String>
    </ConceptName>
    <CASN1Name>Dodecanethioic acid, S-(2-hydroxyethyl) ester</CASN1Name>
    <RegistryNumber>51097-82-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081954</TermUI>
      <String>S-lauroylmercaptoethanol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C089855</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-(acetyloxy)-4-phenyl-2-azetidinone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>11</Month>
   <Day>09</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>a taxol side-chain synthon; structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001384</DescriptorUI>
     <DescriptorName>
      <String>Azetidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biotechnol Appl Biochem 1994 Aug;20(Pt 1):23-33</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0237535</ConceptUI>
    <ConceptName>
     <String>3-(acetyloxy)-4-phenyl-2-azetidinone</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0237535</Concept1UI>
     <Concept2UI>M0237533</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T267540</TermUI>
      <String>3-(acetyloxy)-4-phenyl-2-azetidinone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T267539</TermUI>
      <String>3-AcO-4-Ph-2-azetidinone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0237533</ConceptUI>
    <ConceptName>
     <String>(3R-cis)-3-(acetyloxy)-4-phenyl-2-azetidinone</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0237535</Concept1UI>
     <Concept2UI>M0237533</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T267538</TermUI>
      <String>(3R-cis)-3-(acetyloxy)-4-phenyl-2-azetidinone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C551956</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4'-(pyridin-4-ylmethyl)biphenyl-3,4-diol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2010</Year>
   <Month>09</Month>
   <Day>07</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001713</DescriptorUI>
     <DescriptorName>
      <String>Biphenyl Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011725</DescriptorUI>
     <DescriptorName>
      <String>Pyridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D013254</DescriptorUI>
     <DescriptorName>
      <String>Steroid 17-alpha-Hydroxylase</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
     <QualifierName>
      <String>antagonists &amp; inhibitors</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Med Chem 2010 Aug 12;53(15):5749-58</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0549674</ConceptUI>
    <ConceptName>
     <String>4'-(pyridin-4-ylmethyl)biphenyl-3,4-diol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T776918</TermUI>
      <String>4'-(pyridin-4-ylmethyl)biphenyl-3,4-diol</String>
      <DateCreated>
       <Year>2010</Year>
       <Month>09</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2010)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C471277</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>claviridenone E</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>02</Month>
   <Day>21</Day>
  </DateCreated>
  <Note>from soft coral Clavularia viridis; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011453</DescriptorUI>
     <DescriptorName>
      <String>Prostaglandins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2002 Nov;65(11):1535-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0445894</ConceptUI>
    <ConceptName>
     <String>claviridenone E</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T533268</TermUI>
      <String>claviridenone E</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>02</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C025125</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Stingose</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>07</Month>
   <Day>02</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>09</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>an aqueous solution of 20% aluminum sulphate and 1.1% surfactant used in first-aid for wide range of marine, insect &amp; plant bites &amp; stings; aluminum precipitates proteins and distorts structure of polysaccharides in venoms
  </Note>
  <Frequency>7</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ALUMINUM (1980-2003)</PreviousIndexing>
   <PreviousIndexing>*SURFACE-ACTIVE AGENTS (1980-2003)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000534</DescriptorUI>
     <DescriptorName>
      <String>Alum Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Med J Aust 1980;1(6):284</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0084138</ConceptUI>
    <ConceptName>
     <String>Stingose</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="TRD"  RecordPreferredTermYN="Y">
      <TermUI>T114141</TermUI>
      <String>Stingose</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008269</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>leuconolide-A(3)-5,18-hemiacetal</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>aglycone from leucomycin A3; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ANTIBIOTICS (74-76)</PreviousIndexing>
   <PreviousIndexing>ACETALS (74-76)</PreviousIndexing>
   <PreviousIndexing>LACTONES (74-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007933</DescriptorUI>
     <DescriptorName>
      <String>Leucomycins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiot (Tokyo) 27(2):147;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051976</ConceptUI>
    <ConceptName>
     <String>leuconolide-A(3)-5,18-hemiacetal</String>
    </ConceptName>
    <RegistryNumber>52442-90-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081979</TermUI>
      <String>leuconolide-A(3)-5,18-hemiacetal</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008272</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>levan sulfate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>inhibitor of Cycl AMP phosphodiesterase
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*POLYSACCHARIDES (74-75)</PreviousIndexing>
   <PreviousIndexing>FRUCTOSE (74-75)</PreviousIndexing>
   <PreviousIndexing>SULFURIC ACIDS (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005630</DescriptorUI>
     <DescriptorName>
      <String>Fructans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Res Commun Chem Path Pharmacol 7(3):557;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0051980</ConceptUI>
    <ConceptName>
     <String>levan sulfate</String>
    </ConceptName>
    <CASN1Name>Levan, hydrogen sulfate</CASN1Name>
    <RegistryNumber>50815-13-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T081983</TermUI>
      <String>levan sulfate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C031325</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>syntamid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>09</Month>
   <Day>10</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>09</Month>
   <Day>02</Day>
  </DateRevised>
  <Note>RN given refers to cpd with unknown MF
  </Note>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SURFACE-ACTIVE AGENTS (1981-2003)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009930</DescriptorUI>
     <DescriptorName>
      <String>Organic Chemicals</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Gig Sanit 1981;(6):49</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0098507</ConceptUI>
    <ConceptName>
     <String>syntamid</String>
    </ConceptName>
    <RegistryNumber>37191-51-8</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>12679-83-3 (syntamid 5)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0098507</Concept1UI>
     <Concept2UI>M0319196</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T128511</TermUI>
      <String>syntamid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T128510</TermUI>
      <String>syntamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T128509</TermUI>
      <String>sintamid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0319196</ConceptUI>
    <ConceptName>
     <String>syntamid, syntamid 5</String>
    </ConceptName>
    <RegistryNumber>12679-83-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0098507</Concept1UI>
     <Concept2UI>M0319196</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T349196</TermUI>
      <String>syntamid, syntamid 5</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008284</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>lindenianine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>lupin alkaloid from Lupinous lindenianus; structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ALKALOIDS (75-76)</PreviousIndexing>
   <PreviousIndexing>QUINOLIZINES (75-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013034</DescriptorUI>
     <DescriptorName>
      <String>Sparteine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 39(24):3584;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0052001</ConceptUI>
    <ConceptName>
     <String>lindenianine</String>
    </ConceptName>
    <CASN1Name>13-beta-hydroxy-10-oxosparteine</CASN1Name>
    <RegistryNumber>52539-65-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T082004</TermUI>
      <String>lindenianine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008289</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>lipomaiz</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>fatty emulsion used in kidney disease therapy
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>EMULSIONS (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008055</DescriptorUI>
     <DescriptorName>
      <String>Lipids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Vrach Delo 7(0):45;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0052011</ConceptUI>
    <ConceptName>
     <String>lipomaiz</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T082014</TermUI>
      <String>lipomaiz</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008304</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>macedonic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*FATTY ACIDS, UNSATURATED (74-75)</PreviousIndexing>
   <PreviousIndexing>FATTY ALCOHOLS (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009828</DescriptorUI>
     <DescriptorName>
      <String>Oleanolic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biol Nauki 120(12):41;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0052032</ConceptUI>
    <ConceptName>
     <String>macedonic acid</String>
    </ConceptName>
    <CASN1Name>3,19-dihydroxy-oleana-11,13(18)dien-28-oic acid</CASN1Name>
    <RegistryNumber>26553-68-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T082035</TermUI>
      <String>macedonic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008319</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>manganese hemoglobin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006454</DescriptorUI>
     <DescriptorName>
      <String>Hemoglobins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009942</DescriptorUI>
     <DescriptorName>
      <String>Organometallic Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D008345</DescriptorUI>
     <DescriptorName>
      <String>Manganese</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Am Chem Soc 96(16):5259;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0052050</ConceptUI>
    <ConceptName>
     <String>manganese hemoglobin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T082053</TermUI>
      <String>manganese hemoglobin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008321</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>9-alpha-D-mannofuranosyladenine 6'-phosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>08</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>inhibitor of adenylate kinase; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ADENINE NUCLEOTIDES (74-75)</PreviousIndexing>
   <PreviousIndexing>MANNOSE (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000249</DescriptorUI>
     <DescriptorName>
      <String>Adenosine Monophosphate</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D000263</DescriptorUI>
     <DescriptorName>
      <String>Adenylate Kinase</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
     <QualifierName>
      <String>antagonists &amp; inhibitors</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Carbohydr Res 30(1):133;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0052052</ConceptUI>
    <ConceptName>
     <String>9-alpha-D-mannofuranosyladenine 6'-phosphate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T082055</TermUI>
      <String>9-alpha-D-mannofuranosyladenine 6'-phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C531290</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>(3R,4R)-(-)-6-methoxy-1-oxo-3-pentyl-3,4-dihydro-1 H-isochromen-4-yl acetate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2008</Year>
   <Month>09</Month>
   <Day>11</Day>
  </DateCreated>
  <Note>an aromatase inhibitor from aerial parts of Xyris pterygoblephara; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D049934</DescriptorUI>
     <DescriptorName>
      <String>Isocoumarins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2008 Jun;71(6):1082-4</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0524683</ConceptUI>
    <ConceptName>
     <String>(3R,4R)-(-)-6-methoxy-1-oxo-3-pentyl-3,4-dihydro-1 H-isochromen-4-yl acetate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T725527</TermUI>
      <String>(3R,4R)-(-)-6-methoxy-1-oxo-3-pentyl-3,4-dihydro-1 H-isochromen-4-yl acetate</String>
      <DateCreated>
       <Year>2008</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2008)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T725528</TermUI>
      <String>MOPDIA cpd</String>
      <DateCreated>
       <Year>2008</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2008)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008327</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>marcescin A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>bacteriocin isolated from Serratia marcescens HY
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001430</DescriptorUI>
     <DescriptorName>
      <String>Bacteriocins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Gen Genet 124(3):197;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0052059</ConceptUI>
    <ConceptName>
     <String>marcescin A</String>
    </ConceptName>
    <RegistryNumber>50815-23-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T082062</TermUI>
      <String>marcescin A</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C088133</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>A1494 protein, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>08</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>10</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>a putative thiol protease isolated from Arabidopsis thaliana; induced by wilting and abscisic acid; amino acid sequence in first source; GenBank X74359
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PLANT PROTEINS (1994-2002)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D003546</DescriptorUI>
     <DescriptorName>
      <String>Cysteine Endopeptidases</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Plant Mol Biol 1994 May;25(2):259-70</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0233286</ConceptUI>
    <ConceptName>
     <String>A1494 protein, Arabidopsis</String>
    </ConceptName>
    <RegistryNumber>EC 3.4.22.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T503621</TermUI>
      <String>A1494 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>07</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C412451</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>FimR protein, Porphyromonas gingivalis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>25</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>11</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>part a two-component signal transduction system involved in fimbriation of Porphyromonas gingivalis; amino acid sequence in first source; GenBank AB025360
  </Note>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Microbiol Immunol 2000 ;44(4):279-82</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0368583</ConceptUI>
    <ConceptName>
     <String>FimR protein, Porphyromonas gingivalis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T504961</TermUI>
      <String>FimR protein, Porphyromonas gingivalis</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>07</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C035927</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SGB 483</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1982</Year>
   <Month>11</Month>
   <Day>16</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>07</Month>
   <Day>11</Day>
  </DateRevised>
  <Note>RN given refers to parent cpd; structure given in first source
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010879</DescriptorUI>
     <DescriptorName>
      <String>Piperazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nippon Yakurigaku Zasshi 1982;79(5):441</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0109784</ConceptUI>
    <ConceptName>
     <String>SGB 483</String>
    </ConceptName>
    <CASN1Name>1-Piperazineheptanoic acid, 4-(2-methoxyphenyl)-, ethyl ester</CASN1Name>
    <RegistryNumber>81185-85-5</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>81186-01-8 (fumarate (1:1))</RelatedRegistryNumber>
     <RelatedRegistryNumber>81186-02-9 (tartrate(R-(R*,R*))-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>81186-03-0 (HCl)</RelatedRegistryNumber>
     <RelatedRegistryNumber>81186-05-2 (di-HCl)</RelatedRegistryNumber>
     <RelatedRegistryNumber>81196-08-9 (maleate (1:1))</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0109784</Concept1UI>
     <Concept2UI>M0320469</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0109784</Concept1UI>
     <Concept2UI>M0320470</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0109784</Concept1UI>
     <Concept2UI>M0320472</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0109784</Concept1UI>
     <Concept2UI>M0320468</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0109784</Concept1UI>
     <Concept2UI>M0320471</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T139788</TermUI>
      <String>SGB 483</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T139785</TermUI>
      <String>SBG-483</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T139786</TermUI>
      <String>SGB-483</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T139784</TermUI>
      <String>SBG 483</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0320469</ConceptUI>
    <ConceptName>
     <String>SGB 483, tartrate, (R-(R*,R*))-isomer</String>
    </ConceptName>
    <RegistryNumber>81186-02-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0109784</Concept1UI>
     <Concept2UI>M0320469</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T350469</TermUI>
      <String>SGB 483, tartrate, (R-(R*,R*))-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0320470</ConceptUI>
    <ConceptName>
     <String>SGB 483, hydrochloride</String>
    </ConceptName>
    <RegistryNumber>81186-03-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0109784</Concept1UI>
     <Concept2UI>M0320470</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T350470</TermUI>
      <String>SGB 483, hydrochloride</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0320472</ConceptUI>
    <ConceptName>
     <String>SGB 483, maleate (1:1)</String>
    </ConceptName>
    <RegistryNumber>81196-08-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0109784</Concept1UI>
     <Concept2UI>M0320472</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T350472</TermUI>
      <String>SGB 483, maleate (1:1)</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0320468</ConceptUI>
    <ConceptName>
     <String>SGB 483, fumarate (1:1)</String>
    </ConceptName>
    <RegistryNumber>81186-01-8</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0109784</Concept1UI>
     <Concept2UI>M0320468</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T350468</TermUI>
      <String>SGB 483, fumarate (1:1)</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0320471</ConceptUI>
    <ConceptName>
     <String>SGB 483, dihydrochloride</String>
    </ConceptName>
    <RegistryNumber>81186-05-2</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0109784</Concept1UI>
     <Concept2UI>M0320471</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T350471</TermUI>
      <String>SGB 483, dihydrochloride</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T139787</TermUI>
      <String>ethyl-7-(4-(2-methoxyphenyl)-1-piperazinyl)heptanoate dihydrochloride</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C531291</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hyperielliptone HA</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2008</Year>
   <Month>09</Month>
   <Day>11</Day>
  </DateCreated>
  <Note>from the heartwood of Hypericum geminiflorum; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010696</DescriptorUI>
     <DescriptorName>
      <String>Phloroglucinol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2008 Jun;71(6):1027-31</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0524684</ConceptUI>
    <ConceptName>
     <String>hyperielliptone HA</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T725529</TermUI>
      <String>hyperielliptone HA</String>
      <DateCreated>
       <Year>2008</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2008)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C008353</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>meprocalm</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>contains above 2 cpds
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008620</DescriptorUI>
     <DescriptorName>
      <String>Meprobamate</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012110</DescriptorUI>
     <DescriptorName>
      <String>Reserpine</String>
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  <SourceList>
   <Source>Acta Neurol Belg 73(2):88;1973</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0052101</ConceptUI>
    <ConceptName>
     <String>meprocalm</String>
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    <CASN1Name>Meprocalm</CASN1Name>
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     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T082104</TermUI>
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   </Concept>
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 </SupplementalRecord>
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  <SupplementalRecordUI>C467075</SupplementalRecordUI>
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   <String>triethyl-2,5,8- tribenzyltrindane-2,5,8-tricarboxylate</String>
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  <DateCreated>
   <Year>2002</Year>
   <Month>10</Month>
   <Day>28</Day>
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  <Note>structure in first source
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011083</DescriptorUI>
     <DescriptorName>
      <String>Polycyclic Compounds</String>
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  <SourceList>
   <Source>Org Lett 2002 Mar 7;4(5):795-8</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0440849</ConceptUI>
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      <TermUI>T524395</TermUI>
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      <DateCreated>
       <Year>2002</Year>
       <Month>10</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T524396</TermUI>
      <String>T-TB-TC</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>10</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0440850</ConceptUI>
    <ConceptName>
     <String>triethyl cis,cis,cis-2,5,8- tribenzyltrindane-2,5,8-tricarboxylate</String>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0440849</Concept1UI>
     <Concept2UI>M0440850</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T524397</TermUI>
      <String>triethyl cis,cis,cis-2,5,8- tribenzyltrindane-2,5,8-tricarboxylate</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>10</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
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   </Concept>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C494560</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,2,14,14-tetramethyl-8-oxopentadecanedioic acid</String>
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  <DateCreated>
   <Year>2004</Year>
   <Month>12</Month>
   <Day>29</Day>
  </DateCreated>
  <Note>a hypolipidemic agent; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003998</DescriptorUI>
     <DescriptorName>
      <String>Dicarboxylic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 2004 Nov 18;47(24):6082-99</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0478745</ConceptUI>
    <ConceptName>
     <String>2,2,14,14-tetramethyl-8-oxopentadecanedioic acid</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T626475</TermUI>
      <String>2,2,14,14-tetramethyl-8-oxopentadecanedioic acid</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>12</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T626476</TermUI>
      <String>4MeOPDA</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>12</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C103917</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-(5-ethoxycarbonyl-4-ethyl-6-(2-naphthyl)-1,2,3,6-tetrahydro-2-oxopyrimidin-1-yl)ethyl benzoate</String>
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  <DateCreated>
   <Year>1997</Year>
   <Month>02</Month>
   <Day>19</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001565</DescriptorUI>
     <DescriptorName>
      <String>Benzoates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011744</DescriptorUI>
     <DescriptorName>
      <String>Pyrimidinones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Science 1997 Feb 7;275(5301):823-6</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0271583</ConceptUI>
    <ConceptName>
     <String>2-(5-ethoxycarbonyl-4-ethyl-6-(2-naphthyl)-1,2,3,6-tetrahydro-2-oxopyrimidin-1-yl)ethyl benzoate</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T301588</TermUI>
      <String>2-(5-ethoxycarbonyl-4-ethyl-6-(2-naphthyl)-1,2,3,6-tetrahydro-2-oxopyrimidin-1-yl)ethyl benzoate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T301587</TermUI>
      <String>EENTOE-benzoate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011950</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>nicotinamide-(S-methylmercury-thioinosine) dinucleotide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1995</Year>
   <Month>06</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ORGANOMERCURY COMPOUNDS (76-80)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008767</DescriptorUI>
     <DescriptorName>
      <String>Methylmercury Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009243</DescriptorUI>
     <DescriptorName>
      <String>NAD</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Z Naturforsch (C) 30(5):562;1975</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058611</ConceptUI>
    <ConceptName>
     <String>nicotinamide-(S-methylmercury-thioinosine) dinucleotide</String>
    </ConceptName>
    <CASN1Name>Mercury, methyl(6-thioinosine 5'-(trihydrogen diphosphate) 5'-5'-ester with 3-(aminocarbonyl)-1-beta-D-ribofuranosylpyridiniumato(2-))-</CASN1Name>
    <RegistryNumber>57229-26-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088614</TermUI>
      <String>nicotinamide-(S-methylmercury-thioinosine) dinucleotide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C494561</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N3,5'-cyclo-4-ribofuranosyl-vic-triazolo(4,5-b)pyridin-5-one</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>12</Month>
   <Day>29</Day>
  </DateCreated>
  <Note>has anti-hepatitis C virus activity; structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009705</DescriptorUI>
     <DescriptorName>
      <String>Nucleosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
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  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 2004 Nov 18;47(24):6100-0</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0478746</ConceptUI>
    <ConceptName>
     <String>N3,5'-cyclo-4-ribofuranosyl-vic-triazolo(4,5-b)pyridin-5-one</String>
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    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0478746</Concept1UI>
     <Concept2UI>M0478747</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T626477</TermUI>
      <String>N3,5'-cyclo-4-ribofuranosyl-vic-triazolo(4,5-b)pyridin-5-one</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>12</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T626478</TermUI>
      <String>cyclo-RibTPO</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>12</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0478747</ConceptUI>
    <ConceptName>
     <String>N(3),5'-cyclo-4-(beta-D-ribofuranosyl)-vic-triazolo(4,5-b)pyridin-5-one</String>
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    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0478746</Concept1UI>
     <Concept2UI>M0478747</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T626479</TermUI>
      <String>N(3),5'-cyclo-4-(beta-D-ribofuranosyl)-vic-triazolo(4,5-b)pyridin-5-one</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>12</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C104022</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Fluoro-Red</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1997</Year>
   <Month>02</Month>
   <Day>22</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>a mixed pink emulsion including a solution of 0.5% basic-red 1 and 0.5% basic-violet 11
  </Note>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001565</DescriptorUI>
     <DescriptorName>
      <String>Benzoates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Brain Res 1996 Oct 14;736(1-2):61-7</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0271819</ConceptUI>
    <ConceptName>
     <String>Fluoro-Red</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="TRD"  RecordPreferredTermYN="Y">
      <TermUI>T301824</TermUI>
      <String>Fluoro-Red</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C103215</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4,4'-hydrazobenzenedicarboxylic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1997</Year>
   <Month>01</Month>
   <Day>27</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001565</DescriptorUI>
     <DescriptorName>
      <String>Benzoates</String>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006834</DescriptorUI>
     <DescriptorName>
      <String>Hydrazines</String>
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    </DescriptorReferredTo>
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  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Biomed Anal 1996 Aug;14(11):1615-23</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0269944</ConceptUI>
    <ConceptName>
     <String>4,4'-hydrazobenzenedicarboxylic acid</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T299949</TermUI>
      <String>4,4'-hydrazobenzenedicarboxylic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T299948</TermUI>
      <String>4,4'-hydrazo-BDCA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
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   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011964</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6(9)-oxy-11,15-dihydroxy-prosta-7,13-dienoic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PROSTENOIC ACIDS (76-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011458</DescriptorUI>
     <DescriptorName>
      <String>Prostaglandins E</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 424(2):323;1976</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058638</ConceptUI>
    <ConceptName>
     <String>6(9)-oxy-11,15-dihydroxy-prosta-7,13-dienoic acid</String>
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    <RegistryNumber>35121-77-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088641</TermUI>
      <String>6(9)-oxy-11,15-dihydroxy-prosta-7,13-dienoic acid</String>
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       <ThesaurusID>NLM (1976)</ThesaurusID>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C021192</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-fluoro-2'-deoxyuridine 5'-(4-azidophenyl phosphate)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>07</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>potential photoaffinity label of thymidylate synthetase; structure
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  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001386</DescriptorUI>
     <DescriptorName>
      <String>Azides</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005468</DescriptorUI>
     <DescriptorName>
      <String>Fluorodeoxyuridylate</String>
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    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 22(8):953;1979</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0075754</ConceptUI>
    <ConceptName>
     <String>5-fluoro-2'-deoxyuridine 5'-(4-azidophenyl phosphate)</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T105757</TermUI>
      <String>5-fluoro-2'-deoxyuridine 5'-(4-azidophenyl phosphate)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T105756</TermUI>
      <String>5-fluoro-2'-deoxyuridine 5'-(p-azidophenyl phosphate)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C033169</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-((4-azidophenyl)dithio)propionic N-hydroxysuccinimide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>04</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>07</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>cleavable photoactivable heterobifunctional reagent
  </Note>
  <Frequency>11</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SUCCINIMIDES (82-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001386</DescriptorUI>
     <DescriptorName>
      <String>Azides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 1981;20(24):6754</Source>
   <Source>J Immunol 1982;128(1):251</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0103066</ConceptUI>
    <ConceptName>
     <String>3-((4-azidophenyl)dithio)propionic N-hydroxysuccinimide</String>
    </ConceptName>
    <CASN1Name>2,5-Pyrrolidinedione, 1-(3-((4-azidophenyl)dithio)-1-oxopropoxy)-</CASN1Name>
    <RegistryNumber>74676-98-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T133070</TermUI>
      <String>3-((4-azidophenyl)dithio)propionic N-hydroxysuccinimide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T133069</TermUI>
      <String>succinimidyl(4-azidophenyldithio)propionate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T133068</TermUI>
      <String>SADP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T133067</TermUI>
      <String>3-APDTPHS</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C021232</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>peptidyl diazomethyl ketones</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1995</Year>
   <Month>09</Month>
   <Day>29</Day>
  </DateRevised>
  <Frequency>8</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DIAZONIUM COMPOUNDS (80-81)</PreviousIndexing>
   <PreviousIndexing>PEPTIDES (80-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003978</DescriptorUI>
     <DescriptorName>
      <String>Diazomethane</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007659</DescriptorUI>
     <DescriptorName>
      <String>Ketones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 89(4):1354;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0075828</ConceptUI>
    <ConceptName>
     <String>peptidyl diazomethyl ketones</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T105831</TermUI>
      <String>peptidyl diazomethyl ketones</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C021238</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>phytoecdysones</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Frequency>22</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004440</DescriptorUI>
     <DescriptorName>
      <String>Ecdysone</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010840</DescriptorUI>
     <DescriptorName>
      <String>Phytosterols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ukr Biokhim Zh 51(5):560;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0075850</ConceptUI>
    <ConceptName>
     <String>phytoecdysones</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T105853</TermUI>
      <String>phytoecdysones</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C021243</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>polyamine-peptide conjugate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>from human amniotic fluid
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011073</DescriptorUI>
     <DescriptorName>
      <String>Polyamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D011257</DescriptorUI>
     <DescriptorName>
      <String>Pregnancy Proteins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Clin Chim Acta 95(3):461;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0075861</ConceptUI>
    <ConceptName>
     <String>polyamine-peptide conjugate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T105864</TermUI>
      <String>polyamine-peptide conjugate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C413367</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ILME pheromone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>09</Month>
   <Day>20</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>11</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>a waterborne pheromonal peptide released by the eggs of Sepia officinalis
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009842</DescriptorUI>
     <DescriptorName>
      <String>Oligopeptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010675</DescriptorUI>
     <DescriptorName>
      <String>Pheromones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 2000 Aug 18;275(1):217-22</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0369841</ConceptUI>
    <ConceptName>
     <String>ILME pheromone</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T424545</TermUI>
      <String>ILME pheromone</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>09</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T468829</TermUI>
      <String>Ileu-Leu-Met-Glu</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>11</Month>
       <Day>05</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T424546</TermUI>
      <String>ILME peptide</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>09</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C491371</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Madd protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>11</Month>
   <Day>02</Day>
  </DateCreated>
  <DateRevised>
   <Year>2007</Year>
   <Month>10</Month>
   <Day>24</Day>
  </DateRevised>
  <Note>RefSeq NM_145527
  </Note>
  <Frequency>12</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D020662</DescriptorUI>
     <DescriptorName>
      <String>Guanine Nucleotide Exchange Factors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D053418</DescriptorUI>
     <DescriptorName>
      <String>Death Domain Receptor Signaling Adaptor Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0468460</ConceptUI>
    <ConceptName>
     <String>Madd protein, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T594284</TermUI>
      <String>Madd protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T594287</TermUI>
      <String>differentially expressed in normal and neoplastic cells protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T594285</TermUI>
      <String>MAP-kinase activating death domain protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T594286</TermUI>
      <String>DENN protein, mouse</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C021250</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>somatomedin inhibitor</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1984</Year>
   <Month>01</Month>
   <Day>03</Day>
  </DateRevised>
  <Frequency>18</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013002</DescriptorUI>
     <DescriptorName>
      <String>Somatomedins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Diabetes 28(10):919;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0075876</ConceptUI>
    <ConceptName>
     <String>somatomedin inhibitor</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T105879</TermUI>
      <String>somatomedin inhibitor</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C021251</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>S-protein (control)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1989</Year>
   <Month>10</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>acidic control glycoprotein of membrane attack complex of human complement
  </Note>
  <Frequency>33</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*GLYCOPROTEINS (80-87)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008562</DescriptorUI>
     <DescriptorName>
      <String>Membrane Glycoproteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D015938</DescriptorUI>
     <DescriptorName>
      <String>Complement Membrane Attack Complex</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Biol Chem 254(19):9808;1979</Source>
   <Source>J Immunol 1980;124(4):1779</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0075877</ConceptUI>
    <ConceptName>
     <String>S-protein (control)</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T105880</TermUI>
      <String>S-protein (control)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C479523</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>BCH 15046</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>12</Month>
   <Day>10</Day>
  </DateCreated>
  <Note>inhibits endothelial cell proliferation by targeting integrins alphavbeta3, alphavbeta5, and alpha5beta1; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006146</DescriptorUI>
     <DescriptorName>
      <String>Guanidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013449</DescriptorUI>
     <DescriptorName>
      <String>Sulfonamides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Vascul Pharmacol 2003 Feb;40(2):77-89</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0457252</ConceptUI>
    <ConceptName>
     <String>BCH 15046</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T562648</TermUI>
      <String>BCH 15046</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T562650</TermUI>
      <String>BCH15046</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T562649</TermUI>
      <String>BCH-15046</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C494171</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>S130K-HBGAM chimeric protein</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>12</Month>
   <Day>20</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>10</Month>
   <Day>27</Day>
  </DateRevised>
  <Note>synthetic protein; fibroblast growth factor-1 (FGF-1) mutant (S130K) linked it to a heparin-binding growth-associated molecule (HBGAM) to form the chimera S130K-HBGAM; a potent, heparin-independent epithelial cell and smooth muscle cell mitogen
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*RECOMBINANT PROTEINS (2004-2006)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011993</DescriptorUI>
     <DescriptorName>
      <String>Recombinant Fusion Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D016220</DescriptorUI>
     <DescriptorName>
      <String>Fibroblast Growth Factor 1</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Am J Surg 2004 Nov;188(5);575-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0478028</ConceptUI>
    <ConceptName>
     <String>S130K-HBGAM chimeric protein</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
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      <String>S130K-HBGAM chimeric protein</String>
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       <Month>12</Month>
       <Day>20</Day>
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       <Year>2004</Year>
       <Month>12</Month>
       <Day>20</Day>
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   <Year>1980</Year>
   <Month>01</Month>
   <Day>01</Day>
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      <String>analogs &amp; derivatives</String>
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  <SourceList>
   <Source>Eur J Drug Metab Pharmacokinet 4(2):59;1979</Source>
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  <ConceptList>
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    <ConceptUI>M0075909</ConceptUI>
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     <Concept1UI>M0075909</Concept1UI>
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     <Concept1UI>M0075909</Concept1UI>
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      <TermUI>T105912</TermUI>
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   <Concept PreferredConceptYN="N">
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    <ConceptName>
     <String>4-hydroxy-6-mercaptopyrazolo(3,4-d)pyrimidine</String>
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     <Concept1UI>M0075909</Concept1UI>
     <Concept2UI>M0075907</Concept2UI>
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   <Concept PreferredConceptYN="N">
    <ConceptUI>M0075906</ConceptUI>
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     <String>1,4,5,7-tetrahydro-4-thioxo-6H-pyrazolo(3,4-D)pyrimidin-6-one</String>
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     <Concept2UI>M0075908</Concept2UI>
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      <TermUI>T105911</TermUI>
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       <ThesaurusID>NLM (1980)</ThesaurusID>
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  <SupplementalRecordName>
   <String>1-(3-pyridyl)-3,3-diethyltriazene</String>
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  <DateCreated>
   <Year>1984</Year>
   <Month>04</Month>
   <Day>13</Day>
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  <DateRevised>
   <Year>2000</Year>
   <Month>06</Month>
   <Day>06</Day>
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  <Frequency>1</Frequency>
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     <DescriptorUI>*D014226</DescriptorUI>
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      <String>Triazenes</String>
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  <SourceList>
   <Source>Arch Gewulstforsch 1983;53(6):557</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0121212</ConceptUI>
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     <RelatedRegistryNumber>52731-41-6 (cpd with unspecified pyridine locant)</RelatedRegistryNumber>
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     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T151217</TermUI>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T151216</TermUI>
      <String>PYDAT</String>
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       <ThesaurusID>NLM (1984)</ThesaurusID>
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   <String>6'-O-p-E-coumaroyl-8-epi-loganic acid</String>
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  <DateCreated>
   <Year>2007</Year>
   <Month>10</Month>
   <Day>26</Day>
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  <DateRevised>
   <Year>2007</Year>
   <Month>10</Month>
   <Day>29</Day>
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  <Note>iridoid from Scutellaria albida ssp. albida; structure in first source
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    <DescriptorReferredTo>
     <DescriptorUI>*D039823</DescriptorUI>
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      <String>Iridoids</String>
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  <SourceList>
   <Source>Phytochemistry 2007 Jul;68(13):1799-804</Source>
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       <Month>10</Month>
       <Day>26</Day>
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   <String>3-methyl-N,N-diethyl-p-phenylenediamine</String>
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  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>2000</Year>
   <Month>07</Month>
   <Day>31</Day>
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  <Note>RN given refers to parent cpd; structure
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   <PreviousIndexing>*TOLUIDINES (72-77)</PreviousIndexing>
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   <Source>Cutis 18(5):699;1976</Source>
   <Source>Hautarzt 21(6):282;1970</Source>
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     <RelatedRegistryNumber>2051-79-8 (mono-HCl)</RelatedRegistryNumber>
     <RelatedRegistryNumber>24828-38-4 (unspecified HCl)</RelatedRegistryNumber>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061744</Concept1UI>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
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     <String>3-methyl-4-amino-N-diethylaniline</String>
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     <Concept1UI>M0061744</Concept1UI>
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   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312312</ConceptUI>
    <ConceptName>
     <String>3-methyl-N,N-diethyl-p-phenylenediamine monohydrochloride</String>
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     <Concept1UI>M0061744</Concept1UI>
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      <TermUI>T342312</TermUI>
      <String>3-methyl-N,N-diethyl-p-phenylenediamine monohydrochloride</String>
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       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
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       <ThesaurusID>NLM (1972)</ThesaurusID>
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   <Concept PreferredConceptYN="N">
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     <String>CD 2 color developer</String>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T091743</TermUI>
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   <Concept PreferredConceptYN="N">
    <ConceptUI>M0061741</ConceptUI>
    <ConceptName>
     <String>Kodak CD2</String>
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   <Concept PreferredConceptYN="N">
    <ConceptUI>M0061737</ConceptUI>
    <ConceptName>
     <String>2-amino-5-diethylaminotoluol</String>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061744</Concept1UI>
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   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312313</ConceptUI>
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     <String>3-methyl-N,N-diethyl-p-phenylenediamine hydrochloride</String>
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    <RegistryNumber>24828-38-4</RegistryNumber>
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      <String>3-methyl-N,N-diethyl-p-phenylenediamine hydrochloride</String>
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       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
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   <String>N,N'-bis(9-acridinyl)-4-aza-4-(4-azidobenzoyl)-1,7-diaminoheptane</String>
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  <DateCreated>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>03</Day>
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  <DateRevised>
   <Year>2000</Year>
   <Month>07</Month>
   <Day>12</Day>
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  <SourceList>
   <Source>FEBS Lett 1981;135(1):173</Source>
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     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T133449</TermUI>
      <String>N,N'-bis(9-acridinyl)-4-aza-4-(4-azidobenzoyl)-1,7-diaminoheptane</String>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T133448</TermUI>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C033466</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-azidoimipramine</String>
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  <DateCreated>
   <Year>1982</Year>
   <Month>03</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>07</Month>
   <Day>12</Day>
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  <Note>structure given in first source
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  <Frequency>2</Frequency>
  <HeadingMappedToList>
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     <DescriptorUI>*D001386</DescriptorUI>
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      <String>Azides</String>
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  <SourceList>
   <Source>Biochim Biophys Acta 1982;714(1):173</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0103811</ConceptUI>
    <ConceptName>
     <String>2-azidoimipramine</String>
    </ConceptName>
    <CASN1Name>5H-Dibenz(b,f)azepine-5-propanamine, 2-azido-10,11-dihydro-N,N-dimethyl-</CASN1Name>
    <RegistryNumber>80751-44-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T133815</TermUI>
      <String>2-azidoimipramine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C021330</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>succinyladenosine 3',5'-cyclic monophosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>15</Day>
  </DateRevised>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000242</DescriptorUI>
     <DescriptorName>
      <String>Cyclic AMP</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Tohoku J Exp Med 129(1):91;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0076042</ConceptUI>
    <ConceptName>
     <String>succinyladenosine 3',5'-cyclic monophosphate</String>
    </ConceptName>
    <CASN1Name>adenosine, cyclic 3',5'-(hydrogen phosphate) 2'-(hydrogen butanedioate)</CASN1Name>
    <RegistryNumber>36940-87-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T106045</TermUI>
      <String>succinyladenosine 3',5'-cyclic monophosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T106044</TermUI>
      <String>2'-O-succinyl cyclic AMP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C021286</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>alloxanic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>9</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007093</DescriptorUI>
     <DescriptorName>
      <String>Imidazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Dig Dis Sci 24(9):680;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0075965</ConceptUI>
    <ConceptName>
     <String>alloxanic acid</String>
    </ConceptName>
    <CASN1Name>4-hydroxy-2,5-dioxo-4-imidazolidinecarboxylic acid</CASN1Name>
    <RegistryNumber>470-44-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T105968</TermUI>
      <String>alloxanic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C021297</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>16 beta-ethylestradiol-17 beta</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1993</Year>
   <Month>06</Month>
   <Day>08</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004958</DescriptorUI>
     <DescriptorName>
      <String>Estradiol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Steroid Biochem 11(1B):537;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0075981</ConceptUI>
    <ConceptName>
     <String>16 beta-ethylestradiol-17 beta</String>
    </ConceptName>
    <CASN1Name>(16 beta,17 beta)-16-ethylestra-1,3,5(10)-triene-3,17-diol</CASN1Name>
    <RegistryNumber>62633-99-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T105984</TermUI>
      <String>16 beta-ethylestradiol-17 beta</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C479525</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>methyl 1,2,4-tri-O-acetyl-3-O-benzylidopyranouronate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>12</Month>
   <Day>10</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007067</DescriptorUI>
     <DescriptorName>
      <String>Iduronic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Carbohydr Res 2003 Mar 28;338(7):681-6</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0457257</ConceptUI>
    <ConceptName>
     <String>methyl 1,2,4-tri-O-acetyl-3-O-benzylidopyranouronate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0457257</Concept1UI>
     <Concept2UI>M0457258</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T562657</TermUI>
      <String>methyl 1,2,4-tri-O-acetyl-3-O-benzylidopyranouronate</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T562658</TermUI>
      <String>methyl TABI</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0457258</ConceptUI>
    <ConceptName>
     <String>methyl 1,2,4-tri-O-acetyl-3-O-benzyl-beta-L-idopyranouronate</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0457257</Concept1UI>
     <Concept2UI>M0457258</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T562659</TermUI>
      <String>methyl 1,2,4-tri-O-acetyl-3-O-benzyl-beta-L-idopyranouronate</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C066768</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dppA protein, E coli</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1991</Year>
   <Month>02</Month>
   <Day>13</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>08</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>amino acid sequence given in first source
  </Note>
  <Frequency>21</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BACTERIAL PROTEINS (1991-2003)</PreviousIndexing>
   <PreviousIndexing>*CARRIER PROTEINS (1991-2004)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029968</DescriptorUI>
     <DescriptorName>
      <String>Escherichia coli Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D033902</DescriptorUI>
     <DescriptorName>
      <String>Periplasmic Binding Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Bacteriol 1991;173(1):234</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0183193</ConceptUI>
    <ConceptName>
     <String>dppA protein, E coli</String>
    </ConceptName>
    <RegistryNumber>134215-14-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T541040</TermUI>
      <String>dppA protein, E coli</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>05</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T541041</TermUI>
      <String>periplasmic dipeptide binding protein, E coli</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>05</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C494127</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>E1 glycoprotein, Semliki forest virus</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>12</Month>
   <Day>19</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>10</Month>
   <Day>27</Day>
  </DateRevised>
  <Note>GenBank X74425
  </Note>
  <Frequency>16</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008562</DescriptorUI>
     <DescriptorName>
      <String>Membrane Glycoproteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014759</DescriptorUI>
     <DescriptorName>
      <String>Viral Envelope Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Gen Virol 1994 Jun;75(Pt 6):1499-504</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0477984</ConceptUI>
    <ConceptName>
     <String>E1 glycoprotein, Semliki forest virus</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T624675</TermUI>
      <String>E1 glycoprotein, Semliki forest virus</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>12</Month>
       <Day>19</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T685089</TermUI>
      <String>E1 glycoprotein, SFV</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>10</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C479526</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>methyl 3-O-benzyliduronate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>12</Month>
   <Day>10</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007067</DescriptorUI>
     <DescriptorName>
      <String>Iduronic Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Carbohydr Res 2003 Mar 28;338(7):681-6</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0457259</ConceptUI>
    <ConceptName>
     <String>methyl 3-O-benzyliduronate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0457259</Concept1UI>
     <Concept2UI>M0457260</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T562660</TermUI>
      <String>methyl 3-O-benzyliduronate</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0457260</ConceptUI>
    <ConceptName>
     <String>methyl 3-O-benzyl-L-iduronate</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0457259</Concept1UI>
     <Concept2UI>M0457260</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T562661</TermUI>
      <String>methyl 3-O-benzyl-L-iduronate</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>12</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C090454</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>DPY-27 protein, C elegans</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>12</Month>
   <Day>16</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>08</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>a chromosome condensation protein homolog from Caenorhabditis elegans; GenBank L35274
  </Note>
  <Frequency>10</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CARRIER PROTEINS (1995-2004)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009687</DescriptorUI>
     <DescriptorName>
      <String>Nuclear Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029742</DescriptorUI>
     <DescriptorName>
      <String>Caenorhabditis elegans Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cell 1994 Nov 4;79(3):459-74</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0239012</ConceptUI>
    <ConceptName>
     <String>DPY-27 protein, C elegans</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T269017</TermUI>
      <String>DPY-27 protein, C elegans</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C021311</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>mepronizine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>combination of aceprometazine with meprobamate
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*METRONIDAZOLE (80-80)</PreviousIndexing>
   <PreviousIndexing>ACEPROMAZINE/*analogs (80-80)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000075</DescriptorUI>
     <DescriptorName>
      <String>Acepromazine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008620</DescriptorUI>
     <DescriptorName>
      <String>Meprobamate</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D007536</DescriptorUI>
     <DescriptorName>
      <String>Isomerism</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Nouv Presse Med 8(31):2571;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0076006</ConceptUI>
    <ConceptName>
     <String>mepronizine</String>
    </ConceptName>
    <CASN1Name>1-(10-(3-(dimethylamino)propyl)-10H-phenothiazin-2-yl)ethanone, mixture with 2-methyl-2-propyl- 1,3-propanediyl dicarbamate</CASN1Name>
    <RegistryNumber>51848-48-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T106009</TermUI>
      <String>mepronizine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C523852</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>enshuol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>10</Month>
   <Day>29</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004988</DescriptorUI>
     <DescriptorName>
      <String>Ethers, Cyclic</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014315</DescriptorUI>
     <DescriptorName>
      <String>Triterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Angew Chem Int Ed Engl 2007;46(34):6481-4</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0514956</ConceptUI>
    <ConceptName>
     <String>enshuol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T708624</TermUI>
      <String>enshuol</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>10</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C494215</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>unc-64 protein, C elegans</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>10</Month>
   <Day>27</Day>
  </DateRevised>
  <Note>RefSeq NM_067334
  </Note>
  <Frequency>16</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029742</DescriptorUI>
     <DescriptorName>
      <String>Caenorhabditis elegans Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D050827</DescriptorUI>
     <DescriptorName>
      <String>Syntaxin 1</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0201581</ConceptUI>
    <ConceptName>
     <String>unc-64 protein, C elegans</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T612605</TermUI>
      <String>unc-64 protein, C elegans</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>10</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C523842</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>foeniculoside X</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>10</Month>
   <Day>26</Day>
  </DateCreated>
  <DateRevised>
   <Year>2007</Year>
   <Month>10</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>phenolic glycoside from Foeniculum vulgare fruit with antioxidant activity; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006027</DescriptorUI>
     <DescriptorName>
      <String>Glycosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Phytochemistry 2007 Jul;68(13):1805-12</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0514941</ConceptUI>
    <ConceptName>
     <String>foeniculoside X</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T708604</TermUI>
      <String>foeniculoside X</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>10</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C413368</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Sig2 sigma factor</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>09</Month>
   <Day>20</Day>
  </DateCreated>
  <Note>amino acid sequence in first source
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012808</DescriptorUI>
     <DescriptorName>
      <String>Sigma Factor</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Cell Biol Res Commun 1999 Apr;1(1):14-20</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0369843</ConceptUI>
    <ConceptName>
     <String>Sig2 sigma factor</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T424547</TermUI>
      <String>Sig2 sigma factor</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>09</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C021333</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>exotoxin from Mycoplasma neurolyticum</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>12</Month>
   <Day>04</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BACTERIAL TOXINS (77-78)</PreviousIndexing>
   <PreviousIndexing>*TOXINS (76-77)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005098</DescriptorUI>
     <DescriptorName>
      <String>Exotoxins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Infection 4(1 suppl):9;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0076044</ConceptUI>
    <ConceptName>
     <String>exotoxin from Mycoplasma neurolyticum</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T106047</TermUI>
      <String>exotoxin from Mycoplasma neurolyticum</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C039008</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-(4-chlorophenyl)-2-oxo-3-butenoic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1983</Year>
   <Month>09</Month>
   <Day>21</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>06</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>RN given refers to unlabeled cpd without isomeric designation
  </Note>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*FATTY ACIDS, UNSATURATED (83-87)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005229</DescriptorUI>
     <DescriptorName>
      <String>Fatty Acids, Monounsaturated</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D011767</DescriptorUI>
     <DescriptorName>
      <String>Pyruvate Decarboxylase</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
     <QualifierName>
      <String>antagonists &amp; inhibitors</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Biochemistry 1983;22(16):3735</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0117060</ConceptUI>
    <ConceptName>
     <String>4-(4-chlorophenyl)-2-oxo-3-butenoic acid</String>
    </ConceptName>
    <RegistryNumber>33185-97-6</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>42393-06-6 ((E)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>86088-42-8 (1-(14)C-labeled cpd (E)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0117060</Concept1UI>
     <Concept2UI>M0321116</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0117060</Concept1UI>
     <Concept2UI>M0321115</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T147064</TermUI>
      <String>4-(4-chlorophenyl)-2-oxo-3-butenoic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T147063</TermUI>
      <String>4-CPOB</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0321116</ConceptUI>
    <ConceptName>
     <String>4-(4-chlorophenyl)-2-oxo-3-butenoic acid, 1-(14)C-labeled, (E)-isomer</String>
    </ConceptName>
    <RegistryNumber>86088-42-8</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0117060</Concept1UI>
     <Concept2UI>M0321116</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T351116</TermUI>
      <String>4-(4-chlorophenyl)-2-oxo-3-butenoic acid, 1-(14)C-labeled, (E)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0321115</ConceptUI>
    <ConceptName>
     <String>4-(4-chlorophenyl)-2-oxo-3-butenoic acid, (E)-isomer</String>
    </ConceptName>
    <RegistryNumber>42393-06-6</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0117060</Concept1UI>
     <Concept2UI>M0321115</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T351115</TermUI>
      <String>4-(4-chlorophenyl)-2-oxo-3-butenoic acid, (E)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C027339</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-amino-7-iodoquinoline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>12</Month>
   <Day>17</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>06</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>RN given refers to unlabeled cpd; structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000634</DescriptorUI>
     <DescriptorName>
      <String>Aminoquinolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Int J Appl Radiat Isot 1980;31(9):553</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0088948</ConceptUI>
    <ConceptName>
     <String>4-amino-7-iodoquinoline</String>
    </ConceptName>
    <RegistryNumber>40107-16-2</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>74094-93-2 (125I-labeled cpd)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0088948</Concept1UI>
     <Concept2UI>M0317234</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T118951</TermUI>
      <String>4-amino-7-iodoquinoline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0317234</ConceptUI>
    <ConceptName>
     <String>4-amino-7-iodoquinoline, 125I-labeled</String>
    </ConceptName>
    <RegistryNumber>74094-93-2</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0088948</Concept1UI>
     <Concept2UI>M0317234</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T347234</TermUI>
      <String>4-amino-7-iodoquinoline, 125I-labeled</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C021347</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>heparin depolymerase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>26</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>HEPARIN (73-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006026</DescriptorUI>
     <DescriptorName>
      <String>Glycoside Hydrolases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem J 180(3):587;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0076084</ConceptUI>
    <ConceptName>
     <String>heparin depolymerase</String>
    </ConceptName>
    <RegistryNumber>EC 3.2.1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T106087</TermUI>
      <String>heparin depolymerase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009496</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>H protein, Tobacco mosaic virus</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>01</Month>
   <Day>08</Day>
  </DateRevised>
  <Frequency>74</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*VIRAL PROTEINS (1974-2004)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D036022</DescriptorUI>
     <DescriptorName>
      <String>Capsid Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D014027</DescriptorUI>
     <DescriptorName>
      <String>Tobacco Mosaic Virus</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Biochimie 56(1):181;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0054253</ConceptUI>
    <ConceptName>
     <String>H protein, Tobacco mosaic virus</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0054253</Concept1UI>
     <Concept2UI>M0054251</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T084256</TermUI>
      <String>H protein, Tobacco mosaic virus</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T084255</TermUI>
      <String>H protein, TMV</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0054251</ConceptUI>
    <ConceptName>
     <String>TMV coat protein, Tobacco mosaic virus</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0054253</Concept1UI>
     <Concept2UI>M0054251</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T084254</TermUI>
      <String>TMV coat protein, Tobacco mosaic virus</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C053335</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>FR 900482</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1987</Year>
   <Month>09</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>22</Day>
  </DateRevised>
  <Note>isolated from Streptomyces sandaensis; structure given in above source
  </Note>
  <Frequency>29</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>BICYCLO COMPOUNDS (87-88)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010078</DescriptorUI>
     <DescriptorName>
      <String>Oxazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiot (Tokyo) 1987;40(5):600</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0151069</ConceptUI>
    <ConceptName>
     <String>FR 900482</String>
    </ConceptName>
    <CASN1Name>3,9-Epoxy-3H-azirino(2,3-c)(1)benzazocine-5-carboxaldehyde, 8-(((aminocarbonyl)oxy)methyl)-1,1a,2,8,9,9a-hexahydro-7,9-dihydroxy-</CASN1Name>
    <RegistryNumber>102363-08-6</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0151069</Concept1UI>
     <Concept2UI>M0151067</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T181074</TermUI>
      <String>FR 900482</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T181073</TermUI>
      <String>FR-900482</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T432357</TermUI>
      <String>FR900482</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>01</Month>
       <Day>04</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0151067</ConceptUI>
    <ConceptName>
     <String>4-formyl-6,9-dihydroxy-14-oxa-1,11-diazatetracyclo(7.4.1.O(2,7).O(10,12))tetradeca-2,4,6-triene-8-ylmethyl carbamate</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0151069</Concept1UI>
     <Concept2UI>M0151067</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T181072</TermUI>
      <String>4-formyl-6,9-dihydroxy-14-oxa-1,11-diazatetracyclo(7.4.1.O(2,7).O(10,12))tetradeca-2,4,6-triene-8-ylmethyl carbamate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C021354</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hexose oxidase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>16</Day>
  </DateRevised>
  <Frequency>12</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>HEXOSES (73-83)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000429</DescriptorUI>
     <DescriptorName>
      <String>Alcohol Oxidoreductases</String>
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   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0076099</ConceptUI>
    <ConceptName>
     <String>hexose oxidase</String>
    </ConceptName>
    <RegistryNumber>EC 1.1.3.5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T106102</TermUI>
      <String>hexose oxidase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C021356</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hippurate hydrolase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>16</Day>
  </DateRevised>
  <Frequency>6</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>HIPPURATES (74-83)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000581</DescriptorUI>
     <DescriptorName>
      <String>Amidohydrolases</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Experentia 29(12):1573;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0076107</ConceptUI>
    <ConceptName>
     <String>hippurate hydrolase</String>
    </ConceptName>
    <RegistryNumber>EC 3.5.1.32</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T106110</TermUI>
      <String>hippurate hydrolase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C039889</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>L 611744</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1984</Year>
   <Month>01</Month>
   <Day>19</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>22</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009593</DescriptorUI>
     <DescriptorName>
      <String>Nitroimidazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Trans R Soc Trop Med Hyg 1983;77(5):693</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0119103</ConceptUI>
    <ConceptName>
     <String>L 611744</String>
    </ConceptName>
    <RegistryNumber>58211-94-2</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0119103</Concept1UI>
     <Concept2UI>M0119100</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T149107</TermUI>
      <String>L 611744</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1984)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T149106</TermUI>
      <String>L611,744</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1984)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T149105</TermUI>
      <String>L-611744</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1984)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0119100</ConceptUI>
    <ConceptName>
     <String>3a,4,5,6,7,8,9,9a-octahydro-3-(1-methyl-5-nitroimidazol-2-yl)cycloocta(d)isoxazole</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0119103</Concept1UI>
     <Concept2UI>M0119100</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T149104</TermUI>
      <String>3a,4,5,6,7,8,9,9a-octahydro-3-(1-methyl-5-nitroimidazol-2-yl)cycloocta(d)isoxazole</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1984)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C032238</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tetranitrosylruthenate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>12</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>06</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>structure given in first source; RN given refers to di-Na salt
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*RUTHENIUM (81-93)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D017975</DescriptorUI>
     <DescriptorName>
      <String>Ruthenium Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Radioisotopes 1981;30(4):205</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0100732</ConceptUI>
    <ConceptName>
     <String>tetranitrosylruthenate</String>
    </ConceptName>
    <CASN1Name>Ruthenate(2-), hydroxytetrakis(nitrito-N)nitrosyl-, disodium</CASN1Name>
    <RegistryNumber>13859-66-0</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>14167-09-0 (di-K salt)</RelatedRegistryNumber>
     <RelatedRegistryNumber>56960-14-6 (106 Ru labeled di-Na Salt)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0100732</Concept1UI>
     <Concept2UI>M0319502</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0100732</Concept1UI>
     <Concept2UI>M0100731</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0100732</Concept1UI>
     <Concept2UI>M0319503</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T130736</TermUI>
      <String>tetranitrosylruthenate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0319502</ConceptUI>
    <ConceptName>
     <String>tetranitrosylruthenate dipotassium salt</String>
    </ConceptName>
    <RegistryNumber>14167-09-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0100732</Concept1UI>
     <Concept2UI>M0319502</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T349502</TermUI>
      <String>tetranitrosylruthenate dipotassium salt</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0100731</ConceptUI>
    <ConceptName>
     <String>sodium tetranitrosylruthenate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0100732</Concept1UI>
     <Concept2UI>M0100731</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T130735</TermUI>
      <String>sodium tetranitrosylruthenate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0319503</ConceptUI>
    <ConceptName>
     <String>tetranitrosylruthenate sodium salt, (106)Ru-labeled</String>
    </ConceptName>
    <RegistryNumber>56960-14-6</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0100732</Concept1UI>
     <Concept2UI>M0319503</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T349503</TermUI>
      <String>tetranitrosylruthenate sodium salt, (106)Ru-labeled</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C021372</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>horseradish apoperoxidase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>28</Day>
  </DateRevised>
  <Frequency>4</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>APOENZYMES (78-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006735</DescriptorUI>
     <DescriptorName>
      <String>Horseradish Peroxidase</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Dokladi Akad Nauk SSSR 241(4):977;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0076155</ConceptUI>
    <ConceptName>
     <String>horseradish apoperoxidase</String>
    </ConceptName>
    <RegistryNumber>EC 1.11.1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T106158</TermUI>
      <String>horseradish apoperoxidase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C061005</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-methyl-2-((4-aminophenyl)sulfonyl)amino-5-nitroimidazole</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1989</Year>
   <Month>10</Month>
   <Day>16</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>22</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>8</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009593</DescriptorUI>
     <DescriptorName>
      <String>Nitroimidazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013449</DescriptorUI>
     <DescriptorName>
      <String>Sulfonamides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Boll Chim Farm 1989;128(2):71</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0169238</ConceptUI>
    <ConceptName>
     <String>1-methyl-2-((4-aminophenyl)sulfonyl)amino-5-nitroimidazole</String>
    </ConceptName>
    <RegistryNumber>132151-84-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T199243</TermUI>
      <String>1-methyl-2-((4-aminophenyl)sulfonyl)amino-5-nitroimidazole</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T199241</TermUI>
      <String>sulfimidazole</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T199242</TermUI>
      <String>sulphimidazole</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T199240</TermUI>
      <String>MASAN</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C021382</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-hydroxy amine sulfurtransferase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>HYDROXYLAMINES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013466</DescriptorUI>
     <DescriptorName>
      <String>Sulfurtransferases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Res 36(7):2353;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0076192</ConceptUI>
    <ConceptName>
     <String>N-hydroxy amine sulfurtransferase</String>
    </ConceptName>
    <RegistryNumber>EC 2.8.1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T106195</TermUI>
      <String>N-hydroxy amine sulfurtransferase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C021383</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-hydroxyaminoquinoline-1-oxide reductase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>4-HYDROXYAMINOQUINOLINE-1-OXIDE (78-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009247</DescriptorUI>
     <DescriptorName>
      <String>NADH, NADPH Oxidoreductases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Pharm Bull 26(2):497;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0076193</ConceptUI>
    <ConceptName>
     <String>4-hydroxyaminoquinoline-1-oxide reductase</String>
    </ConceptName>
    <RegistryNumber>EC 1.6.6.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T106196</TermUI>
      <String>4-hydroxyaminoquinoline-1-oxide reductase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C070047</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-hexadecyl-N-(9-octadecenyl)-N,N-dimethylammonium</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1991</Year>
   <Month>08</Month>
   <Day>25</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>05</Month>
   <Day>17</Day>
  </DateRevised>
  <Note>fluorescent probe for phospholipids; RN &amp; structure given in first source; RN given refers to chloride; RN for parent cpd not avail 8/91
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000644</DescriptorUI>
     <DescriptorName>
      <String>Quaternary Ammonium Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 1991;30(30):7491</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0190952</ConceptUI>
    <ConceptName>
     <String>N-hexadecyl-N-(9-octadecenyl)-N,N-dimethylammonium</String>
    </ConceptName>
    <RegistryNumber>134311-09-4</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0190952</Concept1UI>
     <Concept2UI>M0190951</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T220957</TermUI>
      <String>N-hexadecyl-N-(9-octadecenyl)-N,N-dimethylammonium</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0190951</ConceptUI>
    <ConceptName>
     <String>N-hexadecyl-N-(9-octadecenyl)-N,N-dimethylammonium chloride</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0190952</Concept1UI>
     <Concept2UI>M0190951</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T220956</TermUI>
      <String>N-hexadecyl-N-(9-octadecenyl)-N,N-dimethylammonium chloride</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T220955</TermUI>
      <String>9-HODMA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C043445</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-propyl-7-hydroxy-1,2,3,4a,5,6-hexahydronaphthoxazine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1984</Year>
   <Month>12</Month>
   <Day>17</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>22</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010078</DescriptorUI>
     <DescriptorName>
      <String>Oxazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Pharmacol 1984;36(9):639</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0127869</ConceptUI>
    <ConceptName>
     <String>4-propyl-7-hydroxy-1,2,3,4a,5,6-hexahydronaphthoxazine</String>
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    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0127869</Concept1UI>
     <Concept2UI>M0127867</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T157874</TermUI>
      <String>4-propyl-7-hydroxy-1,2,3,4a,5,6-hexahydronaphthoxazine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1984)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T157871</TermUI>
      <String>7-PHHNO</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1984)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0127867</ConceptUI>
    <ConceptName>
     <String>N 0499</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0127869</Concept1UI>
     <Concept2UI>M0127867</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T157872</TermUI>
      <String>N 0499</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1984)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T157873</TermUI>
      <String>N-0499</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1984)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C021390</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-hydroxycholanate dehydrogenase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>reduce keto groups to hydroxyl groups reversibly
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*HYDROXYSTEROID DEHYDROGENASES (76-80)</PreviousIndexing>
   <PreviousIndexing>CHOLIC ACIDS (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015096</DescriptorUI>
     <DescriptorName>
      <String>3-Hydroxysteroid Dehydrogenases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer 36(Conference Suppl 6):2387;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0076215</ConceptUI>
    <ConceptName>
     <String>3-hydroxycholanate dehydrogenase</String>
    </ConceptName>
    <RegistryNumber>EC 1.1.1.52</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T106218</TermUI>
      <String>3-hydroxycholanate dehydrogenase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C512320</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>v-ATPase subunit a1, rat</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>08</Month>
   <Day>09</Day>
  </DateCreated>
  <Note>alternative splicing controls neuronal expression of v-ATPase subunit a1 and sorting to nerve terminals
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D025262</DescriptorUI>
     <DescriptorName>
      <String>Vacuolar Proton-Translocating ATPases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D021122</DescriptorUI>
     <DescriptorName>
      <String>Protein Subunits</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Biol Chem 2006 Jun 23;281(25):17164-72</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0500609</ConceptUI>
    <ConceptName>
     <String>v-ATPase subunit a1, rat</String>
    </ConceptName>
    <RegistryNumber>EC 3.6.1.</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T679353</TermUI>
      <String>v-ATPase subunit a1, rat</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>08</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T679354</TermUI>
      <String>v-ATPase a1 subunit, rat</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>08</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C021395</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>trans-4-hydroxycyclohexanecarboxylic acid dehydrogenase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CYCLOHEXANECARBOXYLIC ACIDS (78-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000429</DescriptorUI>
     <DescriptorName>
      <String>Alcohol Oxidoreductases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Bacteriol 134(2):401;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0076232</ConceptUI>
    <ConceptName>
     <String>trans-4-hydroxycyclohexanecarboxylic acid dehydrogenase</String>
    </ConceptName>
    <RegistryNumber>EC 1.1.1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T106235</TermUI>
      <String>trans-4-hydroxycyclohexanecarboxylic acid dehydrogenase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C021396</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>omega-hydroxyfatty acid:NADP oxidoreductase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000429</DescriptorUI>
     <DescriptorName>
      <String>Alcohol Oxidoreductases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D006880</DescriptorUI>
     <DescriptorName>
      <String>Hydroxy Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Biochem Biophys 191(2):452;1978</Source>
   <Source>Arch Biochem Biophys 191(2):466;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0076233</ConceptUI>
    <ConceptName>
     <String>omega-hydroxyfatty acid:NADP oxidoreductase</String>
    </ConceptName>
    <RegistryNumber>EC 1.1.1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T106236</TermUI>
      <String>omega-hydroxyfatty acid:NADP oxidoreductase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C021393</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hydroxycinnamate-CoA ligase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>15</Day>
  </DateRevised>
  <Frequency>4</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CINNAMATES (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003066</DescriptorUI>
     <DescriptorName>
      <String>Coenzyme A Ligases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cytobiologie 17:433;1978</Source>
   <Source>FEBS Lett 42(2):131;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0076227</ConceptUI>
    <ConceptName>
     <String>hydroxycinnamate-CoA ligase</String>
    </ConceptName>
    <RegistryNumber>EC 6.2.1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T106230</TermUI>
      <String>hydroxycinnamate-CoA ligase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T106229</TermUI>
      <String>hydroxycinnamate-coenzyme A ligase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C021402</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hydroxylamine reductase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>30</Day>
  </DateRevised>
  <Frequency>21</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>HYDROXYLAMINES (73-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010088</DescriptorUI>
     <DescriptorName>
      <String>Oxidoreductases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0076244</ConceptUI>
    <ConceptName>
     <String>hydroxylamine reductase</String>
    </ConceptName>
    <RegistryNumber>EC 1.7.99.1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T106247</TermUI>
      <String>hydroxylamine reductase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C512323</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dipyrrolo(3,4-a:3,4-c)carbazole-1,3,4,6-tetraone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>08</Month>
   <Day>09</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002227</DescriptorUI>
     <DescriptorName>
      <String>Carbazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011758</DescriptorUI>
     <DescriptorName>
      <String>Pyrroles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Bioorg Med Chem. 2006 Jun 1;14(11):3825-34</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0500614</ConceptUI>
    <ConceptName>
     <String>dipyrrolo(3,4-a:3,4-c)carbazole-1,3,4,6-tetraone</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T679361</TermUI>
      <String>dipyrrolo(3,4-a:3,4-c)carbazole-1,3,4,6-tetraone</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>08</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T679362</TermUI>
      <String>DPC-T cpd</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>08</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C021407</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6-hydroxymethylbenzo(alpha)pyrene synthetase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>07</Month>
   <Day>17</Day>
  </DateRevised>
  <Note>catalyzes hydroxymethylation of benzo(alpha)pyrene to the 16-hydroxymethyl derivative
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*TRANSFERASES (76-97)</PreviousIndexing>
   <PreviousIndexing>BENZOPYRENES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D019877</DescriptorUI>
     <DescriptorName>
      <String>Hydroxymethyl and Formyl Transferases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Biochem Biophys 186(2):401;1978</Source>
   <Source>Cancer Res 35(12):3731;1975</Source>
   <Source>Carcinogenesis I W1 CA7624:p171;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0076251</ConceptUI>
    <ConceptName>
     <String>6-hydroxymethylbenzo(alpha)pyrene synthetase</String>
    </ConceptName>
    <RegistryNumber>EC 2.1.2.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T106254</TermUI>
      <String>6-hydroxymethylbenzo(alpha)pyrene synthetase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C021408</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-(4'-hydroxy-3'-methylbut-2'-enyl)-L-tryptophan synthetase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>11</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>enzymatic synthesis of above cpd from isopentenylpyrophosphate &amp; tryptophan
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ALCOHOLS, AMYL (78-82)</PreviousIndexing>
   <PreviousIndexing>TRYPTOPHAN (78-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008025</DescriptorUI>
     <DescriptorName>
      <String>Ligases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>FEBS Lett 82(1):55;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0076252</ConceptUI>
    <ConceptName>
     <String>4-(4'-hydroxy-3'-methylbut-2'-enyl)-L-tryptophan synthetase</String>
    </ConceptName>
    <RegistryNumber>EC 6.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T106255</TermUI>
      <String>4-(4'-hydroxy-3'-methylbut-2'-enyl)-L-tryptophan synthetase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C021409</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-hydroxymethyldeoxycytidylate kinase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1993</Year>
   <Month>08</Month>
   <Day>18</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PHOSPHOTRANSFERASES (72-74)</PreviousIndexing>
   <PreviousIndexing>*PHOSPHOTRANSFERASES, ATP (74-80)</PreviousIndexing>
   <PreviousIndexing>CYTIDINE MONOPHOSPHATE/analogs (75-82)</PreviousIndexing>
   <PreviousIndexing>CYTOSINE NUCLEOTIDES (72-80)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009703</DescriptorUI>
     <DescriptorName>
      <String>Nucleoside-Phosphate Kinase</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0076253</ConceptUI>
    <ConceptName>
     <String>5-hydroxymethyldeoxycytidylate kinase</String>
    </ConceptName>
    <RegistryNumber>EC 2.7.4.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T106256</TermUI>
      <String>5-hydroxymethyldeoxycytidylate kinase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C106237</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>PrsE protein, Rhizobium leguminosarum</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1997</Year>
   <Month>06</Month>
   <Day>20</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>01</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>prs - protein secretion; isolated from Rhizobium leguminosarum; amino acid sequence in first source; GenBank U44387
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D018528</DescriptorUI>
     <DescriptorName>
      <String>ATP-Binding Cassette Transporters</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Microbiology 1997 Apr;143( Pt 4):1389-94</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0276901</ConceptUI>
    <ConceptName>
     <String>PrsE protein, Rhizobium leguminosarum</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T306906</TermUI>
      <String>PrsE protein, Rhizobium leguminosarum</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C512322</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>(2R)-2-(3'-phosphonobicyclo(1.1.1)pentyl)glycine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>08</Month>
   <Day>09</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>08</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001643</DescriptorUI>
     <DescriptorName>
      <String>Bridged Bicyclo Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005998</DescriptorUI>
     <DescriptorName>
      <String>Glycine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Bioorg Med Chem. 2006 Jun 1;14(11):3811-7</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0500612</ConceptUI>
    <ConceptName>
     <String>(2R)-2-(3'-phosphonobicyclo(1.1.1)pentyl)glycine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0500612</Concept1UI>
     <Concept2UI>M0500613</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T679359</TermUI>
      <String>(2R)-2-(3'-phosphonobicyclo(1.1.1)pentyl)glycine</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>08</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0500613</ConceptUI>
    <ConceptName>
     <String>(2S)-2-(3'-phosphonobicyclo(1.1.1)pentyl)glycine</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0500612</Concept1UI>
     <Concept2UI>M0500613</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T679360</TermUI>
      <String>(2S)-2-(3'-phosphonobicyclo(1.1.1)pentyl)glycine</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>08</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C021413</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6-hydroxy-D-nicotine oxidase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>06</Month>
   <Day>02</Day>
  </DateRevised>
  <Frequency>35</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*OXIDOREDUCTASES, N-DEMETHYLATING (73-76)</PreviousIndexing>
   <PreviousIndexing>NICOTINE (73-76)</PreviousIndexing>
   <PreviousIndexing>NICOTINE/analogs (76-80)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010088</DescriptorUI>
     <DescriptorName>
      <String>Oxidoreductases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Microbiol 119(1):65;1978</Source>
   <Source>Eur J Biochem 29(1):143;1972</Source>
   <Source>Eur J Biochem 92(2):449;1978</Source>
   <Source>Eur J Biochem1980;104(2):391</Source>
   <Source>FEBS Lett 86(2):243;1978</Source>
   <Source>Horiz Biochem Biophys 1:62;1974</Source>
   <Source>J Biol Chem 250(19):7747;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0076270</ConceptUI>
    <ConceptName>
     <String>6-hydroxy-D-nicotine oxidase</String>
    </ConceptName>
    <RegistryNumber>EC 1.5.3.6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T106273</TermUI>
      <String>6-hydroxy-D-nicotine oxidase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C512324</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Ixodidin, Boophilus microplus</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>08</Month>
   <Day>09</Day>
  </DateCreated>
  <Note>antimicrobial peptide from the hemocytes of the cattle tick Boophilus microplus with inhibitory activity against serine proteinases; amino acid sequence in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D023181</DescriptorUI>
     <DescriptorName>
      <String>Antimicrobial Cationic Peptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Peptides 2006 Apr;27(4):667-74</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0500615</ConceptUI>
    <ConceptName>
     <String>Ixodidin, Boophilus microplus</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T679363</TermUI>
      <String>Ixodidin, Boophilus microplus</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>08</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T679364</TermUI>
      <String>Ixodidin, B microplus</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>08</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C512325</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>urotensin II receptor, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>08</Month>
   <Day>09</Day>
  </DateCreated>
  <Note>G-protein-coupled receptor that binds urotensin II; RefSeq NM_145440
  </Note>
  <Frequency>19</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D043562</DescriptorUI>
     <DescriptorName>
      <String>Receptors, G-Protein-Coupled</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Peptides 2006 Apr;27(4):858-63</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0500616</ConceptUI>
    <ConceptName>
     <String>urotensin II receptor, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T679365</TermUI>
      <String>urotensin II receptor, mouse</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>08</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T679367</TermUI>
      <String>urotensin 2 receptor, mouse</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>08</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T679366</TermUI>
      <String>Uts2r protein, mouse</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>08</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C025014</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-oxa-4,5,6-nor-(3,7-inter)-3-phenyleneprostaglandin E1 methyl ester</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>06</Month>
   <Day>26</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>10</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000527</DescriptorUI>
     <DescriptorName>
      <String>Alprostadil</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D011459</DescriptorUI>
     <DescriptorName>
      <String>Prostaglandins E, Synthetic</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Steroids 1980;19(1):123</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0083890</ConceptUI>
    <ConceptName>
     <String>3-oxa-4,5,6-nor-(3,7-inter)-3-phenyleneprostaglandin E1 methyl ester</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T113893</TermUI>
      <String>3-oxa-4,5,6-nor-(3,7-inter)-3-phenyleneprostaglandin E1 methyl ester</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T113892</TermUI>
      <String>OI-PGE1-methyl ester</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T113891</TermUI>
      <String>3-oxa-4,5,6-nor-3,7-inter-m-phenylene-PGE1 methyl ester</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C094228</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>polyandrol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>07</Month>
   <Day>21</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>08</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>quassinoid isolated from root bark of Castela polyandra; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BENZOPYRANS (95)</PreviousIndexing>
   <PreviousIndexing>*BICYCLO COMPOUNDS (95)</PreviousIndexing>
   <PreviousIndexing>GLAUCARUBIN/*AA (1995-2002)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D036702</DescriptorUI>
     <DescriptorName>
      <String>Quassins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D029641</DescriptorUI>
     <DescriptorName>
      <String>Simaroubaceae</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Phytochemistry 1995 Apr;38(6):1463-5</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0248285</ConceptUI>
    <ConceptName>
     <String>polyandrol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T278290</TermUI>
      <String>polyandrol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C024976</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>12-hydroxymethyl-7-methylbenz(a)anthracene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>07</Month>
   <Day>09</Day>
  </DateCreated>
  <DateRevised>
   <Year>1984</Year>
   <Month>08</Month>
   <Day>16</Day>
  </DateRevised>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D015127</DescriptorUI>
     <DescriptorName>
      <String>9,10-Dimethyl-1,2-benzanthracene</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 1980;93(3):782</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0083795</ConceptUI>
    <ConceptName>
     <String>12-hydroxymethyl-7-methylbenz(a)anthracene</String>
    </ConceptName>
    <CASN1Name>Benz(a)anthracene-12-methanol, 7-methyl-</CASN1Name>
    <RegistryNumber>568-70-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T113798</TermUI>
      <String>12-hydroxymethyl-7-methylbenz(a)anthracene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C047028</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dicarboxylic acid-CoA oxidase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1985</Year>
   <Month>12</Month>
   <Day>03</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>23</Day>
  </DateRevised>
  <Note>oxidizes dicarboxylic acid CoA esters using molecular oxygen &amp; producing hydrogen peroxide, ultimately producing a dicarboxylic acid with 2 fewer carbon atoms
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010088</DescriptorUI>
     <DescriptorName>
      <String>Oxidoreductases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem J 1985;230(3):683</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0135993</ConceptUI>
    <ConceptName>
     <String>dicarboxylic acid-CoA oxidase</String>
    </ConceptName>
    <RegistryNumber>EC 1.3.3.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T165998</TermUI>
      <String>dicarboxylic acid-CoA oxidase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T165997</TermUI>
      <String>dicarboxylyl-CoA oxidase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T165996</TermUI>
      <String>dicarboxylic acid-coenzyme A oxidase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C024981</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cysteine decarboxylase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>07</Month>
   <Day>10</Day>
  </DateCreated>
  <Frequency>8</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002262</DescriptorUI>
     <DescriptorName>
      <String>Carboxy-Lyases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Cell Biochem 1980;30(1):7</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0083804</ConceptUI>
    <ConceptName>
     <String>cysteine decarboxylase</String>
    </ConceptName>
    <RegistryNumber>EC 4.1.1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T113807</TermUI>
      <String>cysteine decarboxylase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C077171</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>HIVEP2 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1992</Year>
   <Month>11</Month>
   <Day>05</Day>
  </DateCreated>
  <DateRevised>
   <Year>2013</Year>
   <Month>05</Month>
   <Day>15</Day>
  </DateRevised>
  <Note>RefSeq NM_006734
  </Note>
  <Frequency>47</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004268</DescriptorUI>
     <DescriptorName>
      <String>DNA-Binding Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014157</DescriptorUI>
     <DescriptorName>
      <String>Transcription Factors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D008285</DescriptorUI>
     <DescriptorName>
      <String>Major Histocompatibility Complex</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D016335</DescriptorUI>
     <DescriptorName>
      <String>Zinc Fingers</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Proc Natl Acad Sci U S A 1992 Oct 1;89(19):8971-5</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0207341</ConceptUI>
    <ConceptName>
     <String>HIVEP2 protein, human</String>
    </ConceptName>
    <RegistryNumber>148770-78-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T576590</TermUI>
      <String>HIVEP2 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>03</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T610332</TermUI>
      <String>HIV-enhancer binding protein EP2, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T610331</TermUI>
      <String>HIV-EP2 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>21</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T576591</TermUI>
      <String>human immunodeficiency virus type I enhancer binding protein 2, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>03</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T237345</TermUI>
      <String>MHC-binding protein 2, human</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T594479</TermUI>
      <String>MIBP1 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T594480</TermUI>
      <String>Myc-intron-binding peptide, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T844160</TermUI>
      <String>schnurri-2 protein, human</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>05</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T594481</TermUI>
      <String>c-myc intron binding protein 1, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>02</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T237346</TermUI>
      <String>major histocompatibility complex-binding protein 2, human</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010015</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>beta-aletheine oxalate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*MERCAPTOETHYLAMINES (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000409</DescriptorUI>
     <DescriptorName>
      <String>Alanine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Physiol Chem Phys 7(2):115;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055232</ConceptUI>
    <ConceptName>
     <String>beta-aletheine oxalate</String>
    </ConceptName>
    <CASN1Name>3-amino-N-(2-mercaptoethyl)propionamide oxalate</CASN1Name>
    <RegistryNumber>6170-04-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085235</TermUI>
      <String>beta-aletheine oxalate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010018</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>althiomycin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>02</Month>
   <Day>15</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013844</DescriptorUI>
     <DescriptorName>
      <String>Thiazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiotics 27(11):897;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055237</ConceptUI>
    <ConceptName>
     <String>althiomycin</String>
    </ConceptName>
    <RegistryNumber>12656-40-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085240</TermUI>
      <String>althiomycin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010022</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-amino-3-methylguanidine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>AMINES (75-78)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008760</DescriptorUI>
     <DescriptorName>
      <String>Methylguanidine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Kitasato Arch Exp Med 46(3-4):43;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055241</ConceptUI>
    <ConceptName>
     <String>1-amino-3-methylguanidine</String>
    </ConceptName>
    <RegistryNumber>31106-59-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085244</TermUI>
      <String>1-amino-3-methylguanidine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010023</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-amino-3-phenylisocarbostyril</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007546</DescriptorUI>
     <DescriptorName>
      <String>Isoquinolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Soc Jpn 94(10):1322;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055242</ConceptUI>
    <ConceptName>
     <String>2-amino-3-phenylisocarbostyril</String>
    </ConceptName>
    <RegistryNumber>54613-38-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085245</TermUI>
      <String>2-amino-3-phenylisocarbostyril</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C055484</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>BRL 34778</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1988</Year>
   <Month>05</Month>
   <Day>11</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>structure given in first source; potent and specific dopamine D2 receptor antagonist
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BICYCLO COMPOUNDS (88-95)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001549</DescriptorUI>
     <DescriptorName>
      <String>Benzamides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D019086</DescriptorUI>
     <DescriptorName>
      <String>Bridged Bicyclo Compounds, Heterocyclic</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Psychopharmacology 1988;94(3):350</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0156206</ConceptUI>
    <ConceptName>
     <String>BRL 34778</String>
    </ConceptName>
    <CASN1Name>Benzamide, 4-amino-5-chloro-N-(9-((4-fluorophenyl)methyl)-9-azabicyclo(3.3.1)non-3-yl)-2-methoxy-, exo-</CASN1Name>
    <RegistryNumber>86580-77-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0156206</Concept1UI>
     <Concept2UI>M0156204</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T186211</TermUI>
      <String>BRL 34778</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T186210</TermUI>
      <String>BRL-34778</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0156204</ConceptUI>
    <ConceptName>
     <String>4-amino-5-chloro-2-methoxy-N-(9-(fluorophenylmethyl)-9-azabicyclo(3.3.1)non-3-yl)benzamide</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0156206</Concept1UI>
     <Concept2UI>M0156204</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T186209</TermUI>
      <String>4-amino-5-chloro-2-methoxy-N-(9-(fluorophenylmethyl)-9-azabicyclo(3.3.1)non-3-yl)benzamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C516039</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Me-BP7033</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>01</Month>
   <Day>10</Day>
  </DateCreated>
  <Note>analog of BP7033 that inhibits angiogenesis and growth of human epidermoid carcinoma xenograft in nude mice; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001592</DescriptorUI>
     <DescriptorName>
      <String>Benzyl Alcohols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004164</DescriptorUI>
     <DescriptorName>
      <String>Diphosphonates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Anticancer Drugs 2006 Apr;17(4):479-85</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0505366</ConceptUI>
    <ConceptName>
     <String>Me-BP7033</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0505366</Concept1UI>
     <Concept2UI>M0505367</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T689077</TermUI>
      <String>Me-BP7033</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>01</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0505367</ConceptUI>
    <ConceptName>
     <String>(1-hydroxy-1-(hydroxymethoxyphosphoryl)-2-phenylethyl)phosphonic acid</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0505366</Concept1UI>
     <Concept2UI>M0505367</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T689078</TermUI>
      <String>(1-hydroxy-1-(hydroxymethoxyphosphoryl)-2-phenylethyl)phosphonic acid</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>01</Month>
       <Day>10</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010037</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>atropine-N-octylbromide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1969</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ATROPINE (69-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001286</DescriptorUI>
     <DescriptorName>
      <String>Atropine Derivatives</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Jpn J Smooth Muscle Res 10(3):219;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055273</ConceptUI>
    <ConceptName>
     <String>atropine-N-octylbromide</String>
    </ConceptName>
    <RegistryNumber>5843-82-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085276</TermUI>
      <String>atropine-N-octylbromide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1969)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C581065</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Fam129b protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>05</Month>
   <Day>15</Day>
  </DateCreated>
  <Note>RefSeq NM_146119
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010750</DescriptorUI>
     <DescriptorName>
      <String>Phosphoproteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biochem. 2012 Dec;152(6):549-55</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0584767</ConceptUI>
    <ConceptName>
     <String>Fam129b protein, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T844162</TermUI>
      <String>Fam129b protein, mouse</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>05</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T844164</TermUI>
      <String>family with sequence similarity 129, member B, mouse</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>05</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T844163</TermUI>
      <String>Minerva protein, mouse</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>05</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010039</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-aziridinecarboxamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>AZIRIDINES (75-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014508</DescriptorUI>
     <DescriptorName>
      <String>Urea</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Exp Zool 192(1):73;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055276</ConceptUI>
    <ConceptName>
     <String>1-aziridinecarboxamide</String>
    </ConceptName>
    <CASN1Name>1,1-ethyleneurea</CASN1Name>
    <RegistryNumber>3715-65-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085279</TermUI>
      <String>1-aziridinecarboxamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C073197</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-((methylsulfonyl)amino)-N-((4-phenylpiperazin-2-yl)methyl)benzamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1992</Year>
   <Month>03</Month>
   <Day>31</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>RN given refers to parent cpd; RN &amp; structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001549</DescriptorUI>
     <DescriptorName>
      <String>Benzamides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010879</DescriptorUI>
     <DescriptorName>
      <String>Piperazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 1992 Feb 21;35(4):743-50</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0197993</ConceptUI>
    <ConceptName>
     <String>4-((methylsulfonyl)amino)-N-((4-phenylpiperazin-2-yl)methyl)benzamide</String>
    </ConceptName>
    <RegistryNumber>135036-03-2</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>135036-12-3 (HCl)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0197993</Concept1UI>
     <Concept2UI>M0325602</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T227998</TermUI>
      <String>4-((methylsulfonyl)amino)-N-((4-phenylpiperazin-2-yl)methyl)benzamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T227997</TermUI>
      <String>4-MAPPMB</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0325602</ConceptUI>
    <ConceptName>
     <String>4-((methylsulfonyl)amino)-N-((4-phenylpiperazin-2-yl)methyl)benzamide hydrochloride</String>
    </ConceptName>
    <RegistryNumber>135036-12-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0197993</Concept1UI>
     <Concept2UI>M0325602</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T355602</TermUI>
      <String>4-((methylsulfonyl)amino)-N-((4-phenylpiperazin-2-yl)methyl)benzamide hydrochloride</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C084477</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,3-dimethoxy-N-(1-(4-fluorobenzyl)piperidin-4-yl)benzamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1993</Year>
   <Month>12</Month>
   <Day>27</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>structure given in first source; has affinity for D2 receptors
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001549</DescriptorUI>
     <DescriptorName>
      <String>Benzamides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010880</DescriptorUI>
     <DescriptorName>
      <String>Piperidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D005462</DescriptorUI>
     <DescriptorName>
      <String>Fluorine Radioisotopes</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Med Chem 1993 Nov 12;36(23):3707-20</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0224410</ConceptUI>
    <ConceptName>
     <String>2,3-dimethoxy-N-(1-(4-fluorobenzyl)piperidin-4-yl)benzamide</String>
    </ConceptName>
    <RegistryNumber>152128-14-8</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0224410</Concept1UI>
     <Concept2UI>M0224408</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T254415</TermUI>
      <String>2,3-dimethoxy-N-(1-(4-fluorobenzyl)piperidin-4-yl)benzamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T254414</TermUI>
      <String>2,3-DiMeO-FBzPB</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0224408</ConceptUI>
    <ConceptName>
     <String>(18F)MBP</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0224410</Concept1UI>
     <Concept2UI>M0224408</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T254413</TermUI>
      <String>(18F)MBP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C581066</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>zinc finger protein 141, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>05</Month>
   <Day>15</Day>
  </DateCreated>
  <Note>RefSeq NM_003441
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004268</DescriptorUI>
     <DescriptorName>
      <String>DNA-Binding Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D016335</DescriptorUI>
     <DescriptorName>
      <String>Zinc Fingers</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Med Genet. 2013 Jan;50(1);47-53</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0584768</ConceptUI>
    <ConceptName>
     <String>zinc finger protein 141, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T844165</TermUI>
      <String>zinc finger protein 141, human</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>05</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T844166</TermUI>
      <String>ZNF141 protein, human</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>05</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010048</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bis(hexafluoroacetonyl)acetone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>11</Month>
   <Day>09</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*HYDROCARBONS, FLUORINATED (75-77)</PreviousIndexing>
   <PreviousIndexing>ACETONE/analogs (75-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005466</DescriptorUI>
     <DescriptorName>
      <String>Fluorocarbons</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>FEBS Lett 52(1):30;1975</Source>
   <Source>J Biol Chem 1980;255(8):3245</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055290</ConceptUI>
    <ConceptName>
     <String>bis(hexafluoroacetonyl)acetone</String>
    </ConceptName>
    <RegistryNumber>30902-53-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085293</TermUI>
      <String>bis(hexafluoroacetonyl)acetone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011117</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>sulfoglycolipids</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>includes sulfuric acid esters of glycolipids other than ceramides
  </Note>
  <Frequency>115</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006017</DescriptorUI>
     <DescriptorName>
      <String>Glycolipids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D013433</DescriptorUI>
     <DescriptorName>
      <String>Sulfoglycosphingolipids</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Postepy Biochem 21(3):319;1975</Source>
   <Source>Seikagaku 50(3):145;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057162</ConceptUI>
    <ConceptName>
     <String>sulfoglycolipids</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087165</TermUI>
      <String>sulfoglycolipids</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T087164</TermUI>
      <String>sulfated glycolipids</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010054</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,3-butanedione trimer</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>prepared from diacetyl; structure
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DIOXOLES (75-79)</PreviousIndexing>
   <PreviousIndexing>FURANS (75-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003931</DescriptorUI>
     <DescriptorName>
      <String>Diacetyl</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Can J Biochem 53(3):275;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055300</ConceptUI>
    <ConceptName>
     <String>2,3-butanedione trimer</String>
    </ConceptName>
    <CASN1Name>Ethanone, 1,1'-(tetrahydro-6a-hydroxy-2,3a,5-trimethylfuro(2,3-d)-1,3-dioxole-2,5-diyl)bis-</CASN1Name>
    <RegistryNumber>18114-49-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0055300</Concept1UI>
     <Concept2UI>M0055298</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0055300</Concept1UI>
     <Concept2UI>M0055299</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085303</TermUI>
      <String>2,3-butanedione trimer</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0055298</ConceptUI>
    <ConceptName>
     <String>2,3-diacetyl-3 alpha,5,6,6 alpha-tetrahydro-6 alpha-hydroxy-2,3 alpha,5-trimethylfuro(2,3-d)-1,3-dioxile</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0055300</Concept1UI>
     <Concept2UI>M0055298</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085301</TermUI>
      <String>2,3-diacetyl-3 alpha,5,6,6 alpha-tetrahydro-6 alpha-hydroxy-2,3 alpha,5-trimethylfuro(2,3-d)-1,3-dioxile</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0055299</ConceptUI>
    <ConceptName>
     <String>diacetyl trimer</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0055300</Concept1UI>
     <Concept2UI>M0055299</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085302</TermUI>
      <String>diacetyl trimer</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010058</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>canavaninosuccinic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>01</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SUCCINATES (75-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002172</DescriptorUI>
     <DescriptorName>
      <String>Canavanine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Anal Biochem 65(1-2):60;1975</Source>
   <Source>Clin Chem 21(12):1777;1975</Source>
   <Source>Comp Biochem Physiol 52(1):105;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055302</ConceptUI>
    <ConceptName>
     <String>canavaninosuccinic acid</String>
    </ConceptName>
    <RegistryNumber>24764-65-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085305</TermUI>
      <String>canavaninosuccinic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010066</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-(4'-carboxyphenylazo)estriol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>01</Month>
   <Day>19</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>AZO COMPOUNDS (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004964</DescriptorUI>
     <DescriptorName>
      <String>Estriol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Clin Endocrinol Metab 40(6):970;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055313</ConceptUI>
    <ConceptName>
     <String>2-(4'-carboxyphenylazo)estriol</String>
    </ConceptName>
    <CASN1Name>Benzoic acid, 4-(((16alpha,17beta)-3,16,17-trihydroxyestra-1,3,5(10)-trien-2-yl)azo)-</CASN1Name>
    <RegistryNumber>57266-76-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085316</TermUI>
      <String>2-(4'-carboxyphenylazo)estriol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010077</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>chloromercuriferrocene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>08</Month>
   <Day>15</Day>
  </DateRevised>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*MERCURY (75-79)</PreviousIndexing>
   <PreviousIndexing>*ORGANOMETALLIC COMPOUNDS (75-82)</PreviousIndexing>
   <PreviousIndexing>CYCLOPENTANES (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009941</DescriptorUI>
     <DescriptorName>
      <String>Organomercury Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Histochem Cytochem 23(5):390;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055325</ConceptUI>
    <ConceptName>
     <String>chloromercuriferrocene</String>
    </ConceptName>
    <RegistryNumber>1273-75-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085328</TermUI>
      <String>chloromercuriferrocene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C116903</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>des-4-amino-3-I(125)iodozacopride</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1999</Year>
   <Month>02</Month>
   <Day>04</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001549</DescriptorUI>
     <DescriptorName>
      <String>Benzamides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D019086</DescriptorUI>
     <DescriptorName>
      <String>Bridged Bicyclo Compounds, Heterocyclic</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharmacol Exp Ther 1999 Jan;288(1):221-31</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0300331</ConceptUI>
    <ConceptName>
     <String>des-4-amino-3-I(125)iodozacopride</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T330336</TermUI>
      <String>des-4-amino-3-I(125)iodozacopride</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T330335</TermUI>
      <String>I(125)DAIZAC</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T330334</TermUI>
      <String>(S)des-4-amino-3-I(125)iodozacopride</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010079</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-chloro-2-pyrimidinyl dantrolene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>01</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DANTROLENE/analogs (75-80)</PreviousIndexing>
   <PreviousIndexing>PYRIMIDINES (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003620</DescriptorUI>
     <DescriptorName>
      <String>Dantrolene</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 64(2):337;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055330</ConceptUI>
    <ConceptName>
     <String>5-chloro-2-pyrimidinyl dantrolene</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0055330</Concept1UI>
     <Concept2UI>M0055329</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085333</TermUI>
      <String>5-chloro-2-pyrimidinyl dantrolene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0055329</ConceptUI>
    <ConceptName>
     <String>1-((5-(5-chloro-2-pyrimidinyl)furfurylidene)amino)hydantoin</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0055330</Concept1UI>
     <Concept2UI>M0055329</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085332</TermUI>
      <String>1-((5-(5-chloro-2-pyrimidinyl)furfurylidene)amino)hydantoin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010107</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,8-dibenzylcyclooctanone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>07</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>RN given refers to cpd without isomeric designation; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>BENZYL COMPOUNDS (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003516</DescriptorUI>
     <DescriptorName>
      <String>Cycloparaffins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Pharmacol 25(13):1537;1976</Source>
   <Source>J Pharm Sci 64(2):235;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055378</ConceptUI>
    <ConceptName>
     <String>2,8-dibenzylcyclooctanone</String>
    </ConceptName>
    <RegistryNumber>38104-15-3</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>34403-32-2 ((cis)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>34403-33-3 ((trans)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0055378</Concept1UI>
     <Concept2UI>M0311046</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0055378</Concept1UI>
     <Concept2UI>M0311045</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085381</TermUI>
      <String>2,8-dibenzylcyclooctanone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0311046</ConceptUI>
    <ConceptName>
     <String>2,8-dibenzylcyclooctanone, (trans)-isomer</String>
    </ConceptName>
    <RegistryNumber>34403-33-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0055378</Concept1UI>
     <Concept2UI>M0311046</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T341046</TermUI>
      <String>2,8-dibenzylcyclooctanone, (trans)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0311045</ConceptUI>
    <ConceptName>
     <String>2,8-dibenzylcyclooctanone, (cis)-isomer</String>
    </ConceptName>
    <RegistryNumber>34403-32-2</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0055378</Concept1UI>
     <Concept2UI>M0311045</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T341045</TermUI>
      <String>2,8-dibenzylcyclooctanone, (cis)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C581067</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>GAT1_2.1 protein, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>05</Month>
   <Day>15</Day>
  </DateCreated>
  <Note>a class I glutamine amidotransferase that represses shoot branching
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D019884</DescriptorUI>
     <DescriptorName>
      <String>Nitrogenous Group Transferases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Plant Physiol. 2012 Dec;160(4):1770-80</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0584769</ConceptUI>
    <ConceptName>
     <String>GAT1_2.1 protein, Arabidopsis</String>
    </ConceptName>
    <RegistryNumber>EC 2.6.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T844167</TermUI>
      <String>GAT1_2.1 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>05</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010090</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>collinusin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1993</Year>
   <Month>10</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>lignan lactone extract from highly poisonous plant Cleitanthus collinus (Roxb); structure
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DIOXOLES (75-79)</PreviousIndexing>
   <PreviousIndexing>FURANS (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009281</DescriptorUI>
     <DescriptorName>
      <String>Naphthalenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D017705</DescriptorUI>
     <DescriptorName>
      <String>Lignans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Chromatogr 107(1):230;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055353</ConceptUI>
    <ConceptName>
     <String>collinusin</String>
    </ConceptName>
    <CASN1Name>9-(1,3-benzodioxol-5-yl)-3a,4-dihydro-6,7-dimethoxynaphtho(2,3-c)furan-1(3H)-one</CASN1Name>
    <RegistryNumber>17990-72-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085356</TermUI>
      <String>collinusin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010093</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cryptosporiopsin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>07</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>fungitoxic metabolite from Phialophora asteris f.sp. helianthi; structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003517</DescriptorUI>
     <DescriptorName>
      <String>Cyclopentanes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Experientia 32(3):331;1976</Source>
   <Source>J Can Biochem 53(2):149;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055356</ConceptUI>
    <ConceptName>
     <String>cryptosporiopsin</String>
    </ConceptName>
    <CASN1Name>3,5-dichloro-1-hydroxy-4-oxo-2-(1-propenyl)-2-cyclopentene-1-carboxylic acid methyl ester</CASN1Name>
    <RegistryNumber>25707-30-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085359</TermUI>
      <String>cryptosporiopsin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010094</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cystathionine sulfoxide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>03</Day>
  </DateRevised>
  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>SULFOXIDES (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003540</DescriptorUI>
     <DescriptorName>
      <String>Cystathionine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Physiol Chem Phys 7(2):147;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055357</ConceptUI>
    <ConceptName>
     <String>cystathionine sulfoxide</String>
    </ConceptName>
    <RegistryNumber>54927-81-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085360</TermUI>
      <String>cystathionine sulfoxide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C007206</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-cyclopropylmethyl-5-dimethyl-7-methoxybenzazepine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>07</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CYCLOPROPANES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001552</DescriptorUI>
     <DescriptorName>
      <String>Benzazepines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Jap J Pharmacol (Suppl) 24:86;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0050250</ConceptUI>
    <ConceptName>
     <String>N-cyclopropylmethyl-5-dimethyl-7-methoxybenzazepine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0050250</Concept1UI>
     <Concept2UI>M0050249</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T080253</TermUI>
      <String>N-cyclopropylmethyl-5-dimethyl-7-methoxybenzazepine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T080251</TermUI>
      <String>CPM-DM-MB</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0050249</ConceptUI>
    <ConceptName>
     <String>N-cyclopropylmethyl-5-dimethyl-7-methoxybenzazepine hydrochloride</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0050250</Concept1UI>
     <Concept2UI>M0050249</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T080252</TermUI>
      <String>N-cyclopropylmethyl-5-dimethyl-7-methoxybenzazepine hydrochloride</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010103</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>depochlormadinone acetate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1995</Year>
   <Month>07</Month>
   <Day>27</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ACETIC ACIDS (75-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002715</DescriptorUI>
     <DescriptorName>
      <String>Chlormadinone Acetate</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Obstet Gynecol 1975 Apr;45(4):443-50</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055373</ConceptUI>
    <ConceptName>
     <String>depochlormadinone acetate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085376</TermUI>
      <String>depochlormadinone acetate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011228</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dihydrocubebin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>extract of leaves of Piper guineense Schum. &amp; Thonn.; structure
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ALCOHOL, PROPYL/*analogs (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004148</DescriptorUI>
     <DescriptorName>
      <String>Dioxolanes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D017705</DescriptorUI>
     <DescriptorName>
      <String>Lignans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 38(4):343;1975</Source>
   <Source>J Nat Prod 39(1):60;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057360</ConceptUI>
    <ConceptName>
     <String>dihydrocubebin</String>
    </ConceptName>
    <CASN1Name>1,4-Butanediol, 2,3-bis(1,3-benzodioxol-5-ylmethyl)-, (R-(R*,R*))-</CASN1Name>
    <RegistryNumber>24563-03-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087363</TermUI>
      <String>dihydrocubebin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T087362</TermUI>
      <String>1,4-Butanediol, 2,3-bis(1,3-benzodioxol-5-ylmethyl)-, (R*,R*)-(-)-</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010106</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>diacetylaminocyclohexenone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>04</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CYCLOHEXYLAMINES (75-79)</PreviousIndexing>
   <PreviousIndexing>CYCLOHEXYLAMINES (79-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003512</DescriptorUI>
     <DescriptorName>
      <String>Cyclohexanones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Vopr Virusol 1:75;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055377</ConceptUI>
    <ConceptName>
     <String>diacetylaminocyclohexenone</String>
    </ConceptName>
    <RegistryNumber>17578-85-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085380</TermUI>
      <String>diacetylaminocyclohexenone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C411204</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dendronesterol B</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>07</Month>
   <Day>26</Day>
  </DateCreated>
  <Note>a polyhydroxylated sterol from the octocoral Dendronephthya gigantea; structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013261</DescriptorUI>
     <DescriptorName>
      <String>Sterols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2000 May;63(5):670-2</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0366672</ConceptUI>
    <ConceptName>
     <String>dendronesterol B</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T420011</TermUI>
      <String>dendronesterol B</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>07</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010108</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>O,S-dicarbethoxythiamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ETHYL ETHERS (75-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013831</DescriptorUI>
     <DescriptorName>
      <String>Thiamine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>ORL 36(6):344;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055379</ConceptUI>
    <ConceptName>
     <String>O,S-dicarbethoxythiamine</String>
    </ConceptName>
    <CASN1Name>O,S-bis(ethoxycarbonyl)thiamine</CASN1Name>
    <RegistryNumber>137-76-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085382</TermUI>
      <String>O,S-dicarbethoxythiamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C050770</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>phoU protein, E coli</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1986</Year>
   <Month>12</Month>
   <Day>22</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>05</Month>
   <Day>14</Day>
  </DateRevised>
  <Note>Phosphate transport system protein; negative DNA-binding transcriptional regulator for high affinity phosphate uptake, under phosphate excess PhoU downregulates the PHO regulon; MW 27 kDa; from E coli K-12; located in cytoplasm &amp; inner membrane; Do not confuse with N-methyl-N-2-(methylsulfinyl)ethylpropionic acid amide (NMPA)
  </Note>
  <Frequency>21</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BACTERIAL PROTEINS (1986-2003)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014157</DescriptorUI>
     <DescriptorName>
      <String>Transcription Factors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D026901</DescriptorUI>
     <DescriptorName>
      <String>Membrane Transport Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029968</DescriptorUI>
     <DescriptorName>
      <String>Escherichia coli Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Bacteriol 1986;168(2):631</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0144777</ConceptUI>
    <ConceptName>
     <String>phoU protein, E coli</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T540659</TermUI>
      <String>phoU protein, E coli</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>05</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T540660</TermUI>
      <String>phoT protein, E coli</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>05</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T540661</TermUI>
      <String>NmpA protein, E coli</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>05</Month>
       <Day>13</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C411205</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dendronesterol A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>07</Month>
   <Day>26</Day>
  </DateCreated>
  <Note>a polyhydroxylated sterol from the octocoral Dendronephthya gigantea; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013261</DescriptorUI>
     <DescriptorName>
      <String>Sterols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2000 May;63(5):670-2</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0366673</ConceptUI>
    <ConceptName>
     <String>dendronesterol A</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T420012</TermUI>
      <String>dendronesterol A</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>07</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011234</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3,11-dimethylnonacosanone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>contact courting pheromone in German cockroach
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007659</DescriptorUI>
     <DescriptorName>
      <String>Ketones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 40(23):3456;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057368</ConceptUI>
    <ConceptName>
     <String>3,11-dimethylnonacosanone</String>
    </ConceptName>
    <RegistryNumber>53623-10-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087371</TermUI>
      <String>3,11-dimethylnonacosanone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T087370</TermUI>
      <String>3,11,-dimethylnonacosan-2-one</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010122</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dimethyl-benz-dithionaphthene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>08</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>THIOPHENES (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009281</DescriptorUI>
     <DescriptorName>
      <String>Naphthalenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Cancer 11(1):1;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055408</ConceptUI>
    <ConceptName>
     <String>dimethyl-benz-dithionaphthene</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085411</TermUI>
      <String>dimethyl-benz-dithionaphthene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011280</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>7 alpha-hydroxy-5,11-diketotetranorprostane-1,16-dioic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>urinary metabolite of PGE
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011466</DescriptorUI>
     <DescriptorName>
      <String>Prostanoic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D011458</DescriptorUI>
     <DescriptorName>
      <String>Prostaglandins E</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000378</QualifierUI>
     <QualifierName>
      <String>metabolism</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Chromatogr 143(4):401;1977</Source>
   <Source>J Chromatogr 1980;181(1):85</Source>
   <Source>N E J Med 293(25):1278;1975</Source>
   <Source>Prostaglandins 12(5):785;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057458</ConceptUI>
    <ConceptName>
     <String>7 alpha-hydroxy-5,11-diketotetranorprostane-1,16-dioic acid</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087461</TermUI>
      <String>7 alpha-hydroxy-5,11-diketotetranorprostane-1,16-dioic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T087460</TermUI>
      <String>HDKNP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C046774</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Ro 22-8515</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1985</Year>
   <Month>11</Month>
   <Day>08</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>ligand used for benzodiazepine receptor binding
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001552</DescriptorUI>
     <DescriptorName>
      <String>Benzazepines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Pharmacol 1985;113(1):147</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0135380</ConceptUI>
    <ConceptName>
     <String>Ro 22-8515</String>
    </ConceptName>
    <RegistryNumber>89052-67-5</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0135380</Concept1UI>
     <Concept2UI>M0135378</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T165385</TermUI>
      <String>Ro 22-8515</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T165384</TermUI>
      <String>Ro-22-8515</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0135378</ConceptUI>
    <ConceptName>
     <String>8-chloro-6-(2-chlorophenyl)-1,4-dihydropyrrolo(3,4-D)(2)benzazepin-3-(2H)one</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0135380</Concept1UI>
     <Concept2UI>M0135378</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T165383</TermUI>
      <String>8-chloro-6-(2-chlorophenyl)-1,4-dihydropyrrolo(3,4-D)(2)benzazepin-3-(2H)one</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011285</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hydroxythreonine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>present in hydrolysate of actinomycin Z
  </Note>
  <Frequency>8</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013912</DescriptorUI>
     <DescriptorName>
      <String>Threonine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Antibiot (Tokyo) 27(12):952;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057468</ConceptUI>
    <ConceptName>
     <String>hydroxythreonine</String>
    </ConceptName>
    <CASN1Name>L-Threonic acid, 2-amino-3,4-dihydroxy-, (S-(R*,R*))-</CASN1Name>
    <RegistryNumber>21768-45-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087471</TermUI>
      <String>hydroxythreonine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T087470</TermUI>
      <String>alpha-amino-beta,gamma-dihydroxybutyric acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010131</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>distarch glycerol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>10</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>DIGLYCERIDES (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006017</DescriptorUI>
     <DescriptorName>
      <String>Glycolipids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Fd Cosmet Toxicol 12(2):201;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055420</ConceptUI>
    <ConceptName>
     <String>distarch glycerol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085423</TermUI>
      <String>distarch glycerol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C051269</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>BN 50341</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1987</Year>
   <Month>02</Month>
   <Day>26</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>antithrombotic platelet activating factor inhibitor
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001552</DescriptorUI>
     <DescriptorName>
      <String>Benzazepines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Agents Actions (Suppl) 1986;20:259</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0145962</ConceptUI>
    <ConceptName>
     <String>BN 50341</String>
    </ConceptName>
    <CASN1Name>3H-3-Benzazepine-3-propanamine, N-(2-(3,4-dimethoxyphenyl)ethyl)-1,2-dihydro-7,8-dimethoxy-N-methyl-1-phenyl-, monohydrochloride</CASN1Name>
    <RegistryNumber>107550-66-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0145962</Concept1UI>
     <Concept2UI>M0145960</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T175967</TermUI>
      <String>BN 50341</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T175966</TermUI>
      <String>BN-50341</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0145960</ConceptUI>
    <ConceptName>
     <String>1-phenyl-7,8-dimethoxy-(N-(3,4-dimethoxyphenethyl)-N-methyl)-3-propylamino-1H-3-benzazepine chlorhydrate monohydrate</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0145962</Concept1UI>
     <Concept2UI>M0145960</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T175965</TermUI>
      <String>1-phenyl-7,8-dimethoxy-(N-(3,4-dimethoxyphenethyl)-N-methyl)-3-propylamino-1H-3-benzazepine chlorhydrate monohydrate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010135</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>8-doxylpalmitoylcholine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>03</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CHOLINE/*analogs (75-81)</PreviousIndexing>
   <PreviousIndexing>PALMITIC ACIDS (75-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003497</DescriptorUI>
     <DescriptorName>
      <String>Cyclic N-Oxides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D013113</DescriptorUI>
     <DescriptorName>
      <String>Spin Labels</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Proc Nat Acad Sci USA 1975;72(3):1087</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055426</ConceptUI>
    <ConceptName>
     <String>8-doxylpalmitoylcholine</String>
    </ConceptName>
    <CASN1Name>8-(4',4'-dimethyloxazolidine-N-oxyl)palmitoylcholine</CASN1Name>
    <RegistryNumber>55620-99-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085429</TermUI>
      <String>8-doxylpalmitoylcholine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010136</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>androsta-2,4-diene-17 beta-ol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000737</DescriptorUI>
     <DescriptorName>
      <String>Androstenols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Steroids 25(5):673;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055427</ConceptUI>
    <ConceptName>
     <String>androsta-2,4-diene-17 beta-ol</String>
    </ConceptName>
    <CASN1Name>Androsta-2,4-dien-17-ol, (17beta)-</CASN1Name>
    <RegistryNumber>7244-00-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085430</TermUI>
      <String>androsta-2,4-diene-17 beta-ol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010148</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-ethyl-5-propyl-1-N-methylbarbituric acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001463</DescriptorUI>
     <DescriptorName>
      <String>Barbiturates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Pharmazie 308(4):313;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055444</ConceptUI>
    <ConceptName>
     <String>5-ethyl-5-propyl-1-N-methylbarbituric acid</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085447</TermUI>
      <String>5-ethyl-5-propyl-1-N-methylbarbituric acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010162</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>10-formyltetrahydropteroyl-gamma-glutamylglutamic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>11</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*TETRAHYDROFOLATES (75-76)</PreviousIndexing>
   <PreviousIndexing>FORMIC ACID ESTERS (75-76)</PreviousIndexing>
   <PreviousIndexing>GLUTAMATES (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005575</DescriptorUI>
     <DescriptorName>
      <String>Formyltetrahydrofolates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 14(11):2424;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055473</ConceptUI>
    <ConceptName>
     <String>10-formyltetrahydropteroyl-gamma-glutamylglutamic acid</String>
    </ConceptName>
    <CASN1Name>L-Glutamic acid, N-(N-(4-(((2-amino-1,4,5,6,7,8-hexahydro-4-oxo-6-pteridinyl)methyl)formylamino)benzoyl)-L-gamma-glutamyl)-</CASN1Name>
    <RegistryNumber>29552-62-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085476</TermUI>
      <String>10-formyltetrahydropteroyl-gamma-glutamylglutamic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010163</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Forssman glycolipid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1985</Year>
   <Month>04</Month>
   <Day>23</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>56</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CEREBROSIDES (74-79)</PreviousIndexing>
   <PreviousIndexing>*CEREBROSIDES (75-79)</PreviousIndexing>
   <PreviousIndexing>*GLYCOSPHINGOLIPIDS (74-83)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005915</DescriptorUI>
     <DescriptorName>
      <String>Globosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D005577</DescriptorUI>
     <DescriptorName>
      <String>Forssman Antigen</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Cancer Res 35(7):1723;1975</Source>
   <Source>J Biochem (Tokyo) 75(1):197;1974</Source>
   <Source>Jap J Exptl Med 45(4):293;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055478</ConceptUI>
    <ConceptName>
     <String>Forssman glycolipid</String>
    </ConceptName>
    <CASN1Name>Forssman globoside</CASN1Name>
    <RegistryNumber>60267-39-2</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0055478</Concept1UI>
     <Concept2UI>M0055474</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0055478</Concept1UI>
     <Concept2UI>M0055475</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0055478</Concept1UI>
     <Concept2UI>M0055477</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0055478</Concept1UI>
     <Concept2UI>M0055476</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085481</TermUI>
      <String>Forssman glycolipid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0055474</ConceptUI>
    <ConceptName>
     <String>GL-4</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0055478</Concept1UI>
     <Concept2UI>M0055474</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085477</TermUI>
      <String>GL-4</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0055475</ConceptUI>
    <ConceptName>
     <String>GL-5</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0055478</Concept1UI>
     <Concept2UI>M0055475</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085478</TermUI>
      <String>GL-5</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0055477</ConceptUI>
    <ConceptName>
     <String>para-Forssman glycolipid</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0055478</Concept1UI>
     <Concept2UI>M0055477</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085480</TermUI>
      <String>para-Forssman glycolipid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0055476</ConceptUI>
    <ConceptName>
     <String>globopentaosylceramide</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0055478</Concept1UI>
     <Concept2UI>M0055476</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085479</TermUI>
      <String>globopentaosylceramide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010167</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>galline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>protamine from rooster sperm nuclei
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011479</DescriptorUI>
     <DescriptorName>
      <String>Protamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Int J Peptide Protein Res 7(1):31;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055483</ConceptUI>
    <ConceptName>
     <String>galline</String>
    </ConceptName>
    <CASN1Name>Galline</CASN1Name>
    <RegistryNumber>52012-17-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085486</TermUI>
      <String>galline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010168</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>delta-globulin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012712</DescriptorUI>
     <DescriptorName>
      <String>Serum Globulins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Brit Poultry Sci 16(3):241;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055484</ConceptUI>
    <ConceptName>
     <String>delta-globulin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085487</TermUI>
      <String>delta-globulin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010181</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>herbadine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>related chemically to ajmaline; isolated from Vinca libanotica; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>INDOLES (75-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000404</DescriptorUI>
     <DescriptorName>
      <String>Ajmaline</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014748</DescriptorUI>
     <DescriptorName>
      <String>Vinca Alkaloids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharmaceut Sci 64(2):341;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055500</ConceptUI>
    <ConceptName>
     <String>herbadine</String>
    </ConceptName>
    <RegistryNumber>38485-12-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085503</TermUI>
      <String>herbadine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010248</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>mono(4-azobenzenearsonic acid)tyrosylphosphatidylethanolamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>26</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ARSENICALS (75-76)</PreviousIndexing>
   <PreviousIndexing>AZO COMPOUNDS (75-82)</PreviousIndexing>
   <PreviousIndexing>TYROSINE/analogs (75-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010714</DescriptorUI>
     <DescriptorName>
      <String>Phosphatidylethanolamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 14(11):2331;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055609</ConceptUI>
    <ConceptName>
     <String>mono(4-azobenzenearsonic acid)tyrosylphosphatidylethanolamine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085612</TermUI>
      <String>mono(4-azobenzenearsonic acid)tyrosylphosphatidylethanolamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085611</TermUI>
      <String>mono(4-azobenzenearsonic acid)tyrosyl-sn-glycero-3-phosphoethanolamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085610</TermUI>
      <String>MABATPE</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010190</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>allo-gamma-hydroxyglutamic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>27</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>HYDROXY ACIDS (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005971</DescriptorUI>
     <DescriptorName>
      <String>Glutamates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Med 44(4):438;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055512</ConceptUI>
    <ConceptName>
     <String>allo-gamma-hydroxyglutamic acid</String>
    </ConceptName>
    <CASN1Name>threo-4-hydroxy-L-glutamic acid</CASN1Name>
    <RegistryNumber>3913-68-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085515</TermUI>
      <String>allo-gamma-hydroxyglutamic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010191</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hydroxylunine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>06</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>alkaloid found in Ptelea trifoliata; structure
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*QUINOLINES (75-81)</PreviousIndexing>
   <PreviousIndexing>DIOXOLANES (75-76)</PreviousIndexing>
   <PreviousIndexing>FURANS (75-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000470</DescriptorUI>
     <DescriptorName>
      <String>Alkaloids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 38(2):109;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055513</ConceptUI>
    <ConceptName>
     <String>hydroxylunine</String>
    </ConceptName>
    <CASN1Name>1,3-Dioxolo(4,5-h)furo(2,3-b)quinolin-6(8H)-one, 7,10-dihydro-8-(1-hydroxy-1-methylethyl)-10-methyl-, (S)-</CASN1Name>
    <RegistryNumber>25488-60-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085516</TermUI>
      <String>hydroxylunine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C079365</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>technetium Tc 99m trihydrazidophosphine oxide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1993</Year>
   <Month>02</Month>
   <Day>22</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>26</Day>
  </DateRevised>
  <Note>cpd has excellent stability in both acqueous NaCl at neutral pH &amp; in human serum at 37C; may be used as a basis for the development of imaging agents; structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ORGANOPHOSPHORUS COMPOUNDS (93-97)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010720</DescriptorUI>
     <DescriptorName>
      <String>Phosphines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015609</DescriptorUI>
     <DescriptorName>
      <String>Organotechnetium Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nucl Biol Med 1992 Jul-Sep;36(3):296-300</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0212460</ConceptUI>
    <ConceptName>
     <String>technetium Tc 99m trihydrazidophosphine oxide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T242465</TermUI>
      <String>technetium Tc 99m trihydrazidophosphine oxide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T242464</TermUI>
      <String>Tc-99m-THP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T242463</TermUI>
      <String>99mTC THP</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010198</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Ildamen-Novodigal</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>contains beta-acetyldigoxin &amp; oxyfedrine
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>DIGOXIN/*analogs (75-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000113</DescriptorUI>
     <DescriptorName>
      <String>Acetyldigoxins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010099</DescriptorUI>
     <DescriptorName>
      <String>Oxyfedrine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ther Ggw 113(11):1921;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055525</ConceptUI>
    <ConceptName>
     <String>Ildamen-Novodigal</String>
    </ConceptName>
    <CASN1Name>3 beta-((O-4-O-acetyl-2,6-dideoxy-beta-D-ribo-hexopyranosyl-(1-4)-O-2,6-dideoxy-beta-D-ribo-hexopyranosyl-(1-4)-2,6-dideoxy-beta-D-ribo-hexopyranosyl)oxy)-12 beta,14-dihydroxy-5 beta-card-20(22)-enolide mixt. with 3-((2-hydroxy-1-methyl-2-phenyleth yl)amino)-1-(3-methoxyphenyl)-1-propanone.HCl</CASN1Name>
    <RegistryNumber>57607-36-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085528</TermUI>
      <String>Ildamen-Novodigal</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C009965</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>GD-131</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>26</Day>
  </DateRevised>
  <Note>inhibitor of extraneural uptake; RN given refers to parent cpd
  </Note>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CYCLOHEXANES (80-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004048</DescriptorUI>
     <DescriptorName>
      <String>Diethylamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Am J Physiol 228(6):1702;1975</Source>
   <Source>Br J Pharmacol 53(2):267;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055100</ConceptUI>
    <ConceptName>
     <String>GD-131</String>
    </ConceptName>
    <CASN1Name>N-(2-chloroethyl)-N-ethylcyclohexanemethanamine</CASN1Name>
    <RegistryNumber>3772-64-3</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>21658-44-6 (HCl)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0055100</Concept1UI>
     <Concept2UI>M0055099</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0055100</Concept1UI>
     <Concept2UI>M0310980</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T085103</TermUI>
      <String>GD-131</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085101</TermUI>
      <String>GD 131</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0055099</ConceptUI>
    <ConceptName>
     <String>N-cyclohexylmethyl-N-ethyl-beta-chloroethylamine</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0055100</Concept1UI>
     <Concept2UI>M0055099</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085102</TermUI>
      <String>N-cyclohexylmethyl-N-ethyl-beta-chloroethylamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0310980</ConceptUI>
    <ConceptName>
     <String>GD-131 hydrochloride</String>
    </ConceptName>
    <RegistryNumber>21658-44-6</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0055100</Concept1UI>
     <Concept2UI>M0310980</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T340980</TermUI>
      <String>GD-131 hydrochloride</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010202</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>iotetroxide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>EHTYL ETHERS (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007458</DescriptorUI>
     <DescriptorName>
      <String>Iodipamide</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Jpn J Clin Radiol 20(2):127;1975</Source>
   <Source>Jpn J Clin Radiol 21(6):497;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055533</ConceptUI>
    <ConceptName>
     <String>iotetroxide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085536</TermUI>
      <String>iotetroxide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010277</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Florox Reagent</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>04</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>reagent for analysis of ketosteroids; structure
  </Note>
  <Frequency>55</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>FLUOROBENZENES (75-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006898</DescriptorUI>
     <DescriptorName>
      <String>Hydroxylamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
    <PharmacologicalActionList>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D007202</DescriptorUI>
        <DescriptorName>
         <String>Indicators and Reagents</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
    </PharmacologicalActionList>
  <SourceList>
   <Source>J Chromatogr Sci 13(2):97;1975</Source>
   <Source>J Pharm Sci 65(4):625;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055662</ConceptUI>
    <ConceptName>
     <String>Florox Reagent</String>
    </ConceptName>
    <CASN1Name>Hydroxylamine, O-((pentafluorophenyl)methyl)-, hydrochloride</CASN1Name>
    <RegistryNumber>57981-02-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0055662</Concept1UI>
     <Concept2UI>M0055661</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0055662</Concept1UI>
     <Concept2UI>M0055656</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0055662</Concept1UI>
     <Concept2UI>M0055660</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="TRD"  RecordPreferredTermYN="Y">
      <TermUI>T085665</TermUI>
      <String>Florox Reagent</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0055661</ConceptUI>
    <ConceptName>
     <String>pentafluorobenzyloxylammonium</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0055662</Concept1UI>
     <Concept2UI>M0055661</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085664</TermUI>
      <String>pentafluorobenzyloxylammonium</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0055656</ConceptUI>
    <ConceptName>
     <String>O-(2,3,4,5,6-pentafluorobenzyl)hydroxylamine.HCl</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0055662</Concept1UI>
     <Concept2UI>M0055656</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085659</TermUI>
      <String>O-(2,3,4,5,6-pentafluorobenzyl)hydroxylamine.HCl</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085661</TermUI>
      <String>PFBHOX</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085660</TermUI>
      <String>PFBHA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0055660</ConceptUI>
    <ConceptName>
     <String>pentafluorobenzyloxylamine</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0055662</Concept1UI>
     <Concept2UI>M0055660</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085663</TermUI>
      <String>pentafluorobenzyloxylamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085662</TermUI>
      <String>PFBOA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C090758</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>diethylmethylamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>01</Month>
   <Day>03</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>26</Day>
  </DateRevised>
  <Frequency>7</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004048</DescriptorUI>
     <DescriptorName>
      <String>Diethylamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 1994 Dec 9;269(49):30869-79</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0239783</ConceptUI>
    <ConceptName>
     <String>diethylmethylamine</String>
    </ConceptName>
    <RegistryNumber>616-39-7</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>51211-54-2 (HCl)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0239783</Concept1UI>
     <Concept2UI>M0326788</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T269788</TermUI>
      <String>diethylmethylamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T269786</TermUI>
      <String>N-ethyl-N-methyl-ethylamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T269787</TermUI>
      <String>N-methyl-diethylamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0326788</ConceptUI>
    <ConceptName>
     <String>diethylmethylamine hydrochloride</String>
    </ConceptName>
    <RegistryNumber>51211-54-2</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0239783</Concept1UI>
     <Concept2UI>M0326788</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T356788</TermUI>
      <String>diethylmethylamine hydrochloride</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C082539</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SB 204144</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1993</Year>
   <Month>09</Month>
   <Day>06</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>26</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ORGANOPHOSPHORUS COMPOUNDS (93)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010721</DescriptorUI>
     <DescriptorName>
      <String>Phosphinic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014633</DescriptorUI>
     <DescriptorName>
      <String>Valine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 1993 Aug 10;32(31):7972-80</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0219897</ConceptUI>
    <ConceptName>
     <String>SB 204144</String>
    </ConceptName>
    <RegistryNumber>141396-10-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T249902</TermUI>
      <String>SB 204144</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T249901</TermUI>
      <String>SB204144</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T249900</TermUI>
      <String>SB-204144</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C117601</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>diazepam-binding inhibitor (51-70)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1999</Year>
   <Month>03</Month>
   <Day>10</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>26</Day>
  </DateRevised>
  <Note>amino acid sequence known
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009479</DescriptorUI>
     <DescriptorName>
      <String>Neuropeptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010446</DescriptorUI>
     <DescriptorName>
      <String>Peptide Fragments</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Neurosci Res 1998 Dec 1;54(5):673-80</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0301795</ConceptUI>
    <ConceptName>
     <String>diazepam-binding inhibitor (51-70)</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T331800</TermUI>
      <String>diazepam-binding inhibitor (51-70)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T331799</TermUI>
      <String>DBI (51-70)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010218</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-mercaptopolycytidylic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>06</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>4</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CYTOSINE NUCLEOTIDES (75-79)</PreviousIndexing>
   <PreviousIndexing>POLYNUCLEOTIDES (75-79)</PreviousIndexing>
   <PreviousIndexing>SULFHYDRYL COMPOUNDS (75-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011066</DescriptorUI>
     <DescriptorName>
      <String>Poly C</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013873</DescriptorUI>
     <DescriptorName>
      <String>Thionucleotides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 1979;18(25):5630</Source>
   <Source>FEBS Lett 53(1):10;1975</Source>
   <Source>QZ 200.3 N101a:528;1978</Source>
   <Source>QZ 200.3 N101a:577;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055563</ConceptUI>
    <ConceptName>
     <String>5-mercaptopolycytidylic acid</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0055563</Concept1UI>
     <Concept2UI>M0055562</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0055563</Concept1UI>
     <Concept2UI>M0055560</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0055563</Concept1UI>
     <Concept2UI>M0055561</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085566</TermUI>
      <String>5-mercaptopolycytidylic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0055562</ConceptUI>
    <ConceptName>
     <String>thiolated polycytidylic acid</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0055563</Concept1UI>
     <Concept2UI>M0055562</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085565</TermUI>
      <String>thiolated polycytidylic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0055560</ConceptUI>
    <ConceptName>
     <String>mercapto-poly C</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0055563</Concept1UI>
     <Concept2UI>M0055560</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085563</TermUI>
      <String>mercapto-poly C</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0055561</ConceptUI>
    <ConceptName>
     <String>thiolated poly C</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0055563</Concept1UI>
     <Concept2UI>M0055561</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085564</TermUI>
      <String>thiolated poly C</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C052269</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>L protein, lizard</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1987</Year>
   <Month>06</Month>
   <Day>03</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>MW 19 kD; major androgen-dependent protein of lizard epididymis
  </Note>
  <Frequency>4</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*Proteins (1987-2005)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D030162</DescriptorUI>
     <DescriptorName>
      <String>Reptilian Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D008116</DescriptorUI>
     <DescriptorName>
      <String>Lizards</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Biol Cell 1986;58(3):201</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0148428</ConceptUI>
    <ConceptName>
     <String>L protein, lizard</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T178433</TermUI>
      <String>L protein, lizard</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010225</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-methyl-3-carbomethoxy-piperidone-4</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>METHYL ETHERS (75-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010881</DescriptorUI>
     <DescriptorName>
      <String>Piperidones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Pol Med Sci Hist Bull 15(5):417;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055569</ConceptUI>
    <ConceptName>
     <String>1-methyl-3-carbomethoxy-piperidone-4</String>
    </ConceptName>
    <RegistryNumber>13221-89-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085572</TermUI>
      <String>1-methyl-3-carbomethoxy-piperidone-4</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010226</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-methylcyclobarbital</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1994</Year>
   <Month>09</Month>
   <Day>19</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BARBITURATES (75-77)</PreviousIndexing>
   <PreviousIndexing>CYCLOBARBITAL/*analogs (78-94)</PreviousIndexing>
   <PreviousIndexing>CYCLOHEXANES (75-77)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001463</DescriptorUI>
     <DescriptorName>
      <String>Barbiturates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Pharm 308(4):308;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055570</ConceptUI>
    <ConceptName>
     <String>N-methylcyclobarbital</String>
    </ConceptName>
    <RegistryNumber>726-78-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085573</TermUI>
      <String>N-methylcyclobarbital</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C531298</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>apratoxin D</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2008</Year>
   <Month>09</Month>
   <Day>11</Day>
  </DateCreated>
  <Note>a potent cytotoxic cyclodepsipeptide from papua new guinea collections of the marine cyanobacteria Lyngbya majuscula and Lyngbya sordida; structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D047630</DescriptorUI>
     <DescriptorName>
      <String>Depsipeptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2008 Jun;71(6):1099-103</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0524691</ConceptUI>
    <ConceptName>
     <String>apratoxin D</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T725536</TermUI>
      <String>apratoxin D</String>
      <DateCreated>
       <Year>2008</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2008)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011012</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>lincospectin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Frequency>8</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>DRUG COMBINATIONS (76-88)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000198</DescriptorUI>
     <DescriptorName>
      <String>Spectinomycin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008034</DescriptorUI>
     <DescriptorName>
      <String>Lincomycin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Can J Comp Med 39(4):416;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0056992</ConceptUI>
    <ConceptName>
     <String>lincospectin</String>
    </ConceptName>
    <RegistryNumber>57456-42-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T086995</TermUI>
      <String>lincospectin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C512963</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Rps6ka1 protein, rat</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>09</Month>
   <Day>22</Day>
  </DateCreated>
  <Note>RefSeq NM_031107
  </Note>
  <Frequency>30</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D038744</DescriptorUI>
     <DescriptorName>
      <String>Ribosomal Protein S6 Kinases, 90-kDa</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0491939</ConceptUI>
    <ConceptName>
     <String>Rps6ka1 protein, rat</String>
    </ConceptName>
    <RegistryNumber>EC 2.7.11.1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T659637</TermUI>
      <String>Rps6ka1 protein, rat</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>11</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T659639</TermUI>
      <String>Rsk-1 protein, rat</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>11</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T659638</TermUI>
      <String>ribosomal protein S6 kinase polypeptide 1, rat</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>11</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C515097</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dehydrosilybin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>11</Month>
   <Day>28</Day>
  </DateCreated>
  <Note>inhibits cytochrome P450 1A1 catalytic activity; structure in first source
  </Note>
  <Frequency>24</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012838</DescriptorUI>
     <DescriptorName>
      <String>Silymarin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cell Biol Toxicol 2006 Mar;22(2):81-90</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0504272</ConceptUI>
    <ConceptName>
     <String>dehydrosilybin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T686786</TermUI>
      <String>dehydrosilybin</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>11</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011025</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>16-methylene-17 alpha-acetoxyprogesterone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006908</DescriptorUI>
     <DescriptorName>
      <String>Hydroxyprogesterones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Pharmazie 30(8):509;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057022</ConceptUI>
    <ConceptName>
     <String>16-methylene-17 alpha-acetoxyprogesterone</String>
    </ConceptName>
    <RegistryNumber>6815-51-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087025</TermUI>
      <String>16-methylene-17 alpha-acetoxyprogesterone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011026</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,3-methylenedioxynaphthalene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>DIOXOLANES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009281</DescriptorUI>
     <DescriptorName>
      <String>Naphthalenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Yakugaku Zasshi 95(4):439;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057023</ConceptUI>
    <ConceptName>
     <String>2,3-methylenedioxynaphthalene</String>
    </ConceptName>
    <RegistryNumber>269-43-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087026</TermUI>
      <String>2,3-methylenedioxynaphthalene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011027</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>16-methylene-17 alpha-hydroxyprogesterone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006908</DescriptorUI>
     <DescriptorName>
      <String>Hydroxyprogesterones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Pharmazie 30(8):506;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057024</ConceptUI>
    <ConceptName>
     <String>16-methylene-17 alpha-hydroxyprogesterone</String>
    </ConceptName>
    <CASN1Name>Pregn-4-ene-3,20-dione, 17-hydroxy-16-methylene-</CASN1Name>
    <RegistryNumber>3965-17-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087027</TermUI>
      <String>16-methylene-17 alpha-hydroxyprogesterone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011029</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>methyl-4-phenylmandelic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>metabolite of 4-isopropylbiphenyl responsible for nephrotoxicity
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008333</DescriptorUI>
     <DescriptorName>
      <String>Mandelic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Vet Pathol 12(1):69;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057028</ConceptUI>
    <ConceptName>
     <String>methyl-4-phenylmandelic acid</String>
    </ConceptName>
    <RegistryNumber>6244-54-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087031</TermUI>
      <String>methyl-4-phenylmandelic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011036</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>neoleucorite</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>phenol formaldehyde resin
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>FORMALDEHYDE/analogs (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012117</DescriptorUI>
     <DescriptorName>
      <String>Resins, Synthetic</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Gig Tr Prof Zabol 8:37;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057038</ConceptUI>
    <ConceptName>
     <String>neoleucorite</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087041</TermUI>
      <String>neoleucorite</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011037</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>nepetaefolin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>spiro dihydrofuran diterpene component of Leonotis nepetaefolia extract which showed antineoplastic action; structure
  </Note>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ANTINEOPLASTIC AGENTS (76-79)</PreviousIndexing>
   <PreviousIndexing>SPIRO COMPOUNDS (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004224</DescriptorUI>
     <DescriptorName>
      <String>Diterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Am Chem Soc 97(21):6236;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057039</ConceptUI>
    <ConceptName>
     <String>nepetaefolin</String>
    </ConceptName>
    <CASN1Name>Trispiro(furan-3(2H),2'(5'H)-furan-5',8''-(8H-4,8a)propano(1H-2)benzopyran-7''(3''H),2'''-oxiran)-3''-one, 5''-(acetyloxy)-3',4',4'',4''a,5'',6''-hexahydro-4''-methyl-, (4''S-(4''alpha,4''aalpha,5''beta,7''beta,8''alpha(S*),8''aalpha))-</CASN1Name>
    <RegistryNumber>29606-32-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087042</TermUI>
      <String>nepetaefolin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011040</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-nitrophenyl 4-sulfamylbenzoate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>12</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>SULFONAMIDES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009578</DescriptorUI>
     <DescriptorName>
      <String>Nitrobenzenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 66(3):949;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057048</ConceptUI>
    <ConceptName>
     <String>4-nitrophenyl 4-sulfamylbenzoate</String>
    </ConceptName>
    <CASN1Name>Benzoic acid, 4-(aminosulfonyl)-, 4-nitrophenyl ester</CASN1Name>
    <RegistryNumber>57230-00-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0057048</Concept1UI>
     <Concept2UI>M0057046</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0057048</Concept1UI>
     <Concept2UI>M0057045</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0057048</Concept1UI>
     <Concept2UI>M0057047</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087051</TermUI>
      <String>4-nitrophenyl 4-sulfamylbenzoate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0057046</ConceptUI>
    <ConceptName>
     <String>p-nitrophenyl p-sulfamylbenzoate</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0057048</Concept1UI>
     <Concept2UI>M0057046</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T087049</TermUI>
      <String>p-nitrophenyl p-sulfamylbenzoate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0057045</ConceptUI>
    <ConceptName>
     <String>4-nitrophenyl p-sulfamylbenzoate</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0057048</Concept1UI>
     <Concept2UI>M0057045</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T087048</TermUI>
      <String>4-nitrophenyl p-sulfamylbenzoate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0057047</ConceptUI>
    <ConceptName>
     <String>para-nitrophenyl p-sulfamylbenzoate</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0057048</Concept1UI>
     <Concept2UI>M0057047</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T087050</TermUI>
      <String>para-nitrophenyl p-sulfamylbenzoate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C524020</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Opalin protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>11</Month>
   <Day>05</Day>
  </DateCreated>
  <DateRevised>
   <Year>2008</Year>
   <Month>09</Month>
   <Day>11</Day>
  </DateRevised>
  <Note>RefSeq NM_033207
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009185</DescriptorUI>
     <DescriptorName>
      <String>Myelin Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D015415</DescriptorUI>
     <DescriptorName>
      <String>Biomarkers</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Neurochem 2007 Sep;102(5):1533-47</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0515236</ConceptUI>
    <ConceptName>
     <String>Opalin protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T709055</TermUI>
      <String>Opalin protein, human</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>11</Month>
       <Day>05</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T554032</TermUI>
      <String>transmembrane protein TMP10, human</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>10</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T554030</TermUI>
      <String>TMP10 protein, human</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>10</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T556856</TermUI>
      <String>transmembrane protein 10, human</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>11</Month>
       <Day>04</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T556855</TermUI>
      <String>TMEM10 protein, human</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>11</Month>
       <Day>04</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T554031</TermUI>
      <String>HTMP10 protein, human</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>10</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011044</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>norketobemidone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007540</DescriptorUI>
     <DescriptorName>
      <String>Isonipecotic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010636</DescriptorUI>
     <DescriptorName>
      <String>Phenols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Proc West Pharmacol Soc 18:298;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057059</ConceptUI>
    <ConceptName>
     <String>norketobemidone</String>
    </ConceptName>
    <RegistryNumber>15847-72-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087062</TermUI>
      <String>norketobemidone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011045</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Normacol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>27</Day>
  </DateRevised>
  <Note>sterculia bulk-forming agent
  </Note>
  <Frequency>6</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PLANTS, MEDICINAL (76-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010936</DescriptorUI>
     <DescriptorName>
      <String>Plant Extracts</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Br J Surg 62(8):657;1975</Source>
   <Source>Med Chim Dig 6(2):109;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057060</ConceptUI>
    <ConceptName>
     <String>Normacol</String>
    </ConceptName>
    <RegistryNumber>57828-29-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087063</TermUI>
      <String>Normacol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C114910</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Y1 protein, Dugesia japonica</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>10</Month>
   <Day>23</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>02</Month>
   <Day>27</Day>
  </DateRevised>
  <Note>Dj = Dugesia japonica; contains cold shock domain &amp; RG repeat motifs, targeted to sites of regeneration in planarians; amino acid sequence in first source; GenBank X99748
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006360</DescriptorUI>
     <DescriptorName>
      <String>Heat-Shock Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014157</DescriptorUI>
     <DescriptorName>
      <String>Transcription Factors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D012038</DescriptorUI>
     <DescriptorName>
      <String>Regeneration</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Dev Biol 1998 Sep 15;201(2):217-29</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0296117</ConceptUI>
    <ConceptName>
     <String>Y1 protein, Dugesia japonica</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T326122</TermUI>
      <String>Y1 protein, Dugesia japonica</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T326121</TermUI>
      <String>DjY1 protein, Dugesia japonica</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011058</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>pentafluorostannite sodium</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1994</Year>
   <Month>05</Month>
   <Day>13</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*FLUORIDES (75-77)</PreviousIndexing>
   <PreviousIndexing>*TIN (75-77)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014002</DescriptorUI>
     <DescriptorName>
      <String>Tin Fluorides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Toxicol Appl Pharmacol 33(1):21;1975</Source>
   <Source>Toxicol Appl Pharmacol 35(1):21;1976</Source>
   <Source>Toxicol Appl Pharmacol 37(2):363;1976</Source>
   <Source>Toxicol Appl Pharmacol 37(3):445;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057081</ConceptUI>
    <ConceptName>
     <String>pentafluorostannite sodium</String>
    </ConceptName>
    <CASN1Name>sodium mu-fluorotetrafluorodistannate(1-)</CASN1Name>
    <RegistryNumber>22578-17-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087084</TermUI>
      <String>pentafluorostannite sodium</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011059</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>pentagastrin meglumine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>04</Month>
   <Day>16</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008536</DescriptorUI>
     <DescriptorName>
      <String>Meglumine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010418</DescriptorUI>
     <DescriptorName>
      <String>Pentagastrin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Hepatogastroenterol (Stuttg) 22(4):256;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057082</ConceptUI>
    <ConceptName>
     <String>pentagastrin meglumine</String>
    </ConceptName>
    <CASN1Name>N-((1,1-dimethylethoxy)carbonyl)-beta-alanyl-L-tryptophyl-L-methionyl-L-alpha-aspartyl-L-phenyl alaninamide compd. with 1-deoxy-1-(methylamino)-D-glucitol</CASN1Name>
    <RegistryNumber>57448-84-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087085</TermUI>
      <String>pentagastrin meglumine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C500757</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>azukisaponin V</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>05</Month>
   <Day>26</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>05</Month>
   <Day>26</Day>
  </DateRevised>
  <Note>a saponin isolated from Melilotus elegans; structure in first source
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012503</DescriptorUI>
     <DescriptorName>
      <String>Saponins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Pharmazie. 2005 Apr;60(4):310-2</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0485262</ConceptUI>
    <ConceptName>
     <String>azukisaponin V</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T641690</TermUI>
      <String>azukisaponin V</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>05</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C500758</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>HOT protein, bacteriophage P1</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>05</Month>
   <Day>26</Day>
  </DateCreated>
  <Note>homolog of the theta subunit of E. coli DNA polymerase III; Databank PDB/1SE7
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004258</DescriptorUI>
     <DescriptorName>
      <String>DNA Polymerase III</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014764</DescriptorUI>
     <DescriptorName>
      <String>Viral Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Structure (Camb) 2004 Dec;12(12):2221-31</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0485263</ConceptUI>
    <ConceptName>
     <String>HOT protein, bacteriophage P1</String>
    </ConceptName>
    <RegistryNumber>EC 2.7.7.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T641691</TermUI>
      <String>HOT protein, bacteriophage P1</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>05</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011071</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>picramine-epsilon</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>08</Month>
   <Day>28</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009282</DescriptorUI>
     <DescriptorName>
      <String>Naphthalenesulfonates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Gig Sanit 2:115;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057097</ConceptUI>
    <ConceptName>
     <String>picramine-epsilon</String>
    </ConceptName>
    <CASN1Name>8-hydroxy-7-((2-hydroxy-3,5-dinitrophenyl)azo) 1,6-naphthalenedisulfonic acid</CASN1Name>
    <RegistryNumber>29844-04-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087100</TermUI>
      <String>picramine-epsilon</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011072</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>pillaromycin A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1995</Year>
   <Month>09</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>anthracycline glycoside; member of group with daunomycin &amp; adriamycin
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ANTIBIOTICS, ANTHRACYCLINE (89-95)</PreviousIndexing>
   <PreviousIndexing>ANTHRAQUINONES (76-79)</PreviousIndexing>
   <PreviousIndexing>NAPHTHACENES (80-88)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D018943</DescriptorUI>
     <DescriptorName>
      <String>Anthracyclines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Am Chem Soc 97(21):6250;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057098</ConceptUI>
    <ConceptName>
     <String>pillaromycin A</String>
    </ConceptName>
    <RegistryNumber>30361-37-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087101</TermUI>
      <String>pillaromycin A</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011074</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>plasminogen proactivator</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>23</Day>
  </DateRevised>
  <Frequency>15</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004792</DescriptorUI>
     <DescriptorName>
      <String>Enzyme Precursors</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010960</DescriptorUI>
     <DescriptorName>
      <String>Plasminogen Activators</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Jpn Chir 46(3):258;1977</Source>
   <Source>J Physiol Soc Jpn 36(8-9):368;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057101</ConceptUI>
    <ConceptName>
     <String>plasminogen proactivator</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087104</TermUI>
      <String>plasminogen proactivator</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011078</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>poly-alpha-cyanoglycine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>18</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*NITRILES (76-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005998</DescriptorUI>
     <DescriptorName>
      <String>Glycine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011108</DescriptorUI>
     <DescriptorName>
      <String>Polymers</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Science 190(4212):387;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057110</ConceptUI>
    <ConceptName>
     <String>poly-alpha-cyanoglycine</String>
    </ConceptName>
    <CASN1Name>Acetic acid, aminocyano-, homopolymer</CASN1Name>
    <RegistryNumber>57570-05-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087113</TermUI>
      <String>poly-alpha-cyanoglycine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011081</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>polyisoprenyl-beta-D-mannopyranosyl phosphates</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1993</Year>
   <Month>08</Month>
   <Day>25</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*HEXOSEPHOSPHATES (76-78)</PreviousIndexing>
   <PreviousIndexing>*TERPENES (76-78)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008358</DescriptorUI>
     <DescriptorName>
      <String>Mannose</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011103</DescriptorUI>
     <DescriptorName>
      <String>Polyisoprenyl Phosphate Monosaccharides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 250(20):8069;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057113</ConceptUI>
    <ConceptName>
     <String>polyisoprenyl-beta-D-mannopyranosyl phosphates</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087116</TermUI>
      <String>polyisoprenyl-beta-D-mannopyranosyl phosphates</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011082</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>polyprenyl monophosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>07</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>cpd not in Chemline 7/20/83
  </Note>
  <Frequency>7</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*TERPENES (76-79)</PreviousIndexing>
   <PreviousIndexing>PHOSPHATES, ORGANIC (76-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011106</DescriptorUI>
     <DescriptorName>
      <String>Polyisoprenyl Phosphates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Biochem Biophys 181(2):393;1977</Source>
   <Source>Biochem Biophys Res Commun 66(3):980;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057114</ConceptUI>
    <ConceptName>
     <String>polyprenyl monophosphate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087117</TermUI>
      <String>polyprenyl monophosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011083</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>polyproline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>05</Month>
   <Day>26</Day>
  </DateRevised>
  <Note>RN given refers to (L)-isomer
  </Note>
  <Frequency>634</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PROLINE (76-79)</PreviousIndexing>
   <PreviousIndexing>PROLINE/analogs (79-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010455</DescriptorUI>
     <DescriptorName>
      <String>Peptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biopolymers 15(1):15;1976</Source>
   <Source>Immunology 36(4):879;1979</Source>
   <Source>J Am Chem Soc 97(18):5100;1975</Source>
   <Source>Mol Immunol 1979;16(9):651</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057117</ConceptUI>
    <ConceptName>
     <String>polyproline</String>
    </ConceptName>
    <RegistryNumber>25191-13-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0057117</Concept1UI>
     <Concept2UI>M0057116</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0057117</Concept1UI>
     <Concept2UI>M0057115</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087120</TermUI>
      <String>polyproline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0057116</ConceptUI>
    <ConceptName>
     <String>poly(L-proline)</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0057117</Concept1UI>
     <Concept2UI>M0057116</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T087119</TermUI>
      <String>poly(L-proline)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0057115</ConceptUI>
    <ConceptName>
     <String>poly(DL-proline)</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0057117</Concept1UI>
     <Concept2UI>M0057115</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T087118</TermUI>
      <String>poly(DL-proline)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011091</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>prunuside</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>extract from Prunus japonica Thunb; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*GLYCOSIDES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005419</DescriptorUI>
     <DescriptorName>
      <String>Flavonoids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Soc Jpn 5(4):484;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057130</ConceptUI>
    <ConceptName>
     <String>prunuside</String>
    </ConceptName>
    <RegistryNumber>55835-08-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087133</TermUI>
      <String>prunuside</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011094</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>alpha-5-pyridoxalacetic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011730</DescriptorUI>
     <DescriptorName>
      <String>Pyridoxal</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Boll Soc Ital Biol Sper 50(23-24):2005;1975</Source>
   <Source>Experientia 31(9):1017;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057136</ConceptUI>
    <ConceptName>
     <String>alpha-5-pyridoxalacetic acid</String>
    </ConceptName>
    <RegistryNumber>16133-22-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087139</TermUI>
      <String>alpha-5-pyridoxalacetic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C418566</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>enediynol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>22</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011743</DescriptorUI>
     <DescriptorName>
      <String>Pyrimidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D053281</DescriptorUI>
     <DescriptorName>
      <String>Enediynes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Org Lett 2000 Nov 30;2(24):3761-4</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0376876</ConceptUI>
    <ConceptName>
     <String>enediynol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T433768</TermUI>
      <String>enediynol</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>01</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011109</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>serratimannan</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008070</DescriptorUI>
     <DescriptorName>
      <String>Lipopolysaccharides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Pharm Bull (Tokyo) 23(1):163;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057152</ConceptUI>
    <ConceptName>
     <String>serratimannan</String>
    </ConceptName>
    <CASN1Name>Serratimannan</CASN1Name>
    <RegistryNumber>52439-65-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087155</TermUI>
      <String>serratimannan</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011196</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-(4-chlorophenylsulfonyl)-2-imidazolidinone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>09</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SULFONES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007093</DescriptorUI>
     <DescriptorName>
      <String>Imidazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Yakugaku Zasshi 95(7):793;1975</Source>
   <Source>Yakugaku Zasshi 95(7):803;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057304</ConceptUI>
    <ConceptName>
     <String>1-(4-chlorophenylsulfonyl)-2-imidazolidinone</String>
    </ConceptName>
    <RegistryNumber>56524-75-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087307</TermUI>
      <String>1-(4-chlorophenylsulfonyl)-2-imidazolidinone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T087306</TermUI>
      <String>1-(p-chlorophenylsulfonyl)-2-imidazolidinone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011211</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dansyl-arginine-methylpiperidine amide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>05</Day>
  </DateRevised>
  <Frequency>6</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PIPERIDINES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D001120</DescriptorUI>
     <DescriptorName>
      <String>Arginine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Thromb Diath Haemorrh 34(1):347;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057325</ConceptUI>
    <ConceptName>
     <String>dansyl-arginine-methylpiperidine amide</String>
    </ConceptName>
    <CASN1Name>Piperazine, 1-(5-((aminoiminomethyl)amino)-2-(((5-(dimethylamino)-1-naphthalenyl)sulfonyl)amino)-1-oxopentyl)-4-methyl-, (S)-, diacetate</CASN1Name>
    <RegistryNumber>55381-97-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0057325</Concept1UI>
     <Concept2UI>M0057323</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087328</TermUI>
      <String>dansyl-arginine-methylpiperidine amide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T087327</TermUI>
      <String>dansyl-arginine-4-methylpiperidide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0057323</ConceptUI>
    <ConceptName>
     <String>No. 189</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0057325</Concept1UI>
     <Concept2UI>M0057323</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T087326</TermUI>
      <String>No. 189</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011148</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>RMI 61,144</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1994</Year>
   <Month>06</Month>
   <Day>22</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PIPERAZINES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003990</DescriptorUI>
     <DescriptorName>
      <String>Dibenzoxepins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arzneim Forsch (Drug Res) 25(9):1436;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057235</ConceptUI>
    <ConceptName>
     <String>RMI 61,144</String>
    </ConceptName>
    <CASN1Name>N-(8-methoxy-dibenzo(b,f)oxepin-10-yl)-N'-methylpiperazine maleate</CASN1Name>
    <RegistryNumber>56958-57-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087238</TermUI>
      <String>RMI 61,144</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011149</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>RMI 61,140</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1994</Year>
   <Month>06</Month>
   <Day>15</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PIPERAZINES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003990</DescriptorUI>
     <DescriptorName>
      <String>Dibenzoxepins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arzneim Forsch 25(9):1436;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057236</ConceptUI>
    <ConceptName>
     <String>RMI 61,140</String>
    </ConceptName>
    <CASN1Name>N-(8-chloro-dibenzo(b,f)oxepin-10-yl)-N'-methyl- piperazine maleate</CASN1Name>
    <RegistryNumber>24140-98-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087239</TermUI>
      <String>RMI 61,140</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011150</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>RMI 61,280</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1994</Year>
   <Month>06</Month>
   <Day>22</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PIPERAZINES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003990</DescriptorUI>
     <DescriptorName>
      <String>Dibenzoxepins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arzneim Forsch (Drug Res) 25(9):1436;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057237</ConceptUI>
    <ConceptName>
     <String>RMI 61,280</String>
    </ConceptName>
    <CASN1Name>N-(8-fluoro-dibenzo(b,f)oxepin-10-yl)-N'-methyl- piperazine maleate</CASN1Name>
    <RegistryNumber>57342-05-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087240</TermUI>
      <String>RMI 61,280</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011151</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>70026</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>06</Month>
   <Day>18</Day>
  </DateRevised>
  <Note>used for synchronizing estrus in rats
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>THIOSEMICARBAZONES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013876</DescriptorUI>
     <DescriptorName>
      <String>Thiophenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Reprod Fertil 44(3):421;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057238</ConceptUI>
    <ConceptName>
     <String>70026</String>
    </ConceptName>
    <CASN1Name>5-bromo-2-thienylethylketone</CASN1Name>
    <RegistryNumber>23576-95-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087241</TermUI>
      <String>70026</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011155</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3 beta-acetoxy-6-nitrocholestene-5</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002788</DescriptorUI>
     <DescriptorName>
      <String>Cholesterol Esters</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Steroids 26(2):251;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057245</ConceptUI>
    <ConceptName>
     <String>3 beta-acetoxy-6-nitrocholestene-5</String>
    </ConceptName>
    <RegistryNumber>1912-54-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087248</TermUI>
      <String>3 beta-acetoxy-6-nitrocholestene-5</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C010121</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Org NA13</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ANDROSTANES (75-80)</PreviousIndexing>
   <PreviousIndexing>DIMETHYLAMINES (75-77)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000732</DescriptorUI>
     <DescriptorName>
      <String>Androstanols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Brit J Pharmacol 54(1):3;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0055407</ConceptUI>
    <ConceptName>
     <String>Org NA13</String>
    </ConceptName>
    <RegistryNumber>18668-43-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T085410</TermUI>
      <String>Org NA13</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T085409</TermUI>
      <String>3 alpha-dimethylamino-5 alpha-androstan-2 beta-ol-17-one</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011160</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-(5'-adenosyl)-N'-(5'-thymidyl)azelaamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ADENSOINE/*analogs (76-88)</PreviousIndexing>
   <PreviousIndexing>THYMIDINES/*analogs (76-88)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015224</DescriptorUI>
     <DescriptorName>
      <String>Dideoxynucleosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ann N Y Acad Sci 255:332;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057255</ConceptUI>
    <ConceptName>
     <String>N-(5'-adenosyl)-N'-(5'-thymidyl)azelaamide</String>
    </ConceptName>
    <CASN1Name>Adenosine, 5'-amino-5'-deoxy-, 5'-amide with 5'-((8-carboxy-1-oxooctyl)amino)-5'-deoxythymidine</CASN1Name>
    <RegistryNumber>58461-78-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087258</TermUI>
      <String>N-(5'-adenosyl)-N'-(5'-thymidyl)azelaamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011163</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>allylpropylmalonylurea</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>used therapeutically for psychogenic headache
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014508</DescriptorUI>
     <DescriptorName>
      <String>Urea</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Munch Med Wschr 117:38;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057257</ConceptUI>
    <ConceptName>
     <String>allylpropylmalonylurea</String>
    </ConceptName>
    <RegistryNumber>7296-17-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087260</TermUI>
      <String>allylpropylmalonylurea</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011165</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-aminouridine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014529</DescriptorUI>
     <DescriptorName>
      <String>Uridine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Pharm Bull 23(4):844;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057259</ConceptUI>
    <ConceptName>
     <String>3-aminouridine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087262</TermUI>
      <String>3-aminouridine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011167</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>androstenedione 3-enol glucosiduronate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>11</Month>
   <Day>18</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>GLURONATES (76-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000735</DescriptorUI>
     <DescriptorName>
      <String>Androstenedione</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Pharm Bull (Tokyo) 22(11):2530;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057261</ConceptUI>
    <ConceptName>
     <String>androstenedione 3-enol glucosiduronate</String>
    </ConceptName>
    <CASN1Name>beta-D-Glucopyranosiduronic acid, 17-oxoandrosta-3,5-dien-3-yl</CASN1Name>
    <RegistryNumber>7649-05-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087264</TermUI>
      <String>androstenedione 3-enol glucosiduronate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011169</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>annulenone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001952</DescriptorUI>
     <DescriptorName>
      <String>Bridged-Ring Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Topic Current Chem 57:111;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057266</ConceptUI>
    <ConceptName>
     <String>annulenone</String>
    </ConceptName>
    <RegistryNumber>34070-63-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087269</TermUI>
      <String>annulenone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011192</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-(4-chlorophenyl)-beta-(4-hydroxymethylphenoxy)ethylurethane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>induced sulfhemoglobinemia
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014520</DescriptorUI>
     <DescriptorName>
      <String>Urethane</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Folia Pharmacol Jpn 71(4):351;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0057300</ConceptUI>
    <ConceptName>
     <String>N-(4-chlorophenyl)-beta-(4-hydroxymethylphenoxy)ethylurethane</String>
    </ConceptName>
    <CASN1Name>Carbamic acid, (4-chlorophenyl)-, 2-(4-(hydroxymethyl)phenoxy)ethyl ester</CASN1Name>
    <RegistryNumber>52073-58-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T087303</TermUI>
      <String>N-(4-chlorophenyl)-beta-(4-hydroxymethylphenoxy)ethylurethane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C433907</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2'-O-acetyl-27-deoxyactein</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>09</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>08</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>cyclolanostane from the roots of Cimicifuga foetida (Ranunculaceae); structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012503</DescriptorUI>
     <DescriptorName>
      <String>Saponins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014315</DescriptorUI>
     <DescriptorName>
      <String>Triterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2001 May;64(5):627-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0397210</ConceptUI>
    <ConceptName>
     <String>2'-O-acetyl-27-deoxyactein</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T459966</TermUI>
      <String>2'-O-acetyl-27-deoxyactein</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>09</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T507963</TermUI>
      <String>2'-O-acetyl-27-deoxy-actein</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>07</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014778</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>S-propylmercaptocysteine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003545</DescriptorUI>
     <DescriptorName>
      <String>Cysteine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Hokkaido J Med Sci 51(6):507;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063584</ConceptUI>
    <ConceptName>
     <String>S-propylmercaptocysteine</String>
    </ConceptName>
    <CASN1Name>L-Alanine, 3-(propyldithio)-</CASN1Name>
    <RegistryNumber>2280-26-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093587</TermUI>
      <String>S-propylmercaptocysteine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014790</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>quarelin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>contains dipyrone, drotaverine &amp; caffeine
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004177</DescriptorUI>
     <DescriptorName>
      <String>Dipyrone</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010208</DescriptorUI>
     <DescriptorName>
      <String>Papaverine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ther Hung 25(1):32;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063594</ConceptUI>
    <ConceptName>
     <String>quarelin</String>
    </ConceptName>
    <RegistryNumber>62201-28-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093597</TermUI>
      <String>quarelin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014791</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-quinolinecarbonitrile N-oxide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1986</Year>
   <Month>01</Month>
   <Day>17</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003497</DescriptorUI>
     <DescriptorName>
      <String>Cyclic N-Oxides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011804</DescriptorUI>
     <DescriptorName>
      <String>Quinolines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Yakugaku Zasshi 97(2):123;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063595</ConceptUI>
    <ConceptName>
     <String>3-quinolinecarbonitrile N-oxide</String>
    </ConceptName>
    <CASN1Name>3-Quinolinecarbonitrile, 1-oxide</CASN1Name>
    <RegistryNumber>63124-13-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093598</TermUI>
      <String>3-quinolinecarbonitrile N-oxide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C016289</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>carminazone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>17</Day>
  </DateRevised>
  <Note>RN given refers to (2S-cis)-isomer
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002360</DescriptorUI>
     <DescriptorName>
      <String>Carubicin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Antibiotiki 23(4):356;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0066206</ConceptUI>
    <ConceptName>
     <String>carminazone</String>
    </ConceptName>
    <CASN1Name>Benzoic acid, (1-(4-((3-amino-2,3,6-trideoxy-alpha-L-lyxo-hexopyranosyl)oxy)-1,2,3,4,6,11-hexahydro-2,5,7,12-tetrahydroxy-6,11-dioxo-2-naphthacenyl)ethylidene)hydrazide, monohydrochloride, (2S-cis)-</CASN1Name>
    <RegistryNumber>69428-33-7</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>66921-16-2 (mono-HCl(2S-cis)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0066206</Concept1UI>
     <Concept2UI>M0313146</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T096209</TermUI>
      <String>carminazone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T096208</TermUI>
      <String>carminomycin benzoyl hydrazone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0313146</ConceptUI>
    <ConceptName>
     <String>carminazone monohydrochloride, (2S-cis)-isomer</String>
    </ConceptName>
    <RegistryNumber>66921-16-2</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0066206</Concept1UI>
     <Concept2UI>M0313146</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T343146</TermUI>
      <String>carminazone monohydrochloride, (2S-cis)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014872</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tris(4-aminophenyl)carbonium pamoate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>11</Day>
  </DateRevised>
  <Note>shows suppressive activity against Trypanosoma cruzi
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014320</DescriptorUI>
     <DescriptorName>
      <String>Trityl Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 20(6):741;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063700</ConceptUI>
    <ConceptName>
     <String>tris(4-aminophenyl)carbonium pamoate</String>
    </ConceptName>
    <CASN1Name>tris(4-aminophenyl)methylium,with 4,4'-methylenebis(3-hydroxy-2-naphthalene carboxylic acid)(2:1)</CASN1Name>
    <RegistryNumber>2706-47-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093703</TermUI>
      <String>tris(4-aminophenyl)carbonium pamoate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T093702</TermUI>
      <String>TAC pamoate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014809</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>selenohomocystamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1991</Year>
   <Month>07</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SELENIUM (77-91)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003538</DescriptorUI>
     <DescriptorName>
      <String>Cystamine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D016566</DescriptorUI>
     <DescriptorName>
      <String>Organoselenium Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Boll Soc Ital Biol Sper 52(12):917;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063622</ConceptUI>
    <ConceptName>
     <String>selenohomocystamine</String>
    </ConceptName>
    <CASN1Name>3,3'-diselenobis-1-propanamine</CASN1Name>
    <RegistryNumber>51541-77-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093625</TermUI>
      <String>selenohomocystamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014810</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>selenohomolanthionamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1991</Year>
   <Month>05</Month>
   <Day>23</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SELENIUM (77-91)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003959</DescriptorUI>
     <DescriptorName>
      <String>Diamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D016566</DescriptorUI>
     <DescriptorName>
      <String>Organoselenium Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Boll Soc Ital Biol Sper 52(12):917;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063623</ConceptUI>
    <ConceptName>
     <String>selenohomolanthionamine</String>
    </ConceptName>
    <CASN1Name>1-Propanamine, 3,3'-selenobis-</CASN1Name>
    <RegistryNumber>58114-53-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093626</TermUI>
      <String>selenohomolanthionamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C491113</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Nsmaf protein, rat</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>09</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>12</Month>
   <Day>15</Day>
  </DateRevised>
  <Note>a WD-repeat protein that couples the TNFR1 receptor to neural sphingomyelinase; RefSeq NM_181389
  </Note>
  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PROTEINS (2004-2006)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D047908</DescriptorUI>
     <DescriptorName>
      <String>Intracellular Signaling Peptides and Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0468272</ConceptUI>
    <ConceptName>
     <String>Nsmaf protein, rat</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T593654</TermUI>
      <String>Nsmaf protein, rat</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>06</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T593657</TermUI>
      <String>FAN protein, rat</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>06</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T538105</TermUI>
      <String>neutral sphingomyelinase (N-SMase) activation associated factor, rat</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>04</Month>
       <Day>14</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T593656</TermUI>
      <String>factor associated with neutral sphingomyelinase activation protein, rat</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>06</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014873</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>trisulfapyrimidine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>RN given refers to above drug combination; RR:65567-91-1 refers to Na salt of each of the components; contains above 3 cpds
  </Note>
  <Frequency>23</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PYRIMIDINES (77-79)</PreviousIndexing>
   <PreviousIndexing>*SULFONAMIDES (77-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013411</DescriptorUI>
     <DescriptorName>
      <String>Sulfadiazine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013416</DescriptorUI>
     <DescriptorName>
      <String>Sulfamerazine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013418</DescriptorUI>
     <DescriptorName>
      <String>Sulfamethazine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Clin Chem 25(6):1186;1979</Source>
   <Source>J Indian Med Assoc 67(11):252;1976</Source>
   <Source>J Pharm Sci 68(6):699;1979</Source>
   <Source>South Med J 71(12):1494;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063702</ConceptUI>
    <ConceptName>
     <String>trisulfapyrimidine</String>
    </ConceptName>
    <CASN1Name>4-amino-N-(4,6-dimethyl-2-pyrimidinyl)benzenesulfonamide, mixt. with 4-amino-N-(4-methyl-2- pyrimidinyl)benzenesulfonamide &amp; 4-amino-N-2- pyrimidinylbenzenesulfonamide</CASN1Name>
    <RegistryNumber>8017-57-0</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>65567-91-1 (Na salt)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0063702</Concept1UI>
     <Concept2UI>M0312662</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093705</TermUI>
      <String>trisulfapyrimidine</String>
      <ThesaurusIDlist>
       <ThesaurusID>USAN (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T093704</TermUI>
      <String>triple sulfa</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312662</ConceptUI>
    <ConceptName>
     <String>trisulfapyrimidine sodium salt</String>
    </ConceptName>
    <RegistryNumber>65567-91-1</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0063702</Concept1UI>
     <Concept2UI>M0312662</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342662</TermUI>
      <String>trisulfapyrimidine sodium salt</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014824</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>spasmocalm</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>mono-oxalate salt of synonym; RN given refers to parent cpd; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AMINOBUTYRIC ACIDS (77-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005680</DescriptorUI>
     <DescriptorName>
      <String>gamma-Aminobutyric Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Akush Ginekol (Mosk) 16(1):8;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063646</ConceptUI>
    <ConceptName>
     <String>spasmocalm</String>
    </ConceptName>
    <RegistryNumber>1613-24-7</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>17341-99-0 (oxalate)</RelatedRegistryNumber>
     <RelatedRegistryNumber>41688-59-9 (maleate[1:1])</RelatedRegistryNumber>
     <RelatedRegistryNumber>42100-99-2 (HCl)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0063646</Concept1UI>
     <Concept2UI>M0312647</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0063646</Concept1UI>
     <Concept2UI>M0312646</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0063646</Concept1UI>
     <Concept2UI>M0312648</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093649</TermUI>
      <String>spasmocalm</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T093648</TermUI>
      <String>2-benzyl-4-diethylaminobutyric acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312647</ConceptUI>
    <ConceptName>
     <String>spasmocalm maleate (1:1)</String>
    </ConceptName>
    <RegistryNumber>41688-59-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0063646</Concept1UI>
     <Concept2UI>M0312647</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342647</TermUI>
      <String>spasmocalm maleate (1:1)</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312646</ConceptUI>
    <ConceptName>
     <String>spasmocalm oxalate</String>
    </ConceptName>
    <RegistryNumber>17341-99-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0063646</Concept1UI>
     <Concept2UI>M0312646</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342646</TermUI>
      <String>spasmocalm oxalate</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312648</ConceptUI>
    <ConceptName>
     <String>spasmocalm hydrochloride</String>
    </ConceptName>
    <RegistryNumber>42100-99-2</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0063646</Concept1UI>
     <Concept2UI>M0312648</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342648</TermUI>
      <String>spasmocalm hydrochloride</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014826</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>spirodecanone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>7</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013141</DescriptorUI>
     <DescriptorName>
      <String>Spiro Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Pharmacol 43(3):253;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063647</ConceptUI>
    <ConceptName>
     <String>spirodecanone</String>
    </ConceptName>
    <CASN1Name>1-phenyl-1,3,8-triazaspiro(4,5)decan-4-one</CASN1Name>
    <RegistryNumber>1021-25-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093650</TermUI>
      <String>spirodecanone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014829</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>strigosine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011763</DescriptorUI>
     <DescriptorName>
      <String>Pyrrolizidine Alkaloids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Chem Soc (Perkin I) 5:544;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063648</ConceptUI>
    <ConceptName>
     <String>strigosine</String>
    </ConceptName>
    <RegistryNumber>33981-76-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093651</TermUI>
      <String>strigosine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C057254</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>McbE protein, E coli</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1988</Year>
   <Month>10</Month>
   <Day>31</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>03</Month>
   <Day>18</Day>
  </DateRevised>
  <Note>predicted MW 27.9 kDa; amino acid sequence given in first source; integral membrane protein
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BACTERIAL PROTEINS (1988-2003)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008565</DescriptorUI>
     <DescriptorName>
      <String>Membrane Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029968</DescriptorUI>
     <DescriptorName>
      <String>Escherichia coli Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Embo J 1988;7(6):1853</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0160273</ConceptUI>
    <ConceptName>
     <String>McbE protein, E coli</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T535825</TermUI>
      <String>McbE protein, E coli</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>03</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014836</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>sulfonazo III</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>01</Month>
   <Day>02</Day>
  </DateRevised>
  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*NAPHTHOLS (77-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001391</DescriptorUI>
     <DescriptorName>
      <String>Azo Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 75(3):532;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063657</ConceptUI>
    <ConceptName>
     <String>sulfonazo III</String>
    </ConceptName>
    <RegistryNumber>1738-02-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093660</TermUI>
      <String>sulfonazo III</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014838</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>surgumycin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>06</Month>
   <Day>15</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011090</DescriptorUI>
     <DescriptorName>
      <String>Polyenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biokhimiia 42(4):653;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063659</ConceptUI>
    <ConceptName>
     <String>surgumycin</String>
    </ConceptName>
    <CASN1Name>Surgumycin</CASN1Name>
    <RegistryNumber>51938-50-2</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0063659</Concept1UI>
     <Concept2UI>M0063658</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093662</TermUI>
      <String>surgumycin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0063658</ConceptUI>
    <ConceptName>
     <String>28-hydro-23-dehydroxy-24,29-dihydroxyflavofungin</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0063659</Concept1UI>
     <Concept2UI>M0063658</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T093661</TermUI>
      <String>28-hydro-23-dehydroxy-24,29-dihydroxyflavofungin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014840</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,3,5,6-tetramethyl-1,4-dinitrosopiperazine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>06</Month>
   <Day>18</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PIPERAZINES (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009602</DescriptorUI>
     <DescriptorName>
      <String>Nitrosamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Z Krebsforsch 89(1):31;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063661</ConceptUI>
    <ConceptName>
     <String>2,3,5,6-tetramethyl-1,4-dinitrosopiperazine</String>
    </ConceptName>
    <RegistryNumber>63441-59-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093664</TermUI>
      <String>2,3,5,6-tetramethyl-1,4-dinitrosopiperazine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014848</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tetrahydroxyaminopterin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000630</DescriptorUI>
     <DescriptorName>
      <String>Aminopterin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>JNCI 59(1):245;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063667</ConceptUI>
    <ConceptName>
     <String>tetrahydroxyaminopterin</String>
    </ConceptName>
    <CASN1Name>L-Glutamic acid, N-(4-(((2,4-diamino-1,5,6,7-tetrahydro-6-pteridinyl)methyl)amino)benzoyl)-</CASN1Name>
    <RegistryNumber>14231-41-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093670</TermUI>
      <String>tetrahydroxyaminopterin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014854</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3 beta-thioacetyl-14 beta-hydroxy-5 beta-card-20(22)-enolide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>thioacetyl analog of digitoxigenin.; structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004073</DescriptorUI>
     <DescriptorName>
      <String>Digitoxigenin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 66(4):602;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063673</ConceptUI>
    <ConceptName>
     <String>3 beta-thioacetyl-14 beta-hydroxy-5 beta-card-20(22)-enolide</String>
    </ConceptName>
    <RegistryNumber>61971-99-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093676</TermUI>
      <String>3 beta-thioacetyl-14 beta-hydroxy-5 beta-card-20(22)-enolide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C094313</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>p60 tumor necrosis factor receptor-associated kinase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>07</Month>
   <Day>28</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>12</Month>
   <Day>15</Day>
  </DateRevised>
  <Note>interacts with &amp; causes phosphorylation of the cytoplasmic domain of the TNFR1 receptor
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D017346</DescriptorUI>
     <DescriptorName>
      <String>Protein-Serine-Threonine Kinases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D018124</DescriptorUI>
     <DescriptorName>
      <String>Receptors, Tumor Necrosis Factor</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Biol Chem 1995 Jun 23;270(25):14867-70</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0248506</ConceptUI>
    <ConceptName>
     <String>p60 tumor necrosis factor receptor-associated kinase</String>
    </ConceptName>
    <RegistryNumber>EC 2.7.1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T278511</TermUI>
      <String>p60 tumor necrosis factor receptor-associated kinase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T278509</TermUI>
      <String>p60 TNF receptor-associated kinase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T278510</TermUI>
      <String>p60-TRAK</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C085228</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>echitamidine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>02</Month>
   <Day>08</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>09</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>structure given in first source; isolated from Winchia calophylla (Apocynaceae), a medicinal plant used to treat trachitis
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002227</DescriptorUI>
     <DescriptorName>
      <String>Carbazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D029062</DescriptorUI>
     <DescriptorName>
      <String>Apocynaceae</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Yao Hsueh Hsueh Pao 1993;28(7):512-5</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0226270</ConceptUI>
    <ConceptName>
     <String>echitamidine</String>
    </ConceptName>
    <CASN1Name>Curan-17-oic acid, 2,16-didehydro-19-hydroxy-, methyl ester, (19S)-</CASN1Name>
    <RegistryNumber>38681-90-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T256275</TermUI>
      <String>echitamidine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C089912</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hupK protein, Rhizobium leguminosarum</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>11</Month>
   <Day>11</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>03</Month>
   <Day>18</Day>
  </DateRevised>
  <Note>a hydrogenase-ancillary protein; isolated from Rhizobium leguminosarum; has been sequenced
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Microbiol 1993 Sep;9(6):1305-6</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0237643</ConceptUI>
    <ConceptName>
     <String>hupK protein, Rhizobium leguminosarum</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T535716</TermUI>
      <String>hupK protein, Rhizobium leguminosarum</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>03</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014868</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4',5,7-trihydroxy-3,6-dimethoxyflavone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005419</DescriptorUI>
     <DescriptorName>
      <String>Flavonoids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 460(2):364;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063692</ConceptUI>
    <ConceptName>
     <String>4',5,7-trihydroxy-3,6-dimethoxyflavone</String>
    </ConceptName>
    <CASN1Name>5,7-dihydroxy-2-(4-hydroxyphenyl)-3,6-dimethoxy- 4H-1-benzopyran-4-one</CASN1Name>
    <RegistryNumber>22697-65-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093695</TermUI>
      <String>4',5,7-trihydroxy-3,6-dimethoxyflavone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011971</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>pentylethanolamine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004983</DescriptorUI>
     <DescriptorName>
      <String>Ethanolamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Psychoneuroendocrinology WL 102 1657p:307;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058648</ConceptUI>
    <ConceptName>
     <String>pentylethanolamine</String>
    </ConceptName>
    <RegistryNumber>35161-67-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088651</TermUI>
      <String>pentylethanolamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011976</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-phenazinylthioureidotyrosine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>09</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PHENAZINES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014443</DescriptorUI>
     <DescriptorName>
      <String>Tyrosine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mikrobiol Zh 37(4):500;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058651</ConceptUI>
    <ConceptName>
     <String>2-phenazinylthioureidotyrosine</String>
    </ConceptName>
    <RegistryNumber>57355-21-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088654</TermUI>
      <String>2-phenazinylthioureidotyrosine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011979</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>phenylalanyl-alanyl-lysine chloromethyl ketone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>11</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*KETONES (76-77)</PreviousIndexing>
   <PreviousIndexing>*PEPTIDES (76-77)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000590</DescriptorUI>
     <DescriptorName>
      <String>Amino Acid Chloromethyl Ketones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 251(4):1097;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058660</ConceptUI>
    <ConceptName>
     <String>phenylalanyl-alanyl-lysine chloromethyl ketone</String>
    </ConceptName>
    <CASN1Name>L-Alaninamide, L-phenylalanyl-N-(5-amino-1-(chloroacetyl)pentyl)-, (S)-</CASN1Name>
    <RegistryNumber>52780-81-1</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0058660</Concept1UI>
     <Concept2UI>M0058659</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088663</TermUI>
      <String>phenylalanyl-alanyl-lysine chloromethyl ketone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0058659</ConceptUI>
    <ConceptName>
     <String>Phe-Ala-Lys-chloromethyl ketone</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0058660</Concept1UI>
     <Concept2UI>M0058659</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T088662</TermUI>
      <String>Phe-Ala-Lys-chloromethyl ketone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011982</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>(phenylglyoxal bis(4-methyl-3-thiosemicarbazone)) copper(II) chelates</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>01</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009942</DescriptorUI>
     <DescriptorName>
      <String>Organometallic Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013882</DescriptorUI>
     <DescriptorName>
      <String>Thiosemicarbazones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D003300</DescriptorUI>
     <DescriptorName>
      <String>Copper</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Med Chem 19(1):131;1976</Source>
   <Source>J Med Chem 21(8):804;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058665</ConceptUI>
    <ConceptName>
     <String>(phenylglyoxal bis(4-methyl-3-thiosemicarbazone)) copper(II) chelates</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088668</TermUI>
      <String>(phenylglyoxal bis(4-methyl-3-thiosemicarbazone)) copper(II) chelates</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C017587</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>osimol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>contains sodium propionate, citric acid, cobalt SO(4) copper sulfate, magnesium sulfate
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CITRATES (78-96)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008670</DescriptorUI>
     <DescriptorName>
      <String>Metals</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011422</DescriptorUI>
     <DescriptorName>
      <String>Propionates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013431</DescriptorUI>
     <DescriptorName>
      <String>Sulfates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D019343</DescriptorUI>
     <DescriptorName>
      <String>Citric Acid</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Veterinariia (7):72;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0068466</ConceptUI>
    <ConceptName>
     <String>osimol</String>
    </ConceptName>
    <RegistryNumber>60440-51-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T098469</TermUI>
      <String>osimol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011989</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>phthioic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005227</DescriptorUI>
     <DescriptorName>
      <String>Fatty Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Jpn J Bacteriol 30(1):177;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058673</ConceptUI>
    <ConceptName>
     <String>phthioic acid</String>
    </ConceptName>
    <CASN1Name>3,13,19-trimethyltricosanoic acid</CASN1Name>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088676</TermUI>
      <String>phthioic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C494562</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cyclohexaicosaose</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>12</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>12</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003505</DescriptorUI>
     <DescriptorName>
      <String>Cyclodextrins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Carbohydr Res 2004 Jun 1;339(8):1427-37</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0478748</ConceptUI>
    <ConceptName>
     <String>cyclohexaicosaose</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T626480</TermUI>
      <String>cyclohexaicosaose</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>12</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T626481</TermUI>
      <String>CA26 cyclodextrin</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>12</Month>
       <Day>29</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011992</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>pimafutri</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1994</Year>
   <Month>02</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>combination of the above
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>DRUG COMBINATIONS (76-88)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010118</DescriptorUI>
     <DescriptorName>
      <String>Oxytetracycline</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010866</DescriptorUI>
     <DescriptorName>
      <String>Natamycin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Ther Ggw 114(8):1268;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058677</ConceptUI>
    <ConceptName>
     <String>pimafutri</String>
    </ConceptName>
    <CASN1Name>Pimaricin, mixt. with (4S-(4alpha,4aalpha,5alpha,5aalpha,6beta,12aalpha))-4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,6,10,12,12a-hexahydroxy-6-methyl-1,11-dioxo-2-naphthacenecarboxamide</CASN1Name>
    <RegistryNumber>78436-01-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088680</TermUI>
      <String>pimafutri</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012009</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>S 10</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>RN is from 9th CI, Molecular Formula Index; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PIPERAZINES (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010880</DescriptorUI>
     <DescriptorName>
      <String>Piperidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Pol Med Sci Hist Bull 15(3):275;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058707</ConceptUI>
    <ConceptName>
     <String>S 10</String>
    </ConceptName>
    <RegistryNumber>59173-24-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0058707</Concept1UI>
     <Concept2UI>M0058705</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T088710</TermUI>
      <String>S 10</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T088709</TermUI>
      <String>S-10</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0058705</ConceptUI>
    <ConceptName>
     <String>4-propionyl-4-(3-chlorophenyl)-(3-(4-methylpiperazine)propyl)piperidine trihydrochloride</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0058707</Concept1UI>
     <Concept2UI>M0058705</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T088708</TermUI>
      <String>4-propionyl-4-(3-chlorophenyl)-(3-(4-methylpiperazine)propyl)piperidine trihydrochloride</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C011998</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>poly(dimethylaminoethylglutamine)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>18</Day>
  </DateRevised>
  <Note>polycationic modified polypeptide enhancing poly I:C-induced viral resistance
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>GLUTAMINE/analogs (76-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010455</DescriptorUI>
     <DescriptorName>
      <String>Peptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Experientia 31(10):1165;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058690</ConceptUI>
    <ConceptName>
     <String>poly(dimethylaminoethylglutamine)</String>
    </ConceptName>
    <RegistryNumber>57418-09-4</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0058690</Concept1UI>
     <Concept2UI>M0058689</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088693</TermUI>
      <String>poly(dimethylaminoethylglutamine)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0058689</ConceptUI>
    <ConceptName>
     <String>poly(DMAE-glutamine)</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0058690</Concept1UI>
     <Concept2UI>M0058689</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T088692</TermUI>
      <String>poly(DMAE-glutamine)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012070</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,4,6-triaminopyrimidine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>see also 2,4,6-triaminopyridinium (cation)
  </Note>
  <Frequency>37</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011743</DescriptorUI>
     <DescriptorName>
      <String>Pyrimidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Am J Physiol 236(5):C221;1979</Source>
   <Source>Biochim Biophys Acta 448(3):411;1976</Source>
   <Source>Biochim Biophys Acta 448(3):426;1976</Source>
   <Source>J Membr Biol 49(4):363;1979</Source>
   <Source>J Pharmacol Exp Ther 204(1):175;1978</Source>
   <Source>J Pharmacol Exp Ther 206(1):201;1978</Source>
   <Source>J Physiol 266(1):68P;1977</Source>
   <Source>J Physiol 290:331;1979</Source>
   <Source>J Physiol 290:351;1979</Source>
   <Source>J Physiol 290:367;1979</Source>
   <Source>Pfluegers Arch 379(3):287;1979</Source>
   <Source>Vopr Onkol 21(12):68;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058804</ConceptUI>
    <ConceptName>
     <String>2,4,6-triaminopyrimidine</String>
    </ConceptName>
    <CASN1Name>2,4,6-pyrimidinetriamine</CASN1Name>
    <RegistryNumber>1004-38-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088807</TermUI>
      <String>2,4,6-triaminopyrimidine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012004</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>poly(1-vinyluracil)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>06</Day>
  </DateRevised>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>URACIL/*analogs (76-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011145</DescriptorUI>
     <DescriptorName>
      <String>Polyvinyls</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Res 36(4):1273;1976</Source>
   <Source>J Med Chem 20(3):356;1977</Source>
   <Source>Mol Pharmacol 11(6):708;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058695</ConceptUI>
    <ConceptName>
     <String>poly(1-vinyluracil)</String>
    </ConceptName>
    <RegistryNumber>25750-74-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088698</TermUI>
      <String>poly(1-vinyluracil)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C119413</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hemoglobin Khartoum</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1999</Year>
   <Month>06</Month>
   <Day>18</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>arginine replaces proline at position 124(H2) of the beta subunit
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006455</DescriptorUI>
     <DescriptorName>
      <String>Hemoglobins, Abnormal</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Hemoglobin 1999 Feb;23(1):33-45</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0305731</ConceptUI>
    <ConceptName>
     <String>hemoglobin Khartoum</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T335736</TermUI>
      <String>hemoglobin Khartoum</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T335735</TermUI>
      <String>Hb Khartoum</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C119414</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hemoglobin Schlierbach</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1999</Year>
   <Month>06</Month>
   <Day>18</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>isoleucine replaces asparagine at position 108(G10) of the beta subunit
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006455</DescriptorUI>
     <DescriptorName>
      <String>Hemoglobins, Abnormal</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Hemoglobin 1999 Feb;23(1):83-7</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0305733</ConceptUI>
    <ConceptName>
     <String>hemoglobin Schlierbach</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T335738</TermUI>
      <String>hemoglobin Schlierbach</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T335737</TermUI>
      <String>Hb Schlierbach</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C119415</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hemoglobin Brent</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1999</Year>
   <Month>06</Month>
   <Day>18</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>asparagine replaces histidine at position 117(G19) of the beta subunit
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006455</DescriptorUI>
     <DescriptorName>
      <String>Hemoglobins, Abnormal</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Hemoglobin 1999 Feb;23(1):89-93</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0305735</ConceptUI>
    <ConceptName>
     <String>hemoglobin Brent</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T335740</TermUI>
      <String>hemoglobin Brent</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T335739</TermUI>
      <String>Hb Brent</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C059200</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-nitrophenylgalactoside</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1989</Year>
   <Month>05</Month>
   <Day>22</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>RN refers to (beta-D)-isomer
  </Note>
  <Frequency>90</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009598</DescriptorUI>
     <DescriptorName>
      <String>Nitrophenylgalactosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
    <PharmacologicalActionList>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D019920</DescriptorUI>
        <DescriptorName>
         <String>Photoaffinity Labels</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
    </PharmacologicalActionList>
  <SourceList>
   <Source>Biochem J 1989;258(2):389</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0164760</ConceptUI>
    <ConceptName>
     <String>4-nitrophenylgalactoside</String>
    </ConceptName>
    <RegistryNumber>3150-24-1</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>7493-95-0 ((alpha-D)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0164760</Concept1UI>
     <Concept2UI>M0164755</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0164760</Concept1UI>
     <Concept2UI>M0164759</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0164760</Concept1UI>
     <Concept2UI>M0324112</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T194765</TermUI>
      <String>4-nitrophenylgalactoside</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T194761</TermUI>
      <String>PNPG</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0164755</ConceptUI>
    <ConceptName>
     <String>4-nitrophenyl-alpha-galactoside</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0164760</Concept1UI>
     <Concept2UI>M0164755</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T194760</TermUI>
      <String>4-nitrophenyl-alpha-galactoside</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T194763</TermUI>
      <String>p-nitrophenyl-alpha-galactoside</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0164759</ConceptUI>
    <ConceptName>
     <String>para-nitrophenyl-beta-D-galactoside</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0164760</Concept1UI>
     <Concept2UI>M0164759</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T194764</TermUI>
      <String>para-nitrophenyl-beta-D-galactoside</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0324112</ConceptUI>
    <ConceptName>
     <String>4-nitrophenylgalactoside, (alpha-D)-isomer</String>
    </ConceptName>
    <RegistryNumber>7493-95-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0164760</Concept1UI>
     <Concept2UI>M0324112</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T354112</TermUI>
      <String>4-nitrophenylgalactoside, (alpha-D)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T194762</TermUI>
      <String>p-nitrophenyl-alpha-D-galactopyranoside</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1989)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012028</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>scanalka</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>mineral preparation
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  <Frequency>1</Frequency>
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  <SourceList>
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  <ConceptList>
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  <DateCreated>
   <Year>1991</Year>
   <Month>08</Month>
   <Day>07</Day>
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  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>12</Day>
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  <Note>nitrogen-containing heterocyclic compound; Russian patent; antiatherogenic; used for treatment of burns; used on varicose ulcer
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  <Frequency>47</Frequency>
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    <DescriptorReferredTo>
     <DescriptorUI>*D011743</DescriptorUI>
     <DescriptorName>
      <String>Pyrimidines</String>
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    <PharmacologicalActionList>
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     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D000960</DescriptorUI>
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     <PharmacologicalAction>
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       <DescriptorUI>D016587</DescriptorUI>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T220145</TermUI>
      <String>1-(beta-hydroxyethyl)-4,6-dimethyl-1,2-dihydro-2-oxopyrimidine</String>
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       <ThesaurusID>NLM (1991)</ThesaurusID>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T220146</TermUI>
      <String>N-(2-hydroxyethyl)-4,6-dimethyl-2-dehydropyrimidone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
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  <SupplementalRecordUI>C012030</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-selenoethylguanidine</String>
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  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>1992</Year>
   <Month>05</Month>
   <Day>14</Day>
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  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>SELENIUM (76-92)</PreviousIndexing>
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     <DescriptorUI>*D006146</DescriptorUI>
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   <HeadingMappedTo>
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     <DescriptorUI>*D016566</DescriptorUI>
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      <String>Organoselenium Compounds</String>
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  <SourceList>
   <Source>Strahlentherapie 151(1):78;1976</Source>
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  <ConceptList>
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     <String>2-selenoethylguanidine</String>
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    <RegistryNumber>57897-99-1</RegistryNumber>
    <TermList>
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      <TermUI>T088737</TermUI>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C078265</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-(2,3,5-trichlorophenyl)pyrimidine-2,4-diamine ethane sulfonate</String>
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  <DateCreated>
   <Year>1992</Year>
   <Month>12</Month>
   <Day>22</Day>
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  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>02</Day>
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  <Frequency>19</Frequency>
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    <DescriptorReferredTo>
     <DescriptorUI>*D011743</DescriptorUI>
     <DescriptorName>
      <String>Pyrimidines</String>
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  <SourceList>
   <Source>Neurosci Lett 1992 Aug 31;143(1-2):229-32</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0209846</ConceptUI>
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     <String>5-(2,3,5-trichlorophenyl)pyrimidine-2,4-diamine ethane sulfonate</String>
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    <CASN1Name>Ethanesulfonic acid, compd. with 5-(2,3,5-trichlorophenyl)-2,4-pyrimidinediamine (1:1)</CASN1Name>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0209846</Concept1UI>
     <Concept2UI>M0209848</Concept2UI>
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    <TermList>
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      <TermUI>T239851</TermUI>
      <String>5-(2,3,5-trichlorophenyl)pyrimidine-2,4-diamine ethane sulfonate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
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   <Concept PreferredConceptYN="N">
    <ConceptUI>M0209848</ConceptUI>
    <ConceptName>
     <String>BW 1003C87</String>
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     <Concept1UI>M0209846</Concept1UI>
     <Concept2UI>M0209848</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T239853</TermUI>
      <String>BW 1003C87</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T239852</TermUI>
      <String>BW-1003C87</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012032</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>sepharose-N-6-aminohexanoyl-2-amino-2-deoxy-D-glucopyranose</String>
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  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>09</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>used in affinity chromatography
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SEPHAROSE/analogs (82-83)</PreviousIndexing>
   <PreviousIndexing>GLUCOSAMINE/*analogs (76-82)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D012685</DescriptorUI>
     <DescriptorName>
      <String>Sepharose</String>
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    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
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    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem J 153(2):351;1976</Source>
   <Source>Biochem J 153(2):363;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058737</ConceptUI>
    <ConceptName>
     <String>sepharose-N-6-aminohexanoyl-2-amino-2-deoxy-D-glucopyranose</String>
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    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0058737</Concept1UI>
     <Concept2UI>M0058736</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088740</TermUI>
      <String>sepharose-N-6-aminohexanoyl-2-amino-2-deoxy-D-glucopyranose</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
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     </Term>
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   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0058736</ConceptUI>
    <ConceptName>
     <String>sepharose-AADG</String>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0058737</Concept1UI>
     <Concept2UI>M0058736</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T088739</TermUI>
      <String>sepharose-AADG</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
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     </Term>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C411649</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>zinedin</String>
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  <DateCreated>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>07</Day>
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  <Note>a WD repeat protein expressed mainly in the brain; amino acid sequence in first source
  </Note>
  <Frequency>8</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002148</DescriptorUI>
     <DescriptorName>
      <String>Calmodulin-Binding Proteins</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009419</DescriptorUI>
     <DescriptorName>
      <String>Nerve Tissue Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 2000 Jun 30;275(26):19970-7</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0367368</ConceptUI>
    <ConceptName>
     <String>zinedin</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T421016</TermUI>
      <String>zinedin</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>08</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C519773</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>pyrazine-N,N'-dioxide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2007</Year>
   <Month>05</Month>
   <Day>23</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003497</DescriptorUI>
     <DescriptorName>
      <String>Cyclic N-Oxides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011719</DescriptorUI>
     <DescriptorName>
      <String>Pyrazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Spectrochim Acta A Mol Biomol Spectrosc 2007 Apr;66(4-5):964-71</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0509863</ConceptUI>
    <ConceptName>
     <String>pyrazine-N,N'-dioxide</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T698094</TermUI>
      <String>pyrazine-N,N'-dioxide</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>05</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012038</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>spiro(cyclohexane-1,2'-indan)-1',4-dione</String>
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  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>potentiates estrogenic activity of stilbestrol; structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007189</DescriptorUI>
     <DescriptorName>
      <String>Indans</String>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013141</DescriptorUI>
     <DescriptorName>
      <String>Spiro Compounds</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 19(3):438;1976</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058746</ConceptUI>
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     <String>spiro(cyclohexane-1,2'-indan)-1',4-dione</String>
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    <RegistryNumber>56868-14-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088749</TermUI>
      <String>spiro(cyclohexane-1,2'-indan)-1',4-dione</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
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     </Term>
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   </Concept>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012039</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>sporotrichin</String>
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  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1993</Year>
   <Month>02</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>peptido-rhamnomannan extracted from Sporothrix
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  <Frequency>19</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006025</DescriptorUI>
     <DescriptorName>
      <String>Glycosaminoglycans</String>
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   </HeadingMappedTo>
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  <SourceList>
   <Source>Jpn J Dermatol 85(11):633;1975</Source>
   <Source>Nippon Hifuka Gakkai Zasshi 89(6):391;1979</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C080151</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>methyl laminarabioside</String>
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  <DateCreated>
   <Year>1993</Year>
   <Month>04</Month>
   <Day>09</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>structure given in first source
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  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004187</DescriptorUI>
     <DescriptorName>
      <String>Disaccharides</String>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005960</DescriptorUI>
     <DescriptorName>
      <String>Glucosides</String>
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  <SourceList>
   <Source>Carbohydr Res 1992 Dec 31;237:33-43</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0214277</ConceptUI>
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     <String>methyl laminarabioside</String>
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    <RegistryNumber>147217-24-1</RegistryNumber>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0214277</Concept1UI>
     <Concept2UI>M0214274</Concept2UI>
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    <TermList>
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      <TermUI>T244282</TermUI>
      <String>methyl laminarabioside</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
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   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0214276</ConceptUI>
    <ConceptName>
     <String>methyl laminarabioside monohydrate</String>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0214277</Concept1UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T244281</TermUI>
      <String>methyl laminarabioside monohydrate</String>
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       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0214274</ConceptUI>
    <ConceptName>
     <String>methyl 3-O-beta-D-glucopyranosyl-beta-D-glucopyranoside</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0214277</Concept1UI>
     <Concept2UI>M0214274</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T244279</TermUI>
      <String>methyl 3-O-beta-D-glucopyranosyl-beta-D-glucopyranoside</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T244280</TermUI>
      <String>methyl beta-D-laminarabioside</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C119418</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-(4-chlorophenyl)amino-2-(4-pyridyl)ethane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1999</Year>
   <Month>06</Month>
   <Day>18</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000814</DescriptorUI>
     <DescriptorName>
      <String>Aniline Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011725</DescriptorUI>
     <DescriptorName>
      <String>Pyridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Biomed Anal 1998 Nov;18(3):403-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0305741</ConceptUI>
    <ConceptName>
     <String>2-(4-chlorophenyl)amino-2-(4-pyridyl)ethane</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T335746</TermUI>
      <String>2-(4-chlorophenyl)amino-2-(4-pyridyl)ethane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T335745</TermUI>
      <String>AAP-Cl</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012048</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Sulfapral</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>07</Month>
   <Day>07</Day>
  </DateRevised>
  <Note>RN from 9th CI; cpd not in Chemline 7/83
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013419</DescriptorUI>
     <DescriptorName>
      <String>Sulfamethizole</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013421</DescriptorUI>
     <DescriptorName>
      <String>Sulfamethoxypyridazine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Curr Ther Res 19(2):216;1976</Source>
   <Source>Eur J Clin Pharmacol 11:439;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058764</ConceptUI>
    <ConceptName>
     <String>Sulfapral</String>
    </ConceptName>
    <RegistryNumber>8059-46-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088767</TermUI>
      <String>Sulfapral</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012050</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>sulfocamphocaine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>09</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>cardiovascular agent; contains novocaine &amp; sulfocamphoric acid
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002164</DescriptorUI>
     <DescriptorName>
      <String>Camphor</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011343</DescriptorUI>
     <DescriptorName>
      <String>Procaine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Farmatsiia 24(4):93;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058768</ConceptUI>
    <ConceptName>
     <String>sulfocamphocaine</String>
    </ConceptName>
    <RegistryNumber>62683-42-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088771</TermUI>
      <String>sulfocamphocaine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012053</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tempalgin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>combination of analgin and tempidon
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004177</DescriptorUI>
     <DescriptorName>
      <String>Dipyrone</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010881</DescriptorUI>
     <DescriptorName>
      <String>Piperidones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Khirurgiia (Sofiia) 28(1):24;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058776</ConceptUI>
    <ConceptName>
     <String>tempalgin</String>
    </ConceptName>
    <RegistryNumber>39296-38-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088779</TermUI>
      <String>tempalgin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C119420</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-amino-4-(2-chlorophenyl)-6-nitrocarbostyril</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1999</Year>
   <Month>06</Month>
   <Day>18</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>30</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015363</DescriptorUI>
     <DescriptorName>
      <String>Quinolones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Biomed Anal 1998 Nov;18(3):453-60</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0305744</ConceptUI>
    <ConceptName>
     <String>3-amino-4-(2-chlorophenyl)-6-nitrocarbostyril</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T335749</TermUI>
      <String>3-amino-4-(2-chlorophenyl)-6-nitrocarbostyril</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T335748</TermUI>
      <String>3-amino-4-ClPhNCS</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1999)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C035763</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5,5'-bis(8-(phenylamino)-1-naphthalenesulfonate)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2007</Year>
   <Month>05</Month>
   <Day>23</Day>
  </DateRevised>
  <Frequency>208</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000817</DescriptorUI>
     <DescriptorName>
      <String>Anilino Naphthalenesulfonates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
    <PharmacologicalActionList>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D005456</DescriptorUI>
        <DescriptorName>
         <String>Fluorescent Dyes</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
    </PharmacologicalActionList>
  <SourceList>
   <Source>Biochemistry 1982;21(17):4031</Source>
   <Source>Naturwissenschaft 65(6):336;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0109378</ConceptUI>
    <ConceptName>
     <String>5,5'-bis(8-(phenylamino)-1-naphthalenesulfonate)</String>
    </ConceptName>
    <CASN1Name>(1,1'-Binaphthalene)-5,5'-disulfonic acid, 4,4'-bis(phenylamino)-</CASN1Name>
    <RegistryNumber>63741-13-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T139382</TermUI>
      <String>5,5'-bis(8-(phenylamino)-1-naphthalenesulfonate)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T139376</TermUI>
      <String>4,4'-BANS</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T139377</TermUI>
      <String>4,4'-bis(1-anilino-8-naphthalenesulfonate)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T698097</TermUI>
      <String>4,4'-dianilino-1,1'-bisnaphthyl-5,5' disulfonic acid</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>05</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T139379</TermUI>
      <String>5,5-bis(ANS)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T139380</TermUI>
      <String>bis(1,8-anilinonaphthalenesulfonate)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T139381</TermUI>
      <String>bis-ANS</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T139375</TermUI>
      <String>1,1'-bis(4-anilino-5-naphthalenesulfonic acid)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T139378</TermUI>
      <String>4,4'-bis(8-phenylamino)naphthalene-1-sulfonate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C411652</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>IC 261</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>07</Day>
  </DateCreated>
  <Note>a caseine kinase-1 inhibitor; structure in first source
  </Note>
  <Frequency>28</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007211</DescriptorUI>
     <DescriptorName>
      <String>Indoles</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010696</DescriptorUI>
     <DescriptorName>
      <String>Phloroglucinol</String>
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    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
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   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 2000 Jun 30;275(26):20052-60</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0367371</ConceptUI>
    <ConceptName>
     <String>IC 261</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T421021</TermUI>
      <String>IC 261</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>08</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T421023</TermUI>
      <String>IC261</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>08</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T421024</TermUI>
      <String>3-((2,4,6-trimethoxyphenyl)methylidenyl)indolin-2-one</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>08</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T421022</TermUI>
      <String>IC-261</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>08</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012084</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,1,4-trimethyldiethylenetrimine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1986</Year>
   <Month>01</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011073</DescriptorUI>
     <DescriptorName>
      <String>Polyamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Pol Pharm 32(6):663;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058837</ConceptUI>
    <ConceptName>
     <String>1,1,4-trimethyldiethylenetrimine</String>
    </ConceptName>
    <CASN1Name>1,2-Ethanediamine, N-(2-aminoethyl)-N,N',N'-trimethyl-</CASN1Name>
    <RegistryNumber>33451-85-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088840</TermUI>
      <String>1,1,4-trimethyldiethylenetrimine</String>
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       <ThesaurusID>NLM (1976)</ThesaurusID>
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   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012114</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ASI-222</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>07</Month>
   <Day>14</Day>
  </DateRevised>
  <Note>semisynthetic cardiac glycoside; RN given refers to (3beta,5beta)-isomer; structure
  </Note>
  <Frequency>16</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DIGITOXIGENIN/analogs (76-78)</PreviousIndexing>
   <PreviousIndexing>AMINOGLYCOSIDES (76-81)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004073</DescriptorUI>
     <DescriptorName>
      <String>Digitoxigenin</String>
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    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D002301</DescriptorUI>
     <DescriptorName>
      <String>Cardiac Glycosides</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D004071</DescriptorUI>
     <DescriptorName>
      <String>Digitalis Glycosides</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Arch Int Pharmacodyn Ther 227:220;1977</Source>
   <Source>Circ Res 43(6):847;1978</Source>
   <Source>J Pharmacol Exp Ther 197(1):19;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058912</ConceptUI>
    <ConceptName>
     <String>ASI-222</String>
    </ConceptName>
    <CASN1Name>(3 beta,5 beta)-3-((4-amino-4,6-dideoxy-beta-D-galactopyranosyl)oxy)-14-hydroxycard-20(22)-enolide</CASN1Name>
    <RegistryNumber>59006-00-7</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>63938-94-3 (dihydrate)</RelatedRegistryNumber>
     <RelatedRegistryNumber>65411-64-5 (HCl)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0058912</Concept1UI>
     <Concept2UI>M0311739</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0058912</Concept1UI>
     <Concept2UI>M0311740</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0058912</Concept1UI>
     <Concept2UI>M0058910</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T088915</TermUI>
      <String>ASI-222</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T088914</TermUI>
      <String>ASI 222</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0311739</ConceptUI>
    <ConceptName>
     <String>ASI-222 dihydrate</String>
    </ConceptName>
    <RegistryNumber>63938-94-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0058912</Concept1UI>
     <Concept2UI>M0311739</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T341739</TermUI>
      <String>ASI-222 dihydrate</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0311740</ConceptUI>
    <ConceptName>
     <String>ASI-222 hydrochloride</String>
    </ConceptName>
    <RegistryNumber>65411-64-5</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0058912</Concept1UI>
     <Concept2UI>M0311740</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T341740</TermUI>
      <String>ASI-222 hydrochloride</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0058910</ConceptUI>
    <ConceptName>
     <String>3 beta-O-(4-amino-4,6-dideoxy-beta-D-galactopyranosyl)digitoxigenin</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0058912</Concept1UI>
     <Concept2UI>M0058910</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T088913</TermUI>
      <String>3 beta-O-(4-amino-4,6-dideoxy-beta-D-galactopyranosyl)digitoxigenin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C036321</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>apolipoprotein F</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1982</Year>
   <Month>12</Month>
   <Day>06</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>03</Month>
   <Day>13</Day>
  </DateRevised>
  <Note>may be identical to leukemia virus-inactivating factor; minor apolipoprotein from sera; apo F &amp; LTIP are identical
  </Note>
  <Frequency>35</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001053</DescriptorUI>
     <DescriptorName>
      <String>Apolipoproteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 1982;21(21):5347</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0110748</ConceptUI>
    <ConceptName>
     <String>apolipoprotein F</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T140752</TermUI>
      <String>apolipoprotein F</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T140751</TermUI>
      <String>lipid transfer inhibitor protein (LTIP)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T140750</TermUI>
      <String>apo F</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012096</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>vincathicine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>dimeric indole alkaloid; structure
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*VINCA ALKALOIDS (76-79)</PreviousIndexing>
   <PreviousIndexing>INDOLES (76-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014747</DescriptorUI>
     <DescriptorName>
      <String>Vinblastine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 41(6):1001;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058864</ConceptUI>
    <ConceptName>
     <String>vincathicine</String>
    </ConceptName>
    <RegistryNumber>57665-10-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088867</TermUI>
      <String>vincathicine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C074252</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>TthV protein, wheat</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1992</Year>
   <Month>05</Month>
   <Day>27</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>06</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>amino acid sequence given in first source; specifically expressed in developing wheat endosperm
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010940</DescriptorUI>
     <DescriptorName>
      <String>Plant Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D023181</DescriptorUI>
     <DescriptorName>
      <String>Antimicrobial Cationic Peptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Mol Biol 1992 Apr 20;224(4):1003-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0200547</ConceptUI>
    <ConceptName>
     <String>TthV protein, wheat</String>
    </ConceptName>
    <RegistryNumber>147205-78-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T230550</TermUI>
      <String>TthV protein, wheat</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T230551</TermUI>
      <String>thionin protein, Triticum aestivum</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T230552</TermUI>
      <String>neutral (type V) thionin, wheat</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012110</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>USVP E-142</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>06</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>substituted amino propiophenone oxime with MW 405
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011427</DescriptorUI>
     <DescriptorName>
      <String>Propiophenones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Curr Ther Res 19(3):343;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0058905</ConceptUI>
    <ConceptName>
     <String>USVP E-142</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T088908</TermUI>
      <String>USVP E-142</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C513830</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Psg-22 protein, mouse</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>10</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>has been sequenced
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006023</DescriptorUI>
     <DescriptorName>
      <String>Glycoproteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011257</DescriptorUI>
     <DescriptorName>
      <String>Pregnancy Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Reproduction 2006 Apr;131(4):721-32</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0502295</ConceptUI>
    <ConceptName>
     <String>Psg-22 protein, mouse</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T682583</TermUI>
      <String>Psg-22 protein, mouse</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>10</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T682584</TermUI>
      <String>pregnancy-specific glycoprotein 22, mouse</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>10</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002968</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dolichol-D-glucosylmonophosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>07</Month>
   <Day>16</Day>
  </DateRevised>
  <Frequency>34</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*TERPENES (73-78)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011103</DescriptorUI>
     <DescriptorName>
      <String>Polyisoprenyl Phosphate Monosaccharides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Biochem Biophys 188(2):385;1978</Source>
   <Source>Biochem Soc Trans 7(2):370;1979</Source>
   <Source>C R Acad Sci(D) (Paris) 1980;290(5):413</Source>
   <Source>Carbohydr Res 26(2):393;1973</Source>
   <Source>J Biol Chem 1979;254(20):10037</Source>
   <Source>J Dairy Sci 1979;62(11):1726</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043832</ConceptUI>
    <ConceptName>
     <String>dolichol-D-glucosylmonophosphate</String>
    </ConceptName>
    <CASN1Name>beta-D-Glucopyranose, 1-ester with dolichol dihydrogen phosphate</CASN1Name>
    <RegistryNumber>55607-88-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0043832</Concept1UI>
     <Concept2UI>M0043831</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073835</TermUI>
      <String>dolichol-D-glucosylmonophosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073831</TermUI>
      <String>dolichyl monophosphate glucose</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073829</TermUI>
      <String>Dol-P-Glc</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073833</TermUI>
      <String>glucosylphosphodolichol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073830</TermUI>
      <String>dolichol monophosphate glucose</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073832</TermUI>
      <String>dolichylglucose phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0043831</ConceptUI>
    <ConceptName>
     <String>glucosylphosphoryldolicholbeta-D-Glucopyranose, 1-ester with dolichol dihydrogen phosphate</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0043832</Concept1UI>
     <Concept2UI>M0043831</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073834</TermUI>
      <String>glucosylphosphoryldolicholbeta-D-Glucopyranose, 1-ester with dolichol dihydrogen phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C511112</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>7-hydroxymethyl-8,8-dimethyl-4,8-dihydrobenzol(1, 4)thiazine-3,5-dione-(2-O-caffeoyl)-beta-D-glucopyranoside</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>06</Month>
   <Day>19</Day>
  </DateCreated>
  <Note>A thiazinedione from Xanthium strumarium; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009005</DescriptorUI>
     <DescriptorName>
      <String>Monosaccharides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013843</DescriptorUI>
     <DescriptorName>
      <String>Thiazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Fitoterapia. 2006 Apr;77(3):236-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0499082</ConceptUI>
    <ConceptName>
     <String>7-hydroxymethyl-8,8-dimethyl-4,8-dihydrobenzol(1, 4)thiazine-3,5-dione-(2-O-caffeoyl)-beta-D-glucopyranoside</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T676255</TermUI>
      <String>7-hydroxymethyl-8,8-dimethyl-4,8-dihydrobenzol(1, 4)thiazine-3,5-dione-(2-O-caffeoyl)-beta-D-glucopyranoside</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>06</Month>
       <Day>19</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T676256</TermUI>
      <String>7-HMDM-DHBT-G</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>06</Month>
       <Day>19</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C487766</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ABT724</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>07</Month>
   <Day>15</Day>
  </DateCreated>
  <Note>dopamine D4 receptors agonist; structure in first source
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001562</DescriptorUI>
     <DescriptorName>
      <String>Benzimidazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010879</DescriptorUI>
     <DescriptorName>
      <String>Piperazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011725</DescriptorUI>
     <DescriptorName>
      <String>Pyridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Proc Natl Acad Sci U S A 2004 Apr 27;101(17):6758-63</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0469119</ConceptUI>
    <ConceptName>
     <String>ABT724</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0469119</Concept1UI>
     <Concept2UI>M0469120</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T597005</TermUI>
      <String>ABT724</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T597006</TermUI>
      <String>ABT-724</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0469120</ConceptUI>
    <ConceptName>
     <String>2-((4-pyridin-2-ylpiperazine-1-yl)methyl)-1H-benzimidazole</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0469119</Concept1UI>
     <Concept2UI>M0469120</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T597007</TermUI>
      <String>2-((4-pyridin-2-ylpiperazine-1-yl)methyl)-1H-benzimidazole</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C043849</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-mercaptopyridine-2-sulfonamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1985</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>06</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011725</DescriptorUI>
     <DescriptorName>
      <String>Pyridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013449</DescriptorUI>
     <DescriptorName>
      <String>Sulfonamides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Belg 1984;39(4):217</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0128602</ConceptUI>
    <ConceptName>
     <String>3-mercaptopyridine-2-sulfonamide</String>
    </ConceptName>
    <CASN1Name>2-Pyridinesulfonamide, 3-mercapto-, (1R-(1alpha(Z),2beta(1E,3S*),5alpha))-</CASN1Name>
    <RegistryNumber>99780-72-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T158607</TermUI>
      <String>3-mercaptopyridine-2-sulfonamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T158606</TermUI>
      <String>MPSA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1985)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C055187</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>beta-lactamase PSE-2</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1988</Year>
   <Month>04</Month>
   <Day>14</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>nucleotide &amp; amino acid sequence of PSE-2 lactamase gene given in first source; hydrolyzes both carbenicillin &amp; oxacillin; contains 266 amino acid residues
  </Note>
  <Frequency>19</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001618</DescriptorUI>
     <DescriptorName>
      <String>beta-Lactamases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Antimicrob Agents Chemother 1988;32(1):134</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0155503</ConceptUI>
    <ConceptName>
     <String>beta-lactamase PSE-2</String>
    </ConceptName>
    <RegistryNumber>EC 3.5.2.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T185508</TermUI>
      <String>beta-lactamase PSE-2</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T185506</TermUI>
      <String>OXA-10</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T185507</TermUI>
      <String>PSE-2 beta-lactamase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1988)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C513833</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Hit1 protein, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>10</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>may be involved in dealing with high temperatures and water stress; amino acid sequence in first source
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D006360</DescriptorUI>
     <DescriptorName>
      <String>Heat-Shock Proteins</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Planta 2006 Jul;224(2):330-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0502298</ConceptUI>
    <ConceptName>
     <String>Hit1 protein, Arabidopsis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0502298</Concept1UI>
     <Concept2UI>M0502299</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T682587</TermUI>
      <String>Hit1 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>10</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T682588</TermUI>
      <String>heat-intolerant 1 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>10</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0502299</ConceptUI>
    <ConceptName>
     <String>Hit1-1 protein, Arabidopsis</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0502298</Concept1UI>
     <Concept2UI>M0502299</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T682589</TermUI>
      <String>Hit1-1 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>10</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012161</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N'-acetyl-N'-methyl-4'-amino-N,N-dimethyl-4-aminoazobenzene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1985</Year>
   <Month>04</Month>
   <Day>02</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>DIMETHYLAMINOAZOBENZENE/*analogs (76-84)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008749</DescriptorUI>
     <DescriptorName>
      <String>Methyldimethylaminoazobenzene</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Formosan Med Assn 74(8):18;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059033</ConceptUI>
    <ConceptName>
     <String>N'-acetyl-N'-methyl-4'-amino-N,N-dimethyl-4-aminoazobenzene</String>
    </ConceptName>
    <CASN1Name>Acetamide, N-(4-((4-(dimethylamino)phenyl)azo)phenyl)-N-methyl-</CASN1Name>
    <RegistryNumber>33804-48-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089036</TermUI>
      <String>N'-acetyl-N'-methyl-4'-amino-N,N-dimethyl-4-aminoazobenzene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015477</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>porphobilin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>dark brown, almost black pigment derived from porphobilinogen; probably a dipyrrylmethene
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011166</DescriptorUI>
     <DescriptorName>
      <String>Porphyrins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Experientia 33(7):873;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064758</ConceptUI>
    <ConceptName>
     <String>porphobilin</String>
    </ConceptName>
    <CASN1Name>Porphobilin</CASN1Name>
    <RegistryNumber>64176-86-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094761</TermUI>
      <String>porphobilin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015479</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-propoxy-17-methoxyestradiol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004958</DescriptorUI>
     <DescriptorName>
      <String>Estradiol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Can J Biochem 55(10):1096;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064761</ConceptUI>
    <ConceptName>
     <String>3-propoxy-17-methoxyestradiol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094764</TermUI>
      <String>3-propoxy-17-methoxyestradiol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015486</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>quinquangulin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>naphthopyrone from Cassia Quinquangulata; structure
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009284</DescriptorUI>
     <DescriptorName>
      <String>Naphthols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011753</DescriptorUI>
     <DescriptorName>
      <String>Pyrones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Lloydia 40(4):347;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064786</ConceptUI>
    <ConceptName>
     <String>quinquangulin</String>
    </ConceptName>
    <RegistryNumber>64894-58-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094789</TermUI>
      <String>quinquangulin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015492</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ribo-oligonucleotide A(7)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1995</Year>
   <Month>06</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>obtained by alkaline hydrolysis of poly A
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000227</DescriptorUI>
     <DescriptorName>
      <String>Adenine Nucleotides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009843</DescriptorUI>
     <DescriptorName>
      <String>Oligoribonucleotides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biophys Chem 7(3):205;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064791</ConceptUI>
    <ConceptName>
     <String>ribo-oligonucleotide A(7)</String>
    </ConceptName>
    <CASN1Name>Adenosine, adenylyl-(3'-5')-adenylyl-(3'-5')-adenylyl-(3'-5')-adenylyl-(3'-5')-adenylyl-(3'-5')-adenylyl-(3'-5')-</CASN1Name>
    <RegistryNumber>17185-35-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094794</TermUI>
      <String>ribo-oligonucleotide A(7)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C018261</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>insulin, des(tetrapeptide)(B1-B4)-</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>13</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007328</DescriptorUI>
     <DescriptorName>
      <String>Insulin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochemistry 17(21):4550;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0069607</ConceptUI>
    <ConceptName>
     <String>insulin, des(tetrapeptide)(B1-B4)-</String>
    </ConceptName>
    <CASN1Name>Insulin, 1B-de-L-phenylalanine-2B-de-L-valine-3B-de-L-asparagine-4B-de-L-glutamine-</CASN1Name>
    <RegistryNumber>50645-80-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T099610</TermUI>
      <String>insulin, des(tetrapeptide)(B1-B4)-</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T099609</TermUI>
      <String>des(tetrapeptide)(B1-B4)-insulin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C487865</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>isopanduratin A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>07</Month>
   <Day>20</Day>
  </DateCreated>
  <Note>isolated from Kaempferia pandurata; structure in first source
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010936</DescriptorUI>
     <DescriptorName>
      <String>Plant Extracts</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Int J Antimicrob Agents. 2004 Apr;23(4):377-81</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0469367</ConceptUI>
    <ConceptName>
     <String>isopanduratin A</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T597975</TermUI>
      <String>isopanduratin A</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>20</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015500</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>(4R)-5,10-secoestra-4,5-diene-3,10,17-trione</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SECOSTEROIDS (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004963</DescriptorUI>
     <DescriptorName>
      <String>Estrenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Steroid Biochem 8(4):307;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064805</ConceptUI>
    <ConceptName>
     <String>(4R)-5,10-secoestra-4,5-diene-3,10,17-trione</String>
    </ConceptName>
    <CASN1Name>1H-Cyclodec(e)indene-3,6,9(2H)-trione, 11,12-didehydro-3a,4,5,5a,7,8,12,13,13a,13b-decahydro-3a-methyl-, stereoisomer</CASN1Name>
    <RegistryNumber>60398-18-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094808</TermUI>
      <String>(4R)-5,10-secoestra-4,5-diene-3,10,17-trione</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015502</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>septacidin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>10</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>19</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011684</DescriptorUI>
     <DescriptorName>
      <String>Purine Nucleosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Antibiotiki 23(7):579;1978</Source>
   <Source>J Med Chem 20(11):1362;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064812</ConceptUI>
    <ConceptName>
     <String>septacidin</String>
    </ConceptName>
    <CASN1Name>L-glycero-beta-L-gluco-Heptopyranosylamine, 4-deoxy-4-((((14-methyl-1-oxopentadecyl)amino)acetyl)amino)-N-1H-purin-6-yl-</CASN1Name>
    <RegistryNumber>62362-59-8</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0064812</Concept1UI>
     <Concept2UI>M0064810</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0064812</Concept1UI>
     <Concept2UI>M0064808</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0064812</Concept1UI>
     <Concept2UI>M0064811</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0064812</Concept1UI>
     <Concept2UI>M0064809</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094815</TermUI>
      <String>septacidin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0064810</ConceptUI>
    <ConceptName>
     <String>LIA-0101 B</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0064812</Concept1UI>
     <Concept2UI>M0064810</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T094813</TermUI>
      <String>LIA-0101 B</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0064808</ConceptUI>
    <ConceptName>
     <String>2'-epi-septacidin</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0064812</Concept1UI>
     <Concept2UI>M0064808</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T094811</TermUI>
      <String>2'-epi-septacidin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0064811</ConceptUI>
    <ConceptName>
     <String>spicamycin</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0064812</Concept1UI>
     <Concept2UI>M0064811</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T094814</TermUI>
      <String>spicamycin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0064809</ConceptUI>
    <ConceptName>
     <String>LIA-0101</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0064812</Concept1UI>
     <Concept2UI>M0064809</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T094812</TermUI>
      <String>LIA-0101</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015506</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>sirenin (Allomyces)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>03</Month>
   <Day>21</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001643</DescriptorUI>
     <DescriptorName>
      <String>Bridged Bicyclo Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Exp Cell Res 109(1):43;1977</Source>
   <Source>Exp Cell Res 113(1):161;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064820</ConceptUI>
    <ConceptName>
     <String>sirenin (Allomyces)</String>
    </ConceptName>
    <CASN1Name>7-(5-hydroxy-4-methyl-3-pentenyl)-7-methylbicyclo(4.1.0.)hept-2-ene-3-methanol</CASN1Name>
    <RegistryNumber>19888-27-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094823</TermUI>
      <String>sirenin (Allomyces)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015513</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>sturin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>06</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>see also sturin A &amp; sturin B
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011479</DescriptorUI>
     <DescriptorName>
      <String>Protamines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biokhimiia 42(9):1668;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064831</ConceptUI>
    <ConceptName>
     <String>sturin</String>
    </ConceptName>
    <CASN1Name>Sturin</CASN1Name>
    <RegistryNumber>59141-16-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094834</TermUI>
      <String>sturin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015517</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>sulfoacetaldehyde</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>06</Month>
   <Day>23</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>26</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ALKYL SULFONATES (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000079</DescriptorUI>
     <DescriptorName>
      <String>Acetaldehyde</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biochem (Tokyo) 81(6):1911;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064847</ConceptUI>
    <ConceptName>
     <String>sulfoacetaldehyde</String>
    </ConceptName>
    <CASN1Name>Ethanesulfonic acid, 2-oxo-</CASN1Name>
    <RegistryNumber>32797-12-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094850</TermUI>
      <String>sulfoacetaldehyde</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015521</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>suprasterol(2) I</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>07</Month>
   <Day>10</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CYCLOSTEROIDS (78-80)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013261</DescriptorUI>
     <DescriptorName>
      <String>Sterols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nutr Sci Vitaminol 4(23):291;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064851</ConceptUI>
    <ConceptName>
     <String>suprasterol(2) I</String>
    </ConceptName>
    <CASN1Name>7,19:8,19-Dicyclo-9,10-secoergosta-5(10),22-dien-2-ol, (2alpha,7alpha,8S,19alpha,22E)-</CASN1Name>
    <RegistryNumber>42763-68-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094854</TermUI>
      <String>suprasterol(2) I</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015522</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>suprasterol(2) II</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CYCLOSTEROIDS (78-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013261</DescriptorUI>
     <DescriptorName>
      <String>Sterols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nutr Sci Vitaminol 4(23):291;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064852</ConceptUI>
    <ConceptName>
     <String>suprasterol(2) II</String>
    </ConceptName>
    <RegistryNumber>562-71-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094855</TermUI>
      <String>suprasterol(2) II</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015532</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tetrakis(3-N-methylpyridyl)porphinecobalt(III)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008665</DescriptorUI>
     <DescriptorName>
      <String>Metalloporphyrins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D003035</DescriptorUI>
     <DescriptorName>
      <String>Cobalt</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Bioinorg Chem 7(3):267;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064875</ConceptUI>
    <ConceptName>
     <String>tetrakis(3-N-methylpyridyl)porphinecobalt(III)</String>
    </ConceptName>
    <CASN1Name>Cobalt(5+), ((3,3',3'',3'''-(21H,23H-porphine-5,10,15,20-tetrayl)tetrakis(1-methylpyridiniumato))(2-)-N21,N22,N23,N24)-, (SP-4-1)-</CASN1Name>
    <RegistryNumber>63947-81-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094878</TermUI>
      <String>tetrakis(3-N-methylpyridyl)porphinecobalt(III)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015533</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,2,6,6-tetramethyl-4-bromoacetoxypiperidine-1-oxyl</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>06</Month>
   <Day>15</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PIPERIDINES (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003497</DescriptorUI>
     <DescriptorName>
      <String>Cyclic N-Oxides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biokhimiia 42(6):1117;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064876</ConceptUI>
    <ConceptName>
     <String>2,2,6,6-tetramethyl-4-bromoacetoxypiperidine-1-oxyl</String>
    </ConceptName>
    <CASN1Name>1-Piperidinyloxy, 4-((bromoacetyl)oxy)-2,2,6,6-tetramethyl-</CASN1Name>
    <RegistryNumber>39967-58-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094879</TermUI>
      <String>2,2,6,6-tetramethyl-4-bromoacetoxypiperidine-1-oxyl</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015538</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-(2-thienyl)valeric acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>06</Month>
   <Day>16</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>THIOPHENES (78-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010421</DescriptorUI>
     <DescriptorName>
      <String>Pentanoic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 499:315;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064885</ConceptUI>
    <ConceptName>
     <String>5-(2-thienyl)valeric acid</String>
    </ConceptName>
    <RegistryNumber>21010-06-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094888</TermUI>
      <String>5-(2-thienyl)valeric acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015544</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tiaramide N-oxide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>06</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>tertiary amine N-oxide
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*THIAZOLES (78-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010879</DescriptorUI>
     <DescriptorName>
      <String>Piperazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 77(4):1143;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064896</ConceptUI>
    <ConceptName>
     <String>tiaramide N-oxide</String>
    </ConceptName>
    <RegistryNumber>54439-76-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094899</TermUI>
      <String>tiaramide N-oxide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015546</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tolypomycinone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>related to rifamycin S
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012294</DescriptorUI>
     <DescriptorName>
      <String>Rifamycins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 20(10):1287;1977</Source>
   <Source>Mol Pharmacol 14(4):693;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064902</ConceptUI>
    <ConceptName>
     <String>tolypomycinone</String>
    </ConceptName>
    <CASN1Name>4-de((tetrahydro-6-hydroxy-2-methyl-2H-pyran-2- yl)imino)-4-oxotolypomycin Y</CASN1Name>
    <RegistryNumber>22356-23-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094905</TermUI>
      <String>tolypomycinone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000287</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bis(3-hydroxypropyl)trisulfide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>12</Month>
   <Day>17</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ALCOHOL, PROPYL (71-75)</PreviousIndexing>
   <PreviousIndexing>ALCOHOL, PROPYL/analogs (75-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013440</DescriptorUI>
     <DescriptorName>
      <String>Sulfides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040361</ConceptUI>
    <ConceptName>
     <String>bis(3-hydroxypropyl)trisulfide</String>
    </ConceptName>
    <RegistryNumber>29229-36-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070363</TermUI>
      <String>bis(3-hydroxypropyl)trisulfide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000291</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>AY 9928</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>07</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>RN &amp; NM refers to di-HCl
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*METHYLAMINES (73-80)</PreviousIndexing>
   <PreviousIndexing>CYCLOHEXANES (73-80)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003510</DescriptorUI>
     <DescriptorName>
      <String>Cyclohexanes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040371</ConceptUI>
    <ConceptName>
     <String>AY 9928</String>
    </ConceptName>
    <CASN1Name>1,4-cyclohexanedimethanamine, N,N'-bis(1-naphthalenylmethyl)-, dihydrochloride</CASN1Name>
    <RegistryNumber>1257-14-3</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>7303-04-0 (di-HCl(cis)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>7303-05-1 (di-HCl(trans)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0040371</Concept1UI>
     <Concept2UI>M0307401</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0040371</Concept1UI>
     <Concept2UI>M0040370</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0040371</Concept1UI>
     <Concept2UI>M0307400</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T070373</TermUI>
      <String>AY 9928</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T070371</TermUI>
      <String>AY-9928</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0307401</ConceptUI>
    <ConceptName>
     <String>AY 9928, dihydrochloride, (trans)-isomer</String>
    </ConceptName>
    <RegistryNumber>7303-05-1</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0040371</Concept1UI>
     <Concept2UI>M0307401</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T337401</TermUI>
      <String>AY 9928, dihydrochloride, (trans)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0040370</ConceptUI>
    <ConceptName>
     <String>N,N'-bis(1-naphthylmethyl)-1,4-cyclohexanebis(methylamine).2HCl</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0040371</Concept1UI>
     <Concept2UI>M0040370</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T070372</TermUI>
      <String>N,N'-bis(1-naphthylmethyl)-1,4-cyclohexanebis(methylamine).2HCl</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0307400</ConceptUI>
    <ConceptName>
     <String>AY 9928, dihydrochloride, (cis)-isomer</String>
    </ConceptName>
    <RegistryNumber>7303-04-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0040371</Concept1UI>
     <Concept2UI>M0307400</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T337400</TermUI>
      <String>AY 9928, dihydrochloride, (cis)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000293</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bisnoryangonin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>12</Month>
   <Day>17</Day>
  </DateRevised>
  <Note>extract from mushrooms
  </Note>
  <Frequency>4</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PYRANS (72-75)</PreviousIndexing>
   <PreviousIndexing>PLANT EXTRACTS (73-76)</PreviousIndexing>
   <PreviousIndexing>STYRENES (72-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011753</DescriptorUI>
     <DescriptorName>
      <String>Pyrones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Biochem Biophys 169:84;1975</Source>
   <Source>J Pharm Sci 61(2):318;1972</Source>
   <Source>J Pharm Sci 67(4):485;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040372</ConceptUI>
    <ConceptName>
     <String>bisnoryangonin</String>
    </ConceptName>
    <CASN1Name>4-hydroxy-6-(4-hydroxystyryl)-2-pyrone</CASN1Name>
    <RegistryNumber>13709-27-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070374</TermUI>
      <String>bisnoryangonin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000277</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>EL 241</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>24</Day>
  </DateRevised>
  <Note>RN given refers to parent compound; presence in urine characteristic of aspartylgluucosaminuria; structure.
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>ALCOHOL, METHYL (71-75)</PreviousIndexing>
   <PreviousIndexing>CHLOROBENZENES (74-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011725</DescriptorUI>
     <DescriptorName>
      <String>Pyridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040352</ConceptUI>
    <ConceptName>
     <String>EL 241</String>
    </ConceptName>
    <CASN1Name>alpha-alpha-bis(p-chlorophenyl)-3-pyridine methanol</CASN1Name>
    <RegistryNumber>17781-31-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070354</TermUI>
      <String>EL 241</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T070353</TermUI>
      <String>EL-241</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001054</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N,N-dimethyl-2-phenylaziridinium</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1970</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>07</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>RN given refers to parent cpd without isomeric designation
  </Note>
  <Frequency>10</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AZIRINES (70-75)</PreviousIndexing>
   <PreviousIndexing>DIMETHYLAMINES (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001388</DescriptorUI>
     <DescriptorName>
      <String>Aziridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041134</ConceptUI>
    <ConceptName>
     <String>N,N-dimethyl-2-phenylaziridinium</String>
    </ConceptName>
    <RegistryNumber>2641-72-7</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>18945-82-9 (bromide.HBr)</RelatedRegistryNumber>
     <RelatedRegistryNumber>7244-65-7 ((-)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0041134</Concept1UI>
     <Concept2UI>M0307545</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0041134</Concept1UI>
     <Concept2UI>M0041133</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0041134</Concept1UI>
     <Concept2UI>M0307546</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071137</TermUI>
      <String>N,N-dimethyl-2-phenylaziridinium</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T071135</TermUI>
      <String>N,N-DM2PA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0307545</ConceptUI>
    <ConceptName>
     <String>N,N-dimethyl-2-phenylaziridinium, hydrobromide</String>
    </ConceptName>
    <RegistryNumber>18945-82-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0041134</Concept1UI>
     <Concept2UI>M0307545</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T337545</TermUI>
      <String>N,N-dimethyl-2-phenylaziridinium, hydrobromide</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0041133</ConceptUI>
    <ConceptName>
     <String>N,N-dimethyl-2-phenylaziridinium ion</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0041134</Concept1UI>
     <Concept2UI>M0041133</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T071136</TermUI>
      <String>N,N-dimethyl-2-phenylaziridinium ion</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0307546</ConceptUI>
    <ConceptName>
     <String>N,N-dimethyl-2-phenylaziridinium, (-)-isomer</String>
    </ConceptName>
    <RegistryNumber>7244-65-7</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0041134</Concept1UI>
     <Concept2UI>M0307546</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T337546</TermUI>
      <String>N,N-dimethyl-2-phenylaziridinium, (-)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1970)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C000297</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bithionol sulfoxide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1971</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>17</Day>
  </DateRevised>
  <Note>RN given refers to parent cpd; structure
  </Note>
  <Frequency>8</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PHENOLS (71-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D001735</DescriptorUI>
     <DescriptorName>
      <String>Bithionol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Res. Vet. Sci 18(1):109;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0040388</ConceptUI>
    <ConceptName>
     <String>bithionol sulfoxide</String>
    </ConceptName>
    <RegistryNumber>844-26-8</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>55511-30-3 (mono-Na salt)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0040388</Concept1UI>
     <Concept2UI>M0040385</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0040388</Concept1UI>
     <Concept2UI>M0307408</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T070390</TermUI>
      <String>bithionol sulfoxide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T070389</TermUI>
      <String>bis(3,5-dichloro-2-hydroxyphenyl)sulfoxide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T070388</TermUI>
      <String>bis(2-hydroxy-3,5-dichlorophenyl)sulfoxide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0040385</ConceptUI>
    <ConceptName>
     <String>Bitin-S</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0040388</Concept1UI>
     <Concept2UI>M0040385</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="TRD"  RecordPreferredTermYN="N">
      <TermUI>T070387</TermUI>
      <String>Bitin-S</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0307408</ConceptUI>
    <ConceptName>
     <String>bithionol sulfoxide, monosodium salt</String>
    </ConceptName>
    <RegistryNumber>55511-30-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0040388</Concept1UI>
     <Concept2UI>M0307408</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T337408</TermUI>
      <String>bithionol sulfoxide, monosodium salt</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1971)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C511819</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>PICALM-MLLT10 fusion protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>07</Month>
   <Day>18</Day>
  </DateCreated>
  <Note>fusion in acute monocytic leukemia; MLLT - myeloid/lymphoid or mixed-lineage leukemia; PICALM - clathrin assembly protein-like lymphoid leukemia
  </Note>
  <Frequency>7</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015514</DescriptorUI>
     <DescriptorName>
      <String>Oncogene Proteins, Fusion</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D007948</DescriptorUI>
     <DescriptorName>
      <String>Leukemia, Monocytic, Acute</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Genes Chromosomes Cancer 2006 Jun;45(6):575-82</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0499950</ConceptUI>
    <ConceptName>
     <String>PICALM-MLLT10 fusion protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T678062</TermUI>
      <String>PICALM-MLLT10 fusion protein, human</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>07</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C418763</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2',3'-dideoxy-3'-fluorocytidine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003841</DescriptorUI>
     <DescriptorName>
      <String>Deoxycytidine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Carbohydr Res 2000 Aug 18;328(1):49-59</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0377131</ConceptUI>
    <ConceptName>
     <String>2',3'-dideoxy-3'-fluorocytidine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T434049</TermUI>
      <String>2',3'-dideoxy-3'-fluorocytidine</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>01</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T434050</TermUI>
      <String>2',3'-dideoxy-3'-fluoro-alpha-L-cytidine</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>01</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T434051</TermUI>
      <String>3-FLT cpd</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>01</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C414177</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SLC7A2 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>10</Month>
   <Day>10</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>07</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>RefSeq NM_003046
  </Note>
  <Frequency>30</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CALCIUM CHANNELS (2000-2006)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D026923</DescriptorUI>
     <DescriptorName>
      <String>Amino Acid Transport Systems, Basic</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 2000 Sep 8;275(36):28186-94</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0370965</ConceptUI>
    <ConceptName>
     <String>SLC7A2 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T650201</TermUI>
      <String>SLC7A2 protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>09</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T437556</TermUI>
      <String>hCAT-2 transport protein</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>02</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T437555</TermUI>
      <String>CAT-2 transport protein, human</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>02</Month>
       <Day>28</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T650202</TermUI>
      <String>solute carrier family 7 (cationic amino acid transporter, y+ system), member 2 protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>09</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T443147</TermUI>
      <String>CAT-2 transporter, human</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>04</Month>
       <Day>17</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C097501</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>acetyl coenzyme A-salutaridinol-7-O-acetyltransferase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>02</Month>
   <Day>06</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>25</Day>
  </DateRevised>
  <Note>catalyzes the transfer of acetyl from acetyl coenzyme A to the 7-OH group of salutaridinol which yields salutaridinol-7-O-acetate, an intermediate in morphine biosynthesis; from Papaver somniferum plant cell cultures
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000123</DescriptorUI>
     <DescriptorName>
      <String>Acetyltransferases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 1995 Dec 29;270(52):31091-6</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0256301</ConceptUI>
    <ConceptName>
     <String>acetyl coenzyme A-salutaridinol-7-O-acetyltransferase</String>
    </ConceptName>
    <RegistryNumber>EC 2.3.1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T286306</TermUI>
      <String>acetyl coenzyme A-salutaridinol-7-O-acetyltransferase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T286305</TermUI>
      <String>salutaridinol-7-O-acetyltransferase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T286304</TermUI>
      <String>acetyl CoA-salutaridinol-7-O-acetyltransferase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C581069</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Nup160 protein, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>05</Month>
   <Day>15</Day>
  </DateCreated>
  <Note>required for disease resistance
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D028861</DescriptorUI>
     <DescriptorName>
      <String>Nuclear Pore Complex Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Plant Signal Behav. 2012 Oct 1;7(10):1212-4</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0584771</ConceptUI>
    <ConceptName>
     <String>Nup160 protein, Arabidopsis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T844169</TermUI>
      <String>Nup160 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>05</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T844170</TermUI>
      <String>nucleoporin Nup160, Arabidopsis</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>05</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C581070</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>DRB3 protein, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>05</Month>
   <Day>15</Day>
  </DateCreated>
  <Note>RefSeq NM_113606
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D016601</DescriptorUI>
     <DescriptorName>
      <String>RNA-Binding Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Plant Signal Behav. 2012 Oct 1;7(10):1224-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0584772</ConceptUI>
    <ConceptName>
     <String>DRB3 protein, Arabidopsis</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T844171</TermUI>
      <String>DRB3 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>05</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T844172</TermUI>
      <String>dsRNA-binding protein 3, Arabidopsis</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>05</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C067184</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-(cyclohexylmethylamino)-1,2-naphthoquinone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1991</Year>
   <Month>03</Month>
   <Day>09</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009285</DescriptorUI>
     <DescriptorName>
      <String>Naphthoquinones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Pharm Res 1990;7(10):1071</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0184237</ConceptUI>
    <ConceptName>
     <String>4-(cyclohexylmethylamino)-1,2-naphthoquinone</String>
    </ConceptName>
    <RegistryNumber>25107-73-7</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0184237</Concept1UI>
     <Concept2UI>M0184239</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T214242</TermUI>
      <String>4-(cyclohexylmethylamino)-1,2-naphthoquinone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0184239</ConceptUI>
    <ConceptName>
     <String>CGS 19213</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0184237</Concept1UI>
     <Concept2UI>M0184239</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T214244</TermUI>
      <String>CGS 19213</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T214243</TermUI>
      <String>CGS-19213</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C029959</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>benzyloxycarbonylalanine chloromethyl ketone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>06</Month>
   <Day>24</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>inhibits the processing of prolipoprotein of E coli; RN given refers to (S)-(-)-isomer
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000590</DescriptorUI>
     <DescriptorName>
      <String>Amino Acid Chloromethyl Ketones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 1981;256(10):4712</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0095153</ConceptUI>
    <ConceptName>
     <String>benzyloxycarbonylalanine chloromethyl ketone</String>
    </ConceptName>
    <CASN1Name>carbamic acid, (3-chloro-1-methyl-2-oxopropyl)-, phenylmethyl ester, (S)-</CASN1Name>
    <RegistryNumber>41036-43-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T125156</TermUI>
      <String>benzyloxycarbonylalanine chloromethyl ketone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T125154</TermUI>
      <String>Z-Ala-chloromethyl ketone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T125155</TermUI>
      <String>benzyloxycarbonyl-Ala-chloromethyl ketone</String>
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       <ThesaurusID>NLM (1981)</ThesaurusID>
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   <Year>1969</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>1998</Year>
   <Month>01</Month>
   <Day>07</Day>
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  <PreviousIndexingList>
   <PreviousIndexing>*CYCLIC P-OXIDES (69-75)</PreviousIndexing>
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   <Source>J Dent Res 1980;59(1):77</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0046316</ConceptUI>
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      <TermUI>T076319</TermUI>
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   <Month>01</Month>
   <Day>06</Day>
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  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>12</Day>
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  <Note>antibiotic complex from Streptomyces aculeolatus
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   <Source>Biochem Pharmacol 1991;42(10):2019-26</Source>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
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    <TermList>
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   <String>2,4-dimethoxybenzhydrylamine</String>
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  <DateCreated>
   <Year>1993</Year>
   <Month>07</Month>
   <Day>12</Day>
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   <Year>2000</Year>
   <Month>12</Month>
   <Day>15</Day>
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     <DescriptorUI>*D001559</DescriptorUI>
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  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D012116</DescriptorUI>
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      <String>Resins, Plant</String>
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  <SourceList>
   <Source>J Med Chem 1993 Jun 11;36(12):1681-8</Source>
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   <Concept PreferredConceptYN="Y">
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    <RegistryNumber>106864-38-4</RegistryNumber>
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      <TermUI>T247774</TermUI>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T247773</TermUI>
      <String>2,4-DMBHA</String>
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       <ThesaurusID>NLM (1993)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C023845</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-ethyl-N-hydroxyethylnitrosamine</String>
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  <DateCreated>
   <Year>1980</Year>
   <Month>05</Month>
   <Day>06</Day>
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  <DateRevised>
   <Year>2000</Year>
   <Month>12</Month>
   <Day>15</Day>
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  <Frequency>64</Frequency>
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    <DescriptorReferredTo>
     <DescriptorUI>D004052</DescriptorUI>
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      <String>Diethylnitrosamine</String>
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     <QualifierUI>*Q000031</QualifierUI>
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      <String>analogs &amp; derivatives</String>
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      <DescriptorReferredTo>
       <DescriptorUI>D002273</DescriptorUI>
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         <String>Carcinogens</String>
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   <Source>Gan 1979;70(6):817</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0081530</ConceptUI>
    <ConceptName>
     <String>N-ethyl-N-hydroxyethylnitrosamine</String>
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    <CASN1Name>2-(ethylnitrosamino)ethanol</CASN1Name>
    <RegistryNumber>13147-25-6</RegistryNumber>
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     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T111533</TermUI>
      <String>N-ethyl-N-hydroxyethylnitrosamine</String>
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       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T111532</TermUI>
      <String>N-nitrosoethyl-2-hydroxyethylamine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T111531</TermUI>
      <String>N-ethyl-N-(2-hydroxyethyl)nitrosamine</String>
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       <ThesaurusID>NLM (1980)</ThesaurusID>
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  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C581071</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>DRB5 protein, Arabidopsis</String>
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  <DateCreated>
   <Year>2013</Year>
   <Month>05</Month>
   <Day>15</Day>
  </DateCreated>
  <Note>RefSeq NM_123472
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  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D016601</DescriptorUI>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
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  <SourceList>
   <Source>Plant Signal Behav. 2012 Oct 1;7(10):1224-9</Source>
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   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0584773</ConceptUI>
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      <DateCreated>
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       <Month>05</Month>
       <Day>15</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T844174</TermUI>
      <String>dsRNA-binding protein 5, Arabidopsis</String>
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       <Month>05</Month>
       <Day>15</Day>
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  <SupplementalRecordUI>C080506</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-(2-(bis(4-fluorophenyl)methylthio)ethyl)-N-methyl-N-(2-phenyl)ethylamine</String>
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  <DateCreated>
   <Year>1993</Year>
   <Month>04</Month>
   <Day>29</Day>
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  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
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  <Note>structure given in first source; calmodulin antagonist
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  <Frequency>1</Frequency>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001559</DescriptorUI>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003543</DescriptorUI>
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      <String>Cysteamine</String>
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     <DescriptorReferredTo>
    <DescriptorUI>D008024</DescriptorUI>
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  <SourceList>
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    <CASN1Name>Benzeneethanamine, N-(2-((bis(4-fluorophenyl)methyl)thio)ethyl)-N-methyl-3-(trifluoromethyl)-</CASN1Name>
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      <TermUI>T245099</TermUI>
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       <ThesaurusID>NLM (1993)</ThesaurusID>
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   <Concept PreferredConceptYN="N">
    <ConceptUI>M0215096</ConceptUI>
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     <Concept2UI>M0215096</Concept2UI>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
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  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>1980</Year>
   <Month>12</Month>
   <Day>30</Day>
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  <Note>yeast preparation
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  <Frequency>2</Frequency>
  <HeadingMappedToList>
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    <DescriptorReferredTo>
     <DescriptorUI>*D015002</DescriptorUI>
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   <Source>Radiol Clin Biol 42(3):222;1973</Source>
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      <TermUI>T076370</TermUI>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
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  <SupplementalRecordName>
   <String>2-deoxy-6-phosphogluconate</String>
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  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>08</Day>
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  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>DEOXY SUGARS (73-76)</PreviousIndexing>
   <PreviousIndexing>HEXOSEPHOSPHATES (73-82)</PreviousIndexing>
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    <DescriptorReferredTo>
     <DescriptorUI>*D005942</DescriptorUI>
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      <String>Gluconates</String>
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   <Source>J Biol Chem 248(14):4920;1973</Source>
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    <CASN1Name>D-arabino-Hexonic acid, 2-deoxy-, 6-(dihydrogen phosphate)</CASN1Name>
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<SupplementalRecord SCRClass = "1">
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   <String>succinyl-alanyl-alanyl-prolyl-valine chloromethyl ketone</String>
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  <DateCreated>
   <Year>1981</Year>
   <Month>08</Month>
   <Day>20</Day>
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  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
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  <Frequency>3</Frequency>
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    <DescriptorReferredTo>
     <DescriptorUI>*D000590</DescriptorUI>
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   <IndexingInformation>
     <DescriptorReferredTo>
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    <QualifierUI>Q000037</QualifierUI>
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   <Source>Am Rev Respir Dis 1981;124(1):56</Source>
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    <CASN1Name>L-Prolinamide, N-(3-carboxy-1-oxopropyl)-L-alanyl-L-alanyl-N-(3-chloro-1-(1-methylethyl)-2-oxopropyl)-, (S)-</CASN1Name>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T128046</TermUI>
      <String>Suc-Ala-Ala-Pro-Val-chloromethyl ketone</String>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T128045</TermUI>
      <String>SAAPVC</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C030924</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>uropod inhibitory protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>08</Month>
   <Day>17</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>protein factor from human serum or plasma that inhibits uropod formation in T-lymphocytes
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001798</DescriptorUI>
     <DescriptorName>
      <String>Blood Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008894</DescriptorUI>
     <DescriptorName>
      <String>Milk Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biphys Res Commun 1981;100(1):139</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0097540</ConceptUI>
    <ConceptName>
     <String>uropod inhibitory protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T521705</TermUI>
      <String>uropod inhibitory protein, human</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>10</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006772</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,7,12,17-tetraethyl-3,8,13,18-tetramethyl-21H,23H-porphine rhodium complex</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>luminescing porphyrin; RN given refers to chloride dihydrate
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009942</DescriptorUI>
     <DescriptorName>
      <String>Organometallic Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011166</DescriptorUI>
     <DescriptorName>
      <String>Porphyrins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D012238</DescriptorUI>
     <DescriptorName>
      <String>Rhodium</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Am Chem Soc 95(15):4822;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049515</ConceptUI>
    <ConceptName>
     <String>2,7,12,17-tetraethyl-3,8,13,18-tetramethyl-21H,23H-porphine rhodium complex</String>
    </ConceptName>
    <CASN1Name>Rhodium(1+), bis(N-methylmethanamine)(2,7,12,17-tetraethyl-3,8,13,18-tetramethyl-21H,23H-porphinato(2-)-N(21),N(22),N(23),N(24))-, chloride, dihydrate, (OC-6-12)-</CASN1Name>
    <RegistryNumber>50773-64-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079518</TermUI>
      <String>2,7,12,17-tetraethyl-3,8,13,18-tetramethyl-21H,23H-porphine rhodium complex</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T079517</TermUI>
      <String>bis(dimethylamine)etio(I)porphinatorhodium(III) chloride dihydrate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005076</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hexanoylcholine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1984</Year>
   <Month>12</Month>
   <Day>11</Day>
  </DateRevised>
  <Note>RN given refers to parent cpd
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CHOLINE (73-75)</PreviousIndexing>
   <PreviousIndexing>CAPROATES (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002794</DescriptorUI>
     <DescriptorName>
      <String>Choline</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Jpn J Pharmacol 22(6):777;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0046392</ConceptUI>
    <ConceptName>
     <String>hexanoylcholine</String>
    </ConceptName>
    <CASN1Name>N,N,N-trimethyl-2-((1-oxohexyl)oxy)ethanaminium</CASN1Name>
    <RegistryNumber>16639-00-2</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>18885-38-6 (iodide)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0046392</Concept1UI>
     <Concept2UI>M0308897</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0046392</Concept1UI>
     <Concept2UI>M0046391</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T076395</TermUI>
      <String>hexanoylcholine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0308897</ConceptUI>
    <ConceptName>
     <String>iodide of hexanoylcholine</String>
    </ConceptName>
    <RegistryNumber>18885-38-6</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0046392</Concept1UI>
     <Concept2UI>M0308897</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T338897</TermUI>
      <String>iodide of hexanoylcholine</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0046391</ConceptUI>
    <ConceptName>
     <String>caprylylcholine</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0046392</Concept1UI>
     <Concept2UI>M0046391</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T076394</TermUI>
      <String>caprylylcholine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C088404</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-methoxymethyl-1,4-naphthoquinone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>08</Month>
   <Day>15</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>a bioreductive alkylating agent; structure given in first source; name given in first source (2-methylmethoxy....) is incorrect
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009285</DescriptorUI>
     <DescriptorName>
      <String>Naphthoquinones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem J 1994 Jul 1;301(Pt 1):21-30</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0233995</ConceptUI>
    <ConceptName>
     <String>2-methoxymethyl-1,4-naphthoquinone</String>
    </ConceptName>
    <RegistryNumber>39510-88-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T264000</TermUI>
      <String>2-methoxymethyl-1,4-naphthoquinone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T263998</TermUI>
      <String>2-MOM-1,4-naphthoquinone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T263999</TermUI>
      <String>2-methylmethoxy-1,4-naphthoquinone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C100451</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>NSC 117027</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>08</Month>
   <Day>22</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009285</DescriptorUI>
     <DescriptorName>
      <String>Naphthoquinones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 1996 Jun 21;39(13):2472-81</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0263717</ConceptUI>
    <ConceptName>
     <String>NSC 117027</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0263717</Concept1UI>
     <Concept2UI>M0263715</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T293722</TermUI>
      <String>NSC 117027</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T293721</TermUI>
      <String>NSC-117027</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0263715</ConceptUI>
    <ConceptName>
     <String>1,4-bis((di-(3-hydroxy-1,4-dioxo-1,4-dihydronaphthalen-2-yl))methyl)benzene</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0263717</Concept1UI>
     <Concept2UI>M0263715</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T293720</TermUI>
      <String>1,4-bis((di-(3-hydroxy-1,4-dioxo-1,4-dihydronaphthalen-2-yl))methyl)benzene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C033481</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-formylnorleucyl-leucyl-phenylalanine chloromethyl ketone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1982</Year>
   <Month>03</Month>
   <Day>05</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>chemotactic for &amp; induces lysosomal enzyme release from rabbit peritoneal neutrophils
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000590</DescriptorUI>
     <DescriptorName>
      <String>Amino Acid Chloromethyl Ketones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Cell Biochem 1981;41:19</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0103842</ConceptUI>
    <ConceptName>
     <String>N-formylnorleucyl-leucyl-phenylalanine chloromethyl ketone</String>
    </ConceptName>
    <CASN1Name>L-Leucinamide, N-formyl-L-norleucyl-N-(3-chloro-2-oxo-1-(phenylmethyl)propyl)-, (S)-</CASN1Name>
    <RegistryNumber>81134-56-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T133846</TermUI>
      <String>N-formylnorleucyl-leucyl-phenylalanine chloromethyl ketone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T133845</TermUI>
      <String>N-formyl-Nle-Leu-Phe-chloromethyl ketone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T133844</TermUI>
      <String>FNLPCK</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C095014</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>RPM1 protein, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>09</Month>
   <Day>08</Day>
  </DateCreated>
  <DateRevised>
   <Year>2002</Year>
   <Month>12</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>from Arabidopsis thaliana; shares molecular features with single-specificity disease resistance (R) genes; amino acid sequence given in first source; GenBank X87851; do not confuse with RPM-1 protein
  </Note>
  <Frequency>56</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PLANT PROTEINS (1995-2002)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Science 1995 Aug 11;269(5225):843-6</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0250253</ConceptUI>
    <ConceptName>
     <String>RPM1 protein, Arabidopsis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T517540</TermUI>
      <String>RPM1 protein, Arabidopsis</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>08</Month>
       <Day>26</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C033597</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>phenylalanyl-alanyl-arginine chloromethyl ketone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1982</Year>
   <Month>03</Month>
   <Day>15</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>urokinase active site inhibitor
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000590</DescriptorUI>
     <DescriptorName>
      <String>Amino Acid Chloromethyl Ketones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Invest Ophthalmol Vis Sci 1982;22(2):191</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0104163</ConceptUI>
    <ConceptName>
     <String>phenylalanyl-alanyl-arginine chloromethyl ketone</String>
    </ConceptName>
    <CASN1Name>L-Alaninamide, L-phenylalanyl-N-(4-((aminoiminomethyl)amino)-1-(chloroacetyl)butyl)-, (S)-</CASN1Name>
    <RegistryNumber>65319-55-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T134167</TermUI>
      <String>phenylalanyl-alanyl-arginine chloromethyl ketone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T134165</TermUI>
      <String>Phe-Ala-Arg-CK</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T134166</TermUI>
      <String>Phe-Ala-Arg-chloromethyl ketone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C039809</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2',3'-cyclic nucleotide 2'-phosphodiesterase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1983</Year>
   <Month>12</Month>
   <Day>13</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>10</Month>
   <Day>27</Day>
  </DateRevised>
  <Note>catalyzes the hydrolysis of the 2'-phosphodiesterase bond to yield nucleoside 3'phosphate
  </Note>
  <Frequency>13</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015087</DescriptorUI>
     <DescriptorName>
      <String>2',3'-Cyclic-Nucleotide Phosphodiesterases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0118944</ConceptUI>
    <ConceptName>
     <String>2',3'-cyclic nucleotide 2'-phosphodiesterase</String>
    </ConceptName>
    <RegistryNumber>EC 3.1.4.16</RegistryNumber>
    <RelatedRegistryNumberList>
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      <TermUI>T148948</TermUI>
      <String>2',3'-cyclic nucleotide 2'-phosphodiesterase</String>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T148947</TermUI>
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       <ThesaurusID>NLM (1983)</ThesaurusID>
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   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
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   <Month>01</Month>
   <Day>01</Day>
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  <SourceList>
   <Source>Biochemistry 12(15):2829;1973</Source>
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  <ConceptList>
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      <TermUI>T076489</TermUI>
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   <String>brilliant black</String>
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  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
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  <Frequency>7</Frequency>
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    <DescriptorReferredTo>
     <DescriptorUI>*D001391</DescriptorUI>
     <DescriptorName>
      <String>Azo Compounds</String>
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  <SourceList>
   <Source>Acta Histochem 45(2):317;1973</Source>
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      <TermUI>T079562</TermUI>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
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   <Concept PreferredConceptYN="N">
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     <String>C.I. 27260</String>
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     <Concept1UI>M0049559</Concept1UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T079561</TermUI>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005158</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>diaminodurene</String>
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  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <Note>structure
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  <Frequency>9</Frequency>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010655</DescriptorUI>
     <DescriptorName>
      <String>Phenylenediamines</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>BBA 449:125;1976</Source>
   <Source>Biochim Biophys Acta 305(1):105;1973</Source>
   <Source>Biochim Biophys Acta 396(2):310;1975</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0046502</ConceptUI>
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    <RegistryNumber>3102-87-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T076505</TermUI>
      <String>diaminodurene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
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     </Term>
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   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C038768</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>methoxysuccinate-alanyl-alanyl-valine chloromethyl ketone</String>
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  <DateCreated>
   <Year>1983</Year>
   <Month>09</Month>
   <Day>14</Day>
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  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000590</DescriptorUI>
     <DescriptorName>
      <String>Amino Acid Chloromethyl Ketones</String>
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   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D010196</DescriptorUI>
     <DescriptorName>
      <String>Pancreatic Elastase</String>
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     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
     <QualifierName>
      <String>antagonists &amp; inhibitors</String>
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  </IndexingInformationList>
  <SourceList>
   <Source>Mol Immunol 1983;20(6):623</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0116513</ConceptUI>
    <ConceptName>
     <String>methoxysuccinate-alanyl-alanyl-valine chloromethyl ketone</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T146517</TermUI>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T146516</TermUI>
      <String>methoxysuccinate-Ala-Ala-Val-chloromethyl ketone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T146515</TermUI>
      <String>MSAVCK</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1983)</ThesaurusID>
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     </Term>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005161</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>poly(N(6)-benzoyldeoxyadenylate)</String>
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  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*POLY A (76-79)</PreviousIndexing>
   <PreviousIndexing>*POLYNUCLEOTIDES (74-76)</PreviousIndexing>
   <PreviousIndexing>ADENINE NUCLEOTIDES (74-78)</PreviousIndexing>
   <PreviousIndexing>DEOXYRIBONUCLEOTIDES (74-78)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003838</DescriptorUI>
     <DescriptorName>
      <String>Deoxyadenine Nucleotides</String>
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   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011089</DescriptorUI>
     <DescriptorName>
      <String>Polydeoxyribonucleotides</String>
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  <SourceList>
   <Source>Biochim Biophys Acta 308(1):35;1973</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0046508</ConceptUI>
    <ConceptName>
     <String>poly(N(6)-benzoyldeoxyadenylate)</String>
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    <CASN1Name>5'-Adenylic acid, N-benzoyl-2'-deoxy-, homopolymer</CASN1Name>
    <RegistryNumber>59033-76-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T076511</TermUI>
      <String>poly(N(6)-benzoyldeoxyadenylate)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
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     </Term>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005162</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>poly(N(4)-anisoyldeoxycytidylate)</String>
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  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*POLYDEOXYRIBONUCLEOTIDES</PreviousIndexing>
   <PreviousIndexing>*POLYNUCLEOTIDES (74-76)</PreviousIndexing>
   <PreviousIndexing>CYTOSINE NUCLEOTIDES (74-75)</PreviousIndexing>
   <PreviousIndexing>DEOXYRIBONUCLEOTIDES (74-75)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003843</DescriptorUI>
     <DescriptorName>
      <String>Deoxycytidine Monophosphate</String>
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  <SourceList>
   <Source>Biochim Biophys Acta 308(1):35;1973</Source>
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    <ConceptUI>M0046509</ConceptUI>
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     <String>poly(N(4)-anisoyldeoxycytidylate)</String>
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    <CASN1Name>Cytidine, 2'-deoxy-N-(4-methoxybenzoyl)-, homopolymer</CASN1Name>
    <RegistryNumber>41911-89-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T076512</TermUI>
      <String>poly(N(4)-anisoyldeoxycytidylate)</String>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C041051</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dansylalanyllysine chloromethyl ketone</String>
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  <DateCreated>
   <Year>1984</Year>
   <Month>05</Month>
   <Day>29</Day>
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  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
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  <Note>fluorescent probe for localization of acrosin activity
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  <Frequency>1</Frequency>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000590</DescriptorUI>
     <DescriptorName>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003619</DescriptorUI>
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      <String>Dansyl Compounds</String>
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  <SourceList>
   <Source>J Histochem Cytochem 1984;32(5):526</Source>
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    <CASN1Name>Propanamide, N-(5-amino-1-(chloroacetyl)pentyl)-2-(((5-(dimethylamino)-1-naphthalenyl)sulfonyl)amino)-, (S-(R*,R*))-</CASN1Name>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T151913</TermUI>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
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       <ThesaurusID>NLM (1984)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005167</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,5-bis(2-chloroethylsulfonyl)pyrrole-3,4-dicarbonitrile</String>
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  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>07</Day>
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  <Note>lipolytic agent
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  <Frequency>0</Frequency>
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   <PreviousIndexing>ACETONITRILES (75-76)</PreviousIndexing>
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   <Source>J Lipid Res 14(2):250;1973</Source>
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    <RegistryNumber>40380-34-5</RegistryNumber>
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<SupplementalRecord SCRClass = "1">
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  <SupplementalRecordName>
   <String>2,4-diamino-6-butoxy-s-triazine</String>
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  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>07</Day>
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  <Note>lipolytic agent
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   <PreviousIndexing>DIAMINES (74-76)</PreviousIndexing>
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  <SourceList>
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  <DateCreated>
   <Year>1986</Year>
   <Month>01</Month>
   <Day>30</Day>
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  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
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   <Source>Biomed Biochim Acta 1985;44(7-8):1089</Source>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
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       <ThesaurusID>NLM (1986)</ThesaurusID>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T167158</TermUI>
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  <SupplementalRecordName>
   <String>glutamyl-glycyl-arginine chloromethyl ketone</String>
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  <DateCreated>
   <Year>1987</Year>
   <Month>03</Month>
   <Day>12</Day>
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  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
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  <Note>RN given refers to (S)-isomer
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    <DescriptorReferredTo>
     <DescriptorUI>*D000590</DescriptorUI>
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   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D014568</DescriptorUI>
     <DescriptorName>
      <String>Urokinase-Type Plasminogen Activator</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
     <QualifierName>
      <String>antagonists &amp; inhibitors</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Eur J Biochem 1987;162(2):351</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0146133</ConceptUI>
    <ConceptName>
     <String>glutamyl-glycyl-arginine chloromethyl ketone</String>
    </ConceptName>
    <RegistryNumber>65113-67-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0146133</Concept1UI>
     <Concept2UI>M0146132</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T176138</TermUI>
      <String>glutamyl-glycyl-arginine chloromethyl ketone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T176136</TermUI>
      <String>GGACK</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0146132</ConceptUI>
    <ConceptName>
     <String>Glu-Gly-Arg-chloromethane</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0146133</Concept1UI>
     <Concept2UI>M0146132</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T176137</TermUI>
      <String>Glu-Gly-Arg-chloromethane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1987)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005188</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Mandrax</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1968</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>06</Day>
  </DateRevised>
  <Note>contains methaqualone; diphenhydramine
  </Note>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004155</DescriptorUI>
     <DescriptorName>
      <String>Diphenhydramine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008702</DescriptorUI>
     <DescriptorName>
      <String>Methaqualone</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0046552</ConceptUI>
    <ConceptName>
     <String>Mandrax</String>
    </ConceptName>
    <RegistryNumber>8076-99-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T076555</TermUI>
      <String>Mandrax</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1968)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006801</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>brocillin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PENICILLIN (74-75)</PreviousIndexing>
   <PreviousIndexing>PHENYL ETHERS (74-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010404</DescriptorUI>
     <DescriptorName>
      <String>Penicillin V</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Lille Med 19(2):204;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049575</ConceptUI>
    <ConceptName>
     <String>brocillin</String>
    </ConceptName>
    <RegistryNumber>1245-44-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079578</TermUI>
      <String>brocillin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T079577</TermUI>
      <String>alpha-phenoxy propylpenicillin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005202</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-methyl-4-aminoazobenzene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1968</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>19</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AZO COMPOUNDS (68-76)</PreviousIndexing>
   <PreviousIndexing>ANILINE COMPOUNDS (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010128</DescriptorUI>
     <DescriptorName>
      <String>p-Aminoazobenzene</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Res 1979;39(9):3411</Source>
   <Source>Cancer Res 36(3):1196;1976</Source>
   <Source>J Biol Chem 252(11):3970;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0046577</ConceptUI>
    <ConceptName>
     <String>N-methyl-4-aminoazobenzene</String>
    </ConceptName>
    <RegistryNumber>621-90-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T076580</TermUI>
      <String>N-methyl-4-aminoazobenzene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1968)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C497937</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>STXBP1 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateCreated>
  <DateRevised>
   <Year>2008</Year>
   <Month>09</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>RefSeq NM_003165
  </Note>
  <Frequency>120</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D051938</DescriptorUI>
     <DescriptorName>
      <String>Munc18 Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0468856</ConceptUI>
    <ConceptName>
     <String>STXBP1 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T595795</TermUI>
      <String>STXBP1 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T595801</TermUI>
      <String>Munc-18 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T595800</TermUI>
      <String>n-sec1 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T595796</TermUI>
      <String>syntaxin binding protein 1, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T595799</TermUI>
      <String>p67 neuronal-specific protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T595798</TermUI>
      <String>rbSec1 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T595797</TermUI>
      <String>SEC1 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T595806</TermUI>
      <String>hUNC18 protein, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T595802</TermUI>
      <String>neuronal-specific protein, 67.5-kDa, human</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>07</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005215</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Fast Red S</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1969</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>01</Month>
   <Day>05</Day>
  </DateRevised>
  <Frequency>6</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>NAPHTHALENESULFONATES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001391</DescriptorUI>
     <DescriptorName>
      <String>Azo Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0046592</ConceptUI>
    <ConceptName>
     <String>Fast Red S</String>
    </ConceptName>
    <CASN1Name>4-(2-hydroxy-1-naphthylazo)-1-naphthalenesulfonic acid</CASN1Name>
    <RegistryNumber>1658-56-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T076595</TermUI>
      <String>Fast Red S</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1969)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C024223</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>vitamin MK 8</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>05</Month>
   <Day>14</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>09</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>isoprenoid acetone-soluble lipid
  </Note>
  <Frequency>332</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*LIPIDS (1980-1980)</PreviousIndexing>
   <PreviousIndexing>VITAMIN K/*analogs &amp; derivatives (1979-2001)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D024482</DescriptorUI>
     <DescriptorName>
      <String>Vitamin K 2</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Can J Microbiol 1979;25(11):1288</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0082192</ConceptUI>
    <ConceptName>
     <String>vitamin MK 8</String>
    </ConceptName>
    <CASN1Name>(all-E)-2-methyl-3-(3,7,11,15,19,23,27,31-octamethyl-2,6,10,14,18,22,26,30-dotriacontaoctaenyl)-1,4-naphthalenedione</CASN1Name>
    <RegistryNumber>523-38-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T112195</TermUI>
      <String>vitamin MK 8</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T112194</TermUI>
      <String>menaquinone 8</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C063351</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>isoleucyl-phenylalanyl-lysine chloromethyl ketone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1990</Year>
   <Month>04</Month>
   <Day>11</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>RN given is for cpd with L-Ile
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000590</DescriptorUI>
     <DescriptorName>
      <String>Amino Acid Chloromethyl Ketones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D007610</DescriptorUI>
     <DescriptorName>
      <String>Kallikreins</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000037</QualifierUI>
     <QualifierName>
      <String>antagonists &amp; inhibitors</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Chem Pharm Bull 1989;37(11):3108</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0174922</ConceptUI>
    <ConceptName>
     <String>isoleucyl-phenylalanyl-lysine chloromethyl ketone</String>
    </ConceptName>
    <RegistryNumber>126642-86-2</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>126583-13-9 (D-Ile)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0174922</Concept1UI>
     <Concept2UI>M0324618</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T204927</TermUI>
      <String>isoleucyl-phenylalanyl-lysine chloromethyl ketone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T204926</TermUI>
      <String>Ile-Phe-Lys-CH2Cl</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0324618</ConceptUI>
    <ConceptName>
     <String>isoleucyl-phenylalanyl-lysine chloromethyl ketone, D-Ile isomer</String>
    </ConceptName>
    <RegistryNumber>126583-13-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0174922</Concept1UI>
     <Concept2UI>M0324618</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T354618</TermUI>
      <String>isoleucyl-phenylalanyl-lysine chloromethyl ketone, D-Ile isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C065676</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>benzyloxycarbonylphenylalanyl-alanine chloromethyl ketone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1990</Year>
   <Month>10</Month>
   <Day>16</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>structure given in first source
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000590</DescriptorUI>
     <DescriptorName>
      <String>Amino Acid Chloromethyl Ketones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 1990;171(2):711</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0180517</ConceptUI>
    <ConceptName>
     <String>benzyloxycarbonylphenylalanyl-alanine chloromethyl ketone</String>
    </ConceptName>
    <RegistryNumber>60525-17-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T210522</TermUI>
      <String>benzyloxycarbonylphenylalanyl-alanine chloromethyl ketone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T210521</TermUI>
      <String>ZPACK</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T210520</TermUI>
      <String>Boc-Phe-Ala-CMK</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1990)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005228</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>methyl-12-hydroxystearate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>4</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*FATTY ACIDS (73-75)</PreviousIndexing>
   <PreviousIndexing>FATTY ALCOHOLS (73-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013228</DescriptorUI>
     <DescriptorName>
      <String>Stearates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0046623</ConceptUI>
    <ConceptName>
     <String>methyl-12-hydroxystearate</String>
    </ConceptName>
    <CASN1Name>methyl-12-hydroxyoctadecanoate</CASN1Name>
    <RegistryNumber>141-23-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T076626</TermUI>
      <String>methyl-12-hydroxystearate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006825</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-bromouridylyl-(3'-5')adenosine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>dinucleoside monophosphate
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*URACIL NUCLEOTIDES (75-88)</PreviousIndexing>
   <PreviousIndexing>ADENOSINE/*analogs (75-88)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D015226</DescriptorUI>
     <DescriptorName>
      <String>Dinucleoside Phosphates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Bact 120(2):831;1974</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0049612</ConceptUI>
    <ConceptName>
     <String>5-bromouridylyl-(3'-5')adenosine</String>
    </ConceptName>
    <CASN1Name>Adenosine, 5-bromouridylyl-(3'-5')-</CASN1Name>
    <RegistryNumber>53892-50-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T079615</TermUI>
      <String>5-bromouridylyl-(3'-5')adenosine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T079614</TermUI>
      <String>BUY-ADO</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1975)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005243</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>morphactins</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1968</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1997</Year>
   <Month>06</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>fluorenol-9-carboxylic acid derivs Chemline lists nine morphactins
  </Note>
  <Frequency>4</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CARBOXYLIC ACIDS (75-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005449</DescriptorUI>
     <DescriptorName>
      <String>Fluorenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Ultrastruct Res 59(2):140;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0046645</ConceptUI>
    <ConceptName>
     <String>morphactins</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T076648</TermUI>
      <String>morphactins</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1968)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C079507</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-formimidoyl fortimicin A synthase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1993</Year>
   <Month>03</Month>
   <Day>04</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>11</Month>
   <Day>24</Day>
  </DateRevised>
  <Note>amino acid sequence given in first source; an oxidase that converts fortimicin A and glycine to N-formimidoyl fortimicin A; requires O2 and FAD
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000594</DescriptorUI>
     <DescriptorName>
      <String>Amino Acid Oxidoreductases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Mol Gen Genet 1992 Dec;236(1):49-59</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0212811</ConceptUI>
    <ConceptName>
     <String>N-formimidoyl fortimicin A synthase</String>
    </ConceptName>
    <RegistryNumber>EC 1.4.3.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T242816</TermUI>
      <String>N-formimidoyl fortimicin A synthase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T242814</TermUI>
      <String>FI-FTMase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1993)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005347</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>alpha-phenyltetrahydrofuranone-2-gamma-carboxylic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>29</Day>
  </DateRevised>
  <Note>RN given refers to parent cpd; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>CARBOXYLIC ACIDS (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005663</DescriptorUI>
     <DescriptorName>
      <String>Furans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Immunol Ther Exp 21(20):309;1973</Source>
   <Source>Arch Immunol Ther Exp 25(6):819;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0046828</ConceptUI>
    <ConceptName>
     <String>alpha-phenyltetrahydrofuranone-2-gamma-carboxylic acid</String>
    </ConceptName>
    <RegistryNumber>22073-32-1</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>13389-96-3 (Na salt)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0046828</Concept1UI>
     <Concept2UI>M0309057</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T076831</TermUI>
      <String>alpha-phenyltetrahydrofuranone-2-gamma-carboxylic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0309057</ConceptUI>
    <ConceptName>
     <String>alpha-phenyltetrahydrofuranone-2-gamma-carboxylic acid, sodium salt</String>
    </ConceptName>
    <RegistryNumber>13389-96-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0046828</Concept1UI>
     <Concept2UI>M0309057</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T339057</TermUI>
      <String>alpha-phenyltetrahydrofuranone-2-gamma-carboxylic acid, sodium salt</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013326</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Ulcrux powder</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>07</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>for treatment of skin ulcers; contains tetracycline, dehydroacetic acid, hydroxypolyethoxydodecane
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>POWDERS (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011092</DescriptorUI>
     <DescriptorName>
      <String>Polyethylene Glycols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013752</DescriptorUI>
     <DescriptorName>
      <String>Tetracycline</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Fortschr Med 94(19):1148;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0060997</ConceptUI>
    <ConceptName>
     <String>Ulcrux powder</String>
    </ConceptName>
    <CASN1Name>2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-, monohydrochloride, (4S-(4alpha,4aalpha,5aalpha,6beta,12aalpha))-, mixt. with 3-acetyl-6-methyl-2H-pyran-2,4(3H)-dione monosodium salt</CASN1Name>
    <RegistryNumber>78891-91-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091000</TermUI>
      <String>Ulcrux powder</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C020268</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dansyl-L-arginine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>07</Month>
   <Day>05</Day>
  </DateRevised>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>DANSYL COMPOUNDS (79-80)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D001120</DescriptorUI>
     <DescriptorName>
      <String>Arginine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biochem (Tokyo) 85(4):961;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0073848</ConceptUI>
    <ConceptName>
     <String>dansyl-L-arginine</String>
    </ConceptName>
    <CASN1Name>N(2)-((5-(dimethylamino)-1-naphthalenyl)sulfonyl)-L-arginine</CASN1Name>
    <RegistryNumber>28217-22-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T103851</TermUI>
      <String>dansyl-L-arginine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C098372</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>P457 carotenoid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>04</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>09</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>isolated from some dinoflagellates; structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002338</DescriptorUI>
     <DescriptorName>
      <String>Carotenoids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D007785</DescriptorUI>
     <DescriptorName>
      <String>Lactose</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 1995 Nov;58(11):1675-82</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0258418</ConceptUI>
    <ConceptName>
     <String>P457 carotenoid</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T288423</TermUI>
      <String>P457 carotenoid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C033275</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SK&amp;F 93479</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1982</Year>
   <Month>03</Month>
   <Day>09</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>inhibits nocturnal acid secretion
  </Note>
  <Frequency>38</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011744</DescriptorUI>
     <DescriptorName>
      <String>Pyrimidinones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
    <PharmacologicalActionList>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D006635</DescriptorUI>
        <DescriptorName>
         <String>Histamine H2 Antagonists</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
    </PharmacologicalActionList>
  <SourceList>
   <Source>Lancet 1982;1(8265):224</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0103321</ConceptUI>
    <ConceptName>
     <String>SK&amp;F 93479</String>
    </ConceptName>
    <CASN1Name>4(1H)-Pyrimidinone, 2-((2-(((5-((dimethylamino)methyl)-2-furanyl)methyl)thio)ethyl)amino)-5-((6-methyl-3-pyridinyl)methyl)-, trihydrochloride</CASN1Name>
    <RegistryNumber>72716-75-7</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0103321</Concept1UI>
     <Concept2UI>M0103318</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T133325</TermUI>
      <String>SK&amp;F 93479</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T133324</TermUI>
      <String>SKF 93479</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T133323</TermUI>
      <String>SK&amp;F-93479</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0103318</ConceptUI>
    <ConceptName>
     <String>2-(2-(5-dimethylaminomethylfuran-2-ylmethylthio)ethylamino)-5-(6-methylpyrid-3-ylmethyl)pyrimid-4-one</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0103321</Concept1UI>
     <Concept2UI>M0103318</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T133322</TermUI>
      <String>2-(2-(5-dimethylaminomethylfuran-2-ylmethylthio)ethylamino)-5-(6-methylpyrid-3-ylmethyl)pyrimid-4-one</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013584</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>lipid peroxidation inhibitor</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1995</Year>
   <Month>09</Month>
   <Day>22</Day>
  </DateRevised>
  <Note>a mixture of free carboxylic acids (major components comprising 92% of the total fatty acids); induced by CCl(4) in rat liver soluble fraction; also glutathione-dependent factor isolated from human red cell membrane
  </Note>
  <Frequency>39</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>LIPID PEROXIDES/*antag (84-94)</PreviousIndexing>
   <PreviousIndexing>LIPIDS/*metab (77-84)</PreviousIndexing>
   <PreviousIndexing>PEROXIDES/*metab (77-84)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005227</DescriptorUI>
     <DescriptorName>
      <String>Fatty Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Res Commun Chem Pathol Pharmacol 17(2):265;1977</Source>
   <Source>Tox Appl Pharm 40(2):283;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061444</ConceptUI>
    <ConceptName>
     <String>lipid peroxidation inhibitor</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091447</TermUI>
      <String>lipid peroxidation inhibitor</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C436824</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1beta,8beta-dihydroxy-eudesman-4(15),7(11)-dien-8alpha,l2-olide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>10</Month>
   <Day>15</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>from Smyrnium olusatrum; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SESQUITERPENES (2001-2003)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007783</DescriptorUI>
     <DescriptorName>
      <String>Lactones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D045787</DescriptorUI>
     <DescriptorName>
      <String>Sesquiterpenes, Eudesmane</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Phytochemistry 2001 Aug;57(8):1197-200</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0401744</ConceptUI>
    <ConceptName>
     <String>1beta,8beta-dihydroxy-eudesman-4(15),7(11)-dien-8alpha,l2-olide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T466135</TermUI>
      <String>1beta,8beta-dihydroxy-eudesman-4(15),7(11)-dien-8alpha,l2-olide</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>10</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T466136</TermUI>
      <String>1,8-dihydroxyeudesman-4(15),7(11)-dien-8,l2-olide</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>10</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013599</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-methoxy-10 beta(tert-butylamino)propionylphenothiazine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010640</DescriptorUI>
     <DescriptorName>
      <String>Phenothiazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Indian J Exp Biol 14(3):340;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061479</ConceptUI>
    <ConceptName>
     <String>2-methoxy-10 beta(tert-butylamino)propionylphenothiazine</String>
    </ConceptName>
    <CASN1Name>10H-Phenothiazine, 10-(2-((1,1-dimethylethyl)amino)-1-oxopropyl)-2-methoxy-</CASN1Name>
    <RegistryNumber>59260-82-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091482</TermUI>
      <String>2-methoxy-10 beta(tert-butylamino)propionylphenothiazine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013601</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-methoxy-1' beta-methyl-1,11 alpha-methano-9 beta-estra-1,3,4(10)- trien-17 beta ol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004963</DescriptorUI>
     <DescriptorName>
      <String>Estrenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Chem Soc (Perkin I) 22:2374;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061480</ConceptUI>
    <ConceptName>
     <String>3-methoxy-1' beta-methyl-1,11 alpha-methano-9 beta-estra-1,3,4(10)- trien-17 beta ol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091483</TermUI>
      <String>3-methoxy-1' beta-methyl-1,11 alpha-methano-9 beta-estra-1,3,4(10)- trien-17 beta ol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013603</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>(9-methyladenine-N(1),N(7))-bis(diisopropylsulfoxide-S)- trans-dichloroplatinum (II)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PLATINUM (77-78)</PreviousIndexing>
   <PreviousIndexing>ADENINE/*analogs (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009944</DescriptorUI>
     <DescriptorName>
      <String>Organoplatinum Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Am Chem Soc 98(24):7865;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061482</ConceptUI>
    <ConceptName>
     <String>(9-methyladenine-N(1),N(7))-bis(diisopropylsulfoxide-S)- trans-dichloroplatinum (II)</String>
    </ConceptName>
    <CASN1Name>Platinum, tetrachloro(mu-(9-methyl-9H-purin-6-amine-N(1):N(7)))bis(2,2'-sulfinylbis(propane)-S)di-, stereoisomer</CASN1Name>
    <RegistryNumber>61458-74-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091485</TermUI>
      <String>(9-methyladenine-N(1),N(7))-bis(diisopropylsulfoxide-S)- trans-dichloroplatinum (II)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013607</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>17-methyl-18-norandrosta-5,13(17)-dien-3 beta-ol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>NORANDROSTANES (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000737</DescriptorUI>
     <DescriptorName>
      <String>Androstenols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 251(23):7336;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061490</ConceptUI>
    <ConceptName>
     <String>17-methyl-18-norandrosta-5,13(17)-dien-3 beta-ol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091493</TermUI>
      <String>17-methyl-18-norandrosta-5,13(17)-dien-3 beta-ol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C417709</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>dimethylallyl diphosphate naringenin 8-dimethylallyltransferase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>06</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>catalyzes the conversion of naringenin and 3,3-dimethylallyl diphosphate to 8-dimethylallylnaringenin
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D019883</DescriptorUI>
     <DescriptorName>
      <String>Alkyl and Aryl Transferases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Phytochemistry 2000 Aug;54(7):649-55</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0375778</ConceptUI>
    <ConceptName>
     <String>dimethylallyl diphosphate naringenin 8-dimethylallyltransferase</String>
    </ConceptName>
    <RegistryNumber>EC 2.5.1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T432463</TermUI>
      <String>dimethylallyl diphosphate naringenin 8-dimethylallyltransferase</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>01</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T432464</TermUI>
      <String>DMAPP naringenin DMAtransferase</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>01</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013627</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>noroxyclothepin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1986</Year>
   <Month>08</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PIPERAZINES (77-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003988</DescriptorUI>
     <DescriptorName>
      <String>Dibenzothiepins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cesk Farm 25(7):227;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061541</ConceptUI>
    <ConceptName>
     <String>noroxyclothepin</String>
    </ConceptName>
    <RegistryNumber>34775-62-7</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061541</Concept1UI>
     <Concept2UI>M0061540</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091544</TermUI>
      <String>noroxyclothepin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0061540</ConceptUI>
    <ConceptName>
     <String>8-chloro-10-(4-hydroxyethyl)piperazino-10,11- dihydrodibenzo(b,f)thiepin</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061541</Concept1UI>
     <Concept2UI>M0061540</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T091543</TermUI>
      <String>8-chloro-10-(4-hydroxyethyl)piperazino-10,11- dihydrodibenzo(b,f)thiepin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013630</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>oligo (dT) poly (A)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1983</Year>
   <Month>08</Month>
   <Day>19</Day>
  </DateRevised>
  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*POLYNUCLEOTIDES (77-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009838</DescriptorUI>
     <DescriptorName>
      <String>Oligodeoxyribonucleotides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011067</DescriptorUI>
     <DescriptorName>
      <String>Poly dA-dT</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Res 36(12):4687;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061561</ConceptUI>
    <ConceptName>
     <String>oligo (dT) poly (A)</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091564</TermUI>
      <String>oligo (dT) poly (A)</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013634</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-oxo-3-phenyl-1,3-oxazetidine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001384</DescriptorUI>
     <DescriptorName>
      <String>Azetidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 73(2):465;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061568</ConceptUI>
    <ConceptName>
     <String>2-oxo-3-phenyl-1,3-oxazetidine</String>
    </ConceptName>
    <CASN1Name>1,3-Oxazetidin-2-one, 3-phenyl-</CASN1Name>
    <RegistryNumber>16877-22-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091571</TermUI>
      <String>2-oxo-3-phenyl-1,3-oxazetidine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013635</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>oxophlorins</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>6</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011166</DescriptorUI>
     <DescriptorName>
      <String>Porphyrins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Soc Trans 4(2):297;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061569</ConceptUI>
    <ConceptName>
     <String>oxophlorins</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091572</TermUI>
      <String>oxophlorins</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013636</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>9-oxo-13-prostenoic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>05</Month>
   <Day>26</Day>
  </DateRevised>
  <Note>RN given refers to (13E)-isomer
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*FATTY ACIDS, UNSATURATED (77-87)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005229</DescriptorUI>
     <DescriptorName>
      <String>Fatty Acids, Monounsaturated</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Appl Environ Microbiol 32(5):726;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061570</ConceptUI>
    <ConceptName>
     <String>9-oxo-13-prostenoic acid</String>
    </ConceptName>
    <RegistryNumber>41302-01-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091573</TermUI>
      <String>9-oxo-13-prostenoic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013681</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>silenal P</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>corrosion inhibitor containing 8% Na2O, 23.8% SiO2, 2% P2O5 &amp; 66% H2O; RN given refers to cpd with unspecified molecular formula
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PHOSPHORUS (77-82)</PreviousIndexing>
   <PreviousIndexing>SILICA (77-82)</PreviousIndexing>
   <PreviousIndexing>SODIUM (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010087</DescriptorUI>
     <DescriptorName>
      <String>Oxides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Roczw Panstw Zakl Hig 27(5):563;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061628</ConceptUI>
    <ConceptName>
     <String>silenal P</String>
    </ConceptName>
    <RegistryNumber>55128-11-5</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>55128-12-6 (silenal S)</RelatedRegistryNumber>
     <RelatedRegistryNumber>55128-13-7 (silenal Z)</RelatedRegistryNumber>
     <RelatedRegistryNumber>55128-14-8 (silenal ZB)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0061628</Concept1UI>
     <Concept2UI>M0312281</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0061628</Concept1UI>
     <Concept2UI>M0312282</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0061628</Concept1UI>
     <Concept2UI>M0312280</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091631</TermUI>
      <String>silenal P</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312281</ConceptUI>
    <ConceptName>
     <String>silenal Z</String>
    </ConceptName>
    <RegistryNumber>55128-13-7</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0061628</Concept1UI>
     <Concept2UI>M0312281</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342281</TermUI>
      <String>silenal Z</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312282</ConceptUI>
    <ConceptName>
     <String>silenal ZB</String>
    </ConceptName>
    <RegistryNumber>55128-14-8</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0061628</Concept1UI>
     <Concept2UI>M0312282</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342282</TermUI>
      <String>silenal ZB</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312280</ConceptUI>
    <ConceptName>
     <String>silenal S</String>
    </ConceptName>
    <RegistryNumber>55128-12-6</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0061628</Concept1UI>
     <Concept2UI>M0312280</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342280</TermUI>
      <String>silenal S</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C027085</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>O-(2-chloroethyl)choline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>11</Month>
   <Day>26</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>affect muscarinic &amp; nicotinic receptors
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002794</DescriptorUI>
     <DescriptorName>
      <String>Choline</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Toxicol Appl Pharmacol 1980;54(2):265</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0088350</ConceptUI>
    <ConceptName>
     <String>O-(2-chloroethyl)choline</String>
    </ConceptName>
    <CASN1Name>Ethanaminium, 2-(2-chloroethoxy)-N,N,N-trimethyl-</CASN1Name>
    <RegistryNumber>74886-55-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T118353</TermUI>
      <String>O-(2-chloroethyl)choline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T118352</TermUI>
      <String>(2-chloroethyl)choline ether</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C103681</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>kaempferol 3-O-rhamnopyranosyl(1-2)-galactopyranoside-7-O-arabinofuranoside</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1997</Year>
   <Month>02</Month>
   <Day>10</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>a flavonol triglycoside; isolated from the flowers of Indigofera hebepetala; structure given in first source
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>QUERCETIN/*AA (1997-2002)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D044949</DescriptorUI>
     <DescriptorName>
      <String>Kaempferols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Phytochemistry 1996 Nov;43(5):1115-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0271034</ConceptUI>
    <ConceptName>
     <String>kaempferol 3-O-rhamnopyranosyl(1-2)-galactopyranoside-7-O-arabinofuranoside</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0271034</Concept1UI>
     <Concept2UI>M0271032</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T301039</TermUI>
      <String>kaempferol 3-O-rhamnopyranosyl(1-2)-galactopyranoside-7-O-arabinofuranoside</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T301038</TermUI>
      <String>kaempferol 3-Rha(1-2)Gal-7-Ara</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0271032</ConceptUI>
    <ConceptName>
     <String>kaempferol 3-O-alpha-L-rhamnopyrnosyl(1-2)-beta-D-galactopyranoside-7-O-alpha-L-arabinofuranoside</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0271034</Concept1UI>
     <Concept2UI>M0271032</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T301037</TermUI>
      <String>kaempferol 3-O-alpha-L-rhamnopyrnosyl(1-2)-beta-D-galactopyranoside-7-O-alpha-L-arabinofuranoside</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C417707</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>fibronectin peptide V</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>06</Day>
  </DateCreated>
  <Note>administration increases survival of nigral grafts in the brain
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005353</DescriptorUI>
     <DescriptorName>
      <String>Fibronectins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Neuroscience 2000;100(3):521-30</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0375776</ConceptUI>
    <ConceptName>
     <String>fibronectin peptide V</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T432457</TermUI>
      <String>fibronectin peptide V</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>01</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T432459</TermUI>
      <String>tryptophyl-glutaminyl-prolyl-prolyl-arginyl-alanyl-arginyl-isoleucyl-tyrosine</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>01</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T432460</TermUI>
      <String>FN-C H-V peptide</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>01</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T432458</TermUI>
      <String>WQPPRARIY</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>01</Month>
       <Day>06</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C027086</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>O-(2-bromoethyl)choline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>11</Month>
   <Day>26</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>affects muscarinic &amp; nicotinic receptors
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002794</DescriptorUI>
     <DescriptorName>
      <String>Choline</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Toxicol Appl Pharmacol 1980;54(2):265</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0088352</ConceptUI>
    <ConceptName>
     <String>O-(2-bromoethyl)choline</String>
    </ConceptName>
    <RegistryNumber>76584-54-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T118355</TermUI>
      <String>O-(2-bromoethyl)choline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T118354</TermUI>
      <String>(2-bromoethyl)choline ether</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013662</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>pyrecol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>purified water-soluble lipopolysaccharides from nonpathogenic colibacteria
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008070</DescriptorUI>
     <DescriptorName>
      <String>Lipopolysaccharides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D011135</DescriptorUI>
     <DescriptorName>
      <String>Polysaccharides, Bacterial</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Z Gesamte Inn Med 31(17):707;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061611</ConceptUI>
    <ConceptName>
     <String>pyrecol</String>
    </ConceptName>
    <RegistryNumber>65099-16-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091614</TermUI>
      <String>pyrecol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013663</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>pyridazino(2,3-a)-s-triazino-2,4-dione</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>related to fervenulin; structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011724</DescriptorUI>
     <DescriptorName>
      <String>Pyridazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014227</DescriptorUI>
     <DescriptorName>
      <String>Triazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 65(10):1505;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061612</ConceptUI>
    <ConceptName>
     <String>pyridazino(2,3-a)-s-triazino-2,4-dione</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091615</TermUI>
      <String>pyridazino(2,3-a)-s-triazino-2,4-dione</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013671</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-(9-beta-D-ribofuranosylpurin-6-yl)glycyl-1-alanine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>05</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>RN given for sesquihydrate; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DIPEPTIDES (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011684</DescriptorUI>
     <DescriptorName>
      <String>Purine Nucleosides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Am Chem Soc 98(26):8472;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061617</ConceptUI>
    <ConceptName>
     <String>N-(9-beta-D-ribofuranosylpurin-6-yl)glycyl-1-alanine</String>
    </ConceptName>
    <CASN1Name>L-Alanine, N-(N-(9-beta-D-ribofuranosyl-9H-purin-6-yl)glycyl)-, sesquihydrate</CASN1Name>
    <RegistryNumber>61088-71-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091620</TermUI>
      <String>N-(9-beta-D-ribofuranosylpurin-6-yl)glycyl-1-alanine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013676</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>sclerin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>sclerotina metabolite; structure
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BENZOPYRANS (77-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003374</DescriptorUI>
     <DescriptorName>
      <String>Coumarins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Chem Soc (Perkin I)19:2077;1976</Source>
   <Source>Lloydia 40(3):301;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061623</ConceptUI>
    <ConceptName>
     <String>sclerin</String>
    </ConceptName>
    <CASN1Name>(+)-8-hydroxy-4,5,6,7-tetramethyl-1H-2-benzopyran-1,3(4H)-dione</CASN1Name>
    <RegistryNumber>13277-76-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091626</TermUI>
      <String>sclerin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013677</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>selenobiotin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1991</Year>
   <Month>07</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>replaces biotin as a growth factor for several microorganisms; incorporated into carboxymethylases without loss of enzyme activity; with E. coli, the selenoacetyl-CoA carboxylase is as active as the normal enzyme; structure
  </Note>
  <Frequency>3</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SELENIUM (77-91)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D001710</DescriptorUI>
     <DescriptorName>
      <String>Biotin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D016566</DescriptorUI>
     <DescriptorName>
      <String>Organoselenium Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Biophys Res Commun 73(3):773;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061624</ConceptUI>
    <ConceptName>
     <String>selenobiotin</String>
    </ConceptName>
    <CASN1Name>1H-Selenolo(3,4-d)imidazole-4-pentanoic acid, hexahydro-2-oxo-, (3aS-(3aalpha,4beta,6aalpha))-</CASN1Name>
    <RegistryNumber>57956-29-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091627</TermUI>
      <String>selenobiotin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C473501</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Tn10 transposase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateCreated>
  <Frequency>13</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D019895</DescriptorUI>
     <DescriptorName>
      <String>Transposases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cell 1983 Mar;32(3):799-807</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0029542</ConceptUI>
    <ConceptName>
     <String>Tn10 transposase</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T059252</TermUI>
      <String>Tn10 transposase</String>
      <DateCreated>
       <Year>1997</Year>
       <Month>02</Month>
       <Day>14</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013679</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>sialotonin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012471</DescriptorUI>
     <DescriptorName>
      <String>Salivary Proteins and Peptides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Physiol (Lond) 261(3):523;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061626</ConceptUI>
    <ConceptName>
     <String>sialotonin</String>
    </ConceptName>
    <CASN1Name>Sialotonin</CASN1Name>
    <RegistryNumber>61537-16-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091629</TermUI>
      <String>sialotonin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013680</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>silanol salicylate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SILICON (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012459</DescriptorUI>
     <DescriptorName>
      <String>Salicylates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Lille Med 21(8):640;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061627</ConceptUI>
    <ConceptName>
     <String>silanol salicylate</String>
    </ConceptName>
    <CASN1Name>Benzoic acid, 2-hydroxy-, silyl ester</CASN1Name>
    <RegistryNumber>61925-82-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091630</TermUI>
      <String>silanol salicylate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C027087</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>O-(2-iodoethyl)choline</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>11</Month>
   <Day>26</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>affect muscarinic &amp; nicotinic receptors
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002794</DescriptorUI>
     <DescriptorName>
      <String>Choline</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Toxicol Appl Pharmacol 1980;54(2):265</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0088354</ConceptUI>
    <ConceptName>
     <String>O-(2-iodoethyl)choline</String>
    </ConceptName>
    <CASN1Name>Ethanaminium, 2-(2-iodoethoxy)-N,N,N-trimethyl-</CASN1Name>
    <RegistryNumber>76584-53-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T118357</TermUI>
      <String>O-(2-iodoethyl)choline</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T118356</TermUI>
      <String>(2-iodoethyl)choline ether</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C047374</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-((3-(4,5-dihydro-5,5-dimethyl-4-oxo-2-furanyl)-2-butenyl)oxy)-9H-xanthen-9-one</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1986</Year>
   <Month>02</Month>
   <Day>06</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>xanthone analog of geiparvarin; structure given in first source; RN given is for (E)-isomer
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*XANTHENES (1997-2003)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D044004</DescriptorUI>
     <DescriptorName>
      <String>Xanthones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Pharm (Weinheim) 1985;318(10):923</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0136856</ConceptUI>
    <ConceptName>
     <String>3-((3-(4,5-dihydro-5,5-dimethyl-4-oxo-2-furanyl)-2-butenyl)oxy)-9H-xanthen-9-one</String>
    </ConceptName>
    <RegistryNumber>102275-60-5</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>102275-61-6 ((Z)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0136856</Concept1UI>
     <Concept2UI>M0322594</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T166861</TermUI>
      <String>3-((3-(4,5-dihydro-5,5-dimethyl-4-oxo-2-furanyl)-2-butenyl)oxy)-9H-xanthen-9-one</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1986)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T166860</TermUI>
      <String>DDOFBX</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1986)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0322594</ConceptUI>
    <ConceptName>
     <String>3-((3-(4,5-dihydro-5,5-dimethyl-4-oxo-2-furanyl)-2-butenyl)oxy)-9H-xanthen-9-one, (Z)-isomer</String>
    </ConceptName>
    <RegistryNumber>102275-61-6</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0136856</Concept1UI>
     <Concept2UI>M0322594</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T352594</TermUI>
      <String>3-((3-(4,5-dihydro-5,5-dimethyl-4-oxo-2-furanyl)-2-butenyl)oxy)-9H-xanthen-9-one, (Z)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1986)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013683</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>sodium nucleinate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1996</Year>
   <Month>01</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>extracts from yeast; RNA preparation
  </Note>
  <Frequency>146</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009696</DescriptorUI>
     <DescriptorName>
      <String>Nucleic Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D012331</DescriptorUI>
     <DescriptorName>
      <String>RNA, Fungal</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
    <PharmacologicalActionList>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D000276</DescriptorUI>
        <DescriptorName>
         <String>Adjuvants, Immunologic</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D000897</DescriptorUI>
        <DescriptorName>
         <String>Anti-Ulcer Agents</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D007369</DescriptorUI>
        <DescriptorName>
         <String>Interferon Inducers</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D011749</DescriptorUI>
        <DescriptorName>
         <String>Pyrogens</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
    </PharmacologicalActionList>
  <SourceList>
   <Source>Acta Virol 21:338;1977</Source>
   <Source>Antibiotiki 23(6):520;1978</Source>
   <Source>Antibiotiki 24(11):853;1979</Source>
   <Source>Antibiotiki 24(9):697;1979</Source>
   <Source>Biull Eksp Biol Med 87(3):256;1979</Source>
   <Source>Dev Biol Stand 34:85;1977</Source>
   <Source>Vestn Khir 119(10):75;1977</Source>
   <Source>Zentralbl Veterinaermed 23(8):697;1976</Source>
   <Source>Zh Mikrobiol Epidemiol Immunobiol 4:43;1979</Source>
   <Source>Zh Nevropatol Psikhiatr 79(5):623;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061633</ConceptUI>
    <ConceptName>
     <String>sodium nucleinate</String>
    </ConceptName>
    <CASN1Name>Nucleic acids, sodium salts</CASN1Name>
    <RegistryNumber>9010-05-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061633</Concept1UI>
     <Concept2UI>M0061632</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061633</Concept1UI>
     <Concept2UI>M0061631</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091636</TermUI>
      <String>sodium nucleinate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0061632</ConceptUI>
    <ConceptName>
     <String>sodium ribonucleinate</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061633</Concept1UI>
     <Concept2UI>M0061632</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T091635</TermUI>
      <String>sodium ribonucleinate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0061631</ConceptUI>
    <ConceptName>
     <String>nucleinate</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061633</Concept1UI>
     <Concept2UI>M0061631</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T091634</TermUI>
      <String>nucleinate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013711</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2'-thio-2'-deoxycytidine 2',3'-phosphorothioate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1993</Year>
   <Month>08</Month>
   <Day>19</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*CYTOSINE NUCLEOTIDES (77-80)</PreviousIndexing>
   <PreviousIndexing>*ORGANOTHIOPHOSPHORUS COMPOUNDS (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003563</DescriptorUI>
     <DescriptorName>
      <String>Cyclic CMP</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013873</DescriptorUI>
     <DescriptorName>
      <String>Thionucleotides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nucleic Acid Res ((10):2437;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061686</ConceptUI>
    <ConceptName>
     <String>2'-thio-2'-deoxycytidine 2',3'-phosphorothioate</String>
    </ConceptName>
    <CASN1Name>Cytidine, 2'-thio-, cyclic 2',3'-(hydrogen phosphate)</CASN1Name>
    <RegistryNumber>61734-36-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091689</TermUI>
      <String>2'-thio-2'-deoxycytidine 2',3'-phosphorothioate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013712</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-thio-2-hydroxypropyldextran</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>DEXTRAN/*analogs (77-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D003911</DescriptorUI>
     <DescriptorName>
      <String>Dextrans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Polon Pharm 33(5):617;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061687</ConceptUI>
    <ConceptName>
     <String>3-thio-2-hydroxypropyldextran</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091690</TermUI>
      <String>3-thio-2-hydroxypropyldextran</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013805</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-aminobenzonorbornene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>RN given refers to (endo, 1alpha,2beta,4alpha)-isomer
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009636</DescriptorUI>
     <DescriptorName>
      <String>Norbornanes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Pharmacol 28 Suppl:80;1976</Source>
   <Source>Res Commun Chem Pathol Pharmacol 21(1):169;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061889</ConceptUI>
    <ConceptName>
     <String>2-aminobenzonorbornene</String>
    </ConceptName>
    <RegistryNumber>58742-04-4</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>62624-26-4 ((exo, 1alpha,2alpha,4alpha)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061889</Concept1UI>
     <Concept2UI>M0061887</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061889</Concept1UI>
     <Concept2UI>M0061888</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061889</Concept1UI>
     <Concept2UI>M0312326</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091892</TermUI>
      <String>2-aminobenzonorbornene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0061887</ConceptUI>
    <ConceptName>
     <String>endo-2-aminobenzonorbornene</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061889</Concept1UI>
     <Concept2UI>M0061887</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T091890</TermUI>
      <String>endo-2-aminobenzonorbornene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0061888</ConceptUI>
    <ConceptName>
     <String>exo-2-aminobenzonorbornene</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061889</Concept1UI>
     <Concept2UI>M0061888</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T091891</TermUI>
      <String>exo-2-aminobenzonorbornene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312326</ConceptUI>
    <ConceptName>
     <String>2-aminobenzonorbornene, (exo, 1alpha,2alpha,4alpha)-isomer</String>
    </ConceptName>
    <RegistryNumber>62624-26-4</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0061889</Concept1UI>
     <Concept2UI>M0312326</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342326</TermUI>
      <String>2-aminobenzonorbornene, (exo, 1alpha,2alpha,4alpha)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013722</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6-trimethylaminohexanoyl-L-carnitine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002331</DescriptorUI>
     <DescriptorName>
      <String>Carnitine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Biochem 69(1):299;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061712</ConceptUI>
    <ConceptName>
     <String>6-trimethylaminohexanoyl-L-carnitine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091715</TermUI>
      <String>6-trimethylaminohexanoyl-L-carnitine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013723</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>11-trimethylaminoundecanoyl-L-carnitine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002331</DescriptorUI>
     <DescriptorName>
      <String>Carnitine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Eur J Biochem 69(1):299;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061713</ConceptUI>
    <ConceptName>
     <String>11-trimethylaminoundecanoyl-L-carnitine</String>
    </ConceptName>
    <CASN1Name>1-Undecanaminium, 11-(1-(carboxymethyl)-2-(trimethylammonio)ethoxy)-N,N,N-trimethyl-11-oxo-, monohydroxide, inner salt, (R)-</CASN1Name>
    <RegistryNumber>61102-30-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091716</TermUI>
      <String>11-trimethylaminoundecanoyl-L-carnitine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C006210</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>AH 7079</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1974</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>08</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>anti-allergy cpd used in treatment of allergic bronchial asthma &amp; rhinitis; structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*XANTHENES (1974-2003)</PreviousIndexing>
   <PreviousIndexing>TETRAZOLES (74-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D044004</DescriptorUI>
     <DescriptorName>
      <String>Xanthones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cas Lek Ces 116(48):1481;1977</Source>
   <Source>Int Arch Allergy Appl Immunol 45(5):697;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0048505</ConceptUI>
    <ConceptName>
     <String>AH 7079</String>
    </ConceptName>
    <CASN1Name>9H-xanthen-9-one, 2-methoxy-7-(1H-tetrazol-5-yl)-</CASN1Name>
    <RegistryNumber>33440-58-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0048505</Concept1UI>
     <Concept2UI>M0048504</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T078508</TermUI>
      <String>AH 7079</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0048504</ConceptUI>
    <ConceptName>
     <String>7-methoxy-2-(1H-tetrazol-5-yl)xanthen-9-one</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0048505</Concept1UI>
     <Concept2UI>M0048504</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T078507</TermUI>
      <String>7-methoxy-2-(1H-tetrazol-5-yl)xanthen-9-one</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1974)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C474661</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>acetylpyridine benzoyl hydrazine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>06</Month>
   <Day>16</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>06</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006834</DescriptorUI>
     <DescriptorName>
      <String>Hydrazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011725</DescriptorUI>
     <DescriptorName>
      <String>Pyridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Bioorg Med Chem Lett 2003 Jan 6;13(1):51-5</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0450446</ConceptUI>
    <ConceptName>
     <String>acetylpyridine benzoyl hydrazine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T543345</TermUI>
      <String>acetylpyridine benzoyl hydrazine</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>06</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T543346</TermUI>
      <String>APBH cpd</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>06</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C456359</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>PSMG2 protein, human</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>06</Month>
   <Day>12</Day>
  </DateCreated>
  <DateRevised>
   <Year>2008</Year>
   <Month>09</Month>
   <Day>11</Day>
  </DateRevised>
  <Note>RefSeq NM_020232
  </Note>
  <Frequency>4</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PROTEINS (2002-2008)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D018833</DescriptorUI>
     <DescriptorName>
      <String>Chaperonins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D006528</DescriptorUI>
     <DescriptorName>
      <String>Carcinoma, Hepatocellular</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>World J Gastroenterol 2001 Dec;7(6):821-5</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0426789</ConceptUI>
    <ConceptName>
     <String>PSMG2 protein, human</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T725555</TermUI>
      <String>PSMG2 protein, human</String>
      <DateCreated>
       <Year>2008</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2008)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T498181</TermUI>
      <String>HCCA3 protein, human</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>06</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T725556</TermUI>
      <String>proteasome (prosome, macropain) assembly chaperone 2, human</String>
      <DateCreated>
       <Year>2008</Year>
       <Month>09</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2008)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T696147</TermUI>
      <String>proteasome-assembling chaperone 2, human</String>
      <DateCreated>
       <Year>2007</Year>
       <Month>04</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2007)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T639608</TermUI>
      <String>tumor necrosis factor superfamily, member 5-induced protein 1, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>05</Month>
       <Day>04</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T639607</TermUI>
      <String>TNFSF5IP1 protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>05</Month>
       <Day>04</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T498183</TermUI>
      <String>hepatocellular carcinoma 3 protein, human</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>06</Month>
       <Day>12</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C095811</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Fortify sealant</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1995</Year>
   <Month>10</Month>
   <Day>25</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>a surface-penetrating sealant (SPS)
  </Note>
  <Frequency>21</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*DENTAL CEMENTS (95-97)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D019279</DescriptorUI>
     <DescriptorName>
      <String>Resin Cements</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Quintessence Int 1994 Nov;25(11):767-71</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0252254</ConceptUI>
    <ConceptName>
     <String>Fortify sealant</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T282259</TermUI>
      <String>Fortify sealant</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1995)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C097249</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Psk1 protein, S pombe</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>01</Month>
   <Day>24</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>01</Month>
   <Day>20</Day>
  </DateRevised>
  <Note>from Schizosaccharomyces pombe; mutation of psk1 confers resistance to phenylarsine oxide; amino acid sequence given in first source; GenBank D45401
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*FUNGAL PROTEINS (1996-2003)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D017346</DescriptorUI>
     <DescriptorName>
      <String>Protein-Serine-Threonine Kinases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029702</DescriptorUI>
     <DescriptorName>
      <String>Schizosaccharomyces pombe Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Gene 1995 dec 1;166(1):155-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0255661</ConceptUI>
    <ConceptName>
     <String>Psk1 protein, S pombe</String>
    </ConceptName>
    <RegistryNumber>EC 2.7.1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T550439</TermUI>
      <String>Psk1 protein, S pombe</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>09</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T285666</TermUI>
      <String>SPCC4G3.08 protein, S pombe</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C483322</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>complementary human autoantigen proteinase-3 (105-201)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>04</Month>
   <Day>07</Day>
  </DateCreated>
  <Note>a recombinant antisense PR-3 peptide that triggers autoimmunity
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010446</DescriptorUI>
     <DescriptorName>
      <String>Peptide Fragments</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nat Med 2004 Jan;10(1):72-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0463858</ConceptUI>
    <ConceptName>
     <String>complementary human autoantigen proteinase-3 (105-201)</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T581517</TermUI>
      <String>complementary human autoantigen proteinase-3 (105-201)</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>04</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T581518</TermUI>
      <String>cPR-3 (105-201)</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>04</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C113683</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>AxRNBP protein, Ambystoma mexicanum</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>08</Month>
   <Day>18</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>01</Month>
   <Day>21</Day>
  </DateRevised>
  <Note>from the Mexican axolotl; a 16kDa polypeptide; amino acid sequence in first source; GenBank U71299
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D016601</DescriptorUI>
     <DescriptorName>
      <String>RNA-Binding Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029845</DescriptorUI>
     <DescriptorName>
      <String>Amphibian Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D000558</DescriptorUI>
     <DescriptorName>
      <String>Ambystoma mexicanum</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Biochim Biophys Acta 1998 Jul 9;1398(3):265-74</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0293486</ConceptUI>
    <ConceptName>
     <String>AxRNBP protein, Ambystoma mexicanum</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T492385</TermUI>
      <String>AxRNBP protein, Ambystoma mexicanum</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>05</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T323491</TermUI>
      <String>AxRBP protein, Ambystoma mexicanum</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C489113</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>diosgenyl 3-O-(alpha-L-rhamnopyranosyl-(1-2)-(beta-D-xylopyranosyl-(1-3))-beta-D-galactopyranoside)</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2004</Year>
   <Month>09</Month>
   <Day>03</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>11</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>natural saponin from Solanum indicum L., and containing 2,3-branched sugar moieties; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004144</DescriptorUI>
     <DescriptorName>
      <String>Diosgenin</String>
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    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D012503</DescriptorUI>
     <DescriptorName>
      <String>Saponins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 2004 Aug 6;69(16):5497-500</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0472050</ConceptUI>
    <ConceptName>
     <String>diosgenyl 3-O-(alpha-L-rhamnopyranosyl-(1-2)-(beta-D-xylopyranosyl-(1-3))-beta-D-galactopyranoside)</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T607971</TermUI>
      <String>diosgenyl 3-O-(alpha-L-rhamnopyranosyl-(1-2)-(beta-D-xylopyranosyl-(1-3))-beta-D-galactopyranoside)</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T607972</TermUI>
      <String>DRXG cpd</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014168</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-propyl-2-pentenoic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>valproate metabolite; RN given refers to parent cpd
  </Note>
  <Frequency>55</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*FATTY ACIDS, UNSATURATED (77-87)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005229</DescriptorUI>
     <DescriptorName>
      <String>Fatty Acids, Monounsaturated</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
    <PharmacologicalActionList>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D000927</DescriptorUI>
        <DescriptorName>
         <String>Anticonvulsants</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
     <PharmacologicalAction>
      <DescriptorReferredTo>
       <DescriptorUI>D013723</DescriptorUI>
        <DescriptorName>
         <String>Teratogens</String>
        </DescriptorName>
      </DescriptorReferredTo>
     </PharmacologicalAction>
    </PharmacologicalActionList>
  <SourceList>
   <Source>C R Soc Biol (Paris) 172(4):707;1978</Source>
   <Source>Psychopharmacology (Berlin) 50(1):53;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0062492</ConceptUI>
    <ConceptName>
     <String>2-propyl-2-pentenoic acid</String>
    </ConceptName>
    <RegistryNumber>60218-41-9</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>33786-46-8 ((Z)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>33786-47-9 ((E)-isomer)</RelatedRegistryNumber>
     <RelatedRegistryNumber>69827-64-1 (Na salt)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062492</Concept1UI>
     <Concept2UI>M0312412</Concept2UI>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062492</Concept1UI>
     <Concept2UI>M0062490</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062492</Concept1UI>
     <Concept2UI>M0062486</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062492</Concept1UI>
     <Concept2UI>M0312414</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062492</Concept1UI>
     <Concept2UI>M0312413</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062492</Concept1UI>
     <Concept2UI>M0062487</Concept2UI>
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    </ConceptRelationList>
    <TermList>
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      <TermUI>T092495</TermUI>
      <String>2-propyl-2-pentenoic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T092486</TermUI>
      <String>2-enVPA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T092488</TermUI>
      <String>2-n-propylpent-2-enoic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T092487</TermUI>
      <String>2-envalproic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312412</ConceptUI>
    <ConceptName>
     <String>2-propyl-2-pentenoic acid, (Z)-isomer</String>
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    <RegistryNumber>33786-46-8</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062492</Concept1UI>
     <Concept2UI>M0312412</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342412</TermUI>
      <String>2-propyl-2-pentenoic acid, (Z)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0062490</ConceptUI>
    <ConceptName>
     <String>trans-2-en-valproate</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062492</Concept1UI>
     <Concept2UI>M0062490</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T092493</TermUI>
      <String>trans-2-en-valproate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T092494</TermUI>
      <String>trans-2-ene-valproic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T092492</TermUI>
      <String>trans-2-en-VPA</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0062486</ConceptUI>
    <ConceptName>
     <String>E-delta(2)-valproic acid</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062492</Concept1UI>
     <Concept2UI>M0062486</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T092489</TermUI>
      <String>E-delta(2)-valproic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312414</ConceptUI>
    <ConceptName>
     <String>2-propyl-2-pentenoic acid, sodium salt</String>
    </ConceptName>
    <RegistryNumber>69827-64-1</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062492</Concept1UI>
     <Concept2UI>M0312414</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342414</TermUI>
      <String>2-propyl-2-pentenoic acid, sodium salt</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312413</ConceptUI>
    <ConceptName>
     <String>2-propyl-2-pentenoic acid, (E)-isomer</String>
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    <RegistryNumber>33786-47-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062492</Concept1UI>
     <Concept2UI>M0312413</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342413</TermUI>
      <String>2-propyl-2-pentenoic acid, (E)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T092485</TermUI>
      <String>(E)-2-ene valproic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0062487</ConceptUI>
    <ConceptName>
     <String>delta2,3 VPE</String>
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    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0062492</Concept1UI>
     <Concept2UI>M0062487</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T092490</TermUI>
      <String>delta2,3 VPE</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T092491</TermUI>
      <String>delta2-valproic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C026611</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>guanidino propyl piperazine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>10</Month>
   <Day>21</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>07</Month>
   <Day>26</Day>
  </DateRevised>
  <Note>anti-plaque agent; RN given refers to dimethanesulfonate; structure given in first source
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006146</DescriptorUI>
     <DescriptorName>
      <String>Guanidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010879</DescriptorUI>
     <DescriptorName>
      <String>Piperazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Scand J Dent Res 1980;88(3):210</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0087239</ConceptUI>
    <ConceptName>
     <String>guanidino propyl piperazine</String>
    </ConceptName>
    <CASN1Name>urea, N,N''-(1,4-piperazinediylbis(3,1-propanediyliminocarbonimidoyl))bis(N'-hexyl-), dimethanesulfonate</CASN1Name>
    <RegistryNumber>69017-90-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0087239</Concept1UI>
     <Concept2UI>M0087236</Concept2UI>
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    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T117242</TermUI>
      <String>guanidino propyl piperazine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T117238</TermUI>
      <String>1,4-bis(3-(n-hexylcarbamylguanidino)propyl)piperazine dimethanesulfonic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0087236</ConceptUI>
    <ConceptName>
     <String>CK 0569 A</String>
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    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0087239</Concept1UI>
     <Concept2UI>M0087236</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T117239</TermUI>
      <String>CK 0569 A</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T117241</TermUI>
      <String>CKO 569A</String>
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       <ThesaurusID>NLM (1980)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T117240</TermUI>
      <String>CK 569A</String>
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       <ThesaurusID>NLM (1980)</ThesaurusID>
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   </Concept>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C544271</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-hydroxy-5-methyl-O-methyltyrosine</String>
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  <DateCreated>
   <Year>2009</Year>
   <Month>10</Month>
   <Day>15</Day>
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  <Note>structure in first source
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    <DescriptorReferredTo>
     <DescriptorUI>*D008781</DescriptorUI>
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      <String>Methyltyrosines</String>
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  <SourceList>
   <Source>J Microbiol Biotechnol. 2009 May;19(5):439-46</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0540096</ConceptUI>
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     <String>3-hydroxy-5-methyl-O-methyltyrosine</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T759516</TermUI>
      <String>3-hydroxy-5-methyl-O-methyltyrosine</String>
      <DateCreated>
       <Year>2009</Year>
       <Month>10</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2009)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T759517</TermUI>
      <String>3h5mOmTyr</String>
      <DateCreated>
       <Year>2009</Year>
       <Month>10</Month>
       <Day>15</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2009)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C106725</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Rootcal</String>
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  <DateCreated>
   <Year>1997</Year>
   <Month>07</Month>
   <Day>18</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>contains calcium hydroxide and the radioopaque agent barium sulfate
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  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002126</DescriptorUI>
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      <String>Calcium Hydroxide</String>
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  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D012387</DescriptorUI>
     <DescriptorName>
      <String>Root Canal Filling Materials</String>
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     </DescriptorReferredTo>
   </IndexingInformation>
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  <SourceList>
   <Source>Int Endod J 1996 Jul;29(4):271-9</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0277971</ConceptUI>
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     <String>Rootcal</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="TRD"  RecordPreferredTermYN="Y">
      <TermUI>T307976</TermUI>
      <String>Rootcal</String>
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       <ThesaurusID>NLM (1997)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C490697</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>beta-lactamase VIM-5, Pseudomonas aeruginosa</String>
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  <DateCreated>
   <Year>2004</Year>
   <Month>09</Month>
   <Day>25</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>11</Month>
   <Day>05</Day>
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  <Frequency>7</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001426</DescriptorUI>
     <DescriptorName>
      <String>Bacterial Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001618</DescriptorUI>
     <DescriptorName>
      <String>beta-Lactamases</String>
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    </DescriptorReferredTo>
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  </HeadingMappedToList>
  <SourceList>
   <Source>J Antimicrob Chemother 2004 Jul;54(1):282-3</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0473096</ConceptUI>
    <ConceptName>
     <String>beta-lactamase VIM-5, Pseudomonas aeruginosa</String>
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    <RegistryNumber>EC 3.5.2.6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T610837</TermUI>
      <String>beta-lactamase VIM-5, Pseudomonas aeruginosa</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T610839</TermUI>
      <String>bla(VIM-5), Pseudomonas aeruginosa</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T610838</TermUI>
      <String>VIM-5 beta-lactamase, Pseudomonas aeruginosa</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013780</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Abbott 40174</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>08</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>tetrahydropyridobenzopyran derived from cannabinoid nucleus; structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PYRIDINES (77-81)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001578</DescriptorUI>
     <DescriptorName>
      <String>Benzopyrans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Therapeutic potential of Marihuana QV 109 T398:440-457;1975</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061826</ConceptUI>
    <ConceptName>
     <String>Abbott 40174</String>
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    <RegistryNumber>26685-57-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091829</TermUI>
      <String>Abbott 40174</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013794</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>adenosine 2',3'-cyclic phosphate 5'-phosphate</String>
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  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1993</Year>
   <Month>09</Month>
   <Day>07</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000242</DescriptorUI>
     <DescriptorName>
      <String>Cyclic AMP</String>
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    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
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   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>BBA 480:376;1977</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061860</ConceptUI>
    <ConceptName>
     <String>adenosine 2',3'-cyclic phosphate 5'-phosphate</String>
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    <RegistryNumber>4527-92-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091863</TermUI>
      <String>adenosine 2',3'-cyclic phosphate 5'-phosphate</String>
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       <ThesaurusID>NLM (1977)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C489140</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>phenylalanyl-phenylalanyl-norleucyl-argininamide</String>
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  <DateCreated>
   <Year>2004</Year>
   <Month>09</Month>
   <Day>03</Day>
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  <DateRevised>
   <Year>2004</Year>
   <Month>11</Month>
   <Day>05</Day>
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  <Frequency>2</Frequency>
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    <DescriptorReferredTo>
     <DescriptorUI>*D009842</DescriptorUI>
     <DescriptorName>
      <String>Oligopeptides</String>
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  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D017473</DescriptorUI>
     <DescriptorName>
      <String>Receptors, Opioid, kappa</String>
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    <QualifierUI>Q000819</QualifierUI>
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      <String>agonists</String>
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  <SourceList>
   <Source>J Pharmacol Exp Ther 2004 Jul;310(1):326-33</Source>
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  <ConceptList>
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    <ConceptUI>M0472079</ConceptUI>
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     <Concept1UI>M0472079</Concept1UI>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0472079</Concept1UI>
     <Concept2UI>M0472080</Concept2UI>
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      <TermUI>T608072</TermUI>
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       <Year>2004</Year>
       <Month>09</Month>
       <Day>03</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T608073</TermUI>
      <String>Phe-Phe-Nle-Arg-NH2</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>03</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
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   <Concept PreferredConceptYN="N">
    <ConceptUI>M0475204</ConceptUI>
    <ConceptName>
     <String>FE 200041</String>
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     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0472079</Concept1UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T608075</TermUI>
      <String>FE 200041</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>03</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T608077</TermUI>
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      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>03</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T608076</TermUI>
      <String>FE-200041</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>03</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
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   <Concept PreferredConceptYN="N">
    <ConceptUI>M0472080</ConceptUI>
    <ConceptName>
     <String>D-Phe-D-Phe-D-Nle-D-Arg-NH2</String>
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    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0472079</Concept1UI>
     <Concept2UI>M0472080</Concept2UI>
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T608074</TermUI>
      <String>D-Phe-D-Phe-D-Nle-D-Arg-NH2</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>03</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C490713</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>beta-alanine-oxoglutarate aminotransferase, rat</String>
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  <DateCreated>
   <Year>2004</Year>
   <Month>09</Month>
   <Day>25</Day>
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  <DateRevised>
   <Year>2004</Year>
   <Month>11</Month>
   <Day>05</Day>
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  <Frequency>1</Frequency>
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    <DescriptorReferredTo>
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  <SourceList>
   <Source>FEBS Lett 2004 Aug 13;572(1-3):251-5</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0473113</ConceptUI>
    <ConceptName>
     <String>beta-alanine-oxoglutarate aminotransferase, rat</String>
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    <RegistryNumber>EC 2.6.1.-</RegistryNumber>
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     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T610869</TermUI>
      <String>beta-alanine-oxoglutarate aminotransferase, rat</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T610870</TermUI>
      <String>beta-AlaAT 1, rat</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>09</Month>
       <Day>25</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013821</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>axillarine</String>
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  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <Note>structure
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  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011763</DescriptorUI>
     <DescriptorName>
      <String>Pyrrolizidine Alkaloids</String>
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  <SourceList>
   <Source>Helv Chim Acta 59(6):2168;1976</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061913</ConceptUI>
    <ConceptName>
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    <RegistryNumber>19637-66-2</RegistryNumber>
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     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C013822</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>4-azidobenzimidate</String>
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  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1999</Year>
   <Month>07</Month>
   <Day>21</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AZIDES (77-80)</PreviousIndexing>
   <PreviousIndexing>AZIDES (80-81)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007096</DescriptorUI>
     <DescriptorName>
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   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 252(23):8524;1977</Source>
   <Source>J Biol Chem 252(5):1566;1977</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0061914</ConceptUI>
    <ConceptName>
     <String>4-azidobenzimidate</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T091917</TermUI>
      <String>4-azidobenzimidate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
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     </Term>
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   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C507743</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>cyclo-tri-Phen</String>
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  <DateCreated>
   <Year>2006</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>structure in first source
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010618</DescriptorUI>
     <DescriptorName>
      <String>Phenanthrolines</String>
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    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chembiochem. 2005 Nov;6(11):1976-80</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0494833</ConceptUI>
    <ConceptName>
     <String>cyclo-tri-Phen</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T666089</TermUI>
      <String>cyclo-tri-Phen</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>02</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002045</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>hydroxycyprazine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*HERBICIDES (73-75)</PreviousIndexing>
   <PreviousIndexing>CYCLOPROPANES (75-76)</PreviousIndexing>
   <PreviousIndexing>PROPYLAMINES (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014227</DescriptorUI>
     <DescriptorName>
      <String>Triazines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Agr Food Chem 20(6):1286;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0042503</ConceptUI>
    <ConceptName>
     <String>hydroxycyprazine</String>
    </ConceptName>
    <CASN1Name>2-hydroxy-4-cyclopropylamino-6-isopropylamino-s- triazine</CASN1Name>
    <RegistryNumber>39095-16-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T072506</TermUI>
      <String>hydroxycyprazine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002073</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>taurinophenetidine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>26</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ANILINE COMPOUNDS (73-75)</PreviousIndexing>
   <PreviousIndexing>*TAURINE (73-75)</PreviousIndexing>
   <PreviousIndexing>ETHYL ETHER (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D010628</DescriptorUI>
     <DescriptorName>
      <String>Phenetidine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013654</DescriptorUI>
     <DescriptorName>
      <String>Taurine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 61(11):1791;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0042541</ConceptUI>
    <ConceptName>
     <String>taurinophenetidine</String>
    </ConceptName>
    <RegistryNumber>22103-30-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T072544</TermUI>
      <String>taurinophenetidine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T072543</TermUI>
      <String>aminoethanesulfonylphenetidine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002047</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>bis(chloromethyl) sulfone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>affects rumen fermentation
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013450</DescriptorUI>
     <DescriptorName>
      <String>Sulfones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Agr Food Chem 20(6):1252;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0042506</ConceptUI>
    <ConceptName>
     <String>bis(chloromethyl) sulfone</String>
    </ConceptName>
    <RegistryNumber>37557-97-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T072509</TermUI>
      <String>bis(chloromethyl) sulfone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002053</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tetritol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SUGAR ALCOHOLS (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013780</DescriptorUI>
     <DescriptorName>
      <String>Tetroses</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>FEBS Lett 23(1):69;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0042517</ConceptUI>
    <ConceptName>
     <String>tetritol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T072520</TermUI>
      <String>tetritol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002054</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>umecyanin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>copper-containing protein from horseradish root
  </Note>
  <Frequency>13</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PLANT PROTEINS (73-76)</PreviousIndexing>
   <PreviousIndexing>COPPER (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D008667</DescriptorUI>
     <DescriptorName>
      <String>Metalloproteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>FEBS Lett 23(1):41;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0042518</ConceptUI>
    <ConceptName>
     <String>umecyanin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T072521</TermUI>
      <String>umecyanin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C001308</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>glycolaldehyde phosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2006</Year>
   <Month>02</Month>
   <Day>09</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>9</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*SUGAR PHOSPHATES (75-76)</PreviousIndexing>
   <PreviousIndexing>*TETROSES (72-76)</PreviousIndexing>
   <PreviousIndexing>ORGANOPHOSPHORUS CPDS (73-75)</PreviousIndexing>
   <PreviousIndexing>PHOSPHORIC ACIDS (72-73)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000079</DescriptorUI>
     <DescriptorName>
      <String>Acetaldehyde</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 247(10):3262;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0041430</ConceptUI>
    <ConceptName>
     <String>glycolaldehyde phosphate</String>
    </ConceptName>
    <RegistryNumber>870-55-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0041430</Concept1UI>
     <Concept2UI>M0494835</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T071433</TermUI>
      <String>glycolaldehyde phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0494835</ConceptUI>
    <ConceptName>
     <String>bis(glycolaldehyde) phosphate</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="REL">
     <Concept1UI>M0041430</Concept1UI>
     <Concept2UI>M0494835</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T666091</TermUI>
      <String>bis(glycolaldehyde) phosphate</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>02</Month>
       <Day>09</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002414</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>25-azacholesterol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>26</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>AZA STEROIDS (75-76)</PreviousIndexing>
   <PreviousIndexing>CHOLESTEROL (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002784</DescriptorUI>
     <DescriptorName>
      <String>Cholesterol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Poultry Sci 51(2):449;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0042978</ConceptUI>
    <ConceptName>
     <String>25-azacholesterol</String>
    </ConceptName>
    <CASN1Name>Chol-5-en-3-ol, 24-(dimethylamino)-, (3beta)-</CASN1Name>
    <RegistryNumber>1973-61-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T072981</TermUI>
      <String>25-azacholesterol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T072980</TermUI>
      <String>24-(dimethylamino)chol-5-en-3 beta-ol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C012451</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>diisobutylnaphthalenesulfonate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>08</Month>
   <Day>17</Day>
  </DateRevised>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009282</DescriptorUI>
     <DescriptorName>
      <String>Naphthalenesulfonates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Zentralbl Bakteriol (Orig A) 234(3):393;1976</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0059478</ConceptUI>
    <ConceptName>
     <String>diisobutylnaphthalenesulfonate</String>
    </ConceptName>
    <RegistryNumber>52627-01-7</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>27213-90-7 (Na salt)</RelatedRegistryNumber>
     <RelatedRegistryNumber>53578-91-9 (Ca salt)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0059478</Concept1UI>
     <Concept2UI>M0311861</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0059478</Concept1UI>
     <Concept2UI>M0311860</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0059478</Concept1UI>
     <Concept2UI>M0059479</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T089481</TermUI>
      <String>diisobutylnaphthalenesulfonate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0311861</ConceptUI>
    <ConceptName>
     <String>diisobutylnaphthalenesulfonate, calcium salt</String>
    </ConceptName>
    <RegistryNumber>53578-91-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0059478</Concept1UI>
     <Concept2UI>M0311861</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T341861</TermUI>
      <String>diisobutylnaphthalenesulfonate, calcium salt</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0311860</ConceptUI>
    <ConceptName>
     <String>diisobutylnaphthalenesulfonate, sodium salt</String>
    </ConceptName>
    <RegistryNumber>27213-90-7</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0059478</Concept1UI>
     <Concept2UI>M0311860</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T341860</TermUI>
      <String>diisobutylnaphthalenesulfonate, sodium salt</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0059479</ConceptUI>
    <ConceptName>
     <String>Nekal BX</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0059478</Concept1UI>
     <Concept2UI>M0059479</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="TRD"  RecordPreferredTermYN="N">
      <TermUI>T089482</TermUI>
      <String>Nekal BX</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1976)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C470940</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>7-bromo-6-methoxy-2-N-methylamino-1H,4H,5H,8H-9,10-dihydro-9,10-(1',2')benzenoanthracene-1,4,5,8-tetraone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>02</Month>
   <Day>08</Day>
  </DateCreated>
  <Note>an antineoplastic agent; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000880</DescriptorUI>
     <DescriptorName>
      <String>Anthraquinones</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001952</DescriptorUI>
     <DescriptorName>
      <String>Bridged-Ring Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Anticancer Drugs 2002 Jul;13(6):567-81</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0445524</ConceptUI>
    <ConceptName>
     <String>7-bromo-6-methoxy-2-N-methylamino-1H,4H,5H,8H-9,10-dihydro-9,10-(1',2')benzenoanthracene-1,4,5,8-tetraone</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T532331</TermUI>
      <String>7-bromo-6-methoxy-2-N-methylamino-1H,4H,5H,8H-9,10-dihydro-9,10-(1',2')benzenoanthracene-1,4,5,8-tetraone</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>02</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T532332</TermUI>
      <String>TT24-2 cpd</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>02</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
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   </Concept>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C470941</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-(2-(acetylamino)-4-(diethylamino)-5-methoxyphenyl)-5-amino-7-bromo-4-chloro-2H-benzotriazole</String>
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  <DateCreated>
   <Year>2003</Year>
   <Month>02</Month>
   <Day>08</Day>
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  <Note>a mutagen; structure in first source
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  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000814</DescriptorUI>
     <DescriptorName>
      <String>Aniline Compounds</String>
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   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014230</DescriptorUI>
     <DescriptorName>
      <String>Triazoles</String>
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  <SourceList>
   <Source>Mutagenesis 2002 Jul;17(4):293-9</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0445525</ConceptUI>
    <ConceptName>
     <String>2-(2-(acetylamino)-4-(diethylamino)-5-methoxyphenyl)-5-amino-7-bromo-4-chloro-2H-benzotriazole</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T532333</TermUI>
      <String>2-(2-(acetylamino)-4-(diethylamino)-5-methoxyphenyl)-5-amino-7-bromo-4-chloro-2H-benzotriazole</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>02</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T532334</TermUI>
      <String>PBTA-7</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>02</Month>
       <Day>08</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002076</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>pustulan</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>34</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>PLANT EXTRACTS (73-76)</PreviousIndexing>
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  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011134</DescriptorUI>
     <DescriptorName>
      <String>Polysaccharides</String>
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    </DescriptorReferredTo>
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  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Microbiol 104(2):201;1975</Source>
   <Source>Can J Microbiol 18(10):1543;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0042543</ConceptUI>
    <ConceptName>
     <String>pustulan</String>
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    <RegistryNumber>37331-28-5</RegistryNumber>
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     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T072546</TermUI>
      <String>pustulan</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C021013</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N(6),N(6)-dimethyladenosine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1980</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>26</Day>
  </DateRevised>
  <Frequency>16</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D000241</DescriptorUI>
     <DescriptorName>
      <String>Adenosine</String>
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    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D012315</DescriptorUI>
     <DescriptorName>
      <String>RNA Caps</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Biol Chem 254(18):9085;1979</Source>
   <Source>J Biol Chem 254(18):9090;1979</Source>
   <Source>J Biol Chem 254(18):9094;1979</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0075422</ConceptUI>
    <ConceptName>
     <String>N(6),N(6)-dimethyladenosine</String>
    </ConceptName>
    <RegistryNumber>2620-62-4</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T105425</TermUI>
      <String>N(6),N(6)-dimethyladenosine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T105424</TermUI>
      <String>6-dimethylaminopurine riboside</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T105423</TermUI>
      <String>6-(gamma,gamma-dimethylamino)purine riboside</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1980)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014869</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-(2,4,5-trihydroxyphenethyl)normetazocine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>04</Month>
   <Day>17</Day>
  </DateRevised>
  <Note>RN given refers to HI(2alpha,6alpha,11R*)-isomer; structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001575</DescriptorUI>
     <DescriptorName>
      <String>Benzomorphans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Med Chem 20(5):673;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063693</ConceptUI>
    <ConceptName>
     <String>N-(2,4,5-trihydroxyphenethyl)normetazocine</String>
    </ConceptName>
    <CASN1Name>(2 alpha,6 alpha,11R*)-5-(2-(1,4,5,6-tetrahydro- 8-hydroxy-6,11-dimethyl-2,6-methano-3-benzazocin- 3(2H)-yl)ethyl)-1,2,4-benzenetriol</CASN1Name>
    <RegistryNumber>62228-26-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093696</TermUI>
      <String>N-(2,4,5-trihydroxyphenethyl)normetazocine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C115721</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ANG12 precursor protein, Anopheles gambiae</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1998</Year>
   <Month>12</Month>
   <Day>04</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>02</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>a mosquito protein involved in digestion; has homology with allergens, Bla g 1 &amp; Per a 1; amino acid sequence in first source; GenBank Z22925
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D019476</DescriptorUI>
     <DescriptorName>
      <String>Insect Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem1998 Nov 13;273(46):30801-7</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0297839</ConceptUI>
    <ConceptName>
     <String>ANG12 precursor protein, Anopheles gambiae</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T327844</TermUI>
      <String>ANG12 precursor protein, Anopheles gambiae</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1998)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014879</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-yl-6-hydroxycytosine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>08</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>radical resulting after X-irradiation of cytosine monohydrate
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003596</DescriptorUI>
     <DescriptorName>
      <String>Cytosine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D005609</DescriptorUI>
     <DescriptorName>
      <String>Free Radicals</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Radiat Res 70(2):304;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063707</ConceptUI>
    <ConceptName>
     <String>5-yl-6-hydroxycytosine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093710</TermUI>
      <String>5-yl-6-hydroxycytosine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C506238</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N,N-dimethylbiguanidium</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>12</Month>
   <Day>16</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D008687</DescriptorUI>
     <DescriptorName>
      <String>Metformin</String>
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    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Crystallogr C. 2004 Oct;60(Pt 10):o740-43</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0492975</ConceptUI>
    <ConceptName>
     <String>N,N-dimethylbiguanidium</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T662308</TermUI>
      <String>N,N-dimethylbiguanidium</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>12</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C506239</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-(6-(3-Chlorophenyl)-2,4-dioxoperhydropyrimidin-3-yl)ethyl morpholine-4-carbodithioate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>12</Month>
   <Day>16</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004220</DescriptorUI>
     <DescriptorName>
      <String>Disulfides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D009025</DescriptorUI>
     <DescriptorName>
      <String>Morpholines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Crystallogr C. 2004 Oct;60(Pt 10):o757-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0492976</ConceptUI>
    <ConceptName>
     <String>2-(6-(3-Chlorophenyl)-2,4-dioxoperhydropyrimidin-3-yl)ethyl morpholine-4-carbodithioate</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T662310</TermUI>
      <String>2-(6-(3-Chlorophenyl)-2,4-dioxoperhydropyrimidin-3-yl)ethyl morpholine-4-carbodithioate</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>12</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T662311</TermUI>
      <String>2-(CP)-DOPMC-DT</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>12</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C506240</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>(4-oxo-4H-chromen-2-yl)(phenyl)methyl acetate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>12</Month>
   <Day>16</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000085</DescriptorUI>
     <DescriptorName>
      <String>Acetates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001578</DescriptorUI>
     <DescriptorName>
      <String>Benzopyrans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Crystallogr C. 2004 Oct;60(Pt 10):o762-4</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0492977</ConceptUI>
    <ConceptName>
     <String>(4-oxo-4H-chromen-2-yl)(phenyl)methyl acetate</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T662312</TermUI>
      <String>(4-oxo-4H-chromen-2-yl)(phenyl)methyl acetate</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>12</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T662313</TermUI>
      <String>4-OC-PMA</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>12</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014927</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-amino-5-bromo-6-methyl-4-pyrimidinol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>07</Month>
   <Day>18</Day>
  </DateRevised>
  <Frequency>9</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011743</DescriptorUI>
     <DescriptorName>
      <String>Pyrimidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Am J Vet Res 38(12):1963;1977</Source>
   <Source>Comprehensive Ther 3(7):31;1977</Source>
   <Source>Toxicol Appl Pharmacol 42:603;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063833</ConceptUI>
    <ConceptName>
     <String>2-amino-5-bromo-6-methyl-4-pyrimidinol</String>
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    <RegistryNumber>6307-35-3</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
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    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093836</TermUI>
      <String>2-amino-5-bromo-6-methyl-4-pyrimidinol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0063837</ConceptUI>
    <ConceptName>
     <String>U 25166</String>
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    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0063833</Concept1UI>
     <Concept2UI>M0063837</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
      <TermUI>T093840</TermUI>
      <String>U 25166</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T093839</TermUI>
      <String>U-25166</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T093838</TermUI>
      <String>U-25-166</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T093837</TermUI>
      <String>U 25 166</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
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 </SupplementalRecord>
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   <Month>04</Month>
   <Day>01</Day>
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  <Note>antineoplastic annonaceous acetogenin from the seeds of Asimina triloba possessing a bis-tetrahydrofuran ring; structure in first source
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  <SourceList>
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  <ConceptList>
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       <Month>04</Month>
       <Day>01</Day>
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<SupplementalRecord SCRClass = "1">
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  <SupplementalRecordName>
   <String>roridin M</String>
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  <DateCreated>
   <Year>2002</Year>
   <Month>02</Month>
   <Day>21</Day>
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  <DateRevised>
   <Year>2005</Year>
   <Month>04</Month>
   <Day>01</Day>
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  <Note>structure in first source
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
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  <SourceList>
   <Source>J Antibiot (Tokyo) 2001 Nov;54(11):980-3</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
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      <DateCreated>
       <Year>2002</Year>
       <Month>02</Month>
       <Day>21</Day>
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      <ThesaurusIDlist>
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<SupplementalRecord SCRClass = "1">
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  <SupplementalRecordName>
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  <DateCreated>
   <Year>2002</Year>
   <Month>02</Month>
   <Day>21</Day>
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  <DateRevised>
   <Year>2005</Year>
   <Month>04</Month>
   <Day>01</Day>
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  <Note>structure in first source
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
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  <SourceList>
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  <ConceptList>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
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      <DateCreated>
       <Year>2002</Year>
       <Month>02</Month>
       <Day>21</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014978</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>glycineamide ribonucleotide</String>
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  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>19</Day>
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  <Note>structure
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  <Frequency>12</Frequency>
  <HeadingMappedToList>
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    <DescriptorReferredTo>
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  <SourceList>
   <Source>Biochem Pharmacol 1980;29(2):163</Source>
   <Source>Carbohydrate Res 56:75;1977</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063908</ConceptUI>
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    <CASN1Name>2-amino-(N-D-ribofuranosyl)acetamide 5'-phosphate</CASN1Name>
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      <TermUI>T093911</TermUI>
      <String>glycineamide ribonucleotide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T093909</TermUI>
      <String>5'-phosphoribosylglycineamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T093910</TermUI>
      <String>glycineamideribotide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C447959</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>CP-544372</String>
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  <DateCreated>
   <Year>2002</Year>
   <Month>02</Month>
   <Day>27</Day>
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  <DateRevised>
   <Year>2005</Year>
   <Month>04</Month>
   <Day>01</Day>
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  <Note>structure in first source
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D018942</DescriptorUI>
     <DescriptorName>
      <String>Macrolides</String>
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  <SourceList>
   <Source>Curr Med Chem 2001 Dec;8(14):1727-58</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0415949</ConceptUI>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T483780</TermUI>
      <String>CP-544372</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>02</Month>
       <Day>27</Day>
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      <ThesaurusIDlist>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
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      <DateCreated>
       <Year>2002</Year>
       <Month>02</Month>
       <Day>27</Day>
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      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
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  <DateCreated>
   <Year>2002</Year>
   <Month>03</Month>
   <Day>10</Day>
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  <DateRevised>
   <Year>2005</Year>
   <Month>04</Month>
   <Day>01</Day>
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  <HeadingMappedToList>
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     <DescriptorUI>*D005419</DescriptorUI>
     <DescriptorName>
      <String>Flavonoids</String>
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  <SourceList>
   <Source>J Antibiot (Tokyo) 2001 Dec;54(12):1031-5</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
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      <DateCreated>
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       <Month>03</Month>
       <Day>10</Day>
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      <ThesaurusIDlist>
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 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014943</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-(4-acetamidophenyl)-anti-tricyclo(4.2.2.0)deca-3,9-diene-7,8-endodicarboximide</String>
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  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1981</Year>
   <Month>08</Month>
   <Day>10</Day>
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  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>BRIDGED COMPOUNDS (77-81)</PreviousIndexing>
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  <SourceList>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
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      <ThesaurusIDlist>
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<SupplementalRecord SCRClass = "1">
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  <SupplementalRecordName>
   <String>N-acetoxy-N-2-acetylaminophenanthrene</String>
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  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>02</Month>
   <Day>25</Day>
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  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010616</DescriptorUI>
     <DescriptorName>
      <String>Phenanthrenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Cancer Res 37(11):3887;1977</Source>
   <Source>Chem Biol Interact 1980;29(1):43</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063863</ConceptUI>
    <ConceptName>
     <String>N-acetoxy-N-2-acetylaminophenanthrene</String>
    </ConceptName>
    <RegistryNumber>26541-57-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093866</TermUI>
      <String>N-acetoxy-N-2-acetylaminophenanthrene</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014946</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>acetoxynitroestrone</String>
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  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004970</DescriptorUI>
     <DescriptorName>
      <String>Estrone</String>
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    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Soc Trans 5(3):724;1977</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
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    <ConceptName>
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    <RegistryNumber>22145-20-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
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      <ThesaurusIDlist>
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<SupplementalRecord SCRClass = "1">
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  <SupplementalRecordName>
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  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
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  <Frequency>9</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014315</DescriptorUI>
     <DescriptorName>
      <String>Triterpenes</String>
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  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 66(9):1348;1977</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
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    <ConceptName>
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    <RegistryNumber>28937-85-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
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      <ThesaurusIDlist>
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<SupplementalRecord SCRClass = "1">
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  <SupplementalRecordName>
   <String>benzenesulfonic acid, 4-chloro-N-1H-1,2,4-triazol-3-yl-</String>
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  <DateCreated>
   <Year>1983</Year>
   <Month>06</Month>
   <Day>15</Day>
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  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>02</Day>
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  <Note>leukotriene B4 antagonist
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  <Frequency>1</Frequency>
  <PreviousIndexingList>
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  <HeadingMappedToList>
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   <HeadingMappedTo>
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  <SourceList>
   <Source>Graefes Arch Clin Exp Ohthalmol 1983;220(2):74</Source>
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  <ConceptList>
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    <CASN1Name>Benzenesulfenamide, 4-chloro-N-1H-1,2,4-triazol-3-yl-</CASN1Name>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="N">
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      <ThesaurusIDlist>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C028878</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>ferredoxin-NAD+ reductase</String>
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  <DateCreated>
   <Year>1981</Year>
   <Month>04</Month>
   <Day>17</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>19</Day>
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  <Frequency>52</Frequency>
  <HeadingMappedToList>
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     <DescriptorName>
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  </HeadingMappedToList>
  <SourceList>
   <Source>Anal Biochem 1981;110(1):176</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
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    <ConceptName>
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    <RegistryNumber>EC 1.18.1.3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
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      <String>ferredoxin-NAD+ reductase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
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     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T122544</TermUI>
      <String>NADH-ferredoxin oxidoreductase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014952</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-acetylsulfamethoxypyridazine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D013421</DescriptorUI>
     <DescriptorName>
      <String>Sulfamethoxypyridazine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Boll Chim Farm 116(6):358;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063875</ConceptUI>
    <ConceptName>
     <String>N-acetylsulfamethoxypyridazine</String>
    </ConceptName>
    <RegistryNumber>127-75-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093878</TermUI>
      <String>N-acetylsulfamethoxypyridazine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C452640</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>PLP (40-59) peptide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2002</Year>
   <Month>04</Month>
   <Day>25</Day>
  </DateCreated>
  <Note>used for immunization in mice; peptide sequence in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010446</DescriptorUI>
     <DescriptorName>
      <String>Peptide Fragments</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D018991</DescriptorUI>
     <DescriptorName>
      <String>Myelin Proteolipid Protein</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Proc Natl Acad Sci U S A 2002 Mar 5;99(5):3013-7</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0421590</ConceptUI>
    <ConceptName>
     <String>PLP (40-59) peptide</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T491002</TermUI>
      <String>PLP (40-59) peptide</String>
      <DateCreated>
       <Year>2002</Year>
       <Month>04</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2002)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014962</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>altronic acid</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013400</DescriptorUI>
     <DescriptorName>
      <String>Sugar Acids</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>BBA 483:6;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063889</ConceptUI>
    <ConceptName>
     <String>altronic acid</String>
    </ConceptName>
    <RegistryNumber>24871-35-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093892</TermUI>
      <String>altronic acid</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C029225</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>diethylnitrosamine deethylase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1981</Year>
   <Month>04</Month>
   <Day>30</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>19</Day>
  </DateRevised>
  <Frequency>7</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010088</DescriptorUI>
     <DescriptorName>
      <String>Oxidoreductases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Life Sci 1980;27(23):2149</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0093345</ConceptUI>
    <ConceptName>
     <String>diethylnitrosamine deethylase</String>
    </ConceptName>
    <RegistryNumber>EC 1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T123348</TermUI>
      <String>diethylnitrosamine deethylase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T123347</TermUI>
      <String>DEN-deethylase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1981)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C034919</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>acyl protein synthetase</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1982</Year>
   <Month>07</Month>
   <Day>20</Day>
  </DateCreated>
  <DateRevised>
   <Year>2003</Year>
   <Month>10</Month>
   <Day>10</Day>
  </DateRevised>
  <Note>component of the fatty acid reductase complex of luminescent bacteria
  </Note>
  <Frequency>15</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000217</DescriptorUI>
     <DescriptorName>
      <String>Acyltransferases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biol Chem 1982;257(12):6908</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0107312</ConceptUI>
    <ConceptName>
     <String>acyl protein synthetase</String>
    </ConceptName>
    <RegistryNumber>EC 2.3.1.-</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T137316</TermUI>
      <String>acyl protein synthetase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T137314</TermUI>
      <String>fatty acyl-protein synthetase</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1982)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014976</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1-(2-amino-1-(1-(naphthyloxy)methyl)ethyl)piperidine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>06</Month>
   <Day>01</Day>
  </DateRevised>
  <Note>inhibitor of serotonin; RN given refers to HCl; structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010880</DescriptorUI>
     <DescriptorName>
      <String>Piperidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Int Pharmacodyn 228:322;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063905</ConceptUI>
    <ConceptName>
     <String>1-(2-amino-1-(1-(naphthyloxy)methyl)ethyl)piperidine</String>
    </ConceptName>
    <CASN1Name>1-Piperidineethanamine, beta-((1-naphthalenyloxy)methyl)-, monohydrochloride</CASN1Name>
    <RegistryNumber>65997-94-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093908</TermUI>
      <String>1-(2-amino-1-(1-(naphthyloxy)methyl)ethyl)piperidine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014987</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Anatril</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>contains glucosamine hydroiodide; and glucosamine sulfate; anti-arthritic
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005944</DescriptorUI>
     <DescriptorName>
      <String>Glucosamine</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Electro Diag Therap 14(1):5;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063937</ConceptUI>
    <ConceptName>
     <String>Anatril</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093940</TermUI>
      <String>Anatril</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014988</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,3-anhydroerythritol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>11</Month>
   <Day>18</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>EPOXY COMPOUNDS (77-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004896</DescriptorUI>
     <DescriptorName>
      <String>Erythritol</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Carbohydrate Res 56:43;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063938</ConceptUI>
    <ConceptName>
     <String>2,3-anhydroerythritol</String>
    </ConceptName>
    <RegistryNumber>57302-79-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093941</TermUI>
      <String>2,3-anhydroerythritol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014992</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,3-anhydro-DL-threitol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1980</Year>
   <Month>11</Month>
   <Day>18</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>EPOXY COMPOUNDS (77-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D013402</DescriptorUI>
     <DescriptorName>
      <String>Sugar Alcohols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Carbohydrate Res 56:43;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063943</ConceptUI>
    <ConceptName>
     <String>2,3-anhydro-DL-threitol</String>
    </ConceptName>
    <CASN1Name>2,3-Oxiranedimethanol, trans-(+-)-</CASN1Name>
    <RegistryNumber>63621-92-1</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093946</TermUI>
      <String>2,3-anhydro-DL-threitol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C014996</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>antistaphylococcal gamma globulin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1995</Year>
   <Month>07</Month>
   <Day>26</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>STAPHYLOCOCCUS/immunol (77-81)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005719</DescriptorUI>
     <DescriptorName>
      <String>gamma-Globulins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Antibiotiki 22(9):809;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063953</ConceptUI>
    <ConceptName>
     <String>antistaphylococcal gamma globulin</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093956</TermUI>
      <String>antistaphylococcal gamma globulin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015002</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2',5'-arabinosylcytidine monophosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>01</Month>
   <Day>18</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*NUCLEOTIDES, CYCLIC (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003561</DescriptorUI>
     <DescriptorName>
      <String>Cytarabine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Am Chem Soc 99(16):5471;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063968</ConceptUI>
    <ConceptName>
     <String>2',5'-arabinosylcytidine monophosphate</String>
    </ConceptName>
    <CASN1Name>2(1H)-Pyrimidinone, 4-amino-1-(2,5-O-phosphinico-beta-D-arabinofuranosyl)-</CASN1Name>
    <RegistryNumber>15466-01-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093971</TermUI>
      <String>2',5'-arabinosylcytidine monophosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015005</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>beta-aspartyl methylamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1998</Year>
   <Month>03</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>structure; RN given refers to (L)-isomer
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D001216</DescriptorUI>
     <DescriptorName>
      <String>Asparagine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Pharmacol 26(15):1405;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063969</ConceptUI>
    <ConceptName>
     <String>beta-aspartyl methylamide</String>
    </ConceptName>
    <CASN1Name>L-Asparagine, N-methyl-</CASN1Name>
    <RegistryNumber>7175-34-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093972</TermUI>
      <String>beta-aspartyl methylamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015077</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>chromin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>08</Month>
   <Day>14</Day>
  </DateRevised>
  <Note>contains perfluoroethylcyclohexane sulfonic acid &amp; chromium anhydride
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002857</DescriptorUI>
     <DescriptorName>
      <String>Chromium</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005466</DescriptorUI>
     <DescriptorName>
      <String>Fluorocarbons</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Gig Truda 10:35;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064088</ConceptUI>
    <ConceptName>
     <String>chromin</String>
    </ConceptName>
    <RegistryNumber>1407-01-8</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094091</TermUI>
      <String>chromin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015013</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>azobiotin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D001710</DescriptorUI>
     <DescriptorName>
      <String>Biotin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 66(8):1208;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063987</ConceptUI>
    <ConceptName>
     <String>azobiotin</String>
    </ConceptName>
    <CASN1Name>4-(4-carboxybutyl)hexahydropyrrolo(3,4-d)imidazol-2-one.HCl</CASN1Name>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093990</TermUI>
      <String>azobiotin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015016</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>barnol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014992</DescriptorUI>
     <DescriptorName>
      <String>Xylenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Chem Scand 31(5):391;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0063993</ConceptUI>
    <ConceptName>
     <String>barnol</String>
    </ConceptName>
    <CASN1Name>1,2,3-trihydroxy-4,6-dimethyl-5-ethylbenzene</CASN1Name>
    <RegistryNumber>2151-18-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T093996</TermUI>
      <String>barnol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015027</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-benzyl-L-valine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>RN given refers to parent cpd
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>BENZYL CPDS (78-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014633</DescriptorUI>
     <DescriptorName>
      <String>Valine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Br J Pharmacol 61(1):109;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064014</ConceptUI>
    <ConceptName>
     <String>N-benzyl-L-valine</String>
    </ConceptName>
    <RegistryNumber>15363-84-5</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>22711-85-9 (mono-Na salt)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0064014</Concept1UI>
     <Concept2UI>M0312695</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094017</TermUI>
      <String>N-benzyl-L-valine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0312695</ConceptUI>
    <ConceptName>
     <String>N-benzyl-L-valine monosodium salt</String>
    </ConceptName>
    <RegistryNumber>22711-85-9</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0064014</Concept1UI>
     <Concept2UI>M0312695</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342695</TermUI>
      <String>N-benzyl-L-valine monosodium salt</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C498488</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Secisbp2 protein, rat</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2005</Year>
   <Month>07</Month>
   <Day>29</Day>
  </DateCreated>
  <Note>involved in selenoprotein biosynthesis; RefSeq NM_024002
  </Note>
  <Frequency>18</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D016601</DescriptorUI>
     <DescriptorName>
      <String>RNA-Binding Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0458425</ConceptUI>
    <ConceptName>
     <String>Secisbp2 protein, rat</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T634966</TermUI>
      <String>Secisbp2 protein, rat</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>04</Month>
       <Day>01</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T567504</TermUI>
      <String>SECIS-binding protein 2, rat</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>01</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T567505</TermUI>
      <String>Sbp2 protein, rat</String>
      <DateCreated>
       <Year>2004</Year>
       <Month>01</Month>
       <Day>07</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2004)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015031</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,4-bis(acetomercuri)-2,3-diethoxybutane</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Note>structure
  </Note>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000479</DescriptorUI>
     <DescriptorName>
      <String>Alkylmercury Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Europ J Biochem 77:107;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064018</ConceptUI>
    <ConceptName>
     <String>1,4-bis(acetomercuri)-2,3-diethoxybutane</String>
    </ConceptName>
    <CASN1Name>Mercury, bis(acetato-O)(mu-(2,3-diethoxy-1,4-butanediyl))di-, (R*,S*)-</CASN1Name>
    <RegistryNumber>63865-22-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094021</TermUI>
      <String>1,4-bis(acetomercuri)-2,3-diethoxybutane</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015033</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,3-bis(3-chloro-2-butyl)-1-nitrosourea</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <Frequency>0</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002330</DescriptorUI>
     <DescriptorName>
      <String>Carmustine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Org Chem 42(22):3538;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064019</ConceptUI>
    <ConceptName>
     <String>1,3-bis(3-chloro-2-butyl)-1-nitrosourea</String>
    </ConceptName>
    <CASN1Name>Urea, N,N'-bis(2-chloro-1-methylpropyl)-N-nitroso-</CASN1Name>
    <RegistryNumber>63548-66-3</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094022</TermUI>
      <String>1,3-bis(3-chloro-2-butyl)-1-nitrosourea</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002568</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>3-diazopyrazole-4-carboxamide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>09</Month>
   <Day>08</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*AZO CPDS (73-79)</PreviousIndexing>
   <PreviousIndexing>DIAZONIUM COMPOUNDS (73-82)</PreviousIndexing>
   <PreviousIndexing>FORMAMIDES (75-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011720</DescriptorUI>
     <DescriptorName>
      <String>Pyrazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem Pharmacol 21(15):2141;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043222</ConceptUI>
    <ConceptName>
     <String>3-diazopyrazole-4-carboxamide</String>
    </ConceptName>
    <RegistryNumber>38658-38-7</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073225</TermUI>
      <String>3-diazopyrazole-4-carboxamide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002677</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>biotinyl-4-nitrophenyl ester</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1972</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>01</Month>
   <Day>26</Day>
  </DateRevised>
  <Frequency>5</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BIOTIN (72-76)</PreviousIndexing>
   <PreviousIndexing>NITROPHENOLS (72-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D001710</DescriptorUI>
     <DescriptorName>
      <String>Biotin</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Proc Nat Acad Sci USA 68(10):2604;1971</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043385</ConceptUI>
    <ConceptName>
     <String>biotinyl-4-nitrophenyl ester</String>
    </ConceptName>
    <RegistryNumber>33755-53-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073388</TermUI>
      <String>biotinyl-4-nitrophenyl ester</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073387</TermUI>
      <String>biotin-p-nitrophenyl ester</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1972)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002606</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>neo-cholex powder</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1986</Year>
   <Month>08</Month>
   <Day>05</Day>
  </DateRevised>
  <Note>combination drug used as gallbladder contracting agent; contains vegetable oil, sugar, milk fat, lecithin, casein, cocoa
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*OILS (73-86)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002241</DescriptorUI>
     <DescriptorName>
      <String>Carbohydrates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D002364</DescriptorUI>
     <DescriptorName>
      <String>Caseins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004338</DescriptorUI>
     <DescriptorName>
      <String>Drug Combinations</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010938</DescriptorUI>
     <DescriptorName>
      <String>Plant Oils</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Jpn J Clin Radiol 17(9):502;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043277</ConceptUI>
    <ConceptName>
     <String>neo-cholex powder</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073280</TermUI>
      <String>neo-cholex powder</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C511027</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>diplobifuranylone B</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>06</Month>
   <Day>16</Day>
  </DateCreated>
  <Note>produced by Diplodia corticola, a fungus pathogen of cork oak; structure in first source
  </Note>
  <Frequency>3</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D005663</DescriptorUI>
     <DescriptorName>
      <String>Furans</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2006 Apr;69(4):671-4</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0498985</ConceptUI>
    <ConceptName>
     <String>diplobifuranylone B</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T676045</TermUI>
      <String>diplobifuranylone B</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>06</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C005330</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>gilutensin</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2009</Year>
   <Month>11</Month>
   <Day>12</Day>
  </DateRevised>
  <Note>CNS stimulant, anti-hypotensive agent; RN given refers to parent cpd; structure
  </Note>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*BUTYLAMINES (73-82)</PreviousIndexing>
   <PreviousIndexing>ALKENES (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001597</DescriptorUI>
     <DescriptorName>
      <String>Benzylidene Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D007022</DescriptorUI>
     <DescriptorName>
      <String>Hypotension</String>
      </DescriptorName>
     </DescriptorReferredTo>
    <QualifierReferredTo>
    <QualifierUI>Q000188</QualifierUI>
     <QualifierName>
      <String>drug therapy</String>
      </QualifierName>
     </QualifierReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0046813</ConceptUI>
    <ConceptName>
     <String>gilutensin</String>
    </ConceptName>
    <CASN1Name>2-ethyl-3,3-diphenylpropen-2-ylamine</CASN1Name>
    <RegistryNumber>341-00-4</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>1146-95-8 (HCl)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0046813</Concept1UI>
     <Concept2UI>M0309026</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T076816</TermUI>
      <String>gilutensin</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0309026</ConceptUI>
    <ConceptName>
     <String>gilutensin hydrochloride</String>
    </ConceptName>
    <RegistryNumber>1146-95-8</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0046813</Concept1UI>
     <Concept2UI>M0309026</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T339026</TermUI>
      <String>gilutensin hydrochloride</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C511028</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>florxenilide A</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2006</Year>
   <Month>06</Month>
   <Day>16</Day>
  </DateCreated>
  <Note>xenicane-type diterpene with cytotoxicity from Xenia florida; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004224</DescriptorUI>
     <DescriptorName>
      <String>Diterpenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Nat Prod 2006 Apr;69(4):675-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0498986</ConceptUI>
    <ConceptName>
     <String>florxenilide A</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T676046</TermUI>
      <String>florxenilide A</String>
      <DateCreated>
       <Year>2006</Year>
       <Month>06</Month>
       <Day>16</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2006)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002662</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>prostaglandin-ICI 74205</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>07</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>has two more carbons on lower side chain than PGF2alpha; RN given refers to (3S*)-isomer; structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*PROSTAGLANDINS (73-78)</PreviousIndexing>
   <PreviousIndexing>PGF (78-79)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011461</DescriptorUI>
     <DescriptorName>
      <String>Prostaglandins F, Synthetic</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Prostaglandins 2(5):375;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043351</ConceptUI>
    <ConceptName>
     <String>prostaglandin-ICI 74205</String>
    </ConceptName>
    <RegistryNumber>36950-85-3</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>37497-26-0 ((3R*)-isomer)</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0043351</Concept1UI>
     <Concept2UI>M0308016</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073354</TermUI>
      <String>prostaglandin-ICI 74205</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073353</TermUI>
      <String>PG-ICI 74205</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073352</TermUI>
      <String>PG-ICI 742-5</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073351</TermUI>
      <String>ICI 74205</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0308016</ConceptUI>
    <ConceptName>
     <String>prostaglandin-ICI 74205, (3R*)-isomer</String>
    </ConceptName>
    <RegistryNumber>37497-26-0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0043351</Concept1UI>
     <Concept2UI>M0308016</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T338016</TermUI>
      <String>prostaglandin-ICI 74205, (3R*)-isomer</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C411123</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6-oxocampestanol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>07</Month>
   <Day>25</Day>
  </DateCreated>
  <Note>isolated from Catharanthus roseus; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010840</DescriptorUI>
     <DescriptorName>
      <String>Phytosterols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Phytochemistry 2000 Mar;53(5):549-53</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0366571</ConceptUI>
    <ConceptName>
     <String>6-oxocampestanol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T419889</TermUI>
      <String>6-oxocampestanol</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>07</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C580812</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>thioredoxin z, Arabidopsis</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2013</Year>
   <Month>04</Month>
   <Day>30</Day>
  </DateCreated>
  <Note>RefSeq NM_111553
  </Note>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D029681</DescriptorUI>
     <DescriptorName>
      <String>Arabidopsis Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D054479</DescriptorUI>
     <DescriptorName>
      <String>Chloroplast Thioredoxins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Exp Bot. 2012 Nov;63(18):6315-23.</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0584359</ConceptUI>
    <ConceptName>
     <String>thioredoxin z, Arabidopsis</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T843412</TermUI>
      <String>thioredoxin z, Arabidopsis</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>04</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T843413</TermUI>
      <String>TRX z protein, Arabidopsis</String>
      <DateCreated>
       <Year>2013</Year>
       <Month>04</Month>
       <Day>30</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2013)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C105804</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>transglutaminase 1</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1997</Year>
   <Month>05</Month>
   <Day>28</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>06</Month>
   <Day>22</Day>
  </DateRevised>
  <Note>TRANSGLUTAMINASE 1 (TGM1 or TGK) is a membrane-associated enzyme involved in the formation of the cornified cell envelope of the EPIDERMIS; Mutations in the human gene (14q11) cause autosomal recessive lamellar ICHTHYOSIS;   Distinguish from GAMMA-GLUTAMYLTRANSPEPTIDASE involved with glutathione metabolism and other protein cross-linking transglutaminase; RefSeq NM_019984 (mouse), NM_031659 (rat), NM_000359 (human)
  </Note>
  <Frequency>341</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011503</DescriptorUI>
     <DescriptorName>
      <String>Transglutaminases</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Arch Dermatol Res 1997 Jan;289(2):116-9</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0275883</ConceptUI>
    <ConceptName>
     <String>transglutaminase 1</String>
    </ConceptName>
    <RegistryNumber>EC 2.3.2.13</RegistryNumber>
    <RelatedRegistryNumberList>
     <RelatedRegistryNumber>EC 2.3.2.13</RelatedRegistryNumber>
    </RelatedRegistryNumberList>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0275883</Concept1UI>
     <Concept2UI>M0486196</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0275883</Concept1UI>
     <Concept2UI>M0486197</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0275883</Concept1UI>
     <Concept2UI>M0486195</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T305887</TermUI>
      <String>transglutaminase 1</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T433951</TermUI>
      <String>transglutaminase Type I</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>01</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T433949</TermUI>
      <String>transglutaminase1</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>01</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T644022</TermUI>
      <String>TGM1 protein</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>06</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T305888</TermUI>
      <String>transglutaminase K</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1997)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T433948</TermUI>
      <String>epidermal type I transglutaminase</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>01</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T433947</TermUI>
      <String>keratinocyte transglutaminase K</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>01</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T433950</TermUI>
      <String>transglutaminase i</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>01</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T433952</TermUI>
      <String>transglutaminase TGM1</String>
      <DateCreated>
       <Year>2001</Year>
       <Month>01</Month>
       <Day>23</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2001)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0486196</ConceptUI>
    <ConceptName>
     <String>Tgm1 protein, mouse</String>
    </ConceptName>
    <RegistryNumber>EC 2.3.2.13</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0275883</Concept1UI>
     <Concept2UI>M0486196</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T644027</TermUI>
      <String>Tgm1 protein, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>06</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T644028</TermUI>
      <String>transglutaminase 1, K polypeptide, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>06</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T644029</TermUI>
      <String>TGase 1, mouse</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>06</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0486197</ConceptUI>
    <ConceptName>
     <String>Tgm1 protein, rat</String>
    </ConceptName>
    <RegistryNumber>EC 2.3.2.13</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0275883</Concept1UI>
     <Concept2UI>M0486197</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T644030</TermUI>
      <String>Tgm1 protein, rat</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>06</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T644031</TermUI>
      <String>transglutaminase 1, rat</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>06</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0486195</ConceptUI>
    <ConceptName>
     <String>TGM1 protein, human</String>
    </ConceptName>
    <RegistryNumber>EC 2.3.2.13</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0275883</Concept1UI>
     <Concept2UI>M0486195</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T644023</TermUI>
      <String>TGM1 protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>06</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T644024</TermUI>
      <String>transglutaminase 1 (K polypeptide epidermal type I, protein-glutamine-gamma-glutamyltransferase), human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>06</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T644025</TermUI>
      <String>TGASE, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>06</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T644026</TermUI>
      <String>TGK protein, human</String>
      <DateCreated>
       <Year>2005</Year>
       <Month>06</Month>
       <Day>22</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2005)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002628</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>octadecyldihydroxyacetone phosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1990</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*ACETONE (73-75)</PreviousIndexing>
   <PreviousIndexing>*TRIOSES (73-75)</PreviousIndexing>
   <PreviousIndexing>ETHERS (74-76)</PreviousIndexing>
   <PreviousIndexing>ORGANOPHOSPHORUS COMPOUNDS (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004099</DescriptorUI>
     <DescriptorName>
      <String>Dihydroxyacetone Phosphate</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Pharm Sci 62(2):320;1973</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043307</ConceptUI>
    <ConceptName>
     <String>octadecyldihydroxyacetone phosphate</String>
    </ConceptName>
    <CASN1Name>2-Propanone, 1-(octadecyl-1-14C-oxy)-3-(phosphonooxy)-</CASN1Name>
    <RegistryNumber>40166-27-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073310</TermUI>
      <String>octadecyldihydroxyacetone phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002631</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-(3,5-dimethyl-4-isoxazolylmethyl)phthalimide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>08</Day>
  </DateRevised>
  <Note>structure
  </Note>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*IMIDES (73-75)</PreviousIndexing>
   <PreviousIndexing>*PHTHALIC ACID (73-75)</PreviousIndexing>
   <PreviousIndexing>ISOXAZOLES (75-82)</PreviousIndexing>
   <PreviousIndexing>OXAZOLES (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010797</DescriptorUI>
     <DescriptorName>
      <String>Phthalimides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Endocrinol 72(3):604;1973</Source>
   <Source>Arch Anat Microsc Morphol Exp 64(1):27;1975</Source>
   <Source>Mol Cell Endocrinol 1979;15(2):91</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043316</ConceptUI>
    <ConceptName>
     <String>N-(3,5-dimethyl-4-isoxazolylmethyl)phthalimide</String>
    </ConceptName>
    <CASN1Name>2-((3,5-dimethyl-4-isoxazolyl)methyl)-1H-isoindole-1,3(2H)-dione</CASN1Name>
    <RegistryNumber>39962-28-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073319</TermUI>
      <String>N-(3,5-dimethyl-4-isoxazolylmethyl)phthalimide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002647</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>inositol 1-phosphate</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>02</Day>
  </DateRevised>
  <Frequency>163</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*INOSITOL (73-75)</PreviousIndexing>
   <PreviousIndexing>*ORGANOPHOSPHORUS COMPOUNDS (73-75)</PreviousIndexing>
   <PreviousIndexing>INOSITOL/*analogs (76-85)</PreviousIndexing>
   <PreviousIndexing>SUGAR PHOSPHATES (74-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D007295</DescriptorUI>
     <DescriptorName>
      <String>Inositol Phosphates</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Am Chem Soc 97(23):6810;1975</Source>
   <Source>Nature (New Biol) 240(104):258;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043337</ConceptUI>
    <ConceptName>
     <String>inositol 1-phosphate</String>
    </ConceptName>
    <CASN1Name>D-myo-Inositol, 1-(dihydrogen phosphate)</CASN1Name>
    <RegistryNumber>15421-51-9</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073340</TermUI>
      <String>inositol 1-phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073339</TermUI>
      <String>myoinositol 1-phosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T073338</TermUI>
      <String>inositol 1-monophosphate</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C101916</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>SBS-g-VP copolymer</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>11</Month>
   <Day>25</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>4-vinylpyridine grafted to SBS polymer via radiation-induced copolymerization
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011137</DescriptorUI>
     <DescriptorName>
      <String>Polystyrenes</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011725</DescriptorUI>
     <DescriptorName>
      <String>Pyridines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Biomed Mater Res 1996 Jun;31(2):281-6</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0267033</ConceptUI>
    <ConceptName>
     <String>SBS-g-VP copolymer</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T297038</TermUI>
      <String>SBS-g-VP copolymer</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T297037</TermUI>
      <String>SBS-g-(4-vinylpyridine) copolymer</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C101917</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N,N-(2,3-dihydroxybuta-1,4-diyl)valine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>11</Month>
   <Day>26</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>04</Day>
  </DateRevised>
  <Note>a ring-closed pyrrolidine-structured compound
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D011759</DescriptorUI>
     <DescriptorName>
      <String>Pyrrolidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014633</DescriptorUI>
     <DescriptorName>
      <String>Valine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Biol Interact 1996 Sep 6;101(3):193-205</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0267035</ConceptUI>
    <ConceptName>
     <String>N,N-(2,3-dihydroxybuta-1,4-diyl)valine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T297040</TermUI>
      <String>N,N-(2,3-dihydroxybuta-1,4-diyl)valine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T297039</TermUI>
      <String>N,N-PYRV</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C411124</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>6-deoxacastasterone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2000</Year>
   <Month>07</Month>
   <Day>25</Day>
  </DateCreated>
  <Note>isolated from Catharanthus roseus; structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010840</DescriptorUI>
     <DescriptorName>
      <String>Phytosterols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Phytochemistry 2000 Mar;53(5):549-53</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0366572</ConceptUI>
    <ConceptName>
     <String>6-deoxacastasterone</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T419890</TermUI>
      <String>6-deoxacastasterone</String>
      <DateCreated>
       <Year>2000</Year>
       <Month>07</Month>
       <Day>25</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2000)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C101918</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>N-(2,3,4-trihydroxybutyl)valine</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>11</Month>
   <Day>26</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>04</Month>
   <Day>04</Day>
  </DateRevised>
  <Frequency>4</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014633</DescriptorUI>
     <DescriptorName>
      <String>Valine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Chem Biol Interact 1996 Sep 6;101(3):193-205</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0267037</ConceptUI>
    <ConceptName>
     <String>N-(2,3,4-trihydroxybutyl)valine</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T297042</TermUI>
      <String>N-(2,3,4-trihydroxybutyl)valine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T297041</TermUI>
      <String>N-THBV</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002651</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>18-hydroxytetrahydrodeoxycorticosterone</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*HYDROXYCORTICOSTEROIDS (73-75)</PreviousIndexing>
   <PreviousIndexing>*PREGNANES (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D015070</DescriptorUI>
     <DescriptorName>
      <String>18-Hydroxydesoxycorticosterone</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Rec Prog Horm Res 28:2871;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043339</ConceptUI>
    <ConceptName>
     <String>18-hydroxytetrahydrodeoxycorticosterone</String>
    </ConceptName>
    <CASN1Name>3 alpha,18,21-trihydroxy-5 beta-pregnan-20-one</CASN1Name>
    <RegistryNumber>31935-07-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073342</TermUI>
      <String>18-hydroxytetrahydrodeoxycorticosterone</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002652</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-propyluracil</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1975</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>1</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*URACIL (73-75)</PreviousIndexing>
   <PreviousIndexing>PROPANE (73-75)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014498</DescriptorUI>
     <DescriptorName>
      <String>Uracil</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Biochim Pol 19(3):207;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043340</ConceptUI>
    <ConceptName>
     <String>5-propyluracil</String>
    </ConceptName>
    <RegistryNumber>19030-75-2</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073343</TermUI>
      <String>5-propyluracil</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C002653</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>5-isopropyluracil</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1973</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1976</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateRevised>
  <Frequency>0</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*URACIL (73-75)</PreviousIndexing>
   <PreviousIndexing>PROPANE (73-76)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014498</DescriptorUI>
     <DescriptorName>
      <String>Uracil</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Acta Biochim Pol 19(3):207;1972</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0043341</ConceptUI>
    <ConceptName>
     <String>5-isopropyluracil</String>
    </ConceptName>
    <RegistryNumber>17432-95-0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T073344</TermUI>
      <String>5-isopropyluracil</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1973)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C100315</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>NS1 protein, Flavivirus</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>08</Month>
   <Day>14</Day>
  </DateCreated>
  <DateRevised>
   <Year>2004</Year>
   <Month>08</Month>
   <Day>25</Day>
  </DateRevised>
  <Note>has been sequenced
  </Note>
  <Frequency>161</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D017361</DescriptorUI>
     <DescriptorName>
      <String>Viral Nonstructural Proteins</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D012324</DescriptorUI>
     <DescriptorName>
      <String>RNA-Dependent RNA Polymerase</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>J Gen Virol 1996 Jun;77(Pt 6):1287-94</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0263428</ConceptUI>
    <ConceptName>
     <String>NS1 protein, Flavivirus</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0263428</Concept1UI>
     <Concept2UI>M0263427</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0263428</Concept1UI>
     <Concept2UI>M0263425</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0263428</Concept1UI>
     <Concept2UI>M0263426</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0263428</Concept1UI>
     <Concept2UI>M0263423</Concept2UI>
     </ConceptRelation>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0263428</Concept1UI>
     <Concept2UI>M0353921</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T293433</TermUI>
      <String>NS1 protein, Flavivirus</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0263427</ConceptUI>
    <ConceptName>
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      <TermUI>T293429</TermUI>
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       <Month>08</Month>
       <Day>25</Day>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T293431</TermUI>
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       <ThesaurusID>NLM (1996)</ThesaurusID>
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    <ConceptUI>M0263423</ConceptUI>
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      <TermUI>T605872</TermUI>
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       <Year>2004</Year>
       <Month>08</Month>
       <Day>25</Day>
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    <ConceptUI>M0353921</ConceptUI>
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     <String>NS1 protein, Kunjin virus</String>
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     <Concept1UI>M0263428</Concept1UI>
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      <TermUI>T403035</TermUI>
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       <Month>12</Month>
       <Day>17</Day>
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      <TermUI>T403036</TermUI>
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       <Month>12</Month>
       <Day>17</Day>
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   <Month>09</Month>
   <Day>07</Day>
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       <Month>09</Month>
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       <Year>2010</Year>
       <Month>09</Month>
       <Day>07</Day>
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<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015549</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2,4,5-triamino-6-styrylpyrimidine</String>
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  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>1982</Year>
   <Month>06</Month>
   <Day>28</Day>
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  <Frequency>1</Frequency>
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  <SourceList>
   <Source>Naunyn Schmiedebergs Arch Pharmacol 298(2):157;1977</Source>
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    <CASN1Name>6-(2-phenylethenyl)-2,4,5-pyrimidinetriamine</CASN1Name>
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   <String>Citrikleen</String>
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  <DateCreated>
   <Year>2001</Year>
   <Month>07</Month>
   <Day>31</Day>
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  <DateRevised>
   <Year>2005</Year>
   <Month>08</Month>
   <Day>16</Day>
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  <Note>a commercial emulsifier derived from citrus, candidate for remediation applications
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   <PreviousIndexing>*EMULSIONS (2001-2005)</PreviousIndexing>
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      <String>Emulsions</String>
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  <SupplementalRecordUI>C015556</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>trifluoroacetyl-L-phenylalanine</String>
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  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>1982</Year>
   <Month>02</Month>
   <Day>04</Day>
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      <String>analogs &amp; derivatives</String>
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   <Source>Biochim Biophys Acta 483:172;1977</Source>
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   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
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   <Month>08</Month>
   <Day>15</Day>
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    <ConceptName>
     <String>AL-272, oxalate(1:1) salt</String>
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    <RegistryNumber>27471-76-7</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="NRW">
     <Concept1UI>M0064975</Concept1UI>
     <Concept2UI>M0312895</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T342895</TermUI>
      <String>AL-272, oxalate(1:1) salt</String>
      <DateCreated>
       <Year>1999</Year>
       <Month>08</Month>
       <Day>18</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015565</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>tyramine glucuronide</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1977</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>1982</Year>
   <Month>06</Month>
   <Day>18</Day>
  </DateRevised>
  <Frequency>2</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*GLUCURONATES (77-82)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D014439</DescriptorUI>
     <DescriptorName>
      <String>Tyramine</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochem J 164(3):529;1977</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0064925</ConceptUI>
    <ConceptName>
     <String>tyramine glucuronide</String>
    </ConceptName>
    <CASN1Name>4-(2-aminoethyl)phenyl-beta-D-glucopyranosiduronic acid</CASN1Name>
    <RegistryNumber>27972-85-6</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T094928</TermUI>
      <String>tyramine glucuronide</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1977)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "2">
  <SupplementalRecordUI>C076361</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>CEBA combination</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1992</Year>
   <Month>09</Month>
   <Day>28</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>11</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>chemotherapy protocol consisting of above cpds; used in treatment of abdominal germ cell cancers
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000971</DescriptorUI>
     <DescriptorName>
      <String>Antineoplastic Combined Chemotherapy Protocols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D001761</DescriptorUI>
     <DescriptorName>
      <String>Bleomycin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002945</DescriptorUI>
     <DescriptorName>
      <String>Cisplatin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004317</DescriptorUI>
     <DescriptorName>
      <String>Doxorubicin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D005047</DescriptorUI>
     <DescriptorName>
      <String>Etoposide</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Am J Clin Oncol 1992 Aug;15(4):308-10</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0205406</ConceptUI>
    <ConceptName>
     <String>CEBA combination</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T235411</TermUI>
      <String>CEBA combination</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1992)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C542726</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>1,4-benzylidene-bis(S,S)-4-yl-3,5-bis(1-hydroxyethyl)-1,2,4-triazole</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2009</Year>
   <Month>08</Month>
   <Day>11</Day>
  </DateCreated>
  <Note>structure in first source
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D001597</DescriptorUI>
     <DescriptorName>
      <String>Benzylidene Compounds</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D014230</DescriptorUI>
     <DescriptorName>
      <String>Triazoles</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Dalton Trans. 2008 Nov 28;(44):6103-5</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0538175</ConceptUI>
    <ConceptName>
     <String>1,4-benzylidene-bis(S,S)-4-yl-3,5-bis(1-hydroxyethyl)-1,2,4-triazole</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T756106</TermUI>
      <String>1,4-benzylidene-bis(S,S)-4-yl-3,5-bis(1-hydroxyethyl)-1,2,4-triazole</String>
      <DateCreated>
       <Year>2009</Year>
       <Month>08</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2009)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T756107</TermUI>
      <String>1,4-BHT cpd</String>
      <DateCreated>
       <Year>2009</Year>
       <Month>08</Month>
       <Day>11</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2009)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "2">
  <SupplementalRecordUI>C068920</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>CECA protocol</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1991</Year>
   <Month>06</Month>
   <Day>25</Day>
  </DateCreated>
  <DateRevised>
   <Year>2000</Year>
   <Month>11</Month>
   <Day>30</Day>
  </DateRevised>
  <Note>chemotherapy protocol consisting of the above cpds
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D000971</DescriptorUI>
     <DescriptorName>
      <String>Antineoplastic Combined Chemotherapy Protocols</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D002945</DescriptorUI>
     <DescriptorName>
      <String>Cisplatin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D003520</DescriptorUI>
     <DescriptorName>
      <String>Cyclophosphamide</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D004317</DescriptorUI>
     <DescriptorName>
      <String>Doxorubicin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D011034</DescriptorUI>
     <DescriptorName>
      <String>Podophyllotoxin</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Clin Oncol 1991;9(6):1045</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0188299</ConceptUI>
    <ConceptName>
     <String>CECA protocol</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T218304</TermUI>
      <String>CECA protocol</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1991)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C084611</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>YM 9429</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1994</Year>
   <Month>01</Month>
   <Day>04</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>07</Month>
   <Day>31</Day>
  </DateRevised>
  <Note>a potent and specific teratogen; induces cleft palate in CD rats; inhibits dehydrocholesterol reductase
  </Note>
  <Frequency>5</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D010880</DescriptorUI>
     <DescriptorName>
      <String>Piperidines</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Toxicol Sci 1993 Aug;18(3):171-8</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0224744</ConceptUI>
    <ConceptName>
     <String>YM 9429</String>
    </ConceptName>
    <RegistryNumber>72056-79-2</RegistryNumber>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0224744</Concept1UI>
     <Concept2UI>M0224743</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T254749</TermUI>
      <String>YM 9429</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T254747</TermUI>
      <String>YM9429</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T254746</TermUI>
      <String>YM-9429</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
   <Concept PreferredConceptYN="N">
    <ConceptUI>M0224743</ConceptUI>
    <ConceptName>
     <String>cis-1-(4-(p-monthane-8-yloxy)phenyl)piperidine</String>
    </ConceptName>
    <ConceptRelationList>
     <ConceptRelation RelationName="BRD">
     <Concept1UI>M0224744</Concept1UI>
     <Concept2UI>M0224743</Concept2UI>
     </ConceptRelation>
    </ConceptRelationList>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T254748</TermUI>
      <String>cis-1-(4-(p-monthane-8-yloxy)phenyl)piperidine</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1994)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C015607</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>GPA 1734</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>12</Day>
  </DateRevised>
  <Frequency>9</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*RO 4-1284/analogs (78-87)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D012369</DescriptorUI>
     <DescriptorName>
      <String>2H-Benzo(a)quinolizin-2-ol, 2-Ethyl-1,3,4,6,7,11b-hexahydro-3-isobutyl-9,10-dimethoxy-</String>
     </DescriptorName>
    </DescriptorReferredTo>
    <QualifierReferredTo>
     <QualifierUI>*Q000031</QualifierUI>
     <QualifierName>
      <String>analogs &amp; derivatives</String>
     </QualifierName>
    </QualifierReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Biochim Biophys Acta 538:139;1978</Source>
   <Source>Biochim Biophys Acta 538:328;1978</Source>
   <Source>J Pharmacol Exp Ther 204(2):372;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0065008</ConceptUI>
    <ConceptName>
     <String>GPA 1734</String>
    </ConceptName>
    <CASN1Name>8,9-dihydroxy-7-methylbenzo(b)quinolizinium, bromide</CASN1Name>
    <RegistryNumber>21852-25-5</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="LAB"  RecordPreferredTermYN="Y">
      <TermUI>T095011</TermUI>
      <String>GPA 1734</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T095010</TermUI>
      <String>GPA-1734</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1978)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C098118</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>sodium green</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1996</Year>
   <Month>03</Month>
   <Day>15</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>08</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>a new fluorescent sodium indicator; no further information available 3/96
  </Note>
  <Frequency>16</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*FLUORESCENT DYES (1996-2005)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009930</DescriptorUI>
     <DescriptorName>
      <String>Organic Chemicals</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D005456</DescriptorUI>
     <DescriptorName>
      <String>Fluorescent Dyes</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Cytometry 1995 Nov 1;21(3):248-56</Source>
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  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0257798</ConceptUI>
    <ConceptName>
     <String>sodium green</String>
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    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T287803</TermUI>
      <String>sodium green</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1996)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C018301</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>2-(O-alpha-glucopyranosyl)-galactopyranose</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1979</Year>
   <Month>01</Month>
   <Day>01</Day>
  </DateCreated>
  <DateRevised>
   <Year>2001</Year>
   <Month>02</Month>
   <Day>13</Day>
  </DateRevised>
  <Note>disaccharide unit of collagen
  </Note>
  <Frequency>1</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D004187</DescriptorUI>
     <DescriptorName>
      <String>Disaccharides</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>J Immunol 121(6):2137;1978</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0069669</ConceptUI>
    <ConceptName>
     <String>2-(O-alpha-glucopyranosyl)-galactopyranose</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T099672</TermUI>
      <String>2-(O-alpha-glucopyranosyl)-galactopyranose</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
      <TermUI>T099671</TermUI>
      <String>2-(O-alpha-D-glucopyranosyl)-D-galactopyranose</String>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (1979)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C470600</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>Pongarotene</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>2003</Year>
   <Month>01</Month>
   <Day>27</Day>
  </DateCreated>
  <Note>a rotenoid from Pongamia pinnata; structure in first source
  </Note>
  <Frequency>2</Frequency>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>*D006576</DescriptorUI>
     <DescriptorName>
      <String>Heterocyclic Compounds, 4 or More Rings</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <SourceList>
   <Source>Nat Prod Lett 2002 Oct;16(5):351-7</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0445089</ConceptUI>
    <ConceptName>
     <String>Pongarotene</String>
    </ConceptName>
    <RegistryNumber>0</RegistryNumber>
    <TermList>
     <Term  ConceptPreferredTermYN="Y"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="Y">
      <TermUI>T531092</TermUI>
      <String>Pongarotene</String>
      <DateCreated>
       <Year>2003</Year>
       <Month>01</Month>
       <Day>27</Day>
      </DateCreated>
      <ThesaurusIDlist>
       <ThesaurusID>NLM (2003)</ThesaurusID>
      </ThesaurusIDlist>
     </Term>
    </TermList>
   </Concept>
  </ConceptList>
 </SupplementalRecord>
<SupplementalRecord SCRClass = "1">
  <SupplementalRecordUI>C082445</SupplementalRecordUI>
  <SupplementalRecordName>
   <String>PKH 2 dye</String>
  </SupplementalRecordName>
  <DateCreated>
   <Year>1993</Year>
   <Month>08</Month>
   <Day>31</Day>
  </DateCreated>
  <DateRevised>
   <Year>2005</Year>
   <Month>08</Month>
   <Day>16</Day>
  </DateRevised>
  <Note>fluorescent staining kit; no other info avail 8/93
  </Note>
  <Frequency>7</Frequency>
  <PreviousIndexingList>
   <PreviousIndexing>*FLUORESCENT DYES (1993-2005)</PreviousIndexing>
  </PreviousIndexingList>
  <HeadingMappedToList>
   <HeadingMappedTo>
    <DescriptorReferredTo>
     <DescriptorUI>D009930</DescriptorUI>
     <DescriptorName>
      <String>Organic Chemicals</String>
     </DescriptorName>
    </DescriptorReferredTo>
   </HeadingMappedTo>
  </HeadingMappedToList>
  <IndexingInformationList>
   <IndexingInformation>
     <DescriptorReferredTo>
    <DescriptorUI>D005456</DescriptorUI>
     <DescriptorName>
      <String>Fluorescent Dyes</String>
      </DescriptorName>
     </DescriptorReferredTo>
   </IndexingInformation>
  </IndexingInformationList>
  <SourceList>
   <Source>Endocrinology 1993 Aug;133(2):914-20</Source>
  </SourceList>
  <ConceptList>
   <Concept PreferredConceptYN="Y">
    <ConceptUI>M0219668</ConceptUI>
    <ConceptName>
     <String>PKH 2 dye</String>
    </ConceptName>
    <RegistryNumber>145687-07-6</RegistryNumber>
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  <SourceList>
   <Source>FASEB J 2003 Jun;17(9):1186-8</Source>
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       <Month>06</Month>
       <Day>19</Day>
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  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
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   <String>UVF2274</String>
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  <DateCreated>
   <Year>2003</Year>
   <Month>04</Month>
   <Day>22</Day>
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  <SourceList>
   <Source>J Biol Chem 2003 Feb 14;278(7):5172-8</Source>
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       <Year>2003</Year>
       <Month>04</Month>
       <Day>22</Day>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
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       <Year>2003</Year>
       <Month>04</Month>
       <Day>22</Day>
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  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>1994</Year>
   <Month>06</Month>
   <Day>22</Day>
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   <Year>2006</Year>
   <Month>10</Month>
   <Day>22</Day>
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  <SourceList>
   <Source>Int Clin Psychopharmacol 2006 May;21(3):153-8</Source>
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       <Month>10</Month>
       <Day>22</Day>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
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      <DateCreated>
       <Year>2006</Year>
       <Month>10</Month>
       <Day>22</Day>
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      <ThesaurusIDlist>
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       <Year>2006</Year>
       <Month>10</Month>
       <Day>22</Day>
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      <ThesaurusIDlist>
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  <SupplementalRecordName>
   <String>4-(acetoxymercuric)aniline diazotate</String>
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  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>1998</Year>
   <Month>02</Month>
   <Day>11</Day>
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  <Frequency>0</Frequency>
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     <DescriptorUI>D010662</DescriptorUI>
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     <QualifierUI>*Q000031</QualifierUI>
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  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
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   <Month>06</Month>
   <Day>10</Day>
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  <DateCreated>
   <Year>2003</Year>
   <Month>05</Month>
   <Day>30</Day>
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  <DateRevised>
   <Year>2003</Year>
   <Month>05</Month>
   <Day>30</Day>
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       <Month>05</Month>
       <Day>30</Day>
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     <Term  ConceptPreferredTermYN="N"  IsPermutedTermYN="N"  LexicalTag="NON"  RecordPreferredTermYN="N">
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      <DateCreated>
       <Year>2003</Year>
       <Month>05</Month>
       <Day>30</Day>
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  <DateCreated>
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   <Month>10</Month>
   <Day>22</Day>
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   <Source>Haematologica 2006 Sep;91(9):1287-8</Source>
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       <Month>10</Month>
       <Day>22</Day>
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   <Year>2006</Year>
   <Month>10</Month>
   <Day>22</Day>
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       <Month>10</Month>
       <Day>22</Day>
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<SupplementalRecord SCRClass = "1">
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   <String>Actovegin</String>
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  <DateCreated>
   <Year>1978</Year>
   <Month>01</Month>
   <Day>01</Day>
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  <DateRevised>
   <Year>1996</Year>
   <Month>12</Month>
   <Day>28</Day>
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  <Frequency>124</Frequency>
  <HeadingMappedToList>
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    <DescriptorReferredTo>
     <DescriptorUI>D006418</DescriptorUI>
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      <String>Heme</String>
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      <String>analogs &amp; derivatives</String>
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       <DescriptorUI>D000697</DescriptorUI>
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         <String>Central Nervous System Stimulants</String>
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     <PharmacologicalAction>
      <DescriptorReferredTo>
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