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  <common-name>8-methyl-4-oxochromene-2-carboxamide</common-name>
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  <pubchem-id>214625</pubchem-id>
  <chemical-formula>C11H9NO3</chemical-formula>
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  <melting-point nil="true"/>
  <boiling-point nil="true"/>
  <density nil="true"/>
  <solubility nil="true"/>
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  <target nil="true"/>
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  <metabolism nil="true"/>
  <toxicity nil="true"/>
  <lethaldose nil="true"/>
  <carcinogenicity nil="true"/>
  <use-source nil="true"/>
  <min-risk-level nil="true"/>
  <health-effects nil="true"/>
  <symptoms nil="true"/>
  <treatment nil="true"/>
  <created-at type="dateTime">2026-08-27T18:30:16Z</created-at>
  <updated-at type="dateTime">2026-08-27T18:30:16Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia nil="true"/>
  <uniprot-id nil="true"/>
  <kegg-compound-id nil="true"/>
  <omim-id nil="true"/>
  <chebi-id nil="true"/>
  <biocyc-id nil="true"/>
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  <stitch-id nil="true"/>
  <drugbank-id nil="true"/>
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  <actor-id nil="true"/>
  <organism nil="true"/>
  <export type="boolean">true</export>
  <metabolizing-proteins nil="true"/>
  <transporting-proteins nil="true"/>
  <moldb-smiles>CC1=C2C(=CC=C1)C(=O)C=C(O2)C(=O)N</moldb-smiles>
  <moldb-formula>C11H9NO3</moldb-formula>
  <moldb-inchi>InChI=1S/C11H9NO3/c1-6-3-2-4-7-8(13)5-9(11(12)14)15-10(6)7/h2-5H,1H3,(H2,12,14)</moldb-inchi>
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  <origin nil="true"/>
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  <structure-image-updated-at type="dateTime" nil="true"/>
  <biodb-id nil="true"/>
  <synthesis-reference nil="true"/>
  <structure-image-caption nil="true"/>
  <chemdb-id>CHEM278840</chemdb-id>
  <dsstox-id nil="true"/>
  <toxcast-id nil="true"/>
  <stoff-ident-origin nil="true"/>
  <stoff-ident-id nil="true"/>
  <susdat-id nil="true"/>
  <iupac>8-methyl-4-oxochromene-2-carboxamide</iupac>
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  <moldb-refractivity nil="true"/>
  <moldb-polarizability nil="true"/>
  <moldb-rotatable-bond-count nil="true"/>
  <moldb-acceptor-count nil="true"/>
  <moldb-donor-count nil="true"/>
  <moldb-pka-strongest-acidic nil="true"/>
  <moldb-pka-strongest-basic nil="true"/>
  <moldb-physiological-charge nil="true"/>
  <moldb-number-of-rings nil="true"/>
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  <moldb-alogps-logs nil="true"/>
  <moldb-alogps-solubility nil="true"/>
  <kingdom>Organic compounds</kingdom>
  <superklass>Organoheterocyclic compounds</superklass>
  <klass>Benzopyrans</klass>
  <subklass>1-benzopyrans</subklass>
  <paper-count type="integer" nil="true"/>
  <sync-id>CED0234873</sync-id>
  <structure-inchikey>YAHVDMFRYJHLEN-UHFFFAOYSA-N</structure-inchikey>
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  <structure-pickle>ï¾­Þ������������������������€���`������@(������@(������@(������@h�������@h�������@h�������@(�������(������@h�������@(������@(�������(�������(�������h������������h���h���h���h���h���h���(��	h�	
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�������������</structure-pickle>
  <structure-indexed-at type="dateTime">2026-09-19T04:57:38Z</structure-indexed-at>
</compound>
