CHEBI:77013 - β-naphthoflavone

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ChEBI Name β-naphthoflavone ChEBI ID CHEBI:77013 ChEBI ASCII Name beta-naphthoflavone Definition An extended flavonoid resulting from the formal fusion of a benzene ring with the f side of flavone. Stars This entity has been manually annotated by the ChEBI Team. Supplier Information ChemicalBook:CB0158671, eMolecules:493996, ZINC000000001504 Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Wikipedia License Gallic acid (also known as 3,4,5-trihydroxybenzoic acid) is a trihydroxybenzoic acid with the formula C6H2(OH)3CO2H. It is classified as a phenolic acid. It is found in gallnuts, sumac, witch hazel, tea leaves, oak bark, and other plants. It is a white solid, although samples are typically brown owing to partial oxidation. Salts and esters of gallic acid are termed "gallates". Its name is derived from oak galls, which were historically used to prepare tannic acid. Despite the name, gallic acid does not contain gallium. Read full article at Wikipedia Formula C19H12O2 Net Charge 0 Average Mass 272.29740 Monoisotopic Mass 272.08373 InChI InChI=1S/C19H12O2/c20-16-12-18(14-7-2-1-3-8-14)21-17-11-10-13-6-4-5-9-15(13)19(16)17/h1-12H InChIKey OUGIDAPQYNCXRA-UHFFFAOYSA-N SMILES O=c1cc(oc2ccc3ccccc3c12)-c1ccccc1 Roles Classification Biological Role(s): aryl hydrocarbon receptor agonist An agonist that binds to and activates aryl hydrocarbon receptors (AhRs). View more via ChEBI Ontology ChEBI Ontology Outgoing β-naphthoflavone (CHEBI:77013) has role aryl hydrocarbon receptor agonist (CHEBI:72768) β-naphthoflavone (CHEBI:77013) is a extended flavonoid (CHEBI:71037) β-naphthoflavone (CHEBI:77013) is a naphtho-γ-pyrone (CHEBI:64542) β-naphthoflavone (CHEBI:77013) is a organic heterotricyclic compound (CHEBI:26979) IUPAC Name 3-phenyl-1H-benzo[f]chromen-1-one Synonyms Sources 3-phenyl-1H-naphtho(2,1-b)pyran-1-one ChemIDplus 5,6-benzoflavone ChemIDplus benzo[f]flavone ChEBI β-NF ChemIDplus Manual Xrefs Databases Beta-Naphthoflavone Wikipedia DB06732 DrugBank View more database links Registry Numbers Types Sources 18991 Reaxys Registry Number Reaxys 6051-87-2 CAS Registry Number ChemIDplus 6051-87-2 CAS Registry Number NIST Chemistry WebBook Citations Types Sources 11697852 PubMed citation Europe PMC 16730384 PubMed citation Europe PMC 18535361 PubMed citation Europe PMC 19969063 PubMed citation Europe PMC 20060304 PubMed citation Europe PMC 20843940 PubMed citation Europe PMC 21624442 PubMed citation Europe PMC 22167217 PubMed citation Europe PMC 24163404 PubMed citation Europe PMC 3924427 PubMed citation Europe PMC 8430058 PubMed citation Europe PMC Last Modified 09 March 2020