alpha-naphthoflavone

Synonyms: "7,8-benzoflavone", "alpha-naphthoflavone", "2-phenyl-4H-benzo[h]chromen-4-one", "alpha-naphthylflavone", "2-phenylbenzo[h]chromen-4-one", "benzo(h)flavone", "7,8-BF", "2-phenyl-benzo[h]chromen-4-one", "2-phenyl-4H-naphtho(1,2-b)pyran-4-one", "2-phenylbenzo(h)chromen-4-one", "benzo[h]flavone".

Source: alpha-naphthoflavone is a flavonoid.

Identifiers:

IUPAC Name: 2-phenylbenzo[h]chromen-4-one
CAS Number: 604-59-1
PubChem ID: 11790
InChiKey: VFMMPHCGEFXGIP-UHFFFAOYSA-N
Canonical SMILES: C1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C4=CC=CC=C4C=C3

Structural Properties:

Molecular Formula: C₁₉H₁₂O₂
Molecular Weight: 272.303

Pharmacophore Features:

Number of bond donors: 0
Number of bond acceptors: 2
Number of atoms different from hydrogen: 21

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3D structure (.sdf)
3D structure (.mol2)
3D structure (.pdb)
3D structure (.pdbqt)

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Evidence Supporting This Chemical as an Endocrine Disruptor
TEDX List of Potential Endocrine Disruptors

Campbell DR, Kurzer MS. 1993. Flavonoid inhibition of aromatase enzyme activity in human preadipocytes. J Steroid Biochem Mol Biol 46(3):381-388. DOI: 10.1016/0960-0760(93)90228-O. URL: https://www.sciencedirect.com/science/article/pii/096007609390228OPelissero C, Lenczowski MJP, Chinzi D, Davail-Cuisset B, Sumpter JP, Fostier A. 1996. Effects of flavonoids on aromatase activity, an in vitro study. J Steroid Biochem Mol Biol 57(3-4):215-223. DOI: 10.1016/0960-0760(95)00261-8. URL: https://www.sciencedirect.com/science/article/pii/0960076095002618.