α-Naphthoflavone

α-Naphthoflavone
Names
	IUPAC name Benzo[7,8]flavone
	Systematic IUPAC name 2-Phenyl-4H-naphtho[1,2-b]pyran-4-one
	Other names 7,8-Benzoflavone; ANF; 2-Phenyl-benzo[h]chromen-4-one
Identifiers
CAS Number	604-59-1 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:76995 ;
ChEMBL	ChEMBL283196 ;
ChemSpider	11297 ;
DrugBank	DB07453 ;
ECHA InfoCard	100.009.156
EC Number	210-071-1;
PubChem CID	11790;
UNII	FML65D8PY5;
CompTox Dashboard (EPA)	DTXSID2040650;
	InChI InChI=1S/C19H12O2/c20-17-12-18(14-7-2-1-3-8-14)21-19-15-9-5-4-6-13(15)10-11-16(17)19/h1-12H Key: VFMMPHCGEFXGIP-UHFFFAOYSA-N ; InChI=1/C19H12O2/c20-17-12-18(14-7-2-1-3-8-14)21-19-15-9-5-4-6-13(15)10-11-16(17)19/h1-12H Key: VFMMPHCGEFXGIP-UHFFFAOYAW;
	SMILES O=C\1c4c(O/C(=C/1)c2ccccc2)c3ccccc3cc4;
Properties
Chemical formula	C19H12O2
Molar mass	272.303 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

α-Naphthoflavone, also known as 7,8-benzoflavone and 2-phenyl-benzo[h]chromen-4-one, is a synthetic^[1]^[2] flavone derivative. It can be prepared from 2-naphthol and cinnamaldehyde.^[3]

α-Naphthoflavone is a potent inhibitor of the enzyme aromatase, the enzyme that converts testosterone to estrogen.^[1]^[2] α-Naphthoflavone has been shown to cause abnormal testicular development in young chickens.^[4]

References

^ ^a ^b Campbell, Deborah R.; Kurzer, Mindy S. (1993). "Flavonoid inhibition of aromatase enzyme activity in human preadipocytes". Journal of Steroid Biochemistry and Molecular Biology. 46 (3): 381–388. doi:10.1016/0960-0760(93)90228-O. PMID 9831487. S2CID 25861427.
^ ^a ^b Kellis JT Jr; Vickery LE (1984). "Inhibition of human estrogen synthetase (aromatase) by flavones". Science. 225 (4666): 1032–1034. Bibcode:1984Sci...225.1032K. doi:10.1126/science.6474163. PMID 6474163.
^ Harvey, Ronald G.; Hahn, Jung Tai; Bukowska, Maria; Jackson, Henry (1990). "A new chromone and flavone synthesis and its utilization for the synthesis of potentially antitumorigenic polycyclic chromones and flavones". The Journal of Organic Chemistry. 55 (25): 6161. doi:10.1021/jo00312a023.
^ Trefil, P.; Micakova, A.; Stiborova, M.; Poplstein, M.; Brillard, J.P.; Hodek, P. (2004). "Effects of alpha-naphthoflavone on body growth and gonad development in chickens (Gallus domesticus)". Czech Journal of Animal Science. 49 (6): 231–238. doi:10.17221/4305-CJAS.

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[Campbell-1] Campbell, Deborah R.; Kurzer, Mindy S. (1993). "Flavonoid inhibition of aromatase enzyme activity in human preadipocytes". Journal of Steroid Biochemistry and Molecular Biology. 46 (3): 381–388. doi:10.1016/0960-0760(93)90228-O. PMID 9831487. S2CID 25861427.

[Kellis-2] Kellis JT Jr; Vickery LE (1984). "Inhibition of human estrogen synthetase (aromatase) by flavones". Science. 225 (4666): 1032–1034. Bibcode:1984Sci...225.1032K. doi:10.1126/science.6474163. PMID 6474163.

[3] Harvey, Ronald G.; Hahn, Jung Tai; Bukowska, Maria; Jackson, Henry (1990). "A new chromone and flavone synthesis and its utilization for the synthesis of potentially antitumorigenic polycyclic chromones and flavones". The Journal of Organic Chemistry. 55 (25): 6161. doi:10.1021/jo00312a023.

[4] Trefil, P.; Micakova, A.; Stiborova, M.; Poplstein, M.; Brillard, J.P.; Hodek, P. (2004). "Effects of alpha-naphthoflavone on body growth and gonad development in chickens (Gallus domesticus)". Czech Journal of Animal Science. 49 (6): 231–238. doi:10.17221/4305-CJAS.

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[2]

[3]

[4]

Names

IUPAC name Benzo[7,8]flavone
Systematic IUPAC name 2-Phenyl-4H-naphtho[1,2-b]pyran-4-one
Other names 7,8-Benzoflavone ANF 2-Phenyl-benzo[h]chromen-4-one
Identifiers
CAS Number	604-59-1^N
3D model (JSmol)	Interactive image
ChEBI	CHEBI:76995^Y
ChEMBL	ChEMBL283196^Y
ChemSpider	11297^Y
DrugBank	DB07453^Y
ECHA InfoCard	100.009.156
EC Number	210-071-1
PubChem CID	11790
UNII	FML65D8PY5
CompTox Dashboard (EPA)	DTXSID2040650
InChI InChI=1S/C19H12O2/c20-17-12-18(14-7-2-1-3-8-14)21-19-15-9-5-4-6-13(15)10-11-16(17)19/h1-12H^Y Key: VFMMPHCGEFXGIP-UHFFFAOYSA-N^Y InChI=1/C19H12O2/c20-17-12-18(14-7-2-1-3-8-14)21-19-15-9-5-4-6-13(15)10-11-16(17)19/h1-12H Key: VFMMPHCGEFXGIP-UHFFFAOYAW
SMILES O=C\1c4c(O/C(=C/1)c2ccccc2)c3ccccc3cc4
Properties
Chemical formula	C₁₉H₁₂O₂
Molar mass	272.303 g·mol⁻¹
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is ^YN ?) Infobox references

α-Naphthoflavone

See also

References