Names | |
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IUPAC name Benzoflavone | |
Systematic IUPAC name 2-Phenyl-4H-naphthopyran-4-one | |
Other names
7,8-Benzoflavone ANF 2-Phenyl-benzochromen-4-one | |
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DrugBank | |
ECHA InfoCard | 100.009.156 |
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Properties | |
Chemical formula | C19H12O2 |
Molar mass | 272.303 g·mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). N verify (what is ?) Infobox references |
α-Naphthoflavone, also known as 7,8-benzoflavone and 2-phenyl-benzochromen-4-one, is a synthetic flavone derivative. It can be prepared from 2-naphthol and cinnamaldehyde.
α-Naphthoflavone is a potent inhibitor of the enzyme aromatase, the enzyme that converts testosterone to estrogen. α-Naphthoflavone has been shown to cause abnormal testicular development in young chickens.
See also
References
- ^ 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 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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