Biochanin A
Biochanin A | |
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Biochanin A.svg | |
Biochanin-A-3D-balls.png | |
5,7-Dihydroxy-4′-methoxyisoflavone | |
5,7-Dihydroxy-3-(4-methoxyphenyl)-4H-1-benzopyran-4-one | |
別称 Biochanin 4′-Methylgenistein olmelin Biochanine A Biochanin-A Genistein 4-methyl ether | |
Identifiers | |
491-80-5 ![]() | |
ChEBI | |
ChEMBL | ChEMBL131921 ![]() |
ChemSpider | 4444068 ![]() |
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2829 | |
Jmol-3D images | Image |
KEGG | C00814 |
PubChem | 5280373 |
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UNII | U13J6U390T ![]() |
Properties | |
C16H12O5 | |
Molar mass | 284.267 g·mol−1 |
特記なき場合、データは常温(25 °C)・常圧(100 kPa)におけるものである。 |
Biochanin A is an O-methylated isoflavone. It is a natural organic compound in the class of phytochemicals known as flavonoids. Biochanin A can be found in red clover[1] in soy, in alfalfa sprouts, in peanuts, in chickpea (Cicer arietinum) and in other legumes.
Biochanin A is classified as a phytoestrogen and has putative benefits in dietary cancer prophylaxis.テンプレート:Medcn It has also been found to be a weak inhibitor of fatty acid amide hydrolase in vitro.[2]
Metabolism
The enzyme biochanin-A reductase uses dihydrobiochanin A and NADP+ to produce biochanin A, NADPH, and H+. The enzyme isoflavone-7-O-beta-glucoside 6"-O-malonyltransferase uses malonyl-CoA and biochanin A 7-O-β-D-glucoside to produce CoA and biochanin A 7-O-(6-O-malonyl-β-D-glucoside).
See also
References
- ↑ Medjakovic, S.; Jungbauer, A. (2008). "Red clover isoflavones biochanin A and formononetin are potent ligands of the human aryl hydrocarbon receptor". The Journal of Steroid Biochemistry and Molecular Biology. 108 (1–2): 171–177. doi:10.1016/j.jsbmb.2007.10.001. PMID 18060767. S2CID 206495959.
- ↑ Thors L, Burston JJ, Alter BJ, McKinney MK, Cravatt BF, Ross RA, Pertwee RG, Gereau RW, Wiley JL, Fowler CJ (2010). "Biochanin A, a naturally occurring inhibitor of fatty acid amide hydrolase". British Journal of Pharmacology. 160 (3): 549–560. doi:10.1111/j.1476-5381.2010.00716.x. PMC 2931556. PMID 20590565.
テンプレート:Isoflavones テンプレート:Cannabinoid receptor modulators
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