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Contents

   



(Top)
 


1 Metabolism  





2 See also  





3 References  














Biochanin A






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From Wikipedia, the free encyclopedia
 


Biochanin A
Biochanin A molecule
Names
IUPAC name

5,7-Dihydroxy-4′-methoxyisoflavone

Systematic IUPAC name

5,7-Dihydroxy-3-(4-methoxyphenyl)-4H-1-benzopyran-4-one

Other names

Biochanin
4′-Methylgenistein
olmelin
Biochanine A
Biochanin-A
Genistein 4-methyl ether

Identifiers

CAS Number

3D model (JSmol)

ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.007.041 Edit this at Wikidata

IUPHAR/BPS

KEGG

PubChem CID

UNII

CompTox Dashboard (EPA)

  • InChI=1S/C16H12O5/c1-20-11-4-2-9(3-5-11)12-8-21-14-7-10(17)6-13(18)15(14)16(12)19/h2-8,17-18H,1H3 checkY

    Key: WUADCCWRTIWANL-UHFFFAOYSA-N checkY

  • InChI=1/C16H12O5/c1-20-11-4-2-9(3-5-11)12-8-21-14-7-10(17)6-13(18)15(14)16(12)19/h2-8,17-18H,1H3

    Key: WUADCCWRTIWANL-UHFFFAOYAM

  • O=C\1c3c(O/C=C/1c2ccc(OC)cc2)cc(O)cc3O

Properties

Chemical formula

C16H12O5
Molar mass 284.267 g·mol−1

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

checkY verify (what is checkY☒N ?)

Infobox references

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]insoy, 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.[medical citation needed] It has also been found to be a weak inhibitoroffatty acid amide hydrolase in vitro.[2]

Metabolism[edit]

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[edit]

References[edit]

  1. ^ 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.

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Biochanin_A&oldid=1224337476"

    Categories: 
    Aromatase inhibitors
    O-methylated isoflavones
    Phytoestrogens
    Selective ERβ agonists
    Hidden categories: 
    ECHA InfoCard ID from Wikidata
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    This page was last edited on 17 May 2024, at 19:37 (UTC).

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