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5-O-Methylgenistein

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5-O-Methylgenistein
Chemical structure of 5-O-methylgenistein
5-O-Methylgenistein molecule
Names
IUPAC name 4′,7-Dihydroxy-5-methoxyisoflavone
Systematic IUPAC name 7-Hydroxy-3-(4-hydroxyphenyl)-5-methoxy-4H-1-benzopyran-4-one
Other names Isoprunetin
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.230.624 Edit this at Wikidata
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C16H12O5/c1-20-13-6-11(18)7-14-15(13)16(19)12(8-21-14)9-2-4-10(17)5-3-9/h2-8,17-18H,1H3Key: YSINCDVRUMTOPK-UHFFFAOYSA-N
  • InChI=1/C16H12O5/c1-20-13-6-11(18)7-14-15(13)16(19)12(8-21-14)9-2-4-10(17)5-3-9/h2-8,17-18H,1H3Key: YSINCDVRUMTOPK-UHFFFAOYAD
SMILES
  • COC1=C2C(=CC(=C1)O)OC=C(C2=O)C3=CC=C(C=C3)O
Properties
Chemical formula C16H12O5
Molar mass 284.26 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
Chemical compound

5-O-Methylgenistein is an O-methylated isoflavone. It can be found in Ormosia excelsa, a tropical legume.

References

  1. "5-O-methylgenistein on kanaya.naist.jp/knapsack_jsp". Archived from the original on 2012-02-26. Retrieved 2010-02-26.
  2. Gottlieb, O.R.; Da Rocha, A.I. (1972). "5-O-methylgenistein from Ormosia excelsa". Phytochemistry. 11 (3): 1183. Bibcode:1972PChem..11.1183G. doi:10.1016/S0031-9422(00)88486-1.
Isoflavones and their glycosides
Isoflavones
O-methylated isoflavones
Glycosides
Prenylated isoflavones
Pyranoisoflavones
Derivatives
Synthetic
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