5-O-Methylgenistein

5-O-Methylgenistein
Names


IUPAC name 7-hydroxy-3-(4-hydroxyphenyl)-5-methoxychromen-4-one
Other names 7-Hydroxy-3-(4-hydroxyphenyl)-5-methoxy-4H-1-benzopyran-4-one Isoprunetin^[1]
Identifiers
CAS Number	4569-98-6^Y=
ChemSpider	4678012^N
Jmol interactive 3D	Image
PubChem	5748551
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,1H3^N Key: YSINCDVRUMTOPK-UHFFFAOYSA-N^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,1H3 Key: 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 [77 °F], 100 kPa).
N verify (what is ^YN ?)
Infobox references

5-O-Methylgenistein is an O-methylated isoflavone. It can be found in Ormosia excelsa.^[2]

References

↑ 5-O-methylgenistein on kanaya.naist.jp/knapsack_jsp
↑ 5-O-methylgenistein from Ormosia excelsa. O. R. Gottlieb and A. I. da Rocha, Phytochemistry, Volume 11, Issue 3, March 1972, Page 1183

Isoflavones and their glycosides

Isoflavones	Daidzein Genistein Irilone Orobol Pseudobaptigenin Anagyroidisoflavone A and B

O-methylated isoflavones	Biochanin A Calycosin Formononetin Glycitein Irigenin 5-O-methylgenistein Pratensein Prunetin Psi-tectorigenin Retusin Tectorigenin

Glycosides	Daidzin Genistin Iridin Ononin Puerarin Sophoricoside Tectoridin

Prenylated isoflavones	Bidwillol A Derrubone Luteone 7-O-Methylluteone Wighteone

Pyranoisoflavones	Alpinumisoflavone Barbigerone Di-O-methylalpinumisoflavone 4'-methyl-alpinumisoflavone

Misc	Rotenoids

Synthetic	Ipriflavone

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