Substance
ID:449565
Names and Identifiers
IUPAC name
5,7-dihydroxy-3-(4-methoxyphenyl)-4H-chromen-4-one
Synonyms
Genistein 4'-methyl etherPratensolOlmelinBiochanin A
IUPAC Traditional name
5,7-dihydroxy-3-(4-methoxyphenyl)-4H-chromen-4-one
Registration numbers
CAS Number
Properties
Pharmacology Properties
Mechanism of Action
Estrogen
Product Information
Application(s)
Possesses sl. estrogenic activity
Biological Source
Constit. of clover (Trifolium repens), Dalbergia and Cotoneaster spp.
Widely distributed in the Leguminosae (Papilionoideae), also in Cotoneaster pannosa and Cotoneaster serotina (Rosaceae), Virola caducifolia (Myricaceae) and others
Molecule Details
No Data Available
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Molecular Spectra
No Data Available
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References
• Baker, W. et al., J.C.S., 1953, 1852, (synth)
• Aldrich Library of 13C and 1H FT NMR Spectra, 1992, 2, 920A, (nmr)
• Murthy, M.S.R. et al., Magn. Reson. Chem., 1986, 24, 225, (cmr)
• Sekizaki, H. et al., Chem. Pharm. Bull., 1988, 36, 4876, (synth)
• Bass, R.J. et al., J.C.S. Perkin 1, 1978, 666, (cmr)
• Ashdown, D.H.J. et al., Synthesis, 1978, 843, (synth)
• Pelter, A. et al., Synthesis, 1976, 326, (synth)
• Aparecida dos Santos, S. et al., J. Braz. Chem. Soc., 1995, 6, 349, (pmr, cmr)
• Aldrich Library of FT-IR Spectra, 1st edn., 1985, 2, 95D, (ir)
• Ingham, J.L., Prog. Chem. Org. Nat. Prod., 1983, 43, 1, (rev, occur)
• Diedrich, D.F. et al., J. Chem. Eng. Data, 1977, 22, 448, (pmr)
• Elgamal, M.H.A. et al., J. Prakt. Chem., 1986, 328, 893, (ms)
• Balasubramanian, S. et al., Synth. Commun., 2000, 30, 469-484, (synth, pmr)