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Informazioni sul prodotto
- 4H-1-Benzopyran-4-one
- 5,7-dihydroxy-3-(4-hydroxyphenyl)-
- Genistein (6CI)
- Isoflavone
- 4',5,7-trihydroxy- (8CI)
- 4',5,7-Trihydroxyisoflavone
- 5,7,4'-Trihydroxyisoflavone
- 5,7-Dihydroxy-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
- 5,7-Dihydroxy-3-(4-hydroxyphenyl)-4H-chromen-4-one
- Baichanin A
- Vedi altri sinonimi
- Bonistein
- C.I. 75610
- Climagen F
- FW 635I-2
- GeniVida
- Genisteol
- Genisterin
- Genistin aglycone
- NPI 031L
- NSC 36586
- Prunetol
- SIPI 807-1
- Sophoricol
- 4′,5,7-Trihydroxyisoflavone
- 5,7-Dihidroxi-3-(4-Hidroxifenil)-4-Benzopirona
- 5,7-Dihydroxy-3-(4-hydroxyphenyl)-4-benzopyron
- 5,7-Dihydroxy-3-(4-hydroxyphenyl)-4-benzopyrone
- Bio 300
- Csu 1999
- Fw 635I-2
- Isoflavone, 4',5,7-trihydroxy-
- Isoflavone, 4′,5,7-trihydroxy-
- Npi 031L
- Nsc 36586
- Sipi 807-1
Stability Light Sensitive
Applications Exhibits specific inhibitory activity against tyrosine kinases,including autophosphorylation of epidermal growth factor receptor kinase (IC50 - 2.6uM). Also inhibits other protein kinases through competitive inhibition of ATP. Inhibits tumor cell proliferation and induces tumor cell differentiation. Produces cell-cycle arrest and apoptosis in Jurat T-leukemia cells. However, it prevents anti-CD3 monoclonal antibody-induced thymic apoptosis. Genistein also inhibits topoisomerase II activity in vitro. Genistein has also been shown to inhibit the action of GABA on recombinant GABAA receptors 2. uv(max)ethanol: 262.5 nm (e= 138). moderately sol. in hot alcohol
References Akiyama, T., et al.: J. Biol. Chem., 262, 5592 (1987), O'Dell, T.J., et al.: Nature, 353, 588 (1991), Aharonovits, O., et al.: Biochim Biophys. Acta, 1112, 181 (1992), Platanias, L.C., et al.: J. Biol. Chem., 267, 24053 (1992), Yoshida, H., et al.: Biochim. Biophys. Acta, 1137, 321 (1992), Uckun, F.M., et al.: Science, 267, 886 (1995), Merck Index 12th ed. 4395, Huang, R.Q.; Fang, M.J.; Dillon, G.H., Mol. Brain Res. 67: 177-183 (1999)
Proprietà chimiche
Richiesta tecnica su: TR-G350000 Genistein
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