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Молекулярная структура
Genistein
CAS-номер: 446-72-0 Заказать# RT000380 Заказать Распечатать
Описание
  • Synonyms 4H-1-Benzopyran-4-one, 5, 7-dihydroxy-3- (4-hydroxyphenyl)-; 5,7-dihydroxy-3-(4-hydroxyphenyl)-4H-chromen-4-one; 5,7-dihydroxy-3-(4-hydroxyphenyl)chromen-4-one; Prunetol; Isoflavone, 4,5,7-trihydroxy-; 4H-1-Benzopyran-4-one, 5,7-dihydroxy-3-(4-hydroxyphenyl)-; SIPI 807-1; 5,7-Dihydroxy-3-(4-hydroxyphenyl)-4-benzopyrone; 5-18-04-00594 (Beilstein Handbook Reference); C.I. 75610; NPI 031L; 4,5,7-Trihydroxyisoflavone; 4',5,7-trihydroxyisoflavone; 4,5, 7-Trihydroxyisoflavone; Genisteol; Baichanin A; Differenol A; 4H-1-Benzopyran-4-one,5,7-dihydroxy-3- (4-hydroxyphenyl)-; Genisterin; Sophoricol; 5,7,4-Trihydroxyisoflavone; Genistein 4,5,7-Trihydroxyisoflavone;
  • EINECS207-174-9
  • Molecular FormulaC15H10O5
  • AppearanceYellow Crystalline Solid
  • Molecular Weight270.24
  • Density1.548 g/cm3
  • Boiling Point555.5 °C at 760 mmHg
  • Melting Point297-298℃ Flash Point: 217.1 °C
  • Storage Temperature20°C
  • Refractive index1.732
  • Solubilityinsoluble Biological Activity: Phytoestrogen with a wide range of biological actions. Inhibits protein tyrosine kinases including epidermal growth factor receptor kinase. Also binds to PPAR γ and estrogen receptors and acts as an agonist at GPR30. Also av
  • StabilityNo data.
  • UsageExhibits 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
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