Identification | Back Directory | [Name]
3',6-Di(dimethylallyl)genistein | [CAS]
76754-24-0 | [Synonyms]
Lupalbigenin 6-Di(dimethylallyl)genistein 3'-γ,γ-Dimethylallylwighteone 3',6-Di(dimethylallyl)genistein 5,7,4'-Trihydroxy-6,3'-diprenylisoflavone 5,7-Dihydroxy-3-[4-hydroxy-3-(3-methyl-2-butenyl)phenyl]-6-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one | [Molecular Formula]
C25H26O5 | [MDL Number]
MFCD06796684 | [MOL File]
76754-24-0.mol | [Molecular Weight]
406.47 |
Chemical Properties | Back Directory | [Melting point ]
165 °C(Solv: toluene (108-88-3); ethyl acetate (141-78-6)) | [Boiling point ]
623.6±55.0 °C(Predicted) | [density ]
1.246±0.06 g/cm3(Predicted) | [solubility ]
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | [form ]
powder | [pka]
6.94±0.20(Predicted) | [color ]
Yellow |
Hazard Information | Back Directory | [Uses]
Lupalbigenin is a natural compound with anti-metastatic and pro-apoptotic effects[1]. | [Definition]
ChEBI: Lupalbigenin is a member of isoflavanones. | [target]
ERK | Akt | Topoisomerase | NO | Bcl-2/Bax | [References]
[1] Apisara Ausawasamrit, et al. Lupalbigenin from Derris scandens Sensitizes Detachment-induced Cell Death in Human Lung Cancer Cells. Anticancer Res. 2015 May;35(5):2827-34. PMID:25964563 |
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