ChemicalBook--->CAS DataBase List--->104691-86-3

104691-86-3

104691-86-3 Structure

104691-86-3 Structure
IdentificationBack Directory
[Name]

8-PRENYLGENISTEIN
[CAS]

104691-86-3
[Synonyms]

Lupiwighteone
8-PRENYLGENISTEIN
8-Isopentenylgenistein
4',5,7-Trihydroxy-8-prenylisoflavone
4',5,7-Trihydroxy-8-isopentenylisoflavone
5,7-Dihydroxy-3-(4-hydroxyphenyl)-8-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one
3-(4-Hydroxyphenyl)-5,7-dihydroxy-8-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one
4H-1-Benzopyran-4-one, 5,7-dihydroxy-3-(4-hydroxyphenyl)-8-(3-methyl-2-buten-1-yl)-
[Molecular Formula]

C20H18O5
[MDL Number]

MFCD06796683
[MOL File]

104691-86-3.mol
[Molecular Weight]

338.35
Chemical PropertiesBack Directory
[Melting point ]

133-135℃
[Boiling point ]

583.5±50.0 °C(Predicted)
[density ]

1.351±0.06 g/cm3(Predicted)
[storage temp. ]

4°C, protect from light
[solubility ]

DMSO : 100 mg/mL (295.55 mM; Need ultrasonic)
[form ]

Powder
[pka]

6.62±0.20(Predicted)
[color ]

Off-white to light yellow
Hazard InformationBack Directory
[Uses]

Lupiwighteone is a natural product derivative of Genistein (G350000). Genistein 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.
[Definition]

ChEBI: Lupiwighteone is a member of isoflavones.
[target]

PARP | Bcl-2/Bax | Caspase | Akt | CDK | ROS | P450 (e.g. CYP17)
Spectrum DetailBack Directory
[Spectrum Detail]

8-PRENYLGENISTEIN(104691-86-3)1HNMR
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