8-PRENYLGENISTEIN
8-PRENYLGENISTEIN Basic information
- Product Name:
- 8-PRENYLGENISTEIN
- Synonyms:
-
- 8-PRENYLGENISTEIN
- 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
- 4',5,7-Trihydroxy-8-isopentenylisoflavone
- 4',5,7-Trihydroxy-8-prenylisoflavone
- 8-Isopentenylgenistein
- Lupiwighteone
- 4H-1-Benzopyran-4-one, 5,7-dihydroxy-3-(4-hydroxyphenyl)-8-(3-methyl-2-buten-1-yl)-
- CAS:
- 104691-86-3
- MF:
- C20H18O5
- MW:
- 338.35
- Product Categories:
-
- Miscellaneous Natural Products
- Mol File:
- Mol File
8-PRENYLGENISTEIN Chemical Properties
- 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
8-PRENYLGENISTEIN Usage And Synthesis
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)
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