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8-PRENYLGENISTEIN

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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
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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
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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)

8-PRENYLGENISTEINSupplier

BOC Sciences
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0510-85629785 18013409632
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sales@reading-chemicals.com
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