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Rhapontigenin

SKU: orb1303764

Description

Rhapontigenin is a natural stilbenoid and resveratrol analog that acts as a potent, mechanism-based inactivator of cytochrome P450 1A1 (IC50: 400 nM), inhibiting the metabolic activation of procarcinogens. It exhibits antioxidant properties and demonstrates anti-proliferative activity against various cancer cell lines, such as HL-60 and HepG2, in vitro, supporting research in chemoprevention and oncology.

Research Area

Infectious Disease & Virology, Metabolism Research

Images & Validation

Key Properties

CAS Number500-65-2
MW258.27
Purity99.36% (May vary between batches)
FormulaC15H14O4
SMILESCOc1ccc(\C=C\c2cc(O)cc(O)c2)cc1O
TargetAntifungal|||Antibacterial|||Cytochromes P450
SolubilityChloroform, Dichloromethane, Ethyl Acetate, Acetone, etc.:Soluble;DMSO:131.25 mg/mL (508.19 mM);10% DMSO+40% PEG300+5% Tween 80+45% Saline:2 mg/mL (7.74 mM)

Bioactivity

Target IC50
HL-60R:48 μM|HepG2 cells:48 μM|CYP1A1:400 nM

Storage & Handling

Storage-20°C
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

inhibit, Fungal, hypoglycemic, Inhibitor, Bacterial, anticoagulative, antiangiogenic, antiallergic, CYPs, CYP1A1, Cytochrome P450, purgative, Rhapontigenin, Protigenin

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Quality Guarantee

Quality Guarantee

Explore bioreagents carefree to elevate your research. All our products are rigorously tested for performance. If a product does not perform as described on its datasheet, our scientific support team will provide expert troubleshooting, a prompt replacement, or a refund. For full details, please see our Terms & Conditions and Buying Guide. Contact us at [email protected].

Key Properties

No computed properties available.

Protocol Information

Available Sizes

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1 mg
$ 100.00
5 mg
$ 140.00
10 mg
$ 230.00
25 mg
$ 400.00
50 mg
$ 580.00
100 mg
$ 720.00
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