500-65-2
500-65-2
Chemical Structure
Rhapontigenin
- CAS No.: 500-65-2
- Formula:C15H14O4
- Molecular Weight:258.27
IUPAC Name: (E)-5-(3-hydroxy-4-methoxystyryl)benzene-1,3-diol
InChIKey: PHMHDRYYFAYWEG-NSCUHMNNSA-N
SMILES: OC1=CC(/C=C/C2=CC=C(OC)C(O)=C2)=CC(O)=C1
Biological Activity: Rhapontigenin is a natural analog of resveratrol with anticancer, antioxidant, antifungal and antibacterial activities. Rhapontigenin is amechanism-based, potent and selective cytochrome P450 1A1 inactivator (IC50 = 400 nM). Rhapontigenin exhibits 400-fold and 23-fold selectivity for P450 1A1 over P450 1A2 and P450 1B1, respectively[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Rhapontigenin | 99.66% | Rhapontigenin is a natural analog of resveratrol with anticancer, antioxidant, antifungal and antibacterial activities. Rhapontigenin is amechanism-based, potent and selective cytochrome P450 1A1 inactivator (IC50 = 400 nM). Rhapontigenin exhibits 400-fold and 23-fold selectivity for P450 1A1 over P450 1A2 and P450 1B1, respectively. | ||||||||||||||||||||
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Rhapontigenin (Standard) | ≥98% | Rhapontigenin (Standard) is the analytical standard of Rhapontigenin. This product is intended for research and analytical applications. Rhapontigenin is a natural analog of resveratrol with anticancer, antioxidant, antifungal and antibacterial activities. Rhapontigenin is amechanism-based, potent and selective cytochrome P450 1A1 inactivator (IC50 = 400 nM). Rhapontigenin exhibits 400-fold and 23-fold selectivity for P450 1A1 over P450 1A2 and P450 1B1, respectively. | ||||||||||||||||||||
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