Rhapontigenin - ≥96% , CAS No.500-65-2
Potent, selective cytochrome P450 1A1 inhibitor
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Potent, selective cytochrome P450 1A1 inhibitor
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
| CAS | 500-65-2 |
|---|---|
| Synonyms | AS-68092 | Forst U 46 | HMS3266N10 | (E)-5-(3-Hydroxy-4-methoxystyryl)benzene-1,3-diol | 22BG4NNH6W | AKOS037515600 | Rhapontin genin | Umdipyridyl | 5-((1E)-2-(3-HYDROXY-4-METHOXYPHENYL)ETHENYL)-1,3-BENZENEDIOL | MFCD00017718 | s9163 | SCHEMBL1486816 | D |
| Specifications & Purity | ≥96% |
| Storage | Store at 2-8°C,Argon charged |
| Shipped In | Wet ice |
| Product Description | 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 |
| Pubchem Sid | 504763598 |
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504763598 |
| Sensitivity | Light sensitive ;Air sensitive ;Heat sensitive |
| Mdl Number | MFCD00017718 |
| PubChem CID | 5320954 |