In Vitro Rhapontigenin exhibits a potent and selective inhibition of human P450 1A1 with an IC 50 of 0.4 μM. Rhapontigenin shows 400-fold selectivity for P450 1A1 over P450 1A2 and 23-fold selectivity for P450 1A1 over P450 1B1. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Form:Solid
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Rhapontigenin 3'-O-glucoside
CAS number:94356-22-6 molecular formula:C21H24O9
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| Chinese alias | 土大黄素3'-O-葡萄糖苷 | (2S,3R,4S,5S,6R)-2-(5-((E)-3,5-二羟基苯乙烯基)-2-甲氧基苯氧基)-6-(羟甲基)四氢-2H-吡喃-3,4,5-三醇 | ||
| English alias | (2S,3R,4S,5S,6R)-2-(5-((E)-3,5-Dihydroxystyryl)-2-methoxyphenoxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol | ||
| CAS number | 94356-22-6 | molecular formula | C21H24O9 |
| molecular weight | 420.41 g/mol | Exact mass | - |
| PSA | 149.000 Ų | logp | 0.500 |
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