Chemical Structure : Samatasvir
CAS No.: 1312547-19-5
货号: PC-61524Not For Human Use, Lab Use Only.
Samatasvir (IDX719) is a highly potent, selective inhibitor of HCV NS5A that effectively inhibits HCV genotype 1-5 replicons with EC50 of 2-24 pM.
规格 | 价格 | 库存 | 数量 |
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5 mg | ¥1880 | In stock | |
10 mg | ¥2980 | In stock | |
25 mg | ¥4980 | In stock | |
50 mg | Get quote | ||
100 mg | Get quote |
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Samatasvir (IDX719) is a highly potent, selective inhibitor of HCV NS5A that effectively inhibits HCV genotype 1-5 replicons with EC50 of 2-24 pM.
Samatasvir also retains full activity in the presence of HIV and hepatitis B virus (HBV) antivirals.
Samatasvir demonstrates an overall additive effect when combined with IFN-α, ribavirin, representative HCV protease, and nonnucleoside polymerase inhibitors or the nucleotide prodrug IDX184.
分子量 | 885.062 | |
分子式 | C47H48N8O6S2 | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
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Chemical Name/SMILES |
Methyl N-[(1R)-2-[(2S)-2-[5-[4-[6-[2-[(2S)-1-[(2S)-2-(methoxycarbonylamino)-3-methylbutanoyl]pyrrolidin-2-yl]-3H-benzimidazol-5-yl]thieno[3,2-b]thiophen-3-yl]phenyl]-1H-imidazol-2-yl]pyrrolidin-1-yl]-2-oxo-1-phenylethyl]carbamate |
1. Bilello JP, et al. Antimicrob Agents Chemother. 2014 Aug;58(8):4431-42.
2. Vince B, et al. J Hepatol. 2014 May;60(5):920-7.
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