CAS NO: | 1256388-51-8 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
2mg | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 |
Ledipasvir (GS-5885) is an inhibitor of thehepatitis C virus NS5A, withEC50s of 34 pM and 4 pM against genotype 1a and 1b replicon, respectively. Ledipasvir is also aSARS-CoV3CLproinhibitor with anIC50of 1.62 μM[3]. |
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IC50& Target |
EC50: 34 pM (GT1a), 4 pM (GT1b)[1] |
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体外研究 (In Vitro) |
Ledipasvir has GT1a and 1b EC50values of 31 and 4 pM, respectively, and protein-adjusted EC50values of 210 pM (GT1a) and 27 pM (GT1b) and the intrinsic EC50of 39 is 310 fM for GT1a and 40 fM for GT1b. Ledipasvir is highly protein-bound both in human serum and in the cell-culture medium (containing 10% BSA) of the replicon assay[1]. Ledipasvir exhibits an EC50value of 141 nM against the JFH/3a-NS5A replicon[2].
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体内研究 (In Vivo) |
Ledipasvir is remarkable not only on the basis of its high replicon potency but also on the basis of its low clearance, good bioavailability, and long half-lives in rat, dog, and monkey and low predicted clearance in human. The pharmacokinetics of Ledipasvir is measured in rats and dogs. Ledipasvir shows good half-lives (rat 1.83 ± 0.22 hr, dog 2.63 ± 0.18 hr) in plasma, low systemic clearance (CL), and moderate volumes of distribution (Vss) that are greater than total body water volume[1].
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Clinical Trial |
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分子量 |
889.00 |
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性状 |
Solid |
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Formula |
C49H54F2N8O6 |
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CAS 号 |
1256388-51-8 |
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中文名称 |
雷迪帕韦;来地帕韦 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
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溶解性数据 |
In Vitro:
DMSO : 50 mg/mL(56.24 mM;Need ultrasonic)
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In Vivo:
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