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Paritaprevir
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Paritaprevir图片
CAS NO:1216941-48-8
规格:≥98%
包装与价格:
包装价格(元)
1mg询价
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理化性质和储存条件
Molecular Weight (MW) 765.88
Formula C40H43N7O7S
CAS No. 1216941-48-8
Storage-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)DMSO: ≥ 125 mg/mL
Water: <1 mg/mL
Ethanol: <1 mg/mL
SMILES O=C([C@]([C@]1([H])/C=C\CCCCC[C@@H]2NC(C3=NC=C(C)N=C3)=O)(C1)NC([C@@](C[C@@H](OC4=C5C=CC=CC5=C(C=CC=C6)C6=N4)C7)([H])N7C2=O)=O)NS(=O)(C8CC8)=O
Synonyms ABT 450; Paritaprevir; ABT-450; Veruprevir; ATB450; Brand names: Viekirax; Viekira Pak; Technivie.
实验参考方法
In Vitro

In vitro activity: Paritaprevir (formerly known as ABT-450 and/or Veruprevir), an acylsulfonamide structurally, is a potent non-structural protein 3/4A (NS3/4A) protease inhibitor with EC50 values of 1 and 0.21 nM for HCV 1a and 1b, respectively. It is discovered by Abbott Laboratories that shows promising results as a treatment of hepatitis C. Paritaprevir demonstrates in vitro antiviral activity against HCV GT1-4 and GT6 (EC50 range, 0.09 to 19 nM), with an EC50 of 0.09 nM against GT4a. When given in combination with ritonavir and ribavirin for 12 weeks, the rate of sustained virologic response at 24 weeks after treatment has been estimated to be 95% for those with hepatitis C virus genotype 1. Resistance to treatment with paritaprevir is uncommon, because it targets the binding site, but has been seen to arise due to mutations at positions 155 and 168 in NS3. Paritaprevir is a component of Viekira Pak and Technivie.


Kinase Assay: Paritaprevir demonstrates in vitro antiviral activity against HCV GT1-4 and GT6 (EC50 range, 0.09 to 19 nM), with an EC50 of 0.09 nM against GT4a

In VivoThe combination of paritaprevir, ritonavir, ombitasvir (an NS5A protein inhibitor), and dasabuvir (an NS5B non-nucleoside polymerase inhibitor) with or without RBV has been approved to treat HCV genotype 1 infections1
Animal modelNA
Formulation & DosageNA
References Drug Des Devel Ther. 2015 Nov 13;9:6083-94.Antimicrob Agents Chemother. 2015 Nov;59(11):6807-15.
 
 
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