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1b)野生型和S282T复制子,EC90值分别为0.42和7.8μM[2]。在克隆A复制子测定中,Sofosbuvir(PSI-7977)产生抗HCV活性,EC90值为0.42μM[3]。",{"key":227,"value":228},"细胞实验","将克隆A细胞以约5×10 6个细胞\u002F瓶接种到含有100IU \u002F mL青霉素\u002F100μg\u002F mL链霉素和10％胎牛血清的Dulbecco's改良Eagle培养基（DMEM）中的T75烧瓶中。类似地，将人原代肝细胞以约5×10 6个细胞\u002F瓶接种在细胞平板培养基中的T75烧瓶中。孵育过夜以使细胞附着后，将细胞与50μMPSI-7851，PSI-7976或Sofosbuvir（PSI-7977）在新鲜培养基中培养用于克隆A细胞或在用于原代肝细胞的细胞维持培养基中培养至多24 h在37℃，5％CO 2气氛中。当在研究中使用放射性标记的PSI-7851时，应用相同的程序，除了将每孔1×10 6个细胞接种到6孔板中，并将细胞与5μM[3H] PSI-7851一起孵育。在选定的时间，除去培养基，用冷的磷酸盐缓冲盐水（PBS）洗涤细胞层。胰蛋白酶消化后，计数细胞并以1,200rpm离心5分钟。将细胞沉淀悬浮在1mL冷的60％甲醇中，并在-20℃下温育过夜。将样品以14,000rpm离心5分钟，收集上清液并使用SpeedVac浓缩器干燥，并储存在-20℃直至通过高效液相色谱（HPLC）分析。将残留物悬浮于100μL水中，并将50μL等分试样注入HPLC [1]。",{"key":230,"value":231},"参考文献","[1].\nMurakami E, et al. Mechanism of activation of PSI-7851 and its diastereoisomer PSI-7977.J Biol Chem. 2010 Nov 5;285(45):34337-47.\n[2].\nLam AM, et al. Genotype and subtype profiling of PSI-7977 as a nucleotide inhibitor of hepatitis C virus. Antimicrob Agents Chemother. 2012 Jun;56(6):3359-68.\n[3].\nSofia MJ, et al. Discovery of a β-d-2'-deoxy-2'-α-fluoro-2'-β-C-methyluridine nucleotide prodrug (PSI-7977) for the treatment of hepatitis C virus. J Med Chem. 2010 Oct 14;53(19):7202-18.\n[4].\nZhang X, et al. Discovery and evolution of aloperine derivatives as a new family of HCV inhibitors with novel mechanism. 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