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Discovery of Novel Allosteric HCV NS5B Inhibitors.2. Lactam-Containing Thiophene Carboxylates

机译:发现新型变构HCV NS5B抑制剂。2.含内酰胺的噻吩羧酸盐

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摘要

Lomibuvir (>1) is a non-nucleoside, allosteric inhibitor of the hepatitis C virus NS5B polymerase with demonstrated clinical efficacy. Further development efforts within this class of inhibitor focused on improving the antiviral activity and physicochemical and pharmacokinetic properties. Recently, we reported the development of this series, leading to compound >2, a molecule with comparable potency and an improved physicochemical profile relative to >1. Further exploration of the amino amide-derived side chain led to a series of lactam derivatives, inspired by the X-ray crystal structure of related thiophene carboxylate inhibitors. This series, exemplified by >12f, provided 3–5-fold improvement in potency against HCV replication, as measured by replicon assays. The synthesis, structure–activity relationships, in vitro ADME characterization, and in vivo evaluation of this novel series are discussed.
机译:Lomibuvir(> 1 )是丙型肝炎病毒NS5B聚合酶的一种非核苷变构抑制剂,具有临床疗效。这类抑制剂的进一步开发工作集中在改善抗病毒活性以及理化和药代动力学特性上。最近,我们报道了该系列的开发成果,从而开发出了化合物> 2 ,该分子相对于> 1 具有同等的效价并且理化特性得到了改善。进一步探索源自氨基酰胺的侧链,受到相关噻吩羧酸盐抑制剂的X射线晶体结构的启发,产生了一系列内酰胺衍生物。以> 12f 为例的该系列,通过复制子检测,对HCV复制的效力提高了3-5倍。合成,结构-活性关系,体外ADME表征和体内评估的这个新颖的系列进行了讨论。

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