| Literature DB >> 28197321 |
Pan Li1, Warren Dorsch1, David J Lauffer1, Darius Bilimoria1, Nathalie Chauret2, John J Court1, Sanjoy Kumar Das2, Francois Denis2, Nagraj Mani1, Suganthini Nanthakumar1, Olivier Nicolas2, B Govinda Rao1, Steven Ronkin1, Subajini Selliah2, Rebecca S Shawgo1, Ralph Stearns1, Qing Tang1, Nathan D Waal1, Jeremy Green1.
Abstract
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.Entities:
Keywords: Lomibuvir; NS5B; antiviral activity; hepatitis C; non-nucleoside; polymerase
Year: 2017 PMID: 28197321 PMCID: PMC5304295 DOI: 10.1021/acsmedchemlett.6b00479
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345