| Literature DB >> 14684311 |
Pierre L Beaulieu1, Michael Bös, Yves Bousquet, Gulrez Fazal, Jean Gauthier, James Gillard, Sylvie Goulet, Steven LaPlante, Marc-André Poupart, Sylvain Lefebvre, Ginette McKercher, Charles Pellerin, Volkhard Austel, George Kukolj.
Abstract
Benzimidazole 5-carboxamide derivatives from a combinatorial screening library were discovered as specific inhibitors of the NS5B polymerase of the hepatitis C virus (HCV). Initial hit-to-lead activities taking advantage of high-throughput parallel synthetic techniques, identified a 1,2-disubstituted benzimidazole 5-carboxylic acid scaffold as the minimum core for biological activity. Potent analogues in this series inhibit the polymerase at low micromolar concentrations and provide an attractive "drug-like" lead structure for further optimization and the development of potential HCV therapeutics.Entities:
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Year: 2004 PMID: 14684311 DOI: 10.1016/j.bmcl.2003.10.023
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823