Non-nucleoside inhibitors of the hepatitis C virus NS5B polymerase:: discovery and preliminary SAR of benzimidazole derivatives

被引:102
作者
Beaulieu, PL
Bös, M
Bousquet, Y
Fazal, G
Gauthier, J
Gillard, J
Goulet, S
LaPlante, S
Poupart, MA
Lefebvre, S
McKercher, G
Pellerin, C
Austel, V
Kukolj, G
机构
[1] Boehringer Ingelheim KG, Dept Chem, Res & Dev, Laval, PQ H7S 2G5, Canada
[2] Boehringer Ingelheim KG, Biol Sci, Res & Dev, Laval, PQ H7S 2G5, Canada
[3] Boehringer Ingelheim KG, Dept Chem, Biberach, Germany
关键词
D O I
10.1016/j.bmcl.2003.10.023
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
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. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:119 / 124
页数:6
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