Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1371879 | Bioorganic & Medicinal Chemistry Letters | 2009 | 4 Pages |
Abstract
A new series of NS3/4A protease boronic acid inhibitors is described. The compounds show good biochemical potency and cellular activity. The peptidomimetic inhibitors were evaluated against proteases from different HCV genotypes and clinically relevant NS3/4A mutants. Compound 28 displayed subnanomolar to single digit nanomolar potencies in the enzymatic assays and an EC50 of 25 nM in the replicon cell-based assay.
Graphical abstractThe synthesis and evaluation of a series of peptidomimetic boronic acid inhibitors of the HCV NS3/4A protease is described. Data on their biochemical and cellular activities, mutant protease activity, and genotype coverage is reported.Figure optionsDownload full-size imageDownload as PowerPoint slide
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Amogh Boloor, Denise Hanway, Maria Joshi, David T. Winn, Gabriel Mendez, Marlena Walls, Ping Wei, Fuxin Qian, Xiaoli Zhang, Yuliang Zhang, Michael E. Hepperle, Xinqiang Li, David A. Campbell, Juan M. Betancort,