Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1379080 | Bioorganic & Medicinal Chemistry Letters | 2006 | 5 Pages |
Abstract
Prolonged hepatitis C infection is the leading cause for cirrhosis of the liver and hepatocellular carcinoma. The etiological agent HCV virus codes a single polyprotein of ∼3000 amino acids that is processed with the help of a serine protease NS3A to produce structural and non-structural proteins required for viral replication. Inhibition of NS3 protease can potentially be used to develop drugs for treatment of HCV infections. Herein, we report the development of a series of novel NS3 serine protease inhibitors derived from 2-aza-bicyclo[2.2.1]-heptane carboxylic acid with potential therapeutic use for treatment of HCV infections.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Srikanth Venkatraman, F. George Njoroge, Wanli Wu, Viyyoor Girijavallabhan, Andrew J. Prongay, Nancy Butkiewicz, John Pichardo,