Abstract
Continual genetic variation supports hepatitis C virus (HCV) persistent infection, a leading cause of cirrhosis and hepatocellular carcinoma. The current standard of care has limited efficacy and is associated with severe adverse effects. Efforts to improve patients’ outcomes have focused on the design and development of small molecule compounds targeted towards essential viral proteins. Following the clinical success of HIV protease inhibitors, the HCV NS3-4A protease domain emerged as one of the most successful antiviral drug targets. This mini-review describes several HCV protease inhibitors in the various stages of clinical trials, and discusses their antiviral activities, pharmacokinetic properties, side effects and resistance profiles.
Keywords: Drug resistance, hepatitis C, HCV, NS3, protease inhibitor.
Anti-Infective Agents
Title:The Development of Novel HCV NS3-4A Protease Inhibitors
Volume: 11 Issue: 2
Author(s): Chang-Ye Hui, Xiao-Bing Xie, Hong Cao and Sheng-He Huang
Affiliation:
Keywords: Drug resistance, hepatitis C, HCV, NS3, protease inhibitor.
Abstract: Continual genetic variation supports hepatitis C virus (HCV) persistent infection, a leading cause of cirrhosis and hepatocellular carcinoma. The current standard of care has limited efficacy and is associated with severe adverse effects. Efforts to improve patients’ outcomes have focused on the design and development of small molecule compounds targeted towards essential viral proteins. Following the clinical success of HIV protease inhibitors, the HCV NS3-4A protease domain emerged as one of the most successful antiviral drug targets. This mini-review describes several HCV protease inhibitors in the various stages of clinical trials, and discusses their antiviral activities, pharmacokinetic properties, side effects and resistance profiles.
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Cite this article as:
Hui Chang-Ye, Xie Xiao-Bing, Cao Hong and Huang Sheng-He, The Development of Novel HCV NS3-4A Protease Inhibitors, Anti-Infective Agents 2013; 11 (2) . https://dx.doi.org/10.2174/2211352511311020006
DOI https://dx.doi.org/10.2174/2211352511311020006 |
Print ISSN 2211-3525 |
Publisher Name Bentham Science Publisher |
Online ISSN 2211-3533 |
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