Abstract:
:Hepatitis C virus (HCV) is the most prevalent viral pathogen that infects more than 185 million people worldwide. HCV infection leads to chronic liver diseases such as liver cirrhosis and hepatocellular carcinoma. Direct-acting antivirals (DAAs) are the recent combination therapy for HCV infection with reduced side effects than prior therapies. Sustained virological response (SVR) acts as a gold standard marker to monitor the success of antiviral treatment. Older treatment therapies attain 50-55% of SVR compared with DAAs which attain around 90-95%. The current review emphasizes the recent chemogenomic updates that have been unfolded through structure-based drug design of HCV drug target proteins (NS3/4A, NS5A, and NS5B) and ligand-based drug design of DAAs in achieving a stable HCV viral treatment strategies.
journal_name
J Cell Biochemjournal_title
Journal of cellular biochemistryauthors
Venkatesan A,Prabhu Dass J Fdoi
10.1002/jcb.28581subject
Has Abstractpub_date
2019-08-01 00:00:00pages
12167-12181issue
8eissn
0730-2312issn
1097-4644journal_volume
120pub_type
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