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Nesbuvir is a small molecule non-nucleoside inhibitor of the hepatitis C virus (HCV) NS5B RNA-dependent RNA polymerase. It binds to the palm site II pocket of the NS5B polymerase and inhibits viral genome replication. Nesbuvir demonstrated potent anti-HCV activity in vitro and in animal models, with low nanomolar inhibitory concentrations against genotype 1a and 1b replicons. The drug was investigated for use in combination therapy for hepatitis C but its clinical development was terminated during phase II trials due to safety concerns[1][2][3][4][5][7].
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