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MK-3281 is a potent, orally bioavailable small molecule inhibitor of the hepatitis C virus (HCV) NS5B RNA-dependent RNA polymerase. It is a non-nucleoside inhibitor that binds to an allosteric site on the thumb domain of the NS5B polymerase, interfering with viral replication. Preclinical studies demonstrated efficacy in cell-based assays against HCV genotypes 1 and 3, as well as in vivo activity in chimeric mouse and chimpanzee models of HCV infection. The drug was developed for chronic HCV infection and reached Phase I clinical trials, where it showed good pharmacokinetic properties and was generally well tolerated[2][4][5][7].
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