UK-1 and structural analogs are potent inhibitors of hepatitis C virus replication

UK-1 and structural analogs are potent inhibitors of hepatitis C virus replication In silico identification, design and synthesis of novel piperazine-based antiviral agents targeting the hepatitis C virus helicase Synthesis of New Acridone Derivatives, Inhibitors of NS3 Helicase, Which Efficiently and Specifically Inhibit Subgenomic HCV Replication N-Naphthoyl-substituted indole thio-barbituric acid analogs inhibit the helicase activity of the hepatitis C virus NS3 Comparative In Vitro Anti-Hepatitis C Virus Activities of a Selected Series of Polymerase, Protease, and Helicase Inhibitors Studies on the anti-hepatitis C virus activity of newly synthesized tropolone derivatives: Identification of NS3 helicase inhibitors that specifically inhibit subgenomic HCV replication Integrated Strategies for Identifying Leads That Target the NS3 Helicase of the Hepatitis C Virus Hexahydro-pyrrolo- and hexahydro-1H-pyrido[1,2-b]pyridazin-2-ones as potent inhibitors of HCV NS5B polymerase Computer-aided identification, synthesis and evaluation of substituted thienopyrimidines as novel inhibitors of HCV replication C-6 aryl substituted 4-quinolone-3-carboxylic acids as inhibitors of hepatitis C virus