RESUMO
The discovery and optimization of a novel class of quinolone small-molecules that inhibit NS5B polymerase, a key enzyme of the HCV viral life-cycle, is described. Our research led to the replacement of a hydrolytically labile ester functionality with bio-isosteric heterocycles. An X-ray crystal structure of a key analog bound to NS5B facilitated the optimization of this series of compounds to afford increased activity against the target enzyme and in the cell-based replicon assay system.
Assuntos
Antivirais/farmacologia , Química Farmacêutica/métodos , Hepacivirus/enzimologia , Quinolonas/farmacologia , Proteínas não Estruturais Virais/antagonistas & inibidores , Sítio Alostérico , Antivirais/síntese química , Sítios de Ligação , Cristalografia por Raios X/métodos , Desenho de Fármacos , Ligação de Hidrogênio , Hidrólise , Concentração Inibidora 50 , Modelos Químicos , Conformação Molecular , Quinolonas/síntese química , Relação Estrutura-Atividade , Proteínas não Estruturais Virais/química , Raios XRESUMO
Hepatitis C virus (HCV) infection is treated with a combination of peginterferon alfa-2a/b and ribavirin. To address the limitations of this therapy, numerous small molecule agents are in development, which act by directly affecting key steps in the viral life-cycle. Herein we describe our discovery of quinolone derivatives, novel small-molecules that inhibit NS5b polymerase, a key enzyme of the viral life-cycle. A crystal structure of a quinoline analog bound to NS5B reveals that this class of compounds binds to allosteric site-II (non-nucleoside inhibitor-site 2, NNI-2) of this protein.