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    • 5. 发明申请
    • SUBSTITUTED PYRROLIDINE AS ANTI-INFECTIVES
    • 替代吡咯烷作为抗感染剂
    • WO2009003009A1
    • 2008-12-31
    • PCT/US2008/068130
    • 2008-06-25
    • ENANTA PHARMACEUTICALS, INC.OR, Yat, SunYING, LuWANG, CeLONG, JiangQUI, Yao-Ling
    • OR, Yat, SunYING, LuWANG, CeLONG, JiangQUI, Yao-Ling
    • A61K31/4025C07D403/06
    • C07D417/14A61K38/21C07D401/14C07D403/06C07D405/14C07D409/14C07D413/04C07D417/04A61K2300/00
    • The present invention discloses compounds of Formulae (A), or pharmaceutically acceptable salts, esters, or prodrugs thereof: Formula (A), which inhibit RNA-containing virus, particularly the hepatitis C virus (HCV). Consequently, the compounds of the present invention interfere with the life cycle of the hepatitis C virus and are also useful as antiviral agents. The present invention further relates to pharmaceutical compositions comprising the aforementioned compounds for administration to a subject suffering from HCV infection. The invention also relates to methods of treating an HCV infection in a subject by administering a pharmaceutical composition comprising the compounds of the present invention. The present invention relates to novel antiviral compounds represented herein above, pharmaceutical compositions comprising such compounds, and methods for the treatment or prophylaxis of viral (particularly HCV infection in a subject in need of such therapy with said compounds.
    • 本发明公开了式(A)或其药学上可接受的盐,酯或前药的化合物:抑制含RNA病毒,特别是丙型肝炎病毒(HCV)的式(A)。 因此,本发明的化合物干扰丙型肝炎病毒的生命周期,也可用作抗病毒剂。 本发明还涉及药物组合物,其包含用于给患有HCV感染的受试者施用的上述化合物。 本发明还涉及通过施用包含本发明化合物的药物组合物来治疗受试者的HCV感染的方法。 本发明涉及上述新型抗病毒化合物,包含这些化合物的药物组合物,以及用于治疗或预防病毒(特别是需要用所述化合物治疗的受试者的HCV感染)的方法。