NS5A inhibitors useful for treating HCV
    4.
    发明授权
    NS5A inhibitors useful for treating HCV 有权
    用于治疗HCV的NS5A抑制剂

    公开(公告)号:US08835456B1

    公开(公告)日:2014-09-16

    申请号:US13423935

    申请日:2012-03-19

    IPC分类号: A61K31/44 C07D451/02

    CPC分类号: C07D471/08 A61K45/06

    摘要: The invention provides compounds of Formula I and the pharmaceutically salts thereof. These compounds may be generally described as bridged-bicyclo indole-containing compounds. The variables shown in Formula I are defined herein. Certain compounds of Formula I are useful as antiviral agents. Compounds as disclosed herein are potent and/or selective inhibitors of viral replication, particularly Hepatitis C virus replication. The invention also provides pharmaceutical compositions containing one or more compounds of Formula I and at least one pharmaceutically acceptable carrier. Such pharmaceutical compositions may contain a compound of Formula I as the only active agent or may contain a combination of a compound of Formula I and one or more other pharmaceutically active agents. The invention also provides methods for treating viral infections, including Hepatitis C infections, in patients.

    摘要翻译: 本发明提供式I化合物及其药学上可接受的盐。 这些化合物通常可以被描述为含桥连双环吲哚的化合物。 式I中所示的变量在本文中定义。 某些式I化合物可用作抗病毒剂。 本文公开的化合物是病毒复制的有效和/或选择性抑制剂,特别是丙型肝炎病毒复制。 本发明还提供含有一种或多种式I化合物和至少一种药学上可接受的载体的药物组合物。 这样的药物组合物可以含有式I化合物作为唯一的活性剂,或者可以含有式I化合物与一种或多种其它药物活性剂的组合。 本发明还提供了用于治疗患者中的病毒感染(包括丙型肝炎感染)的方法。

    4-AMINO-4-OXOBUTANOYL PEPTIDE CYCLIC ANALOGUES, INHIBITORS OF VIRAL REPLICATION
    7.
    发明申请
    4-AMINO-4-OXOBUTANOYL PEPTIDE CYCLIC ANALOGUES, INHIBITORS OF VIRAL REPLICATION 审中-公开
    4-氨基-4-氧杂多酚类环状类似物,病毒复制抑制剂

    公开(公告)号:US20100152103A1

    公开(公告)日:2010-06-17

    申请号:US12635049

    申请日:2009-12-10

    IPC分类号: A61K38/12 C07K5/12 A61P31/12

    摘要: The invention provides 4-amino-4-oxobutanoyl peptides and cyclic analogues thereof of Formula I and the pharmaceutically salts thereof.The variables are defined herein. Certain compounds of Formula I are useful as antiviral agents. 4-amino-4-oxobutanoyl peptide cyclic analogues as disclosed herein are potent and/or selective inhibitors of viral replication, particularly Hepatitis C virus replication. The invention also provides pharmaceutical compositions containing one or more 4-amino-4-oxobutanoyl peptide cyclic analogues and one or more pharmaceutically acceptable carriers. Such pharmaceutical compositions may contain a 4-amino-4-oxobutanoyl peptide cyclic analogue as the only active agent or may contain a combination of a 4-amino-4-oxobutanoyl peptide cyclic analogue and one or more other pharmaceutically active agents. The invention also provides methods for treating viral infections, including Hepatitis C infections, in patients.

    摘要翻译: 本发明提供了式I的4-氨基-4-氧代丁酰基肽及其环状类似物及其药学上可接受的盐。 变量在此定义。 某些式I化合物可用作抗病毒剂。 本文公开的4-氨基-4-氧代丁酰基肽环类似物是病毒复制,特别是丙型肝炎病毒复制的有效和/或选择性抑制剂。 本发明还提供含有一种或多种4-氨基-4-氧代丁酰基肽环状类似物和一种或多种药学上可接受的载体的药物组合物。 这样的药物组合物可以含有4-氨基-4-氧代丁酰基肽环类似物作为唯一的活性剂,或者可以含有4-氨基-4-氧代丁酰基肽环类似物和一种或多种其它药物活性剂的组合。 本发明还提供了用于治疗患者中的病毒感染(包括丙型肝炎感染)的方法。