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    • 4. 发明授权
    • Inhibitors of serine proteases, particularly HCV NS3-NS4A protease
    • 丝氨酸蛋白酶抑制剂,特别是HCV NS3-NS4A蛋白酶
    • US07109172B2
    • 2006-09-19
    • US10893748
    • 2004-07-16
    • Shawn D. BrittKevin M. CottrellRobert B. PerniJanos Pitlik
    • Shawn D. BrittKevin M. CottrellRobert B. PerniJanos Pitlik
    • A61K38/00
    • C07K7/06
    • The present invention relates to compounds of formula I or formula Ia or pharmaceutically acceptable salts thereof, that inhibit serine protease activity, particularly the activity of hepatitis C virus NS3–NS4A protease. As such, they act by interfering with the life cycle of the hepatitis C virus and are useful as antiviral agents. The invention further relates to pharmaceutically acceptable compositions comprising said compounds either for ex vivo use or for administration to a patient suffering from HCV infection and processes for preparing the compounds. The invention also relates to methods of treating an HCV infection in a patient by administering a pharmaceutical composition comprising a compound of this invention.
    • 本发明涉及抑制丝氨酸蛋白酶活性,特别是丙型肝炎病毒NS3-NS4A蛋白酶活性的式I或式Ia化合物或其药学上可接受的盐。 因此,它们通过干扰丙型肝炎病毒的生命周期起作用,并且作为抗病毒剂是有用的。 本发明还涉及包含用于离体使用或用于给予HCV感染的患者的所述化合物的药学上可接受的组合物和用于制备所述化合物的方法。 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患者HCV感染的方法。
    • 7. 发明授权
    • Inhibitors of serine proteases, particularly HCV NS3-NS4A protease
    • 丝氨酸蛋白酶抑制剂,特别是HCV NS3-NS4A蛋白酶
    • US08039623B2
    • 2011-10-18
    • US11716248
    • 2007-03-09
    • Kevin M. CottrellRobert B. PerniJanos Pitlik
    • Kevin M. CottrellRobert B. PerniJanos Pitlik
    • C07D241/02A61K31/495
    • C07K7/06A61K38/08
    • The present invention relates to compounds of formula I: or a pharmaceutically acceptable salt or mixtures thereof that inhibit serine protease activity, particularly the activity of hepatitis C virus NS3-NS4A protease. As such, they act by interfering with the life cycle of the hepatitis C virus and are also useful as antiviral agents. The invention further relates to compositions comprising these compounds either for ex vivo use or for administration to a patient suffering from HCV infection and to processes for preparing the compounds. The invention also relates to methods of treating an HCV infection in a patient by administering a composition comprising a compound of this invention. The invention further relates to processes for preparing these compounds.
    • 本发明涉及抑制丝氨酸蛋白酶活性,特别是丙型肝炎病毒NS3-NS4A蛋白酶活性的式I化合物或其药学上可接受的盐或混合物。 因此,它们通过干扰丙型肝炎病毒的生命周期起作用,也可用作抗病毒剂。 本发明还涉及包含用于离体使用或用于给予HCV感染患者的这些化合物的组合物和制备该化合物的方法。 本发明还涉及通过施用包含本发明化合物的组合物来治疗患者HCV感染的方法。 本发明还涉及制备这些化合物的方法。