发明名称 Arylsulfonamide based matrix metalloprotease inhibitors
摘要 The present invention provides a compound of formula (I):; said compound is inhibitor of MMP-2, and/or MMP-8, and/or MMP-9, and/or MMP-12 and/or MMP-13, and thus can be employed for the treatment of a disorder or disease characterized by abnormal activity of MMP-2, and/or MMP-8, and/or MMP-9, and/or MMP-12 and/or MMP-13. Accordingly, the compound of formula (I) can be used in treatment of disorders or diseases mediated by MMP-2, and/or MMP-8, and/or MMP-9, and/or MMP-12, and/or MMP-13. Finally, the present invention also provides a pharmaceutical composition.
申请公布号 US8975439(B2) 申请公布日期 2015.03.10
申请号 US201213690274 申请日期 2012.11.30
申请人 Novartis AG 发明人 Tommasi Ruben Alberto;Shultz Michael David;McQuire Leslie Wighton;Rigollier Pascal;Rogel Olivier;Ehrhardt Claus
分类号 C07C311/16;A61K31/18;C07D207/333;C07D209/12;C07C317/24;C07D295/112;A61K45/06;C07D403/04;C07D409/04;A61K31/55;C07D209/82;C07D235/06;C07D241/04;C07C323/67;C07D211/14;C07D265/30;C07D211/06;C07D213/61;C07D213/50;C07D471/04;C07D209/14;C07D211/24;C07D209/08;C07D209/10;C07D333/22;A61K31/4402;C07D401/04;C07D295/116;C07C311/46;C07D223/04;C07D333/18;C07D413/04;C07D221/16;C07D295/192;C07D207/20;A61K31/451;C07D209/80;A61K31/437;C07D213/40;C07C311/29;C07D487/04;C07D231/56;A61K31/495;C07C311/39;C07D235/08;A61K31/5375 主分类号 C07C311/16
代理机构 代理人 Binet-Cross Sophie
主权项 1. A compound of formula (II) wherein R′1 is selected from cycloakyl, R5C(O)—, R6SO2—, and (R8)(R9)N—, aryl, heteroaryl, heterocycloalkyl, said aryl, heteroaryl, and heterocycloalkyl are optionally substituted by one or two substituents selected from hydroxy, halo, alkyl, carboxyl, alkoxycarbonyl, and HC(O)—; wherein R4, R5, R6, R8 and R9 are independently alkyl or aryl each of which is optionally substituted by one to five substituents selected from the group consisting of (C1-C7) alkyl, halo, hydroxyl, (C1-C7) alkoxy, and aryl; R2 and R3 are independently hydrogen, or (C1-C7) alkyl; X is selected from cyano, halogen, nitro, alkyl-S—, alkyl-SO—, alkyl-SO2—, H2N—SO2—, R5—C(O)—, alkyl, and R4—O, wherein R4 and R5 are independently alkyl or aryl each of which is optionally substituted by substituents selected from the group consisting of (C1-C7) alkyl, halo, hydroxyl, (C1-C7) alkoxy, and aryl; or a pharmaceutically acceptable salt thereof, or an optical isomer thereof; or a mixture of optical isomers.
地址 Basel CH