NOVEL COMPOUNDS
    12.
    发明公开
    NOVEL COMPOUNDS 有权
    新ROUTES

    公开(公告)号:EP1539731A1

    公开(公告)日:2005-06-15

    申请号:EP03738863.4

    申请日:2003-07-15

    申请人: AstraZeneca AB

    CPC分类号: C07D333/38

    摘要: There are provided novel compounds of formula (I) wherein R1, R2, R3, R4, R5, R6, R7, M, T, U, Y, V and W are as defined in the specification and pharmaceutically acceptable salts thereof; together with processes for their preparation, compositions containing them and their use in therapy. The compounds are inhibitors of nitric oxide synthase and are thereby particularly useful in the treatment or prophylaxis of inflammatory disease and pain.

    QUINICLIDINE DERIVATIVES OF (HETERO) ARYLCYCLOHEPTANECARBOXYLIC ACID AS MUSCARINIC RECEPTOR ANTAGONISTS
    14.
    发明公开
    QUINICLIDINE DERIVATIVES OF (HETERO) ARYLCYCLOHEPTANECARBOXYLIC ACID AS MUSCARINIC RECEPTOR ANTAGONISTS 有权
    (杂芳基)芳基环庚烷羧酸作为麦考酚酸受体拮抗剂的喹吖啶衍生物

    公开(公告)号:EP2094694A1

    公开(公告)日:2009-09-02

    申请号:EP07824574.3

    申请日:2007-11-13

    申请人: AstraZeneca AB

    IPC分类号: C07D453/02 A61K31/439

    CPC分类号: C07D453/02

    摘要: The invention provides compounds of formula (I) wherein R4 is a group of formula (II) or (IIIa) or (IIIb) and R1, R2, R3, R5, a, b and X are as defined in the specification, a process for their preparation, pharmaceutical compositions containing them, a process for preparing pharmaceutical compositions, their use in therapy and intermediates of use in their preparation (I), (II), (IIIa), (IIIb).

    摘要翻译: 本发明提供了其中R 4为式(II)或(IIIa)或(IIIb)的基团且R 1,R 2,R 3,R 5,a,b和X如说明书中所定义的式 它们的制备,含有它们的药物组合物,制备药物组合物的方法,它们在治疗中的用途以及在其制备(I),(II),(IIIa),(IIIb)中使用的中间体。

    NOVEL COMPOUNDS
    15.
    发明授权

    公开(公告)号:EP1539731B9

    公开(公告)日:2008-08-20

    申请号:EP03738863.4

    申请日:2003-07-15

    申请人: AstraZeneca AB

    CPC分类号: C07D333/38

    摘要: There are provided novel compounds of formula (I) wherein R1, R2, R3, R4, R5, R6, R7, M, T, U, Y, V and W are as defined in the specification and pharmaceutically acceptable salts thereof; together with processes for their preparation, compositions containing them and their use in therapy. The compounds are inhibitors of nitric oxide synthase and are thereby particularly useful in the treatment or prophylaxis of inflammatory disease and pain.

    NOVEL PHENYLHETEROALKYLAMINE DERIVATIVES
    18.
    发明公开
    NOVEL PHENYLHETEROALKYLAMINE DERIVATIVES 有权
    新的苯基高铁烷基胺衍生物

    公开(公告)号:EP1263714A1

    公开(公告)日:2002-12-11

    申请号:EP01906490.6

    申请日:2001-02-20

    申请人: AstraZeneca AB

    摘要: There are provided novel compounds of formula (I), wherein R1, R2, X, Y, V, W and Z are as defined in the specification, and pharmaceutically acceptable salts thereof, and enantiomers and racemates thereof; together with processes for their preparation, compositions containing them and their use in therapy. The compounds are inhibitors of nitric oxide synthase and are thereby particularly useful in the treatment or prophylaxis of inflammatory disease and pain.

    摘要翻译: 提供了式(I)的新化合物,其中R 1,R 2,X,Y,V,W和Z如说明书中所定义,及其药学上可接受的盐,以及其对映体和外消旋体; 以及它们的制备方法,含有它们的组合物以及它们在治疗中的用途。 这些化合物是一氧化氮合酶的抑制剂,因此特别适用于治疗或预防炎性疾病和疼痛。