Compounds having BETA2 adrenergic receptor agonist and muscarinic receptor antagonist activity
    14.
    发明授权
    Compounds having BETA2 adrenergic receptor agonist and muscarinic receptor antagonist activity 失效
    具有BETA2肾上腺素能受体激动剂和毒蕈碱受体拮抗剂活性的化合物

    公开(公告)号:US08247564B2

    公开(公告)日:2012-08-21

    申请号:US12903365

    申请日:2010-10-13

    Abstract: The invention is directed to compounds of formula I: wherein R1, R2, R3, R4, R5, R6, R7a, R7b, W, G1, G2, a, b, c, d and m are as defined in the specification, or a pharmaceutically acceptable salt or solvate or stereoisomer thereof. The invention is also directed to pharmaceutical compositions comprising such compounds; methods of using such compounds; and process and intermediates for preparing such compounds.

    Abstract translation: 本发明涉及式I化合物:其中R1,R2,R3,R4,R5,R6,R7a,R7b,W,G1,G2,a,b,c,d和m如说明书中所定义, 其药学上可接受的盐或溶剂合物或立体异构体。 本发明还涉及包含这些化合物的药物组合物; 使用这些化合物的方法; 以及制备这些化合物的方法和中间体。

    Diphenylmethyl compounds useful as muscarinic receptor antagonists
    18.
    发明授权
    Diphenylmethyl compounds useful as muscarinic receptor antagonists 有权
    用作毒蕈碱受体拮抗剂的二苯甲基化合物

    公开(公告)号:US07071224B2

    公开(公告)日:2006-07-04

    申请号:US11076658

    申请日:2005-03-10

    Abstract: This invention provides compounds of formula I: wherein a, b, c, e, m, R1, R2, R3, R4a, R4b, R5, R6, R7 and R8are as defined in the specification. The compounds of formula I are muscarinic receptor antagonists. The invention also provides pharmaceutical compositions containing such compounds, processes and intermediates for preparing such compounds and methods of using such compounds to treat pulmonary disorders.

    Abstract translation: 本发明提供了式I化合物:其中a,b,c,e,m,R 1,R 2,R 3,R R 4a,R 4b,R 5,R 6,R 7和R 7,R 7, 在说明书中定义。 式I化合物是毒蕈碱受体拮抗剂。 本发明还提供含有这些化合物的药物组合物,用于制备这些化合物的方法和中间体以及使用这些化合物治疗肺部疾病的方法。

    Compounds having beta2 adrenergic receptor agonist and muscarinic receptor antagonist activity
    19.
    发明申请
    Compounds having beta2 adrenergic receptor agonist and muscarinic receptor antagonist activity 有权
    具有β2肾上腺素能受体激动剂和毒蕈碱受体拮抗剂活性的化合物

    公开(公告)号:US20080097105A1

    公开(公告)日:2008-04-24

    申请号:US12001362

    申请日:2007-12-11

    Abstract: The invention is directed to compounds of formula I: wherein R1, R2, R3, R4, R5, R6, R7a, R7b, W, G1, G2, a, b, c, d and m are as defined in the specification, or a pharmaceutically acceptable salt or solvate or stereoisomer thereof. The invention is also directed to pharmaceutical compositions comprising such compounds; methods of using such compounds; and process and intermediates for preparing such compounds.

    Abstract translation: 本发明涉及式I化合物:其中R 1,R 2,R 3,R 4, R 5,R 6,R 7a,R 7b,W,G 1, A,B,C,D和m如说明书中所定义,或其药学上可接受的盐或溶剂合物或立体异构体。 本发明还涉及包含这些化合物的药物组合物; 使用这些化合物的方法; 以及制备这些化合物的方法和中间体。

    Diphenylmethyl compounds useful as muscarinic receptor antagonists
    20.
    发明授权
    Diphenylmethyl compounds useful as muscarinic receptor antagonists 有权
    用作毒蕈碱受体拮抗剂的二苯甲基化合物

    公开(公告)号:US07208515B2

    公开(公告)日:2007-04-24

    申请号:US11543622

    申请日:2006-10-05

    Abstract: This invention provides compounds of formula I: wherein a, b, c, e, m, R1, R2, R3, R4a, R4b, R5, R6, R7, and R8 are as defined in the specification. The compounds of formula I are muscarinic receptor antagonists. The invention also provides pharmaceutical compositions containing such compounds, processes and intermediates for preparing such compounds and methods of using such compounds to treat pulmonary disorders.

    Abstract translation: 本发明提供了式I化合物:其中a,b,c,e,m,R 1,R 2,R 3,R R 4a,R 4b,R 5,R 6,R 7和/或R 4, R 8如本说明书中所定义。 式I化合物是毒蕈碱受体拮抗剂。 本发明还提供含有这些化合物的药物组合物,用于制备这些化合物的方法和中间体以及使用这些化合物治疗肺部疾病的方法。

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