TETRAHYDROQUINOLINE ANALOGUES AS MUSCARINIC AGONISTS
    1.
    发明授权
    TETRAHYDROQUINOLINE ANALOGUES AS MUSCARINIC AGONISTS 有权
    四氢喹啉类似物作为麦考酚酸激动剂

    公开(公告)号:EP1461318B9

    公开(公告)日:2005-12-28

    申请号:EP02794441.2

    申请日:2002-12-23

    IPC分类号: C07D215/00

    摘要: The present invention relates to tetrahydroquinoline compounds as formulas I, as well as salts and isomers thereof wherein m is 0, 1 or 2; C3-C4 is CH2-CH or CH=Cor C4 is CH and C3 is absent; L1 and L2 are biradicals independently selected from the group consisting of -C(R6)=C(R7), -C(R6)=N, -N=C(R6)-, -S-, -NH- and -O-; wherein only one of L1 and L2 may be selected from the group consisting of -S-, NH - and O; Y is selected from the group consisting of O, S, and H2; X is a biradical as muscarinic receptor agonists; compositions comprising the same; methods of inhibiting an activity of a muscarinic receptor with said compounds; methods of treating a disease condition associated with a muscarinic receptor using said compounds; and methods for identifying a subject suitable for treatment using said compounds.

    摘要翻译: 本发明涉及式I的四氢喹啉化合物及其盐和异构体,其中m为0,1或2; C 3 -C 4是CH 2 -CH或CH = C 1 -C 4是CH且C 3不存在; L1和L2是独立地选自-C(R6)= C(R7),-C(R6)= N,-N = C(R6) - , - S - , - NH-和-O- - ; 其中L1和L2中只有一个可以选自-S-,NH-和O; Y选自O,S和H 2; X是一种双基作为毒蕈碱受体激动剂; 包含其的组合物; 用所述化合物抑制毒蕈碱受体活性的方法; 使用所述化合物治疗与毒蕈碱受体相关的疾病状况的方法; 以及使用所述化合物鉴定适于治疗的受试者的方法。

    TETRAHYDROQUINOLINE ANALOGUES AS MUSCARINIC AGONISTS
    2.
    发明授权
    TETRAHYDROQUINOLINE ANALOGUES AS MUSCARINIC AGONISTS 有权
    四氢ALS毒蕈碱激动剂

    公开(公告)号:EP1461318B1

    公开(公告)日:2005-09-14

    申请号:EP02794441.2

    申请日:2002-12-23

    IPC分类号: C07D215/00

    摘要: The present invention relates to tetrahydroquinoline compounds as formulas I, as well as salts and isomers thereof wherein m is 0, 1 or 2; C3-C4 is CH2-CH or CH=Cor C4 is CH and C3 is absent; L1 and L2 are biradicals independently selected from the group consisting of -C(R6)=C(R7), -C(R6)=N, -N=C(R6)-, -S-, -NH- and -O-; wherein only one of L1 and L2 may be selected from the group consisting of -S-, NH - and O; Y is selected from the group consisting of O, S, and H2; X is a biradical as muscarinic receptor agonists; compositions comprising the same; methods of inhibiting an activity of a muscarinic receptor with said compounds; methods of treating a disease condition associated with a muscarinic receptor using said compounds; and methods for identifying a subject suitable for treatment using said compounds.

    TETRAHYDROQUINOLINE ANALOGUES AS MUSCARINIC AGONISTS
    3.
    发明公开
    TETRAHYDROQUINOLINE ANALOGUES AS MUSCARINIC AGONISTS 有权
    四氢ALS毒蕈碱激动剂

    公开(公告)号:EP1461318A2

    公开(公告)日:2004-09-29

    申请号:EP02794441.2

    申请日:2002-12-23

    IPC分类号: C07D215/00

    摘要: The present invention relates to tetrahydroquinoline compounds as formulas I, as well as salts and isomers thereof wherein m is 0, 1 or 2; C3-C4 is CH2-CH or CH=Cor C4 is CH and C3 is absent; L1 and L2 are biradicals independently selected from the group consisting of -C(R6)=C(R7), -C(R6)=N, -N=C(R6)-, -S-, -NH- and -O-; wherein only one of L1 and L2 may be selected from the group consisting of -S-, NH - and O; Y is selected from the group consisting of O, S, and H2; X is a biradical as muscarinic receptor agonists; compositions comprising the same; methods of inhibiting an activity of a muscarinic receptor with said compounds; methods of treating a disease condition associated with a muscarinic receptor using said compounds; and methods for identifying a subject suitable for treatment using said compounds.