Substituted bicycloalkylamine derivatives as modulators of chemokine receptor activity
    5.
    发明申请
    Substituted bicycloalkylamine derivatives as modulators of chemokine receptor activity 有权
    取代的双环烷基胺衍生物作为趋化因子受体活性的调节剂

    公开(公告)号:US20050192276A1

    公开(公告)日:2005-09-01

    申请号:US11059771

    申请日:2005-02-17

    CPC分类号: C07D403/14 C07D403/04

    摘要: The present application describes modulators of MCP-1 of formula (I): or stereoisomers or pharmaceutically acceptable salts thereof, wherein X, Z, a, b, c, d, bond g, n, s, R1, R2, R4, R5, R10, R12, and R13, are as defined above. In addition, methods of treating and preventing inflammatory diseases such as asthma and allergic diseases, as well as autoimmune pathologies such as rheumatoid arthritis and atherosclerosis using said modulators are disclosed.

    摘要翻译: 本申请描述了式(I)的MCP-1的调节剂:其立体异构体或其药学上可接受的盐,其中X,Z,a,b,c,d,键g,n,s,R 1, R 2,R 2,R 4,R 5,R 10,R 12, SUP>和R 13,如上所定义。 此外,公开了使用所述调节剂治疗和预防炎症性疾病如哮喘和过敏性疾病以及自身免疫病态如类风湿性关节炎和动脉粥样硬化的方法。

    Substituted bicycloalkylamine derivatives as modulators of chemokine receptor activity
    6.
    发明申请
    Substituted bicycloalkylamine derivatives as modulators of chemokine receptor activity 有权
    取代的双环烷基胺衍生物作为趋化因子受体活性的调节剂

    公开(公告)号:US20050227960A1

    公开(公告)日:2005-10-13

    申请号:US11060250

    申请日:2005-02-17

    CPC分类号: C07D209/52 C07D403/12

    摘要: The present application describes modulators of MCP-1 of formula (I): or stereoisomers or pharmaceutically acceptable salts thereof, wherein X, Z, a, b, c, d, n, R1, R2, R3, R4, R5, R10, R10a, and R12, are as defined herein. In addition, methods of treating and preventing inflammatory diseases such as asthma and allergic diseases, as well as autoimmune pathologies such as rheumatoid arthritis and atherosclerosis using said modulators are disclosed.

    摘要翻译: 本申请描述了式(I)的MCP-1的调节剂:其立体异构体或其药学上可接受的盐,其中X,Z,a,b,c,d,n,R 1, R 2,R 3,R 4,R 5,R 10,R 10, SUP> 10a<<< 12>,如本文所定义。 此外,公开了使用所述调节剂治疗和预防炎症性疾病如哮喘和过敏性疾病以及自身免疫病态如类风湿性关节炎和动脉粥样硬化的方法。

    Substituted fused bicyclic amines as modulators of chemokine receptor activity
    7.
    发明申请
    Substituted fused bicyclic amines as modulators of chemokine receptor activity 有权
    取代的稠合双环胺作为趋化因子受体活性的调节剂

    公开(公告)号:US20050197373A1

    公开(公告)日:2005-09-08

    申请号:US11060483

    申请日:2005-02-17

    摘要: The present application describes modulators of CCR3 of formula (Ia) and (Ib): or pharmaceutically acceptable salt forms thereof, wherein Z, R1, R2, R3, R4, R5, R5′, R6, a, b, c, d, and u are as defined herein. In addition, methods of treating and preventing inflammatory diseases such as asthma and allergic diseases, as well as autoimmune pathologies such as rheumatoid arthritis and atherosclerosis using said modulators are disclosed.

    摘要翻译: 本申请描述了式(Ia)和(Ib)的CCR3的调节剂:或其药学上可接受的盐形式,其中Z,R 1,R 2,R SUP R 3,R 4,R 5,R 5,R 6,S 6, b,c,d和u如本文所定义。 此外,公开了使用所述调节剂治疗和预防炎症性疾病如哮喘和过敏性疾病以及自身免疫病态如类风湿性关节炎和动脉粥样硬化的方法。

    Substituted spiro azabicyclics as modulators of chemokine receptor activity
    8.
    发明申请
    Substituted spiro azabicyclics as modulators of chemokine receptor activity 有权
    取代的螺氮氮杂双环作为趋化因子受体活性的调节剂

    公开(公告)号:US20050197325A1

    公开(公告)日:2005-09-08

    申请号:US11060246

    申请日:2005-02-17

    摘要: The present application describes modulators of CCR3 of formula (Ia) and (Ib): or pharmaceutically acceptable salt forms thereof, wherein Z, R1, R2, R3, R4, R5, R5′, R6, a, b, c, d, and u are as defined herein. In addition, methods of treating and preventing inflammatory diseases such as asthma and allergic diseases, as well as autoimmune pathologies such as rheumatoid arthritis and atherosclerosis using said modulators are disclosed.

    摘要翻译: 本申请描述了式(Ia)和(Ib)的CCR3的调节剂:或其药学上可接受的盐形式,其中Z,R 1,R 2,R SUP R 3,R 4,R 5,R 5,R 6,S 6, b,c,d和u如本文所定义。 此外,公开了使用所述调节剂治疗和预防炎症性疾病如哮喘和过敏性疾病以及自身免疫病态如类风湿性关节炎和动脉粥样硬化的方法。