OXO-imidazolidines as modulators of chemokine receptors
    5.
    发明授权
    OXO-imidazolidines as modulators of chemokine receptors 有权
    OXO-咪唑啉作为趋化因子受体的调节剂

    公开(公告)号:US07786157B2

    公开(公告)日:2010-08-31

    申请号:US12048814

    申请日:2008-03-14

    IPC分类号: A01N43/50

    摘要: The present invention provides compounds having formula (I): or pharmaceutically acceptable salts and N-oxides thereof, wherein the subscript m is an integer from 0-4; Ar is an optionally substituted aryl; B is an optionally substituted aryl; L1 is an optionally substituted linking group selected from the group consisting of C1-4 alkylene, C1-4 heteroalkylene, C2-4 alkenylene and —CH2N(Ru)X5—; and L2 is a bond or C1-3 alkylene. The compounds act as potent antagonists of the CCR1 receptor, and have in vivo anti-inflammatory activity.

    摘要翻译: 本发明提供具有式(I)的化合物或其药学上可接受的盐和N-氧化物,其中下标m是0-4的整数; Ar是任选取代的芳基; B是任选取代的芳基; L1是选自C1-4亚烷基,C1-4亚杂烷基,C2-4亚烯基和-CH2N(Ru)X5-的任选取代的连接基团; 并且L 2是键或C 1-3亚烷基。 该化合物作为CCR1受体的有效拮抗剂,具有体内抗炎活性。