INDOLE DERIVATIVES AS CRTH2 RECEPTOR ANTAGONISTS
    23.
    发明公开
    INDOLE DERIVATIVES AS CRTH2 RECEPTOR ANTAGONISTS 审中-公开
    吲哚衍生物作为CRTH2受体拮抗剂

    公开(公告)号:EP2342201A1

    公开(公告)日:2011-07-13

    申请号:EP09813944.7

    申请日:2009-09-17

    申请人: Merck Canada Inc.

    发明人: WANG, Zhaoyin

    IPC分类号: C07D471/04 A61K31/437

    CPC分类号: C07D471/04

    摘要: The compound (+) {7R-[[(4-fluorophenyl)sulfonyl](methyl)ammo]-6,7,8,9-tetrahydropyrido[1,2-a]mdol-10-yl}acetic acid and pharmaceutically acceptable salts thereof are antagonists of the PGD2 receptor, CRTH2, and as such are useful in the treatment and/or prevention of CRTH2-meidated diseases such as asthma.

    摘要翻译: (+){7R - [[(4-氟苯基)磺酰基](甲基)氨基] -6,7,8,9-四氢吡啶并[1,2-a]吲哚-10-基}乙酸和药学上可接受的 它们的盐是PGD 2受体CRTH 2的拮抗剂,并且因此可用于治疗和/或预防CRTH 2 - 中间体疾病如哮喘。