CRTH2 receptor ligands for medicinal uses
    8.
    发明授权
    CRTH2 receptor ligands for medicinal uses 失效
    用于药用的CRTH2受体配体

    公开(公告)号:US08022063B2

    公开(公告)日:2011-09-20

    申请号:US11597873

    申请日:2005-05-30

    IPC分类号: A01N43/00 C07D231/00

    摘要: Compounds of formula (I) are useful for the treatment of disease responsive to modulation of CRTH2 receptor activity, such as asthma, rhinitis, allergic airway syndrome, and allergic rhinobronchitis, wherein A represents a carboxyl group —COON, or a carboxyl bioisostere; A1, is hydrogen or methyl; ring Ar1 is an optionally substituted phenyl ring 5- or 6-membered monocyclic heteroaryl ring, in which AA1CHO— and L2 are linked to adjacent ring atoms; rings Are2, Ar3 each independently represent a phenyl or 5- or 6-membered monocyclic heteroaryl ring, or a bicyclic ring system consisting of a 5- or 6-membered carbocyclic or heterocyclic ring which is benz-fused or fused to a 5- or 6-membered monocyclic heteroaryl ring, said ring or ring system being optionally substituted; t is 0 or 1; L2 and L3 are linker radicals as defined in the description.

    摘要翻译: 式(I)化合物可用于治疗对CRTH2受体活性调节作用的疾病,例如哮喘,鼻炎,过敏性气道综合征和过敏性鼻炎支原体,其中A表示羧基-COON或羧基生物电子等排体; A1,是氢或甲基; 环Ar1是任选取代的苯环5-或6-元单环杂芳基环,其中AA1CHO-和L2与相邻的环原子连接; 环A 2,Ar 3各自独立地表示苯基或5-或6-元单环杂芳基环,或由5-或6-元碳环或杂环组成的双环系统,其被苯并稠合或稠合至5-或 6元单环杂芳基环,所述环或环系统任选被取代; t为0或1; L2和L3是如说明书中定义的连接基团。