2,6-Disubstituted piperiddines as modulators
    3.
    发明申请
    2,6-Disubstituted piperiddines as modulators 失效
    2,6-二取代的哌啶作为调节剂

    公开(公告)号:US20070179158A1

    公开(公告)日:2007-08-02

    申请号:US10586765

    申请日:2005-01-14

    摘要: The present invention is further directed to compounds of formula (I): wherein R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, R16, R17, R18, R19, R20, R21 and R22 are as defined herein) which are modulators of chemokine receptor activity and are useful in the prevention or treatment of certain inflammatory and immunoregulatory disorders and diseases, allergic diseases, atopic conditions including allergic rhinitis, dermatitis, conjunctivitis, and asthma, as well as autoimmune pathologies such as rheumatoid arthritis and atherosclerosis. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which chemokine receptors are involved.

    摘要翻译: 本发明还涉及式(I)的化合物:其中R 1,R 2,R 3,R 4, R 5,R 6,R 7,R 8,R 9,R 9, R 10,R 16,R 17,R 18,R 19,R 16, R 20,R 21,R 22和R 22如本文所定义),其是趋化因子受体活性的调节剂,并且可用于 预防或治疗某些炎性和免疫调节性疾病和疾病,过敏性疾病,特应性病症,包括过敏性鼻炎,皮炎,结膜炎和哮喘,以及自身免疫病态如类风湿性关节炎和动脉粥样硬化。 本发明还涉及包含这些化合物的药物组合物以及这些化合物和组合物在预防或治疗涉及趋化因子受体的疾病中的用途。

    Benzoxazinyl-amidocyclopentyl-heterocyclic modulators of chemokine receptors
    7.
    发明申请
    Benzoxazinyl-amidocyclopentyl-heterocyclic modulators of chemokine receptors 审中-公开
    趋化因子受体的苯并恶嗪基酰胺基环戊基 - 杂环调节剂

    公开(公告)号:US20070238723A1

    公开(公告)日:2007-10-11

    申请号:US10536092

    申请日:2004-10-15

    摘要: Cyclopentyl compounds linked to a benzoxazinyl group through an amido moiety utilizing the ring nitrogen of the benzoxazine, and further substituted with a heterocyclic moiety, such compounds represented by formula I: which are used to modulate the CCR-2 chemokine receptor to prevent or treat inflammatory and immunoregulatory disorders and diseases, allergic diseases, atopic conditions including allergic rhinitis, dermatitis, conjunctivitis, and asthma, as well as autoimmune pathologies such as rheumatoid arthritis and atherosclerosis; and pharmaceutical compositions comprising these compounds and the use of these compounds and compositions.

    摘要翻译: 通过使用苯并恶嗪的环氮通过酰胺部分连接到苯并恶嗪基的环戊基化合物,并进一步被杂环部分取代,由式I表示的化合物:其用于调节CCR-2趋化因子受体以预防或治疗炎症 和免疫调节性疾病和疾病,过敏性疾病,特应性病症,包括过敏性鼻炎,皮炎,结膜炎和哮喘,以及自身免疫性病态如类风湿性关节炎和动脉粥样硬化; 和包含这些化合物的药物组合物以及这些化合物和组合物的用途。