INHIBITORS OF TRANSCRIPTION FACTOR NF-$g(k)B
    98.
    发明公开
    INHIBITORS OF TRANSCRIPTION FACTOR NF-$g(k)B 审中-公开
    转录因子NF- $ g(k)B的抑制剂

    公开(公告)号:EP1085872A1

    公开(公告)日:2001-03-28

    申请号:EP99930459.5

    申请日:1999-06-18

    摘要: The present invention provides amino-indanone inhibitors of transcription factor NF-λB and pharmaceutically acceptable salts, hydrates and solvates thereof, pharmaceutical compositions of such compounds, and methods for treating diseases in which activation of NF-λB is implicated. More specifically, the present invention provides methods of treatment of a variety of diseases associated with NF-λB activation including inflammatory disorders; particularly rheumatoid arthritis, inflammatory bowel disease, and asthma; dermatosis, including psoriasis and acute dermatosis; autoimmune diseases; tissue and organ rejection; Alzheimer's disease; stroke; atherosclerosis; restenosis; cancer, including Hodgkins disease; and certain viral infections, including AIDS; osteoarthritis; osteoporosis; and Ataxia Telangiestasia by administering to a patient in need thereof a compound of the present invention.

    摘要翻译: 本发明提供转录因子NF-λB的氨基 - 茚酮抑制剂及其药学上可接受的盐,水合物和溶剂合物,这些化合物的药物组合物,以及治疗其中涉及NF-λB活化的疾病的方法。 更具体地说,本发明提供了治疗与NF-λB激活有关的多种疾病的方法,包括炎性疾病; 特别是类风湿性关节炎,炎症性肠病和哮喘; 皮肤病,包括牛皮癣和急性皮肤病; 自身免疫性疾病; 组织和器官排斥; 阿尔茨海默氏病; 行程; 动脉粥样硬化; 再狭窄; 癌症,包括霍奇金病; 和某些病毒感染,包括艾滋病; 骨关节炎; 骨质疏松症; 和共济失调毛细血管扩张症的方法,其通过向有需要的患者施用本发明的化合物来实现。

    INHIBITORS OF TRANSCRIPTION FACTOR NF-KAPPA B
    99.
    发明公开
    INHIBITORS OF TRANSCRIPTION FACTOR NF-KAPPA B 有权
    转录因子NF-κB的抑制剂的

    公开(公告)号:EP1085848A2

    公开(公告)日:2001-03-28

    申请号:EP99930345.6

    申请日:1999-06-18

    IPC分类号: A61K6/00

    CPC分类号: A61K31/165 C07C235/64

    摘要: The present invention provides pharmaceutical compositions of salicylanilide inhibitors of transcription factor NF-λB, and methods for treating diseases in which activation of NF-λB is implicated. More specifically, the present invention provides methods of treatment of a variety of diseases associated with NF-λB activation including inflammatory disorders; particularly rheumatoid arthritis, inflammatory bowel disease, and asthma; dermatosis, including psoriasis and atopic dermatitis; autoimmune diseases; tissue and organ rejection; Alzheimer's disease; stroke; atherosclerosis; restenosis; cancer, including Hodgkin's disease; certain viral infections, including AIDS; osteoarthritis; osteoporosis; and Ataxia Telangiestasia by administering to a patient in need thereof a compound of the present invention.