Furanopyrimidines
    5.
    发明申请
    Furanopyrimidines 有权
    呋喃并嘧啶

    公开(公告)号:US20060040961A1

    公开(公告)日:2006-02-23

    申请号:US11169312

    申请日:2005-06-29

    IPC分类号: A61K31/519 C07D491/02

    CPC分类号: C07D491/04 C07D495/04

    摘要: The present invention relates to furanopyrimidine compounds having the general Formula I: and stereoisomers, tautomers, solvates, pharmaceutically acceptable salts and derivatives, and prodrugs thereof. The invention also includes pharmaceutical compositions comprising a compound of Formula I, methods of treating various diseases and conditions in a mammal, including inflammation, inhibition of T cell activation, proliferation, arthritis, organ transplant, ischemic or reperfusion injury, myocardial infarction, stroke, multiple sclerosis, inflammatory bowel disease, Crohn's disease, lupus, hypersensitivity, type 1 diabetes, psoriasis, dermatitis, Hashimoto's thyroiditis, Sjogren's syndrome, autoimmune hyperthyroidism, Addison's disease, autoimmune diseases, glomerulonephritis, allergic diseases, asthma, hayfever, eczema, cancer, colon carcinoma and thymoma, comprising administering to the mammal a therapeutically effective amount of a compound of Formula I. The invention also relates to methods of manufacturing medicaments, which comprise one or more compounds of Formula I.

    摘要翻译: 本发明涉及具有通式I的呋喃并嘧啶化合物及其立体异构体,互变异构体,溶剂合物,药用盐和衍生物及其前药。 本发明还包括药物组合物,其包含式I化合物,治疗哺乳动物各种疾病和病症的方法,包括炎症,抑制T细胞活化,增殖,关节炎,器官移植,缺血或再灌注损伤,心肌梗塞,中风, 多发性硬化,炎性肠病,克罗恩病,狼疮,超敏反应,1型糖尿病,牛皮癣,皮炎,桥本氏甲状腺炎,干燥综合征,自身免疫性甲状腺功能亢进,艾迪生病,自身免疫性疾病,肾小球性肾炎,过敏性疾病,哮喘,干草病,湿疹, 结肠癌和胸腺瘤,包括向哺乳动物施用治疗有效量的式I化合物。本发明还涉及制备药物的方法,其包含一种或多种式I化合物。

    PHARMACEUTICAL COMPOUNDS
    6.
    发明申请
    PHARMACEUTICAL COMPOUNDS 有权
    药物化合物

    公开(公告)号:US20110065701A1

    公开(公告)日:2011-03-17

    申请号:US12840070

    申请日:2010-07-20

    CPC分类号: A61K31/5355 C07D495/04

    摘要: A thienopyrimidine of formula (I): and the pharmaceutically acceptable salts thereof have activity as inhibitors of PI3K with selectivity for the P110α subtype, and may be used to treat diseases and disorders arising from abnormal cell growth, function or behaviour, particularly those associated with PI3 kinase such as cancer, immune disorders, cardiovascular disease, viral infection, inflammation, metabolism/endocrine disorders and neurological disorders. Processes for synthesizing the compounds are also described.

    摘要翻译: 式(I)的噻吩并嘧啶及其药学上可接受的盐具有作为P110α亚型选择性的PI3K抑制剂的活性,并且可用于治疗由异常细胞生长,功能或行为引起的疾病和障碍,特别是与 PI3激酶如癌症,免疫疾病,心血管疾病,病毒感染,炎症,代谢/内分泌障碍和神经障碍。 还描述了合成化合物的方法。