3-Substituted benzofurans as therapeutic agents
    2.
    发明申请
    3-Substituted benzofurans as therapeutic agents 审中-公开
    3-取代的苯并呋喃作为治疗剂

    公开(公告)号:US20050020631A1

    公开(公告)日:2005-01-27

    申请号:US10860527

    申请日:2004-06-03

    CPC分类号: C07D405/12 C07D405/14

    摘要: The present invention provides benzofurans of Formula I: wherein R1, R2, R3, and L have any of the values defined therefor in the specification, and pharmaceutically acceptable salts thereof, that are useful as agents in the treatment of diseases and conditions, including inflammatory diseases, cardiovascular diseases, and cancers. Also provided are pharmaceutical compositions comprising one or more compounds of Formula I.

    摘要翻译: 本发明提供式I的苯并呋喃:其中R 1,R 2,R 3和L具有本说明书中定义的任何值及其药学上可接受的盐,其可用作 治疗疾病和病症,包括炎性疾病,心血管疾病和癌症。 还提供了包含一种或多种式I化合物的药物组合物。

    4-Phenylamino-quinazolin-6-yl-amides
    3.
    发明申请
    4-Phenylamino-quinazolin-6-yl-amides 有权
    4-苯基氨基 - 喹唑啉-6-基 - 酰胺

    公开(公告)号:US20050250761A1

    公开(公告)日:2005-11-10

    申请号:US11122345

    申请日:2005-05-05

    摘要: This invention provides quinazoline compounds of the formula: wherein: R1 is halo; R2 is H or halo; R3 is a) C1-C3 alkyl, optionally substituted by halo; or b) —(CH2)n-morpholino, —(CH2)n-piperidine, —(CH2)n-piperazine, —(CH2)n—-piperazine-N(C1-C3 alkyl), —(CH2)n-pyrrolidine, or —(CH2)n-imidazole; n is 1 to 4; R4 is —(CH2)m-Het; Het is morpholine, piperidine, piperazine, piperazine-N(C1-C3 alkyl), imidazole, pyrrolidine, azepane, 3,4-dihydro-2H-pyridine, or 3,6-dihydro-2H-pyridine, each optionally substituted by alkyl, halo, OH, NH2, NH(C1-C3 alkyl) or N (C1-C3 alkyl)2; m is 1-3; and X is O, S or NH; or a pharmaceutically acceptable salt thereof, as well as processes and intermediate compounds for making them, useful pharmaceutical compositions and methods of using the compounds in the treatment of proliferative diseases.

    摘要翻译: 本发明提供下式的喹唑啉化合物:其中:R 1是卤素; R 2是H或卤素; R 3是a)任选被卤素取代的C 1 -C 3 - 烷基; 或b) - (CH 2)n - 吗啉代, - (CH 2)n - 哌啶, - (CH 2)n - 哌嗪, - (CH 2)n - 哌嗪-N(C < 或 - (CH 2)n - 吡咯烷,或 - (CH 2)n - 2 N) - 咪唑; n为1〜4; R 4是 - (CH 2 CH 2)m -Het; Het是吗啉,哌啶,哌嗪,哌嗪-N(C 1 -C 3烷基),咪唑,吡咯烷,氮杂环庚烷,3,4-二氢-2H-吡啶, 或3,6-二氢-2H-吡啶,各自任选被烷基,卤素,OH,NH 2,NH(C 1 -C 3) (C 1 -C 6烷基)或N(C 1 -C 3烷基)2。 m为1-3; X为O,S或NH; 或其药学上可接受的盐,以及制备它们的方法和中间体化合物,有用的药物组合物和使用该化合物治疗增殖性疾病的方法。

    Antidiabetic agents
    4.
    发明授权
    Antidiabetic agents 失效
    抗糖尿病药

    公开(公告)号:US06716842B2

    公开(公告)日:2004-04-06

    申请号:US10390465

    申请日:2003-03-17

    IPC分类号: A61K315377

    CPC分类号: C07D413/12 C07D263/32

    摘要: Compounds of formula I: wherein X, E, and R′ have any of the values defined in the specification, and their pharmaceutically acceptable salts, lower blood glucose levels and are useful for treating diseases in mammals such as Non-Insulin Dependent Diabetes Mellitus. Also disclosed are pharmaceutical compositions, processes for preparing compounds of formula (I) and intermediates useful for preparing compounds of formula I.

    摘要翻译: 式I化合物:其中X,E和R'具有说明书中定义的任何值,及其药学上可接受的盐,降低血糖水平,并且可用于治疗哺乳动物如非胰岛素依赖性糖尿病中的疾病。 还公开了药物组合物,制备式(I)化合物的方法和可用于制备式I化合物的中间体。