Ortho-substituted benzoic acid derivatives for the treatment of insulin resistance
    6.
    发明授权
    Ortho-substituted benzoic acid derivatives for the treatment of insulin resistance 失效
    正离子取代的苯甲酸衍生物用于治疗胰岛素抵抗

    公开(公告)号:US07351858B2

    公开(公告)日:2008-04-01

    申请号:US10519376

    申请日:2003-06-17

    申请人: Lanna Li

    发明人: Lanna Li

    IPC分类号: C07C229/00 A61K31/195

    CPC分类号: C07C235/20

    摘要: The present invention provides a compound of formula (I), wherein n is 0, 1 or 2; R1 represents halo, a C1-4alkyl group which is optionally substituted by one or more fluoro, a C1-4alkoxy group which is optionally substituted by one or more fluoro and wherein when n is 2 the substituents R1 may be the same or different; R2 represents an unbranched C2-7alkyl group; R3 represents H or OCH3; and W represents O or S and pharmaceutically acceptable salts and prodrugs thereof, to processes for preparing such compounds, to their utility in treating clinical conditions associated with insulin resistance, to methods for their therapeutic use and to pharmaceutical compositions containing them.

    摘要翻译: 本发明提供式(I)化合物,其中n为0,1或2; R 1表示卤素,任选被一个或多个氟C 1-4烷氧基取代的C 1-4烷基, 其任选被一个或多个氟取代,并且其中当n为2时,取代基R 1可以相同或不同; R 2表示无支链的C 2-7烷基; R 3表示H或OCH 3; W表示O或S及其药学上可接受的盐和前药,用于制备此类化合物的方法,用于治疗与胰岛素抵抗相关的临床病症,其治疗用途的方法和含有它们的药物组合物。

    Ortho-substituted benzoic acid derivatives for the treatment of insulin resistance
    8.
    发明申请
    Ortho-substituted benzoic acid derivatives for the treatment of insulin resistance 失效
    正离子取代的苯甲酸衍生物用于治疗胰岛素抵抗

    公开(公告)号:US20050222261A1

    公开(公告)日:2005-10-06

    申请号:US10519376

    申请日:2003-06-17

    申请人: Lanna Li

    发明人: Lanna Li

    CPC分类号: C07C235/20

    摘要: The present invention provides a compound of formula (I), wherein n is 0, 1 or 2; R1 represents halo, a C1-4alkyl group which is optionally substituted by one or more fluoro, a C1-4alkoxy group which is optionally substituted by one or more fluoro and wherein when n is 2 the substituents R1 may be the same or different; R2 represents an unbranched C2-7alkyl group; R3 represents H or OCH3; and W represents O or S and pharmaceutically acceptable salts and prodrugs thereof, to processes for preparing such compounds, to their utility in treating clinical conditions associated with insulin resistance, to methods for their therapeutic use and to pharmaceutical compositions containing them.

    摘要翻译: 本发明提供式(I)化合物,其中n为0,1或2; R 1表示卤素,任选被一个或多个氟C 1-4烷氧基取代的C 1-4烷基, 其任选被一个或多个氟取代,并且其中当n为2时,取代基R 1可以相同或不同; R 2表示无支链的C 2-7烷基; R 3表示H或OCH 3; W表示O或S及其药学上可接受的盐和前药,用于制备此类化合物的方法,用于治疗与胰岛素抵抗相关的临床病症,其治疗用途的方法和含有它们的药物组合物。

    5-Thioxo-1,5-Dihydro-2H-Pyrrol-2-One Derivatives As Liver X Receptor Modulators
    10.
    发明申请
    5-Thioxo-1,5-Dihydro-2H-Pyrrol-2-One Derivatives As Liver X Receptor Modulators 审中-公开
    5-硫代-1,5-二氢-2H-吡咯-2-酮衍生物作为肝X受体调节剂

    公开(公告)号:US20080255207A1

    公开(公告)日:2008-10-16

    申请号:US11813467

    申请日:2006-01-09

    申请人: Patrik Holm Lanna Li

    发明人: Patrik Holm Lanna Li

    IPC分类号: A61K31/4439 C07D401/12

    摘要: The present invention relates to certain novel compounds of the Formula (I) to processes for preparing such compounds, to their the utility in modulation of nuclear hormone receptors Liver X Receptor (LXR) α(NR1H3) and/or β(NR1H2) and in treating clinical conditions including cardiovascular diseases such as atherosclerosis; inflammatory diseases, Alzheimer's disease, lipid disorders (dyslipidemias) whether or not associated with insulin resistance, type 2 diabetes and other manifestations of the metabolic syndrome, to methods for their therapeutic use and to pharmaceutical compositions containing them.

    摘要翻译: 本发明涉及式(I)的某些新型化合物,用于制备这些化合物,用于调节核激素受体肝X受体(LXR)α(NR1H3)和/或β(NR1H2)和在 治疗包括心血管疾病如动脉粥样硬化的临床病症; 炎性疾病,阿尔茨海默病,与胰岛素抵抗相关的脂质紊乱(血脂异常),2型糖尿病和代谢综合征的其他表现,其治疗用途的方法和含有它们的药物组合物。