Non-Anilinic Derivatives Of Isothiazol-3(2H)-Thione 1,1-Dioxides As Liver X Receptor Modulators
    2.
    发明申请
    Non-Anilinic Derivatives Of Isothiazol-3(2H)-Thione 1,1-Dioxides As Liver X Receptor Modulators 审中-公开
    异噻唑啉-3(2H) - 二氧化铅的非苯胺衍生物作为肝X受体调节剂

    公开(公告)号:US20080139616A1

    公开(公告)日:2008-06-12

    申请号:US11813458

    申请日:2006-01-09

    CPC分类号: C07D275/03 C07D417/14

    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 and/or preventing 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)的某些新化合物,其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 治疗和/或预防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。

    Non-Anilinic Derivatives of Isothiazol-3(2H)-Thione 1,1-Dioxides As Liver X Receptor Modulators
    5.
    发明申请
    Non-Anilinic Derivatives of Isothiazol-3(2H)-Thione 1,1-Dioxides As Liver X Receptor Modulators 审中-公开
    异噻唑啉-3(2H) - 二氧化硫作为肝X受体调节剂的非苯胺衍生物

    公开(公告)号:US20080319017A2

    公开(公告)日:2008-12-25

    申请号:US11813458

    申请日:2007-07-06

    CPC分类号: C07D275/03 C07D417/14

    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 and/or preventing 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)的某些新化合物,其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 治疗和/或预防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。

    Derivatives of Isothiazol-3(2H)-Thione 1,1-Dioxides as Liver X Receptor Modulators
    6.
    发明申请
    Derivatives of Isothiazol-3(2H)-Thione 1,1-Dioxides as Liver X Receptor Modulators 审中-公开
    作为肝X受体调节剂的异噻唑-3(2H) - 硫酮-1,2-二氧化物的衍生物

    公开(公告)号:US20080125396A1

    公开(公告)日:2008-05-29

    申请号:US11813489

    申请日:2006-01-09

    CPC分类号: C07D275/03

    摘要: The present invention relates to certain novel compounds of 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 and/or preventing 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: 本发明涉及某些新的式(I)化合物,其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)和治疗 和/或预防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。

    Non-Anilinic Derivatives of Isothiazol-3(2H)-Thione 1,1-Dioxides As Liver X Receptor Modulators
    9.
    发明申请
    Non-Anilinic Derivatives of Isothiazol-3(2H)-Thione 1,1-Dioxides As Liver X Receptor Modulators 审中-公开
    异噻唑啉-3(2H) - 二氧化硫作为肝X受体调节剂的非苯胺衍生物

    公开(公告)号:US20090029945A2

    公开(公告)日:2009-01-29

    申请号:US11813489

    申请日:2007-07-06

    CPC分类号: C07D275/03

    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 and/or preventing 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)的某些新化合物,其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 治疗和/或预防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。