Non-anilinic derivatives of isothiazol-3(2H)-one 1,1-dioxides as liver X receptor modulators
申请人:AstraZeneca AB
公开号:US07960380B2
公开(公告)日:2011-06-14
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.
本发明涉及某些新型化合物(I)的公式,以制备这些化合物的过程,以及它们在调节核激素受体肝X受体(LXR)α (NR1H3)和/或β (NR1H2)以及治疗和/或预防包括心血管疾病(如动脉粥样硬化)、炎症性疾病、阿尔茨海默病、脂质紊乱(无论是否与胰岛素抵抗有关)、2型糖尿病和代谢综合征的其他表现在内的临床病症方面的用途,以及它们的治疗用途的方法和含有它们的制药组合物。