[EN] QUINOXALINE-BASED LXR MODULATORS<br/>[FR] MODULATEURS DE LXR À BASE DE QUINOXALINE
申请人:WYETH LLC
公开号:WO2010054229A1
公开(公告)日:2010-05-14
Disclosed are quinoxaline-based modulators of Liver X receptors (LXRs) and related methods. The modulators include compounds of formula (I): wherein: each of L1 and L2 is, independently, a bond, -O- or -NH-; R2 is C6-C10 aryl or heteroaryl including 5-10 ring atoms, each of which is (i) substituted with 1 R9, and (ii) optionally further substituted with from 1-4 Re; and each of R4 and R5 is, independently (i) hydrogen; or (ii) halo; or (iii) C1-C6 alkyl or C1-C6 haloalkyl, each of which is optionally substituted with from 1-3 Ra; and R1, R3, R6, R9, Ra and Re are defined herein. In general, these compounds can be used for treating or preventing one or more diseases, disorders, conditions or symptoms mediated by LXRs.
本发明涉及基于喹哚醌的肝X受体(LXR)调节剂及相关方法。这些调节剂包括式(I)的化合物:其中:L1和L2中的每一个独立地是一个键,-O-或-NH-;R2是C6-C10芳基或杂环芳基,包括5-10个环原子,每个原子(i)被1个R9取代,并且(ii)可以进一步选择地被1-4个Re取代;R4和R5中的每一个独立地是(i)氢;或(ii)卤素;或(iii)C1-C6烷基或C1-C6卤代烷基,每一个取代基可以选择地被1-3个Ra取代;R1、R3、R6、R9、Ra和Re在此定义。一般来说,这些化合物可用于治疗或预防LXR介导的一种或多种疾病、障碍、症状或条件。