N-Acylthiadiazolines, a New Class of Liver X Receptor Agonists with Selectivity for LXRβ
摘要:
We have identified a novel liver X receptor (LXR) agonist (2) that activates the LXR beta subtype with selectivity over LXR alpha. LXR beta selectivity was confirmed using macrophages derived from LXR mutant mice. Despite its selectivity and modest potency, the compound can induce APO-AI-dependent cholesterol efflux from macrophages with full efficacy. Our results indicate that it is possible to achieve significant LXR beta selectivity in a small molecule while maintaining functional LXR activity.
The invention provides compounds, pharmaceutical compositions comprising such compounds and methods of using such compounds to treat or prevent diseases or disorders associated with the activity of liver X receptors (LXRs).
The invention provides compounds, pharmaceutical compositions comprising such compounds and methods of using such compounds to treat or prevent diseases or disorders associated with the activity of liver X receptors (LXRs).
[EN] COMPOUNDS AND COMPOSITIONS AS LXR MODULATORS<br/>[FR] COMPOSES ET COMPOSITIONS CONVENANT COMME MODULATEURS DES LXR
申请人:IRM LLC
公开号:WO2005077124A2
公开(公告)日:2005-08-25
The invention provides compounds, pharmaceutical compositions comprising such compounds and methods of using such compounds to treat or prevent diseases or disorders associated with the activity of liver X receptors (LXRs).