作者:Jason W. Szewczyk、Shaei Huang、Jayne Chin、Jenny Tian、Lyndon Mitnaul、Raymond L. Rosa、Larry Peterson、Carl P. Sparrow、Alan D. Adams
DOI:10.1016/j.bmcl.2006.02.050
日期:2006.6
Counterscreening compounds from a Merck PPAR program discovered lead 1, as a nanomolar LXR/PPAR dual agonist. SAR optimization developed a series of heterocyclic LXR agonists having excellent selectivity over all PPAR isoforms and possessing high LXR affinity and strong in vivo potency. (c) 2006 Elsevier Ltd. All rights reserved.