Department of Medicinal Chemistry, Merck Research Laboratories, PO Box 2000, Rahway, NJ 07065, USA.
Bioorg Med Chem Lett. 2010 Apr 1;20(7):2074-7. doi: 10.1016/j.bmcl.2010.02.076. Epub 2010 Feb 21.
This Letter describes a series of potent and selective BRS-3 agonists containing a biarylethylimidazole pharmacophore. Extensive SAR studies were carried out with different aryl substitutions. This work led to the identification of a compound 2-{2-[4-(pyridin-2-yl)phenyl]ethyl}-5-(2,2-dimethylbutyl)-1H-imidazole 9 with excellent binding affinity (IC(50)=18 nM, hBRS-3) and functional agonist activity (EC(50)=47 nM, 99% activation). After oral administration, compound 9 had sufficient exposure in diet induced obese mice to demonstrate efficacy in lowering food intake and body weight via BRS-3 activation.
这封信描述了一系列含有双芳基乙基咪唑药效团的强效和选择性 BRS-3 激动剂。通过不同的芳基取代进行了广泛的 SAR 研究。这项工作导致了一种化合物 2-{2-[4-(吡啶-2-基)苯基]乙基}-5-(2,2-二甲基丁基)-1H-咪唑 9 的鉴定,该化合物具有优异的结合亲和力(IC(50)=18 nM,hBRS-3)和功能激动剂活性(EC(50)=47 nM,99%激活)。口服给予化合物 9 后,在饮食诱导肥胖小鼠中具有足够的暴露量,通过 BRS-3 激活显示出降低食物摄入和体重的功效。