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基于 2-联苯乙基咪唑的衍生物的合成及构效关系研究作为肥胖症治疗的囊泡相关膜蛋白 3(BRS-3)激动剂。

Synthesis and SAR of derivatives based on 2-biarylethylimidazole as bombesin receptor subtype-3 (BRS-3) agonists for the treatment of obesity.

机构信息

Department of Medicinal Chemistry, Merck Research Laboratories, PO Box 2000, Rahway, NJ 07065, USA.

出版信息

Bioorg Med Chem Lett. 2010 Apr 1;20(7):2074-7. doi: 10.1016/j.bmcl.2010.02.076. Epub 2010 Feb 21.

Abstract

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.

摘要

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。

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