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二酰甘油酰基转移酶1抑制剂作为抗肥胖和抗糖尿病药物。

DGAT1 inhibitors as anti-obesity and anti-diabetic agents.

作者信息

Birch Alan M, Buckett Linda K, Turnbull Andrew V

机构信息

AstraZeneca plc, Mereside, Alderley Park, Macclesfield, Cheshire, UK.

出版信息

Curr Opin Drug Discov Devel. 2010 Jul;13(4):489-96.

Abstract

Since 2008, significant advances have been made in understanding the role of diacylglycerol acyl transferase-1 (DGAT1) in disease states such as diabetes and obesity. Gene deletion and overexpression studies have provided important new insights into the function of DGAT1, as have the first reports from preclinical models of small-molecule inhibitor effects, which are discussed in this review in relation to the phenotypes of DGAT knockout and overexpression models. The progress of medicinal chemistry efforts has resulted in a new generation of DGAT1 inhibitors that have progressed into clinical development, with the leading compound LCQ-908 (Novartis AG) now in phase II clinical trials. This exciting progress has led researchers to anticipate that an understanding of the human pharmacology of DGAT1 inhibitors, as well as their potential as therapeutic agents for the treatment of diabetes and obesity, will be achieved in the next few years.

摘要

自2008年以来,在了解二酰基甘油酰基转移酶-1(DGAT1)在糖尿病和肥胖等疾病状态中的作用方面取得了重大进展。基因敲除和过表达研究为DGAT1的功能提供了重要的新见解,小分子抑制剂作用的临床前模型的首批报告也是如此,本综述将结合DGAT基因敲除和过表达模型的表型对其进行讨论。药物化学研究的进展产生了新一代已进入临床开发阶段的DGAT1抑制剂,领先化合物LCQ-908(诺华公司)目前正处于II期临床试验阶段。这一令人兴奋的进展使研究人员预计,在未来几年内将实现对DGAT1抑制剂人体药理学及其作为糖尿病和肥胖治疗药物潜力的了解。

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