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发现一种强效、选择性且口服有效的嘧啶并恶嗪基双环辛烷乙酸二酰甘油酰基转移酶-1抑制剂。

Discovery of a potent, selective, and orally efficacious pyrimidinooxazinyl bicyclooctaneacetic acid diacylglycerol acyltransferase-1 inhibitor.

作者信息

Birch Alan M, Birtles Susan, Buckett Linda K, Kemmitt Paul D, Smith Graham J, Smith Tim J D, Turnbull Andrew V, Wang Steven J Y

机构信息

AstraZeneca, Mereside, Alderley Park, Macclesfield, Cheshire SK10 4TG, United Kingdom.

出版信息

J Med Chem. 2009 Mar 26;52(6):1558-68. doi: 10.1021/jm801507v.

Abstract

Inhibition of DGAT-1 is increasingly seen as an attractive mechanism with the potential for treatment of obesity and other elements of the metabolic syndrome. We report here a bicyclooctaneacetic acid derivative in the pyrimidinooxazine structural class of DGAT-1 inhibitors that has good potency, selectivity, and pharmacokinetic characteristics across a variety of species. This compound is an effective inhibitor of DGAT-1 in both intestinal and adipose tissue, which results in a reduction in body weight or body weight gain following oral administration in both mouse and rat models of dietary-induced obesity.

摘要

抑制二酰甘油酰基转移酶-1(DGAT-1)越来越被视为一种有吸引力的机制,具有治疗肥胖症和代谢综合征其他方面的潜力。我们在此报告一种嘧啶并恶嗪结构类的DGAT-1抑制剂中的双环辛烷乙酸衍生物,它在多种物种中具有良好的效力、选择性和药代动力学特征。该化合物在肠道和脂肪组织中都是有效的DGAT-1抑制剂,在饮食诱导肥胖的小鼠和大鼠模型中口服给药后,会导致体重减轻或体重增加减少。

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