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
AstraZeneca, Mereside, Alderley Park, Macclesfield, Cheshire SK10 4TG, United Kingdom.
J Med Chem. 2009 Mar 26;52(6):1558-68. doi: 10.1021/jm801507v.
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.
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。