Synthesis and in Vitro Evaluation of N-Substituted Maleimide Derivatives as Selective Monoglyceride Lipase Inhibitors
作者:Nicolas Matuszak、Giulio G. Muccioli、Geoffray Labar、Didier M. Lambert
DOI:10.1021/jm900461w
日期:2009.12.10
action is quickly terminated via enzymatic hydrolysis catalyzed by monoglyceride lipase (MGL). Regulating its endogenous level could offer therapeutic opportunities; however, few selective MGL inhibitors have been described so far. Here, we describe the synthesis of N-substituted maleimides and their pharmacological evaluation on the recombinant human fatty acid amide hydrolase (FAAH) and on the purified
内源性大麻素2-花生四烯酸甘油酯(2-AG)在许多生理过程中起着重要作用,其作用通过甘油单酯脂肪酶(MGL)催化的酶促水解迅速终止。调节其内源水平可以提供治疗机会;然而,到目前为止,几乎没有描述选择性的MGL抑制剂。在这里,我们描述了N-取代的马来酰亚胺的合成及其对重组人脂肪酸酰胺水解酶(FAAH)和纯化人MGL的药理评价。先前已经描述了一些N-芳基马来酰亚胺(萨里奥(SM);萨洛(OM);Nevalainen,T .;Poso,A。莱蒂宁(JT);贾文恩(T. Jarvinen)Niemi,R.大鼠小脑膜中2-花生四烯酸甘油水解酶中巯基敏感位点的表征。化学 生物学 2005年,12,649-656),为MGL抑制剂,以及沿着这些线路,我们提出一组新的马来酰亚胺衍生物的那显示出低微摩尔的IC 50和朝向MGL VS FAAH高选择性。然后,研究了结构活性关系,例如,1-biphenyl-4