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取代的2-[(4-氨甲基)苯氧基]-2-甲基丙酸PPARα激动剂。1. 新型强效高密度脂蛋白胆固醇升高剂系列的发现。

Substituted 2-[(4-aminomethyl)phenoxy]-2-methylpropionic acid PPARalpha agonists. 1. Discovery of a novel series of potent HDLc raising agents.

作者信息

Sierra Michael L, Beneton Véronique, Boullay Anne-Bénédict, Boyer Thierry, Brewster Andrew G, Donche Frédéric, Forest Marie-Claire, Fouchet Marie-Hélène, Gellibert Françoise J, Grillot Didier A, Lambert Millard H, Laroze Alain, Le Grumelec Christelle, Linget Jean Michel, Montana Valerie G, Nguyen Van-Loc, Nicodème Edwige, Patel Vipul, Penfornis Annie, Pineau Olivier, Pohin Danig, Potvain Florent, Poulain Géraldine, Ruault Cécile Bertho, Saunders Michael, Toum Jérôme, Xu H Eric, Xu Robert X, Pianetti Pascal M

机构信息

Department of Medicinal Chemistry, Laboratoire GlaxoSmithKline, Centre de Recherches, 25-27 avenue du Québec, 91951 Les Ulis, France, USA.

出版信息

J Med Chem. 2007 Feb 22;50(4):685-95. doi: 10.1021/jm058056x. Epub 2007 Jan 23.

Abstract

The peroxisome proliferator activated receptors PPARalpha, PPARgamma, and PPARdelta are ligand-activated transcription factors that play a key role in lipid homeostasis. The fibrates raise circulating levels of high-density lipoprotein cholesterol and lower levels of triglycerides in part through their activity as PPARalpha agonists; however, the low potency and restricted selectivity of the fibrates may limit their efficacy, and it would be desirable to develop more potent and selective PPARalpha agonists. Modification of the selective PPARdelta agonist 1 (GW501516) so as to incorporate the 2-aryl-2-methylpropionic acid group of the fibrates led to a marked shift in potency and selectivity toward PPARalpha agonism. Optimization of the series gave 25a, which shows EC50 = 4 nM on PPARalpha and at least 500-fold selectivity versus PPARdelta and PPARgamma. Compound 25a (GW590735) has been progressed to clinical trials for the treatment of diseases of lipid imbalance.

摘要

过氧化物酶体增殖物激活受体PPARα、PPARγ和PPARδ是配体激活的转录因子,在脂质稳态中起关键作用。贝特类药物部分通过作为PPARα激动剂的活性来提高循环中高密度脂蛋白胆固醇水平并降低甘油三酯水平;然而,贝特类药物的低效性和有限的选择性可能会限制其疗效,因此开发更有效和更具选择性的PPARα激动剂是很有必要的。对选择性PPARδ激动剂1(GW501516)进行修饰,使其并入贝特类药物的2-芳基-2-甲基丙酸基团,导致其效力和对PPARα激动作用的选择性发生显著转变。对该系列进行优化得到了25a,其对PPARα的EC50 = 4 nM,对PPARδ和PPARγ的选择性至少为500倍。化合物25a(GW590735)已进入治疗脂质失衡疾病的临床试验阶段。

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