首页> 外国专利> SUBSTITUTED ARYLALCANOIC ACID DERIVATIVES AS PPAR PAN AGONISTS WITH POTENT ANTIHYPERGLYCEMIC AND ANTIHYPERLIPIDEMIC ACTIVITY

SUBSTITUTED ARYLALCANOIC ACID DERIVATIVES AS PPAR PAN AGONISTS WITH POTENT ANTIHYPERGLYCEMIC AND ANTIHYPERLIPIDEMIC ACTIVITY

机译:取代的芳酸衍生物,具有强的抗高血糖和抗高脂血症活性

摘要

Disclosed is the preparation and pharmaceutical use of substitutedarylalcanoic acid derivatives of Formula I, wherein ring A, ring B, Rl, R2,R3, R4, R5, X, Alkl, Alk2, Arl, and Ar2 are as defined in the specification.These compounds, as selective agonists activating peroxisome proliferator-activated receptors (PPAR), in particularly the RXR/PPARalpha, RXR/PPARgamma,and RXRJPPARdelta heterodimers, are useful in the treatment and/or preventionof type 2 diabetes and associated metabolic syndrome such as hypertension,obesity, insulin resistance, hyperlipidemia, hyperglycemia,hypercholesterolemia, atherosclerosis, coronary artery disease, and othercardiovascular disorders with improved side effects profile commonlyassociated with conventional PPARgamma agonists.
机译:公开了取代的制备和药物用途式I的芳基烷酸衍生物,其中环A,环B,R1,R2,R3,R4,R5,X,Alk1,Alk2,Arl和Ar2如说明书中所定义。这些化合物作为激活过氧化物酶体增殖物的选择性激动剂,激活受体(PPAR),尤其是RXR / PPARalpha,RXR / PPARgamma,和RXRJPPARδ异二聚体,可用于治疗和/或预防2型糖尿病和相关的代谢综合征(例如高血压)肥胖,胰岛素抵抗,高脂血症,高血糖症,高胆固醇血症,动脉粥样硬化,冠状动脉疾病等通常具有改善的副作用的心血管疾病与传统的PPARγ激动剂有关。

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