The present invention comprises phenyl and pyridinyl 1,2,4-oxadiazolone compounds their physiologically acceptable salts and physiologically functional derivatives that exhibit peroxisome proliferator activator receptor (PPAR) delta agonist activity. Also described and claimed are processes for their preparation and their use as pharmaceuticals. These are compounds of formula I,
in which the R-group substituents are defined herein. The compounds are suitable for the treatment and/or prevention of disorders of fatty acid metabolism and glucose utilization disorders as well as of disorders in which insulin resistance is involved and de-myelinating and other neurodegenerative disorders of the central and peripheral nervous system.
本发明涉及苯基和
吡啶基1,2,4-
噁二唑酮化合物及其生理上可接受的盐和生理功能衍
生物,其表现出
过氧化物酶体增殖物激活受体(
PPAR)δ激动剂活性。还描述和声明了它们的制备过程以及它们作为药物的用途。这些化合物的
化学式为I,其中R基取代基在此定义。这些化合物适用于治疗和/或预防
脂肪酸代谢障碍和
葡萄糖利用障碍以及
胰岛素抵抗涉及的疾病,以及中枢和外周神经系统的去髓鞘和其他神经退行性疾病。