The invention relates to phenyl-1,2,4-oxadiazolone derivatives with phenyl group and to their physiologically acceptable salts and physiologically functional derivatives showing PPARdelta agonist activity.
What are described are compounds of the formula I,
in which the radicals are as defined, and their physiologically acceptable salts and processes for their preparations. 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 demyelinating and other neurodegenerative disorders of the central and peripheral nervous system.
本发明涉及具有苯基的苯基-1,2,4-
噁二唑酮衍
生物及其生理上可接受的盐和生理上功能衍
生物,显示
PPARδ激动剂活性。所描述的是式I的化合物,其中基团如定义所述,以及它们的生理上可接受的盐和它们的制备方法。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
胰岛素抵抗涉及的障碍以及中枢和外周神经系统的脱髓鞘和其他神经退行性疾病。