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AGONISTS OF RECEPTORS ACTIVATED BY PEROXISOMAL PROLIFERATOR

机译:过氧化物酶体增殖剂激活的受体激动剂

摘要

The present invention relates to compounds represented by the following structural formula (I): and their pharmaceutically acceptable salts, solvates and hydrates, where n is 2, 3 or 4 and W is CH, CH (OH), C (O) or O; R1 is unsubstituted or substituted aryl, heteroaryl, cycloalkyl, heterocycloalkyl, arylalkyl, heteroarylalkyl, cycloalkylalkyl or t-butyl; R2 is H, alkyl, haloalkyl or phenyl; Y is unsubstituted or substituted thiophene-2,5-diyl or phenylene; R3 is alkyl or haloalkyl; R4 is a substituted or unsubstituted phenyl, naphthyl, 1,2,3,4-tetrahydronaphthyl, quinolyl, pyridyl, or benzo [1,3] dioxol-5-yl group; and R5 is H, alkyl or aminoalkyl; which are used to modulate a peroxisomal proliferator-activated receptor, in particular for the treatment of diabetes mellitus. The international application was published along with an international search report.
机译:本发明涉及由以下结构式(I)表示的化合物:及其药学上可接受的盐,溶剂化物和水合物,其中n为2、3或4,并且W为CH,CH(OH),C(O)或O ; R1是未取代或取代的芳基,杂芳基,环烷基,杂环烷基,芳基烷基,杂芳基烷基,环烷基烷基或叔丁基; R 2为H,烷基,卤代烷基或苯基; Y为未取代或取代的噻吩-2,5-二基或亚苯基; R3是烷基或卤代烷基; R4是取代或未取代的苯基,萘基,1,2,3,4-四氢萘基,喹啉基,吡啶基或苯并[1,3]二氧杂-5-基; R5为H,烷基或氨基烷基;它们被用于调节过氧化物酶体增殖物激活的受体,特别是用于治疗糖尿病。国际申请与国际检索报告一同发布。

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