Several thiazolidinedione derivatives (3-7) were designed and synthesized as candidate thyromimetic drugs. Among them, the dihydrogenated compounds, such as 5-2-[[4-(3-tert-butyl-4-hydroxyphenyl)oxy-3, 5-diiodophenyl]ethyl]-2, 4-thiazolidine-dione (6d) and its 3-isopropyl analog (7b), exhibited potent thyroid hormone receptor α1 (TRα1) activation activity.
我们设计并合成了几种
噻唑烷二酮衍
生物(3-7),作为甲状腺仿生药物的候选药物。其中,5-2-[[4-(3-叔丁基-
4-羟基苯基)氧基-3,5-二
碘苯基]乙基]-2,4-
噻唑烷二酮(6d)及其 3-异丙基类似物(7b)等二氢化化合物表现出了强大的甲状腺激素受体 α1(TRα1)激活活性。