Comparison of the hypolipidemic activity of cyclic vs. acyclic imides
作者:P. Josee Voorstad、J. M. Chapman、G. H. Cocolas、S. D. Wyrick、Iris H. Hall
DOI:10.1021/jm00379a003
日期:1985.1
cyclic and acyclic imides were examined for hypolipidemic activity in mice after dosing for 16 days at a dose of 20 mg/kg per day. The hypolipidemic activity of the unsubstituted, N-butyl, N-3-oxobutyl, and N-2-carboxyethyl derivatives of diacetimide and succinimide were compared as well as the unsubstituted and N-substituted dibenzimide and diphenimide. It was shown that an imide functionality incorporated
以每天20 mg / kg的剂量给药16天后,检查了两个系列的氮取代的环状和非环状酰亚胺在小鼠中的降血脂活性。比较了二乙酰亚胺和琥珀酰亚胺的未取代的,N-丁基,N-3-氧丁基和N-2-羧乙基衍生物的降血脂活性,以及未取代的和N-取代的二苯并亚胺和二苯酰亚胺。已经表明,并入环中的酰亚胺官能团对于降胆固醇活性不是必需的。在一系列无环和环状酰亚胺中均观察到良好的降胆固醇活性。但是,环状亚氨基结构是良好的降甘油三酸酯活性的必要条件。当将环状酰亚胺与其各自的非环状同类物进行比较时,注意到甘油三酸酯的活性降低。