Novel Orally Active Analgesic and Anti-Inflammatory Cyclohexyl-N-Acylhydrazone Derivatives
作者:Tiago Fernandes Silva、Walfrido Bispo Júnior、Magna Suzana Alexandre-Moreira、Fanny Nascimento Costa、Carlos Monteiro、Fabio Furlan Ferreira、Regina Cely Rodrigues Barroso、François Noël、Roberto Takashi Sudo、Gisele Zapata-Sudo、Lídia Moreira Lima、Eliezer Barreiro
DOI:10.3390/molecules20023067
日期:——
representing a new class of cycloalkyl analogues. Compounds 10–26 and their conformationally restricted analogue 9 were synthetized and evaluated as analgesic and anti-inflammatory agents in classical pharmacologic protocols. The cyclohexyl-N-acylhydrazones 10–26 and the cyclohexenyl analogue 9 showed great anti-inflammatory and/or analgesic activities, but compound 13 stood out as a new prototype to
N-酰基腙 (NAH) 部分被认为是一种特权结构,存在于许多具有不同药理活性的化合物中。在归因于 NAH 衍生物的活动中,抗炎和镇痛的活动是反复出现的。作为旨在设计新型镇痛和抗炎先导候选药物的研究计划的一部分,一系列环己基-N-酰基腙 10-26 是从原型 LASSBio-294 的分子修饰结构设计的,代表了一类新的环烷基类似物。化合物 10-26 及其构象限制类似物 9 被合成并评估为经典药理学方案中的镇痛和抗炎剂。环己基-N-酰基腙10-26和环己烯基类似物9显示出很好的抗炎和/或镇痛活性,