Synthesis and preliminary pharmacological screening of novel imidazo[2,1-f]theophylline derivatives
作者:Maciej Pawłowski、Jacek Katlabi、Sławomir Jurczyk、Danuta Malec、Jerzy Modzelewski
DOI:10.1016/s0014-827x(02)01224-7
日期:2002.9
The three different kinds of imidazo[2,1-f]theophylline derivatives were synthesized and tested for their CNS activity. A series of alkoxy-alkylamides and amino-alkylamides with basic function, derived from 8-benzyl-6,7-dihydroimidazo[2,1-f]theophylline-7-carboxylic acid showed stimulating influence on CNS as they increased the locomotor activity (compound 8 and 10) or enhanced amphetamine and apomorphine
合成了三种不同的咪唑并[2,1-f]茶碱衍生物,并测试了它们的中枢神经系统活性。衍生自8-苄基-6,7-二氢咪唑并[2,1-f]茶碱-7-羧酸的一系列具有基本功能的烷氧基烷基酰胺和氨基烷基酰胺对中枢神经系统有刺激作用,因为它们增加了运动活性(化合物8和10)或增强的苯丙胺和阿扑吗啡对小鼠的作用(化合物3、4和9)。在戊四唑试验中,化合物1、5、8-10和12具有抗惊厥活性;具有带碘化咪唑-7-on环(内酰胺结构)的12个具有镇静作用和抗血清素作用。