Synthesis and pharmacological properties of soft drug derivatives related to perhexiline
作者:Gilbert Marciniak、Dominique Decolin、Gerard Leclerc、Nicole Decker、Jean Schwartz
DOI:10.1021/jm00120a007
日期:1988.12
cyclohexylaralkylamines II based on the "soft drug" concept and incorporating an amide function were synthesized. In a preliminary screening, compounds were evaluated for their alpha-adrenolytic activities. Several derivatives, especially N-(cyclohexylphenylmethyl)-2-(cyclohexyl-methylamino)acetamide (3), N-(cyclohexylphenylmethyl)-2-(homoveratrylmethylamino)acetam ide (7), and N-[2-(cyclohexylamino)ethyl]-alpha-
为了减少哌克昔林的毒性,合成了一系列基于“软药物”概念并结合酰胺功能的27种环己基烷基胺II。在初步筛选中,对化合物的α-肾上腺素分解活性进行了评估。几种衍生物,尤其是N-(环己基苯基甲基)-2-(环己基甲基氨基)乙酰胺(3),N-(环己基苯基甲基)-2-(全过甲基甲基氨基)乙酰胺(7)和N- [2-(环己基氨基)乙基] -α-环己基苯乙酰胺(23)在大鼠主动脉条中的体外活性范围与哌己昔林相同。然后研究了这三种分子的体外代谢,并将其与哌己昔林进行了比较。研究了在II上引入各种N-芳烷基胺基对α-肾上腺素解活性的影响。