Suppr超能文献

2-(4-(4-取代苄氧基)-3-甲氧基苄基)-1,4-二氮杂环庚烷-1-基)-N-(4,5-二氢-1-甲基[1,2,4]三唑并[4,3-a]喹啉-7-基)-乙酰胺的合成与正性肌力评价

Synthesis and positive inotropic evaluation of 2-(4-(4-substituted benzyloxy)-3-methoxybenzyl)-1,4-diazepan-1-yl)-N-(4,5-dihydro-1-methyl[1,2,4]triazolo[4,3-a]quinolin-7-yl)-acetamides.

作者信息

Li Jing-Yuan, Cui Xun, Liu Xue-Kun, Hong Lan, Quan Zhe-Shan, Piao Hu-Ri

机构信息

Key Laboratory of Natural Resources and Functional Molecules of Changbai Mountain, Affiliated Ministry of Education, Yanbian University College of Pharmacy, Yanji, Jilin, PR China.

出版信息

Arch Pharm (Weinheim). 2008 Dec;341(12):794-9. doi: 10.1002/ardp.200800132.

Abstract

In an attempt to search for more potent positive inotropic agents, a series of 2-(4-(4-substituted benzyloxy)-3-methoxybenzyl)-1,4-diazepan-1-yl)-N-(4,5-dihydro-1-methyl[1,2,4]triazolo[4,3-a]quinolin-7-yl)acetamides was synthesized and their positive inotropic activities were evaluated by measuring left atrium stroke volume on isolated rabbit-heart preparations. Several compounds showed favorable activity compared with the standard drug Milrinone among which 2-(4-(4-(2-chlorobenzyloxy)-3-methoxybenzyl)-1,4-diazepan-1-yl)-N-(4,5-dihydro-1-methyl-[1,2,4]triazolo[4,3-a]quinolin-7-yl)acetamide 6e was found to have the most desirable potency with the 6.79 +/- 0.18% increased stroke volume (Milrinone: 1.67 +/- 0.64%) at a concentration of 1 x 10(-5) M in our in-vitro study. The chronotropic effects of those compounds having inotropic effects were also evaluated in this work.

摘要

为了寻找更有效的正性肌力药物,合成了一系列2-(4-(4-取代苄氧基)-3-甲氧基苄基)-1,4-二氮杂环庚烷-1-基)-N-(4,5-二氢-1-甲基[1,2,4]三唑并[4,3-a]喹啉-7-基)乙酰胺,并通过测量离体兔心标本的左心房搏出量来评估它们的正性肌力活性。与标准药物米力农相比,几种化合物表现出良好的活性,其中2-(4-(4-(2-氯苄氧基)-3-甲氧基苄基)-1,4-二氮杂环庚烷-1-基)-N-(4,5-二氢-1-甲基-[1,2,4]三唑并[4,3-a]喹啉-7-基)乙酰胺6e在我们的体外研究中,在1×10(-5) M的浓度下具有最理想的效力,使搏出量增加6.79±0.18%(米力农:1.67±0.64%)。在这项工作中还评估了那些具有正性肌力作用的化合物的变时作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验