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新型喹唑啉衍生物的合成及其支气管扩张活性

Synthesis and bronchodilator activity of new quinazolin derivative.

作者信息

Zabeer A, Bhagat A, Gupta O P, Singh G D, Youssouf M S, Dhar K L, Suri O P, Suri K A, Satti N K, Gupta B D, Qazi G N

机构信息

Department of Pharmacology, Regional Research Laboratory (CSIR), Jammu, India.

出版信息

Eur J Med Chem. 2006 Mar;41(3):429-34. doi: 10.1016/j.ejmech.2005.09.010. Epub 2006 Jan 23.

Abstract

Taking lead from a naturally occurring quinazolin vasicine, a number of compounds were developed and evaluated for bronchodilator and anti-allergic activities. One of these compounds was 2,4-diethoxy-6,7,8,9,10,12-hexahydroazepino[2,1-b]quinazolin-12-one, hereinafter named 95-4, exhibited marked bronchodilator activity evaluated on contracted trachea or constricted tracheo-bronchial tree. On intestinal smooth muscle too it showed relaxant effect. Tracheal relaxant effect was not found to be mediated through beta-adrenoceptors. Cumulative dose-response study with acetylcholine and histamine indicated for its non-specific direct effect on smooth muscles. 95-4 was found to be more potent than theophylline and less to that of salbutamol on dose basis. Tested by a number of experimental models, it was found devoid of anti-allergic activity. It was also found to be free from any adverse effect. 95-4 due to its marked bronchial muscle relaxant effect can find use in conditions associated with spasm of bronchial muscles.

摘要

以天然存在的喹唑啉类化合物鸭嘴花碱为先导,开发并评估了多种具有支气管扩张和抗过敏活性的化合物。其中一种化合物是2,4 - 二乙氧基 - 6,7,8,9,10,12 - 六氢氮杂环庚并[2,1 - b]喹唑啉 - 12 - 酮,以下简称95 - 4,在收缩的气管或狭窄的气管 - 支气管树上评估时表现出显著的支气管扩张活性。在肠道平滑肌上它也显示出松弛作用。发现气管松弛作用不是通过β - 肾上腺素能受体介导的。用乙酰胆碱和组胺进行累积剂量 - 反应研究表明其对平滑肌有非特异性直接作用。在剂量基础上发现95 - 4比茶碱更有效,比沙丁胺醇效力稍低。通过多种实验模型测试,发现它没有抗过敏活性。还发现它没有任何不良反应。由于其显著的支气管肌肉松弛作用,95 - 4可用于与支气管肌肉痉挛相关的病症。

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