文章基本信息

标题：Synthesis and pharmacological investigation of novel 4-(3-ethylphenyl)-1-substituted-4H-[1,2,4]triazolo[4,3-a] quinazolin-5-ones as a new class of H1-antihistaminic agents
本地全文：下载
作者：VEERACHAMY ALAGARSAMY ; KUNCHU KAVITHA ; MANI RUPESHKUMAR 等
期刊名称：Acta Pharmaceutica
电子版ISSN：1846-9558
出版年度：2009
卷号：59
期号：1
页码：97-106
DOI：10.2478/v10007-009-0003-1
语种：English
出版社：Sciendo
摘要：A series of novel 4-(3-ethylphenyl)-1-substituted-4H-[1,2,4] triazolo[4,3-a]quinazolin-5-ones (4a-j) were synthesized by the cyclization of 3-(3-ethylphenyl)-2-hydrazino-3H- -quinazolin-4-one (3) with various one-carbon donors.The starting material,compound 3,was synthesized from 3-ethyl aniline by a new innovative route with improved yield.When tested for their in vivo H1-antihistaminic activity on conscious guinea pigs,all test compounds protected the animals from histamine induced bronchospasm significantly.Compound 4-(3-ethylphenyl)-1-methyl-4H - -[1,2,4]triazolo[4,3-a]quinazolin-5-one (4b) emerged as the most active compound of the series and it is more potent (74.6 % protection) compared to the reference standard chlorpheniramine maleate (71 % protection).Compound 4b shows negligible sedation (10 %) compared to chlorpheniramine maleate (30 %).Therefore compound 4b can serve as the leading compound for further development of a new class of H1-antihistamines.
关键词：quinazolin-5-ones;sedation;H1-antihistaminic agents