Synthesis and antifungal activities in vitro of novel pyrazino [2,1-a] isoquinolin derivatives
作者:Hui Tang、Canhui Zheng、Jiaguo Lv、Juan Wu、Yanan Li、Hui Yang、Bingyue Fu、Chuntong Li、Youjun Zhou、Ju Zhu
DOI:10.1016/j.bmcl.2009.12.050
日期:2010.2
A series of novel pyrazino[2,1-a]isoquinolin compounds were designed and synthesized, and their antifungal activities in vitro were evaluated. The results showed that all of the compounds exhibited antifungal activities. Some of them exhibited stronger antifungal activities than that of lead compounds and among them compound 11b was the most potent one, which showed more potent than that of the active
设计并合成了一系列新颖的吡嗪并[2,1- a ]异喹啉化合物,并对其体外抗真菌活性进行了评价。结果表明,所有化合物均表现出抗真菌活性。它们中的一些表现出比先导化合物更强的抗真菌活性,并且其中化合物11b是最有效的一种,对5种被测真菌中的4种,其显示出比活性对照氟康唑更强的抗真菌活性。本文介绍的研究为新型抗真菌剂的开发提供了一种新的结构类型。