Evaluation of N-(2-Thienylidene)amines, N-(2-Hydroxybenzylidene)amines and 3-Iminoindolin-2-ones as Antileishmanial Agents
作者:Yasser M.S.A. Al-Kahraman、Girija S. Singh、Masoom Yasinzai
DOI:10.2174/157018011795514221
日期:2011.6.1
The paper describes the synthesis and antileishmanial activity of N-substituted imines, obtained from the reactions of primary amines with three biologically important aldehydes/ketones, thiophene-2-carbaldehyde, 2- hydroxybenzaldehyde (salicylaldehyde) and indoline-2,3-dione. Of the fourteen compounds screened from three classes, five compounds showed significant antileishmanial activity. Among the three classes of imines, the class of N-(2- thienylidene)amines showed much better activity than the other two classes. N-(2-Thienylidene)benzhydrylamine showed IC50 value of 0.51 μg/ml. The effect of substituents on the bioactivity is discussed.
论文描述了通过一级胺与三种生物学上重要的醛/酮(噻吩-2-甲醛、2-羟基苯甲醛(水杨醛)和吲哚啉-2,3-二酮)反应获得的N-取代亚胺的合成及其抗利什曼活性。从三个类别中筛选出的十四个化合物中,有五个显示出显著的抗利什曼活性。在三种亚胺类别中,N-(2-噻吩亚基)胺类显示出比其他两类更好的活性。N-(2-噻吩亚基)二苯甲基胺的IC50值为0.51 μg/ml。讨论了取代基对生物活性的影响。