首页> 外文期刊>Beni-Suef University Journal of Basic and Applied Sciences >Microwave-assisted synthesis, structural activity relationship and biological activity of some new quinoxaline Schiff base derivatives as highly potent spirochete bactericidal agents
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Microwave-assisted synthesis, structural activity relationship and biological activity of some new quinoxaline Schiff base derivatives as highly potent spirochete bactericidal agents

机译:微波辅助合成,一些新的喹喔啉席夫碱衍生物作为高效螺环蛇杀菌剂的结构活性关系和生物活性

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The main aim of this work was to synthesise a new (E)-3-(4-or3-Aminophenylimino) quinoxaline-2(3H)-one oxime Schiff base derivatives and evaluate the anti-leptospiral activity against Leptospira icterohaemorrhagiae. The mentioned derivatives were prepared by performing microwave-assisted condensation reactions of (E)-3-(4-or3-Aminophenyl imino)quinoxaline-2(3H)-one and aromatic aldehydes. The structures of these interesting compounds were characterised by FT-IR, 1H NMR and mass spectroscopy. Furthermore, these compounds were screened for spirocidal activity against Leptospira icterohaemorrhagiae by using in vitro and in vivo method. The anti-leptospiral activity result reveals that most of the compounds were exhibiting considerable activity against Leptospira icterohaemorrhagiae. Compound 6c demonstrated remarkable activity at low concentration against the Leptospira icterohaemorrhagiae as compared to the standard drugs.
机译:这项工作的主要目的是合成一种新的(E)-3-(4-或3-氨基苯基亚氨基)喹喔啉-2(3H)-一种肟席夫碱衍生物,并评估其对钩端螺旋体出血性钩端螺旋体的抗钩体活性。通过进行(E)-3-(4-或3-氨基苯基亚氨基)喹喔啉-2(3H)-一和芳族醛的微波辅助缩合反应来制备上述衍生物。这些有趣的化合物的结构通过FT-IR,1H NMR和质谱进行了表征。此外,通过体外和体内方法筛选了这些化合物对黄腐螺旋体的杀菌活性。抗钩端螺旋体活性的结果表明,大多数化合物都具有抗黄腐螺旋体的显着活性。与标准药物相比,化合物6c在低浓度下表现出了出色的抗钩端螺旋体出血性活性。

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