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首页> 外文期刊>RSC Advances >Malononitrile-activated synthesis and anti-cholinesterase activity of styrylquinoxalin-2(1H)-ones
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Malononitrile-activated synthesis and anti-cholinesterase activity of styrylquinoxalin-2(1H)-ones

机译:Styrylquinoxalin-2(1H)-2(1H) - 酮的丙二腈活化合成和抗胆碱酯酶活性

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摘要

Herein, we report a base-free malononitrile activated condensation of 3-methylquinoxaline-2(1H)-one (3MQ) 1 with aryl aldehydes 3a-3ad for synthesis of styrylquinoxalin-2(1H)-ones (SQs) 4a-4ad with excellent yields. In this reaction, malononitrile activates the aldehyde via Knoevenagel condensation towards reaction with 3MQ 1 and gets liberated during the course of reaction to yield the desired SQs 4a-4ad. The SQs were evaluated for in vitro cholinesterase inhibition and 4n was found to display a mixed type of inhibition of AChE, which was supported by molecular modelling studies. This study has led to the discovery of a new chemotype for cholinesterase inhibition which might be useful in finding a remedy for Alzheimer's disease.
机译:在此,我们通过芳基醛3A-3AD报告3-甲基喹喔啉-2(1H)-ONE(3MQ)1的无基丙二腈活化缩合,用于合成芳烯酮-2(1H) - 4A-4AD 优异的产量。 在该反应中,丙二腈通过Knoevenagel缩合与3MQ 1反应激活醛并在反应过程中释放,得到所需的SQS 4a-4Ad。 评估SQS的体外胆碱酯酶抑制作用,4N被发现显示出疼痛的混合类型,这是通过分子建模研究的支持。 该研究导致对胆碱酯酶抑制的新趋化型发现,这可能是用于寻找阿尔茨海默病的补救措施。

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