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Acetylcholinesterase enzyme inhibitor activity of some novel pyrazinamide condensed 1234-tetrahydropyrimidines

机译:某些新型吡嗪酰胺缩合的1234-四氢嘧啶类化合物的乙酰胆碱酯酶酶抑制剂活性

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摘要

A new series of some novel pyrazinamide condensed 1,2,3,4-tetrahydropyrimidines was prepared by reacting of N-(3-oxobutanoyl)pyrazine-2-carboxamide with urea/thiourea and appropriate aldehyde in the presence of catalytic amount of laboratory made p-toluenesulfonic acid as an efficient catalyst. Confirmation of the chemical structure of the synthesized compounds (4a–l) was substantiated by TLC, different spectral data IR, 1H NMR, mass spectra and elemental analysis. The synthesized compounds were evaluated for acetyl and butyl cholinesterase (AChE and BuChE) inhibitor activity. The titled compounds exhibited weak, moderate or high AChE and BuChE inhibitor activity. Especially, compound (4l) showed the best AChE and BuChE inhibitory activity of all the 1,2,3,4-tetrahydropyrimidine derivatives, with an IC50 value of 0.11 μM and 3.4 μM.
机译:在催化量的实验室条件下,通过使N-(3-氧代丁酰基)吡嗪-2-羧酰胺与脲/硫脲和适当的醛反应,制备了一系列新的稠合的1,2,3,4-四氢嘧啶的吡嗪酰胺。对甲苯磺酸是一种有效的催化剂。薄层色谱,不同光谱数据IR, 1 1 H NMR,质谱和元素分析证实了合成化合物(4a-1)的化学结构。评价合成的化合物的乙酰胆碱酯酶和丁基胆碱酯酶(AChE和BuChE)抑制剂的活性。标题化合物表现出弱,中等或高的AChE和BuChE抑制剂活性。特别是化合物(4l)在所有1,2,3,4-四氢嘧啶衍生物中均表现出最好的AChE和BuChE抑制活性,IC50值为0.11μM和3.4μM。

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