首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis, molecular docking and biological evaluation of Schiff base transition metal complexes as potential urease inhibitors.
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Synthesis, molecular docking and biological evaluation of Schiff base transition metal complexes as potential urease inhibitors.

机译:席夫碱过渡金属配合物作为潜在脲酶抑制剂的合成,分子对接和生物学评估。

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摘要

Six transition metal compounds of Schiff base ligands were evaluated for the inhibitory activity on jack bean urease, of which compounds 2-6 were determined by single crystal X-ray analysis. It was found that copper(II) complexes 1 and 4 showed strong inhibitory activity against jack bean urease (IC(50) = 0.52 and 0.46 microM), compared with acetohydroxamic acid (IC(50) = 42.12 microM) as a positive reference. Cobalt(II), nickel(II) and zinc(II) compounds also exhibited potent inhibitory activity (IC(50) = 3.88-25.20 microM). A docking analysis using the AUTODOCK 4.0 program could explain the inhibitory activities of 1 and 4 against urease.
机译:评价了六种席夫碱配体的过渡金属化合物对波克豆脲酶的抑制活性,其中化合物2-6通过单晶X射线分析确定。发现铜(II)配合物1和4对菜豆脲酶(IC(50)= 0.52和0.46 microM)表现出强抑制活性,而乙酰氧肟酸(IC(50)= 42.12 microM)则为阳性参考。钴(II),镍(II)和锌(II)化合物也显示出有效的抑制活性(IC(50)= 3.88-25.20 microM)。使用AUTODOCK 4.0程序进行的对接分析可以解释1和4对脲酶的抑制活性。

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