首页> 外文期刊>Journal of enzyme inhibition and medicinal chemistry. >Syntheses and spectroscopic characterization of some phosphoramidates as reversible inhibitors of human acetylcholinesterase and determination of their potency.
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Syntheses and spectroscopic characterization of some phosphoramidates as reversible inhibitors of human acetylcholinesterase and determination of their potency.

机译:作为人乙酰胆碱酯酶可逆抑制剂的某些氨基磷酸酯的合成和光谱表征及其效力的测定。

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The ability of phosphoramidates Me2NP(O)(Cl)(p-NHC6H4NO2) 1, Me2NP(O)(p-NHC6H4NO2)2 2, (CH3C6H4O-p)P(O)(p-NHC6H4NO2)2 3 and (CH3C6H40-p)2P(O)(p-NHC6H4NO2) 4 to inhibit human acetylcholinesterase (hAChE) has been evaluated by a modified Ellman's method and spectrophotometric measurements. Results showed that compounds 1 and 2 do not have any inhibitory potency, whereas compounds 3 and 4 were reversible mixed inhibitors. The IC50 values for inhibitors 3 and 4 were 0.143 and 0.581 mM, respectively. The previously unknown compounds 3 and 4 were synthesized and characterized by 1H, 13C, 31P NMR and IR spectroscopy and elemental analysis.
机译:氨基磷酸酯Me2NP(O)(Cl)(p-NHC6H4NO2)1,Me2NP(O)(p-NHC6H4NO2)2 2,(CH3C6H4O-p)P(O)(p-NHC6H4NO2)2 3和(CH3C6H40-已通过改良的Ellman方法和分光光度法评估了抑制人乙酰胆碱酯酶(hAChE)的p)2P(O)(p-NHC6H4NO2)4。结果表明,化合物1和2没有任何抑制作用,而化合物3和4是可逆的混合抑制剂。抑制剂3和4的IC50值分别为0.143和0.581 mM。合成了先前未知的化合物3和4,并通过1H,13C,31P NMR和IR光谱及元素分析对其进行了表征。

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