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S-取代谷胱甘肽对乙二醛酶抑制作用的定量构效关系

QSAR of the inhibition of glyoxalase by S-substituted glutathiones.

作者信息

Silipo C, Hansch C

出版信息

Farmaco Sci. 1979 Jan;34(1):3-10.

PMID:553818
Abstract

A quantitative structure-activity relationship (QSAR) has been formulated for the inhibition of glyoxalase I from yeast by 37 S-substituted glutathiones: log 1/C = 1.23 pi' + 1.20 MR4 - 0.67 I1 - 0.14 pi'2 + 1.85 C in this expression is the molar concentration of inhibitor producing 50% inhibition, pi' is the usual hydrophobic parameter modified for certain substituents, MR4 is the molar refractivity of certain p-phenyl substituents, and I1 is an indicator variable for those congeners with an acetylated alpha-amino group. This equation should be of help in the design of more effective inhibitors which may be of value in cancer chemotherapy.

摘要

已针对37种S-取代谷胱甘肽对酵母乙二醛酶I的抑制作用建立了定量构效关系(QSAR):log 1/C = 1.23π'+ 1.20 MR4 - 0.67 I1 - 0.14π'² + 1.85 在此表达式中,C是产生50%抑制作用的抑制剂的摩尔浓度,π'是针对某些取代基修正的常用疏水参数,MR4是某些对苯基取代基的摩尔折射度,I1是具有乙酰化α-氨基的同系物的指示变量。该方程应有助于设计更有效的抑制剂,这在癌症化疗中可能具有价值。

相似文献

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Inhibition of glyoxalase I by new squaric acid derivatives.
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