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儿茶酚氧位甲基转移酶。8. 8-羟基喹啉抑制作用的构效关系。

Catechol O-methyltransferase. 8. Structure-activity relationships for inhibtion by 8-hydroxyquinolines.

作者信息

Borchardt R T, Thakker D R, Warner V D, Mirth D B, Sane J N

出版信息

J Med Chem. 1976 Apr;19(4):558-60. doi: 10.1021/jm00226a025.

Abstract

A series of 5- and 7-substituted 8-hydroxyquinolines was evaluated as inhibitors of catechol O-methyltransferase (COMT, E.C. 2.1.1.6). The electronic character of the substituents in the 5 position appeared to have only a small effect if any on the inhibitory activity of these compounds. A significant factor which contributes to the inhibitory activity of these compounds appears to be the nature of the 7-substituent. The structure-activity relationship for this series of inhibitors is discussed relative to the nature of the enzymatic binding site.

摘要

对一系列5-和7-取代的8-羟基喹啉作为儿茶酚O-甲基转移酶(COMT,E.C. 2.1.1.6)抑制剂进行了评估。5位取代基的电子特性对这些化合物的抑制活性似乎仅有微小影响(若有影响的话)。对这些化合物抑制活性有显著贡献的一个因素似乎是7-取代基的性质。相对于酶结合位点的性质,讨论了该系列抑制剂的构效关系。

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