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基于酶底物特异性的物理化学性质修饰策略III:阿司匹林衍生物的羧肽酶A水解

Physicochemical property modification strategies based on enzyme substrate specificities III: carboxypeptidase A hydrolysis of aspirin derivatives.

作者信息

Banerjee P K, Amidon G L

出版信息

J Pharm Sci. 1981 Dec;70(12):1307-9. doi: 10.1002/jps.2600701204.

Abstract

The aspirin derivatives aspirin phenylalanine and aspirin phenyllactic acid were studied as substrates for carboxypeptidase A. The phenyllactic acid derivative (an ester) was the best substrate but showed considerable product inhibition. The kinetic parameters for both substrates were in the range expected on the basis of other known substrates. The results indicate that the acylamide substituent (drug) has only a small effect on the enzyme kinetic parameters. Consequently, carboxypeptidase A may serve as a reconversion site for many drug derivatives.

摘要

对阿司匹林衍生物阿司匹林苯丙氨酸和阿司匹林苯乳酸作为羧肽酶A的底物进行了研究。苯乳酸衍生物(一种酯)是最佳底物,但表现出相当程度的产物抑制作用。两种底物的动力学参数都在基于其他已知底物预期的范围内。结果表明,酰胺基取代基(药物)对酶动力学参数的影响很小。因此,羧肽酶A可能是许多药物衍生物的再转化位点。

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