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依那普利对兔肺血管紧张素转换酶的抑制作用。

Inhibition of rabbit lung angiotensin converting enzyme by idrapril.

作者信息

Lippi A, Criscuoli M, Sardelli G, Subissi A

机构信息

Department of Pharmacology, Laboratori Guidotti SpA, Pisa, Italy.

出版信息

Biochem Pharmacol. 1993 Mar 24;45(6):1358-62. doi: 10.1016/0006-2952(93)90291-4.

Abstract

Idrapril, the prototype of a new class of angiotensin converting enzyme (ACE) inhibitors, competitively inhibited, with nanomolar apparent Ki, the hydrolysis of hippuryl-glycyl-glycine by rabbit lung ACE. The pre-steady-state analysis of this tight-binding inhibition showed it to be characterized by slow kinetics, but at variance with what was found for enalaprilat in the same conditions, idrapril appeared to act through a simple, single step mechanism. Kinetic Ki and k(on) and k(off) values were 470 pM, 3.0 +/- 1.5 x 10(6) M-1 sec-1 and 1.4 +/- 0.3 x 10(-3) sec-1, respectively.

摘要

依那普利拉是新型血管紧张素转换酶(ACE)抑制剂的原型,它以纳摩尔级的表观 Ki 值竞争性抑制兔肺 ACE 对马尿酰 - 甘氨酰 - 甘氨酸的水解。这种紧密结合抑制的稳态前分析表明其具有慢动力学特征,但与在相同条件下依那普利拉的情况不同,依那普利拉似乎通过简单的单步机制起作用。动力学 Ki 值以及 k(on) 和 k(off) 值分别为 470 pM、3.0 +/- 1.5 x 10(6) M-1 秒-1 和 1.4 +/- 0.3 x 10(-3) 秒-1。

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