CHEMICAL DESIGN OF CILAZAPRIL

被引：8

作者：

ATTWOOD, MR

机构：

来源：

BRITISH JOURNAL OF CLINICAL PHARMACOLOGY | 1989年 / 27卷

关键词：

D O I：

10.1111/j.1365-2125.1989.tb03474.x

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

引用

页码：S133 / S137

页数：5

共 9 条

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[2]

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[4]

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[5] STRUCTURE OF A MERCAPTAN THERMOLYSIN COMPLEX ILLUSTRATES MODE OF INHIBITION OF ZINC PROTEASES BY SUBSTRATE-ANALOG MERCAPTANS [J].

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[6] BINDING OF N-CARBOXYMETHYL DIPEPTIDE INHIBITORS TO THERMOLYSIN DETERMINED BY X-RAY CRYSTALLOGRAPHY - A NOVEL CLASS OF TRANSITION-STATE ANALOGS FOR ZINC PEPTIDASES [J].

MONZINGO, AF ;

MATTHEWS, BW .

BIOCHEMISTRY, 1984, 23 (24) :5724-5729

[7] DESIGN OF SPECIFIC INHIBITORS OF ANGIOTENSIN-CONVERTING ENZYME - NEW CLASS OF ORALLY ACTIVE ANTIHYPERTENSIVE AGENTS [J].

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[8]

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[9] THE EXISTENCE OF 2 FORMS OF HYPERTENSIN [J].

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