MECHANISM-BASED ISOCOUMARIN INHIBITORS FOR TRYPSIN AND BLOOD-COAGULATION SERINE PROTEASES - NEW ANTICOAGULANTS

被引：83

作者：

KAM, CM

FUJIKAWA, K

POWERS, JC

机构：

[1] GEORGIA INST TECHNOL,DEPT CHEM,ATLANTA,GA 30332

[2] UNIV WASHINGTON,DEPT BIOCHEM,SEATTLE,WA 98195

来源：

BIOCHEMISTRY | 1988年 / 27卷 / 07期

关键词：

D O I：

10.1021/bi00407a042

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

页码：2547 / 2557

页数：11

共 48 条

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[26] INHIBITION OF HUMAN-LEUKOCYTE ELASTASE, CATHEPSIN-G, CHYMOTRYPSIN-A-ALPHA, AND PORCINE PANCREATIC ELASTASE WITH SUBSTITUTED ISOBENZOFURANONES AND BENZOPYRANDIONES
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[27] MECHANISM-BASED ISOCOUMARIN INHIBITORS FOR TRYPSIN-LIKE SERINE PROTEASES INVOLVED IN BLOOD-COAGULATION
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[29] ACTIVATION OF HUMAN FACTOR-XI (PLASMA THROMBOPLASTIN ANTECEDENT) BY FACTOR-XIIA (ACTIVATED HAGEMAN-FACTOR)
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