Synthesis and in vitro evaluation of new azaphenylalanine derivatives as serine protease inhibitors

被引：0

作者：

Obreza, A ^{[1
]}

Stegnar, M ^{[1
]}

Trampus-Bakija, A ^{[1
]}

Prezelj, A ^{[1
]}

Urleb, U ^{[1
]}

机构：

[1] Univ Ljubljana, Fac Pharm, Ljubljana, Slovenia

来源：

PHARMAZIE | 2004年 / 59卷 / 10期

关键词：

D O I：

暂无

中图分类号：

R914 [药物化学];

学科分类号：

100701 ;

摘要：

New inhibitors of serine proteases with azaphenylalanine scaffold were synthesized and their activity was evaluated in vitro. We studied the effect of different substituents in the part of a molecule that binds in the distal pocket of the thrombin active site. Modifications generally led to decreased activity, however two derivatives are promising lead compounds as new thrombin and dual thrombin-factor Xa inhibitors.

引用

页码：739 / 743

页数：5

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