S-1 heterocyclic thrombin inhibitors

被引:21
作者
Dominguez, C
Carini, DJ
Weber, PC
Knabb, RM
Alexander, RS
Kettner, CA
Wexler, RR
机构
[1] DuPont Merck Pharmaceutical Company, Experimental Station, Wilmington, DE 19880-0500
[2] Schering Plough Res. Institute, Kenilworth, NJ 07033
关键词
D O I
10.1016/S0960-894X(96)00584-7
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of boropeptides have previously been described by Kettner et al. to be potent thrombin inhibitors. DuP 714 is a representative of this class of compounds with a K-i = 0.040 nM, but this inhibitor has undesireable side effects. New and selective boronic acid thrombin inhibitors have been developed by replacing the guanidine of the boroarginine side chain with various heterocycles ranging in size and basicity. Copyright (C) 1996 Elsevier Science Ltd
引用
收藏
页码:79 / 84
页数:6
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