EFFICIENT INHIBITION OF HUMAN-LEUKOCYTE ELASTASE AND CATHEPSIN-G BY SACCHARIN DERIVATIVES

被引:56
作者
GROUTAS, WC
HOUSERARCHIELD, N
CHONG, LS
VENKATARAMAN, R
EPP, JB
HUANG, H
MCCLENAHAN, JJ
机构
[1] Department of Chemistry, Wichita State University, Wichita
关键词
D O I
10.1021/jm00073a019
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of saccharin derivatives I has been synthesized and evaluated for their inhibitory activity toward human leukocyte elastase and cathepsin G. Most of the compounds were found to be efficient and time-dependent inhibitors of elastase. Inactivated elastase was found to regain its activity almost fully after 24 h (80-90 % activity) and the half-lives of reactivation ranged between 12-15 h. Addition of hydroxylamine to fully-inactivated enzyme led to rapid and complete recovery of enzymatic activity. A tentative mechanism of action is proposed on the basis of biochemical and model studies.
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页码:3178 / 3181
页数:4
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