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Efficient inhibition of human leukocyte elastase and cathepsin G by saccharin derivatives.

作者信息

Groutas W C, Houser-Archield N, Chong L S, Venkataraman R, Epp J B, Huang H, McClenahan J J

机构信息

Department of Chemistry, Wichita State University, Kansas 67260.

出版信息

J Med Chem. 1993 Oct 15;36(21):3178-81. doi: 10.1021/jm00073a019.

Abstract

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.

摘要

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