Inhibition of human leukocyte elastase. 1. Inhibition by C-7-substituted cephalosporin tert-butyl esters

James B. Doherty, Bonnie M. Ashe, Peter L. Barker, Thomas J. Blacklock, John W. Butcher, Gilbert O. Chandler, Mary Ellen Dahlgren, Philip R. Davies, Conrad P. Dorn

Journal of Medicinal Chemistry · 1990 · 73 citations · 0 references

DOIFull text

Open access

Concepts

Abstract

Time-dependent inhibitors of the enzyme human leukocyte elastase have been developed based on the cephem nucleus. A series of cephalosporin tert-butyl esters has been examined, and the activity of these compounds has been found to be very sensitive to C-7 substituents, with small, alpha-oriented, electron-withdrawing groups showing greatest activity. Additionally, the oxidation state of the sulfur atom has been found to play a role in potency, with sulfones showing considerably greater activity than the corresponding sulfides or beta-sulfoxides. The alpha-sulfoxides were inactive.