@article{ref1,
title="Functionalized N-aryl azetidinones as novel mechanism-based inhibitors of neutrophil elastase",
journal="FEBS letters",
year="1991",
author="Wakselman, M. and Joyeau, R. and Kobaiter, R. and Boggetto, N. and Vergely, I. and Maillard, J. and Okochi, V. and Montagne, J. J. and Reboud-Ravaux, M.",
volume="282",
number="2",
pages="377-381",
abstract="A functionalized N-aryl azetidinone has been shown to inactivate human leukocyte elastase (HLE) and porcine pancreatic elastase (PPE) by an enzyme-mediated process. The inactivation is characterized by the following kinetic constants at pH 8.0 and 37 degrees C: kinact = 0.035 s-1, KI = 1.2 x 10(-4) M for HLE, 0.08 s-1 and 2.7 x 10(-4) M for PPE, respectively. Two parent molecules devoid of the latent leaving group failed to inactivate HLE and PPE and behaved as substrates of these enzymes. A suicide mechanism is postulated involving the formation of an acyl-enzyme and the simultaneous unmasking of a latent quinonimmonium methide ion which irreversibly reacts with an active site nucleophile. Moreover, the inhibitor is still effective at inhibiting elastase preabsorbed onto elastin.<p /><p>Language: en</p>",
language="en",
issn="0014-5793",
doi="10.1016/0014-5793(91)80517-7",
url="http://dx.doi.org/10.1016/0014-5793(91)80517-7"
}