| Literature DB >> 8691456 |
L Pochet1, C Doucet, M Schynts, N Thierry, N Boggetto, B Pirotte, K Y Jiang, B Masereel, P de Tullio, J Delarge, M Reboud-Ravaux.
Abstract
A series of esters and amides of 6-(chloromethyl)-2-oxo-2H-1-benzopyran-3-carboxylic acid were synthesized and evaluated in vitro for their inhibitory activity toward bovine alpha-chymotrypsin and human leukocyte elastase. Both series behaved as time-dependent inhibitors of alpha-chymotrypsin, but ester-type coumarins were clearly more efficient than the corresponding amides in inactivating the serine proteinase. The best inactivations were observed with "aromatic" esters, in particular with meta-substituted phenyl esters such as m-chlorophenyl 6-(chloromethyl)-2-oxo-2H-1-benzopyran-3-carboxylate, which appears to be one of the most powerful inactivators of alpha-chymotrypsin yet reported (kinact/KI = 760,000 M-1 S-1 at pH 7.5 and 25 degrees C). Usually, the coumarin derivatives failed to inhibit significantly human leukocyte elastase. As a result, the reported series of aromatic coumarinic esters behaves as a new chemical family of selective alpha-chymotrypsin inhibitors.Entities:
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Year: 1996 PMID: 8691456 DOI: 10.1021/jm960090b
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446