Mechanism-based inhibition of human leukocyte elastase and cathepsin G by substituted dihydrouracils

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Authors
Groutas, William C.
Huang, He
Epp, Jeffrey B.
Venkataraman, Radhika
McClenahan, Jerry J.
Tagusagawa, F.
Issue Date
1994-11-29
Type
Article
Language
eng
Keywords
Research Support, U.S. Gov't, P.H.S.
Research Projects
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Abstract

A series of dihydrouracil derivatives has been synthesized and investigated for their in vitro inhibitory activity toward human leukocyte elastase (HLE) and cathepsin G (Cath G). Alkyl [sulfonyl(oxy)] uracils 1-2 were found to be efficient, time-dependent inhibitors of elastase (kobs/[I] M-1 s-1 values ranged between 480 and 8110). These compounds formed acyl enzymes that exhibited variable hydrolytic stability which appeared to be dependent on the nature of the R1 group (believed to be accommodated at the primary specificity site, S1). The acyl enzymes formed with cathepsin G deacylated rapidly, leading to a significant regain of enzymatic activity. In sharp contrast, the corresponding phosphorus compounds 3-4 were found to be potent, time-dependent irreversible inhibitors of HLE. Furthermore, the results of the structure-activity relationship studies suggest that the binding modes of compounds 1-2 and 3-4 may be different.

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Citation
Biochimica et biophysica acta. 1994 Nov 29; 1227(3): 130-6.
Publisher
Elsevier
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ISSN
0006-3002
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