Aryl-substituted tetronic acids, tetramic acids, and cyclic beta-dicarbonyl moieties were evaluated as leaving groups in the peptidyl-COCH2-X type inhibitor iii. Tripeptidyl aspartyl alpha-((tetronoyl)oxy)- and alpha-((tetramoyl)oxy)methyl ketone derivatives demonstrate potent time-dependent inhibition (k(obs)/[T] 100,000-250,000 M(-1)s(-1)) of the cysteine protease ICE. Copyright (C) 1996 Elsevier Science Ltd
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DOLLE, RE
SINGH, J
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SINGH, J
WHIPPLE, D
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OSIFO, IK
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SPEIER, G
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SPEIER, G
GRAYBILL, TL
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GRAYBILL, TL
GREGORY, JS
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HARRIS, AL
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DOLLE, RE
SINGH, J
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SINGH, J
WHIPPLE, D
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OSIFO, IK
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SPEIER, G
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SPEIER, G
GRAYBILL, TL
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GREGORY, JS
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HARRIS, AL
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HELASZEK, CT
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MILLER, RE
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