Journal of Medicinal Chemistry · 2002 · 63 citations · 13 references
Life SciencesMedicinal ChemistryPharmacologyDrug DiscoveryEnzymologyStructure-activity RelationshipsCaspase ActivationEnzyme InhibitionEnzyme KineticsPeptide Drug DiscoveryProteolytic EnzymesCathepsin ActivityCysteine ProteasesProtease InhibitorsProtease SelectivityRate ConstantsReaction Rate Constants
Aza-peptide epoxides, a new class of irreversible protease inhibitors, are specific for the clan CD cysteine proteases. The inhibitors have second-order rate constants up to 10(5) M(-1) s(-1), with the most potent epoxides having the S,S stereochemistry. The aza-Asn derivatives are effective legumain inhibitors, while the aza-Asp epoxides were specific for caspases. The inhibitors have little or no inhibition with other proteases such as chymotrypsin, papain, or cathepsin B.
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The Handbook of proteolytic enzymes
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Structure and mechanism of interleukin-lβ converting enzyme
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