Abstract
A new class of inhibitors for cysteine proteases cathepsin B, L, K and S is described. These inhibitors are based on the beta-lactam ring designed to interact with the nucleophilic thiol of the cysteine in the active site of cysteine proteases. Some 3-acylamino-azetidin-2-one derivatives showed very potent inhibition activities for cathepsins L, K and S at the nanomolar or subnanomolar IC(50) values.
MeSH terms
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Azetidines / chemical synthesis*
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Azetidines / pharmacology
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Cathepsin B / antagonists & inhibitors
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Cathepsin K
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Cathepsin L
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Cathepsins / antagonists & inhibitors
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Cysteine Endopeptidases
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Cysteine Proteinase Inhibitors / chemical synthesis*
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Cysteine Proteinase Inhibitors / pharmacology
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Drug Design
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Humans
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Inhibitory Concentration 50
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Lactams / chemistry
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Leukocyte Elastase / antagonists & inhibitors
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Structure-Activity Relationship
Substances
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Azetidines
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Cysteine Proteinase Inhibitors
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Lactams
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Cathepsins
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Leukocyte Elastase
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Cysteine Endopeptidases
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Cathepsin B
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CTSL protein, human
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Cathepsin L
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cathepsin S
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CTSK protein, human
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Cathepsin K