Abstract
A novel dioxo-triazine series of cathepsin K inhibitors was identified from HTS. A rapid exploratory programme led to the discovery of potent and selective cathepsin K inhibitors, typified by compound 24 which displayed IC(50) values of 17nM against catK and >10,000nM in catL, catB and catS assays.
Copyright 2010 Elsevier Ltd. All rights reserved.
MeSH terms
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Binding Sites
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Catalytic Domain
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Cathepsin K / antagonists & inhibitors*
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Cathepsin K / metabolism
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Crystallography, X-Ray
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Cysteine Proteinase Inhibitors / chemical synthesis
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Cysteine Proteinase Inhibitors / chemistry*
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Cysteine Proteinase Inhibitors / pharmacology
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High-Throughput Screening Assays
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Humans
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Structure-Activity Relationship
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Triazines / chemical synthesis
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Triazines / chemistry*
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Triazines / pharmacology
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Uracil / analogs & derivatives
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Uracil / chemical synthesis
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Uracil / chemistry
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Uracil / pharmacology
Substances
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Cysteine Proteinase Inhibitors
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Triazines
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Uracil
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Cathepsin K