Abstract
A clickable, affinity-based probe (AfBP), which was modified from staurosporine (a natural product kinase inhibitor), has been synthesized and used in situ for activity-based proteome profiling of potential cellular targets of staurosporine in HepG2 cancer cells.
This journal is © The Royal Society of Chemistry 2011
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Click Chemistry*
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Hep G2 Cells
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Humans
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Molecular Probes / chemical synthesis
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Molecular Probes / chemistry*
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Molecular Probes / metabolism*
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Permeability
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Protein Kinase Inhibitors / metabolism*
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Protein Kinases / metabolism
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Proteomics / methods*
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Staurosporine / metabolism*
Substances
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Molecular Probes
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Protein Kinase Inhibitors
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Protein Kinases
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Staurosporine