Abstract
Until now, a lack of inhibitors with high potency and selectivity in vivo has hampered investigation of the p38 mitogen-activated protein kinase (MAPK) signaling pathway. We describe the design of skepinone-L, which is, to our knowledge, the first ATP-competitive p38 MAPK inhibitor with excellent in vivo efficacy and selectivity. Therefore, skepinone-L is a valuable probe for chemical biology research, and it may foster the development of a unique class of kinase inhibitors.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adenosine Triphosphate
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Animals
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Binding, Competitive
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Dibenzocycloheptenes / chemistry*
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Drug Design
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Mice
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Models, Molecular
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Protein Interaction Domains and Motifs
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Protein Kinase Inhibitors / chemistry*
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p38 Mitogen-Activated Protein Kinases / antagonists & inhibitors*
Substances
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Dibenzocycloheptenes
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Protein Kinase Inhibitors
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skepinone-L
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Adenosine Triphosphate
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p38 Mitogen-Activated Protein Kinases
Associated data
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PDB/3QUE
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PDB/3ZYA
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PubChem-Substance/131287876
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PubChem-Substance/131287877
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PubChem-Substance/131287878
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PubChem-Substance/131287879
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PubChem-Substance/131287880
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PubChem-Substance/131287881
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PubChem-Substance/131287882
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PubChem-Substance/131287883
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PubChem-Substance/131287884
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PubChem-Substance/131287885
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PubChem-Substance/131287886
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PubChem-Substance/131287887
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PubChem-Substance/131287888