Abstract
Biochemical and structural studies provide information on the mode of action of FGF401 as a selective, reversible covalent inhibitor of FGFR4. Kinase and proliferation assays reveal that FGF401 has the ability to overcome gatekeeper mutations in FGFR4.
MeSH terms
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Amino Acid Sequence
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Animals
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Cell Line, Transformed
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Cell Proliferation / drug effects
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Humans
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Inhibitory Concentration 50
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Mass Spectrometry
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Mutation
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Piperazines / pharmacology*
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Protein Kinase Inhibitors / pharmacology
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Pyridines / pharmacology*
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Receptor, Fibroblast Growth Factor, Type 4 / antagonists & inhibitors*
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Receptor, Fibroblast Growth Factor, Type 4 / chemistry
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Receptor, Fibroblast Growth Factor, Type 4 / genetics
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Sequence Homology, Amino Acid
Substances
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Piperazines
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Protein Kinase Inhibitors
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Pyridines
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FGFR4 protein, human
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Receptor, Fibroblast Growth Factor, Type 4
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roblitinib