Publication | Open Access
Discovery of a Highly Potent and Selective MEK Inhibitor: GSK1120212 (JTP-74057 DMSO Solvate)
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References
2011
Year
Chemoprevention StrategySelective Mek InhibitorNew GenerationChemical BiologyTumor BiologyMolecular PharmacologyMedicinal ChemistryReceptor Tyrosine KinaseHighly PotentAnti-cancer AgentRadiation OncologyCell SignalingInhibitory ActivityCancer ResearchBiochemistryLead Compound 2Mechanism Of ActionJtp-74057 Dmso SolvateTumor TargetingPharmacologyTumor MicroenvironmentNatural SciencesMedicineCellular Mek InhibitionDrug Discovery
Inhibition of mitogen-activated protein kinase/extracellular signal-regulated kinase kinase (MEK) represents a promising strategy for the discovery of a new generation of anticancer chemotherapeutics. Our synthetic efforts, beginning from the lead compound 2, were directed at improving antiproliferative activity against cancer cells as well as various drug properties. These efforts led to the discovery of N-{3-[3-cyclopropyl-5-(2-fluoro-4-iodophenylamino)-6,8-dimethyl-2,4,7-trioxo-3,4,6,7-tetrahydro-2H-pyrido[4,3-d]pyrimidin-1-yl]phenyl}acetamide dimethylsulfoxide solvate (GSK1120212, JTP-74057 DMSO solvate; 1), a selective and highly potent MEK inhibitor with improved drug properties. We further confirmed that the antiproliferative activity correlates with cellular MEK inhibition and observed significant antitumor activity with daily oral dosing of 1 in a tumor xenograft model. These qualities led to the selection of 1 for clinical development.
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