Journal of Medicinal Chemistry · 2011 · 56 citations · 31 references
MedicineMedicinal ChemistryPharmacologyCancer PharmacologyDrug DiscoveryPharmacodynamicsMitotic InhibitorsPharmacodynamics Of Anticancer AgentsPharmacodynamics Of Anticancer DrugsPharmacokinetics Of Anticancer DrugsCancer Cell Proliferation InhibitionKinase Signaling InhibitorsPharmacokinetic-pharmacodynamic OptimizationPolo-like Kinase InhibitionPolo-like Kinase InhibitorsProtein Kinase InhibitorsTherapy-induced Growth Inhibition
This article describes the discovery of a series of potent inhibitors of Polo-like kinase 1 (PLK1). Optimization of this benzolactam-derived chemical series produced an orally bioavailable inhibitor of PLK1 (12c, MLN0905). In vivo pharmacokinetic-pharmacodynamic experiments demonstrated prolonged mitotic arrest after oral administration of 12c to tumor bearing nude mice. A subsequent efficacy study in nude mice achieved tumor growth inhibition or regression in a human colon tumor (HT29) xenograft model.
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BI 2536, a Potent and Selective Inhibitor of Polo-like Kinase 1, Inhibits Tumor Growth In Vivo
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Prognostic significance of polo-like kinase (PLK) expression in non-small cell lung cancer
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