Publication | Open Access
Pyranonaphthoquinone Lactones: A New Class of AKT Selective Kinase Inhibitors Alkylate a Regulatory Loop Cysteine
72
Citations
24
References
2009
Year
Chemical BiologyPharmaceutical ChemistryDrug ResistanceMedicinal ChemistrySynthetic PnqsAnti-cancer AgentInhibitory ActivityBiochemistryMedicineDrug DevelopmentPharmacologySerine-threonine Kinase AktRegulatory Loop CysteineNatural SciencesPyranonaphthoquinone LactonesRational Drug DesignNew ClassPreliminary SarDrug Discovery
The naturally occurring pyranonaphthoquinone (PNQ) antibiotic lactoquinomycin and related aglycones were found to be selective inhibitors of the serine-threonine kinase AKT. A set of synthetic PNQs were prepared and a minimum active feature set and preliminary SAR were determined. PNQ lactones inhibit the proliferation of human tumor cell lines containing constitutively activated AKT and show expected effects on cellular biomarkers. Biochemical data are presented supporting a proposed bioreductive alkylation mechanism of action.
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