Concise synthesis and CDK/GSK inhibitory activity of the missing 9-azapaullones
David P Power1, Olivier Lozach, Laurent Meijer
1Centre for Synthesis and Chemical Biology, School of Chemistry, University of Dublin, Trinity College, Dublin 2, Ireland.
Bioorganic & Medicinal Chemistry Letters
|July 13, 2010
Abstract:
A remarkably concise, chromatography-free route to the parent compound of the paullone family of cyclin-dependent kinase (CDK) inhibitors is reported. A similar strategy allowed the synthesis of the hitherto missing 9-azapaullone and its protonated, N-oxidised and N-alkylated derivatives. Screening studies identified an active and strongly selective inhibitor of CDK9/cyclin T.
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