- Thienopyridine ureas as dual inhibitors of the VEGF and Aurora kinase families.
Thienopyridine ureas as dual inhibitors of the VEGF and Aurora kinase families.
Bioorganic & medicinal chemistry letters (2012-04-03)
Michael L Curtin, Robin R Frey, H Robin Heyman, Niru B Soni, Patrick A Marcotte, Lori J Pease, Keith B Glaser, Terrance J Magoc, Paul Tapang, Daniel H Albert, Donald J Osterling, Amanda M Olson, Jennifer J Bouska, Zhiwen Guan, Lee C Preusser, James S Polakowski, Kent D Stewart, Chris Tse, Steven K Davidsen, Michael R Michaelides
PMID22465635
ABSTRACT
In an effort to identify multi-targeted kinase inhibitors with a novel spectrum of kinase activity, a screen of Abbott proprietary KDR inhibitors against a broad panel of kinases was conducted and revealed a series of thienopyridine ureas with promising activity against the Aurora kinases. Modification of the diphenyl urea and C7 moiety of these compounds provided potent inhibitors with good pharmacokinetic profiles that were efficacious in mouse tumor models after oral dosing. Compound 2 (ABT-348) of this series is currently undergoing Phase I clinical trials in solid and hematological cancer populations.
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