Organic & Biomolecular Chemistry · 2010 · 60 citations · 39 references
PharmacyMedicinal ChemistryPharmacologyDrug DesignDrug DiscoveryMolecular PharmacologyEnzyme InhibitionHit-to-lead OptimizationLigand-based DesignMolecular Targets Of DrugsReceptor Tyrosine Kinase SignalingTyrosine Kinase InhibitorsKinase Inhibitor Library DesignPyrimidine AnalogsPyrimidine AnaloguesPyrimidine ChemistrySmall Molecule Tyrosine Kinase InhibitorsTriazole ChemistryTyrosine Kinase InhibitionTyrosine Kinase Receptors
A library of pyrido[2,3-d]pyrimidines was designed as inhibitors of FGFR3 tyrosine kinase allowing possible interactions with an unexploited region of the ATP binding-site. This library was built-up with an efficient step of click-chemistry giving easy access to triazole-based compounds bearing a large panel of substituents. Among the 27 analogues synthesized, more than half exhibited 55-89% inhibition of in vitro FGFR3 kinase activity at 2 microM and one (19g) was able to inhibit auto-phosphorylation of mutant FGFR3-K650M in transfected HEK cells.
39
Frequent activating mutations of FGFR3 in human bladder and cervix carcinomas
David Cappellen, Catherine De Oliveira, David Ricol et al. · Nature Genetics · 1999 · 705 citations