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Identification of aminopyrazolopyridine ureas as potent VEGFR/PDGFR multitargeted kinase inhibitors
Authors:Dai Yujia  Hartandi Kresna  Soni Niru B  Pease Lori J  Reuter David R  Olson Amanda M  Osterling Donald J  Doktor Stella Z  Albert Daniel H  Bouska Jennifer J  Glaser Keith B  Marcotte Patrick A  Stewart Kent D  Davidsen Steven K  Michaelides Michael R
Affiliation:Cancer Research, Global Pharmaceutical Research and Development, Abbott Laboratories, 100 Abbott Park Road, Abbott Park, IL 60064-6100, USA. yujia.dai@abbott.com
Abstract:Tumor angiogenesis is mediated by KDR and other VEGFR and PDGFR kinases. Their inhibition presents an attractive approach for developing anticancer therapeutics. Here, we report a series of aminopyrazolopyridine ureas as potent VEGFR/PDGFR multitargeted kinase inhibitors. A number of compounds have been identified to be orally bioavailable and efficacious in the mouse edema model.
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