Omega-carboxypyridyl substituted ureas as Raf kinase inhibitors

Omega-carboxypyridyl substituted ureas as Raf kinase inhibitors Design, synthesis and antitumor activities of novel bis-aryl ureas derivatives as Raf kinase inhibitors Design and Synthesis of Orally Bioavailable Benzimidazoles as Raf Kinase Inhibitors Design and synthesis of isoquinolines and benzimidazoles as RAF kinase inhibitors Arylcarboxyamino-substituted diaryl ureas as potent and selective FLT3 inhibitors 4-Quinazolinyloxy-diaryl ureas as novel BRAFV600E inhibitors Design, synthesis and biological evaluation of bis-aryl ureas and amides based on 2-amino-3-purinylpyridine scaffold as DFG-out B-Raf kinase inhibitors Synthesis of amide and urea derivatives of benzothiazole as Raf-1 inhibitor Design, synthesis and biological evaluation of β-carboline derivatives as novel inhibitors targeting B-Raf kinase Virtual screening for Raf-1 kinase inhibitors based on pharmacophore model of substituted ureas