| Cat. No. | Product Name / Activity | 
          
            | 5860 | 7rh | 
          
            |  | Potent and selective DDR1 inhibitor; orally bioavailable | 
          
            | 5013 | AC 710 | 
          
            |  | Potent and selective PDGFR family inhibitor | 
          
            | 8023 | AZ 14145845 | 
          
            |  | Dual Mer/Axl inhibitor | 
          
            | 6579 | BAY 826 | 
          
            |  | Potent Tie2 inhibitor | 
          
            | 5077 | DDR1-IN-1 dihydrochloride | 
          
            |  | Selective DDR1 inhibitor | 
          
            | 5673 | GW 2580 | 
          
            |  | Selective cFMS kinase inhibitor; orally bioavailable | 
          
            | 5260 | KG 5 | 
          
            |  | PDGFRβ, B-Raf, c-Raf, FLT3 and KIT inhibitor; antiangiogenic | 
          
            | 4481 | Ki 20227 | 
          
            |  | c-Fms inhibitor; suppresses osteolysis and osteoclast accumulation | 
          
            | 5592 | LCB 03-0110 dihydrochloride | 
          
            |  | Potent discoidin domain receptor 2 (DDR2) tyrosine kinase inhibitor; also inhibits BTK, c-Src and Syk | 
          
            | 7705 | Masitinib | 
          
            |  | Potent colony-stimulating factor 1 receptor (CSF-1R) tyroine kinase inhibitor | 
          
            | 7590 | Pexidartinib | 
          
            |  | Potent CSF-1R inhibitor | 
          
            | 7696 | Selpercatinib | 
          
            |  | Potent and selective RET inhibitor | 
          
            | 5391 | SPP 86 | 
          
            |  | Potent RET inhibitor | 
          
            | 3037 | SU 5416 | 
          
            |  | Inhibitor of VEGFR, KIT, RET, MET and FLT3 | 
          
            | 3768 | Sunitinib malate | 
          
            |  | Potent VEGFR, PDGFRβ and KIT inhibitor | 
          
            | 6537 | UNC 2881 | 
          
            |  | Potent Mer kinase inhibitor | 
          
            | 7728 | VU 6015929 | 
          
            |  | Potent and selective discoidin domain receptor 1/2 inhibitor | 
          
            | 7791 | WS 6 | 
          
            |  | Predicted tyrosine kinase inhibitor; induces hippocampal neurogenesis; also maintains totipotent stem cells, induces islet β cell growth | 
          
            | 5422 | XL 184 | 
          
            |  | Inhibits VEGFR, c-Met, KIT, FLT4, AXL, FLT3, FLT1 and Tie2 | 
          
            | 6821 | ZAP 180013 | 
          
            |  | Zap70 inhibitor; inhibits interaction with ITAMs |