|
| 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 New |
| 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 |
| 3894 |
PP 121 |
| Dual kinase inhibitor; inhibits receptor tyrosine kinases |
| 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 |