T3466 |
FIIN-3
|
|
EGFR
,
FGFR
|
|
FIIN-3 is an irreversible inhibitor of FGFR. |
T60108 |
PDGFR Tyrosine Kinase Inhibitor III
|
PDGF Receptor Tyrosine Kinase Inhibitor III |
PDGFR
|
|
PDGFR Tyrosine Kinase Inhibitor III (PDGF Receptor Tyrosine Kinase Inhibitor III), a multikinase inhibitor, inhibits PDG... |
T2496 |
(Z)-Semaxinib
|
SU5416 |
VEGFR
|
|
Semaxanib (SU5416) is a potent and selective VEGFR(Flk-1/KDR) inhibitor (IC50: 1.23 μM), 20-fold more selective for VEGF... |
T2215 |
Ferulic Acid
|
Coniferic acid , Fumalic Acid |
FGFR
,
Endogenous Metabolite
|
|
Ferulic Acid is a highly abundant phenolic phytochemical and a type of organic compound found in the Ferula assafoetida ... |
T19355 |
Heparan Sulfate
|
|
Endogenous Metabolite
,
Wnt/beta-catenin
,
FGFR
|
|
Heparan Sulfate is a complex and linear polysaccharide, exists as part of glycoproteins named heparan sulfate proteoglyc... |
T6996 |
SU 5402
|
SU5402 |
VEGFR
,
FGFR
,
PDGFR
|
|
SU5402 is a potent multi-targeted receptor tyrosine kinase inhibitor with IC50 of 20 nM, 30 nM, and 510 nM for VEGFR2, F... |
T0520 |
Lenvatinib
|
E7080 |
VEGFR
,
FGFR
,
c-RET
,
PDGFR
,
c-Kit
|
|
Lenvatinib is a Kinase Inhibitor. The mechanism of action of lenvatinib is as a Receptor Tyrosine Kinase Inhibitor. |
T60185 |
FGFR2-IN-3
|
|
FGFR
|
|
FGFR2-IN-3 is an orally active selective inhibitor of FGFR2 [1]. |
T39001 |
FGFR-IN-1
|
|
|
|
FGFR-IN-1 is a potent FGFR inhibitor with an IC 50 of <100 nM for FGFR1, FGFR2, and FGFR3, respectively (patent US201303... |
T61528 |
FGFR-IN-7
|
|
|
|
FGFR-IN-7 (compound 17) is an orally active, potent and BBB-penetrated FGFR (fibroblast growth factor receptor) modulato... |
T39682 |
Gunagratinib
|
ICP-192 |
|
|
Gunagratinib (ICP-192) is a low toxicity and orally active pan-FGFR (fibroblast growth factor receptors) inhibitor that ... |
T30168 |
ASP5878 HCl
|
ASP-5878 , ASP5878 , ASP 5878 |
|
|
ASP5878 is an oral bioavailable fibroblast growth factor receptor (FGFR) inhibitor with potential anti-tumor activity. |
T61666 |
SUN13837
|
|
|
|
SUN13837 is an orally active, potent and BBB-penetrated FGFR (fibroblast growth factor receptor) modulator. SUN13837 sho... |
T39992 |
FGFR1 inhibitor-2
|
|
|
|
FGFR1 inhibitor-2 is a FGFR1 inhibitor ( IC 50 is 4.55 μM in MDA-MB-231 cells). FGFR1 inhibitor-2 can be used for the re... |
T61473 |
FGFR2-IN-2
|
|
|
|
FGFR2-IN-2 is a selective FGFR2 inhibitor with an IC 50 of 29 nM. |
T62794 |
FGFR-IN-5
|
|
|
|
FGFR-IN-5 is a potent inhibitor of FGFR. FGFR-IN-5 has potential for research in cancer diseases (information from paten... |
T62522 |
FGFR-IN-4
|
|
|
|
FGFR-IN-4 is a potent inhibitor of FGFR. FGFR-IN-4 has potential for cancer disease studies (information from patent WO2... |
T62391 |
FGFR-IN-6
|
|
|
|
FGFR-IN-6 (Compound 5) is an FGFR inhibitor. |
T61660 |
FGFR-IN-3
|
|
|
|
FGFR-IN-3 (compound 6) is an orally active, potent and BBB-penetrated FGFR (fibroblast growth factor receptor) modulator... |
T64125 |
FGFR-IN-8
|
|
|
|
FGFR-IN-8 is a potent, orally active FGFR inhibitor that inhibits both wild-type and mutant FGFR. FGFR-IN-8 acts on FGFR... |