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23 results for "Additional RTK Inhibitors" in Products

Additional RTK Inhibitors

c-Fms inhibitor; suppresses osteolysis and osteoclast accumulation

Chemical Name:
N-[4-[(6,7-Dimethoxy-4-quinolinyl)oxy]-2-methoxyphenyl]-N'-[1-(2-thiazolyl)ethyl]urea
Purity:
≥97%
c-Fms inhibitor; suppresses osteolysis and osteoclast accumulation

VEGFR inhibitor. Also inhibits KIT, RET, MET and FLT3

Alternate Names:
Semaxinib
Chemical Name:
3-[(3,5-Dimethyl-1H-pyrrol-2-yl)methylene]-1,3-dihydro-2H-indol-2-one
Purity:
≥98%
VEGFR inhibitor. Also inhibits KIT, RET, MET and FLT3

Potent and selective PDGFR family inhibitor

Chemical Name:
N-[4-[[[[5-(1,1-Dimethethylethyl)-3-isoxazolyl]amino]carbonyl]amino]phenyl]-5-[(1-ethyl-2,2,6,6-tetramethyl-4-piperidinyl)oxy]-2-pyridinecarboxamide
Purity:
≥98%
Potent and selective PDGFR family inhibitor

Selective DDR1 inhibitor

Chemical Name:
N-[3-[(2,3-Dihydro-2-oxo-1H-indol-5-yl)oxy]-4-methylphenyl]-4-[(4-ethyl-1-piperazinyl)methyl]-3-(trifluoromethyl)benzamide dihydrochloride
Purity:
≥98%
Selective DDR1 inhibitor

Potent CSF-1R inhibitor

Chemical Name:
N-[5-[(5-Chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)methyl]-2-pyridinyl]-6-(trifluoromethyl)-3-pyridinemethanamine
Purity:
≥98%
Potent CSF-1R inhibitor

Potent and selective FGFR inhibitor

Chemical Name:
rel-N-[5-[2-(3,5-Dimethoxyphenyl)ethyl]-1H-pyrazol-3-yl]-4-[(3R,5S)-3,5-dimethyl-1-piperazinyl]benzamide
Purity:
≥98%
Potent and selective FGFR inhibitor

Potent VEGFR, PDGFRβ and KIT inhibitor

Alternate Names:
SU 11248
Chemical Name:
N-[2-(Diethylamino)ethyl]-5-[(Z)-(5-fluoro-1,2-dihydro-2-oxo-3H-indol-3-ylidine)methyl]-2,4-dimethyl-1H-pyrrole-3-carboxamide (2S)-2-hydroxybutanedioate salt
Purity:
≥98%
Potent VEGFR, PDGFRβ and KIT inhibitor

PDGFRβ, B-Raf, c-Raf, FLT3 and KIT inhibitor

Chemical Name:
2-(Methylthio)-6-[4-[5-[[3-(trifluoromethyl)phenyl]amino]-1H-1,2,4-triazol-3-yl]phenoxy]-4-pyrimidinamine
Purity:
≥98%
PDGFRβ, B-Raf, c-Raf, FLT3 and KIT inhibitor

Potent RET inhibitor

Chemical Name:
1-(1-Methylethyl)-3-(2-phenylethynyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine
Purity:
≥98%
Potent RET inhibitor

PDGFRβ, B-Raf, c-Raf, FLT3 and KIT inhibitor

Chemical Name:
2-(Methylthio)-6-[4-[5-[[3-(trifluoromethyl)phenyl]amino]-1H-1,2,4-triazol-3-yl]phenoxy]-4-pyrimidinamine
Purity:
≥98%
PDGFRβ, B-Raf, c-Raf, FLT3 and KIT inhibitor

Potent c-SRC kinase inhibitor; also inhibits DDR2, BTK and Syk

Chemical Name:
3-[[2-[3-(4-Morpholinylmethyl)phenyl]thieno[3,2-b]pyridin-7-yl]amino]phenol dihydrochloride
Purity:
≥98%
Potent c-SRC kinase inhibitor; also inhibits DDR2, BTK and Syk

Selective cFMS kinase inhibitor; orally bioavailable

Chemical Name:
5-[[3-Methoxy-4-[(4-methoxyphenyl)methoxy]phenyl]methyl]-2,4-pyrimidinediamine
Purity:
≥98%
Selective cFMS kinase inhibitor; orally bioavailable

Potent and selective DDR1 inhibitor; orally bioavailable

Chemical Name:
4-Ethyl-N-[3-[(4-methyl-1-piperazinyl)methyl]-5-(trifluoromethyl)phenyl]-3-(2-pyrazolo[1,5-a]pyrimidin-6-ylethynyl)benzamide
Purity:
≥98%
Potent and selective DDR1 inhibitor; orally bioavailable

Potent Mer kinase inhibitor

Chemical Name:
2-(Butylamino)-4-[(trans-4-hydroxycyclohexyl)amino]-N-[[4-(1H-imidazol-1-yl)phenyl]methyl]-5-pyrimidinecarboxamide
Purity:
≥98%
Potent Mer kinase inhibitor

Potent Tie2 inhibitor

Chemical Name:
[3-Cyano-5-[[[2,4-dimethyl-5-[6-(3-pyridinyl)-1H-imidazo[1,2-b]pyrazol-1-yl]phenyl]amino]carbonyl]phenyl]pentafluorosulfur
Purity:
≥98%
Potent Tie2 inhibitor

Zap70 inhibitor; inhibits interaction with ITAMs

Chemical Name:
5-Chloro-N-[(4-chlorophenyl)methyl]-2-(ethylsulfonyl)-N-(2-furanylmethyl)-4-pyrimidinecarboxamide
Purity:
≥98%
Zap70 inhibitor; inhibits interaction with ITAMs

Potent and selective dual inhibitor of the IGF-1 receptor and insulin receptor

Chemical Name:
cis-3-[8-Amino-1-(2-phenyl-7-quinolinyl)imidazo[1,5-a]pyrazin-3-yl]-1-methylcyclobutanol
Purity:
≥98%
Potent and selective dual inhibitor of the IGF-1 receptor and insulin receptor

Potent and selective RET inhibitor

Chemical Name:
6-(2-Hydroxy-2-methylpropoxy)-4-[6-[6-[(6-methoxy-3-pyridinyl)methyl]-3,6-diazabicyclo[3.1.1]hept-3-yl]-3-pyridinyl]pyrazolo[1,5-a]pyridine-3-carbonitrile
Purity:
≥98%
Potent and selective RET inhibitor

PDGFRβ, B-Raf, c-Raf, FLT3 and KIT inhibitor

Chemical Name:
2-(Methylthio)-6-[4-[5-[[3-(trifluoromethyl)phenyl]amino]-1H-1,2,4-triazol-3-yl]phenoxy]-4-pyrimidinamine
Purity:
≥98%
PDGFRβ, B-Raf, c-Raf, FLT3 and KIT inhibitor

Potent and selective discoidin domain receptor 1/2 inhibitor

Chemical Name:
4-Fluoro-3-[[[5-(1-methyl-1H-pyrazol-3-yl)-3-pyridinyl]methyl]amino]-N-[3-(trifluoromethoxy)phenyl]benzamide
Purity:
≥98%
Potent and selective discoidin domain receptor 1/2 inhibitor

Potent inhibitor of VEGFR, PDGFR and FGFR

Chemical Name:
4-[(4-Fluoro-2-methyl-1H-indol-5-yl)oxy]-6-methoxy-7-[3-(1-pyrrolidinyl)propoxy]quinazoline
Purity:
≥98%
Potent inhibitor of VEGFR, PDGFR and FGFR

Induces growth and proliferation of pancreatic islet cells, murine totipotent stem cells, GABAergic neurons and hippocampal neurons

Chemical Name:
4-[[6-[(Cyclopropylcarbonyl)amino]-4-pyrimidinyl]oxy]-N-[4-[(4-methyl-1-piperazinyl)methyl]-3-(trifluoromethyl)phenyl]benzeneacetamide
Purity:
≥98%
Induces growth and proliferation of pancreatic islet cells, murine totipotent stem cells, GABAergic neurons and hippocampal neurons

Dual Mer/Axl inhibitor

Chemical Name:
3-[4-[(Dimethylamino)methyl]phenyl]-N-methyl-N-[5-[3-methyl-5-(1,3,5-trimethyl-1H-pyrazol-4-yl)-2-pyridinyl]-1,3,4-oxadiazol-2-yl]imidazo[1,2-a]pyridine-6-methanamine
Purity:
≥97%
Mer/Axl Dual inhibitor
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