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VEGFR2/KDR/Flk-1: Small Molecules and Peptides

VEGFR2/KDR/Flk-1 (vascular endothelial growth factor receptor 2) is a transmembrane receptor tyrosine kinase that mediates the angiogenic effects of VEGF-A and VEGF-C. It is expressed primarily on vascular endothelial cells and endothelial cell progenitors.

It is also expressed on endometrial epithelium, hematopoietic stem cells, liver sinusoidal endothelial cells, Sertoli cells and Leydig cells, platelets and megakaryocytes, sensory and autonomic neurons, Schwann cells, Muller glial cells, retinal progenitors, and osteoblasts. VEGFR2 can be associated with VEGFR1, and a soluble form of VEGFR2 can circulate in the serum.

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17 results for "VEGFR2/KDR/Flk-1 Small Molecules and Peptides" in Products

17 results for "VEGFR2/KDR/Flk-1 Small Molecules and Peptides" in Products

VEGFR2/KDR/Flk-1: Small Molecules and Peptides

VEGFR2/KDR/Flk-1 (vascular endothelial growth factor receptor 2) is a transmembrane receptor tyrosine kinase that mediates the angiogenic effects of VEGF-A and VEGF-C. It is expressed primarily on vascular endothelial cells and endothelial cell progenitors.

It is also expressed on endometrial epithelium, hematopoietic stem cells, liver sinusoidal endothelial cells, Sertoli cells and Leydig cells, platelets and megakaryocytes, sensory and autonomic neurons, Schwann cells, Muller glial cells, retinal progenitors, and osteoblasts. VEGFR2 can be associated with VEGFR1, and a soluble form of VEGFR2 can circulate in the serum.

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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% (HPLC)
VEGFR inhibitor. Also inhibits KIT, RET, MET and FLT3

Potent VEGFR, PDGFR and FGFR inhibitor

Chemical Name: Methyl (Z)-3-[[[4-(N-methyl-2-(4-methylpiperazin-1-yl)acetamido)phenyl)amino)(phenyl)methylene]-2-oxoindoline-6-carboxylate
Purity: ≥98%
Potent VEGFR, PDGFR and FGFR inhibitor

Potent inhibitor of PDGFRβ, KDR, FLT3 and CSF-1R

Chemical Name: N-[4-(3-Amino-1H-indazol-4-yl)phenyl]-N'-(2-fluoro-5-methylphenyl)urea
Purity: ≥98% (HPLC)
Potent inhibitor of PDGFRβ, KDR, FLT3 and CSF-1R

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% (HPLC)
Potent VEGFR, PDGFRβ and KIT inhibitor

Potent VEGFR-1, -2 and -3 inhibitor

Chemical Name: N-Methyl-[[3[(1E)-2-(2-pyridinyl)ethenyl]-1H-indazol-6-yl]thio]-benzamide
Purity: ≥98% (HPLC)
Potent VEGFR-1, -2 and -3 inhibitor

Potent Raf-1 inhibitor; also inhibits VEGFR-2, VEGFR-3, PDGFR-β, Flt-3 and cKIT

Chemical Name: 4-[4-[[[[4-Chloro-3-(trifluoromethyl)phenyl]amino]carbonyl]amino]phenoxy]-N-methyl-2-pyridinecarboxamide
Purity: ≥98% (HPLC)
Potent Raf-1 inhibitor; also inhibits VEGFR-2, VEGFR-3, PDGFR-β, Flt-3 and cKIT

Potent, selective inhibitor of VEGFR-2

Chemical Name: 5-((7-Benzyloxyquinazolin-4-yl)amino)-4-fluoro-2-methylphenol hydrochloride
Purity: ≥98% (HPLC)
Potent, selective inhibitor of VEGFR-2

Potent, selective VEGFR-2 inhibitor

Chemical Name: N-(2,4-Difluorophenyl)-N'-[4-[(6,7-dimethoxy-4-quinolinyl)oxy]-2-fluorophenyl]urea
Purity: ≥97% (HPLC)
Potent, selective VEGFR-2 inhibitor

Dual site Src kinase inhibitor

Chemical Name: 6,7-Dimethoxy-N-(4-phenoxyphenyl)-4-quinazolinamine
Purity: ≥98% (HPLC)
Dual site Src kinase inhibitor

Src tyrosine kinase inhibitor

Chemical Name: N-(2-Chloro-5-methoxyphenyl)-6-methoxy
Purity: ≥98% (HPLC)
Src tyrosine kinase inhibitor

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% (HPLC)
c-Fms inhibitor; suppresses osteolysis and osteoclast accumulation

Potent VEGFR inhibitor; also aromatase inhibitor

Alternate Names: CGP 79787D,PTK787/ZK222584
Chemical Name: N-(4-Chlorophenyl)-4-(4-pyridinylmethyl)-1-phthalazinamine succinate
Purity: ≥98% (HPLC)
Potent VEGFR inhibitor; also aromatase inhibitor

Potent VEGFR inhibitor; also inhibits other RTKs

Alternate Names: Cabozantinib,BMS 907351
Chemical Name: N-[4-[(6,7-Dimethoxy-4-quinolinyl)oxy]phenyl]-N-(4-fluorophenyl)-1,1-cyclopropanedicarboxamide
Purity: ≥98% (HPLC)
Potent VEGFR inhibitor; also inhibits other RTKs

Potent EGFR and VEGFR inhibitor

Chemical Name: 6-[4-[(4-Ethyl-1-piperazinyl)methyl]phenyl]-N-[(1R)-1-phenylethyl]-7H-pyrrolo[2,3-d]pyrimidin-4-amine
Purity: ≥98% (HPLC)
Potent EGFR and VEGFR inhibitor

Potent VEGFR-2 inhibitor, also inhibits EGFR and RET oncoproteins activity

Chemical Name: N-(4-Bromo-2-fluorophenyl)-6-methoxy-7-[(1-methyl-4-piperidinyl)methoxy]-4-quinazolinamine
Purity: ≥98% (HPLC)
Potent VEGFR-2 inhibitor, also inhibits EGFR and RET oncoproteins activity

Inhibitor of mutant β-catenin signaling in hepatocellular carcinoma

Chemical Name: 4-[3-Fluoro-4-[[[[4-(1,1,2,2,2-pentafluoroethyl)phenyl]amino]carbonyl]amino]phenoxy]-N-methyl-2-pyridinecarboxamide
Purity: ≥98% (HPLC)
Inhibitor of mutant β-catenin signaling in hepatocellular carcinoma

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% (HPLC)
Potent inhibitor of VEGFR, PDGFR and FGFR
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