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8 results for "VEGFR1, VEGFR2, VEGFR3" in Products

VEGFR1, VEGFR2, VEGFR3 Products

VEGFR1 (Flt-1), VEGFR2 (KDR/Flk-1), and VEGFR3 (Flt-4) belong to the class III subfamily of receptor tyrosine kinases (RTKs). All three receptors contain seven immunoglobulin-like repeats in their extracellular domain and kinase insert domains in their intracellular region. They are best known for regulating VEGF family-mediated vasculogenesis, angiogenesis, and lymphangiogenesis. They are also mediators of neurotrophic activity and regulators of hematopoietic development. VEGFR2 is thought to be the primary inducer of VEGF-mediated blood vessel growth, while VEGFR3 plays a significant role in VEGF-C and VEGF-D-mediated lymphangiogenesis.

Potent FGFR and VEGFR inhibitor

Alternate Names:
PF-02969207,PNU-0290908
Chemical Name:
2-[(1,2-Dihydro-2-oxo-3H-indol-3-ylidene)methyl]-4-methyl-1H-pyrrole-3-propanoic acid
Purity:
≥95%
Potent FGFR and VEGFR inhibitor

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 VEGFR-1, -2 and -3 inhibitor

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

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%
Potent EGFR and VEGFR 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 VEGFR inhibitor; also aromatase inhibitor

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

1 vial each of PE-conjugated anti-VEGF R1 (clone 49560), VEGF R2 (clone 89106), and VEGF R3 (clone 54733)

Reactivity:
Human
Details:
Mouse IgG1 Monoclonal Clone #89106, 49560, 54733
Applications:
Flow
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