Chemical Structure : TAK-593
CAS No.: 1005780-62-0
Catalog No.: PC-25522Not For Human Use, Lab Use Only.
TAK-593 is a potent, selective and ATP-competitive inhibitor of tyrosine kinases VEGFR and PDGFR with IC50s of 3.2, 0.95, 1.1, 4.3 and 13 nM for VEGFR1, VEGFR2, VEGFR3, PDFGRα and PDFGRβ, respectively.
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TAK-593 is a potent, selective and ATP-competitive inhibitor of tyrosine kinases VEGFR and PDGFR with IC50s of 3.2, 0.95, 1.1, 4.3 and 13 nM for VEGFR1, VEGFR2, VEGFR3, PDFGRα and PDFGRβ, respectively.
TAK-593 strongly suppresses proliferation of VEGF-stimulated human umbilical vein endothelial cells with an IC50 of 0.30 nM。
TAK-593 potently inhibits VEGF- and PDGF-stimulated cellular phosphorylation and proliferation of human umbilical vein endothelial cells and human coronary artery smooth muscle cells.
TAK-593 exhibits strong anti-tumor effects against various human cancer xenografts.
TAK-593 shows anti-proliferative and pro-apoptotic effects on tumors along with a decrease of vessel density and inhibition of pericyte recruitment to microvessels in vivo.
M.Wt | 445.48 | |
Formula | C23H23N7O3 | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
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Chemical Name/SMILES |
N-(5-((2-(Cyclopropanecarboxamido)imidazo[1,2-b]pyridazin-6-yl)oxy)-2-methylphenyl)-1,3-dimethyl-1H-pyrazole-5-carboxamide |
1. Iwata H, et al. Biochemistry. 2011 Feb 8;50(5):738-51.
2. Awazu Y, et al. Cancer Sci. 2013 Apr;104(4):486-94.
3. Miyamoto N, et al. Bioorg Med Chem. 2013 Apr 15;21(8):2333-2345.
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