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SU 5402, 1mg, potent VEGFR and FGFR inhibitor, >95% purity

SU 5402, 1mg, potent VEGFR and FGFR inhibitor, >95% purity

SU 5402, 1mg, potent VEGFR and FGFR inhibitor, IC50: 0.02 M (VEGFR2), 0.03 M (FGFR1), 0.51 M (PDGFR), 100 M (EGFR), >95% purity, CAS: 215543-92-3, C17H16N2O3, IUPAC Name: 3-[4-methyl-2-[(Z)-(2-oxo-1H-indol-3-ylidene)methyl]-1H-pyrrol-3-yl]propanoic a

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Product Name	Description	Item#	QTY
SU-5402 1MG	SU-5402 1MG - 1645-1, 1 mg	3279-16451	EA
NEC-1SA POTENT NECROPTOSIS INHIBITOR 1MG	NEC-1SA POTENT NECROPTOSIS INHIBITOR 1MG - 2535-1, 1 mg	3279-25351	EA
SU 5416, VEGFR inhibitor, inhibits KIT, RET, MET, FLT3, 50mg	SU 5416, VEGFR inhibitor, also inhibits KIT, RET, MET, FLT3. No activity vs EGFR, HER2, IGF1R, PDGFR. Inhibits tumor vascularization and growth. 50mg, >99%, C15H14N2O, CAS 204005-46-9	2946-303750	EA
3-Deazaneplanocin A hydrochloride, EZH2 inhibitor, 1mg, >98% purity	3-Deazaneplanocin A hydrochloride, EZH2 histone methyltransferase and SAH hydrolase inhibitor; blocks H3K27 and H4K20 trimethylation in vitro; induces apoptosis in cancer cell lines; 1mg, >98% purity, CAS: 120964-45-6, MW: 298.727, Tocris Bioscience	2946-47031	EA
BzATP triethylammonium salt, 1mg, Tocris Bioscience, >95% purity	BzATP triethylammonium salt, 1mg, >95% purity, prototypic P2X7 receptor agonist, EC50: 3.6, 7, 285 M (rat, human, mouse); partial agonist at P2X1 (pEC50=8.7) and P2Y1; photoaffinity label for ATPase; isomer mixture, Tocris Bioscience, CAS: 112898-15-	2946-33121	EA

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SU 5402, 1mg, potent VEGFR and FGFR inhibitor, >95% purity

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