Product apis-protein-tyrosine-kinase

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Catalog	name	Description	price
R-C-2712	WZ4002 CAS:1213269-23-8	WZ4002 is a mutant selective EGFR inhibitor with IC50s of 2,8,3 and 2nM for EGFRL858R,EGFRL858R/T790M,EGFRE746-A750 and EGFRE746-A750/T790M,respectively.	price>
R-C-2713	WZ8040 CAS:1214265-57-2	WZ8040 is an irreversible mutated EGFR T790M inhibitor and inhibits EGFR phosphorylation.WZ8040 displays 100-fold greater activity against the mutated EGFR than the normal.	price>
R-C-2717	OSI-420 CAS:183320-51-6	OSI-420(Desmethyl Erlotinib,CP-473420)is an orally active EGFR tyrosin kinase inhibitor,which inhibits receptor tyrosine kinases(TKs)by inhibition of the intercellular domain .	price>
R-C-2718	Butein CAS:487-52-5	Butein is a cAMP-specific PDE inhibitor with an IC50 of 10.4μM for PDE4. Butein is a specific protein tyrosine kinase inhibitor with IC50s of 16 and 65 μM for EGFR and p60c-src in HepG2 cells.Butein sensitizes HeLa cells to Cisplatin through AKT and ERK/p38 MAPK pathways by targeting FoxO3a.Butein is a SIRT1 activator(STAC).	price>
R-C-2722	CP-724714 CAS:537705-08-1	CP-724714 is a potent,selective and orally active ErbB2(HER2)tyrosine kinase inhibitor,with an IC50 of 10nM.CP-724714 displays a marked selectivity against EGFR kinase(IC50=6400nM).CP-724714 potently inhibits ErbB2 receptor autophosphorylation in intact cells.Antitumor activities.	price>
R-C-3076	SU 5205 CAS:3476-86-6	SU5205 is an inhibitor of VEGF receptor 2 (VEGFR2/FLK-1) with IC50 of 9.6 µM.Only for scientific research, not for human body.	price>
R-C-3077	SU-5408 CAS:15966-93-5	SU5408 (VEGFR2 Kinase Inhibitor I) is a potent and selective inhibitor of VEGFR2 Kinase with IC50 of 70 nM.Only for scientific research, not for human body.	price>
R-C-3078	SU 5214 CAS:186611-04-1	SU5214 is a inhibitor of VEGF receptor 2 (VEGFR2/FLK-1) with IC50 of 14.8 µM and EGFR with IC50 of 36.7 µm, respectively.Only for scientific research, not for human body.	price>
R-C-3079	Ranibizumab cas:347396-82-1	Ranibizumab is a monoclonal antibody that inhibits angiogenesis by inhibiting Vascular endothelial growth factor A.Only for scientific research, not for human body.	price>
R-C-3080	ACC-789(NVP-ACC789)	ACC-789, also known as NVP-ACC789 and ZK-202650, is a potent, selective and orally active inhibitor of the VEGF receptor tyrosine kinases with potential anticancer activity.Only for scientific research, not for human body.	price>

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