Chemical Structure : Surufatinib
CAS No.: 1308672-74-3
Catalog No.: PC-42960Not For Human Use, Lab Use Only.
Surufatinib (Sulfatinib, HMPL-012) is a potent, multi-targeted tyrosine kinase inhibitor of VEGFR-1/2/3, FGFR1, CSF1R with IC50 of 2/24/1 nM, 15 nM, 4 nM, respectively.
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	Surufatinib (Sulfatinib, HMPL-012) is a potent, multi-targeted tyrosine kinase inhibitor of VEGFR-1/2/3, FGFR1, CSF1R with IC50 of 2/24/1 nM, 15 nM, 4 nM, respectively.
	Sulfatinib (HMPL-012) also potently inhibits TrkB and FLT-3 with IC50 of 41 and 67 nM, shows little to no activity against other 278 other kinases (IC50>150 nM).
	Sulfatinib (HMPL-012) targets tumor angiogenesis and immune modulation, exhibits an acceptable safety profile and encouraging antitumor activity in clinical investigations.
| M.Wt | 480.5825 | |
| Formula | C24H28N6O3S | |
| Appearance | Solid | |
| Storage | 
                            
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| Solubility | 
                             DMSO: ≥ 30 mg/mL  | 
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| Chemical Name/SMILES | 
                             Benzenemethanesulfonamide, N-[2-(dimethylamino)ethyl]-3-[[4-[(2-methyl-1H-indol-5-yl)oxy]-2-pyrimidinyl]amino]-  | 
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1. Xu JM, et al. Oncotarget. 2017 Jun 27;8(26):42076-42086.

                
                
                
                
                
                
                
                
            
            
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