Sorafenib Tosylate , ≥99% , 475207-59-1
CAS NO.:475207-59-1
Empirical Formula: C28H24ClF3N4O6S
Molecular Weight: 637.03
MDL number: MFCD08235032
EINECS: 641-758-8
Pack Size | Price | Stock | Quantity |
50MG | RMB15.20 | In Stock |
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100mg | RMB24.00 | In Stock |
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250MG | RMB36.00 | In Stock |
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1G | RMB88.00 | In Stock |
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5G | RMB288.80 | In Stock |
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25g | RMB1011.20 | In Stock |
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others | Enquire |
PRODUCT Properties
Melting point: | 229-232°C |
storage temp. | 2-8°C(protect from light) |
solubility | Soluble in DMSO (up to 200 mg/ml) or in Ethanol (up to 3 mg/ml). |
form | solid |
color | Off-white |
Stability: | Stable for 2 years from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20° for up to 1 month. |
InChIKey | IVDHYUQIDRJSTI-UHFFFAOYSA-N |
SMILES | S(C1C=CC(C)=CC=1)(O)(=O)=O.O(C1C=CC(NC(=O)NC2C=CC(Cl)=C(C(F)(F)F)C=2)=CC=1)C1=CC=NC(C(=O)NC)=C1 |
CAS DataBase Reference | 475207-59-1(CAS DataBase Reference) |
Description and Uses
Sorafenib (475207-59-1) was initially developed as a Raf kinase inhibitor, IC50 = 6 nM, but has been shown to inhibit many receptor tyrosine kinases including BRAF (IC50 = 22 nM); VEGFR-2 (IC50 = 90 nM); VEGFR-3 (IC50 = 20 nM); PDGFR-β (IC50 = 57 nM); Flt3 (IC50 = 58 nM); c-KIT (IC50 = 68 nM); FGFR-1 (IC50 = 580 nM).1?Paradoxically more potent in a cellular assay (IC50 = 20 nM) compared to an isolated enzyme assay (IC50 = 107 nM) for c-Fms.2?Inhibits activation of MAPK pathway and ERK phosphorylation.3?Induces caspase-independent apoptosis in melanoma cells.4?Sorafenib is a clinically useful anticancer agent.
Sorafenib Tosylate (Bay 43-9006, Nexavar) is a small molecular inhibitor of VEGFR, PDGFR, c-Raf and B-Raf with IC50s of 18 nM, 10 nM, 3 nM and 15 nM, respectively.
Safety
Symbol(GHS) | GHS08,GHS09 |
Signal word | Danger |
Hazard statements | H360FD-H362-H372-H410 |
Precautionary statements | P201-P202-P260-P263-P273-P308+P313 |
Risk Statements | 36/37/38 |
Safety Statements | 28-26 |
HS Code | 29159000 |