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284461-73-0 2-Pyridinecarboxamide,4-[4-[[[[4-chloro-3-(trifluoromethyl)phenyl]amino]carbonyl]amino]phenoxy]-N-methyl Sorafenib
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Product name:sorafenib
synonyms:bay43-9006;n-[4-chloro-3-(trifluoromethyl)phenyl]-n'-[4-[2-(n-methylcarbamoyl)-4-pyridyloxy]phenyl]urea
specification: 98%
cas no.:284461-73-0
appearance: white crystalline powder
molecular weight: 464.82
molecular formula:c21h16clf3n4o3
items |
specifications |
results |
appearance |
off white powder to white powder |
off-white powder |
identification |
h-nmr, ms |
complies |
water content |
< 0.5% |
0.06% |
loss on drying |
<1.0% |
0.02% |
related impurity by hplc |
total impurity ≤1.0% single impurity≤0.3% |
0.05% 0.04% |
purity (hplc) |
≥99% |
99.95% |
function and application:
sorafenib is a raf kinase inhibitor which suppresses erk phosphorylation. studies indicate that sorafenib induces c-raf phosphorylation
at both ser-43 and ser-259. when combined with vitamin k1 phosphorylation is increased at these serine residues. sorafenib also induces the phosphorylation of pka. in addition, sorafenib induces c-met phosphorylation at tyr-1349, which consequently induces pi3k-akt phosphorylation. studies determined that sorafenib inhibits other kinases such as flk-1 (vegfr2), platelet-derived growth factor receptor (pdgfr), flt3, ret, and c-kit.
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