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Sorafenib tosylate

 - BAY 43-9006  - Nexavar
Axon 1397
  • Parent CAS:  284461-73-0
Purity:  99%
  • Soluble in DMSO
  • MF:  C21H16ClF3N4O3.C7H8O3S
  • MW:  637.03

Description

Sorafenib tosylate is an orally active multikinase inhibitor that targets RAF kinases as well as pro-angiogenic receptor tyrosine kinases including VEGFR and PDGFR.

Sorafenib inhibits RAF–MEK–ERK signaling and tumor angiogenesis, linking direct antiproliferative effects with vascular pathway suppression. It is used in oncology research to study multikinase pharmacology, pathway adaptation and resistance.

Key Features

  • Multikinase inhibitor of RAF and angiogenic RTKs
  • Suppresses RAF–MEK–ERK pathway signaling
  • Inhibits VEGFR- and PDGFR-dependent angiogenesis
  • Clinically validated antineoplastic pharmacology

Applications

  • RAF kinase and MAPK pathway studies
  • Angiogenesis and VEGFR signaling assays
  • Tumor-cell proliferation models
  • Multikinase resistance and combination research

More Information

Parent CAS No. 284461-73-0
Chemical Name 4-[4-[[4-chloro-3-(trifluoromethyl)phenyl]carbamoylamino]phenoxy]-N-methyl-pyridine-2-carboxamide
SMILES N1C=CC(OC2C=CC(NC(=O)NC3C=C(C(F)(F)F)C(Cl)=CC=3)=CC=2)=CC=1C(=O)NC.C1C=C(C)C=CC=1S(O)(=O)=O
MFCD MFCD08235032
InChi InChI=1S/C21H16ClF3N4O3.C7H8O3S/c1-26-19(30)18-11-15(8-9-27-18)32-14-5-2-12(3-6-14)28-20(31)29-13-4-7-17(22)16(10-13)21(23,24)25;1-6-2-4-7(5-3-6)11(8,9)10/h2-11H,1H3,(H,26,30)(H2,28,29,31);2-5H,1H3,(H,8,9,10)
InChiKey IVDHYUQIDRJSTI-UHFFFAOYSA-N
CID 406563
Short Description Raf inhibitor

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