Raf inhibitor Regorafenib, Purity ≥98%

Cat. No.: X23-10-ZQ185

Raf inhibitor Regorafenib, Purity ≥98%

Synonym: 755037-03-7; Regorafenib; BAY 73-4506; Stivarga; 4-(4-(3-(4-Chloro-3-(trifluoromethyl)phenyl)ureido)-3-fluorophenoxy)-N-methylpicolinamide; Raf inhibitor

  • MDL: MFCD16038047
  • CAS Number: 755037-03-7
  • Compound CID: 11167602
Product Size
25 mg; 100 mg
Price
Datasheet
MSDS
Properties
Description
Regorafenib, soluble in DMSO and insoluble in ethanol and water, blocks a MAPK/ERK signaling pathway. It targets B-Raf, B-Raf (V600E), B-Raf (V600E), Kit, Kit, Raf-1, RET, Tie-2, VEGFR1, VEGFR2, and VEGFR3.
Molecular Weight
482.8
Molecular Formula
C21H15ClF4N4O3
Targets
B-Raf: 28 nM; B-Raf (V600E): 19 nM; B-Raf (V600E): 19 nM; Kit: 7 nM; Kit: 7 nM; Raf-1: 2.5 nM; RET: 1.5 nM; Tie-2: 311 nM; VEGFR1: 13 nM; VEGFR2: 4.2 nM; VEGFR3: 46 nM
Form
Lyophilized powder
Purity
≥98%
Solubility
DMSO: 88 mg/mL (182.26 mM); Water: Insoluble; Ethanol: Insoluble
Identity
Confirmed by NMR/HPLC/MS.
Applications
Regorafenib can be employed to investigate its multi-kinase inhibition in cancer therapy.
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