Raf inhibitor Belvarafenib, Purity ≥98%

Cat. No.: X23-10-ZQ967

Raf inhibitor Belvarafenib, Purity ≥98%

Synonym: Belvarafenib; 1446113-23-0; 31M3WLJ3KG; 4-Amino-N-(1-((3-chloro-2-fluorophenyl)amino)-6-methylisoquinolin-5-yl)thieno[3,2-d]pyrimidine-7-carboxamide; Raf inhibitor

  • MDL: MFCD31731098
  • CAS Number: 1446113-23-0
  • Compound CID: 89655386
Product Size
5 mg; 10 mg; 25 mg; 50 mg; 100 mg
Price
Datasheet
MSDS
Properties
Description
Belvarafenib, soluble in DMSO and insoluble in ethanol and water, blocks a MAPK/ERK signaling pathway. It targets B-Raf, B-Raf (V600E), and CRAF.
Molecular Weight
478.93
Molecular Formula
C23H16ClFN6OS
Targets
B-Raf: 56 nM; B-Raf (V600E): 7 nM; CRAF: 5 nM
Form
Lyophilized powder
Purity
≥98%
Solubility
DMSO: 84 mg/mL (175.39 mM); Water: Insoluble; Ethanol: Insoluble
Identity
Confirmed by NMR/HPLC/MS.
Stability
The product is stable for three years when stored at the recommended temperature in lyophilized powder.
Applications
Belvarafenib can be utilized to study its role as a pan-RAF inhibitor in cancer research.
Storage
Store at -20ºC.
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