Raf inhibitor RAF709, Purity ≥98%

Cat. No.: X23-10-ZQ981

Raf inhibitor RAF709, Purity ≥98%

Synonym: RAF709; 1628838-42-5; RAF-709; N-[6-Methyl-5-[5-morpholin-4-yl-6-(oxan-4-yloxy)pyridin-3-yl]pyridin-3-yl]-3-(trifluoromethyl)benzamide; N-(2-Methyl-5'-morpholino-6'-((tetrahydro-2H-pyran-4-yl)oxy)-[3,3'-bipyridin]-5-yl)-3-(trifluoromethyl)benzamide; N-{2-Methyl-5'-(Morpholin-4-Yl)-6'-[(Oxan-4-Yl)oxy][3,3'-Bipyridin]-5-Yl}-3-(Trifluoromethyl)benzamide; Raf inhibitor

  • CAS Number: 1628838-42-5
  • Compound CID: 90408826
Product Size
5 mg; 10 mg; 25 mg; 50 mg; 100 mg
Price
Datasheet
MSDS
Properties
Description
RAF709, soluble in DMSO and ethanol and insoluble in water, blocks a MAPK/ERK signaling pathway. It targets B-Raf and CRAF.
Molecular Weight
542.55
Molecular Formula
C28H29F3N4O4
Targets
B-Raf: 0.4 nM; CRAF: 0.5 nM
Form
Lyophilized powder
Purity
≥98%
Solubility
DMSO: 86 mg/mL (158.51 mM); Water: Insoluble; Ethanol: 86 mg/mL (158.51 mM)
Identity
Confirmed by NMR/HPLC/MS.
Stability
The product is stable for three years when stored at the recommended temperature in lyophilized powder.
Applications
RAF709 can be applied in research studying selective inhibition of RAF kinases in cancer therapy.
Storage
Store at -20ºC.
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