CXCR inhibitor Reparixin, Purity ≥98%

Cat. No.: X23-10-ZQ550

CXCR inhibitor Reparixin, Purity ≥98%

Synonym: Reparixin; 266359-83-5; DF 1681Y; (R)-2-(4-Isobutylphenyl)-N-(methylsulfonyl)propanamide; DF1681Y; Reparixin (Repertaxin); CXCR inhibitor

  • MDL: MFCD18633292
  • CAS Number: 266359-83-5
  • Compound CID: 9838712
Product Size
5 mg; 10 mg; 25 mg; 50 mg; 100 mg
Price
Datasheet
MSDS
Properties
Description
Reparixin, soluble in DMSO and ethanol and insoluble in water, targets the chemokine receptors CXCR, which are part of the GPCR family. It targets CXCR1, CXCR1-Ile43Val, CXCR1-wt, and CXCR2.
Molecular Weight
283.39
Molecular Formula
C14H21NO3S
Targets
CXCR1: 1 nM; CXCR1-Ile43Val: 80 nM (In L1.2 cells); CXCR1-wt: 5.6 nM (In L1.2 cells); CXCR2: 100 nM (In cells)
Form
Lyophilized powder
Purity
≥98%
Solubility
DMSO: 52 mg/mL (183.49 mM); Water: Insoluble; Ethanol: 52 mg/mL
Identity
Confirmed by NMR/HPLC/MS.
Stability
The product is stable for three years when stored at the recommended temperature in lyophilized powder.
Applications
Reparixin can be used to study its effects as a CXCR1/2 inhibitor in inflammation and cancer research.
Storage
Store at -20ºC.
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