Description
A CXCR2 antagonist (IC50 = 0.79 nM in a radioligand binding assay); inhibits CXCL1-induced CD11b expression in and chemotaxis of isolated human neutrophils (pA2s = 6.9 and 9.1, respectively); inhibits BALF neutrophil influx in a rat model of LPS-induced lung neutrophilia and non-allergic airway inflammation at 3 and 10 μmol/kg
Formal name: N-[2-[[(2,3-difluorophenyl)methyl]thio]-6-[(1R,2S)-2,3-dihydroxy-1-methylpropoxy]-4-pyrimidinyl]-1-azetidinesulfonamide
Synonyms:
Molecular weight: 476.5
CAS: 878385-84-3
Purity: ≥98%
Formulation: A crystalline solid