Description
A CXCR3 antagonist; inhibits calcium mobilization induced by CXCL11 in HEK293 cells expressing the human receptor (IC50 = 0.06 µM); selective for CXCR3 over a panel of 14 human G protein-coupled receptors at 10 µM; inhibits CXCR3-mediated migration of isolated human T cells (IC50 = ~100 nM)
Formal name: 4-[2-[(3-chlorobenzoyl)amino]-4-[[[2-(2,4-dichlorophenyl)ethyl]amino]carbonyl]phenyl]-N-ethylhexahydro-1H-1,4-diazepine-1-carboxamide
Synonyms:
Molecular weight: 617
CAS: 870998-13-3
Purity: ≥98%
Formulation: A crystalline solid