Leukotriene B4 photoaffinity probes: design, synthesis and evaluation of new arylazide-1,3-disubstituted cyclohexanes

Abstract The synthesis and the binding affinities of new leukotriene B 4 receptor photoaffinity probes, where a 1,3-disubstitued cyclohexane ring replaces the conjugated Δ 6,7 and Δ 8,9 double bonds of the natural eicosanoid, are described. One enantiomeric compound, 4bα , is specifically cross-linked upon photolysis to the recombinant leukotriene B 4 receptor from human origin (h-BLTR) solubilized in a micellar medium. This probe appears as a good candidate for identifying the ligand binding site of this receptor.