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. 2013 Dec 17;170(8):1459–1581. doi: 10.1111/bph.12445
Nomenclature FPR2/ALX OXE receptor
HGNC, UniProt FPR2, P25090 OXER1, Q8TDS5
Principal transduction Gi 1078 Gi/o 1070,1071,1074,1083
Rank order of potency LXA4=aspirin triggered lipoxin A4=ATLa2>LTC4=LTD4>>15-deoxy-LXA4>>fMet-Leu-Phe 1060,1061,1063,1065,1098 5-oxo-ETE, 5-oxo-C20:3, 5-oxo-ODE > 5-oxo-15-HETE > 5S-HPETE > 5S-HETE 1070,1074,1086
Endogenous agonists (pKi) aspirin triggered lipoxin A4 (Selective), LXA4 (Selective) (pEC50 ∼12.0) 1075, resolvin D1 (Selective) (pEC50 ∼11.9) 1075 5-oxo-ETE (Selective) (pEC50 8.3–8.5) 1064,1084,1086,1089,1094
Selective antagonists (pKi) ATLa2 1066
Radioligands (Kd) [3H]LXA4 (Agonist, Full agonist) (5×10−10 – 7×10−10 M) 1061,1062 [3H]5-oxo-ETE (Agonist) (3.8×10−9 M) 1084
Comment The agonist activity of the lipid mediators described has been questioned 1067,1088, which may derive from batch-to-batch differences, partial agonism or biased agonism.