For example, the dual FPR1/2 agonist compound 17b has been reported to exert anti‐inflammatory effects and protect mice from myocardial infarction injury,59 whereas another compound (Bristol Meyers‐Squibb; BMS‐986235) has proceeded into a clinical phase I study as a selective FPR2 agonist for prevention of heart failure.60 This evidence concerns the gene FPR1 and myocardial infarction.