Identification and characterization of pyrrolidine diastereoisomers as potent functional agonists and antagonists of the human melanocortin-4 receptor

Abstract A series of trans -4-phenylpyrrolidine-3-carboxamides were synthesized and characterized as potent ligands of the human melanocortin-4 receptor. Interestingly, a pair of diastereoisomers 13b displayed potent functional agonist and antagonist activity, respectively. Thus, the 3 S ,4 R -pyrrolidine 13b-1 possessed a K i of 1.0 nM and an EC 50 of 3.8 nM, while its 3 R ,4 S -isomer 13b-2 exhibited a K i of 4.7 and an IC 50 of 64 nM. Both compounds were highly selective over other melanocortin receptor subtypes. The MC4R agonist 13b-1 also demonstrated efficacy in a diet-induced obesity model in rats.