Synthesis and Biological Evaluation of a Novel Series of Heterobivalent Muscarinic Ligands Based on Xanomeline and 1?[3-(4-Butylpiperidin-1-yl)propyl]-1,2,3,4-tetrahydroquinolin-2-one (77-LH-28-1)

摘要

Novel bitopic hybrids, based on the M_1/M_4 muscarinic acetylcholine receptor (mAChR) orthosteric agonist xanomeline (1) and the putative M_1 mAChR allosteric agonist 1-[3-(4-butylpiperidin-1-yl)propyl]-1,2,3,4-tetrahydroquinolin-2-one (77-LH-28-1, 3) connected by an aliphatic linker of variable length, were prepared. The novel heterobivalent hybrids 4a-f along with the intermediate alcohols 5a-f were pharmacologically evaluated in radioligand binding assays and some of them for their functional efficacies in bioluminescence resonance energy transfer (BRET)-based assays to give an insight into the structure-activity relationships of bivalent and linkerattached compounds in mAChRs. The hybrid 4d exhibited high efficacy for β-arrestin2 engagement in M_1 mAChR and alcohol 5c behaved much like 3 at M_1 mAChR and showed full antagonism in both G_i activation and β-arrestin2 engagement at M_4 mAChR. Moreover, docking simulations on the M1 mAChR model were performed to elucidate how the binding mode of the proposed compounds is influenced by the linker length.