While the muscarinic acetylcholine receptor mAChR subtype 5 (M) has been studied over decades, recent findings suggest that more in-depth research is required to elucidate a thorough understanding of its physiological function related to neurological and psychiatric disorders. Our efforts to identify potent, selective, and pharmaceutically favorable next-generation M antagonist tool compounds have led to the discovery of a novel triazolopyridine-based series. In particular, () showed exquisite potency (human M IC = 20 nM), good subtype selectivity (>500 fold selectivity against human M), desirable brain exposure ( = 0.68, = 0.65), and high oral bioavailability (% > 100%). () and its close analogues will support further studies of M as advanced antagonist tool compounds and play an important role in the emerging biology of M.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11345818 | PMC |
http://dx.doi.org/10.1021/acs.jmedchem.4c01193 | DOI Listing |
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