Further optimization of the M1 PAM VU0453595: Discovery of novel heterobicyclic core motifs with improved CNS penetration

• Published in: Bioorganic & medicinal chemistry letters Vol. 26; no. 15; pp. 3822 - 3825
• Main Authors: Panarese, Joseph D., Cho, Hykeyung P., Adams, Jeffrey J., Nance, Kellie D., Garcia-Barrantes, Pedro M., Chang, Sichen, Morrison, Ryan D., Blobaum, Anna L., Niswender, Colleen M., Stauffer, Shaun R., Conn, P. Jeffrey, Lindsley, Craig W.
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.08.2016
• Subjects: Allosteric Regulation - drug effects; Animals; Central Nervous System - drug effects; Central Nervous System Agents - chemical synthesis; Central Nervous System Agents - chemistry; Central Nervous System Agents - pharmacology; CNS penetration; Dose-Response Relationship, Drug; Drug Discovery; Heterocyclic Compounds - chemical synthesis; Heterocyclic Compounds - chemistry; Heterocyclic Compounds - pharmacology; Molecular Structure; Muscarinic acetylcholine receptor; Positive allosteric modulator (PAM); Pyridines - chemical synthesis; Pyridines - chemistry; Pyridines - pharmacology; Pyrroles - chemical synthesis; Pyrroles - chemistry; Pyrroles - pharmacology; Rats; Receptor, Muscarinic M1 - metabolism; Structure-Activity Relationship; Structure–activity relationship (SAR); Structure–activity relationship (SAR); M1; Positive allosteric modulator (PAM); CNS penetration; Muscarinic acetylcholine receptor; M
• ISSN: 0960-894X; 1464-3405
• DOI: 10.1016/j.bmcl.2016.04.083

[Display omitted] This Letter describes the continued chemical optimization of the VU0453595 series of M1 positive allosteric modulators (PAMs). By surveying alternative 5,6- and 6,6-heterobicylic cores for the 6,7-dihydro-5H-pyrrolo[3,4-b]pyridine-5-one core of VU453595, we found new cores that engendered not only comparable or improved M1 PAM potency, but significantly improved CNS distribution (Kps 0.3–3.1). Moreover, this campaign provided fundamentally distinct M1 PAM chemotypes, greatly expanding the available structural diversity for this valuable CNS target, devoid of hydrogen-bond donors.