Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1369523 | Bioorganic & Medicinal Chemistry Letters | 2016 | 5 Pages |
Abstract
Optimization of a benzimidazolone template for potency and physical properties revealed 5-aryl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-ones as a key template on which to develop a new series of mGlu2 positive allosteric modulators (PAMs). Systematic investigation of aryl-SAR led to the identification of compound 27 as a potent and highly selective mGlu2 PAM with sufficient pharmacokinetics to advance to preclinical models of psychosis. Gratifyingly, compound 27 showed full efficacy in the PCP- and MK-801-induced hyperlocomotion assay in rats at CSF concentrations consistent with mGlu2 PAM potency.
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Related Topics
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Organic Chemistry
Authors
Mark E. Layton, Alexander J. Reif, Timothy J. Hartingh, Kevin Rodzinak, Vadim Dudkin, Cheng Wang, Ken Arrington, Michael J. Kelly III, Robert M. Garbaccio, Julie A. O’Brien, Brian C. Magliaro, Jason M. Uslaner, Sarah L. Huszar, Kerry L. Fillgrove,