| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1371778 | Bioorganic & Medicinal Chemistry Letters | 2012 | 4 Pages |
Abstract
A series of fused tricyclic mGluR1 antagonists containing a pyridone ring were synthesized. In vitro, these antagonists were potent against both human and rat isozymes, as well as selective for inhibiting mGluR1 over mGluR5. When dosed orally, several examples were active in vivo in a rat SNL test.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Chad E. Bennett, Duane A. Burnett, William J. Greenlee, Chad E. Knutson, Peter Korakas, Cheng Li, Deen Tulshian, Wen-Lian Wu, Rosalia Bertorelli, Silva Fredduzzi, Mariagrazia Grilli, Gianluca Lozza, Angelo Reggiani, Alessio Veltri,