Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1372449 | Bioorganic & Medicinal Chemistry Letters | 2010 | 5 Pages |
Abstract
Imidazo[1,2-a]pyridines were identified via their shape and electrostatic similarity as novel positive allosteric modulators of the metabotropic glutamate 2 receptor. The subsequent synthesis and SAR are described. Potent, selective and metabolically stable compounds were found representing a promising avenue for current further studies.
Graphical abstractShape and electrostatic virtual screening identified the imidazopyridine as highly similar to the pyridone mGluR2 PAM scaffold. Example compounds were synthesized and show good primary activity and promise for future work.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
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Authors
Gary Tresadern, Jose María Cid, Gregor J. Macdonald, Juan Antonio Vega, Ana Isabel de Lucas, Aránzazu García, Encarnación Matesanz, María Lourdes Linares, Daniel Oehlrich, Hilde Lavreysen, Ilse Biesmans, Andrés A. Trabanco,