Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1377241 | Bioorganic & Medicinal Chemistry Letters | 2006 | 5 Pages |
Abstract
Several β-amino tetrazole analogs of gabapentin 1 and pregabalin 2 were prepared by one of two convergent, highly efficient routes, and their affinity for the α2–δ protein examined. Two select compounds with potent affinity for α2–δ, 8a and 16a, were subsequently tested in vivo in an audiogenic seizure model and found to elicit protective effects.
Graphical abstractTruncation and acid replacement with tetrazole furnished a compound with a similar pattern of activity to pregabalin.Figure optionsDownload full-size imageDownload as PowerPoint slide
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Jacob B. Schwarz, Norman L. Colbry, Zhijian Zhu, Brian Nichelson, Nancy S. Barta, Kristin Lin, Raymond A. Hudack, Sian E. Gibbons, Paul Galatsis, Russell J. DeOrazio, David D. Manning, Mark G. Vartanian, Jack J. Kinsora, Susan M. Lotarski, Zheng Li,