Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1375227 | Bioorganic & Medicinal Chemistry Letters | 2008 | 5 Pages |
Abstract
Compounds with various activities and selectivities were discovered through structure–activity relationship studies of bicifadine analogs as monoamine transporter inhibitors. The norepinephrine-selective 2-thienyl compound S-6j was efficacious in a rodent pain model.
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Related Topics
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Chemistry
Organic Chemistry
Authors
Mingzhu Zhang, Florence Jovic, Troy Vickers, Brian Dyck, Junko Tamiya, Jonathan Grey, Joe A. Tran, Beth A. Fleck, Rebecca Pick, Alan C. Foster, Chen Chen,