Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1377387 | Bioorganic & Medicinal Chemistry Letters | 2007 | 5 Pages |
Abstract
A series of N-alkylbenzenesulfonamides were developed from a high throughput screening hit. Classic and parallel synthesis strategies were employed to produce compounds with good in vitro and in vivo γ-secretase activity.
Graphical abstractA series of N-alkylbenzenesulfonamides were developed from a high throughput screening hit. Classic and parallel synthesis strategies were employed to produce compounds with good in vitro and in vivo γ-secretase activity.Figure optionsDownload full-size imageDownload as PowerPoint slide
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Michael F. Parker, Donna M. Barten, Carl P. Bergstrom, Joanne J. Bronson, Jason A. Corsa, Milind S. Deshpande, Kevin M. Felsenstein, Valerie L. Guss, Steven B. Hansel, Graham Johnson, Daniel J. Keavy, Wai Y. Lau, Jeremy Mock, C.V.C. Prasad,