Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1376303 | Bioorganic & Medicinal Chemistry Letters | 2007 | 5 Pages |
Abstract
High throughput screening led to the discovery of a novel series of 1,3-diaminopropan-2-ol sulfonamides as selective GlyT-1 inhibitors. Structure–activity relationships of this novel series and optimisation of the initial hit that led to the identification of (2), a potent and selective GlyT-1 inhibitor, are also presented.
Graphical abstractHigh throughput screening led to the discovery of a novel series of 1,3-diaminopropan-2-ol sulfonamides as selective GlyT-1 inhibitors. Structure–activity relationships of this novel series and optimisation of the initial hit that led to the identification of (2), a potent and selective GlyT-1 inhibitor, are also presented.Figure optionsDownload full-size imageDownload as PowerPoint slide
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Shahzad S. Rahman, Steven Coulton, Hugh J. Herdon, Graham F. Joiner, Jian Jin, Roderick A. Porter,