| Literature DB >> 20817006 |
Graeme Horne1, Francis X Wilson, Jon Tinsley, David H Williams, Richard Storer.
Abstract
Iminosugars comprise the most attractive class of carbohydrate mimetics reported to date and are ideally positioned to take advantage of our increasing understanding of glycobiology in the search for new medicines. First-generation iminosugar drugs suffered from lack of adequate selectivity, resulting in considerable side-effects in the clinic. Current efforts directed towards second-generation compounds, encompassing a much greater range of structures and addressing a wider selection of biochemical targets, are enabling the identification and development of suitable candidates that benefit from improved activity and selectivity. Furthermore, second-generation compounds can address a variety of established targets that have previously proved refractory to other compound classes. This review focuses on the breadth of opportunities provided by second-generation leads from iminosugars (Seglins™).Entities:
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Year: 2010 PMID: 20817006 DOI: 10.1016/j.drudis.2010.08.017
Source DB: PubMed Journal: Drug Discov Today ISSN: 1359-6446 Impact factor: 7.851