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Synthesis of potent BACE-1 inhibitors incorporating a hydroxyethylene isostere as central core
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2010 (English)In: European Journal of Medicinal Chemistry, ISSN 0223-5234, E-ISSN 1768-3254, Vol. 45, no 3, 870-882 p.Article in journal (Refereed) Published
Abstract [en]

We herein describe the design and synthesis of a series of BACE-1 inhibitors incorporating a P1-substituted hydroxyl ethylene transition state isostere. The synthetic route starting from commercially available carbohydrates yielded a pivotal lactone intermediate with excellent stereochemical control which subsequently could be diversified at the PI-position. The final inhibitors were optimized using three different amines to provide the residues in the P2'-P3' position and three different acids affording the residues in the P2-P3 position. In addition we report on the stereochemical preference of the P1'-methyl substituent in the synthesized inhibitors. All inhibitors were evaluated in an in vitro BACE-I assay where the most potent inhibitor, 34-(R), exhibited a BACE-1 IC50 Value of 3.1 nM.

Place, publisher, year, edition, pages
2010. Vol. 45, no 3, 870-882 p.
Keyword [en]
Alzheimer's disease, BACE-1 inhibitors, Hydroxylethylene, Transition state isostere
National Category
Natural Sciences
Identifiers
URN: urn:nbn:se:su:diva-50312DOI: 10.1016/j.ejmech.2009.11.013ISI: 000275404900003OAI: oai:DiVA.org:su-50312DiVA: diva2:380774
Note
authorCount :10Available from: 2010-12-22 Created: 2010-12-22 Last updated: 2017-12-11Bibliographically approved

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