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Discovery of cyclic sulfoxide hydroxyethylamines as potent and selective β-site APP-cleaving enzyme 1 (BACE1) inhibitors: Structure based design and in vivo reduction of amyloid β-peptides

Crossref DOI link: https://doi.org/10.1016/j.bmcl.2013.07.071

Published Print: 2013-10

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

Rueeger, Heinrich

Lueoend, Rainer

Machauer, Rainer

Veenstra, Siem Jacob

Jacobson, Laura Helen

Staufenbiel, Matthias

Desrayaud, Sandrine

Rondeau, Jean-Michel

Möbitz, Henrik

Neumann, Ulf
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Text and Data Mining valid from 2013-10-01
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This article is maintained by: Elsevier

Article Title: Discovery of cyclic sulfoxide hydroxyethylamines as potent and selective β-site APP-cleaving enzyme 1 (BACE1) inhibitors: Structure based design and in vivo reduction of amyloid β-peptides

Journal Title: Bioorganic & Medicinal Chemistry Letters

CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.bmcl.2013.07.071

Content Type: article

Copyright: Copyright © 2013 Elsevier Ltd. All rights reserved.

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