| Literature DB >> 21924610 |
Thomas Lübbers1, Alexander Flohr, Synese Jolidon, Pascale David-Pierson, Helmut Jacobsen, Laurence Ozmen, Karlheinz Baumann.
Abstract
We herein report the discovery of a new γ-secretase modulator class with an aminothiazole core starting from a HTS hit (3). Synthesis and SAR of this series are discussed. These novel compounds demonstrate moderate to good in vitro potency in inhibiting amyloid beta (Aβ) peptide production. Overall γ-secretase is not inhibited but the formation of the aggregating, toxic Aβ42 peptide is shifted to smaller non-aggregating Aβ peptides. Compound 15 reduced brain Aβ42 in vivo in APPSwe transgenic mice at 30mg/kg p.o.Entities:
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Year: 2011 PMID: 21924610 DOI: 10.1016/j.bmcl.2011.08.060
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823