Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1375687 | Bioorganic & Medicinal Chemistry Letters | 2009 | 4 Pages |
Abstract
Accumulation of beta-amyloid (Aβ), produced by the proteolytic cleavage of amyloid precursor protein (APP) by β- and γ-secretase, is widely believed to be associated with Alzheimer’s disease (AD). Research around the high-throughput screening hit (S)-4-chlorophenylsulfonyl isoleucinol led to the identification of the Notch-1-sparing (9.5-fold) γ-secretase inhibitor (S)-N-(5-chlorothiophene-2-sulfonyl)-β,β-diethylalaninol 7.b.2 (Aβ 40/42 EC50 = 28 nM), which is efficacious in reduction of Aβ production in vivo.
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Related Topics
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Authors
Derek C. Cole, Joseph R. Stock, Anthony F. Kreft, Madelene Antane, Suzan H. Aschmies, Kevin P. Atchison, David S. Casebier, Thomas A. Comery, George Diamantidis, John W. Ellingboe, Boyd L. Harrison, Yun Hu, Mei Jin, Dennis M. Kubrak, Peimin Lu,