Abstract
The development of a novel series of purines as gamma-secretase modulators for potential use in the treatment of Alzheimer's disease is disclosed herein. Optimization of a previously disclosed pyrimidine series afforded a series of potent purine-based gamma-secretase modulators with 300- to 2000-fold in vitro selectivity over inhibition of Notch cleavage and that selectively reduces Alphabeta42 in an APP-YAC transgenic mouse model.
2010 Elsevier Ltd. All rights reserved.
MeSH terms
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Alzheimer Disease / drug therapy*
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Amyloid Precursor Protein Secretases / genetics
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Amyloid Precursor Protein Secretases / metabolism*
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Amyloid beta-Peptides / antagonists & inhibitors*
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Amyloid beta-Peptides / metabolism
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Animals
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Humans
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Mice
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Mice, Transgenic
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Peptide Fragments / antagonists & inhibitors*
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Peptide Fragments / metabolism
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Purines / chemistry*
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Purines / pharmacology
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Purines / therapeutic use*
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Receptors, Notch / metabolism
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Structure-Activity Relationship
Substances
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Amyloid beta-Peptides
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Peptide Fragments
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Purines
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Receptors, Notch
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amyloid beta-protein (40-42)
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Amyloid Precursor Protein Secretases