ABSTRACT
Inhibiting aggregation of the amyloid-beta (Aß) peptide may be an effective strategy for combating Alzheimer's disease. As the high-resolution structure of the toxic Aß aggregate is unknown, rational design of small molecule inhibitors is not possible, and inhibitors are best isolated by high-throughput screening. We applied high-throughput screening to a collection of 65,000 compounds to identify compound D737 as an inhibitor of Aß aggregation. D737 diminished the formation of oligomers and fibrils, and reduced Aß42-induced cytotoxicity. Most importantly, D737 increased the life span and locomotive ability of transgenic flies in a Drosophila melanogaster model of Alzheimer's disease (J Biol Chem, 287, 2012, 38992). To explore the chemical features that make D737 an effective inhibitor of Aß42 aggregation and toxicity, we tested a small collection of eleven analogues of D737. Overall, the ability of a compound to inhibit Aß aggregation was a good predictor of its efficacy in prolonging the life span and locomotive ability of transgenic flies expressing human Aß42 in the central nervous system. Two compounds (D744 and D830) with fluorine substitutions on an aromatic ring were effective inhibitors of Aß42 aggregation and increased the longevity of transgenic flies beyond that observed for the parent compound, D737.
