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164SFAD were grown in high glucose (4.5 g/L) DMEM (Invitrogen) media supplemented with 10% FBS, 100 μ g/mL pen-strep, 2 mM glutamine, and 100 μg/mL geneticin. Cells were aliquoted into a 96 well plate, and after attachment the medium was replaced with Ultraculture (Whittaker Bioproducts) containing individual compounds of interest (final DMSO concentration of 1%. After an overnight incubation the conditioned medium was removed and evaluated for the presence of Aβ in a sandwich ELISA using a monoclonal C-terminal Aβ40 specific capture antibody and an HRP labeled monoclonal antibody to the N-teminus of Aβ for detection. The endpoint measurement of Aβ1-40 level was developed using TMB reagent followed by the addition of 1 M phosphoric acid. The plates were read at 450 nm
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3): 0.80-1.25 (m, 12H), 1.88-2.05 (m, 1H), 3.25-3.49 (s, 5H), 4.32-4.52 (m, 2H), 5.18 (m, 1H), 6.08-6.18 (m, 1H) 5.09-5.10 (d, 1H), 6.66-7.80 (m, 7H); MS (ESI) 501.23 (M+H)
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