Design, synthesis, and evaluation of resveratrol derivatives as Aß1–42 aggregation inhibitors, antioxidants, and neuroprotective agents

C Lu, Y Guo, J Li, M Yao, Q Liao, Z Xie, X Li - Bioorganic & medicinal …, 2012 - Elsevier
C Lu, Y Guo, J Li, M Yao, Q Liao, Z Xie, X Li
Bioorganic & medicinal chemistry letters, 2012Elsevier
A series of novel resveratrol derivatives were designed, synthesised and evaluated as
potential therapeutic agents for the treatment of Alzheimer's disease. Among these
compounds, compound 7l,(E)-5-(4-(isopropylamino) styryl) benzene-1, 3-diol, exhibited
potent ß-amyloid aggregation inhibition activity, which was confirmed by a ThT fluorescence
assay (71.65% at 20μM) and transmission electron microscopy (TEM). Compound 7l also
exhibited good antioxidant activity (4.12 Trolox equivalents in an oxygen radical absorbance …
A series of novel resveratrol derivatives were designed, synthesised and evaluated as potential therapeutic agents for the treatment of Alzheimer’s disease. Among these compounds, compound 7l, (E)-5-(4-(isopropylamino)styryl)benzene-1,3-diol, exhibited potent ß-amyloid aggregation inhibition activity, which was confirmed by a ThT fluorescence assay (71.65% at 20μM) and transmission electron microscopy (TEM). Compound 7l also exhibited good antioxidant activity (4.12 Trolox equivalents in an oxygen radical absorbance capacity assay and a 37% reduction in reactive oxygen species in cells at 10μM). The cytotoxicity analysis of compounds 7f, 7i, 7j and 7l indicated that these compounds have lower toxicities than resveratrol at 60μM.
Elsevier
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