کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1394362 1501155 2013 15 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Structure-based optimization of oxadiazole-based GSK-3 inhibitors
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آلی
پیش نمایش صفحه اول مقاله
Structure-based optimization of oxadiazole-based GSK-3 inhibitors
چکیده انگلیسی

Inhibition of glycogen synthase kinase-3 (GSK-3) induces neuroprotective effects, e.g. decreases β-amyloid production and reduces tau hyperphosphorylation, which are both associated with Alzheimer's disease (AD). The two isoforms of GSK-3 in mammalians are GSK-3α and β, which share 98% homology in their catalytic domains. We investigated GSK-3 inhibitors based on 2 different scaffolds in order to elucidate the demands of the ATP-binding pocket [1]. Particularly, the oxadiazole scaffold provided potent and selective GSK-3 inhibitors. For example, the most potent inhibitor of the present series, the acetamide 26d, is characterized by an IC50 of 2 nM for GSK-3α and 17 nM for GSK-3β. In addition, the benzodioxane 8g showed up to 27-fold selectivity for GSK-3α over GSK-3β, with an IC50 of 35 nM for GSK-3α. Two GSK-3 inhibitors were further profiled for efficacy and toxicity in the wild-type (wt) zebrafish embryo assay to evaluate simultaneously permeability and safety.

Graphical AbstractFigure optionsDownload as PowerPoint slideHighlights
► Synthesis of GSK-3 inhibitors with oxadiazole scaffold.
► Interplay of different substituents on the second phenyl ring is adequate to gain selectivity for one GSK-3 isoform.
► These compounds were found to exhibit remarkable activities and selectivities.
► The most active compounds were selected to be evaluated on a zebrafish embryo assay.
► One inhibitor showed up to 27-fold selectivity for GSK-3α over GSK-3β.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: European Journal of Medicinal Chemistry - Volume 61, March 2013, Pages 26–40
نویسندگان
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