کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1394252 1501140 2014 13 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Development and characterization of 3-(benzylsulfonamido)benzamides as potent and selective SIRT2 inhibitors
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آلی
پیش نمایش صفحه اول مقاله
Development and characterization of 3-(benzylsulfonamido)benzamides as potent and selective SIRT2 inhibitors
چکیده انگلیسی


• Inhibitors of SIRT2 are protective in models of Huntington's disease (HD).
• Inhibitors of SIRT2 decrease polyglutamine aggregation in HD.
• Sulfobenzoic acid derivatives shown to be selective SIRT2 inhibitors.
• Bioactive in α-tubulin K40 acetylation in two neuronal cell lines.
• Bioactive in polyglutamine aggregation assay.

Inhibitors of sirtuin-2 deacetylase (SIRT2) have been shown to be protective in various models of Huntington's disease (HD) by decreasing polyglutamine aggregation, a hallmark of HD pathology. The present study was directed at optimizing the potency of SIRT2 inhibitors containing the neuroprotective sulfobenzoic acid scaffold and improving their pharmacology. To achieve that goal, 176 analogues were designed, synthesized, and tested in deacetylation assays against the activities of major human sirtuins SIRT1-3. This screen yielded 15 compounds with enhanced potency for SIRT2 inhibition and 11 compounds having SIRT2 inhibition equal to reference compound AK-1. The newly synthesized compounds also demonstrated higher SIRT2 selectivity over SIRT1 and SIRT3. These candidates were subjected to a dose–response bioactivity assay, measuring an increase in α-tubulin K40 acetylation in two neuronal cell lines, which yielded five compounds bioactive in both cell lines and eight compounds bioactive in at least one of the cell lines tested. These bioactive compounds were subsequently tested in a tertiary polyglutamine aggregation assay, which identified five inhibitors. ADME properties of the bioactive SIRT2 inhibitors were assessed, which revealed a significant improvement of the pharmacological properties of the new entities, reaching closer to the goal of a clinically-viable candidate.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: European Journal of Medicinal Chemistry - Volume 76, 9 April 2014, Pages 414–426
نویسندگان
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