5-((3-Amidobenzyl)oxy)nicotinamides as Sirtuin 2 Inhibitors

Teng Ai, Daniel J. Wilson, Swati S. More, Jiashu Xie, Liqiang Chen

Research output: Contribution to journalArticlepeer-review

22 Scopus citations


Derived from our previously reported human sirtuin 2 (SIRT2) inhibitors that were based on a 5-aminonaphthalen-1-yloxy nicotinamide core structure, 5-((3-amidobenzyl)oxy)nicotinamides offered excellent activity against SIRT2 and high isozyme selectivity over SIRT1 and SIRT3. Selected compounds also exhibited generally favorable in vitro absorption, distribution, metabolism, and excretion properties. Kinetic studies revealed that a representative SIRT2 inhibitor acted competitively against both NAD+ and the peptide substrate, an inhibitory modality that was supported by our computational study. More importantly, two selected compounds exhibited significant protection against α-synuclein aggregation-induced cytotoxicity in SH-SY5Y cells. Therefore, 5-((3-amidobenzyl)oxy)nicotinamides represent a new class of SIRT2 inhibitors that are attractive candidates for further lead optimization in our continued effort to explore selective inhibition of SIRT2 as a potential therapy for Parkinson's disease.

Original languageEnglish (US)
Pages (from-to)2928-2941
Number of pages14
JournalJournal of medicinal chemistry
Issue number7
StatePublished - Apr 28 2016


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