| Literature DB >> 29577959 |
Han Dai1, David A Sinclair2, James L Ellis1, Clemens Steegborn3.
Abstract
The NAD+-dependent protein lysine deacylases of the Sirtuin family regulate various physiological functions, from energy metabolism to stress responses. The human Sirtuin isoforms, SIRT1-7, are considered attractive therapeutic targets for aging-related diseases, such as type 2 diabetes, inflammatory diseases and neurodegenerative disorders. We review the status of Sirtuin-targeted drug discovery and development. Potent and selective pharmacological Sirt1 activators and inhibitors are available, and initial clinical trials have been carried out. Several promising inhibitors and activators have also been described for other isoforms. Progress in understanding the mechanisms of Sirtuin modulation by such compounds provides a rational basis for further drug development.Entities:
Keywords: Activation; Deacetylase; Deacylase; Drug discovery and development; Inhibition
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Year: 2018 PMID: 29577959 PMCID: PMC6342514 DOI: 10.1016/j.pharmthera.2018.03.004
Source DB: PubMed Journal: Pharmacol Ther ISSN: 0163-7258 Impact factor: 12.310