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Current Trends in Sirtuin Activator and Inhibitor Development

Karina Bursch, Christopher J. Goetz, Brian C. Smith

Molecules · 2024 · ▲ 54 citations

Abstract

-dependent protein deacylases and key metabolic regulators, coupling the cellular energy state with selective lysine deacylation to regulate many downstream cellular processes. Humans encode seven sirtuin isoforms (Sirt1-7) with diverse subcellular localization and deacylase targets. Sirtuins are considered protective anti-aging proteins since increased sirtuin activity is canonically associated with lifespan extension and decreased activity with developing aging-related diseases. However, sirtuins can also assume detrimental cellular roles where increased activity contributes to pathophysiology. Modulation of sirtuin activity by activators and inhibitors thus holds substantial potential for defining the cellular roles of sirtuins in health and disease and developing therapeutics. Instead of being comprehensive, this review discusses the well-characterized sirtuin activators and inhibitors available to date, particularly those with demonstrated selectivity, potency, and cellular activity. This review also provides recommendations regarding the best-in-class sirtuin activators and inhibitors for practical research as sirtuin modulator discovery and refinement evolve.

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Provenance

Source
OpenAlex
DOI
10.3390/molecules29051185
Canonical
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Fetched
2026-06-29 MST

Cite this

APA
Bursch, K., Goetz, C.J., &amp; Smith, B.C. (2024). Current Trends in Sirtuin Activator and Inhibitor Development. <em>Molecules</em>. https://doi.org/10.3390/molecules29051185
Vancouver
Bursch K, Goetz CJ, Smith BC. Current Trends in Sirtuin Activator and Inhibitor Development. Molecules. 2024. doi:10.3390/molecules29051185.
BibTeX
@article{karina2024Curren, title = {Current Trends in Sirtuin Activator and Inhibitor Development}, author = {Karina Bursch and Christopher J. Goetz and Brian C. Smith}, journal = {Molecules}, year = {2024}, doi = {10.3390/molecules29051185}, }

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