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Recent advances in the development of histone deacylase SIRT2 inhibitors
Sirtuin 2 (SIRT2) is an important and special member of the atypical histone deacetylase Sirtuin (SIRT) family. Due to its extensive catalytic effects, SIRT2 can regulate autophagy, myelination, immunity, inflammation and other physiological processes. Recent evidence revealed that dysregulation of...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9057128/ https://www.ncbi.nlm.nih.gov/pubmed/35521274 http://dx.doi.org/10.1039/d0ra06316a |
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author | Yang, Wenyu Chen, Wei Su, Huilin Li, Rong Song, Chen Wang, Zhouyu Yang, Lingling |
author_facet | Yang, Wenyu Chen, Wei Su, Huilin Li, Rong Song, Chen Wang, Zhouyu Yang, Lingling |
author_sort | Yang, Wenyu |
collection | PubMed |
description | Sirtuin 2 (SIRT2) is an important and special member of the atypical histone deacetylase Sirtuin (SIRT) family. Due to its extensive catalytic effects, SIRT2 can regulate autophagy, myelination, immunity, inflammation and other physiological processes. Recent evidence revealed that dysregulation of human SIRT2 activity is associated with the pathogenesis and prognosis of cancers, Parkinson's disease and other disorders; thus SIRT2 is a promising target for potential therapeutic intervention. This review presents a systematic summary of nine chemotypes of small-molecule SIRT2 inhibitors, particularly including the discovery and structural optimization strategies, which will be useful for future efforts to develop new inhibitors targeting SIRT2 and associated target proteins. |
format | Online Article Text |
id | pubmed-9057128 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90571282022-05-04 Recent advances in the development of histone deacylase SIRT2 inhibitors Yang, Wenyu Chen, Wei Su, Huilin Li, Rong Song, Chen Wang, Zhouyu Yang, Lingling RSC Adv Chemistry Sirtuin 2 (SIRT2) is an important and special member of the atypical histone deacetylase Sirtuin (SIRT) family. Due to its extensive catalytic effects, SIRT2 can regulate autophagy, myelination, immunity, inflammation and other physiological processes. Recent evidence revealed that dysregulation of human SIRT2 activity is associated with the pathogenesis and prognosis of cancers, Parkinson's disease and other disorders; thus SIRT2 is a promising target for potential therapeutic intervention. This review presents a systematic summary of nine chemotypes of small-molecule SIRT2 inhibitors, particularly including the discovery and structural optimization strategies, which will be useful for future efforts to develop new inhibitors targeting SIRT2 and associated target proteins. The Royal Society of Chemistry 2020-10-09 /pmc/articles/PMC9057128/ /pubmed/35521274 http://dx.doi.org/10.1039/d0ra06316a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Yang, Wenyu Chen, Wei Su, Huilin Li, Rong Song, Chen Wang, Zhouyu Yang, Lingling Recent advances in the development of histone deacylase SIRT2 inhibitors |
title | Recent advances in the development of histone deacylase SIRT2 inhibitors |
title_full | Recent advances in the development of histone deacylase SIRT2 inhibitors |
title_fullStr | Recent advances in the development of histone deacylase SIRT2 inhibitors |
title_full_unstemmed | Recent advances in the development of histone deacylase SIRT2 inhibitors |
title_short | Recent advances in the development of histone deacylase SIRT2 inhibitors |
title_sort | recent advances in the development of histone deacylase sirt2 inhibitors |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9057128/ https://www.ncbi.nlm.nih.gov/pubmed/35521274 http://dx.doi.org/10.1039/d0ra06316a |
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