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Synthesis and Evaluation of Novel Benzofuran Derivatives as Selective SIRT2 Inhibitors
A series of benzofuran derivatives were designed and synthesized, and their inhibitory activites were measured against the SIRT1–3. The enzymatic assay showed that all the compounds showed certain anti-SIRT2 activity and selective over SIRT1 and SIRT3 with IC(50) (half maximal inhibitory concentrati...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6152376/ https://www.ncbi.nlm.nih.gov/pubmed/28805748 http://dx.doi.org/10.3390/molecules22081348 |
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author | Zhou, Yumei Cui, Huaqing Yu, Xiaoming Peng, Tao Wang, Gang Wen, Xiaoxue Sun, Yunbo Liu, Shuchen Zhang, Shouguo Hu, Liming Wang, Lin |
author_facet | Zhou, Yumei Cui, Huaqing Yu, Xiaoming Peng, Tao Wang, Gang Wen, Xiaoxue Sun, Yunbo Liu, Shuchen Zhang, Shouguo Hu, Liming Wang, Lin |
author_sort | Zhou, Yumei |
collection | PubMed |
description | A series of benzofuran derivatives were designed and synthesized, and their inhibitory activites were measured against the SIRT1–3. The enzymatic assay showed that all the compounds showed certain anti-SIRT2 activity and selective over SIRT1 and SIRT3 with IC(50) (half maximal inhibitory concentration) values at the micromolar level. The preliminary structure–activity relationships were analyzed and the binding features of compound 7e (IC(50) 3.81 µM) was predicted using the CDOCKER program. The results of this research could provide informative guidance for further optimizing benzofuran derivatives as potent SIRT2 inhibitors. |
format | Online Article Text |
id | pubmed-6152376 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61523762018-11-13 Synthesis and Evaluation of Novel Benzofuran Derivatives as Selective SIRT2 Inhibitors Zhou, Yumei Cui, Huaqing Yu, Xiaoming Peng, Tao Wang, Gang Wen, Xiaoxue Sun, Yunbo Liu, Shuchen Zhang, Shouguo Hu, Liming Wang, Lin Molecules Article A series of benzofuran derivatives were designed and synthesized, and their inhibitory activites were measured against the SIRT1–3. The enzymatic assay showed that all the compounds showed certain anti-SIRT2 activity and selective over SIRT1 and SIRT3 with IC(50) (half maximal inhibitory concentration) values at the micromolar level. The preliminary structure–activity relationships were analyzed and the binding features of compound 7e (IC(50) 3.81 µM) was predicted using the CDOCKER program. The results of this research could provide informative guidance for further optimizing benzofuran derivatives as potent SIRT2 inhibitors. MDPI 2017-08-14 /pmc/articles/PMC6152376/ /pubmed/28805748 http://dx.doi.org/10.3390/molecules22081348 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Zhou, Yumei Cui, Huaqing Yu, Xiaoming Peng, Tao Wang, Gang Wen, Xiaoxue Sun, Yunbo Liu, Shuchen Zhang, Shouguo Hu, Liming Wang, Lin Synthesis and Evaluation of Novel Benzofuran Derivatives as Selective SIRT2 Inhibitors |
title | Synthesis and Evaluation of Novel Benzofuran Derivatives as Selective SIRT2 Inhibitors |
title_full | Synthesis and Evaluation of Novel Benzofuran Derivatives as Selective SIRT2 Inhibitors |
title_fullStr | Synthesis and Evaluation of Novel Benzofuran Derivatives as Selective SIRT2 Inhibitors |
title_full_unstemmed | Synthesis and Evaluation of Novel Benzofuran Derivatives as Selective SIRT2 Inhibitors |
title_short | Synthesis and Evaluation of Novel Benzofuran Derivatives as Selective SIRT2 Inhibitors |
title_sort | synthesis and evaluation of novel benzofuran derivatives as selective sirt2 inhibitors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6152376/ https://www.ncbi.nlm.nih.gov/pubmed/28805748 http://dx.doi.org/10.3390/molecules22081348 |
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