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Novel benzamido derivatives as PTP1B inhibitors with anti-hyperglycemic and lipid-lowering efficacy
Based on a non-competitive and selective PTP1B inhibitor reported by us previously, thirty-nine benzamido derivatives were designed and synthesized as novel PTP1B inhibitors. Among them, twelve compounds exhibited IC(50) values at micromolar level against human recombinant PTP1B, and most of them ex...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251817/ https://www.ncbi.nlm.nih.gov/pubmed/30505661 http://dx.doi.org/10.1016/j.apsb.2018.05.001 |
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author | Tang, Yanbo Zhang, Xiaolin Chen, Zheng Yin, Wenwen Nan, Guanglei Tian, Jinying Ye, Fei Xiao, Zhiyan |
author_facet | Tang, Yanbo Zhang, Xiaolin Chen, Zheng Yin, Wenwen Nan, Guanglei Tian, Jinying Ye, Fei Xiao, Zhiyan |
author_sort | Tang, Yanbo |
collection | PubMed |
description | Based on a non-competitive and selective PTP1B inhibitor reported by us previously, thirty-nine benzamido derivatives were designed and synthesized as novel PTP1B inhibitors. Among them, twelve compounds exhibited IC(50) values at micromolar level against human recombinant PTP1B, and most of them exhibited significant selectivity to PTP1B over TC-PTP and CD45. Further evaluation of the most potent compound 27 on high-fat diet (HFD)-induced insulin-resistant (IR) obese mice indicated that 27 could modulate glucose metabolism and ameliorate dyslipidemia simultaneously. |
format | Online Article Text |
id | pubmed-6251817 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-62518172018-11-30 Novel benzamido derivatives as PTP1B inhibitors with anti-hyperglycemic and lipid-lowering efficacy Tang, Yanbo Zhang, Xiaolin Chen, Zheng Yin, Wenwen Nan, Guanglei Tian, Jinying Ye, Fei Xiao, Zhiyan Acta Pharm Sin B Original article Based on a non-competitive and selective PTP1B inhibitor reported by us previously, thirty-nine benzamido derivatives were designed and synthesized as novel PTP1B inhibitors. Among them, twelve compounds exhibited IC(50) values at micromolar level against human recombinant PTP1B, and most of them exhibited significant selectivity to PTP1B over TC-PTP and CD45. Further evaluation of the most potent compound 27 on high-fat diet (HFD)-induced insulin-resistant (IR) obese mice indicated that 27 could modulate glucose metabolism and ameliorate dyslipidemia simultaneously. Elsevier 2018-10 2018-05-08 /pmc/articles/PMC6251817/ /pubmed/30505661 http://dx.doi.org/10.1016/j.apsb.2018.05.001 Text en © 2018 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original article Tang, Yanbo Zhang, Xiaolin Chen, Zheng Yin, Wenwen Nan, Guanglei Tian, Jinying Ye, Fei Xiao, Zhiyan Novel benzamido derivatives as PTP1B inhibitors with anti-hyperglycemic and lipid-lowering efficacy |
title | Novel benzamido derivatives as PTP1B inhibitors with anti-hyperglycemic and lipid-lowering efficacy |
title_full | Novel benzamido derivatives as PTP1B inhibitors with anti-hyperglycemic and lipid-lowering efficacy |
title_fullStr | Novel benzamido derivatives as PTP1B inhibitors with anti-hyperglycemic and lipid-lowering efficacy |
title_full_unstemmed | Novel benzamido derivatives as PTP1B inhibitors with anti-hyperglycemic and lipid-lowering efficacy |
title_short | Novel benzamido derivatives as PTP1B inhibitors with anti-hyperglycemic and lipid-lowering efficacy |
title_sort | novel benzamido derivatives as ptp1b inhibitors with anti-hyperglycemic and lipid-lowering efficacy |
topic | Original article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251817/ https://www.ncbi.nlm.nih.gov/pubmed/30505661 http://dx.doi.org/10.1016/j.apsb.2018.05.001 |
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