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Synthesis, characterization and in vitro biological evaluation of two matrine derivatives
Matrine is a traditional Chinese medicine and botanical pesticide with broad biological activities, including pharmacological and agricultural activities. In present work, two matrine derivatives have been successfully synthesized via introducing indole and cyclohexylamino to 13 position of matrine,...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6200782/ https://www.ncbi.nlm.nih.gov/pubmed/30356148 http://dx.doi.org/10.1038/s41598-018-33908-8 |
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author | Cheng, Xingan Ye, Jingmin He, Huiqing Liu, Zhanmei Xu, Chunbao (Charles) Wu, Bo Xiong, Xialing Shu, Xugang Jiang, Xuhong Qin, Xiangjing |
author_facet | Cheng, Xingan Ye, Jingmin He, Huiqing Liu, Zhanmei Xu, Chunbao (Charles) Wu, Bo Xiong, Xialing Shu, Xugang Jiang, Xuhong Qin, Xiangjing |
author_sort | Cheng, Xingan |
collection | PubMed |
description | Matrine is a traditional Chinese medicine and botanical pesticide with broad biological activities, including pharmacological and agricultural activities. In present work, two matrine derivatives have been successfully synthesized via introducing indole and cyclohexylamino to 13 position of matrine, respectively, with sophocarpine as starting material, and structurally characterized via infrared spectroscopy(IR), MS, 1 H NMR, 13 C NMR and X-ray crystal diffraction. The results of the in vitro biological activity tests showed that these two matrine derivatives exhibited even better activities against human cancer cells Hela229 and insect cell line Sf9 from Spodoptera frugiperda (J. E. Smith) than that of parent matrine, suggesting that the heterocyclic or cyclic group can dramatically increase the biological activity of matrine. It is worth to mention that 13-indole-matrine could possibly inhibit the growth of insect cells or human cancer cells by inducing cell apoptosis. The results of the present study provide useful information for further structural modifications of these compounds and for exploring new, potent anti-cancer agents and environment friendly pesticides. |
format | Online Article Text |
id | pubmed-6200782 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62007822018-10-26 Synthesis, characterization and in vitro biological evaluation of two matrine derivatives Cheng, Xingan Ye, Jingmin He, Huiqing Liu, Zhanmei Xu, Chunbao (Charles) Wu, Bo Xiong, Xialing Shu, Xugang Jiang, Xuhong Qin, Xiangjing Sci Rep Article Matrine is a traditional Chinese medicine and botanical pesticide with broad biological activities, including pharmacological and agricultural activities. In present work, two matrine derivatives have been successfully synthesized via introducing indole and cyclohexylamino to 13 position of matrine, respectively, with sophocarpine as starting material, and structurally characterized via infrared spectroscopy(IR), MS, 1 H NMR, 13 C NMR and X-ray crystal diffraction. The results of the in vitro biological activity tests showed that these two matrine derivatives exhibited even better activities against human cancer cells Hela229 and insect cell line Sf9 from Spodoptera frugiperda (J. E. Smith) than that of parent matrine, suggesting that the heterocyclic or cyclic group can dramatically increase the biological activity of matrine. It is worth to mention that 13-indole-matrine could possibly inhibit the growth of insect cells or human cancer cells by inducing cell apoptosis. The results of the present study provide useful information for further structural modifications of these compounds and for exploring new, potent anti-cancer agents and environment friendly pesticides. Nature Publishing Group UK 2018-10-24 /pmc/articles/PMC6200782/ /pubmed/30356148 http://dx.doi.org/10.1038/s41598-018-33908-8 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Cheng, Xingan Ye, Jingmin He, Huiqing Liu, Zhanmei Xu, Chunbao (Charles) Wu, Bo Xiong, Xialing Shu, Xugang Jiang, Xuhong Qin, Xiangjing Synthesis, characterization and in vitro biological evaluation of two matrine derivatives |
title | Synthesis, characterization and in vitro biological evaluation of two matrine derivatives |
title_full | Synthesis, characterization and in vitro biological evaluation of two matrine derivatives |
title_fullStr | Synthesis, characterization and in vitro biological evaluation of two matrine derivatives |
title_full_unstemmed | Synthesis, characterization and in vitro biological evaluation of two matrine derivatives |
title_short | Synthesis, characterization and in vitro biological evaluation of two matrine derivatives |
title_sort | synthesis, characterization and in vitro biological evaluation of two matrine derivatives |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6200782/ https://www.ncbi.nlm.nih.gov/pubmed/30356148 http://dx.doi.org/10.1038/s41598-018-33908-8 |
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