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Natural phenolic derivatives based on piperine scaffold as potential antifungal agents
Piperine is a natural alkaloid with a wide range of biological functions. Natural phenolic compounds existed in many essential oils (EOs) are plant-derived aroma compounds with broad range of biological activities, however, their actions are slow, and they are typically unstable to light or heat, di...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7106752/ https://www.ncbi.nlm.nih.gov/pubmed/32259136 http://dx.doi.org/10.1186/s13065-020-00676-4 |
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author | Wang, Jingjing Wang, Wenlong Xiong, Haojin Song, Di Cao, Xiufang |
author_facet | Wang, Jingjing Wang, Wenlong Xiong, Haojin Song, Di Cao, Xiufang |
author_sort | Wang, Jingjing |
collection | PubMed |
description | Piperine is a natural alkaloid with a wide range of biological functions. Natural phenolic compounds existed in many essential oils (EOs) are plant-derived aroma compounds with broad range of biological activities, however, their actions are slow, and they are typically unstable to light or heat, difficult to extract and so on. In order to find high-potential fungicides derived from piperine, a series of piperine-directed essential oil derivatives were designed and synthesized. The structures of all molecules were confirmed by satisfied spectral data, including (1)H NMR, (13)C NMR and ESIMS. The target compounds were screened for their potential fungicidal activities against six species of plant pathogen fungi, including Rhizoctonia solani, Fusarium graminearum, Phomopsis adianticola, Alternaria tenuis Nees, Phytophthora capsici and Gloeosporium theae-sinensis. Some of target compounds exhibited moderate and broad-spectrum activity against tested fungi compared to the parental piperine. Further studies have shown that some different concentrations of compounds have significant inhibitory activity against Alternaria tenuis Nees and Phytophthora capsici compared to commercial carbendazim, and compound 2b exhibited particularly significant broad-spectrum fungicidal activity. [Image: see text] |
format | Online Article Text |
id | pubmed-7106752 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-71067522020-04-01 Natural phenolic derivatives based on piperine scaffold as potential antifungal agents Wang, Jingjing Wang, Wenlong Xiong, Haojin Song, Di Cao, Xiufang BMC Chem Research Article Piperine is a natural alkaloid with a wide range of biological functions. Natural phenolic compounds existed in many essential oils (EOs) are plant-derived aroma compounds with broad range of biological activities, however, their actions are slow, and they are typically unstable to light or heat, difficult to extract and so on. In order to find high-potential fungicides derived from piperine, a series of piperine-directed essential oil derivatives were designed and synthesized. The structures of all molecules were confirmed by satisfied spectral data, including (1)H NMR, (13)C NMR and ESIMS. The target compounds were screened for their potential fungicidal activities against six species of plant pathogen fungi, including Rhizoctonia solani, Fusarium graminearum, Phomopsis adianticola, Alternaria tenuis Nees, Phytophthora capsici and Gloeosporium theae-sinensis. Some of target compounds exhibited moderate and broad-spectrum activity against tested fungi compared to the parental piperine. Further studies have shown that some different concentrations of compounds have significant inhibitory activity against Alternaria tenuis Nees and Phytophthora capsici compared to commercial carbendazim, and compound 2b exhibited particularly significant broad-spectrum fungicidal activity. [Image: see text] Springer International Publishing 2020-03-30 /pmc/articles/PMC7106752/ /pubmed/32259136 http://dx.doi.org/10.1186/s13065-020-00676-4 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Wang, Jingjing Wang, Wenlong Xiong, Haojin Song, Di Cao, Xiufang Natural phenolic derivatives based on piperine scaffold as potential antifungal agents |
title | Natural phenolic derivatives based on piperine scaffold as potential antifungal agents |
title_full | Natural phenolic derivatives based on piperine scaffold as potential antifungal agents |
title_fullStr | Natural phenolic derivatives based on piperine scaffold as potential antifungal agents |
title_full_unstemmed | Natural phenolic derivatives based on piperine scaffold as potential antifungal agents |
title_short | Natural phenolic derivatives based on piperine scaffold as potential antifungal agents |
title_sort | natural phenolic derivatives based on piperine scaffold as potential antifungal agents |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7106752/ https://www.ncbi.nlm.nih.gov/pubmed/32259136 http://dx.doi.org/10.1186/s13065-020-00676-4 |
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