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Synthesis and characteristics of (Hydrogenated) ferulic acid derivatives as potential antiviral agents with insecticidal activity
BACKGROUND: Plant viruses cause many serious plant diseases and are currently suppressed with the simultaneous use of virucides and insecticides. The use of such materials, however, increases the amounts of pollutants in the environment. To reduce environmental contaminants, virucides with insectici...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3599306/ https://www.ncbi.nlm.nih.gov/pubmed/23409923 http://dx.doi.org/10.1186/1752-153X-7-33 |
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author | Huang, Guang-Ying Cui, Can Wang, Zhi-Peng Li, Yong-Qiang Xiong, Li-Xia Wang, Li-Zhong Yu, Shu-Jing Li, Zheng-Ming Zhao, Wei-Guang |
author_facet | Huang, Guang-Ying Cui, Can Wang, Zhi-Peng Li, Yong-Qiang Xiong, Li-Xia Wang, Li-Zhong Yu, Shu-Jing Li, Zheng-Ming Zhao, Wei-Guang |
author_sort | Huang, Guang-Ying |
collection | PubMed |
description | BACKGROUND: Plant viruses cause many serious plant diseases and are currently suppressed with the simultaneous use of virucides and insecticides. The use of such materials, however, increases the amounts of pollutants in the environment. To reduce environmental contaminants, virucides with insecticidal activity is an attractive option. RESULTS: A series of substituted ferulic acid amide derivatives 7 and the corresponding hydrogenated ferulic acid amide derivatives 13 were synthesized and evaluated for their antiviral and insecticidal activities. The majority of the synthesized compounds exhibited good levels of antiviral activity against the tobacco mosaic virus (TMW), with compounds 7a, 7b and 7d in particular providing higher levels of protective and curative activities against TMV at 500 μg/mL than the control compound ribavirin. Furthermore, these compounds displayed good insecticidal activities against insects with piercing-sucking mouthparts, which can spread plant viruses between and within crops. CONCLUSIONS: Two series of ferulic acid derivatives have been synthesized efficiently. The bioassay showed title compounds not only inhibit the plant viral infection, but also prevented the spread of plant virus by insect vectors. These findings therefore demonstrate that the ferulic acid amides represent a new template for future antiviral studies. |
format | Online Article Text |
id | pubmed-3599306 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35993062013-08-07 Synthesis and characteristics of (Hydrogenated) ferulic acid derivatives as potential antiviral agents with insecticidal activity Huang, Guang-Ying Cui, Can Wang, Zhi-Peng Li, Yong-Qiang Xiong, Li-Xia Wang, Li-Zhong Yu, Shu-Jing Li, Zheng-Ming Zhao, Wei-Guang Chem Cent J Research Article BACKGROUND: Plant viruses cause many serious plant diseases and are currently suppressed with the simultaneous use of virucides and insecticides. The use of such materials, however, increases the amounts of pollutants in the environment. To reduce environmental contaminants, virucides with insecticidal activity is an attractive option. RESULTS: A series of substituted ferulic acid amide derivatives 7 and the corresponding hydrogenated ferulic acid amide derivatives 13 were synthesized and evaluated for their antiviral and insecticidal activities. The majority of the synthesized compounds exhibited good levels of antiviral activity against the tobacco mosaic virus (TMW), with compounds 7a, 7b and 7d in particular providing higher levels of protective and curative activities against TMV at 500 μg/mL than the control compound ribavirin. Furthermore, these compounds displayed good insecticidal activities against insects with piercing-sucking mouthparts, which can spread plant viruses between and within crops. CONCLUSIONS: Two series of ferulic acid derivatives have been synthesized efficiently. The bioassay showed title compounds not only inhibit the plant viral infection, but also prevented the spread of plant virus by insect vectors. These findings therefore demonstrate that the ferulic acid amides represent a new template for future antiviral studies. BioMed Central 2013-02-14 /pmc/articles/PMC3599306/ /pubmed/23409923 http://dx.doi.org/10.1186/1752-153X-7-33 Text en Copyright © 2013 Huang et al; licensee Chemistry Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Huang, Guang-Ying Cui, Can Wang, Zhi-Peng Li, Yong-Qiang Xiong, Li-Xia Wang, Li-Zhong Yu, Shu-Jing Li, Zheng-Ming Zhao, Wei-Guang Synthesis and characteristics of (Hydrogenated) ferulic acid derivatives as potential antiviral agents with insecticidal activity |
title | Synthesis and characteristics of (Hydrogenated) ferulic acid derivatives as potential antiviral agents with insecticidal activity |
title_full | Synthesis and characteristics of (Hydrogenated) ferulic acid derivatives as potential antiviral agents with insecticidal activity |
title_fullStr | Synthesis and characteristics of (Hydrogenated) ferulic acid derivatives as potential antiviral agents with insecticidal activity |
title_full_unstemmed | Synthesis and characteristics of (Hydrogenated) ferulic acid derivatives as potential antiviral agents with insecticidal activity |
title_short | Synthesis and characteristics of (Hydrogenated) ferulic acid derivatives as potential antiviral agents with insecticidal activity |
title_sort | synthesis and characteristics of (hydrogenated) ferulic acid derivatives as potential antiviral agents with insecticidal activity |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3599306/ https://www.ncbi.nlm.nih.gov/pubmed/23409923 http://dx.doi.org/10.1186/1752-153X-7-33 |
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