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Germacrone Derivatives as new Insecticidal and Acaricidal Compounds: A Structure-Activity Relationship
Currently, the use of synthetic pesticides is the main method of plant protection applied in agri- and horticulture. However, its excessive use leads to the development of pesticide resistance, a contamination of the environment, toxicity to non-target organisms, and risks for human health. With the...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6720995/ https://www.ncbi.nlm.nih.gov/pubmed/31404973 http://dx.doi.org/10.3390/molecules24162898 |
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author | Galisteo Pretel, Alberto Pérez del Pulgar, Helena Guerrero de León, Estela López-Pérez, José Luis Olmeda, A. Sonia Gonzalez-Coloma, Azucena F. Barrero, Alejandro Quílez del Moral, José Francisco |
author_facet | Galisteo Pretel, Alberto Pérez del Pulgar, Helena Guerrero de León, Estela López-Pérez, José Luis Olmeda, A. Sonia Gonzalez-Coloma, Azucena F. Barrero, Alejandro Quílez del Moral, José Francisco |
author_sort | Galisteo Pretel, Alberto |
collection | PubMed |
description | Currently, the use of synthetic pesticides is the main method of plant protection applied in agri- and horticulture. However, its excessive use leads to the development of pesticide resistance, a contamination of the environment, toxicity to non-target organisms, and risks for human health. With the ultimate aim of contributing to the develop of a more sustainable pest management, we used the natural product germacrone (compound 1), reported to possess significant insecticidal activity, as starting material for the generation of molecular diversity (2–24). Some of the generated derivatives are natural compounds, such as 1,10-epoxygermacrone (2), 4,5-epoxygermacrone (3), gajutsulactone A (7), germacrol (11), isogermacrone (14), 9-hydroxyeudesma-3,7(11)dien-6-one (19), eudesma-4,7(11),dien-8-one (20), eudesma-3,7(11)-dien-8-one (21) and eudesma-4(15),7(11)-dien-8-one (22). Compounds, 7,11-9,10-diepoxigermacr-4,5-en-8-ol (17), 7,11-epoxieudesma-4,7(11)-dien-8-one (23) and 7,11-epoxieudesma-3,7(11)-dien-8-one (24) are described for the first time. The biocidal activity of most of these compounds was assayed against the tick Hyalomma lusitanicum. The acaricidal effects of compound 24 were four times higher than that of germacrone (1). Compound 2 is an insect antifeedant a thousand times more potent than germacrone against Rhopalosiphum padi, which makes this substance a promising selective antifeedant against this cereal pest. |
format | Online Article Text |
id | pubmed-6720995 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-67209952019-09-10 Germacrone Derivatives as new Insecticidal and Acaricidal Compounds: A Structure-Activity Relationship Galisteo Pretel, Alberto Pérez del Pulgar, Helena Guerrero de León, Estela López-Pérez, José Luis Olmeda, A. Sonia Gonzalez-Coloma, Azucena F. Barrero, Alejandro Quílez del Moral, José Francisco Molecules Article Currently, the use of synthetic pesticides is the main method of plant protection applied in agri- and horticulture. However, its excessive use leads to the development of pesticide resistance, a contamination of the environment, toxicity to non-target organisms, and risks for human health. With the ultimate aim of contributing to the develop of a more sustainable pest management, we used the natural product germacrone (compound 1), reported to possess significant insecticidal activity, as starting material for the generation of molecular diversity (2–24). Some of the generated derivatives are natural compounds, such as 1,10-epoxygermacrone (2), 4,5-epoxygermacrone (3), gajutsulactone A (7), germacrol (11), isogermacrone (14), 9-hydroxyeudesma-3,7(11)dien-6-one (19), eudesma-4,7(11),dien-8-one (20), eudesma-3,7(11)-dien-8-one (21) and eudesma-4(15),7(11)-dien-8-one (22). Compounds, 7,11-9,10-diepoxigermacr-4,5-en-8-ol (17), 7,11-epoxieudesma-4,7(11)-dien-8-one (23) and 7,11-epoxieudesma-3,7(11)-dien-8-one (24) are described for the first time. The biocidal activity of most of these compounds was assayed against the tick Hyalomma lusitanicum. The acaricidal effects of compound 24 were four times higher than that of germacrone (1). Compound 2 is an insect antifeedant a thousand times more potent than germacrone against Rhopalosiphum padi, which makes this substance a promising selective antifeedant against this cereal pest. MDPI 2019-08-09 /pmc/articles/PMC6720995/ /pubmed/31404973 http://dx.doi.org/10.3390/molecules24162898 Text en © 2019 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 Galisteo Pretel, Alberto Pérez del Pulgar, Helena Guerrero de León, Estela López-Pérez, José Luis Olmeda, A. Sonia Gonzalez-Coloma, Azucena F. Barrero, Alejandro Quílez del Moral, José Francisco Germacrone Derivatives as new Insecticidal and Acaricidal Compounds: A Structure-Activity Relationship |
title | Germacrone Derivatives as new Insecticidal and Acaricidal Compounds: A Structure-Activity Relationship |
title_full | Germacrone Derivatives as new Insecticidal and Acaricidal Compounds: A Structure-Activity Relationship |
title_fullStr | Germacrone Derivatives as new Insecticidal and Acaricidal Compounds: A Structure-Activity Relationship |
title_full_unstemmed | Germacrone Derivatives as new Insecticidal and Acaricidal Compounds: A Structure-Activity Relationship |
title_short | Germacrone Derivatives as new Insecticidal and Acaricidal Compounds: A Structure-Activity Relationship |
title_sort | germacrone derivatives as new insecticidal and acaricidal compounds: a structure-activity relationship |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6720995/ https://www.ncbi.nlm.nih.gov/pubmed/31404973 http://dx.doi.org/10.3390/molecules24162898 |
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