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Design, synthesis, and insecticidal activity of a novel series of flupyrimin analogs bearing 1-aryl-1H-pyrazol-4-yl subunits
To discover new potential insecticides to protect agricultural crops from damage, a series of novel flupyrimin derivatives containing an arylpyrazole core were designed and synthesized. Their structures were confirmed by (1)H NMR, (13)C NMR, and HRMS. Bioassays indicated that the 31 compounds synthe...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9574050/ https://www.ncbi.nlm.nih.gov/pubmed/36262338 http://dx.doi.org/10.3389/fchem.2022.1019573 |
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author | Zhao, Fenghai Tang, Xianjun Huang, Jiaxing Li, Jiaqi Xiao, Yumei Qin, Zhaohai |
author_facet | Zhao, Fenghai Tang, Xianjun Huang, Jiaxing Li, Jiaqi Xiao, Yumei Qin, Zhaohai |
author_sort | Zhao, Fenghai |
collection | PubMed |
description | To discover new potential insecticides to protect agricultural crops from damage, a series of novel flupyrimin derivatives containing an arylpyrazole core were designed and synthesized. Their structures were confirmed by (1)H NMR, (13)C NMR, and HRMS. Bioassays indicated that the 31 compounds synthesized possessed excellent insecticidal activity against Plutella xylostella. Among these target compounds, the lethality of A3, B1-B6, D4, and D6 reached 100% at 400 μg/ml. Moreover, when the concentration dropped to 25 μg/ml, the insecticidal activities against the Plutella xylostella for compounds B2, B3, and B4 still reached more than 70%. The structure–activity relationship of the Plutella xylostella was discussed. The density functional theory analysis of flupyrimin and B4 was carried out to support the abovementioned structure–activity relationship. The possible binding modes between receptor and active groups in title compounds were also verified by docking simulation. These results provided new ideas for the development of these novel candidate insecticides in the future. |
format | Online Article Text |
id | pubmed-9574050 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95740502022-10-18 Design, synthesis, and insecticidal activity of a novel series of flupyrimin analogs bearing 1-aryl-1H-pyrazol-4-yl subunits Zhao, Fenghai Tang, Xianjun Huang, Jiaxing Li, Jiaqi Xiao, Yumei Qin, Zhaohai Front Chem Chemistry To discover new potential insecticides to protect agricultural crops from damage, a series of novel flupyrimin derivatives containing an arylpyrazole core were designed and synthesized. Their structures were confirmed by (1)H NMR, (13)C NMR, and HRMS. Bioassays indicated that the 31 compounds synthesized possessed excellent insecticidal activity against Plutella xylostella. Among these target compounds, the lethality of A3, B1-B6, D4, and D6 reached 100% at 400 μg/ml. Moreover, when the concentration dropped to 25 μg/ml, the insecticidal activities against the Plutella xylostella for compounds B2, B3, and B4 still reached more than 70%. The structure–activity relationship of the Plutella xylostella was discussed. The density functional theory analysis of flupyrimin and B4 was carried out to support the abovementioned structure–activity relationship. The possible binding modes between receptor and active groups in title compounds were also verified by docking simulation. These results provided new ideas for the development of these novel candidate insecticides in the future. Frontiers Media S.A. 2022-10-03 /pmc/articles/PMC9574050/ /pubmed/36262338 http://dx.doi.org/10.3389/fchem.2022.1019573 Text en Copyright © 2022 Zhao, Tang, Huang, Li, Xiao and Qin. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Chemistry Zhao, Fenghai Tang, Xianjun Huang, Jiaxing Li, Jiaqi Xiao, Yumei Qin, Zhaohai Design, synthesis, and insecticidal activity of a novel series of flupyrimin analogs bearing 1-aryl-1H-pyrazol-4-yl subunits |
title | Design, synthesis, and insecticidal activity of a novel series of flupyrimin analogs bearing 1-aryl-1H-pyrazol-4-yl subunits |
title_full | Design, synthesis, and insecticidal activity of a novel series of flupyrimin analogs bearing 1-aryl-1H-pyrazol-4-yl subunits |
title_fullStr | Design, synthesis, and insecticidal activity of a novel series of flupyrimin analogs bearing 1-aryl-1H-pyrazol-4-yl subunits |
title_full_unstemmed | Design, synthesis, and insecticidal activity of a novel series of flupyrimin analogs bearing 1-aryl-1H-pyrazol-4-yl subunits |
title_short | Design, synthesis, and insecticidal activity of a novel series of flupyrimin analogs bearing 1-aryl-1H-pyrazol-4-yl subunits |
title_sort | design, synthesis, and insecticidal activity of a novel series of flupyrimin analogs bearing 1-aryl-1h-pyrazol-4-yl subunits |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9574050/ https://www.ncbi.nlm.nih.gov/pubmed/36262338 http://dx.doi.org/10.3389/fchem.2022.1019573 |
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