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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...

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Autores principales: Zhao, Fenghai, Tang, Xianjun, Huang, Jiaxing, Li, Jiaqi, Xiao, Yumei, Qin, Zhaohai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
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.
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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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