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Design, Synthesis and Bioactivities of Novel Isoxazole-Containing Pyrazole Oxime Derivatives
In this study, in order to find novel biologically active pyrazole oxime derivatives, twenty-eight new pyrazole oxime compounds containing a substituted isoxazole ring were synthesized and evaluated for their acaricidaland insecticidal activities. Bioassays exhibited that some target compounds indic...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149770/ https://www.ncbi.nlm.nih.gov/pubmed/29186906 http://dx.doi.org/10.3390/molecules22122000 |
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author | Dai, Hong Yao, Wei Fang, Yuan Sun, Siyu Shi, Yujun Chen, Jia Jiang, Guoqing Shi, Jian |
author_facet | Dai, Hong Yao, Wei Fang, Yuan Sun, Siyu Shi, Yujun Chen, Jia Jiang, Guoqing Shi, Jian |
author_sort | Dai, Hong |
collection | PubMed |
description | In this study, in order to find novel biologically active pyrazole oxime derivatives, twenty-eight new pyrazole oxime compounds containing a substituted isoxazole ring were synthesized and evaluated for their acaricidaland insecticidal activities. Bioassays exhibited that some target compounds indicated good acaricidal and insecticidal activities against Tetranychus cinnabarinus, Aphis medicaginis, Mythimna separata, and Nilaparvata lugens. Especially, compounds 9c, 9h, 9u, and 9v showed 100.00%, 90.56%, 90.78%, and 90.62% insecticidal activities against A. medicaginis at the concentration of 20 μg/mL, respectively, compounds 9k and 9u had 70.86% and 100.00% insecticidal activities against M. separata at 20 μg/mL, respectively. |
format | Online Article Text |
id | pubmed-6149770 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61497702018-11-13 Design, Synthesis and Bioactivities of Novel Isoxazole-Containing Pyrazole Oxime Derivatives Dai, Hong Yao, Wei Fang, Yuan Sun, Siyu Shi, Yujun Chen, Jia Jiang, Guoqing Shi, Jian Molecules Article In this study, in order to find novel biologically active pyrazole oxime derivatives, twenty-eight new pyrazole oxime compounds containing a substituted isoxazole ring were synthesized and evaluated for their acaricidaland insecticidal activities. Bioassays exhibited that some target compounds indicated good acaricidal and insecticidal activities against Tetranychus cinnabarinus, Aphis medicaginis, Mythimna separata, and Nilaparvata lugens. Especially, compounds 9c, 9h, 9u, and 9v showed 100.00%, 90.56%, 90.78%, and 90.62% insecticidal activities against A. medicaginis at the concentration of 20 μg/mL, respectively, compounds 9k and 9u had 70.86% and 100.00% insecticidal activities against M. separata at 20 μg/mL, respectively. MDPI 2017-11-27 /pmc/articles/PMC6149770/ /pubmed/29186906 http://dx.doi.org/10.3390/molecules22122000 Text en © 2017 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 Dai, Hong Yao, Wei Fang, Yuan Sun, Siyu Shi, Yujun Chen, Jia Jiang, Guoqing Shi, Jian Design, Synthesis and Bioactivities of Novel Isoxazole-Containing Pyrazole Oxime Derivatives |
title | Design, Synthesis and Bioactivities of Novel Isoxazole-Containing Pyrazole Oxime Derivatives |
title_full | Design, Synthesis and Bioactivities of Novel Isoxazole-Containing Pyrazole Oxime Derivatives |
title_fullStr | Design, Synthesis and Bioactivities of Novel Isoxazole-Containing Pyrazole Oxime Derivatives |
title_full_unstemmed | Design, Synthesis and Bioactivities of Novel Isoxazole-Containing Pyrazole Oxime Derivatives |
title_short | Design, Synthesis and Bioactivities of Novel Isoxazole-Containing Pyrazole Oxime Derivatives |
title_sort | design, synthesis and bioactivities of novel isoxazole-containing pyrazole oxime derivatives |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149770/ https://www.ncbi.nlm.nih.gov/pubmed/29186906 http://dx.doi.org/10.3390/molecules22122000 |
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