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N-Substituted 5–Chloro-6-phenylpyridazin-3(2H)-ones: Synthesis, Insecticidal Activity Against Plutella xylostella (L.) and SAR Study
A series of N-substituted 5–chloro-6-phenylpyridazin-3(2H)-one derivatives were synthesized based on our previous work; all compounds were characterized by spectral data and tested for in vitro insecticidal activity against Plutella xylostella. The results showed that the synthesized pyridazin-3(2H)...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268875/ https://www.ncbi.nlm.nih.gov/pubmed/22869161 http://dx.doi.org/10.3390/molecules17089413 |
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author | Wu, Jian Kang, Shenghong Yuan, Qinkun Luo, Lijun Ma, Juan Shi, Qingcai Yang, Song |
author_facet | Wu, Jian Kang, Shenghong Yuan, Qinkun Luo, Lijun Ma, Juan Shi, Qingcai Yang, Song |
author_sort | Wu, Jian |
collection | PubMed |
description | A series of N-substituted 5–chloro-6-phenylpyridazin-3(2H)-one derivatives were synthesized based on our previous work; all compounds were characterized by spectral data and tested for in vitro insecticidal activity against Plutella xylostella. The results showed that the synthesized pyridazin-3(2H)-one compounds possessed good insecticidal activities, especially the compounds 4b, 4d, and 4h which showed >90% activity at 100 mg/L. The structure-activity relationships (SAR) for these compounds were also discussed. |
format | Online Article Text |
id | pubmed-6268875 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62688752018-12-12 N-Substituted 5–Chloro-6-phenylpyridazin-3(2H)-ones: Synthesis, Insecticidal Activity Against Plutella xylostella (L.) and SAR Study Wu, Jian Kang, Shenghong Yuan, Qinkun Luo, Lijun Ma, Juan Shi, Qingcai Yang, Song Molecules Article A series of N-substituted 5–chloro-6-phenylpyridazin-3(2H)-one derivatives were synthesized based on our previous work; all compounds were characterized by spectral data and tested for in vitro insecticidal activity against Plutella xylostella. The results showed that the synthesized pyridazin-3(2H)-one compounds possessed good insecticidal activities, especially the compounds 4b, 4d, and 4h which showed >90% activity at 100 mg/L. The structure-activity relationships (SAR) for these compounds were also discussed. MDPI 2012-08-06 /pmc/articles/PMC6268875/ /pubmed/22869161 http://dx.doi.org/10.3390/molecules17089413 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Wu, Jian Kang, Shenghong Yuan, Qinkun Luo, Lijun Ma, Juan Shi, Qingcai Yang, Song N-Substituted 5–Chloro-6-phenylpyridazin-3(2H)-ones: Synthesis, Insecticidal Activity Against Plutella xylostella (L.) and SAR Study |
title | N-Substituted 5–Chloro-6-phenylpyridazin-3(2H)-ones: Synthesis, Insecticidal Activity Against Plutella xylostella (L.) and SAR Study |
title_full | N-Substituted 5–Chloro-6-phenylpyridazin-3(2H)-ones: Synthesis, Insecticidal Activity Against Plutella xylostella (L.) and SAR Study |
title_fullStr | N-Substituted 5–Chloro-6-phenylpyridazin-3(2H)-ones: Synthesis, Insecticidal Activity Against Plutella xylostella (L.) and SAR Study |
title_full_unstemmed | N-Substituted 5–Chloro-6-phenylpyridazin-3(2H)-ones: Synthesis, Insecticidal Activity Against Plutella xylostella (L.) and SAR Study |
title_short | N-Substituted 5–Chloro-6-phenylpyridazin-3(2H)-ones: Synthesis, Insecticidal Activity Against Plutella xylostella (L.) and SAR Study |
title_sort | n-substituted 5–chloro-6-phenylpyridazin-3(2h)-ones: synthesis, insecticidal activity against plutella xylostella (l.) and sar study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268875/ https://www.ncbi.nlm.nih.gov/pubmed/22869161 http://dx.doi.org/10.3390/molecules17089413 |
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