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Design, Synthesis and Insecticidal Activity of Novel Phenylurea Derivatives

A series of novel phenylurea derivatives were designed and synthesized according to the method of active groups linkage and the principle of aromatic groups bioisosterism in this study. The structures of the novel phenylurea derivatives were confirmed based on ESI-MS, IR and (1)H-NMR spectral data....

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Autores principales: Sun, Jialong, Zhou, Yuanming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272132/
https://www.ncbi.nlm.nih.gov/pubmed/25808149
http://dx.doi.org/10.3390/molecules20035050
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author Sun, Jialong
Zhou, Yuanming
author_facet Sun, Jialong
Zhou, Yuanming
author_sort Sun, Jialong
collection PubMed
description A series of novel phenylurea derivatives were designed and synthesized according to the method of active groups linkage and the principle of aromatic groups bioisosterism in this study. The structures of the novel phenylurea derivatives were confirmed based on ESI-MS, IR and (1)H-NMR spectral data. All of the compounds were evaluated for the insecticidal activity against the third instars larvae of Spodoptera exigua Hiibner, Plutella xyllostella Linnaeus, Helicoverpa armigera Hubner and Pieris rapae Linne respectively, at the concentration of 10 mg/L. The results showed that all of the derivatives displayed strong insecticidal activity. Most of the compounds presented higher insecticidal activity against S. exigua than the reference compounds tebufenozide, chlorbenzuron and metaflumizone. Among the synthesized compounds, 3b, 3d, 3f, 4b and 4g displayed broad spectrum insecticidal activity.
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spelling pubmed-62721322018-12-31 Design, Synthesis and Insecticidal Activity of Novel Phenylurea Derivatives Sun, Jialong Zhou, Yuanming Molecules Article A series of novel phenylurea derivatives were designed and synthesized according to the method of active groups linkage and the principle of aromatic groups bioisosterism in this study. The structures of the novel phenylurea derivatives were confirmed based on ESI-MS, IR and (1)H-NMR spectral data. All of the compounds were evaluated for the insecticidal activity against the third instars larvae of Spodoptera exigua Hiibner, Plutella xyllostella Linnaeus, Helicoverpa armigera Hubner and Pieris rapae Linne respectively, at the concentration of 10 mg/L. The results showed that all of the derivatives displayed strong insecticidal activity. Most of the compounds presented higher insecticidal activity against S. exigua than the reference compounds tebufenozide, chlorbenzuron and metaflumizone. Among the synthesized compounds, 3b, 3d, 3f, 4b and 4g displayed broad spectrum insecticidal activity. MDPI 2015-03-19 /pmc/articles/PMC6272132/ /pubmed/25808149 http://dx.doi.org/10.3390/molecules20035050 Text en © 2015 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 license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sun, Jialong
Zhou, Yuanming
Design, Synthesis and Insecticidal Activity of Novel Phenylurea Derivatives
title Design, Synthesis and Insecticidal Activity of Novel Phenylurea Derivatives
title_full Design, Synthesis and Insecticidal Activity of Novel Phenylurea Derivatives
title_fullStr Design, Synthesis and Insecticidal Activity of Novel Phenylurea Derivatives
title_full_unstemmed Design, Synthesis and Insecticidal Activity of Novel Phenylurea Derivatives
title_short Design, Synthesis and Insecticidal Activity of Novel Phenylurea Derivatives
title_sort design, synthesis and insecticidal activity of novel phenylurea derivatives
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272132/
https://www.ncbi.nlm.nih.gov/pubmed/25808149
http://dx.doi.org/10.3390/molecules20035050
work_keys_str_mv AT sunjialong designsynthesisandinsecticidalactivityofnovelphenylureaderivatives
AT zhouyuanming designsynthesisandinsecticidalactivityofnovelphenylureaderivatives