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Synthesis and Larvicidal Activity against Culex pipiens pallens of New Triazole Derivatives of Phrymarolin from Phryma leptostachya L.

Twelve new triazole derivatives of Phrymarolin were prepared from Phrymarolin I and the structures of all the derivatives were fully characterized by (1)H-NMR, (13)C-NMR and MS spectral data analyses. Larvicidal activities against 4rd instar larvae of Culex pipiens pallens of these Phrymarolin analo...

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Detalles Bibliográficos
Autores principales: Zhang, Ji-Wen, Hu, Zhan, Gao, Peng, Wang, Jun-Ru, Hu, Zhao-Nong, Wu, Wen-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3876095/
https://www.ncbi.nlm.nih.gov/pubmed/24336066
http://dx.doi.org/10.3390/ijms141224064
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author Zhang, Ji-Wen
Hu, Zhan
Gao, Peng
Wang, Jun-Ru
Hu, Zhao-Nong
Wu, Wen-Jun
author_facet Zhang, Ji-Wen
Hu, Zhan
Gao, Peng
Wang, Jun-Ru
Hu, Zhao-Nong
Wu, Wen-Jun
author_sort Zhang, Ji-Wen
collection PubMed
description Twelve new triazole derivatives of Phrymarolin were prepared from Phrymarolin I and the structures of all the derivatives were fully characterized by (1)H-NMR, (13)C-NMR and MS spectral data analyses. Larvicidal activities against 4rd instar larvae of Culex pipiens pallens of these Phrymarolin analogues were assayed. Although the triazole derivatives of Phrymarolin showed certain larvicidal activity, they showed lower activity than Phrymarolin I. The typical non-natural groups triazole substituents reduced the larvicidal activity of Phrymarolin derivatives.
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spelling pubmed-38760952013-12-31 Synthesis and Larvicidal Activity against Culex pipiens pallens of New Triazole Derivatives of Phrymarolin from Phryma leptostachya L. Zhang, Ji-Wen Hu, Zhan Gao, Peng Wang, Jun-Ru Hu, Zhao-Nong Wu, Wen-Jun Int J Mol Sci Article Twelve new triazole derivatives of Phrymarolin were prepared from Phrymarolin I and the structures of all the derivatives were fully characterized by (1)H-NMR, (13)C-NMR and MS spectral data analyses. Larvicidal activities against 4rd instar larvae of Culex pipiens pallens of these Phrymarolin analogues were assayed. Although the triazole derivatives of Phrymarolin showed certain larvicidal activity, they showed lower activity than Phrymarolin I. The typical non-natural groups triazole substituents reduced the larvicidal activity of Phrymarolin derivatives. Molecular Diversity Preservation International (MDPI) 2013-12-10 /pmc/articles/PMC3876095/ /pubmed/24336066 http://dx.doi.org/10.3390/ijms141224064 Text en © 2013 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
Zhang, Ji-Wen
Hu, Zhan
Gao, Peng
Wang, Jun-Ru
Hu, Zhao-Nong
Wu, Wen-Jun
Synthesis and Larvicidal Activity against Culex pipiens pallens of New Triazole Derivatives of Phrymarolin from Phryma leptostachya L.
title Synthesis and Larvicidal Activity against Culex pipiens pallens of New Triazole Derivatives of Phrymarolin from Phryma leptostachya L.
title_full Synthesis and Larvicidal Activity against Culex pipiens pallens of New Triazole Derivatives of Phrymarolin from Phryma leptostachya L.
title_fullStr Synthesis and Larvicidal Activity against Culex pipiens pallens of New Triazole Derivatives of Phrymarolin from Phryma leptostachya L.
title_full_unstemmed Synthesis and Larvicidal Activity against Culex pipiens pallens of New Triazole Derivatives of Phrymarolin from Phryma leptostachya L.
title_short Synthesis and Larvicidal Activity against Culex pipiens pallens of New Triazole Derivatives of Phrymarolin from Phryma leptostachya L.
title_sort synthesis and larvicidal activity against culex pipiens pallens of new triazole derivatives of phrymarolin from phryma leptostachya l.
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3876095/
https://www.ncbi.nlm.nih.gov/pubmed/24336066
http://dx.doi.org/10.3390/ijms141224064
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