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Design, Synthesis and Antifungal/Insecticidal Evaluation of Novel Cinnamide Derivatives

Twenty novel cinnamamide derivatives were designed and synthesized using as lead compound pyrimorph, whose morpholine moiety was replaced by β-phenylethylamine. All the compounds were characterized by their spectroscopic data. The fungicidal and insecticidal activities were also evaluated. The preli...

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Detalles Bibliográficos
Autores principales: Xiao, Yumei, Yang, Xiaoli, Li, Bo, Yuan, Huizhu, Wan, Shuqing, Xu, Yanjun, Qin, Zhaohai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264240/
https://www.ncbi.nlm.nih.gov/pubmed/22027951
http://dx.doi.org/10.3390/molecules16118945
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author Xiao, Yumei
Yang, Xiaoli
Li, Bo
Yuan, Huizhu
Wan, Shuqing
Xu, Yanjun
Qin, Zhaohai
author_facet Xiao, Yumei
Yang, Xiaoli
Li, Bo
Yuan, Huizhu
Wan, Shuqing
Xu, Yanjun
Qin, Zhaohai
author_sort Xiao, Yumei
collection PubMed
description Twenty novel cinnamamide derivatives were designed and synthesized using as lead compound pyrimorph, whose morpholine moiety was replaced by β-phenylethylamine. All the compounds were characterized by their spectroscopic data. The fungicidal and insecticidal activities were also evaluated. The preliminary results showed that all the title compounds had certain fungicidal activities against seven plant pathogens at a concentration of 50 μg/mL, and compounds 11a and 11l showed inhibition ratios of up to 90% against R. solani. Most of the title compounds exhibited moderate nematicidal activities. In general, the morpholine ring may be replaced by other amines and a chlorine atom in the pyridine ring is helpful to fungicidal activity.
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spelling pubmed-62642402018-12-10 Design, Synthesis and Antifungal/Insecticidal Evaluation of Novel Cinnamide Derivatives Xiao, Yumei Yang, Xiaoli Li, Bo Yuan, Huizhu Wan, Shuqing Xu, Yanjun Qin, Zhaohai Molecules Article Twenty novel cinnamamide derivatives were designed and synthesized using as lead compound pyrimorph, whose morpholine moiety was replaced by β-phenylethylamine. All the compounds were characterized by their spectroscopic data. The fungicidal and insecticidal activities were also evaluated. The preliminary results showed that all the title compounds had certain fungicidal activities against seven plant pathogens at a concentration of 50 μg/mL, and compounds 11a and 11l showed inhibition ratios of up to 90% against R. solani. Most of the title compounds exhibited moderate nematicidal activities. In general, the morpholine ring may be replaced by other amines and a chlorine atom in the pyridine ring is helpful to fungicidal activity. MDPI 2011-10-25 /pmc/articles/PMC6264240/ /pubmed/22027951 http://dx.doi.org/10.3390/molecules16118945 Text en © 2011 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/3.0/).
spellingShingle Article
Xiao, Yumei
Yang, Xiaoli
Li, Bo
Yuan, Huizhu
Wan, Shuqing
Xu, Yanjun
Qin, Zhaohai
Design, Synthesis and Antifungal/Insecticidal Evaluation of Novel Cinnamide Derivatives
title Design, Synthesis and Antifungal/Insecticidal Evaluation of Novel Cinnamide Derivatives
title_full Design, Synthesis and Antifungal/Insecticidal Evaluation of Novel Cinnamide Derivatives
title_fullStr Design, Synthesis and Antifungal/Insecticidal Evaluation of Novel Cinnamide Derivatives
title_full_unstemmed Design, Synthesis and Antifungal/Insecticidal Evaluation of Novel Cinnamide Derivatives
title_short Design, Synthesis and Antifungal/Insecticidal Evaluation of Novel Cinnamide Derivatives
title_sort design, synthesis and antifungal/insecticidal evaluation of novel cinnamide derivatives
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264240/
https://www.ncbi.nlm.nih.gov/pubmed/22027951
http://dx.doi.org/10.3390/molecules16118945
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