Larvicidal Activity of Cinnamic Acid Derivatives: Investigating Alternative Products for <i>Aedes aegypti</i> L. Control

The mosquito <i>Aedes aegypti</i> transmits the virus that causes dengue, yellow fever, Zika and Chikungunya viruses, and in several regions of the planet represents a vector of great clinical importance. In terms of mortality and morbidity, infections caused by <i>Ae. aegypti</...

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Main Authors: Marianna O. Araújo, Yunierkis Pérez-Castillo, Louise H. G. Oliveira, Fabíola C. Nunes, Damião P. de Sousa
Format: Article
Language:English
Published: MDPI AG 2020-12-01
Series:Molecules
Subjects:
Online Access:https://www.mdpi.com/1420-3049/26/1/61
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author Marianna O. Araújo
Yunierkis Pérez-Castillo
Louise H. G. Oliveira
Fabíola C. Nunes
Damião P. de Sousa
author_facet Marianna O. Araújo
Yunierkis Pérez-Castillo
Louise H. G. Oliveira
Fabíola C. Nunes
Damião P. de Sousa
author_sort Marianna O. Araújo
collection DOAJ
description The mosquito <i>Aedes aegypti</i> transmits the virus that causes dengue, yellow fever, Zika and Chikungunya viruses, and in several regions of the planet represents a vector of great clinical importance. In terms of mortality and morbidity, infections caused by <i>Ae. aegypti</i> are among the most serious arthropod transmitted viral diseases. The present study investigated the larvicidal potential of seventeen cinnamic acid derivatives against fourth stage <i>Ae. aegypti</i> larvae. The larvicide assays were performed using larval mortality rates to determine lethal concentration (LC<sub>50</sub>). Compounds containing the medium alkyl chains butyl cinnamate (<b>7</b>) and pentyl cinnamate (<b>8</b>) presented excellent larvicidal activity with LC<sub>50</sub> values of around 0.21–0.17 mM, respectively. While among the derivatives with aryl substituents, the best LC<sub>50</sub> result was 0.55 mM for benzyl cinnamate (<b>13</b>). The tested derivatives were natural compounds and in pharmacology and antiparasitic studies, many have been evaluated using biological models for environmental and toxicological safety. Molecular modeling analyses suggest that the larvicidal activity of these compounds might be due to a multi-target mechanism of action involving inhibition of a carbonic anhydrase (CA), a histone deacetylase (HDAC2), and two sodium-dependent cation-chloride co-transporters (CCC2 e CCC3).
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spelling doaj.art-1ceb3b26e4fb4a759ea9dfe20b4732302023-11-21T02:30:45ZengMDPI AGMolecules1420-30492020-12-012616110.3390/molecules26010061Larvicidal Activity of Cinnamic Acid Derivatives: Investigating Alternative Products for <i>Aedes aegypti</i> L. ControlMarianna O. Araújo0Yunierkis Pérez-Castillo1Louise H. G. Oliveira2Fabíola C. Nunes3Damião P. de Sousa4Post Graduation Program in Natural and Synthetic Bioactive Products, Federal University of Paraíba, João Pessoa 58051-900, BrazilBio-Cheminformatics Research Group and Escuela de Ciencias Físicas y Matemáticas, Universidad de Las Américas, Quito 170125, EcuadorBiotechnology Center, Federal University of Paraíba, João Pessoa 58051-900, BrazilBiotechnology Center, Federal University of Paraíba, João Pessoa 58051-900, BrazilPost Graduation Program in Natural and Synthetic Bioactive Products, Federal University of Paraíba, João Pessoa 58051-900, BrazilThe mosquito <i>Aedes aegypti</i> transmits the virus that causes dengue, yellow fever, Zika and Chikungunya viruses, and in several regions of the planet represents a vector of great clinical importance. In terms of mortality and morbidity, infections caused by <i>Ae. aegypti</i> are among the most serious arthropod transmitted viral diseases. The present study investigated the larvicidal potential of seventeen cinnamic acid derivatives against fourth stage <i>Ae. aegypti</i> larvae. The larvicide assays were performed using larval mortality rates to determine lethal concentration (LC<sub>50</sub>). Compounds containing the medium alkyl chains butyl cinnamate (<b>7</b>) and pentyl cinnamate (<b>8</b>) presented excellent larvicidal activity with LC<sub>50</sub> values of around 0.21–0.17 mM, respectively. While among the derivatives with aryl substituents, the best LC<sub>50</sub> result was 0.55 mM for benzyl cinnamate (<b>13</b>). The tested derivatives were natural compounds and in pharmacology and antiparasitic studies, many have been evaluated using biological models for environmental and toxicological safety. Molecular modeling analyses suggest that the larvicidal activity of these compounds might be due to a multi-target mechanism of action involving inhibition of a carbonic anhydrase (CA), a histone deacetylase (HDAC2), and two sodium-dependent cation-chloride co-transporters (CCC2 e CCC3).https://www.mdpi.com/1420-3049/26/1/61natural productsmedicinal plantsmosquitoescinnamic esterdengueyellow fever
spellingShingle Marianna O. Araújo
Yunierkis Pérez-Castillo
Louise H. G. Oliveira
Fabíola C. Nunes
Damião P. de Sousa
Larvicidal Activity of Cinnamic Acid Derivatives: Investigating Alternative Products for <i>Aedes aegypti</i> L. Control
Molecules
natural products
medicinal plants
mosquitoes
cinnamic ester
dengue
yellow fever
title Larvicidal Activity of Cinnamic Acid Derivatives: Investigating Alternative Products for <i>Aedes aegypti</i> L. Control
title_full Larvicidal Activity of Cinnamic Acid Derivatives: Investigating Alternative Products for <i>Aedes aegypti</i> L. Control
title_fullStr Larvicidal Activity of Cinnamic Acid Derivatives: Investigating Alternative Products for <i>Aedes aegypti</i> L. Control
title_full_unstemmed Larvicidal Activity of Cinnamic Acid Derivatives: Investigating Alternative Products for <i>Aedes aegypti</i> L. Control
title_short Larvicidal Activity of Cinnamic Acid Derivatives: Investigating Alternative Products for <i>Aedes aegypti</i> L. Control
title_sort larvicidal activity of cinnamic acid derivatives investigating alternative products for i aedes aegypti i l control
topic natural products
medicinal plants
mosquitoes
cinnamic ester
dengue
yellow fever
url https://www.mdpi.com/1420-3049/26/1/61
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