Terpenic Constituents of Essential Oils with Larvicidal Activity against Aedes Aegypti: A QSAR and Docking Molecular Study

Author:

Cruz-Castillo Adrián Ulises1,Rodríguez-Valdez Luz María2ORCID,Correa-Basurto José3ORCID,Nogueda-Torres Benjamín4ORCID,Andrade-Ochoa Sergio1ORCID,Nevárez-Moorillón Guadalupe Virginia2ORCID

Affiliation:

1. Campus Coyoacán, Universidad del Valle de México, Calzada De Tlalpan No. 3016 y 3058, Ex Hacienda Coapa, Delegación Coyoacán, Ciudad de México 04910, Mexico

2. Facultad de Ciencias Químicas, Universidad Autónoma de Chihuahua, Circuito Universitario S/N Campus Universitario II, Chihuahua 31125, Mexico

3. Escuela Superior de Medicina, Instituto Politécnico Nacional, Plan de San Luis y Díaz Mirón S/N Col. Santo Tomas, Ciudad de México 11340, Mexico

4. Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Prolongación de Carpio y Plan de Ayala S/N Col. Santo Tomas, Ciudad de México 11340, Mexico

Abstract

Aedes aegypti is a vector for the arbovirus responsible for yellow fever, Zika and Chikungunya virus. Essential oils and their constituents are known for their larvicidal properties and are strong candidates for mosquito control. This work aimed to develop a quantitative structure–activity study and molecular screening for the search and design of new larvicidal agents. Twenty-five monoterpenes with previously evaluated larvicidal activity were built and optimized using computational tools. QSAR models were constructed through genetic algorithms from the larvicidal activity and the calculation of theoretical descriptors for each molecule. Docking studies on acetylcholinesterase (AChE) and sterol carrier protein (SCP-2) were also carried out. Results demonstrate that the epoxide groups in the structure of terpenes hinder larvicidal activity, while lipophilicity plays an important role in enhancing biological activity. Larvicidal activity correlates with the interaction of the sterol-carrier protein. Of the 25 compounds evaluated, carvacrol showed the highest larvicidal activity with an LC50 of 8.8 µg/mL. The information included in this work contributes to describing the molecular, topological, and quantum mechanical properties related to the larvicidal activity of monoterpenes and their derivatives.

Funder

Consejo Nacional de Ciencia y Tecnología

SIP-COFAA/IPN

Publisher

MDPI AG

Subject

Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science

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