Predicting toxicity of triazole fungicide: A molecular-based insight into triadimefon and triadimenol

Triazole fungicides, such as triadimefon (TF) and its stereoisomeric metabolite, triadimenol (TN), remain cornerstone agrochemicals. However, their stereochemistry may affect shape reactivity, intermolecular recognition, and ecotoxicity in different ways, with potential impacts on non-target species. Objective : This study employs computational methods to describe structural and electronic descriptors, quantify supramolecular interactions, and predict toxicological endpoints in silico for TF and its individual stereoisomer, TN. Methods : Density functional theory calculations were employed to optimize the molecular geometries and calculate reactivity descriptors at the M06-2×/6–311++G(d,p) level of theory. The intermolecular interactions were compared using Hirshfeld surface analysis, quantum theory of atoms in molecules, and natural bond orbital analysis. Chemical reactivity descriptors were calculated to assess reactive sites. Pharmacophore modeling was performed to verify the potential of the six isomers to interact with the lanosterol 14 α -demethylase target. Toxicity was predicted using computational models available online. Results : Differences were found between the electronic properties and intermolecular interactions of TF and TN, due to the presence of –OH or –CO– functional groups. These variations influence the molecular electrostatic potential, reactivity descriptors, and interaction energies, affecting their biological behavior. The results of the pharmacophore modeling suggest that only the 1 R -TF, 1 S ,2 R -TN, and 1 S ,2 S -TN isomers demonstrated potential for interaction with the lanosterol 14 α -demethylase target. Toxicity predictions revealed that some triadimenol stereoisomers exhibit a greater potential for adverse effects on non-target organisms when compared to TF. Conclusion : The findings highlight the crucial role of stereochemistry in modulating the chemical behavior and toxicity of triazole fungicides. Additionally, the use of in silico methods proves effective in predicting the ecotoxicological profiles of such compounds and supports the development of safer and more sustainable agrochemical practices.

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Journal
Results in Chemistry
Published
2026-03-31
DOI
https://doi.org/10.1016/j.rechem.2026.103268
Primary Topic
Fungal Plant Pathogen Control
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article
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article

Predicting toxicity of triazole fungicide: A molecular-based insight into triadimefon and triadimenol

Ronaldo Freitas, Hamilton B. Napolitano, Lucas D. Dias, Leonardo L. Borges et al.
Results in Chemistry
Fungal Plant Pathogen Control
article

Predicting toxicity of triazole fungicide: A molecular-based insight into triadimefon and triadimenol

Ronaldo Freitas, Hamilton B. Napolitano, Lucas D. Dias, Leonardo L. Borges, Antônio S.N. Aguiar, Leonardo R. de Almeida, Lucas B. Ribeiro de Carvalho, Áureo B. Souza, Ana L.M. Monteiro
article en

Abstract

Triazole fungicides, such as triadimefon (TF) and its stereoisomeric metabolite, triadimenol (TN), remain cornerstone agrochemicals. However, their stereochemistry may affect shape reactivity, intermolecular recognition, and ecotoxicity in different ways, with potential impacts on non-target species. Objective : This study employs computational methods to describe structural and electronic descriptors, quantify supramolecular interactions, and predict toxicological endpoints in silico for TF and its individual stereoisomer, TN. Methods : Density functional theory calculations were employed to optimize the molecular geometries and calculate reactivity descriptors at the M06-2×/6–311++G(d,p) level of theory. The intermolecular interactions were compared using Hirshfeld surface analysis, quantum theory of atoms in molecules, and natural bond orbital analysis. Chemical reactivity descriptors were calculated to assess reactive sites. Pharmacophore modeling was performed to verify the potential of the six isomers to interact with the lanosterol 14 α -demethylase target. Toxicity was predicted using computational models available online. Results : Differences were found between the electronic properties and intermolecular interactions of TF and TN, due to the presence of –OH or –CO– functional groups. These variations influence the molecular electrostatic potential, reactivity descriptors, and interaction energies, affecting their biological behavior. The results of the pharmacophore modeling suggest that only the 1 R -TF, 1 S ,2 R -TN, and 1 S ,2 S -TN isomers demonstrated potential for interaction with the lanosterol 14 α -demethylase target. Toxicity predictions revealed that some triadimenol stereoisomers exhibit a greater potential for adverse effects on non-target organisms when compared to TF. Conclusion : The findings highlight the crucial role of stereochemistry in modulating the chemical behavior and toxicity of triazole fungicides. Additionally, the use of in silico methods proves effective in predicting the ecotoxicological profiles of such compounds and supports the development of safer and more sustainable agrochemical practices.

Results in ChemistryVol. 25
Universidade Estadual de Goiás (BR), Pontifícia Universidade Católica de Goiás (BR)
Zero hunger
Openalex Percentile: Top 10%
Fungal Plant Pathogen Control
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