A Cheminformatics Study Regarding the Human Health Risks Assessment of the Stereoisomers of Difenoconazole

• Published in: Molecules (Basel, Switzerland) Switzerland), 2022-07, Vol.27 (15), p.4682
• Main Authors: Voiculescu, Denisa Ioana, Roman, Diana Larisa, Ostafe, Vasile, Isvoran, Adriana
• Format: Article
• Language: English
• Subjects: Agricultural products; Agriculture; Bioavailability; Biological activity; Biological effects; Carcinogenicity; Carcinogens; Cardiotoxicity; Cheminformatics; Cytochrome; Cytochromes; Difenoconazole; Dioxolanes; Drinking water; Endocrine disruptors; Fruits; Fungicides; Health risk assessment; Health risks; Hepatotoxicity; human health; Humans; Hydrogen bonding; Hydrogen bonds; Informatics; Isomers; Laboratory animals; Metabolism; Microbiota; Molecular docking; Molecular Docking Simulation; Mutagenicity; Neurotoxicity; Nuclear receptors; Permeability; Pesticides; Plasma proteins; Probability; Proteins; Risk assessment; Stereoisomerism; Stereoisomers; stereoisomers of difenoconazole; Toxicity; toxicology; Triazoles; Vegetables
• ISSN: 1420-3049; 1420-3049
• DOI: 10.3390/molecules27154682

Difenoconazole is a chemical entity containing two chiral centers and having four stereoisomers: (2 ,4 )-, (2 ,4 )-, (2 ,4 )- and (2 ,4 )-difenoconazole, the marketed product containing a mixture of these isomers. Residues of difenoconazole have been identified in many agricultural products and drinking water. A computational approach has been used to evaluate the toxicological effects of the difenoconazole stereoisomers on humans. It integrates predictions of absorption, distribution, metabolism, excretion and toxicity (ADMET) profiles, prediction of metabolism sites, and assessment of the interactions of the difenoconazole stereoisomers with human cytochromes, nuclear receptors and plasma proteins by molecular docking. Several toxicological effects have been identified for all the difenoconazole stereoisomers: high plasma protein binding, inhibition of cytochromes, possible hepatotoxicity, neurotoxicity, mutagenicity, skin sensitization potential, moderate potential to produce endocrine disrupting effects. There were small differences in the predicted probabilities of producing various biological effects between the distinct stereoisomers of difenoconazole. Furthermore, there were significant differences between the interacting energies of the difenoconazole stereoisomers with plasma proteins and human cytochromes, the spectra of the hydrogen bonds and aromatic donor-acceptor interactions being quite distinct. Some distinguishing results have been obtained for the ( , )-difenoconazole: it registered the highest value for clearance, exposed reasonable probabilities to produce cardiotoxicity and carcinogenicity and negatively affected numerous nuclear receptors.