An in silico investigation of the toxicological effects and biological activities of 3-phenoxybenzoic acid and its metabolite products.
| Autor: | Nguyen HD; Division of Microbiology, Tulane National Private Research Center, Tulane University, Covington, LA, USA., Hoang TL; College of Pharmacy, California Northstate University College of Pharmacy, CA, USA., Vu GH; Department of Public Heath, Hong Bang Health Center, Hai Phong, Vietnam. |
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| Jazyk: | angličtina |
| Zdroj: | Xenobiotica; the fate of foreign compounds in biological systems [Xenobiotica] 2024 Jun; Vol. 54 (6), pp. 322-341. Date of Electronic Publication: 2024 Jun 24. |
| DOI: | 10.1080/00498254.2024.2361457 |
| Abstrakt: | We aimed to elucidate the toxic effects and biological activities of 3-phenoxybenzoic acid (3PBA) and its metabolite products. Numerous in silico methods were used to identify the toxic effects and biological activities of 3PBA, including PASS online, molecular docking, ADMETlab 2.0, ADMESWISS, MetaTox, and molecular dynamic simulation. Ten metabolite products were identified via Phase II reactions (O-glucuronidation, O-sulfation, and methylation). All of the investigated compounds were followed by Lipinski's rule, indicating that they were stimulants or inducers of hazardous processes. Because of their high gastrointestinal absorption and ability to reach the blood-brain barrier, the studied compounds' physicochemical and pharmacokinetic properties matched existing evidence of harmful effects, including haematemesis, reproductive dysfunction, allergic dermatitis, toxic respiration, and neurotoxicity. The studied compounds have been linked to the apoptotic pathway, the reproductivity system, neuroendocrine disruptors, phospholipid-translocating ATPase inhibitors, and JAK2 expression. An O-glucuronidation metabolite product demonstrated higher binding affinity and interaction with CYP2C9, CYP3A4, caspase 3, and caspase 8 than 3PBA and other metabolite products, whereas metabolite products from methylation were predominant and more toxic. Our in silico findings partly meet the 3Rs principle by minimizing animal testing before more study is needed to identify the detrimental effects of 3PBA on other organs (liver, kidneys). Future research directions may involve experimental validation of in silico predictions, elucidation of molecular mechanisms, and exploration of therapeutic interventions. These findings contribute to our understanding of the toxicological profile of 3PBA and its metabolites, which has implications for risk assessment and regulatory decisions. |
| Databáze: | MEDLINE |
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