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The European regulation on chemicals (REACh) places emphasis on reduction of systematic toxicity testing, thus fostering development of alternative methods. Consequently, we analysed acute toxicity data gathered by the Japanese Ministry of Environment for three species belonging to three different trophic levels (i.e., Pseudokirchneriella subcapitata 72-hour EC50, Daphnia magna 48-hour EC50 and Oryzias latipes 96-hour LC50). This paper investigates the relationships between the chemical structure and both the toxicity of the chemicals and the cross-species differences in sensitivity. The physicochemical properties of the chemicals were represented by the categories they belonged to in several widely-used categorisation schemes implemented by the freely available OECD (Q)SAR Toolbox and by quantitative molecular descriptors using DRAGON software. The outputs of these software products were analysed and compared in terms of quality of prediction and biological interpretation. Amongst the categorisations implemented by the OECD Toolbox, those focussing on bioaccumulation or biotransformation appeared to be the most interesting in terms of environmental prediction on a whole set of chemicals, in particular as the predicted biotransformation half-life is strongly dependent on hydrophobicity. In predicting toxicity towards each species, simple linear regression on logP performed better than PLS regression of toxicity on a very large set of molecular descriptors. However, the predictions based on the interspecies correlations performed better than the QSAR predictions. The results in terms of cross-species comparisons encourage the use of test strategies focussing on reducing the number of tests on fish.
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http://dx.doi.org/10.1016/j.scitotenv.2011.05.029 | DOI Listing |
Talanta
August 2025
National Institutes for Food and Drug Control, Beijing, 102629, P.R. China; State Key Laboratory of Drug Regulatory Science, Beijing, 102629, P.R. China. Electronic address:
As concealment methods for illegal cosmetic adulteration advance, identifying non-library or unexpected additives remains challenging. This study presents a novel integrated strategy for rapid, non-targeted detection of reference-standard-free illegal cosmetic additives, especially emerging structural analogs of known prohibited compounds. The quinolone case study validated the strategy's broad applicability to cosmetics.
View Article and Find Full Text PDFMol Divers
August 2025
Drug Discovery and Development Laboratory (DDD Lab), Department of Pharmaceutical Technology, Jadavpur University, Kolkata, 700032, India.
The terminal half-life ( ) is a crucial pharmacokinetic parameter for estimating the dose regimen and duration of action of a drug. Previously, few research papers have been published on the pharmacokinetic parameters that correlate with the chemical structure of pharmaceuticals, but these are time-consuming and costly. The main goal of the current study is to generate a quantitative read-across structure-activity relationship (q-RASAR) for terminal half-life estimation of diverse pharmaceuticals.
View Article and Find Full Text PDFSAR QSAR Environ Res
July 2025
Institute of Physiologically Active Compounds, Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, Chernogolovka, Russia.
The existing QSAR approaches for mammalian acute toxicity have been limited in scope, often relying on small or narrowly focused datasets and on classification endpoints. In contrast, our work leverages a sufficiently large curated dataset (9843 rat oral and 2323 intravenous LD values) to build regression models of acute toxicity. The best-performing QSAR models developed using 2D RDKit descriptors and the Cat Boost method achieve = 0.
View Article and Find Full Text PDFALTEX
July 2025
Department of Veterinary Physiology and Pharmacology, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, TX, USA.
Under the European Union's REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) regulation, the European Chemicals Agency (ECHA) is required to assess the compliance of safety data submitted by chemical registrants. ECHA must check a proportion of registration dossiers for compliance. From 2010 to 2023, 4,854 compliance checks (CCHs) were conducted.
View Article and Find Full Text PDFToxics
July 2025
QSAR Research Unit in Environmental Chemistry and Ecotoxicology, Department of Theoretical and Applied Sciences, University of Insubria, via J.H. Dunant 3, 21100 Varese, Italy.
Per- and polyfluoroalkyl substances (PFAS) are of concern because of their potential thyroid hormone system disruption by binding to human transthyretin (hTTR). However, the amount of experimental data is scarce. In this work, new classification and regression QSARs were developed to predict the hTTR disruption based on experimental data measured for 134 PFAS.
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