QSTR Models in Dioxins and Dioxin-like Compounds Provide Insights into Gene Expression Dysregulation.

ABSTRACT: Polychlorinated dibenzo-p-dioxins and polychlorinated dibenzo-p-furans (PCDD/Fs) are a group of organic chemicals containing three-ring structures that can be substituted with one to eight chlorine atoms, leading to 75 dioxin and 135 furan congeners. As endocrine-disrupting chemicals (EDCs), they can alter physiological processes causing a number of disorders. In this study, quantitative structure-toxicity relationship (QSTR) studies were used to determine the correlations between the PCDD/Fs' molecular structures and various toxicity endpoints. Strong QSTR models, with the coefficients of determination (r²) values greater than 0.95 and ANOVA p-values less than 0.0001 were established between molecular descriptors and the endpoints of bioconcentration, fathead minnow LC50

SUBMITTER: Eleazar EG 

PROVIDER: S-EPMC11359467 | biostudies-literature | 2024 Aug

REPOSITORIES: biostudies-literature