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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/20778
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dc.contributor.authorGoonetilleke, Ashantha-
dc.date.accessioned2026-03-03T08:53:18Z-
dc.date.available2026-03-03T08:53:18Z-
dc.date.issued2020-02-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S235234091931176X-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/20778-
dc.description.abstractSixteen significant physicochemical predictor variables for thirty PAHs and transformed PAH products (TPPs) were retrieved individually prior to collation from ChemSpider.com [1] whilst their corresponding toxicity equivalency factor (TEF) end-point was obtained from published articles by Bortey-Sam, Ikenaka [2] and Wei, Bandowe [3]. In order to achieve a 5:1 ratio of the number of observations to predictors which is vital for an effective quantitative structure-activity relationship (QSAR) modelling, factor analysis was used to reduce the data. Four fundamental predictors were obtained whilst the observations were found to cluster into two main groups of nitro-PAHs and other analytes. It is anticipated that the data presented here is highly relevant for future studies on the toxicity and health effects of the analytes in the environment. Secondly, the fate and distribution patterns of PAHs and TPPs are influenced by the parameters in the dataset. In this regard, studies on the behaviour patterns of these environmental pollutants require this information for a comprehensive evaluation and interpretation of results. Researchers across varied fields of environmental science and toxicology will find this dataset very useful.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectCivil engineeringen_US
dc.subjectQuantitative structure-activity relationshipen_US
dc.subjectPredictor variableen_US
dc.subjectResponse variableen_US
dc.subjectToxicity equivalency factorsen_US
dc.subjectFactor analysisen_US
dc.subjectTransformed PAH productsen_US
dc.titleDataset for the quantitative structure-activity relationship (QSAR) modeling of the toxicity equivalency factors (TEFs) of PAHs and transformed PAH productsen_US
dc.typeArticleen_US
Appears in Collections:Department of Civil Engineering

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