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• W2034382629 abstract "Abstract A sizable number of environmental contaminants and natural products have been found to possess hormonal activity and have been termed endocrine-disrupting chemicals. Due to the vast number (estimated at about 58,000) of environmental contaminants, their potential to adversely affect the endocrine system, and the paucity of health effects data associated with them, the U.S. Congress was led to mandate testing of these compounds for endocrine-disrupting ability. Here we provide evidence that a computational structure–activity relationship (SAR) approach has the potential to rapidly and cost effectively screen and prioritize these compounds for further testing. Our models were based on data for 122 compounds assayed for estrogenicity in the ESCREEN assay. We produced two models, one for relative proliferative effect (RPE) and one for relative proliferative potency (RPP) for chemicals as compared to the effects and potency of 17β-estradiol. The RPE and RPP models achieved an 88 and 72% accurate prediction rate, respectively, for compounds not in the learning sets. The good predictive ability of these models and their basis on simple to understand 2-D molecular fragments indicates their potential usefulness in computational screening methods for environmental estrogens. Keywords: Environmental estrogensXenoestrogensStructure–activity relationship (SAR)Computational modeling Acknowledgements We gratefully acknowledge support for this work from the Congressionally Directed Medical Research Program for Breast Cancer Idea Award DAMD17-01-0376." @default.
• W2034382629 created "2016-06-24" @default.
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• W2034382629 date "2004-02-01" @default.
• W2034382629 modified "2023-10-05" @default.
• W2034382629 title "Structure–Activity Approach to the Identification of Environmental Estrogens: The MCASE Approach" @default.
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• W2034382629 doi "https://doi.org/10.1080/1062936032000169679" @default.
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