کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2593453 1562164 2015 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
QSAR screening of 70,983 REACH substances for genotoxic carcinogenicity, mutagenicity and developmental toxicity in the ChemScreen project
موضوعات مرتبط
علوم زیستی و بیوفناوری علوم محیط زیست بهداشت، سم شناسی و جهش زایی
پیش نمایش صفحه اول مقاله
QSAR screening of 70,983 REACH substances for genotoxic carcinogenicity, mutagenicity and developmental toxicity in the ChemScreen project
چکیده انگلیسی


• QSAR screening of 70,983 REACH substances.
• 16 QSAR models applied to reach predictions of potential effects.
• Genotoxic carcinogenicity, mutagenicity and developmental toxicity.
• Result: 6.5% genotoxic carcinogens, 16.3% mutagens, 11.5% developmental toxicants.
• Results are similar to earlier findings for chemical inventories.

The ChemScreen project aimed to develop a screening system for reproductive toxicity based on alternative methods. QSARs can, if adequate, contribute to the evaluation of chemical substances under REACH and may in some cases be applied instead of experimental testing to fill data gaps for information requirements. As no testing for reproductive effects should be performed in REACH on known genotoxic carcinogens or germ cell mutagens with appropriate risk management measures implemented, a QSAR pre-screen for 70,983 REACH substances was performed. Sixteen models and three decision algorithms were used to reach overall predictions of substances with potential effects with the following result: 6.5% genotoxic carcinogens, 16.3% mutagens, 11.5% developmental toxicants. These results are similar to findings in earlier QSAR and experimental studies of chemical inventories, and illustrate how QSAR predictions may be used to identify potential genotoxic carcinogens, mutagens and developmental toxicants by high-throughput virtual screening.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Reproductive Toxicology - Volume 55, 1 August 2015, Pages 64–72
نویسندگان
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