| Literature DB >> 20113858 |
Benjamin Smith1, Peter Cadby, Jean-Charles Leblanc, R Woodrow Setzer.
Abstract
The weight of evidence points to weak genotoxic activity of methyleugenol, the putative genotoxic carcinogen being 1'-sulphate ester metabolite. Dose response modelling of the data for methyleugenol gave a BMDL10 for male rat liver adenoma or carcinoma (combined) of 7.9 mg/kg-bw/d following adjustment to daily average doses. The MoEs ranged from 100 to 800 depending on the assumptions used in the exposure estimation. Copyright 2009 ILSI Europe. Published by Elsevier Ltd.. All rights reserved.Entities:
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Year: 2010 PMID: 20113858 DOI: 10.1016/j.fct.2009.10.036
Source DB: PubMed Journal: Food Chem Toxicol ISSN: 0278-6915 Impact factor: 6.023