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Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/386

Title: Structural features of alkylphenolic chemicals associated with estrogenic activity
Authors: Routledge, EJ
Sumpter, JP
Publication Date: 1997
Publisher: The American Society for Biochemistry and Molecular Biology, Inc.
Citation: The Journal of Biological Chemistry, Volume 272, Number 6, Issue of February 7, 1997 pp. 3280-3288
Abstract: The ability of certain man-made chemicals to mimic the effects of natural steroid hormones and their potential to disrupt the delicate balance of the endocrine system in animals are of increasing concern. The growing list of reported hormone-mimics includes the alkylphenolic (AP) compounds, a small number of which have been reported to be weakly estrogenic. In their most basic form, APs are composed of an alkyl group, which can vary in size, branching, and position, joined to a phenolic ring. The aim of this project was to identify the important structural features responsible for the estrogenic activity of AP chemicals. This was achieved by incubating APs with different structural features in a medium containing a previously described estrogen-inducible strain of yeast (Saccharomyces cerevisiae) expressing the human estrogen receptor and comparing their activity spectrophotometrically by the resulting color change of the medium. The results were compared to the effects of the main natural estrogen 17-estradiol. The data indicate that both the position (para > meta > ortho) and branching (tertiary > secondary = normal) of the alkyl group affect estrogenicity. Optimal estrogenic activity requires a single tertiary branched alkyl group composed of between 6 and 8 carbons located at the para position on an otherwise unhindered phenol ring. The results are discussed in relation to the purity and composition of the chemicals tested.
URI: http://bura.brunel.ac.uk/handle/2438/386
Appears in Collections:Institute for the Environment Research Papers
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