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Expanding the structural footprint of xenoestrogens

Published Web Location

http://www.tandfonline.com/doi/full/10.4161/23273739.2014.967138
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Abstract

Many synthetic chemicals with structural similarity to estradiol bind to the estrogen receptor and disrupt the normal estrogen physiology in humans and other vertebrates. Most of these xenoestrogens contain a structure that mimics the phenolic A ring on E2.  This phenolic A ring is a defining property of E2 that distinguishes it from aldosterone,cortisol, progesterone and testosterone. However, Delta5-androstenediol, 5alpha-androstanediol and 27-hydroxycholesterolalso have estrogenic activity, despite having important structural differencesin their A rings compared to E2.  Unlike E2, these steroids have a saturated A ring with a 3beta-hydroxyl and a C19 methyl group. An implication of their estrogenic activity is that synthetic chemicals containing a saturated A ring

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