Abstract
Phenols are used world-wide and their presence in the environment is a cause of increasing concern. Despite evidence to suggest that, in general, they bind poorly to estrogen receptors, they are suspected of being endocrine disrupters. Here, we show that 2, x-substituted phenols are potent inhibitors of estrogen sulfotransferase with IC(50) values at low- or sub-micromolar levels. Our results demonstrate a potential non-genomic mechanism of action for these compounds and suggest that, where viable alternatives exist, both phenols substituted in the 2-position and their metabolic precursors should be avoided.
| Original language | English |
|---|---|
| Pages (from-to) | 72-74 |
| Number of pages | 3 |
| Journal | Molecular and Cellular Endocrinology |
| Volume | 244 |
| Issue number | 1-2 |
| DOIs | |
| Publication status | Published - 1 Dec 2005 |
Keywords
- environmental chemical
- structure-activity relationship
- endocrine disrupter
- inhibitor
- chlorinated phenol
- SULT 1E1