4-Hydroxyestriol
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Names | |
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IUPAC name
(8R,9S,13S,14S,16R,17R)-13-Methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,4,16,17-tetrol[1]
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Other names
Estra-1,3,5(10)-triene-3,4,16α,17β-tetrol
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Identifiers | |
3D model (JSmol)
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ChemSpider | |
PubChem CID
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CompTox Dashboard (EPA)
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Properties | |
C18H24O4 | |
Molar mass | 304.386 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Chemical compound
4-Hydroxyestriol, also known as estra-1,3,5(10)-triene-3,4,16α,17β-tetrol, is an endogenous catechol estrogen and metabolite of estriol. It has been found in pregnancy urine.[2]
See also
References
- ^ "(16-A,17-A)-Estra-1,3,5(10)-Triene-3,4,16,17-Tetrol". National Center for Biotechnology Information. 17 December 2016. Archived from the original on 26 December 2016. Retrieved 26 December 2016.
{{cite journal}}
: Cite journal requires|journal=
(help); Unknown parameter|deadurl=
ignored (|url-status=
suggested) (help) - ^ Theodore Fotsis Fotsis; Paula Jervenpee; Herman Adlercreutz (13 January 2009) [1980]. "Identification of 4-Hydroxyestriol in Pregnancy Urine". The Journal of Clinical Endocrinology and Metabolism. 51 (1): 148–151. doi:10.1210/jcem-51-1-148. PMID 6892918. Retrieved 26 December 2016.
ERTooltip Estrogen receptor |
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GPERTooltip G protein-coupled estrogen receptor |
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