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Estriol 3-glucuronide
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Names | |
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IUPAC name
16α,17β-Dihydroxyestra-1,3,5(10)-trien-3-yl β-D-glucopyranosiduronic acid
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Systematic IUPAC name
(2S,3S,4S,5R,6S)-6-{[(1R,2R,3aS,3bR,9bS,11aS)-1,2-Dihydroxy-11a-methyl-2,3,3a,3b,4,5,9b,10,11,11a-decahydro-1H-cyclopenta[a]phenanthren-7-yl]oxy}-3,4,5-trihydroxyoxane-2-carboxylic acid | |
Other names
(16α,17β)-16,17-Dihydroxyestra-1(10),2,4-trien-3-yl β-D-glucopyranosiduronic acid
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Identifiers | |
3D model (JSmol)
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ChEBI | |
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PubChem CID
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CompTox Dashboard (EPA)
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Properties | |
C24H32O9 | |
Molar mass | 464.511 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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Estriol 3-glucuronide, or oestriol 3-glucuronide, also known as estriol 3-β-D-glucosiduronic acid, is a natural, steroidal estrogen and a glucuronic acid (β-D-glucopyranuronic acid) conjugate of estriol. It is found in the urine of women as a reversibly formed metabolite of estriol. The positional isomer of estriol 3-glucuronide, estriol 16α-glucuronide, also occurs as an endogenous metabolite of estriol, but to a much greater extent in comparison.
See also
- Estrogen conjugate
- Estradiol glucuronide
- Estrone glucuronide
- Estradiol sulfate
- Estrone sulfate
- Lipoidal estradiol
- Catechol estrogen
External links
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