Compound
16alpha,17alpha-estriol 17-O-(beta-D-glucuronate)
A steroid glucuronide anion that is the conjugate base of 17-epiestriol 17-O-(β-D-glucuronide) arising from deprotonation of the carboxylic acid function; major species at pH 7.3.
Definition from ChEBI (CHEBI:136883), read 2026-09-23. CC BY 4.0.
Structure
Loading the model…
- Class
- Organic compound, anion
- Formula
- C24H31O9
- Mass
- 463.503 g/mol
- Charge
- -1
- InChIKey
- CZGFLAQOJPXVRV-SQFONMOTSA-M
- SMILES
- [H][C@@]12CCc3cc(O)ccc3[C@@]1([H])CC[C@]1(C)[C@H](O[C@@H]3O[C@H](C(=O)[O-])[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)C[C@@]21[H]
- Look it up
- ChEBIPubChemBy InChIKey
Identity from ChEBI, geometry from PubChem. Not evidence.
What it touches on the way
Mechanistic reach
2 entities
2 entities reached.
0 reported hops2 assembled from the scaffold
What the reference databases state
Statements
2 statements
2 statements · 1 reference database · Subject: 16alpha,17alpha-estriol 17-O-(beta-D-glucuronate) · Sources: Rhea
- 16alpha,17alpha-estriol 17-O-(beta-D-glucuronate) is metabolised by UGT2B4ProteinRhea RHEA:52916Inferred only
- 16alpha,17alpha-estriol 17-O-(beta-D-glucuronate) is metabolised by UGT2B7ProteinRhea RHEA:52916Inferred only
Reactions
1 reaction
16alpha,17alpha-estriol+UDP-alpha-D-glucuronate16alpha,17alpha-estriol 17-O-(beta-D-glucuronate)+UDP+hydron
Reaction pageLeft to rightBalance undeterminable
Rhea RHEA:52916CC BY 4.0Reference data
Other names
4 names
Resolves to: 16alpha,17alpha-estriol 17-O-(beta-D-glucuronate)
- Also called
- (16alpha,17alpha)-3,16-dihydroxyestra-1(10),2,4-trien-17-yl beta-D-glucopyranosiduronate(16α,17α)-3,16-dihydroxyestra-1(10),2,4-trien-17-yl β-D-glucopyranosiduronate
- Systematic name
- 3,16alpha-dihydroxyestra-1(10),2,4-trien-17alpha-yl beta-D-glucopyranosiduronate3,16α-dihydroxyestra-1(10),2,4-trien-17α-yl β-D-glucopyranosiduronate