Compound
16alpha-hydroxyestrone 16-O-(beta-D-glucuronate)
A steroid glucuronide anion that is the conjugate base of 16α-hydroxyestrone 16-O-(β-D-glucuronide) arising from deprotonation of the carboxylic acid function; major species at pH 7.3.
Definition from ChEBI (CHEBI:136636), read 2026-09-23. CC BY 4.0.
Structure
Loading the model…
- Class
- Organic compound, anion
- Formula
- C24H29O9
- Mass
- 461.487 g/mol
- Charge
- -1
- InChIKey
- JLYJQBHANCHTOW-OWYKRJLGSA-M
- SMILES
- [H][C@@]12C[C@@H](O[C@@H]3O[C@H](C(=O)[O-])[C@@H](O)[C@H](O)[C@H]3O)C(=O)[C@@]1(C)CC[C@]1([H])c3ccc(O)cc3CC[C@@]21[H]
- Look it up
- ChEBIPubChemBy InChIKey
Identity from ChEBI, geometry from PubChem. Not evidence.
What it touches on the way
Mechanistic reach
1 entity
1 entities reached.
0 reported hops1 assembled from the scaffold
What the reference databases state
Chemical structure
- 16alpha-hydroxyestrone 16-O-(beta-D-glucuronate) has the functional parent 16alpha-hydroxyestroneCompoundChEBI CHEBI:136636Inferred only
Statements
1 statement
1 statement · 1 reference database · Subject: 16alpha-hydroxyestrone 16-O-(beta-D-glucuronate) · Sources: Rhea
- 16alpha-hydroxyestrone 16-O-(beta-D-glucuronate) is metabolised by UGT2B7ProteinRhea RHEA:52452Inferred only
Reactions
1 reaction
16alpha-hydroxyestrone+UDP-alpha-D-glucuronate16alpha-hydroxyestrone 16-O-(beta-D-glucuronate)+UDP+hydron
Catalysed by UGT2B7
Reaction pageLeft to rightBalance undeterminable
Rhea RHEA:52452CC BY 4.0Reference data
Other names
2 names
Resolves to: 16alpha-hydroxyestrone 16-O-(beta-D-glucuronate)
- Systematic name
- 3-hydroxy-17-oxoestra-1,3,5(10)-trien-16alpha-yl beta-D-glucopyranosiduronate3-hydroxy-17-oxoestra-1,3,5(10)-trien-16α-yl β-D-glucopyranosiduronate