Compound

lithocholoyl-24-O-(beta-D-glucuronate)

A steroid glucuronide anion that is the conjugate base of lithocholic acid 24-O-(β-D-glucuronide) arising from deprotonation of the carboxylic acid function; major species at pH 7.3.

Definition from ChEBI (CHEBI:136902), read 2026-09-23. CC BY 4.0.

CHEBI:136902ChEBI

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Structure

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A generated conformer of lithocholoyl-24-O-(beta-D-glucuronate) — one low-energy arrangement PubChem computed, not a measured structure. Hydrogens are not drawn; the formula counts them.

Class: Organic compound, anion
Formula: C30H47O9
Mass: 551.697 g/mol
Charge: -1
InChIKey: YRGNGOBHHWKRFH-VYACWCJYSA-M
SMILES: [H][C@]12CC[C@]3([H])[C@]([H])(CC[C@@]4(C)[C@@]3([H])CC[C@]4([H])[C@H](C)CCC(=O)O[C@@H]3O[C@H](C(=O)[O-])[C@@H](O)[C@H](O)[C@H]3O)[C@@]1(C)CC[C@@H](O)C2
Look it up: ChEBI PubChem By InChIKey

Identity from ChEBI, geometry from PubChem. Not evidence.

What the reference databases state

Statements

1 statement

1 statement · 1 reference database · Subject: lithocholoyl-24-O-(beta-D-glucuronate) · Sources: Rhea

Order

lithocholate is converted to lithocholoyl-24-O-(beta-D-glucuronate)CompoundRhea RHEA:52952Inferred only

Reactions

1 reaction

lithocholate+UDP-alpha-D-glucuronatelithocholoyl-24-O-(beta-D-glucuronate)+UDP
Catalysed by UGT2A1 or UGT2A2 or UGT1A3
Reaction pageLeft to rightBalanced
Rhea RHEA:52952CC BY 4.0Reference data

Other names

6 names

Resolves to: lithocholoyl-24-O-(beta-D-glucuronate)

Also called: 1-O-[(3alpha,5beta)-3-hydroxy-24-oxocholan-24-yl]-beta-D-glucopyranuronate1-O-[(3α,5β)-3-hydroxy-24-oxocholan-24-yl]-β-D-glucopyranuronateLCA-24G(1-)LCA-24G(1−)
Systematic name: 1-O-(3alpha-hydroxy-24-oxo-5beta-cholan-24-yl)-beta-D-glucopyranuronate1-O-(3α-hydroxy-24-oxo-5β-cholan-24-yl)-β-D-glucopyranuronate