Structure Information
Structure

Compound Identification

SMILES

[H]\C(COS(O)(=O)=O)=C1\S[C@@]([H])(N=C1C)C(=O)OC1([H])OC([H])(C(O)=O)C([H])(O)C([H])(O)C1([H])O

InChIKey

InChIKey=KMPJREXKAWMOGI-AXZSSGOOSA-N

Formula

C13H17NO12S2

Mass

443.39

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organic oxygen compounds

Class

Organooxygen compounds

Subclass

Carbohydrates and carbohydrate conjugates

Intermediate Tree Nodes

Sugar acids and derivatives - Glucuronic acid derivatives - Glucuronides

Direct Parent

O-glucuronides

Alternative Parents

Molecular Framework

Aliphatic heteromonocyclic compounds

Substituents

O-glucuronide - 1-o-glucuronide - Alpha-amino acid ester - Alpha-amino acid or derivatives - Thiazolecarboxylic acid or derivatives - Beta-hydroxy acid - Sulfuric acid ester - Alkyl sulfate - Sulfate-ester - Sulfuric acid monoester - Pyran - Oxane - Monosaccharide - Hydroxy acid - Dicarboxylic acid or derivatives - Meta-thiazoline - Thiazole - Organic sulfuric acid or derivatives - Thioenolether - Secondary alcohol - Ketimine - Carboxylic acid ester - Oxacycle - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Polyol - Carboxylic acid - Carboxylic acid derivative - Acetal - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Imine - Carbonyl group - Alcohol - Aliphatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as o-glucuronides. These are glucuronides in which the aglycone is linked to the carbohydrate unit through an O-glycosidic bond.

External Descriptors

Not available

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