Structure Information
Structure

Compound Identification

SMILES

[Na+].[Na+].CO[C@@H]1O[C@H](CO)[C@H](OS([O-])(=O)=O)[C@H](O[C@@H]2O[C@H]([C@@H](O)[C@H](O)[C@H]2O)C([O-])=O)[C@H]1NC(C)=O

InChIKey

InChIKey=VFJHIBOVYWZXEM-HYGAWUOQSA-L

Formula

C15H23NNa2O15S

Mass

535.38

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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

Aminosaccharides

Direct Parent

N-acyl-alpha-hexosamines

Alternative Parents

Molecular Framework

Aliphatic heteromonocyclic compounds

Substituents

N-acyl-alpha-hexosamine - O-glucuronide - 1-o-glucuronide - Glucuronic acid or derivatives - Short-chain hydroxy acid - Beta-hydroxy acid - Fatty acid - Sulfuric acid ester - Alkyl sulfate - Sulfate-ester - Sulfuric acid monoester - Pyran - Oxane - Monosaccharide - Hydroxy acid - Acetamide - Organic sulfuric acid or derivatives - Secondary alcohol - Carboxylic acid salt - Carboxamide group - Oxacycle - Organic alkali metal salt - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic sodium salt - Organic salt - Organonitrogen compound - Alcohol - Aliphatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as n-acyl-alpha-hexosamines. These are carbohydrate derivatives containing a hexose moiety in which the oxygen atom is replaced by an n-acyl group.

External Descriptors

Not available

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