Structure Information
Structure

Compound Identification

SMILES

[Na+].[Na+].C[C@H](OC[C@H]1OCC[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[C@@]3(C[C@H](O)[C@@H](NC(C)=O)[C@@H](O3)[C@@H](O)[C@H](O)CO)C([O-])=O)[C@H]2O)[C@H]1O)C([O-])=O

InChIKey

InChIKey=YNXIZRMILLEWRB-KRLHDRKVSA-L

Formula

C26H41NNa2O19

Mass

717.582

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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 - Sugar amino acids and derivatives - Pyranoid amino acids and derivatives - Neuraminic acids and derivatives - N-acylneuraminic acids and derivatives

Direct Parent

N-acylneuraminic acids

Alternative Parents

Molecular Framework

Aliphatic heteromonocyclic compounds

Substituents

Oligosaccharide - N-acylneuraminic acid - Neuraminic acid - C-glucuronide - C-glycosyl compound - Glycosyl compound - O-glycosyl compound - Ketal - Dicarboxylic acid or derivatives - Oxane - Pyran - Acetamide - Carboxamide group - Carboxylic acid salt - Secondary carboxylic acid amide - Secondary alcohol - Acetal - Carboxylic acid derivative - Carboxylic acid - Dialkyl ether - Oxacycle - Ether - Organic alkali metal salt - Organoheterocyclic compound - Polyol - Organopnictogen compound - Organic nitrogen compound - Carbonyl group - Organic oxide - Organic sodium salt - Alcohol - Organic salt - Organonitrogen compound - Organic zwitterion - Hydrocarbon derivative - Primary alcohol - Aliphatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as n-acylneuraminic acids. These are neuraminic acids carrying an N-acyl substituent.

External Descriptors

Not available

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