Structure Information
Structure

Compound Identification

SMILES

CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[C@@H]1O[C@H](CO[C@@]2(C[C@H](O)[C@@H](NC(C)=O)[C@@H](O2)[C@H](O)[C@H](O)CO)C(O)=O)[C@@H](O)[C@H](O)[C@@H]1O)[C@H](O)CO

InChIKey

InChIKey=OWSNEDGPBHBCDR-RZCOEOHRSA-N

Formula

C25H42N2O19

Mass

674.606

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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

N-acylneuraminic acid - Neuraminic acid - Fatty acyl glycoside - Fatty acyl glycoside of mono- or disaccharide - C-glucuronide - Alkyl glycoside - C-glycosyl compound - Glycosyl compound - O-glycosyl compound - Ketal - Amino saccharide - Pyran - Oxane - Beta-hydroxy aldehyde - Fatty acyl - Monosaccharide - Acetamide - Secondary carboxylic acid amide - Secondary alcohol - Carboxamide group - Organoheterocyclic compound - Polyol - Monocarboxylic acid or derivatives - Oxacycle - Acetal - Carboxylic acid - Carboxylic acid derivative - Alcohol - Organic oxide - Carbonyl group - Hydrocarbon derivative - Organopnictogen compound - Organonitrogen compound - Organic nitrogen compound - Aldehyde - 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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