Structure Information
Structure

Compound Identification

SMILES

[Na].[Na].[Na].[Na].CCCCCCCCCCCCCCCCCCCCCCOCC(C)(COCCCCCCCCCCCCCCCCCCCCCC)COC(=O)[C@@]1(O)C[C@H](OS(O)(=O)=O)[C@@H](NC(C)=O)[C@@H](O1)[C@H](OS(O)(=O)=O)[C@@H](COS(O)(=O)=O)OS(O)(=O)=O

InChIKey

InChIKey=HQJAFTIITJYEND-SNJYSJBGSA-N

Formula

C60H117NNa4O23S4

Mass

1440.78

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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

Direct Parent

N-acylneuraminic acids and derivatives

Alternative Parents

Molecular Framework

Aliphatic heteromonocyclic compounds

Substituents

N-acylneuraminic acid or derivatives - C-glucuronide - C-glycosyl compound - Glycosyl compound - Oxane - Pyran - Sulfuric acid monoester - Sulfate-ester - Alkyl sulfate - Sulfuric acid ester - Acetamide - Organic sulfuric acid or derivatives - Secondary carboxylic acid amide - Carboxamide group - Hemiacetal - Carboxylic acid ester - Organic alkali metal salt - Organoheterocyclic compound - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Oxacycle - Ether - Dialkyl ether - Carbonyl group - Hydrocarbon derivative - Organonitrogen compound - Organic nitrogen compound - Organic oxide - Aliphatic heteromonocyclic compound

Description

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

External Descriptors

Not available

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