Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCCCCCCCCOC[C@H](CO[C@]1(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)C(O)=O)OS(O)(=O)=O

InChIKey

InChIKey=MQLODQNHWVTYNI-QOEIKJPUSA-N

Formula

C32H61NO26S5

Mass

1036.12

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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 - C-glucuronide - C-glycosyl compound - Glycosyl compound - Ketal - Glycerol ether - Oxane - Pyran - Sulfuric acid monoester - Sulfate-ester - Sulfuric acid ester - Alkyl sulfate - Acetamide - Organic sulfuric acid or derivatives - Secondary carboxylic acid amide - Carboxamide group - Acetal - Carboxylic acid derivative - Carboxylic acid - Dialkyl ether - Ether - Monocarboxylic acid or derivatives - Oxacycle - Organoheterocyclic compound - Organopnictogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organonitrogen compound - 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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