Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCCCCCCCCCC[C@@H](O)C(=O)N[C@@H](CO[C@@H]1OC(CO)[C@@H](O[C@@H]2OC(CO)[C@H](O[C@@H]3OC(CO)[C@H](O)C(OS(O)(=O)=O)C3O)C(O)C2O)C(O)C1O)[C@H](O)[C@H](O)CCCCCCCCCCCC(C)CC

InChIKey

InChIKey=DWRADBKHRGYZKR-FKWJKRBQSA-N

Formula

C59H113NO23S

Mass

1236.6

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Lipids and lipid-like molecules

Class

Sphingolipids

Subclass

Glycosphingolipids

Intermediate Tree Nodes

Not available

Direct Parent

Glycosphingolipids

Alternative Parents

Molecular Framework

Aliphatic heteromonocyclic compounds

Substituents

Glycosphingolipid - Oligosaccharide - Fatty acyl glycoside - Alkyl glycoside - Glycosyl compound - O-glycosyl compound - Fatty amide - N-acyl-amine - Oxane - Sulfuric acid monoester - Sulfate-ester - Alkyl sulfate - Sulfuric acid ester - Fatty acyl - Organic sulfuric acid or derivatives - Secondary alcohol - Carboxamide group - Secondary carboxylic acid amide - Organoheterocyclic compound - Carboxylic acid derivative - Oxacycle - Acetal - Alcohol - Organopnictogen compound - Primary alcohol - Organic nitrogen compound - Carbonyl group - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aliphatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as glycosphingolipids. These are sphingolipids containing a saccharide moiety glycosidically attached to the sphingoid base. Although saccharide moieties are mostly O-glycosidically linked to the ceramide moiety, other sphingolipids with glycosidic bonds of other types (e.g. S-,C-, or N-type) has been reported.

External Descriptors

Not available

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