Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCCCCCCCCCCCCC(O)=NC(COC1OC(CO)C(OC2OC(CO)C(OC3OC(CO)C(O)C(O)C3CC(C)=O)C(OC3(CC(O)C(N=C(C)O)C(O3)C(O)C(O)CO)C(O)=O)C2O)C(O)C1O)C(O)C=CCCCCCCCCCCCCC

InChIKey

InChIKey=WDEAITNWAKFRFR-UHFFFAOYSA-N

Formula

C73H132N2O26

Mass

1453.847

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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 - Neuraminic acid - Fatty acyl glycoside - C-glucuronide - Alkyl glycoside - C-glycosyl compound - Glycosyl compound - O-glycosyl compound - Ketal - Fatty acyl - Pyran - Oxane - Ketone - Secondary alcohol - Acetal - Carboximidic acid - Carboximidic acid derivative - Carboxylic acid derivative - Carboxylic acid - Oxacycle - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Polyol - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Organic oxygen compound - Organopnictogen compound - Carbonyl group - Alcohol - Aldehyde - Organonitrogen compound - Organooxygen compound - Primary alcohol - 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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