Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCCCC=C[C@@H](OC(=O)C1=CC=CC=C1)[C@H](CO[C@H]1O[C@@H]2COC(O[C@@H]2[C@H](OC(=O)C2=CC=CC=C2)[C@H]1OC(=O)C1=CC=CC=C1)C1=CC=CC=C1)[N-][N+]#N

InChIKey

InChIKey=OQLKVEWYHGNHQZ-MRRYJAGRSA-N

Formula

C52H61N3O10

Mass

888.071

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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

Aromatic heteropolycyclic compounds

Substituents

Glycosphingolipid - Fatty acyl glycoside of mono- or disaccharide - Fatty acyl glycoside - Alkyl glycoside - Pyranodioxin - Benzoate ester - Tricarboxylic acid or derivatives - Benzoic acid or derivatives - Benzoyl - Benzenoid - Fatty acyl - Monocyclic benzene moiety - Oxane - Meta-dioxane - Monosaccharide - Carboxylic acid ester - Azo imide - Azo compound - Acetal - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Organic salt - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organic cation - Aromatic heteropolycyclic 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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