Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCCCC[C@@H](O)[C@@H](O)[C@H](CO[C@@H]1O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O[C@]3(C[C@H](O)[C@@H](N=C(C)[O-])[C@@H](O3)[C@H](O)[C@@H](CO)O[C@]3(C[C@H](O)[C@@H](N=C(C)[O-])[C@@H](O3)[C@H](O)[C@@H](CO)O[C@]3(C[C@H](O)[C@@H](N=C(C)[O-])[C@@H](O3)[C@H](O)[C@H](O)COC(C)=O)C(O)=O)C(O)=O)C(O)=O)[C@H]2O)[C@H](O)[C@H]1O)N=C(O)CCCCCCCCCCCCC\C=C\CCCCCCCC

InChIKey

InChIKey=YLUKTNCNLPAZFL-VQNCKUSNSA-K

Formula

C89H153N4O39

Mass

1903.194

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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 - Tetracarboxylic acid or derivatives - Alkyl glycoside - O-glycosyl compound - Glycosyl compound - C-glycosyl compound - Ketal - Fatty acyl - Pyran - Oxane - Secondary alcohol - Carboxylic acid ester - Oxacycle - Organoheterocyclic compound - Carboxylic acid - Carboxylic acid derivative - Carboximidic acid derivative - Carboximidic acid - Acetal - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organonitrogen compound - Carbonyl group - Alcohol - Organic anion - 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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