Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCC[C@H](O)C(=O)NC(CO[C@H]1O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)C(O)=O)C(O)CCCCCCCCC\C=C/CCCCCC

InChIKey

InChIKey=NHXIBOKUMLTPLW-DBJMDDPOSA-N

Formula

C40H75NO10

Mass

730.037

Export to:

JSON SDF CSV

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 - Fatty acyl glycoside - Fatty acyl glycoside of mono- or disaccharide - 1-o-glucuronide - O-glucuronide - Glucuronic acid or derivatives - Alkyl glycoside - Glycosyl compound - O-glycosyl compound - Beta-hydroxy acid - Fatty acyl - Pyran - Fatty amide - Oxane - Hydroxy acid - Monosaccharide - N-acyl-amine - Carboxamide group - Secondary carboxylic acid amide - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Carboxylic acid - Polyol - Monocarboxylic acid or derivatives - Acetal - Organic nitrogen compound - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Alcohol - Carbonyl group - Organopnictogen 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

Previous Back Next