Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCCCCCCCCCCCC(=O)N[C@@H](CO[C@@H]1O[C@H](COP(O)(=O)OCC[N+](C)(C)C)[C@H](O)[C@H](O)[C@H]1O)[C@H](O)CCCCCCCCCCCCCCCCCCC

InChIKey

InChIKey=KSYUDPBZIXGYNP-DFXWQDGCSA-O

Formula

C55H112N2O11P

Mass

1008.477

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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 - Hexose phosphate - Fatty acyl glycoside - Fatty acyl glycoside of mono- or disaccharide - Alkyl glycoside - Glycosyl compound - O-glycosyl compound - Phosphocholine - Monosaccharide phosphate - Dialkyl phosphate - Fatty amide - Monosaccharide - N-acyl-amine - Organic phosphoric acid derivative - Oxane - Phosphoric acid ester - Fatty acyl - Alkyl phosphate - Quaternary ammonium salt - Tetraalkylammonium salt - Secondary carboxylic acid amide - Secondary alcohol - Carboxamide group - Carboxylic acid derivative - Organoheterocyclic compound - Polyol - Acetal - Oxacycle - Organic oxide - Carbonyl group - Organopnictogen compound - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Alcohol - Amine - Organic cation - 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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