Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCCCCC(O)C(O)C(C[C@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O)NC(=O)CCCCCCCCCCC1=CC=C(OC2=CC=C(F)C=C2)C=C1

InChIKey

InChIKey=CNTWXKFHJKZPCS-FTKAIFNHSA-N

Formula

C47H76FNO9

Mass

818.121

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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 heteromonocyclic compounds

Substituents

Glycosphingolipid - Diphenylether - Hexose monosaccharide - Glycosyl compound - Diaryl ether - C-glycosyl compound - Phenoxy compound - Phenol ether - Halobenzene - Fluorobenzene - Fatty acyl - Monocyclic benzene moiety - Fatty amide - Aryl halide - Oxane - N-acyl-amine - Aryl fluoride - Monosaccharide - Benzenoid - Secondary carboxylic acid amide - Secondary alcohol - 1,2-diol - Carboxamide group - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Dialkyl ether - Ether - Polyol - Primary alcohol - Organic oxygen compound - Alcohol - Carbonyl group - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Aromatic 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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