Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCCCCC[C@@H](O)[C@H](CO[C@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O)NC(=O)CCCCCCCCCCNC(=O)CCC1=CC=C(\C=C2/N=C(C)C=C2C)N1B(F)F

InChIKey

InChIKey=PSUYPDKNORSROS-KUIGAIMTSA-N

Formula

C49H83BF2N4O9

Mass

921.03

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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 - Fatty acyl glycoside - Fatty acyl glycoside of mono- or disaccharide - Alkyl glycoside - Hexose monosaccharide - Glycosyl compound - O-glycosyl compound - Fatty amide - Monosaccharide - N-acyl-amine - Oxane - Substituted pyrrole - Fatty acyl - Pyrrole - Heteroaromatic compound - Carboxamide group - Ketimine - Secondary carboxylic acid amide - Secondary alcohol - Azacycle - Organic metalloid salt - Oxacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Acetal - Polyol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Imine - Carbonyl group - Alcohol - Organic nitrogen compound - Primary alcohol - Organonitrogen compound - Organooxygen compound - Organopnictogen 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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