Compound Identification
SMILES
CCCCCCCCCCCCCCC[C@@H](O)C(=O)NC(CC1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C(O)C=CCCC=C(C)CCCCCCCCC
InChIKey
InChIKey=GXOQINIZCVSYDP-MICXNSOHSA-N
Formula
C42H79NO8
Mass
726.093
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
-
Class
Sphingolipids
- Subclass Glycosphingolipids
-
Class
Sphingolipids
-
Superclass
Lipids and lipid-like molecules
Kingdom
Organic compounds
Superclass
Lipids and lipid-like molecules
Class
Sphingolipids
Subclass
Glycosphingolipids
Intermediate Tree Nodes
Not available
Direct Parent
Glycosphingolipids
Alternative Parents
Hexoses C-glycosyl compounds Oxanes N-acyl amines Secondary carboxylic acid amides Secondary alcohols Polyols Oxacyclic compounds Dialkyl ethers Primary alcohols Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aliphatic heteromonocyclic compounds
Substituents
Glycosphingolipid - Hexose monosaccharide - C-glycosyl compound - Glycosyl compound - Fatty amide - Fatty acyl - Monosaccharide - N-acyl-amine - Oxane - Carboxamide group - Secondary carboxylic acid amide - Secondary alcohol - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Organoheterocyclic compound - Polyol - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Carbonyl group - Organic oxygen compound - Primary alcohol - Organonitrogen compound - Organooxygen compound - Alcohol - 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