Compound Identification
SMILES
CCCCCCCCCCCCCC[C@@H](O)[C@@H](O)[C@H](C[C@H]1O[C@H](COCC2=CC=CC=C2)[C@H](OCC2=CC=CC=C2)[C@H](OCC2=CC=CC=C2)[C@H]1OCC1=CC=CC=C1)N=[N+]=[N-]
InChIKey
InChIKey=IOGFJTGEEACZNB-MJJUNOJKSA-N
Formula
C52H71N3O7
Mass
850.154
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
-
Class
Sphingolipids
- Subclass Glycosphingolipids
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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 Benzylethers Oxanes Secondary alcohols Azo imides Azo compounds 1,2-diols Oxacyclic compounds Dialkyl ethers Organic zwitterions Organic salts Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Glycosphingolipid - Hexose monosaccharide - C-glycosyl compound - Glycosyl compound - Benzylether - Monocyclic benzene moiety - Monosaccharide - Oxane - Benzenoid - Secondary alcohol - Azo compound - Azo imide - 1,2-diol - Organoheterocyclic compound - Dialkyl ether - Ether - Oxacycle - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organic zwitterion - Hydrocarbon derivative - Organic salt - Alcohol - 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