Structure Information
Structure

Compound Identification

SMILES

[Na+].CCCCCCCC\C=C/CCCCCCCCOCC(CO[C@@H]1O[C@H](CO)[C@H](OC2O[C@H](CO)[C@H](O)[C@H](OS([O-])(=O)=O)[C@H]2O)[C@H](O[C@@H]2O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]2O)[C@H]1O)OCCCCCCCC\C=C/CCCCCCCC

InChIKey

InChIKey=ZOEXHRQFMWGWQT-OYVYCUNJSA-M

Formula

C57H105NaO20S

Mass

1165.5

Export to:

JSON SDF CSV

Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Lipids and lipid-like molecules

Class

Glycerolipids

Subclass

Glycosylglycerols

Intermediate Tree Nodes

Not available

Direct Parent

Glycosylglycerols

Alternative Parents

Molecular Framework

Aliphatic heteromonocyclic compounds

Substituents

Oligosaccharide - Glycosyldialkylglycerol - Glycosyldiradylglycerol - Glycosylglycerol - Glycosyl compound - O-glycosyl compound - Glycerol ether - Oxane - Sulfuric acid monoester - Sulfate-ester - Sulfuric acid ester - Alkyl sulfate - Organic sulfuric acid or derivatives - Secondary alcohol - Organic alkali metal salt - Dialkyl ether - Ether - Acetal - Organoheterocyclic compound - Polyol - Oxacycle - Organic oxide - Alcohol - Organooxygen compound - Organic salt - Organic sodium salt - Primary alcohol - Organic oxygen compound - Hydrocarbon derivative - Organic cation - Aliphatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as glycosylglycerols. These are glycerolipids structurally characterized by the presence of one or more sugar residues attached to glycerol via a glycosidic linkage.

External Descriptors

Not available

Previous Back Next