Structure Information
Structure

Compound Identification

SMILES

[Na+].CCCCCCCC\C=C/CCCCC\C=C/C(=O)OC[C@@H](O)CO[C@H]1O[C@H](CS([O-])(=O)=O)[C@@H](O)[C@H](O)[C@H]1O

InChIKey

InChIKey=KIVWDOKIGKCJGF-NPUACFAHSA-M

Formula

C27H47NaO11S

Mass

602.71

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Lipids and lipid-like molecules

Class

Glycerolipids

Subclass

Glycosylglycerols

Intermediate Tree Nodes

Glycosylmonoradylglycerols - Glycosylmonoacylglycerols - Sulfoquinovosylmonoacylglycerols

Direct Parent

Sulfoquinovosyl 1-monoacylglycerols

Alternative Parents

Molecular Framework

Aliphatic heteromonocyclic compounds

Substituents

Sulfoquinovosyl 1-monoacylglycerol - Hexose monosaccharide - Glycosyl compound - O-glycosyl compound - Fatty acid ester - Monosaccharide - Oxane - Fatty acyl - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Organosulfonic acid - Sulfonyl - Alkanesulfonic acid - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Carboxylic acid ester - Secondary alcohol - Carboxylic acid derivative - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Oxacycle - Organic alkali metal salt - Polyol - Acetal - Hydrocarbon derivative - Organic oxide - Organic salt - Organooxygen compound - Organosulfur compound - Organic sodium salt - Organic oxygen compound - Alcohol - Carbonyl group - Organic cation - Aliphatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as sulfoquinovosyl 1-monoacylglycerols. These are sulfoquinovosylmonoacylglycerols where the glycerol moiety is 1-O acylated.

External Descriptors

Not available

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