Structure Information
Structure

Compound Identification

SMILES

[Na].CCCCCCCCCCCC(=O)NC1=CC=C(COCCOCCOCCO[C@@H]2O[C@H](CO)[C@@H](O[C@@H]3O[C@H](CO)[C@H](O)[C@H](OS(O)(=O)=O)[C@H]3O)[C@H](O[C@@H]3O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]3O)[C@H]2O)C=C1

InChIKey

InChIKey=VXDGFPBNEPZBGX-LODZOXLHSA-N

Formula

C43H73NNaO22S

Mass

1011.09

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organic oxygen compounds

Class

Organooxygen compounds

Subclass

Carbohydrates and carbohydrate conjugates

Intermediate Tree Nodes

Not available

Direct Parent

Oligosaccharides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Oligosaccharide - Glycosyl compound - O-glycosyl compound - Benzylether - Anilide - N-arylamide - Oxane - Sulfuric acid monoester - Sulfate-ester - Monocyclic benzene moiety - Fatty amide - Fatty acyl - Benzenoid - Sulfuric acid ester - Alkyl sulfate - Organic sulfuric acid or derivatives - Secondary carboxylic acid amide - Carboxamide group - Secondary alcohol - Acetal - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Organic alkali metal salt - Organoheterocyclic compound - Polyol - Organic nitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Carbonyl group - Organic oxide - Primary alcohol - Organonitrogen compound - Alcohol - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds.

External Descriptors

Not available

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