Structure Information
Structure

Compound Identification

SMILES

CC(=O)NC1=C(Cl)C=CC(CO[C@@H]2O[C@H](CSCCCC3=CC=CC=C3)[C@@H](O[C@H]3O[C@@H]4COC(O[C@H]4[C@H](O)[C@H]3O)C3=CC=CC=C3)[C@H](O)[C@H]2O)=C1

InChIKey

InChIKey=VHNQWEQNJMXZLJ-XUEJCKNZSA-N

Formula

C37H44ClNO11S

Mass

746.27

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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

Glycosyl compounds

Direct Parent

O-glycosyl compounds

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

O-haloacetanilide - Haloacetanilide - O-glycosyl compound - Disaccharide - Pyranodioxin - Acetanilide - N-acetylarylamine - Anilide - N-arylamide - Chlorobenzene - Halobenzene - Oxane - Aryl chloride - Benzenoid - Meta-dioxane - Monocyclic benzene moiety - Aryl halide - Acetamide - Carboxamide group - Secondary carboxylic acid amide - Secondary alcohol - Acetal - Oxacycle - Carboxylic acid derivative - Thioether - Sulfenyl compound - Dialkylthioether - Organoheterocyclic compound - Alcohol - Organohalogen compound - Organic nitrogen compound - Carbonyl group - Organochloride - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organosulfur compound - Organonitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.

External Descriptors

Not available

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