Structure Information
Structure

Compound Identification

SMILES

CCC1OC[C@H]2O[C@H](O[C@H]3[C@H](O)[C@@H](O)[C@H](OCC4=CC(NC(C)=O)=C(Cl)C=C4)O[C@@H]3COC(=O)C3=CC=CC=C3)[C@H](O)[C@@H](O)[C@@H]2O1

InChIKey

InChIKey=WUTRKIMIMYHQSW-AMBBSUBFSA-N

Formula

C31H38ClNO13

Mass

668.09

Export to:

JSON SDF CSV

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-glycosyl compound - O-haloacetanilide - Haloacetanilide - Disaccharide - Acetanilide - Pyranodioxin - Benzoate ester - N-acetylarylamine - Benzoic acid or derivatives - Anilide - N-arylamide - Benzoyl - Chlorobenzene - Halobenzene - Aryl halide - Benzenoid - Aryl chloride - Oxane - Meta-dioxane - Monocyclic benzene moiety - Acetamide - Secondary carboxylic acid amide - Carboxamide group - Carboxylic acid ester - Secondary alcohol - Acetal - Oxacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Alcohol - Organic nitrogen compound - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Carbonyl group - Organochloride - 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

Previous Back Next