Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](SC3=CC=C(NC(=O)CCC(=O)NC4=CC=C(S[C@@H]5O[C@H](CO)[C@@H](O[C@@H]6O[C@H](CO)[C@@H](O)[C@H](O)[C@H]6O)[C@H](O)[C@H]5O)C=C4)C=C3)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O

InChIKey

InChIKey=SEXQJLFHXGOQOY-AKLOTGDBSA-N

Formula

C40H56N2O22S2

Mass

981.0

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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

Thioglycosides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Disaccharide - O-glycosyl compound - S-glycosyl compound - Anilide - Aryl thioether - N-arylamide - Monocyclic benzene moiety - Fatty amide - Fatty acyl - Benzenoid - Oxane - Monothioacetal - Carboxamide group - Secondary carboxylic acid amide - Secondary alcohol - Acetal - Carboxylic acid derivative - Oxacycle - Organoheterocyclic compound - Sulfenyl compound - Polyol - Hydrocarbon derivative - Organic oxide - Alcohol - Organic nitrogen compound - Organonitrogen compound - Organosulfur compound - Carbonyl group - Organopnictogen compound - Primary alcohol - Aromatic heteromonocyclic compound

Description

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

External Descriptors

Not available

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