Structure Information
Structure

Compound Identification

SMILES

COC1=C(OC2OC(COC(C)=O)C(OC(C)=O)C(OC(C)=O)C2OC(C)=O)C=CC(=C1)C(=O)N1CCOCC1

InChIKey

InChIKey=KAGLYCBCVFCTRB-UHFFFAOYSA-N

Formula

C26H33NO13

Mass

567.544

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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

Phenolic glycosides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Phenolic glycoside - Tetracarboxylic acid or derivatives - O-glycosyl compound - Benzamide - Morpholine-4-carboxylic acid or derivatives - Benzoic acid or derivatives - Phenoxy compound - Anisole - Benzoyl - Methoxybenzene - Phenol ether - Alkyl aryl ether - Monosaccharide - Monocyclic benzene moiety - Morpholine - Benzenoid - Oxazinane - Oxane - Tertiary carboxylic acid amide - Carboxylic acid ester - Carboxamide group - Acetal - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Dialkyl ether - Ether - Organopnictogen compound - Carbonyl group - Organic oxide - Organonitrogen compound - Hydrocarbon derivative - Organic nitrogen compound - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

External Descriptors

Not available

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