Structure Information
Structure

Compound Identification

SMILES

COC1=CC(O[C@@H]2O[C@H](CO[C@@H]3OC[C@](O)(COC(=O)C4=CC(O)=C(O)C(O)=C4)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O)=C(C=C1)C(C)=O

InChIKey

InChIKey=QNVPMKAFCVXMFH-NDDHQHNUSA-N

Formula

C27H32O16

Mass

612.537

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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 - Galloyl ester - Alkyl-phenylketone - Gallic acid or derivatives - O-glycosyl compound - P-hydroxybenzoic acid alkyl ester - M-hydroxybenzoic acid ester - P-hydroxybenzoic acid ester - Disaccharide - Benzoate ester - Pyrogallol derivative - Acetophenone - Benzenetriol - Phenylketone - Benzoic acid or derivatives - Aryl ketone - Phenoxy compound - Aryl alkyl ketone - Benzoyl - Methoxybenzene - Phenol ether - Anisole - 1-hydroxy-4-unsubstituted benzenoid - Alkyl aryl ether - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Oxane - Benzenoid - Monocyclic benzene moiety - Oxolane - Tertiary alcohol - Secondary alcohol - Ketone - Carboxylic acid ester - Polyol - Monocarboxylic acid or derivatives - Ether - Acetal - Carboxylic acid derivative - Organoheterocyclic compound - Oxacycle - Aldehyde - Organic oxide - Hydrocarbon derivative - Alcohol - 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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