Structure Information
Structure

Compound Identification

SMILES

OCC1OC(OC2=CC=CC=C2COC(=O)C2(O)C=CCCC2=O)C(OC(=O)C2=CC=CC=C2)C(O)C1O

InChIKey

InChIKey=RCKCYCDBDYUIGM-UHFFFAOYSA-N

Formula

C27H28O11

Mass

528.51

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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 - Hexose monosaccharide - O-glycosyl compound - Benzoate ester - Benzyloxycarbonyl - Benzoic acid or derivatives - Phenoxy compound - Benzoyl - Phenol ether - Cyclohexenone - Acyloin - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Benzenoid - Monosaccharide - Oxane - Tertiary alcohol - Ketone - Carboxylic acid ester - Cyclic ketone - Secondary alcohol - Carboxylic acid derivative - Organoheterocyclic compound - Oxacycle - Acetal - Alcohol - Carbonyl group - Hydrocarbon derivative - Organic oxide - Primary 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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