Structure Information
Structure

Compound Identification

SMILES

CC(=O)CC1=CC(=O)C2=C(O1)C([C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1OC(=O)\C=C\C1=CC=C(O)C=C1)=C(O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C=C2C

InChIKey

InChIKey=DHSFJZHHJGPZGG-HCYJAHFRSA-N

Formula

C34H38O16

Mass

702.662

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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 heteropolycyclic compounds

Substituents

Phenolic glycoside - Coumaric acid ester - Cinnamic acid or derivatives - Coumaric acid or derivatives - Hydroxycinnamic acid or derivatives - Cinnamic acid ester - C-glycosyl compound - Chromone - O-glycosyl compound - 1-benzopyran - Benzopyran - Styrene - 1-hydroxy-2-unsubstituted benzenoid - Pyranone - Phenol - Fatty acid ester - Fatty acyl - Pyran - Benzenoid - Monocyclic benzene moiety - Oxane - Monosaccharide - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Heteroaromatic compound - Ketone - Carboxylic acid ester - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Polyol - Acetal - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Ether - Dialkyl ether - Primary alcohol - Aldehyde - Alcohol - Organic oxide - Hydrocarbon derivative - Carbonyl group - Aromatic heteropolycyclic 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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