Structure Information
Structure

Compound Identification

SMILES

COC1=C(O)C(C)=C(CCCCCCCCCCO)C(O[C@H]2O[C@@H]([C@@H](O)[C@H](O)[C@H]2O)C(O)=O)=C1OC

InChIKey

InChIKey=BIJMDRJUMJQGSB-BOLZJEHGSA-N

Formula

C25H40O11

Mass

516.584

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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

Fatty acyl glycoside of mono- or disaccharide - Phenolic glycoside - Fatty acyl glycoside - 1-o-glucuronide - O-glucuronide - Glucuronic acid or derivatives - Alkyl glycoside - O-glycosyl compound - Methoxyphenol - O-dimethoxybenzene - Dimethoxybenzene - Fatty alcohol - 4-alkoxyphenol - Anisole - Methoxybenzene - O-cresol - Phenol ether - Phenoxy compound - Alkyl aryl ether - Phenol - Toluene - Beta-hydroxy acid - Benzenoid - Oxane - Monocyclic benzene moiety - Fatty acyl - Hydroxy acid - Monosaccharide - Pyran - Secondary alcohol - Acetal - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Carboxylic acid - Ether - Monocarboxylic acid or derivatives - Polyol - Carbonyl group - Hydrocarbon derivative - Alcohol - 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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