Structure Information
Structure

Compound Identification

SMILES

CC12CCC3C(CCC4=CC(OC5OC(C(O)C(O)C5O)C(O)=O)=CC=C34)C1COCC2O

InChIKey

InChIKey=BLSGLLHUDSNNBM-UHFFFAOYSA-N

Formula

C24H32O9

Mass

464.511

Export to:

JSON SDF CSV

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

Fatty acyl glycoside of mono- or disaccharide - Phenolic glycoside - Fatty acyl glycoside - Naphthopyran - 1-o-glucuronide - O-glucuronide - Phenanthrene - Glucuronic acid or derivatives - Alkyl glycoside - O-glycosyl compound - Tetralin - Naphthalene - Beta-hydroxy acid - Pyran - Hydroxy acid - Oxane - Monosaccharide - Benzenoid - Fatty acyl - Secondary alcohol - Polyol - Acetal - Organoheterocyclic compound - Oxacycle - Ether - Dialkyl ether - Carboxylic acid - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Carbonyl group - Hydrocarbon derivative - Organic oxide - Alcohol - 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

Previous Back Next