Structure Information
Structure

Compound Identification

SMILES

COC(=O)C1=CO[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]2[C@@](C)(O)[C@H](C[C@]12O)OC(=O)\C=C\C1=CC=C(OC)C=C1

InChIKey

InChIKey=DVQVHBAATHWQAS-OALRNCSFSA-N

Formula

C27H34O14

Mass

582.555

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Lipids and lipid-like molecules

Class

Prenol lipids

Subclass

Terpene glycosides

Intermediate Tree Nodes

Not available

Direct Parent

Iridoid O-glycosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Iridoid o-glycoside - Hexose monosaccharide - Cinnamic acid ester - Cinnamic acid or derivatives - O-glycosyl compound - Iridoid-skeleton - Glycosyl compound - Bicyclic monoterpenoid - Monoterpenoid - Aromatic monoterpenoid - Anisole - Phenol ether - Phenoxy compound - Styrene - Methoxybenzene - Fatty acid ester - Alkyl aryl ether - Fatty acyl - Benzenoid - Dicarboxylic acid or derivatives - Oxane - Monosaccharide - Monocyclic benzene moiety - Vinylogous ester - Cyclic alcohol - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Methyl ester - Tertiary alcohol - Carboxylic acid ester - Secondary alcohol - Ether - Acetal - Carboxylic acid derivative - Organoheterocyclic compound - Oxacycle - Polyol - Organic oxide - Organic oxygen compound - Alcohol - Carbonyl group - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as iridoid o-glycosides. These are iridoid monoterpenes containing a glycosyl (usually a pyranosyl) moiety linked to the iridoid skeleton.

External Descriptors

Not available

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