Structure Information
Structure

Compound Identification

SMILES

COC(=O)C1=CO[C@@H](O[C@@H]2O[C@H](COC(=O)\C=C\C3=CC(OC)=C(O)C(OC)=C3)[C@@H](O)[C@H](O)[C@H]2O)[C@H]2[C@@H]1CC=C2CO

InChIKey

InChIKey=YOFHAHMLGOFXAB-OBCDOPQVSA-N

Formula

C28H34O14

Mass

594.566

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