Structure Information
Structure

Compound Identification

SMILES

COC1=C(OC)C=C(\C=C\C(=O)OCC2=CC[C@@H]3[C@H]2[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)OC=C3C(O)=O)C=C1

InChIKey

InChIKey=DCVLQGZRIUJCDA-OVKUTGNMSA-N

Formula

C27H32O13

Mass

564.54

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