Structure Information
Structure

Compound Identification

SMILES

COC(=O)C1=COC(OC2OC(CO)C(O)C(O)C2O)C2C1C=CC21OC(=O)C(=C1)C(C)OC(=O)C=CC1=CC=C(OC2OC(CO)C(O)C(O)C2O)C=C1

InChIKey

InChIKey=AFYIWKNGSIYXCQ-UHFFFAOYSA-N

Formula

C36H42O19

Mass

778.713

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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 - Terpene lactone - Phenolic glycoside - Cinnamic acid or derivatives - Cinnamic acid ester - Glycosyl compound - Iridoid-skeleton - O-glycosyl compound - Aromatic monoterpenoid - Bicyclic monoterpenoid - Monoterpenoid - Tricarboxylic acid or derivatives - Phenoxy compound - Phenol ether - Styrene - Fatty acid ester - Benzenoid - 2-furanone - Monocyclic benzene moiety - Monosaccharide - Fatty acyl - Oxane - Vinylogous ester - Dihydrofuran - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Methyl ester - Lactone - Secondary alcohol - Carboxylic acid ester - Oxacycle - Polyol - Organoheterocyclic compound - Acetal - Carboxylic acid derivative - Primary alcohol - Carbonyl group - Organic oxide - Organic oxygen compound - 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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