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Structure Information
Structure

Compound Identification

SMILES

COC1=C(OC)C=C(CC2COC(=O)[C@]2(O)CC2=CC(OC)=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C=C2)C=C1

InChIKey

InChIKey=LWYAMIUSVGPFKS-DYOMPVLHSA-N

Formula

C27H34O12

Mass

550.557

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Lignans, neolignans and related compounds

Class

Lignan glycosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Lignan glycosides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Lignan glycoside - Dibenzylbutyrolactone - Lignan lactone - Tetrahydrofuran lignan - 9,9p-epoxylignan - Furanoid lignan - Fatty acyl glycoside of mono- or disaccharide - Fatty acyl glycoside - Phenolic glycoside - Alkyl glycoside - O-glycosyl compound - Glycosyl compound - O-dimethoxybenzene - Dimethoxybenzene - Methoxybenzene - Phenol ether - Anisole - Phenoxy compound - Alkyl aryl ether - Fatty acyl - Oxane - Benzenoid - Monocyclic benzene moiety - Monosaccharide - Gamma butyrolactone - Oxolane - Tertiary alcohol - Lactone - Carboxylic acid ester - Secondary alcohol - Acetal - Oxacycle - Carboxylic acid derivative - Organoheterocyclic compound - Ether - Polyol - Monocarboxylic acid or derivatives - Carbonyl group - Organic oxygen compound - Organic oxide - Primary alcohol - Hydrocarbon derivative - Organooxygen compound - Alcohol - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as lignan glycosides. These are aromatic polycyclic compounds containing a carbohydrate component glycosidically linked to a lignan moiety. They include 1-aryltetralin lactones.

External Descriptors

Not available

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