Structure Information
Structure

Compound Identification

SMILES

OCC1OC(Oc2ccc(C=CC(=O)OCC3OC(Oc4cc(cc(OC5OC(CO)C(O)C(O)C5O)c4O)C4=C(OC5OC(COC(=O)CC(O)=O)C(O)C(O)C5O)C=c5c(O)cc(O)cc5=[O]4)C(O)C(O)C3O)cc2)C(O)C(O)C1O

InChIKey

InChIKey=LUTDPMDCQWGUQF-UHFFFAOYSA-N

Formula

C51H59O32

Mass

1184.001

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Flavonoids

Subclass

Flavonoid glycosides

Intermediate Tree Nodes

Flavonoid O-glycosides

Direct Parent

Flavonoid 3p-O-p-coumaroyl glycosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Flavonoid 3p-o-6-p-coumaroyl-glycoside - 5-hydroxyflavonoid - 7-hydroxyflavonoid - Hydroxyflavonoid - Phenolic glycoside - Cinnamic acid or derivatives - Cinnamic acid ester - Glycosyl compound - O-glycosyl compound - Tricarboxylic acid or derivatives - Phenoxy compound - Phenol ether - Styrene - Fatty acid ester - 1-hydroxy-2-unsubstituted benzenoid - Phenol - 1-hydroxy-4-unsubstituted benzenoid - Monocyclic benzene moiety - Fatty acyl - Monosaccharide - Benzenoid - Oxane - 1,3-dicarbonyl compound - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Secondary alcohol - Carboxylic acid ester - Polyol - Carboxylic acid derivative - Acetal - Carboxylic acid - Oxacycle - Organoheterocyclic compound - Carbonyl group - Primary alcohol - Organic oxide - Organooxygen compound - Hydrocarbon derivative - Alcohol - Organic oxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as flavonoid 3p-o-p-coumaroyl glycosides. These are flavonoid 3p-O-glycosides where the carbohydrate moiety is esterified with a p-coumaric acid. P-coumaric acid is an organic derivative of cinnamic acid, that carries a hydroxyl group at the 4-position of the benzene ring.

External Descriptors

Not available

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