Structure Information
Structure

Compound Identification

SMILES

OCC1OC(Oc2cc(cc(OC3OC(COC(=O)C=Cc4ccc(OC5OC(COC(O)=CC=C6C=CC(=O)C=C6)C(O)C(O)C5O)cc4)C(O)C(O)C3O)c2O)C2=C(OC3OC(COC(=O)CC(O)=O)C(O)C(O)C3O)C=c3c(O)cc(O)cc3=[O]2)C(O)C(O)C1O

InChIKey

InChIKey=YONFWCZNHUJYDU-UHFFFAOYSA-N

Formula

C60H65O34

Mass

1330.146

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