Structure Information
Structure

Compound Identification

SMILES

[H][C@@]1(OC[C@@]2([H])O[C@@]([H])(OC3=C(OC4=CC5=C(OCO5)C(OC)=C4C3=O)C3=CC=C(OC)C=C3)[C@]([H])(O)[C@@]([H])(O)[C@]2([H])O)OC[C@](O)(CO)[C@@]1([H])O

InChIKey

InChIKey=NYWHOVQPVOXJBL-NFVOTNMOSA-N

Formula

C29H32O16

Mass

636.559

Export to:

JSON SDF CSV

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-3-O-glycosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Flavonoid-3-o-glycoside - 4p-methoxyflavonoid-skeleton - 5-methoxyflavonoid-skeleton - Flavone - O-glycosyl compound - Glycosyl compound - Disaccharide - Chromone - 1-benzopyran - Benzopyran - Benzodioxole - Phenol ether - Phenoxy compound - Methoxybenzene - Anisole - Pyranone - Alkyl aryl ether - Monocyclic benzene moiety - Benzenoid - Oxane - Pyran - Heteroaromatic compound - Tertiary alcohol - Tetrahydrofuran - Vinylogous ester - Secondary alcohol - Polyol - Acetal - Oxacycle - Organoheterocyclic compound - Ether - Organooxygen compound - Organic oxygen compound - Alcohol - Primary alcohol - Hydrocarbon derivative - Organic oxide - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as flavonoid-3-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C3-position.

External Descriptors

Not available

Previous Back Next