Structure Information
Structure

Compound Identification

SMILES

[H][C@](C)(O)[C@@]([H])(C)C(O)=N[C@@]1([H])C[C@@]([H])(OC2=C(O)C3=C(C(=O)C[C@]([H])(O3)C3=CC=CC=C3)C(CO)=C2)O[C@]([H])(C)[C@@]1([H])O

InChIKey

InChIKey=IHPAYRWYRVVKSK-WQYRALSXSA-N

Formula

C27H33NO9

Mass

515.559

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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-7-O-glycosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Flavonoid-7-o-glycoside - 8-hydroxyflavonoid - Hydroxyflavonoid - Flavanone - Flavan - Hexose monosaccharide - O-glycosyl compound - Glycosyl compound - Chromone - Benzopyran - Chromane - 1-benzopyran - Aryl ketone - Aryl alkyl ketone - Alkyl aryl ether - Monosaccharide - Benzenoid - Monocyclic benzene moiety - Oxane - Secondary alcohol - Ketone - Acetal - Carboximidic acid - Carboximidic acid derivative - Oxacycle - Ether - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic oxygen compound - Alcohol - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Aromatic alcohol - Primary alcohol - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as flavonoid-7-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position.

External Descriptors

Not available

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