Structure Information
Structure

Compound Identification

SMILES

CC(=O)OCC1OC(OC2=CC(O)=C(C(=O)CC3=CC=C(C=C3)[N+]([O-])=O)C(O)=C2)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O

InChIKey

InChIKey=RLYYLWXCEVBVRV-UHFFFAOYSA-N

Formula

C28H29NO15

Mass

619.532

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Stilbenes

Subclass

Stilbene glycosides

Intermediate Tree Nodes

Not available

Direct Parent

Stilbene glycosides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Stilbene glycoside - Phenolic glycoside - Tetracarboxylic acid or derivatives - Alkyl-phenylketone - O-glycosyl compound - Glycosyl compound - Nitrobenzene - Phenylketone - Phenoxy compound - Phenol ether - Resorcinol - Nitroaromatic compound - Aryl ketone - Aryl alkyl ketone - Benzoyl - Phenol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Oxane - Monosaccharide - Monocyclic benzene moiety - Benzenoid - Vinylogous acid - Ketone - Carboxylic acid ester - Organic nitro compound - C-nitro compound - Acetal - Organoheterocyclic compound - Organic 1,3-dipolar compound - Oxacycle - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organic zwitterion - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organopnictogen compound - Organic oxygen compound - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as stilbene glycosides. These are compounds structurally characterized by the presence of a carbohydrate moiety glycosidically linked to the stilbene skeleton.

External Descriptors

Not available

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