Structure Information
Structure

Compound Identification

SMILES

O[C@@H]1[C@H](O)[C@@H](OC(=O)C2=CC=CC=C2)[C@@H](OC2=CC=C(C=C2)[N+]([O-])=O)O[C@@H]1COC(=O)C1=CC=CC=C1

InChIKey

InChIKey=CTPGKZRJMUOBTP-AALNHBIMSA-N

Formula

C26H23NO10

Mass

509.467

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organic oxygen compounds

Class

Organooxygen compounds

Subclass

Carbohydrates and carbohydrate conjugates

Intermediate Tree Nodes

Glycosyl compounds

Direct Parent

Phenolic glycosides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Phenolic glycoside - O-glycosyl compound - Benzoate ester - Benzoic acid or derivatives - Nitrobenzene - Phenoxy compound - Nitroaromatic compound - Benzoyl - Phenol ether - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Monosaccharide - Oxane - Benzenoid - 1,2-diol - Carboxylic acid ester - Organic nitro compound - C-nitro compound - Secondary alcohol - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Carboxylic acid derivative - Acetal - Oxacycle - Organoheterocyclic compound - Organic oxoazanium - Organic zwitterion - Organic nitrogen compound - Organopnictogen compound - Alcohol - Organic oxide - Organic salt - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

External Descriptors

Not available

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