Structure Information
Structure

Compound Identification

SMILES

COC(=O)c1ccc(O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)c(c1)[N+]([O-])=O

InChIKey

InChIKey=AORKARPAMNXVNO-OIRVYTLQSA-N

Formula

C14H17NO10

Mass

359.287

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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 - Hexose monosaccharide - Nitrobenzoate - O-glycosyl compound - Benzoate ester - Benzoic acid or derivatives - Nitrobenzene - Phenol ether - Phenoxy compound - Nitroaromatic compound - Benzoyl - Sugar acid - Monocyclic benzene moiety - Oxane - Monosaccharide - Benzenoid - Methyl ester - Organic nitro compound - Carboxylic acid ester - Secondary alcohol - C-nitro compound - Acetal - Carboxylic acid derivative - Oxacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Polyol - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Alcohol - Organic zwitterion - Primary alcohol - Organonitrogen compound - Organic nitrogen 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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