Structure Information
Structure

Compound Identification

SMILES

OC1C(O)C(OC2=CC=C(C=C2)[N+]([O-])=O)OC(C1O)C(O)=O

InChIKey

InChIKey=QSUILVWOWLUOEU-UHFFFAOYSA-N

Formula

C12H13NO9

Mass

315.234

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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-glucuronide - 1-o-glucuronide - Glucuronic acid or derivatives - O-glycosyl compound - Nitrobenzene - Phenol ether - Phenoxy compound - Nitroaromatic compound - Beta-hydroxy acid - Monocyclic benzene moiety - Pyran - Oxane - Monosaccharide - Hydroxy acid - Benzenoid - Secondary alcohol - Organic nitro compound - C-nitro compound - Acetal - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Oxacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Polyol - Organopnictogen compound - Carbonyl group - Organic salt - Alcohol - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Organic nitrogen compound - Organic cation - 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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