Structure Information
Structure

Compound Identification

SMILES

COC(=O)c1ccc(O[C@@H]2O[C@H](CO)[C@H](O)[C@H](OCc3nnn[nH]3)[C@H]2O)cc1

InChIKey

InChIKey=WWFRFSBKJRWSEG-QPVMMRRFSA-N

Formula

C16H20N4O8

Mass

396.356

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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 - Phenol ether - Phenoxy compound - Benzoyl - Sugar acid - Monosaccharide - Benzenoid - Oxane - Monocyclic benzene moiety - Methyl ester - Tetrazole - Azole - Heteroaromatic compound - Carboxylic acid ester - Secondary alcohol - Acetal - Oxacycle - Carboxylic acid derivative - Azacycle - Dialkyl ether - Ether - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Alcohol - Primary alcohol - 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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