Structure Information
Structure

Compound Identification

SMILES

[H]\C(=C(\[H])C1=CC(OC)=C(O[C@@]2([H])O[C@@]([H])(C)[C@]([H])(O)[C@@]([H])(O)[C@@]2([H])O)C=C1)C(O)=NCCCCNC(=O)C1=CC=C(O)C=C1

InChIKey

InChIKey=IOMDNBQZRLSOTC-LBFIMLOHSA-N

Formula

C27H34N2O9

Mass

530.574

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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 - O-glycosyl compound - Benzoic acid or derivatives - Benzamide - Phenol ether - Styrene - Phenoxy compound - Benzoyl - Methoxybenzene - Anisole - Alkyl aryl ether - Phenol - 1-hydroxy-2-unsubstituted benzenoid - Oxane - Monosaccharide - Monocyclic benzene moiety - Benzenoid - Secondary alcohol - Secondary carboxylic acid amide - Carboxamide group - Acetal - Oxacycle - Organoheterocyclic compound - Carboximidic acid - Carboximidic acid derivative - Organic 1,3-dipolar compound - Carboxylic acid derivative - Polyol - Propargyl-type 1,3-dipolar organic compound - Ether - Organic oxide - Hydrocarbon derivative - Alcohol - Organic nitrogen compound - Organopnictogen compound - 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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