Structure Information
Structure

Compound Identification

SMILES

[3H]C1=CC=CC=C1N1[C@@H]([C@@H](CC[C@H](O)C2=CC=C(F)C=C2)C1=O)C1=CC=C(O[C@@H]2O[C@@H]([C@@H](O)[C@H](O)[C@H]2O)C(O)=O)C([3H])=C1

InChIKey

InChIKey=QVUSMROKGZCDDR-SUSVGSBASA-N

Formula

C30H30FNO9

Mass

571.583

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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 - Fatty acyl glycoside - Fatty acyl glycoside of mono- or disaccharide - Monobactam - 1-o-glucuronide - O-glucuronide - Glucuronic acid or derivatives - Alkyl glycoside - Hexose monosaccharide - O-glycosyl compound - 1-phenylazetidine - 2-phenylazetidine - Phenoxy compound - Phenol ether - Beta-hydroxy acid - Halobenzene - Fluorobenzene - Benzenoid - Fatty acyl - Oxane - Monosaccharide - Hydroxy acid - Aryl fluoride - Monocyclic benzene moiety - Aryl halide - Pyran - Beta-lactam - Tertiary carboxylic acid amide - Azetidine - Carboxamide group - Secondary alcohol - Lactam - Monocarboxylic acid or derivatives - Acetal - Oxacycle - Azacycle - Carboxylic acid derivative - Carboxylic acid - Organoheterocyclic compound - Polyol - Carbonyl group - Organofluoride - Organohalogen compound - Alcohol - Organopnictogen compound - Organic oxide - Aromatic alcohol - Organic nitrogen compound - 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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