Structure Information
Structure

Compound Identification

SMILES

C\C(=C/C1=C(F)C=C(O[C@@H]2O[C@@H]([C@@H](O)[C@@H]2O)C(\CO)=C\COC2=C(Cl)C=C(Cl)C=C2)C=C1)C(=O)NC1=C(O)C=C2OCOC2=C1O

InChIKey

InChIKey=RDXNDOHNSRXRKC-LUMCDFKHSA-N

Formula

C31H28Cl2FNO11

Mass

680.46

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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 heteropolycyclic compounds

Substituents

Phenolic glycoside - Cinnamic acid or derivatives - Cinnamic acid amide - O-glycosyl compound - Pentose monosaccharide - Benzodioxole - 1,3-dichlorobenzene - Phenoxy compound - Phenol ether - N-arylamide - Fluorobenzene - Chlorobenzene - 1-hydroxy-2-unsubstituted benzenoid - 1-hydroxy-4-unsubstituted benzenoid - Halobenzene - Alkyl aryl ether - Benzenoid - Monosaccharide - Aryl chloride - Monocyclic benzene moiety - Aryl halide - Aryl fluoride - Oxolane - Carboxamide group - Secondary carboxylic acid amide - Secondary alcohol - Ether - Oxacycle - Organoheterocyclic compound - Acetal - Carboxylic acid derivative - Organohalogen compound - Alcohol - Organic nitrogen compound - Carbonyl group - Primary alcohol - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organofluoride - Organochloride - Aromatic heteropolycyclic 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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