Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@@H](OC2=CC=C(C=C2)C2=C(C(=O)C3=CC=C(OCCN4CCCCC4)C=C3)C3=C(S2)C=C(O)C=C3)[C@H](O)[C@@H](O)[C@@H]1O

InChIKey

InChIKey=SMCKNNQQQOVEFY-JPLCMXNCSA-N

Formula

C34H37NO9S

Mass

635.73

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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

Fatty acyl glycoside of mono- or disaccharide - Phenolic glycoside - Fatty acyl glycoside - Aryl-phenylketone - Hexose monosaccharide - 3-aroylthiophene - Alkyl glycoside - O-glycosyl compound - 1-benzothiophene - Benzothiophene - Phenol ether - Phenoxy compound - Thiophene carboxylic acid or derivatives - Aryl ketone - Benzoyl - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - Benzenoid - Oxane - Monosaccharide - Monocyclic benzene moiety - Fatty acyl - Piperidine - Thiophene - Heteroaromatic compound - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - Ketone - Acetal - Oxacycle - Ether - Azacycle - Organoheterocyclic compound - Polyol - Alcohol - Hydrocarbon derivative - Organic oxide - Aldehyde - Organic nitrogen compound - Organopnictogen compound - Primary alcohol - Amine - Organonitrogen compound - 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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