Structure Information
Structure

Compound Identification

SMILES

C[C@@H]1C2CC3=C(C=C(O[C@@H]4O[C@@H]([C@@H](O)[C@H](O)[C@H]4O)C(O)=O)C=C3)[C@@]1(C)CCN2CC=C(C)C

InChIKey

InChIKey=ULCOPPYWWFWQCJ-CZEZGIFXSA-N

Formula

C25H35NO7

Mass

461.555

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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

2,6-dimethyl-3-benzazocine - Fatty acyl glycoside - Fatty acyl glycoside of mono- or disaccharide - Phenolic glycoside - 1-o-glucuronide - O-glucuronide - Glucuronic acid or derivatives - 6,7-benzomorphan - Alkyl glycoside - Hexose monosaccharide - Benzazocine - O-glycosyl compound - Tetralin - Beta-hydroxy acid - Aralkylamine - Fatty acyl - Hydroxy acid - Monosaccharide - Oxane - Piperidine - Pyran - Benzenoid - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - Amino acid or derivatives - Amino acid - Azacycle - Organoheterocyclic compound - Polyol - Carboxylic acid derivative - Carboxylic acid - Oxacycle - Monocarboxylic acid or derivatives - Acetal - Amine - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Alcohol - Organonitrogen compound - Hydrocarbon derivative - Carbonyl group - 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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