Structure Information
Structure

Compound Identification

SMILES

CC1=CC=CC(C)=C1NC(=O)CN1CCN(CC(O)COC2=CC=CC=C2OC2OC(C(O)C(O)C2O)C(O)=O)CC1

InChIKey

InChIKey=YLNYEZQRRIKMQF-UHFFFAOYSA-N

Formula

C29H39N3O10

Mass

589.642

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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 - O-glucuronide - 1-o-glucuronide - Glucuronic acid or derivatives - Hexose monosaccharide - Alpha-amino acid amide - O-glycosyl compound - N-piperazineacetamide - Alpha-amino acid or derivatives - Anilide - Phenol ether - M-xylene - N-arylamide - Phenoxy compound - Xylene - Beta-hydroxy acid - Alkyl aryl ether - N-alkylpiperazine - Hydroxy acid - Monosaccharide - Monocyclic benzene moiety - Benzenoid - 1,4-diazinane - Oxane - Piperazine - Pyran - Amino acid or derivatives - Amino acid - Tertiary amine - 1,2-aminoalcohol - Carboxamide group - Tertiary aliphatic amine - Secondary alcohol - Secondary carboxylic acid amide - Acetal - Oxacycle - Azacycle - Organoheterocyclic compound - Polyol - Carboxylic acid derivative - Carboxylic acid - Ether - Monocarboxylic acid or derivatives - Alcohol - Organopnictogen compound - Carbonyl group - Organic oxide - Hydrocarbon derivative - Amine - Organonitrogen compound - Organic nitrogen 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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