Structure Information
Structure

Compound Identification

SMILES

CO[C@@H]1[C@@H](CNC(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)C)O[C@@H](OC2=CC=CC=C2)[C@H](O)[C@H]1OCC1=CC=CC=C1

InChIKey

InChIKey=WOVVMXFPMYFGGL-CWEZWLNASA-N

Formula

C30H42N2O8

Mass

558.672

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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 - Valine or derivatives - Alpha-amino acid amide - O-glycosyl compound - N-substituted-alpha-amino acid - Alpha-amino acid or derivatives - Benzylether - Phenoxy compound - Phenol ether - Fatty amide - Monosaccharide - N-acyl-amine - Monocyclic benzene moiety - Oxane - Fatty acyl - Benzenoid - Carbamic acid ester - Secondary alcohol - Secondary carboxylic acid amide - Carboxamide group - Dialkyl ether - Oxacycle - Carboxylic acid derivative - Ether - Acetal - Organoheterocyclic compound - Organic nitrogen compound - Carbonyl group - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Alcohol - 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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