Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCC(=O)NC1=CC2=C(C=C1)C1(OC2=O)C2=C(OC3=C1C=CC(O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O)=C3)C=C(O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O)C=C2

InChIKey

InChIKey=LIPJNTJKVBTSSW-CFACPRDNSA-N

Formula

C42H51NO16

Mass

825.861

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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 - Fatty acyl glycoside - Phenolic glycoside - Xanthene - Dibenzopyran - Alkyl glycoside - Hexose monosaccharide - O-glycosyl compound - Diaryl ether - Phthalide - Benzofuranone - Benzopyran - Isobenzofuranone - 1-benzopyran - Isocoumaran - Isobenzofuran - N-arylamide - Fatty acyl - Fatty amide - Benzenoid - Monosaccharide - Oxane - Secondary carboxylic acid amide - Lactone - Secondary alcohol - Carboxamide group - Carboxylic acid ester - Polyol - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Acetal - Ether - Oxacycle - Carboxylic acid derivative - Primary alcohol - Hydrocarbon derivative - Alcohol - Carbonyl group - Organic oxide - Organonitrogen compound - Organopnictogen compound - Organic nitrogen 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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