Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@H](OC2=C(C=C(CCCCOC3=NC(OCCCCC4=CC(=C(O[C@H]5O[C@H](CO)[C@@H](O)[C@@H](O)[C@@H]5O)C=C4)C4=CC(CC(O)=O)=CC=C4)=NC(OCCCCC4=CC(=C(O[C@H]5O[C@H](CO)[C@@H](O)[C@@H](O)[C@@H]5O)C=C4)C4=CC(CC(O)=O)=CC=C4)=N3)C=C2)C2=CC(CC(O)=O)=CC=C2)[C@@H](O)[C@H](O)[C@@H]1O

InChIKey

InChIKey=JZDIYCBIQYVXKY-KUSSPWHVSA-N

Formula

C75H87N3O27

Mass

1462.515

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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

Fatty acyl glycoside of mono- or disaccharide - Fatty acyl glycoside - Phenolic glycoside - Alkyl glycoside - Biphenyl - O-glycosyl compound - Tricarboxylic acid or derivatives - Alkoxy-s-triazine - Phenoxy compound - Phenol ether - Alkyl aryl ether - 1,3,5-triazine - Fatty acyl - Monosaccharide - Benzenoid - Triazine - Oxane - Monocyclic benzene moiety - Heteroaromatic compound - Secondary alcohol - Acetal - Carboxylic acid derivative - Carboxylic acid - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Polyol - Alcohol - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Organonitrogen compound - Carbonyl group - 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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