CC(=O)OC1C(OC2OC=C3C(=O)OCCC3(O)C2C=C)OC(COC#C)C(OC(=O)C2=CC=CC(OC3OC(CO)C(O)C(O)C3O)=C2O)C1OC(C)=O

InChIKey=XOBJGOIGYNBWJM-UHFFFAOYSA-N

C35H40O20

780.685

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Tetracarboxylic acids and derivatives o-Hydroxybenzoic acid esters O-glycosyl compounds Salicylic acid and derivatives Benzoyl derivatives Phenol ethers Phenoxy compounds 1-hydroxy-4-unsubstituted benzenoids Delta valerolactones Sugar acids and derivatives Oxanes Monosaccharides Vinylogous esters Tertiary alcohols Vinylogous acids Enoate esters Secondary alcohols Oxacyclic compounds Acetals Polyols Organic oxides Hydrocarbon derivatives Carbonyl compounds Primary alcohols

Aromatic heteropolycyclic compounds

Phenolic glycoside - Tetracarboxylic acid or derivatives - O-glycosyl compound - O-hydroxybenzoic acid ester - Salicylic acid or derivatives - Benzoate ester - Benzoic acid or derivatives - Benzoyl - Phenoxy compound - Phenol ether - Phenol - Delta_valerolactone - 1-hydroxy-4-unsubstituted benzenoid - Delta valerolactone - Sugar acid - Oxane - Benzenoid - Monosaccharide - Monocyclic benzene moiety - Vinylogous acid - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Vinylogous ester - Tertiary alcohol - Carboxylic acid ester - Secondary alcohol - Lactone - Acetal - Carboxylic acid derivative - Organoheterocyclic compound - Oxacycle - Polyol - Alcohol - Carbonyl group - Hydrocarbon derivative - Organic oxide - Primary alcohol - Aromatic heteropolycyclic compound

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.

Not available