OC[C@H]1O[C@@H](OC2=C(O)C=CC=C2COC(=O)[C@@]2(O)C=CCCC2=O)[C@H](OC(=O)C2=CC=CC=C2)[C@@H](O)[C@@H]1O

InChIKey=KAXLSURJPZQJPA-KPAQMPDBSA-N

C27H28O12

544.509

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Hexoses O-glycosyl compounds Benzyloxycarbonyls Benzoic acid esters Phenoxy compounds Phenol ethers Benzoyl derivatives Cyclohexenones 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Oxanes Dicarboxylic acids and derivatives Acyloins Tertiary alcohols Secondary alcohols Carboxylic acid esters Oxacyclic compounds Acetals Primary alcohols Organic oxides Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

Phenolic glycoside - Hexose monosaccharide - O-glycosyl compound - Benzyloxycarbonyl - Benzoate ester - Benzoic acid or derivatives - Phenoxy compound - Phenol ether - Benzoyl - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Cyclohexenone - Phenol - Benzenoid - Oxane - Monosaccharide - Dicarboxylic acid or derivatives - Monocyclic benzene moiety - Acyloin - Tertiary alcohol - Cyclic ketone - Secondary alcohol - Ketone - Carboxylic acid ester - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Acetal - Organic oxide - Hydrocarbon derivative - Primary alcohol - Carbonyl group - Alcohol - Aromatic heteromonocyclic 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