CC(CO)C1=C(O)C(O[C@@H]2O[C@H](COS(O)(=O)=O)[C@@H](O)[C@H](O)[C@H]2O)=C2COC3=C2C1=CC(C)=C3

InChIKey=ABWBTCIXNWMTSG-BFTMEJOLSA-N

C21H26O12S

502.49

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

O-glycosyl compounds Naphthols and derivatives Monosaccharide sulfates Alkyl aryl ethers Sulfuric acid monoesters Oxanes Alkyl sulfates Secondary alcohols Polyols Oxacyclic compounds Acetals Primary alcohols Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Phenolic glycoside - 2-naphthol - O-glycosyl compound - Naphthalene - Monosaccharide sulfate - Alkyl aryl ether - Monosaccharide - Oxane - Sulfuric acid monoester - Sulfate-ester - Benzenoid - Alkyl sulfate - Sulfuric acid ester - Organic sulfuric acid or derivatives - Secondary alcohol - Polyol - Organoheterocyclic compound - Oxacycle - Ether - Acetal - Alcohol - Primary alcohol - Organic oxide - Hydrocarbon derivative - 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