OC[C@H]1O[C@@H](OC2=CC(\C=C\C3=CC=C(OS([O-])(=O)=O)C=C3)=CC(O)=C2)[C@H](O)[C@@H](O)[C@@H]1O

InChIKey=OPXYKICHKIQGOV-CUYWLFDKSA-M

C20H21O11S

469.44

Organic compounds

Phenylpropanoids and polyketides

Stilbenes

Stilbene glycosides

Not available

Stilbene glycosides

Phenolic glycosides Hexoses O-glycosyl compounds Phenylsulfates Styrenes Phenoxy compounds Phenol ethers 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Sulfuric acid monoesters Oxanes Secondary alcohols Polyols Acetals Oxacyclic compounds Organic oxides Hydrocarbon derivatives Primary alcohols Organic anions

Aromatic heteromonocyclic compounds

Stilbene glycoside - Phenolic glycoside - Hexose monosaccharide - Phenylsulfate - O-glycosyl compound - Glycosyl compound - Arylsulfate - Styrene - Phenoxy compound - Phenol ether - 1-hydroxy-2-unsubstituted benzenoid - 1-hydroxy-4-unsubstituted benzenoid - Phenol - Monosaccharide - Benzenoid - Oxane - Sulfuric acid ester - Sulfate-ester - Sulfuric acid monoester - Monocyclic benzene moiety - Organic sulfuric acid or derivatives - Secondary alcohol - Acetal - Organoheterocyclic compound - Oxacycle - Polyol - Primary alcohol - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Alcohol - Organic anion - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as stilbene glycosides. These are compounds structurally characterized by the presence of a carbohydrate moiety glycosidically linked to the stilbene skeleton.

Not available