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

InChIKey=UPCRMPLOWXXPFK-BNVRZUOOSA-N

C21H22O9

418.398

Organic compounds

Phenylpropanoids and polyketides

Stilbenes

Stilbene glycosides

Not available

Stilbene glycosides

Phenolic glycosides Hexoses O-glycosyl compounds Salicylic acids Benzoic acids Styrenes Phenoxy compounds Phenol ethers Benzoyl derivatives Sugar acids and derivatives 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Oxanes Vinylogous acids Secondary alcohols Polyols Acetals Oxacyclic compounds Monocarboxylic acids and derivatives Carboxylic acids Primary alcohols Organic oxides Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

Stilbene glycoside - Phenolic glycoside - Hexose monosaccharide - O-glycosyl compound - Glycosyl compound - Salicylic acid or derivatives - Salicylic acid - Hydroxybenzoic acid - Benzoic acid - Benzoic acid or derivatives - Styrene - Phenol ether - Phenoxy compound - Benzoyl - 1-hydroxy-2-unsubstituted benzenoid - Sugar acid - 1-hydroxy-4-unsubstituted benzenoid - Phenol - Monocyclic benzene moiety - Benzenoid - Oxane - Monosaccharide - Vinylogous acid - Secondary alcohol - Polyol - Monocarboxylic acid or derivatives - Acetal - Organoheterocyclic compound - Carboxylic acid - Carboxylic acid derivative - Oxacycle - Primary alcohol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Alcohol - Organooxygen compound - 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