OC[C@H]1O[C@@H](OC2=CC(=CC(O)=C2)[C@H]2[C@@H]([C@@H]3[C@@H]4C5=C(C=C(O)C=C5)[C@H]([C@@H](C5=CC(O)=CC(O)=C45)C4=C(O)C=C(O)C2=C34)C2=CC=C(O)C=C2)C2=CC=C(O)C=C2)[C@H](O)[C@@H](O)[C@@H]1O

InChIKey=VJNCSOQWERNPTK-STZBKUPESA-N

C48H42O14

842.85

Organic compounds

Phenylpropanoids and polyketides

Stilbenes

Stilbene glycosides

Not available

Stilbene glycosides

Lignan glycosides Linear diarylheptanoids Dibenzocycloheptenes Phenolic glycosides Hexoses O-glycosyl compounds Indanes Phenol ethers Phenoxy compounds 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Oxanes Secondary alcohols Oxacyclic compounds Polyols Acetals Primary alcohols Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Lignan glycoside - Stilbene glycoside - Linear 1,7-diphenylheptane skeleton - Neolignan skeleton - Dibenzocycloheptene - Phenolic glycoside - Hexose monosaccharide - Glycosyl compound - O-glycosyl compound - Indane - Phenoxy compound - Phenol ether - Phenol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Monocyclic benzene moiety - Oxane - Benzenoid - Monosaccharide - Secondary alcohol - Polyol - Acetal - Organoheterocyclic compound - Oxacycle - Organooxygen compound - Primary alcohol - Organic oxygen compound - Hydrocarbon derivative - Alcohol - Aromatic heteropolycyclic 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