OC[C@H]1OC([C@H](O)[C@@H](O)[C@@H]1O)C1=C(O)C=C(C=C1O)[C@@H]1[C@H](\C(=C/C2=CC=C(O)C=C2)C2=CC(O)=C(C3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C(O)=C12)C1=CC=C(O)C=C1

InChIKey=HYDHYXXMXHPISD-HABDSXGTSA-N

C40H42O16

778.76

Organic compounds

Phenylpropanoids and polyketides

Stilbenes

Stilbene glycosides

Not available

Stilbene glycosides

Lignan glycosides Phenolic glycosides C-glycosyl compounds Indanes Resorcinols 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Oxanes Monosaccharides Benzene and substituted derivatives 1,2-diols Secondary alcohols Oxacyclic compounds Dialkyl ethers Primary alcohols Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Lignan glycoside - Stilbene glycoside - Neolignan skeleton - Phenolic glycoside - C-glycosyl compound - Glycosyl compound - Indane - Resorcinol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Benzenoid - Oxane - Monosaccharide - Monocyclic benzene moiety - Secondary alcohol - 1,2-diol - Polyol - Organoheterocyclic compound - Oxacycle - Dialkyl ether - Ether - Primary alcohol - Alcohol - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - 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