CO[C@H]1[C@H](O)[C@@H](C)O[C@@H](OC2=C(OC)C=CC(=C2)[C@@]23OC4=CC(OC)=CC(OC)=C4[C@]2(O)[C@H](O)C[C@H]3C2=CC=CC=C2)[C@H]1OC(C)=O

InChIKey=QKVLYKATVKEUOR-NAQGKKNMSA-N

C35H40O12

652.693

Organic compounds

Phenylpropanoids and polyketides

Stilbenes

Stilbene glycosides

Not available

Stilbene glycosides

Flavaglines Phenolic glycosides Hexoses O-glycosyl compounds Coumarans Phenoxy compounds Anisoles Methoxybenzenes Alkyl aryl ethers Oxanes Tertiary alcohols Secondary alcohols Carboxylic acid esters Cyclic alcohols and derivatives Acetals Oxacyclic compounds Monocarboxylic acids and derivatives Dialkyl ethers Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aromatic heteropolycyclic compounds

Stilbene glycoside - Flavagline skeleton - Phenolic glycoside - Hexose monosaccharide - Glycosyl compound - O-glycosyl compound - Coumaran - Methoxybenzene - Phenoxy compound - Phenol ether - Anisole - Alkyl aryl ether - Monosaccharide - Monocyclic benzene moiety - Benzenoid - Oxane - Cyclic alcohol - Tertiary alcohol - Carboxylic acid ester - Secondary alcohol - Organoheterocyclic compound - Ether - Dialkyl ether - Oxacycle - Acetal - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Alcohol - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - 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