C[C@H]1O[C@H](OC2=CC(C)=C(C(=O)C3=CC=C(C=C3)C#N)C(C)=C2)[C@@H](O)[C@@H](O)[C@@H]1O

InChIKey=JNRLDFCFBLGLJB-FPECJGDJSA-N

C22H23NO6

397.427

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Fatty acyl glycosides of mono- and disaccharides Benzophenones Aryl-phenylketones Diphenylmethanes Alkyl glycosides Hexoses O-glycosyl compounds m-Xylenes Phenoxy compounds Phenol ethers Benzonitriles Benzoyl derivatives Oxanes Secondary alcohols Nitriles Oxacyclic compounds Acetals Polyols Organic oxides Organopnictogen compounds Aldehydes Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

Phenolic glycoside - Fatty acyl glycoside - Fatty acyl glycoside of mono- or disaccharide - Benzophenone - Aryl-phenylketone - Diphenylmethane - Alkyl glycoside - Hexose monosaccharide - O-glycosyl compound - Phenoxy compound - Benzonitrile - Benzoyl - M-xylene - Xylene - Aryl ketone - Phenol ether - Monocyclic benzene moiety - Fatty acyl - Monosaccharide - Benzenoid - Oxane - Ketone - Secondary alcohol - Nitrile - Carbonitrile - Polyol - Organoheterocyclic compound - Oxacycle - Acetal - Aldehyde - Organic oxide - Cyanide - Organopnictogen compound - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Alcohol - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Not available