OCCOCCOCCOCCOCCOCCCCCCCCCCCSSCCCCCCCCCCCOCCOCCOCCOCCOCCOCCNC(=O)CCC1=CC=C(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C=C1

InChIKey=GNUAWJQQPTWVRE-KAHVGNKNSA-N

C59H109NO19S2

1200.63

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Hexoses O-glycosyl compounds Polyethylene glycols Phenoxy compounds Phenol ethers Fatty amides Oxanes Dialkyldisulfides Secondary carboxylic acid amides Secondary alcohols Acetals Sulfenyl compounds Polyols Oxacyclic compounds Hydrocarbon derivatives Carbonyl compounds Primary alcohols Organic oxides Organonitrogen compounds Organopnictogen compounds

Aromatic heteromonocyclic compounds

Phenolic glycoside - Hexose monosaccharide - O-glycosyl compound - Polyethylene glycol - Phenol ether - Phenoxy compound - Monocyclic benzene moiety - Oxane - Benzenoid - Fatty amide - Fatty acyl - Monosaccharide - Secondary alcohol - Secondary carboxylic acid amide - Organic disulfide - Dialkyldisulfide - Carboxamide group - Acetal - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Organoheterocyclic compound - Sulfenyl compound - Polyol - Organic oxide - Organic nitrogen compound - Hydrocarbon derivative - Carbonyl group - Organopnictogen compound - Alcohol - Organonitrogen compound - Organosulfur compound - Primary 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