OC[C@H]1O[C@@H](O[C@H](C#N)C2=CC=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C=C2)[C@H](O)[C@@H](O)[C@@H]1O

InChIKey=RJPLGQRRNXUSQI-UUGBRMIUSA-N

C20H27NO12

473.431

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Cyanogenic glycosides O-glycosyl compounds Phenoxy compounds Phenol ethers Oxanes Monosaccharides Secondary alcohols Polyols Oxacyclic compounds Nitriles Acetals Primary alcohols Organopnictogen compounds Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

Cyanogenic glycoside - Phenolic glycoside - O-glycosyl compound - Phenoxy compound - Phenol ether - Monocyclic benzene moiety - Monosaccharide - Oxane - Benzenoid - Secondary alcohol - Polyol - Nitrile - Carbonitrile - Acetal - Organoheterocyclic compound - Oxacycle - Primary alcohol - Hydrocarbon derivative - Organonitrogen compound - Organopnictogen compound - Alcohol - Organic nitrogen compound - 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.

CHEBI:8525 : cyanogenic glycoside
KEGG (C08339) : Cyanogenic glucosides derived from thyrosine