C[C@H]1[C@@H](O)[C@@H](O)[C@H](O)CN1CC1=CC=CC=C1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O

InChIKey=MVBRUDGWLYNOPB-HPFOEUPTSA-N

C19H29NO9

415.439

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

N-benzylpiperidines Hexoses O-glycosyl compounds Benzylamines Phenol ethers Phenoxy compounds Phenylmethylamines Aralkylamines Oxanes Secondary alcohols Trialkylamines 1,2-aminoalcohols Oxacyclic compounds Acetals Azacyclic compounds Polyols Organopnictogen compounds Primary alcohols Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

Phenolic glycoside - N-benzylpiperidine - Benzylpiperidine - Hexose monosaccharide - O-glycosyl compound - Benzylamine - Phenoxy compound - Phenol ether - Phenylmethylamine - Aralkylamine - Monocyclic benzene moiety - Monosaccharide - Oxane - Piperidine - Benzenoid - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - 1,2-aminoalcohol - Polyol - Organoheterocyclic compound - Azacycle - Oxacycle - Acetal - Amine - Organopnictogen compound - Organic nitrogen compound - Hydrocarbon derivative - Primary alcohol - 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