CC(C)=CCC1=CC(=CC(CC=C(C)C)=C1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1OC1O[C@@H](CO)[C@H](O)[C@H]1O)C(=O)OCC1CCN2CCC[C@H]12

InChIKey=LLZLNFVFAZZRDM-NYGIAEFMSA-N

C36H53NO12

691.815

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

O-glycosyl compounds Disaccharides Benzoic acid esters Pyrrolizidines Phenoxy compounds Phenol ethers Benzoyl derivatives Oxanes N-alkylpyrrolidines Tetrahydrofurans Trialkylamines Secondary alcohols Carboxylic acid esters Amino acids and derivatives Oxacyclic compounds Monocarboxylic acids and derivatives Azacyclic compounds Acetals Primary alcohols Organopnictogen compounds Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Phenolic glycoside - O-glycosyl compound - Disaccharide - Benzoate ester - Benzoic acid or derivatives - Phenoxy compound - Pyrrolizidine - Phenol ether - Benzoyl - Benzenoid - N-alkylpyrrolidine - Oxane - Monocyclic benzene moiety - Tetrahydrofuran - Pyrrolidine - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - Carboxylic acid ester - Amino acid or derivatives - Oxacycle - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Acetal - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Organonitrogen compound - Amine - Alcohol - Aromatic heteropolycyclic 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