OC(C1CC2CCN1CC2C=C)C1=CC=NC2=CC=CC=C12.OC1C(O)C(OC2=CC=C(C=C2)C2(OC(=O)C3=CC=CC=C23)C2=CC=C(O)C=C2)OC(C1O)C(O)=O

InChIKey=OHZNPMBIHVHDDD-UHFFFAOYSA-N

C45H44N2O11

788.85

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

O-glucuronides O-glycosyl compounds Phthalides Benzofuranones Phenoxy compounds Phenol ethers Beta hydroxy acids and derivatives 1-hydroxy-2-unsubstituted benzenoids Pyrans Oxanes Monosaccharides Dicarboxylic acids and derivatives Secondary alcohols Lactones Carboxylic acid esters Polyols Oxacyclic compounds Carboxylic acids Acetals Organic oxides Hydrocarbon derivatives Carbonyl compounds

Not available

Phenolic glycoside - O-glucuronide - 1-o-glucuronide - Glucuronic acid or derivatives - O-glycosyl compound - Isobenzofuranone - Phthalide - Benzofuranone - Isocoumaran - Phenoxy compound - Phenol ether - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Beta-hydroxy acid - Benzenoid - Pyran - Oxane - Monosaccharide - Hydroxy acid - Dicarboxylic acid or derivatives - Monocyclic benzene moiety - Secondary alcohol - Lactone - Carboxylic acid ester - Oxacycle - Organoheterocyclic compound - Polyol - Carboxylic acid - Carboxylic acid derivative - Acetal - Organic oxide - Hydrocarbon derivative - Carbonyl group - 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