OC[C@H]1O[C@@H](OC2=CC=C(C=C2)C(=O)NC2=CC=C(C=C2)C2=CC(=O)OC2)[C@H](O)[C@@H](O)[C@@H]1O

InChIKey=LIOKFWILDPMTCZ-OXUVVOBNSA-N

C23H23NO9

457.435

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Benzanilides Hexoses O-glycosyl compounds Benzamides Benzoyl derivatives Phenoxy compounds Phenol ethers Butenolides Oxanes Enoate esters Secondary carboxylic acid amides Lactones Secondary alcohols Monocarboxylic acids and derivatives Polyols Acetals Oxacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Primary alcohols Organopnictogen compounds

Aromatic heteromonocyclic compounds

Benzanilide - Phenolic glycoside - Aromatic anilide - Hexose monosaccharide - O-glycosyl compound - Benzoic acid or derivatives - Benzamide - Phenoxy compound - Benzoyl - Phenol ether - 2-furanone - Benzenoid - Monosaccharide - Oxane - Monocyclic benzene moiety - Dihydrofuran - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Carboxamide group - Carboxylic acid ester - Secondary carboxylic acid amide - Lactone - Secondary alcohol - Organoheterocyclic compound - Carboxylic acid derivative - Acetal - Oxacycle - Monocarboxylic acid or derivatives - Polyol - Organic nitrogen compound - Alcohol - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Primary alcohol - Organonitrogen 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.

Not available