COC(=O)C1OC(OC2=C(OC)C(OC)=C3C(CCC(NC(C)=O)C4=CC(=O)C(SC)=CC=C34)=C2)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O

InChIKey=IRRYQXHQELBFIE-UHFFFAOYSA-N

C34H39NO14S

717.74

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

O-glucuronides Tetracarboxylic acids and derivatives O-glycosyl compounds Tropones Anisoles Alkyl aryl ethers Alkylarylthioethers Pyrans Oxanes Monosaccharides Acetamides Methyl esters Secondary carboxylic acid amides Cyclic ketones Sulfenyl compounds Oxacyclic compounds Acetals Organopnictogen compounds Organonitrogen compounds Organic oxides

Aromatic heteropolycyclic compounds

Phenolic glycoside - O-glucuronide - 1-o-glucuronide - Glucuronic acid or derivatives - Tetracarboxylic acid or derivatives - O-glycosyl compound - Tropone - Anisole - Aryl thioether - Alkyl aryl ether - Alkylarylthioether - Monosaccharide - Pyran - Benzenoid - Oxane - Acetamide - Methyl ester - Carboxamide group - Carboxylic acid ester - Cyclic ketone - Secondary carboxylic acid amide - Organoheterocyclic compound - Oxacycle - Ether - Carboxylic acid derivative - Acetal - Sulfenyl compound - Thioether - Organonitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Carbonyl group - Organosulfur compound - 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