CC1=CC(O)=CC(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)=C1CC1=CC=C(\C=C\C(=O)NCCNS(N)(=O)=O)C=C1

InChIKey=HFRABILSAXBLAZ-IBKRAMOPSA-N

C25H33N3O10S

567.61

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Diphenylmethanes Cinnamic acid amides Hexoses O-glycosyl compounds Styrenes Phenoxy compounds Phenol ethers Meta cresols Toluenes 1-hydroxy-2-unsubstituted benzenoids Sulfuric acid diamides Oxanes Secondary carboxylic acid amides Secondary alcohols Acetals Polyols Oxacyclic compounds Organopnictogen compounds Carbonyl compounds Primary alcohols Hydrocarbon derivatives Organonitrogen compounds Organic oxides

Aromatic heteromonocyclic compounds

Phenolic glycoside - Diphenylmethane - Cinnamic acid amide - Cinnamic acid or derivatives - Hexose monosaccharide - O-glycosyl compound - Phenoxy compound - M-cresol - Phenol ether - Styrene - Toluene - Phenol - 1-hydroxy-2-unsubstituted benzenoid - Monocyclic benzene moiety - Benzenoid - Oxane - Monosaccharide - Sulfuric acid diamide - Organic sulfuric acid or derivatives - Secondary carboxylic acid amide - Secondary alcohol - Carboxamide group - Oxacycle - Organoheterocyclic compound - Polyol - Carboxylic acid derivative - Acetal - Carbonyl group - Organic nitrogen compound - Primary alcohol - Hydrocarbon derivative - Organopnictogen compound - Alcohol - Organonitrogen compound - Organic oxide - 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