[Na+].OC[C@H]1O[C@@H](OC2=CC=C(NC(=O)C=C)C=C2)[C@H](O)[C@@H](OS([O-])(=O)=O)[C@H]1O

InChIKey=ZOLIFOSXCCNLMQ-UMJUXCNXSA-M

C15H18NNaO10S

427.36

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Hexoses O-glycosyl compounds Anilides N-arylamides Phenol ethers Phenoxy compounds Oxanes Sulfuric acid monoesters Alkyl sulfates Acrylic acids and derivatives Secondary alcohols Secondary carboxylic acid amides Oxacyclic compounds Acetals Organopnictogen compounds Organic sodium salts Organic oxides Hydrocarbon derivatives Carbonyl compounds Primary alcohols Organic cations

Aromatic heteromonocyclic compounds

Phenolic glycoside - Hexose monosaccharide - O-glycosyl compound - Anilide - Phenoxy compound - Phenol ether - N-arylamide - Monocyclic benzene moiety - Monosaccharide - Oxane - Sulfuric acid monoester - Sulfate-ester - Benzenoid - Sulfuric acid ester - Alkyl sulfate - Acrylic acid or derivatives - Organic sulfuric acid or derivatives - Carboxamide group - Secondary alcohol - Secondary carboxylic acid amide - Organoheterocyclic compound - Carboxylic acid derivative - Oxacycle - Organic alkali metal salt - Acetal - Organic salt - Organopnictogen compound - Organonitrogen compound - Organic sodium salt - Primary alcohol - Hydrocarbon derivative - Organic nitrogen compound - Alcohol - Organic oxide - Carbonyl group - Organic cation - 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