OC[C@H]1O[C@@H](OC2=CC3=C(C=C2)N=C(S3)C2=N[C@H](CS2)C(O)=O)[C@H](O)[C@@H](O)[C@H]1O

InChIKey=OUKXHVUTHGDBNY-VEAFCXQSSA-N

C17H18N2O8S2

442.46

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Hexoses O-glycosyl compounds Alpha amino acids and derivatives Benzothiazoles Oxanes Imidothiolactones Benzenoids Thiazolines Thiazoles Heteroaromatic compounds Secondary alcohols Propargyl-type 1,3-dipolar organic compounds Polyols Oxacyclic compounds Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Acetals Primary alcohols Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aromatic heteropolycyclic compounds

Phenolic glycoside - Hexose monosaccharide - O-glycosyl compound - Alpha-amino acid or derivatives - 1,3-benzothiazole - Imidothiolactone - Benzenoid - Oxane - Monosaccharide - Heteroaromatic compound - Meta-thiazoline - Thiazole - Azole - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Polyol - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Acetal - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Organonitrogen compound - 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