CC(=O)OCC1OC(OC2=CC(O)=C(C=C2)C(=O)CC2=CSC=N2)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O

InChIKey=WAEKSZJQJUDRCQ-UHFFFAOYSA-N

C25H27NO12S

565.55

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Tetracarboxylic acids and derivatives Alkyl-phenylketones O-glycosyl compounds Phenoxy compounds Phenol ethers Aryl alkyl ketones Benzoyl derivatives 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Oxanes Monosaccharides Thiazoles Heteroaromatic compounds Vinylogous acids Carboxylic acid esters Azacyclic compounds Oxacyclic compounds Acetals Hydrocarbon derivatives Organopnictogen compounds Organonitrogen compounds Organic oxides

Aromatic heteromonocyclic compounds

Phenolic glycoside - Tetracarboxylic acid or derivatives - Alkyl-phenylketone - O-glycosyl compound - Phenylketone - Aryl ketone - Aryl alkyl ketone - Phenol ether - Phenoxy compound - Benzoyl - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Benzenoid - Oxane - Monosaccharide - Monocyclic benzene moiety - Heteroaromatic compound - Thiazole - Vinylogous acid - Azole - Carboxylic acid ester - Ketone - Oxacycle - Acetal - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Organonitrogen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organopnictogen compound - Organic nitrogen 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