CC(=O)N[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=C(O)C=C2OC(=O)C=CC2=C1

InChIKey=OTXAWKXSJDFGID-LMHBHQSJSA-N

C17H19NO9

381.337

Organic compounds

Phenylpropanoids and polyketides

Coumarins and derivatives

Coumarin glycosides

Not available

Coumarin glycosides

N-acyl-alpha-hexosamines 7-hydroxycoumarins Hexoses O-glycosyl compounds 1-benzopyrans Pyranones and derivatives 1-hydroxy-2-unsubstituted benzenoids Oxanes Acetamides Heteroaromatic compounds Secondary carboxylic acid amides Secondary alcohols Lactones Oxacyclic compounds Acetals Carbonyl compounds Organonitrogen compounds Primary alcohols Organopnictogen compounds Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Coumarin-6-o-glycoside - Coumarin o-glycoside - N-acyl-alpha-hexosamine - 7-hydroxycoumarin - Hydroxycoumarin - Hexose monosaccharide - Glycosyl compound - O-glycosyl compound - 1-benzopyran - Benzopyran - Pyranone - 1-hydroxy-2-unsubstituted benzenoid - Monosaccharide - Benzenoid - Pyran - Oxane - Heteroaromatic compound - Acetamide - Secondary carboxylic acid amide - Secondary alcohol - Lactone - Carboxamide group - Acetal - Carboxylic acid derivative - Oxacycle - Organoheterocyclic compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Primary alcohol - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as coumarin glycosides. These are aromatic compounds containing a carbohydrate moiety glycosidically bound to a coumarin moiety.

Not available