CC(=O)N[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@H]1[C@H](O)[C@@H](NC(C)=O)[C@H](OC2=CC3=C(C=C2)C(C)=CC(=O)O3)O[C@@H]1CO

InChIKey=UPSFMJHZUCSEHU-JYGUBCOQSA-N

C26H34N2O13

582.559

Organic compounds

Phenylpropanoids and polyketides

Coumarins and derivatives

Coumarin glycosides

Not available

Coumarin glycosides

N-acyl-alpha-hexosamines Disaccharides O-glycosyl compounds 1-benzopyrans Pyranones and derivatives Oxanes Benzenoids Acetamides Heteroaromatic compounds Secondary alcohols Secondary carboxylic acid amides Lactones Oxacyclic compounds Acetals Hydrocarbon derivatives Carbonyl compounds Organic oxides Organonitrogen compounds Organopnictogen compounds Primary alcohols

Aromatic heteropolycyclic compounds

Coumarin-7-o-glycoside - Coumarin o-glycoside - N-acyl-alpha-hexosamine - Disaccharide - Glycosyl compound - O-glycosyl compound - Benzopyran - 1-benzopyran - Pyranone - Oxane - Pyran - Benzenoid - Acetamide - Heteroaromatic compound - Secondary alcohol - Secondary carboxylic acid amide - Carboxamide group - Lactone - Organoheterocyclic compound - Acetal - Carboxylic acid derivative - Oxacycle - Alcohol - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organic nitrogen compound - Primary alcohol - 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