CC(=O)N[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=CC2=C(C=C1)C(=CC(=O)O2)C1=CC=CC=C1

InChIKey=XFHAJXPWZUYJGZ-OKKOYFSCSA-N

C23H23NO8

441.436

Organic compounds

Phenylpropanoids and polyketides

Neoflavonoids

Neoflavonoid 7-O-glycosides

Not available

Neoflavonoid 7-O-glycosides

Coumarin glycosides Neoflavones N-acyl-alpha-hexosamines O-glycosyl compounds 1-benzopyrans Pyranones and derivatives Oxanes Benzene and substituted derivatives Monosaccharides Acetamides Heteroaromatic compounds Secondary alcohols Secondary carboxylic acid amides Lactones Acetals Oxacyclic compounds Hydrocarbon derivatives Organopnictogen compounds Carbonyl compounds Primary alcohols Organonitrogen compounds Organic oxides

Aromatic heteropolycyclic compounds

Neoflavonoid-7-o-glycoside - Coumarin-7-o-glycoside - Coumarin o-glycoside - 4-phenylcoumarin - N-acyl-alpha-hexosamine - Coumarin - Glycosyl compound - O-glycosyl compound - Benzopyran - 1-benzopyran - Pyranone - Monocyclic benzene moiety - Monosaccharide - Oxane - Benzenoid - Pyran - Acetamide - Heteroaromatic compound - Secondary carboxylic acid amide - Secondary alcohol - Carboxamide group - Lactone - Acetal - Organoheterocyclic compound - Oxacycle - Carboxylic acid derivative - Organooxygen compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Hydrocarbon derivative - Alcohol - Carbonyl group - Primary alcohol - Organonitrogen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as neoflavonoid 7-o-glycosides. These are 7-O-glycosylated neoflavonoids. Neoflavonoids are compounds with a structure based on the 4-phenylchromene backbone.

Not available