COC1=CC=C(C=C1)C1=CC(=O)OC2=C1C=CC(OCC(=O)N[C@@H](CCCNC(N)=O)C([O-])=O)=C2

InChIKey=YLWNKQZQXPFSHV-IBGZPJMESA-M

C24H24N3O8

482.47

Organic compounds

Phenylpropanoids and polyketides

Neoflavonoids

Neoflavones

Not available

Neoflavones

N-acyl-L-alpha-amino acids Coumarins and derivatives 1-benzopyrans Phenoxy compounds Anisoles Methoxybenzenes Pyranones and derivatives Alkyl aryl ethers Heteroaromatic compounds Ureas Secondary carboxylic acid amides Carboxylic acid salts Lactones Oxacyclic compounds Carboxylic acids Monocarboxylic acids and derivatives Carbonyl compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Organic anions

Aromatic heteropolycyclic compounds

4-phenylcoumarin - N-acyl-alpha amino acid or derivatives - N-acyl-l-alpha-amino acid - N-acyl-alpha-amino acid - Coumarin - 1-benzopyran - Alpha-amino acid or derivatives - Benzopyran - Phenol ether - Phenoxy compound - Anisole - Methoxybenzene - Pyranone - Alkyl aryl ether - Pyran - Benzenoid - Monocyclic benzene moiety - Heteroaromatic compound - Urea - Lactone - Carboxylic acid salt - Carboxamide group - Secondary carboxylic acid amide - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Carboxylic acid - Ether - Monocarboxylic acid or derivatives - Organic oxide - Organic oxygen compound - Carbonyl group - Organooxygen compound - Hydrocarbon derivative - Organonitrogen compound - Organic nitrogen compound - Organic anion - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as neoflavones. These are neoflavonoids with a structure based on the 4-phenylcoumarin skeleton.

Not available