[H][C@]12CC(=O)O[C@@]1([H])C1=C(C(=O)C3=C(C=CC=C3O)C1=O)[C@]1(O2)O[C@@]([H])(C)C[C@]([H])(OC(C)=O)[C@]1([H])O

InChIKey=DKQCCDMPFPKSEP-CRSIVXOJSA-N

C22H20O10

444.392

Organic compounds

Phenylpropanoids and polyketides

Isochromanequinones

Benzoisochromanequinones

Not available

Benzoisochromanequinones

Naphthopyranones Naphthoquinones Furopyrans Aryl ketones Quinones 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Ketals Pyranones and derivatives Gamma butyrolactones Dicarboxylic acids and derivatives Oxanes Vinylogous acids Tetrahydrofurans Furans Secondary alcohols Carboxylic acid esters Oxacyclic compounds Hydrocarbon derivatives Organic oxides

Aromatic heteropolycyclic compounds

Benzoisochromanequinone - Naphthopyranone - Naphthopyran - Naphthoquinone - Naphthalene - Furopyran - Aryl ketone - Quinone - 1-hydroxy-2-unsubstituted benzenoid - 1-hydroxy-4-unsubstituted benzenoid - Pyranone - Ketal - Dicarboxylic acid or derivatives - Gamma butyrolactone - Benzenoid - Oxane - Pyran - Furan - Vinylogous acid - Tetrahydrofuran - Lactone - Ketone - Carboxylic acid ester - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Acetal - Carboxylic acid derivative - Alcohol - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organic oxygen compound - Organooxygen compound - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as benzoisochromanequinones. These are benzo derivatives of isochromanequinones. Isochromanequinones are structurally characterized by a quinone fused to an isochromane, and forming a naphtho[2,3-c]pyran-6,9-dione skeleton.

Not available