OC(=O)C1=CC2=C(N1)C1=C(N=C(C=C1C(O)=O)C(=O)COCCOCCOCCOCCN=[N+]=[N-])C(=O)C2=O

InChIKey=ZJRDPTHVLHYIHO-UHFFFAOYSA-N

C23H23N5O11

545.461

Organic compounds

Organoheterocyclic compounds

Quinolines and derivatives

Pyrroloquinolines

Not available

Pyrroloquinoline quinones

Quinoline carboxylic acids Indoles and derivatives Pyridinecarboxylic acids Aryl alkyl ketones O-quinones Pyrrole 2-carboxylic acids Substituted pyrroles Vinylogous amides Heteroaromatic compounds Azo imides Azo compounds Azacyclic compounds Dialkyl ethers Carboxylic acids Organic salts Organic oxides Hydrocarbon derivatives Organic zwitterions

Aromatic heteropolycyclic compounds

Pyrroloquinoline quinone - Quinoline-4-carboxylic acid - Indole or derivatives - Pyridine carboxylic acid - Pyridine carboxylic acid or derivatives - O-quinone - Pyrrole-2-carboxylic acid - Pyrrole-2-carboxylic acid or derivatives - Quinone - Aryl ketone - Aryl alkyl ketone - Substituted pyrrole - Pyridine - Heteroaromatic compound - Pyrrole - Vinylogous amide - Azo imide - Azo compound - Ketone - Carboxylic acid derivative - Azacycle - Dialkyl ether - Carboxylic acid - Ether - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Organic zwitterion - Organooxygen compound - Organic oxygen compound - Organic salt - Organic oxide - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as pyrroloquinoline quinones. These are compounds with a structure based on the 2,7,-tricarboxy-1H-pyrrolo[2,3-f ]quinoline-4,5-dione. Pyrroloquinoline Quinones usually bear a carboxylic acid group at the C-2, C-7 and C-9 positions.

Not available