OC1=CC2=C(C=C1)C1=CC3=C(OCO3)C(O)=C1C(=O)N2

InChIKey=UAUYRRWIDUZJMH-UHFFFAOYSA-N

C14H9NO5

271.228

Organic compounds

Alkaloids and derivatives

Amaryllidaceae alkaloids

Phenanthridine- and phenanthridone-type amaryllidaceae alkaloids

Not available

Phenanthridine- and phenanthridone-type amaryllidaceae alkaloids

Phenanthridines and derivatives Hydroquinolones Isoquinolones and derivatives Hydroquinolines Benzodioxoles Pyridinones 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Vinylogous acids Heteroaromatic compounds Lactams Oxacyclic compounds Azacyclic compounds Acetals Organonitrogen compounds Organic oxides Hydrocarbon derivatives Organopnictogen compounds

Aromatic heteropolycyclic compounds

Phenanthridone-type amaryllidaceae alkaloid - Benzoquinoline - Phenanthridine - Dihydroquinolone - Isoquinolone - Dihydroquinoline - Isoquinoline - Quinoline - Benzodioxole - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Pyridinone - Pyridine - Benzenoid - Heteroaromatic compound - Vinylogous acid - Lactam - Organoheterocyclic compound - Azacycle - Oxacycle - Acetal - Organopnictogen compound - Organic oxide - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as phenanthridine- and phenanthridone-type amaryllidaceae alkaloids. These are amaryllidaceae alkaloids compounds based on the phenanthridine or the phenanthridone skeleton. Phenanthridone-type alkaloids have the highest oxygenated C ring in all Amaryllidaceae alkaloids, and they always show an amide group in ring B. On the contrary, alkaloids of the phenanthridine type often show completely aromatic ring system, occasionally with a methylation quaternary nitrogen atom.

Not available