CCN(CC)CCN1C(=O)C2=CC3=C(OCO3)C=C2C2=C1C1=C(C=C2)N=CC=C1

InChIKey=MSIKXLCPZQJRNS-UHFFFAOYSA-N

C23H23N3O3

389.455

Organic compounds

Alkaloids and derivatives

Amaryllidaceae alkaloids

Phenanthridine- and phenanthridone-type amaryllidaceae alkaloids

Not available

Phenanthridine- and phenanthridone-type amaryllidaceae alkaloids

Phenanthrolines Phenanthridines and derivatives Hydroquinolones Isoquinolones and derivatives Hydroquinolines Benzodioxoles Pyridinones Benzenoids Heteroaromatic compounds Trialkylamines Lactams Acetals Oxacyclic compounds Azacyclic compounds Organic oxides Organopnictogen compounds Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Phenanthridone-type amaryllidaceae alkaloid - Benzoquinoline - Phenanthridine - 1,7-phenanthroline - Dihydroquinolone - Isoquinolone - Dihydroquinoline - Isoquinoline - Quinoline - Benzodioxole - Pyridinone - Benzenoid - Pyridine - Heteroaromatic compound - Tertiary aliphatic amine - Tertiary amine - Lactam - Organoheterocyclic compound - Acetal - Azacycle - Oxacycle - Amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - 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