CC(=O)N1[C@H]2C[C@@H]3O[C@@H]3C[C@@H]2C2=CC3=C(OCO3)C=C2C1=O

InChIKey=RILDRRYKOMCFIE-QFEPDWEUSA-N

C16H15NO5

301.298

Organic compounds

Alkaloids and derivatives

Amaryllidaceae alkaloids

Phenanthridine- and phenanthridone-type amaryllidaceae alkaloids

Not available

Phenanthridine- and phenanthridone-type amaryllidaceae alkaloids

Phenanthridines and derivatives Isoquinolones and derivatives Tetrahydroisoquinolines Benzodioxoles Oxepanes N-substituted carboxylic acid imides Benzenoids Acetamides Dicarboximides Oxacyclic compounds Acetals Azacyclic compounds Epoxides Dialkyl ethers Carbonyl compounds Hydrocarbon derivatives Organic oxides Organonitrogen compounds Organopnictogen compounds

Aromatic heteropolycyclic compounds

Phenanthridone-type amaryllidaceae alkaloid - Benzoquinoline - Phenanthridine - Isoquinolone - Quinoline - Tetrahydroisoquinoline - Benzodioxole - Oxepane - Benzenoid - Carboxylic acid imide, n-substituted - Acetamide - Carboxylic acid imide - Dicarboximide - Organoheterocyclic compound - Oxacycle - Azacycle - Carboxylic acid derivative - Acetal - Dialkyl ether - Ether - Oxirane - Hydrocarbon derivative - Organopnictogen compound - Organonitrogen compound - Organooxygen compound - Organic oxide - Carbonyl group - Organic oxygen 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