OC1C[C@@H]2NC(=O)C3=CC4=C(OCO4)C=C3[C@H]2[C@@H](O)[C@@H]1O

InChIKey=HCSZCBCMALXZNJ-OJCQTPOQSA-N

C14H15NO6

293.275

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 Benzenoids Cyclitols and derivatives Lactams Secondary alcohols Secondary carboxylic acid amides Azacyclic compounds Acetals Oxacyclic compounds Polyols Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Phenanthridone-type amaryllidaceae alkaloid - Benzoquinoline - Phenanthridine - Isoquinolone - Tetrahydroisoquinoline - Quinoline - Benzodioxole - Cyclitol or derivatives - Benzenoid - Cyclic alcohol - Carboxamide group - Lactam - Secondary carboxylic acid amide - Secondary alcohol - Acetal - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Polyol - Hydrocarbon derivative - Alcohol - Organic oxide - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organopnictogen 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