CC(=O)O[C@H]1C=C2[C@@H](NC(=O)C3=CC4=C(OCO4)C=C23)[C@H](O)[C@@H]1O

InChIKey=CYXNWMRKQREOBX-YJNKXOJESA-N

C16H15NO7

333.296

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 Secondary carboxylic acid amides Secondary alcohols 1,2-diols Carboxylic acid esters Lactams Oxacyclic compounds Acetals Azacyclic compounds Monocarboxylic acids and derivatives Organonitrogen compounds Carbonyl compounds Organic oxides Organopnictogen compounds Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Phenanthridone-type amaryllidaceae alkaloid - Phenanthridine - Benzoquinoline - Isoquinolone - Quinoline - Tetrahydroisoquinoline - Benzodioxole - Cyclitol or derivatives - Benzenoid - Carboxylic acid ester - 1,2-diol - Lactam - Carboxamide group - Secondary alcohol - Secondary carboxylic acid amide - Acetal - Oxacycle - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Alcohol - Organic oxygen 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