CC(=O)O[C@@H]1CC[C@@]23C[C@@H](O)N(CC4=CC5=C(OCO5)C=C24)[C@H]3C1

InChIKey=OMAXREMMBFIYGY-QRVDHSFSSA-N

C18H21NO5

331.368

Organic compounds

Alkaloids and derivatives

Amaryllidaceae alkaloids

Crinine- and Haemanthamine-type amaryllidaceae alkaloids

Not available

Crinine- and Haemanthamine-type amaryllidaceae alkaloids

Phenanthridines and derivatives Benzazepines Tetrahydroisoquinolines Indoles and derivatives Benzodioxoles Azepines N-alkylpyrrolidines Benzenoids Hemiaminals Carboxylic acid esters Oxacyclic compounds Monocarboxylic acids and derivatives Azacyclic compounds Acetals Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aromatic heteropolycyclic compounds

Hemanthamine/crinine alkaloid skeleton - Phenanthridine - Benzoquinoline - Benzazepine - Tetrahydroisoquinoline - Quinoline - Indole or derivatives - Benzodioxole - Azepine - Benzenoid - N-alkylpyrrolidine - Pyrrolidine - Hemiaminal - Carboxylic acid ester - Oxacycle - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Alkanolamine - Acetal - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as crinine- and haemanthamine-type amaryllidaceae alkaloids. These are amaryllidaceae alkaloids compounds with a structure based on the crinine or haemanthamine backbone. Both backbones have a common 5,10b-ethano bridge moiety in their frameworks, which is a very significant taxonomic feature, and the configurations of the 5,10b-ethano bridge are opposite to each other.

Not available