COc1c2OCOc2cc2c1CN1CC[C@]22[C@H]3O[C@H]3[C@H](O)CC12

InChIKey=HHEOZJCKMANJQV-XGTUGMNXSA-N

C17H19NO5

317.341

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 Anisoles Oxepanes Alkyl aryl ethers Aralkylamines Azepines N-alkylpyrrolidines Trialkylamines Secondary alcohols Cyclic alcohols and derivatives Acetals Oxacyclic compounds Dialkyl ethers Epoxides Azacyclic compounds Hydrocarbon derivatives Organopnictogen compounds

Aromatic heteropolycyclic compounds

Hemanthamine/crinine alkaloid skeleton - Benzoquinoline - Phenanthridine - Benzazepine - Tetrahydroisoquinoline - Quinoline - Benzodioxole - Indole or derivatives - Anisole - Alkyl aryl ether - Azepine - Aralkylamine - Oxepane - Benzenoid - N-alkylpyrrolidine - Cyclic alcohol - Pyrrolidine - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - Ether - Oxirane - Dialkyl ether - Acetal - Organoheterocyclic compound - Azacycle - Oxacycle - Organonitrogen compound - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Amine - Organooxygen compound - Hydrocarbon derivative - Alcohol - 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