CO[C@H]1C[C@@H]2N3C[C@@H](O)[C@@]2(C=C1)c1cc2OCOc2c(OC)c1C3

InChIKey=QAHZAHIPKNLGAS-RIOHULGPSA-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 Anisoles Alkyl aryl ethers Aralkylamines Azepines N-alkylpyrrolidines Trialkylamines Secondary alcohols 1,2-aminoalcohols Oxacyclic compounds Acetals Azacyclic compounds Dialkyl ethers Organopnictogen compounds Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Hemanthamine/crinine alkaloid skeleton - Benzoquinoline - Phenanthridine - Benzazepine - Tetrahydroisoquinoline - Quinoline - Benzodioxole - Indole or derivatives - Anisole - Alkyl aryl ether - Azepine - Aralkylamine - Benzenoid - N-alkylpyrrolidine - Pyrrolidine - Tertiary amine - 1,2-aminoalcohol - Tertiary aliphatic amine - Secondary alcohol - Acetal - Oxacycle - Azacycle - Dialkyl ether - Ether - Organoheterocyclic compound - Hydrocarbon derivative - Organopnictogen compound - Organooxygen compound - Alcohol - Organic nitrogen compound - Amine - Organic oxygen compound - Organonitrogen compound - 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