CO[C@@H]1C[C@H]2N3CC(O)[C@]2([C@H]2O[C@@H]12)C1=CC2=C(OCO2)C(OC)=C1C3

InChIKey=GKZWOVRDMISXTE-OQJUAWBNSA-N

C18H21NO6

347.367

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 1,2-aminoalcohols Oxacyclic compounds Acetals Dialkyl ethers Azacyclic compounds Epoxides Hydrocarbon derivatives Organopnictogen compounds

Aromatic heteropolycyclic compounds

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