COC1=C2CN3CCC4(C=C[C@@H](C[C@@H]34)OC(C)=O)C2=CC2=C1OCO2

InChIKey=SIXXWBHRECGZRD-HAEBDUGBSA-N

C19H21NO5

343.379

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 Azepines Azepanes Aralkylamines Alkyl aryl ethers Piperidines N-alkylpyrrolidines 1,3-dioxoles Trialkylamines Carboxylic acid esters Amino acids and derivatives Oxacyclic compounds Monocarboxylic acids and derivatives Azacyclic compounds Acetals Organopnictogen compounds Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Hemanthamine/crinine alkaloid skeleton - Phenanthridine - Benzoquinoline - Benzazepine - Tetrahydroisoquinoline - Quinoline - Indole or derivatives - Benzodioxole - Anisole - Aralkylamine - Azepine - Azepane - Alkyl aryl ether - Benzenoid - N-alkylpyrrolidine - Piperidine - Pyrrolidine - Meta-dioxole - Tertiary aliphatic amine - Tertiary amine - Carboxylic acid ester - Amino acid or derivatives - Oxacycle - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Ether - Carboxylic acid derivative - Acetal - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Amine - 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