COC1=C2[C@H]3[C@@H]4N(C)CCC4=CC[C@H]3OC(=O)C2=CC2=C1OCO2

InChIKey=HRQKWQANALFRKZ-BYCMXARLSA-N

C18H19NO5

329.352

Organic compounds

Alkaloids and derivatives

Amaryllidaceae alkaloids

Homolycorine-type amaryllidaceae alkaloids

Not available

Homolycorine-type amaryllidaceae alkaloids

Gallic acid and derivatives 2-benzopyrans Benzodioxoles Indoles and derivatives Anisoles Aralkylamines Alkyl aryl ethers N-alkylpyrrolidines Lactones Carboxylic acid esters Trialkylamines Amino acids and derivatives Monocarboxylic acids and derivatives Oxacyclic compounds Azacyclic compounds Acetals Organic oxides Hydrocarbon derivatives Organopnictogen compounds

Aromatic heteropolycyclic compounds

Homolycorine skeleton - Gallic acid or derivatives - Benzopyran - Isochromane - 2-benzopyran - Benzodioxole - Indole or derivatives - Anisole - Alkyl aryl ether - Aralkylamine - Benzenoid - N-alkylpyrrolidine - Pyrrolidine - Tertiary aliphatic amine - Tertiary amine - Lactone - Amino acid or derivatives - Carboxylic acid ester - Azacycle - Acetal - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Oxacycle - Ether - Carboxylic acid derivative - Organooxygen compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Amine - Organonitrogen compound - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as homolycorine-type amaryllidaceae alkaloids. These are amaryllidaceae alkaloids compounds containing the homolycorine skeleton, made up of a [3,4-g]benzopyranone ring due to the oxidation of the hydroxyl group at the C6. They are biogenetically formed through a restructuring of lycorine-type alkaloids.

Not available