CO[C@@H]1C=C2CCN(C)[C@@H]2C2[C@H]1OC(=O)C1=CC3=C(OCO3)C=C21

InChIKey=DITOENWBJBNZSL-XOJKTNQZSA-N

C18H19NO5

329.352

Organic compounds

Alkaloids and derivatives

Amaryllidaceae alkaloids

Homolycorine-type amaryllidaceae alkaloids

Not available

Homolycorine-type amaryllidaceae alkaloids

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

Aromatic heteropolycyclic compounds

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