CO[C@H]1[C@@H]2O[C@@]22CCN(C)[C@H]2C2C1OC(=O)C1=CC(OC)=C(O)C=C21

InChIKey=ODNUSIICQUYOIZ-FXYVQQGDSA-N

C18H21NO6

347.367

Organic compounds

Alkaloids and derivatives

Amaryllidaceae alkaloids

Homolycorine-type amaryllidaceae alkaloids

Not available

Homolycorine-type amaryllidaceae alkaloids

2-benzopyrans Indoles and derivatives Anisoles 1-hydroxy-2-unsubstituted benzenoids Oxepanes Alkyl aryl ethers Aralkylamines N-alkylpyrrolidines Carboxylic acid esters Lactones Trialkylamines Amino acids and derivatives Epoxides Dialkyl ethers Azacyclic compounds Oxacyclic compounds Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Homolycorine skeleton - Benzopyran - Isochromane - 2-benzopyran - Indole or derivatives - Anisole - Phenol ether - Alkyl aryl ether - 1-hydroxy-2-unsubstituted benzenoid - Oxepane - Aralkylamine - Phenol - Benzenoid - N-alkylpyrrolidine - Pyrrolidine - Amino acid or derivatives - Carboxylic acid ester - Lactone - Tertiary aliphatic amine - Tertiary amine - Oxacycle - Ether - Oxirane - Dialkyl ether - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Organonitrogen compound - Organic nitrogen compound - Amine - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organic oxygen 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