CN1CCC2=C[C@H](O)[C@H]3OC(=O)C4=CC(O)=C(O)C=C4[C@H]3[C@H]12

InChIKey=VCMOJZNESSZVCD-BYNSBNAKSA-N

C16H17NO5

303.314

Organic compounds

Alkaloids and derivatives

Amaryllidaceae alkaloids

Homolycorine-type amaryllidaceae alkaloids

Not available

Homolycorine-type amaryllidaceae alkaloids

2-benzopyrans Hydroxybenzoic acid derivatives Indoles and derivatives 1-hydroxy-2-unsubstituted benzenoids Aralkylamines N-alkylpyrrolidines Trialkylamines Secondary alcohols Amino acids and derivatives Lactones Carboxylic acid esters Polyols Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Organic oxides

Aromatic heteropolycyclic compounds

Homolycorine skeleton - Dihydroxybenzoic acid - Benzopyran - Isochromane - 2-benzopyran - Indole or derivatives - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Aralkylamine - Benzenoid - N-alkylpyrrolidine - Pyrrolidine - Amino acid or derivatives - Carboxylic acid ester - Lactone - Secondary alcohol - Tertiary amine - Tertiary aliphatic amine - Azacycle - Oxacycle - Carboxylic acid derivative - Polyol - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Alcohol - Amine - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - 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