OC(=O)\C=C\C(O)=O.COC1=C(O)C=C2C3C4N(C)CCC4=CC(O)C3OC(=O)C2=C1

InChIKey=WYSGJJPVUZCZEQ-WLHGVMLRSA-N

C21H23NO9

433.413

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 Alkyl aryl ethers Aralkylamines Unsaturated fatty acids Dicarboxylic acids and derivatives N-alkylpyrrolidines Trialkylamines Carboxylic acid esters Amino acids and derivatives Secondary alcohols Lactones Carboxylic acids Azacyclic compounds Oxacyclic compounds Carbonyl compounds Organic oxides Hydrocarbon derivatives

Not available

Homolycorine skeleton - Benzopyran - Isochromane - 2-benzopyran - Indole or derivatives - Anisole - Phenol ether - Alkyl aryl ether - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Aralkylamine - Fatty acid - Benzenoid - N-alkylpyrrolidine - Fatty acyl - Unsaturated fatty acid - Dicarboxylic acid or derivatives - Pyrrolidine - Secondary alcohol - Tertiary amine - Tertiary aliphatic amine - Amino acid or derivatives - Lactone - Carboxylic acid ester - Organoheterocyclic compound - Carboxylic acid derivative - Azacycle - Ether - Oxacycle - Carboxylic acid - Alcohol - Organonitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organooxygen compound - Amine - Organic nitrogen 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