COC1=CC2=C(C=C1OC(=O)CC(C)O)C1C3NCCC3=CC(OC(C)=O)C1OC2=O

InChIKey=LFBMHHCFTVOGOT-UHFFFAOYSA-N

C22H25NO8

431.441

Organic compounds

Alkaloids and derivatives

Amaryllidaceae alkaloids

Homolycorine-type amaryllidaceae alkaloids

Not available

Homolycorine-type amaryllidaceae alkaloids

2-benzopyrans Tricarboxylic acids and derivatives Indolines Anisoles Alkyl aryl ethers Fatty acid esters Aralkylamines Beta hydroxy acids and derivatives Pyrrolidines Secondary alcohols Amino acids and derivatives Lactones Carboxylic acid esters Oxacyclic compounds Dialkylamines Azacyclic compounds Hydrocarbon derivatives Organopnictogen compounds Organic oxides Carbonyl compounds

Aromatic heteropolycyclic compounds

Homolycorine skeleton - 2-benzopyran - Isochromane - Benzopyran - Indole or derivatives - Dihydroindole - Tricarboxylic acid or derivatives - Anisole - Aralkylamine - Fatty acid ester - Alkyl aryl ether - Beta-hydroxy acid - Fatty acyl - Benzenoid - Hydroxy acid - Pyrrolidine - Amino acid or derivatives - Lactone - Carboxylic acid ester - Secondary alcohol - Secondary amine - Carboxylic acid derivative - Secondary aliphatic amine - Ether - Organoheterocyclic compound - Azacycle - Oxacycle - Alcohol - Organonitrogen compound - Carbonyl group - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen 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