COC1=C(OC(=O)CC(C)O)C=C2C3[C@@H]4N(C)CCC4=CC(OC(C)=O)C3OC(=O)C2=C1

InChIKey=FBWQZJWDTGIERI-LQBUJFQQSA-N

C23H27NO8

445.468

Organic compounds

Alkaloids and derivatives

Amaryllidaceae alkaloids

Homolycorine-type amaryllidaceae alkaloids

Not available

Homolycorine-type amaryllidaceae alkaloids

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

Aromatic heteropolycyclic compounds

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