CCC1CC2C3N(C1)C(=O)CC31C(NC3=CC=CC=C13)C(C(=O)OC)C2=O

InChIKey=CQJMFRLCGDFUAT-UHFFFAOYSA-N

C21H24N2O4

368.433

Organic compounds

Alkaloids and derivatives

Pandoline alkaloids

Not available

Not available

Pandoline alkaloids

Plumeran-type alkaloids Carbazoles Quinolidines Indolizidines Indolines Secondary alkylarylamines Aralkylamines Pyrrolidine-2-ones Piperidines N-alkylpyrrolidines Benzenoids 1,3-dicarbonyl compounds Tertiary carboxylic acid amides Methyl esters Lactams Ketones Amino acids and derivatives Monocarboxylic acids and derivatives Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Pandoline skeleton - Plumeran-type alkaloid - Carbazole - Quinolidine - Indolizidine - Dihydroindole - Indole or derivatives - Aralkylamine - Secondary aliphatic/aromatic amine - Benzenoid - N-alkylpyrrolidine - 1,3-dicarbonyl compound - 2-pyrrolidone - Pyrrolidone - Piperidine - Methyl ester - Tertiary carboxylic acid amide - Pyrrolidine - Lactam - Ketone - Carboxylic acid ester - Carboxamide group - Amino acid or derivatives - Azacycle - Organoheterocyclic compound - Secondary amine - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Amine - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as pandoline alkaloids. These are alkaloids with a structure that is based on the pentacyclic pandoline skeleton. The Pandoline (pseudoaspidospermidine) (type II indole alkaloid) nucleus is believed to be formed by cyclisation of a secodine derivative.

Not available