CC[C@@H]1C[C@H]2[C@H]3N(CC[C@@]33[C@H](NC4=CC=CC=C34)[C@H](C(=O)OC)C2=O)C1

InChIKey=QUNKEVXMUMPQOU-RVAKVISXSA-N

C21H26N2O3

354.45

Organic compounds

Alkaloids and derivatives

Pandoline alkaloids

Not available

Not available

Pandoline alkaloids

Plumeran-type alkaloids Carbazoles Quinolidines Indolines Indolizidines Aralkylamines Secondary alkylarylamines 1,3-dicarbonyl compounds Benzenoids Piperidines N-alkylpyrrolidines Methyl esters Trialkylamines Amino acids and derivatives Ketones Monocarboxylic acids and derivatives Azacyclic compounds Organic oxides Organopnictogen compounds Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

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