O[C@@H]1[C@H]2[C@@H](CCC[C@@H]2C([O-])=O)C[NH+]2CCC3=C(NC4=CC=CC=C34)[C@@H]12

InChIKey=FAJGWXJPBTUEOP-MSNQJLDKSA-N

C20H24N2O3

340.423

Organic compounds

Alkaloids and derivatives

Corynanthean-type alkaloids

Not available

Not available

Corynanthean-type alkaloids

Beta carbolines Delta amino acids and derivatives 3-alkylindoles Aralkylamines Benzenoids Piperidines Quaternary ammonium salts Pyrroles Heteroaromatic compounds Secondary alcohols Carboxylic acid salts Trialkylamines 1,2-aminoalcohols Carboxylic acids Azacyclic compounds Monocarboxylic acids and derivatives Hydrocarbon derivatives Organic zwitterions Carbonyl compounds Organic oxides Organic salts

Aromatic heteropolycyclic compounds

Corynanthean skeleton - Pyridoindole - Beta-carboline - Delta amino acid or derivatives - 3-alkylindole - Indole - Indole or derivatives - Aralkylamine - Piperidine - Benzenoid - Pyrrole - Quaternary ammonium salt - Heteroaromatic compound - Secondary alcohol - Tertiary aliphatic amine - Carboxylic acid salt - 1,2-aminoalcohol - Carboxylic acid derivative - Carboxylic acid - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Amine - Hydrocarbon derivative - Alcohol - Organic oxide - Organic nitrogen compound - Carbonyl group - Organic salt - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organic zwitterion - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as corynanthean-type alkaloids. These are alkaloids with a structure based on the corynanthean nucleus, which is a tetracycle characterized by an indole fused to a quinolizidine. Additionally, the quinolizidine ring system is substituted to a 2-methylpropyl group and one ethyl group.

Not available