CC[C@H]1C[C@@H]2CN3CCC4=C(NC5=C4C=CC(O)=C5)[C@](C2)([C@H]13)C(=O)OC

InChIKey=GFEUNVMURRUASI-NBEPNCHPSA-N

C21H26N2O3

354.45

Organic compounds

Alkaloids and derivatives

Ibogan-type alkaloids

Not available

Not available

Ibogan-type alkaloids

Pyrroloazepines Hydroxyindoles 3-alkylindoles Piperidinecarboxylic acids 1-hydroxy-2-unsubstituted benzenoids Azepines Aralkylamines Pyrroles Methyl esters Heteroaromatic compounds Trialkylamines Amino acids and derivatives Monocarboxylic acids and derivatives Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides

Aromatic heteropolycyclic compounds

Ibogan skeleton - Catharanthine skeleton - Hydroxyindole - Pyrroloazepine - 3-alkylindole - Indole - Indole or derivatives - Piperidinecarboxylic acid - Azepine - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Aralkylamine - Piperidine - Benzenoid - Methyl ester - Heteroaromatic compound - Pyrrole - Tertiary aliphatic amine - Tertiary amine - Carboxylic acid ester - Amino acid or derivatives - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Organooxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Carbonyl group - Organic oxygen compound - Organic oxide - Amine - Organonitrogen compound - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as ibogan-type alkaloids. These are indole alkaloids with a structure based on the ibogamine skeleton or a derivative thereof. Ibogamine is a pentacyclic heterocyclic compound consisting of an indole fused to an azepane-containing tricyclic moiety ring. Iboga alkaloids arise from the cyclization of a secodine-type precursor through the formation of a 16,21 bond.

Not available