O[C@H]1CC[C@H]2CN3CCC4=C(NC5=CC=CC=C45)[C@@H]3C[C@@H]2[C@H]1C(=O)NCCCCNC(=O)[C@H]1[C@@H](O)CC[C@H]2CN3CCC4=C(NC5=CC=CC=C45)[C@@H]3C[C@H]12

InChIKey=KFMHLMMVJDAMBL-QRMJEQFMSA-N

C44H56N6O4

732.97

Organic compounds

Alkaloids and derivatives

Corynanthean-type alkaloids

Not available

Not available

Corynanthean-type alkaloids

Beta carbolines 3-alkylindoles Aralkylamines Benzenoids Piperidines Heteroaromatic compounds Pyrroles Cyclic alcohols and derivatives Secondary alcohols Trialkylamines Secondary carboxylic acid amides Amino acids and derivatives Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aromatic heteropolycyclic compounds

Corynanthean skeleton - Beta-carboline - Pyridoindole - 3-alkylindole - Indole - Indole or derivatives - Aralkylamine - Piperidine - Benzenoid - Cyclic alcohol - Heteroaromatic compound - Pyrrole - Amino acid or derivatives - Carboxamide group - Tertiary aliphatic amine - Secondary alcohol - Secondary carboxylic acid amide - Tertiary amine - Carboxylic acid derivative - Organoheterocyclic compound - Azacycle - Organooxygen compound - Organonitrogen compound - Organic oxide - Organopnictogen compound - Alcohol - Organic oxygen compound - Amine - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - 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