CCC12CCCN3CCC4(C13)C(CC2)=NC1=C4C=CC(O)=C1C1CC2(CC)CCCN3CCC4=C(C23)N1C1=CC=CC=C41

InChIKey=HWRDULPLRZTZRK-UHFFFAOYSA-N

C38H46N4O

574.813

Organic compounds

Alkaloids and derivatives

Eburnan-type alkaloids

Not available

Not available

Eburnan-type alkaloids

Plumeran-type alkaloids Indolonaphthyridine alkaloids Beta carbolines Quinolidines 3-alkylindoles Naphthyridines Indolizidines 1-hydroxy-2-unsubstituted benzenoids Aralkylamines Piperidines N-alkylpyrrolidines Heteroaromatic compounds Pyrroles Trialkylamines Ketimines Azacyclic compounds Propargyl-type 1,3-dipolar organic compounds Organooxygen compounds Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Eburna alkaloid - Plumeran-type alkaloid - Indolo[3,2-1de][1,5]naphthyridine - Beta-carboline - Pyridoindole - 3-alkylindole - Quinolidine - Naphthyridine - Indole - Indole or derivatives - Indolizidine - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Aralkylamine - Piperidine - Benzenoid - N-alkylpyrrolidine - Heteroaromatic compound - Pyrrole - Pyrrolidine - Tertiary aliphatic amine - Ketimine - Tertiary amine - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organoheterocyclic compound - Azacycle - Organooxygen compound - Organonitrogen compound - Amine - Hydrocarbon derivative - Imine - Organic oxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as eburnan-type alkaloids. These are alkaloids with a structure based on the eburnan skeleton, that arises from rearrangement of the aspidospermidine ring system, involving migration of C-21 from C-7 to C-2, fission of the 2,16-bond, and attachment of C-16 to N-1.

Not available