CCC12CCCN3CCC4(C(CC1)NC1=C(C=CC(O)=C41)C1CC4(CCCN5CCC6=C(C45)N1C1=CC=CC=C61)C(C)(F)F)C23

InChIKey=JJPDLHNPSGZWLA-UHFFFAOYSA-N

C38H46F2N4O

612.81

Organic compounds

Alkaloids and derivatives

Eburnan-type alkaloids

Not available

Not available

Eburnan-type alkaloids

Aspidospermatan-type alkaloids Plumeran-type alkaloids Indolonaphthyridine alkaloids Beta carbolines Carbazoles Quinolidines Naphthyridines 3-alkylindoles Indolizidines Indolines Secondary alkylarylamines Aralkylamines 1-hydroxy-2-unsubstituted benzenoids N-alkylpyrrolidines Piperidines Pyrroles Heteroaromatic compounds Trialkylamines Azacyclic compounds Hydrocarbon derivatives Alkyl fluorides Organofluorides Organooxygen compounds

Aromatic heteropolycyclic compounds

Eburna alkaloid - Aspidosperma alkaloid - Plumeran-type alkaloid - Indolo[3,2-1de][1,5]naphthyridine - Beta-carboline - Carbazole - Pyridoindole - Naphthyridine - 3-alkylindole - Quinolidine - Indolizidine - Dihydroindole - Indole or derivatives - Indole - Secondary aliphatic/aromatic amine - Phenol - Aralkylamine - 1-hydroxy-2-unsubstituted benzenoid - Benzenoid - N-alkylpyrrolidine - Piperidine - Pyrrolidine - Pyrrole - Heteroaromatic compound - Tertiary aliphatic amine - Tertiary amine - Azacycle - Secondary amine - Organoheterocyclic compound - Alkyl halide - Alkyl fluoride - Organohalogen compound - Organofluoride - Hydrocarbon derivative - Organic oxygen compound - Organonitrogen compound - Organic nitrogen compound - Amine - Organooxygen 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