CCOC(=O)[C@@]1(O)C[C@]2(CC)CCC[N+]3([O-])CCC4=C([C@H]23)N1C1=CC=CC=C41

InChIKey=KARGDDHSMSSUQU-VYDXOXBFSA-N

C22H28N2O4

384.476

Organic compounds

Alkaloids and derivatives

Eburnan-type alkaloids

Not available

Not available

Eburnan-type alkaloids

Indolonaphthyridine alkaloids Beta carbolines Alpha amino acids and derivatives Naphthyridines 3-alkylindoles Piperidines Benzenoids Pyrroles Trialkyl amine oxides Heteroaromatic compounds Carboxylic acid esters Alkanolamines Monocarboxylic acids and derivatives Trisubstituted amine oxides and derivatives Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Organic salts Organic zwitterions

Aromatic heteropolycyclic compounds

Eburna alkaloid - Indolo[3,2-1de][1,5]naphthyridine - Beta-carboline - Pyridoindole - Naphthyridine - Alpha-amino acid or derivatives - 3-alkylindole - Indole - Indole or derivatives - Piperidine - Benzenoid - Trialkyl amine oxide - Heteroaromatic compound - Pyrrole - Carboxylic acid ester - Trisubstituted n-oxide - N-oxide - Alkanolamine - Carboxylic acid derivative - Azacycle - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Organic zwitterion - Organic salt - Organic nitrogen compound - Organic oxide - Organonitrogen compound - Carbonyl group - Organooxygen compound - Organic oxygen compound - Hydrocarbon derivative - 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