CC[C@@]12CCCN3CCC4=C([C@H]13)N(C1=CC=CC=C41)C(=C2)C(=O)OCCCCCO[N+]([O-])=O

InChIKey=HCZVNLRMPGXZKW-NOZRDPDXSA-N

C25H31N3O5

453.539

Organic compounds

Alkaloids and derivatives

Eburnan-type alkaloids

Not available

Not available

Eburnan-type alkaloids

Indolonaphthyridine alkaloids Beta carbolines 3-alkylindoles Alpha amino acids and derivatives Naphthyridines Aralkylamines Piperidines Benzenoids Heteroaromatic compounds Enoate esters Alkyl nitrates Pyrroles Organic nitro compounds Trialkylamines Organic nitric acids and derivatives Monocarboxylic acids and derivatives Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Organic salts Organic cations

Aromatic heteropolycyclic compounds

Eburna alkaloid - Indolo[3,2-1de][1,5]naphthyridine - Beta-carboline - Pyridoindole - Alpha-amino acid or derivatives - 3-alkylindole - Naphthyridine - Indole - Indole or derivatives - Aralkylamine - Benzenoid - Piperidine - Organic nitrate - Pyrrole - Alkyl nitrate - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Heteroaromatic compound - Amino acid or derivatives - Carboxylic acid ester - Organic nitro compound - Organic nitric acid or derivatives - Tertiary amine - Tertiary aliphatic amine - Allyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Carboxylic acid derivative - Organoheterocyclic compound - Azacycle - Monocarboxylic acid or derivatives - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Amine - Organic salt - Organonitrogen compound - Organooxygen compound - Organic cation - 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