[Cl-].CC[C@@]12CCC[N+]3=C1C1=C(C4=C(C=CC(Cl)=C4)N1C(=C2)C(=O)OC)C(O)=C3

InChIKey=JVDZUWTWWIMPEZ-BOXHHOBZSA-N

C21H20Cl2N2O3

419.3

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 Indoles Hydroxypyridines Pyridinium derivatives Aryl chlorides Benzenoids Pyrroles Methyl esters Enoate esters Heteroaromatic compounds Azacyclic compounds Monocarboxylic acids and derivatives Organonitrogen compounds Hydrocarbon derivatives Carbonyl compounds Organic chloride salts Organic oxides Organochlorides Organic cations

Aromatic heteropolycyclic compounds

Eburna alkaloid - Indolo[3,2-1de][1,5]naphthyridine - Beta-carboline - Pyridoindole - Alpha-amino acid or derivatives - Naphthyridine - Indole - Indole or derivatives - Hydroxypyridine - Aryl chloride - Aryl halide - Pyridine - Pyridinium - Benzenoid - Methyl ester - Pyrrole - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Heteroaromatic compound - Carboxylic acid ester - Organoheterocyclic compound - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Azacycle - Organic salt - Organic oxygen compound - Organohalogen compound - Organochloride - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organic nitrogen compound - Carbonyl group - Organic chloride salt - 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