CC[C@@]12C=C[C@H](N3CCC4=C([C@H]13)N(C1=CC=CC=C41)C(=C2)C(=O)OC)C1=CN2CCC3=C4[C@@H]2[C@](CC)(C=C(N4C2=CC=CC=C32)C(=O)OC)[C@@H]1O

InChIKey=DESPGBHWBUIOGW-GAABGMJYSA-N

C42H42N4O5

682.821

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 Tetrahydropyridines Aralkylamines Benzenoids Dicarboxylic acids and derivatives Heteroaromatic compounds Enoate esters Pyrroles Methyl esters Trialkylamines Secondary alcohols Enamines Allylamines Azacyclic compounds Carbonyl compounds Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Eburna alkaloid - Indolo[3,2-1de][1,5]naphthyridine - Beta-carboline - Pyridoindole - Alpha-amino acid or derivatives - Naphthyridine - 3-alkylindole - Indole - Indole or derivatives - Aralkylamine - Tetrahydropyridine - Dicarboxylic acid or derivatives - Benzenoid - Alpha,beta-unsaturated carboxylic ester - Methyl ester - Enoate ester - Pyrrole - Heteroaromatic compound - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - Amino acid or derivatives - Carboxylic acid ester - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Enamine - Allylamine - Alcohol - Organooxygen compound - Amine - Carbonyl group - Organic oxygen compound - Organic oxide - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen 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