CCNC(=O)C1=CO[C@@H](C)[C@H]2CN3CCC4=C([C@@H]3C[C@H]12)N(C(=O)OC)C1=CC=CC=C41

InChIKey=ZVSYOXPPKAILOQ-HEFCWWFNSA-N

C24H29N3O4

423.513

Organic compounds

Alkaloids and derivatives

Yohimbine alkaloids

Not available

Not available

Yohimbine alkaloids

Corynanthean-type alkaloids Beta carbolines Indolecarboxylic acids 3-alkylindoles Pyrrole carboxylic acids and derivatives Aralkylamines Benzenoids Substituted pyrroles Piperidines Heteroaromatic compounds Vinylogous esters Secondary carboxylic acid amides Amino acids and derivatives Trialkylamines Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Carbonyl compounds Organic oxides

Aromatic heteropolycyclic compounds

18-oxayohimban - Corynanthean skeleton - Yohimbine alkaloid - Beta-carboline - Pyridoindole - Indolecarboxylic acid - Indolecarboxylic acid derivative - 3-alkylindole - Indole - Indole or derivatives - Pyrrole-1-carboxylic acid or derivatives - Aralkylamine - Substituted pyrrole - Piperidine - Benzenoid - Pyrrole - Vinylogous ester - Heteroaromatic compound - Amino acid or derivatives - Carboxamide group - Tertiary aliphatic amine - Tertiary amine - Secondary carboxylic acid amide - Azacycle - Oxacycle - Carboxylic acid derivative - Organoheterocyclic compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Amine - Organooxygen compound - Organic nitrogen compound - Carbonyl group - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as yohimbine alkaloids. These are alkaloids containing the pentacyclic yohimban skeleton. The Yohimbinoid alkaloids contain a carbocyclic ring E arising through C-17 to C-18 bond formation in a corynantheine precursor.

Not available