CON1C(=O)C2(CC3C4COC2CC4C(CN3C)=CC)C2=CC=CC=C12

InChIKey=SJKRPUOXUNOPOP-UHFFFAOYSA-N

C21H26N2O3

354.45

Organic compounds

Alkaloids and derivatives

Gelsemium alkaloids

Not available

Not available

Gelsemium alkaloids

Indoles and derivatives Oxepanes Aralkylamines Piperidines Oxanes Benzenoids Trialkylamines Amino acids and derivatives Oxacyclic compounds Dialkyl ethers Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aromatic heteropolycyclic compounds

Gelsemium skeleton - Indole or derivatives - Oxepane - Aralkylamine - Oxane - Piperidine - Benzenoid - Amino acid or derivatives - Tertiary amine - Tertiary aliphatic amine - Oxacycle - Azacycle - Carboxylic acid derivative - Dialkyl ether - Ether - Organoheterocyclic compound - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organooxygen compound - Amine - Organic oxygen compound - Carbonyl group - Organic oxide - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as gelsemium alkaloids. These are alkaloids with a structure that is based on the tetracyclic gelsemium skeleton. These alkaloids contain an oxindole function and a cage-like, hydroaromatic residue which is believed to arise from an intermediate related to anhydrovobasinediol by formation of a 6,20 bond and rearrangement to an oxindole. The major alkaloids in this group are related to Gelsemine; however, a smaller group, characterized by Gelsedine, lack the 6,20 bond, and have also lost C-21.

Not available