C\C=C1/CNC2CC3(C4CC1C2CO4)C(=O)NC1=CC=CC=C31

InChIKey=YIOBXNAEUXWNQS-BIIKFXOESA-N

C19H22N2O2

310.397

Organic compounds

Alkaloids and derivatives

Gelsemium alkaloids

Not available

Not available

Gelsemium alkaloids

Indolines Oxepanes Aralkylamines Piperidines Oxanes Benzenoids Secondary carboxylic acid amides Amino acids and derivatives Lactams Oxacyclic compounds Azacyclic compounds Dialkyl ethers Dialkylamines Carbonyl compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Gelsemium skeleton - Indole or derivatives - Dihydroindole - Oxepane - Aralkylamine - Oxane - Piperidine - Benzenoid - Carboxamide group - Lactam - Amino acid or derivatives - Secondary carboxylic acid amide - Oxacycle - Carboxylic acid derivative - Dialkyl ether - Secondary aliphatic amine - Ether - Azacycle - Organoheterocyclic compound - Secondary amine - Organic nitrogen compound - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Amine - Organopnictogen compound - Carbonyl group - 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