CNC(=O)OC1=CC2=C(C=C1)N(C)[C@H]1N(C)CC[C@@]21C.CN1CC2(C=C)C3CC4OCC3C1C2[C@@]41C(=O)NC2=CC=CC=C12

InChIKey=OIUVQDDWCVENEM-BFDSESMSSA-N

C35H43N5O4

597.76

Organic compounds

Alkaloids and derivatives

Gelsemium alkaloids

Not available

Not available

Gelsemium alkaloids

Pyrroloindoles Indoles Isoindolines Indolines Dialkylarylamines Aralkylamines Oxepanes Benzenoids Piperidines Oxanes N-alkylpyrrolidines Pyrroles Carbamate esters Trialkylamines Secondary carboxylic acid amides Lactams Dialkyl ethers Oxacyclic compounds Azacyclic compounds Carbonyl compounds Organic oxides Hydrocarbon derivatives

Not available

Gelsemium skeleton - Pyrroloindole - Indole - Indole or derivatives - Dihydroindole - Isoindoline - Isoindole or derivatives - Dialkylarylamine - Aralkylamine - Oxepane - Benzenoid - N-alkylpyrrolidine - Piperidine - Oxane - Carbamic acid ester - Pyrrolidine - Pyrrole - Amino acid or derivatives - Tertiary aliphatic amine - Tertiary amine - Secondary carboxylic acid amide - Carboxamide group - Lactam - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Dialkyl ether - Ether - Amine - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - 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