CON1C(=O)[C@@]2(C[C@@H]3NC[C@@]4(O[C@@H]4C)[C@@H]4C[C@@H]2OC[C@H]34)C2=C1C=C(OC)C=C2

InChIKey=VSCNFOAMCNRXFZ-DFFYWDIOSA-N

C21H26N2O5

386.448

Organic compounds

Alkaloids and derivatives

Gelsemium alkaloids

Not available

Not available

Gelsemium alkaloids

Indoles and derivatives Anisoles Oxepanes Alkyl aryl ethers Aralkylamines Piperidines Oxanes Amino acids and derivatives Oxacyclic compounds Epoxides Azacyclic compounds Dialkylamines Dialkyl ethers Carbonyl compounds Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Gelsemium skeleton - Indole or derivatives - Anisole - Phenol ether - Alkyl aryl ether - Oxepane - Aralkylamine - Oxane - Benzenoid - Piperidine - Amino acid or derivatives - Carboxylic acid derivative - Dialkyl ether - Secondary aliphatic amine - Oxirane - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Secondary amine - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organic nitrogen compound - Amine - Organic oxygen 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