COC1=CC2=C(C=C1)[C@]1(CC3NC[C@@]4(O[C@H]4C)[C@@H]4C[C@@H]1OC[C@H]34)C(=O)N2

InChIKey=XMZMYHAYGQPXSR-CORRHQHCSA-N

C20H24N2O4

356.422

Organic compounds

Alkaloids and derivatives

Gelsemium alkaloids

Not available

Not available

Gelsemium alkaloids

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

Aromatic heteropolycyclic compounds

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