CC[C@@]1(CO)N[C@H]2C[C@]3([C@H]4C[C@@H]1[C@@H]2CO4)C(=O)NC1=C3C=CC(OC)=C1

InChIKey=VPSRFQGSFLTXAE-SQMWYMQWSA-N

C20H26N2O4

358.438

Organic compounds

Alkaloids and derivatives

Gelsemium alkaloids

Not available

Not available

Gelsemium alkaloids

Indolines Anisoles Oxepanes Alkyl aryl ethers Aralkylamines Oxanes Pyrrolidines Secondary carboxylic acid amides 1,2-aminoalcohols Amino acids and derivatives Lactams Oxacyclic compounds Dialkylamines Azacyclic compounds Dialkyl ethers Primary alcohols Organic oxides Carbonyl compounds Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

C21-norgelsemium skeleton - Indole or derivatives - Dihydroindole - Anisole - Phenol ether - Alkyl aryl ether - Oxepane - Aralkylamine - Oxane - Benzenoid - Pyrrolidine - 1,2-aminoalcohol - Amino acid or derivatives - Carboxamide group - Lactam - Secondary carboxylic acid amide - Secondary amine - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Dialkyl ether - Secondary aliphatic amine - Ether - Oxacycle - Primary alcohol - Alcohol - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Amine - Organonitrogen compound - Organooxygen 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