CCC1(CO)NC2CC3(C4CC1C2CO4)C(=O)N(OC)C1=CC=CC=C31

InChIKey=ZREVWZNVVDYUMA-UHFFFAOYSA-N

C20H26N2O4

358.438

Organic compounds

Alkaloids and derivatives

Gelsemium alkaloids

Not available

Not available

Gelsemium alkaloids

Indoles and derivatives Oxepanes Aralkylamines Oxanes Benzenoids Pyrrolidines 1,2-aminoalcohols Amino acids and derivatives Oxacyclic compounds Azacyclic compounds Dialkyl ethers Dialkylamines Organic oxides Carbonyl compounds Organopnictogen compounds Primary alcohols Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

C21-norgelsemium skeleton - Indole or derivatives - Oxepane - Aralkylamine - Oxane - Benzenoid - Pyrrolidine - Amino acid or derivatives - 1,2-aminoalcohol - Carboxylic acid derivative - Dialkyl ether - Secondary aliphatic amine - Ether - Oxacycle - Azacycle - Secondary amine - Organoheterocyclic compound - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Amine - Organooxygen compound - Carbonyl group - Primary alcohol - Alcohol - Organopnictogen compound - Organic oxide - 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