CCC1=C[N+]([C@H]2C[C@]3([C@H]4C[C@@H]1[C@@H]2CO4)C(=O)NC1=C3C=CC(OC)=C1)=C(OCC(Cl)(Cl)Cl)O[Si](C)(C)C

InChIKey=REDULKRGAARDDI-YNBIHDICSA-O

C26H34Cl3N2O5Si

589.0

Organic compounds

Alkaloids and derivatives

Gelsemium alkaloids

Not available

Not available

Gelsemium alkaloids

Indolines Anisoles Tetrahydropyridines Oxepanes Alkyl aryl ethers Oxanes Trialkylheterosilanes Secondary carboxylic acid amides Lactams Oxacyclic compounds Azacyclic compounds Carboximidic acids and derivatives Dialkyl ethers Organic metalloid salts Alkyl chlorides Organonitrogen compounds Hydrocarbon derivatives Organochlorides Organic oxides Carbonyl compounds Organic cations

Aromatic heteropolycyclic compounds

Gelsemium skeleton - Indole or derivatives - Dihydroindole - Anisole - Phenol ether - Alkyl aryl ether - Oxepane - Tetrahydropyridine - Oxane - Benzenoid - Trialkylheterosilane - Carboxamide group - Lactam - Secondary carboxylic acid amide - Carboximidic acid derivative - Organoheterosilane - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Azacycle - Organic metalloid salt - Organoheterocyclic compound - Organohalogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic metalloid moeity - Organochloride - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Alkyl chloride - Alkyl halide - Organosilicon compound - Organic cation - 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