2-Aryl-3H-indol-3-ones: Synthesis, electrochemical behaviour and antiplasmodial activities

• Synthesis of 2-aryl-3H-indol-3-ones via deoxygenation of indolone-N-oxides.
• Tested for antiplasmodial activity against Plasmodium falciparum.
• Electrochemical behaviour and biological activity were compared to those of N-oxides.
• Compound 7 was most active with IC50 49 nM.

The synthesis of indolone derivatives and their antiplasmodial activity in vitro against Plasmodium falciparum at the blood stage are described. The 2-aryl-3H-indol-3-ones were synthesized via deoxygenation of indolone-N-oxides. Electrochemical behaviour, antiplasmodial activity and cytotoxicity on human tumor cell lines were compared to those of indolone-N-oxides. The antiplasmodial IC50 (concentrations at 50% inhibition) of these compounds ranged between 49 and 1327 nM. Among them, the 2-(4-dimethylaminophenyl)-5-methoxy-indol-3-one, 7, had the best antiplasmodial activity in vitro (IC50 = 49 nM; FcB1 strain) and selectivity index (SI (CC50 MCF7/IC50 FcB1) = 423.4). Thus, the hits identified in this deoxygenated series correspond to their structural homologs in the N-oxide series with comparable electrochemical behaviour at the nitrogen–carbon double bond.

A series of 2-aryl-3H-indol-3-ones was synthesized via deoxygenation of indolone-N-oxides and was evaluated for in vitro activity against chloroquine-resistant strains of Plasmodium falciparum.Figure optionsDownload as PowerPoint slide