Chemotherapy of leishmaniasis part-VIII: Synthesis and bioevaluation of novel chalcones

Some novel dihydro-α-ionone based chalcones have been synthesized and evaluated for their in vitro antileishmanial activity in promastigote and amastigote model. Some of the compounds showed 100% inhibition at 5 and 2 μm/ml concentration.

Some novel dihydro-α-ionone based chalcones have been synthesized and evaluated for their in vitro antileishmanial activity in promastigote and amastigote model. Some of the compounds showed 100% inhibition at 5 and 2 μm/ml concentration.Figure optionsDownload as PowerPoint slide