Chemotherapy of leishmaniasis part-VIII: Synthesis and bioevaluation of novel chalcones
摘要:
Some novel dihydro-a-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 mu m/ml concentration. (C) 2008 Elsevier Masson SAS. All rights reserved.
Some novel dihydro-a-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 mu m/ml concentration. (C) 2008 Elsevier Masson SAS. All rights reserved.