4.7 Article

Antiplasmodial activity of novel keto-enamine chalcone-chloroquine based hybrid pharmacophores

Journal

BIOORGANIC & MEDICINAL CHEMISTRY
Volume 20, Issue 9, Pages 2971-2981

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmc.2012.03.011

Keywords

Synthesis; Quinoline; Keto-enamine; Antimalarial agents

Funding

  1. EMPOWER of CSIR-CDRI [OLP0007]
  2. CSIR
  3. ICMR

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A series of novel keto-enamine chalcone-chloroquine based hybrids were synthesized following new methodology developed in our laboratory. The synthesized compounds were screened against chloroquine sensitive strain (3D7) of Plasmodium falciparum in an in vitro model. Some of the compounds were showing comparable antimalarial activity at par with chloroquine. Compounds with significant in vitro antimalarial activity were then evaluated for their in vivo efficacy in Swiss mice against Plasmodium yoelii (chloroquine resistant N-67 strain), wherein compounds 25 and 27 each showed an in vivo suppression of 99.9% parasitaemia on day 4. Biochemical studies reveal that inhibition of hemozoin formation is the primary mechanism of action of these analogues. (C) 2012 Elsevier Ltd. All rights reserved.

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