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Synthesis of oxalamide and triazine derivatives as a novel class of hybrid 4–aminoquinoline with potent antiplasmodial activity

IR@CDRI: CSIR-Central Drug Research Institute, Lucknow

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Field Value
 
Creator Sunduru, Naresh
Sharma, Moni
Srivastava, Kumkum
Rajakumar, S
Puri, S K
Saxena, J K
Chauhan, P M S
 
Date 2010-09-04T06:33:37Z
2010-09-04T06:33:37Z
2009
 
Identifier Bioorganic & Medicinal chemistry, 17(17), 2009, 6451-6462
http://hdl.handle.net/123456789/576
 
Description Frequency of malaria and its resistance to chemotherapeutic options are emerging rapidly. To counter this problem, a series of 4–aminoquinolines having oxalamide and triazine functionalities in the side chain were synthesized and screened for their antimalarial activities. Triazine derivative 48 found to be the most active against CQ sensitive strain 3D7 of plasmodium falciparum in an in vitro assay with an IC50 of 5.23 ng/mL and oxalamide derivative 13 showed an in vivo suppression of 70.45% on day 4 against CQ resistant strain N–67 of plasmodium yoelii.
 
Format 310494 bytes
application/pdf
 
Language en
 
Subject malaria
Plasmodium falciparum
antimalarial activities
plasmodium yoelii
 
Title Synthesis of oxalamide and triazine derivatives as a novel class of hybrid 4–aminoquinoline with potent antiplasmodial activity
 
Type Article