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  • Title: Antiplasmodial activity of new 4-aminoquinoline derivatives against chloroquine resistant strain.
    Author: Sinha M, Dola VR, Agarwal P, Srivastava K, Haq W, Puri SK, Katti SB.
    Journal: Bioorg Med Chem; 2014 Jul 15; 22(14):3573-86. PubMed ID: 24906512.
    Abstract:
    Emergence and spread of multidrug resistant strains of Plasmodium falciparum has severely limited the antimalarial chemotherapeutic options. In order to overcome the obstacle, a set of new side-chain modified 4-aminoquinolines were synthesized and screened against chloroquine-sensitive (3D7) and chloroquine-resistant (K1) strains of P. falciparum. The key feature of the designed molecules is the use of methylpiperazine linked α, β(3)- and γ-amino acids to generate novel side chain modified 4-aminoquinoline analogues. Among the evaluated compounds, 20c and 30 were found more potent than CQ against K1 and displayed a four-fold and a three-fold higher activity respectively, with a good selectivity index (SI=5846 and 11,350). All synthesized compounds had resistance index between 1.06 and >14.13 as against 47.2 for chloroquine. Biophysical studies suggested that this series of compounds act on heme polymerization target.
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