Kojic acid derived hydroxypyridinone–chloroquine hybrids: Synthesis, crystal structure, antiplasmodial activity and b-haematin inhibition
Abstract
Aminochloroquinoline–kojic acid hybrids were synthesized and evaluated for b-haematin inhibition and
antiplasmodial activity against drug resistant (K1) and sensitive (3D7) strains of Plasmodium falciparum.
Compound 7j was the most potent compound in both strains (IC50
3D7 = 0.004 lM; IC50
K1 = 0.03 lM) and had
the best b-haematin inhibition activity (0.07 IC50 equiv vs 1.91 IC50 equiv for chloroquine). One compound
8c was found to be equipotent in both strains (IC50 = 0.04 lM).
URI
http://dx.doi.org/10.1016/j.bmcl.2014.06.012http://repository.mut.ac.ke:8080/xmlui/handle/123456789/6742
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