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Southeast Asian J Trop Med Public Health ; 2006 Jul; 37(4): 607-12
Article in English | IMSEAR | ID: sea-31224

ABSTRACT

Sixteen antimalarial alkoxylated and hydroxylated chalcones were tested for their ability to inhibit recombinant plasmepsin II in vitro. The best inhibitory compounds had either a chloro or dimethylamino group at the 4-position of phenyl ring A in the chalcone template. Combination of the chalcones with chloroquine showed additivity or mild antagonism of Plasmodium falciparum K1 growth in culture.


Subject(s)
Animals , Antimalarials/pharmacology , Aspartic Acid Endopeptidases/antagonists & inhibitors , Chalcones/chemistry , Chloroquine/toxicity , Inhibitory Concentration 50 , Molecular Structure , Plasmodium falciparum/drug effects
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