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The Korean Journal of Parasitology ; : 123-126, 2005.
Article in English | WPRIM | ID: wpr-115349

ABSTRACT

Each diastereomer of 10-thiophenyl- and 10-benzenesulfonyl-dihydroartemisinin was synthesized from artemisinin in three steps, and screened against chloroquine-resistance and chloroquine-sensitive Plasmodium falciparum. Three of the four tested compounds were found to be effective. Especially, 10 beta-benzenesulfonyl-dihydroartemisinin showed stronger antimalarial activity than artemisinin.


Subject(s)
Animals , Antimalarials/chemistry , Artemisinins/chemistry , Chloroquine/pharmacology , Drug Resistance , Plasmodium falciparum/drug effects
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