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      A clinical drug library screen identifies astemizole as an antimalarial agent.

      Nature chemical biology
      Animals, Antimalarials, adverse effects, metabolism, pharmacology, Astemizole, analogs & derivatives, Chloroquine, Disease Models, Animal, Dose-Response Relationship, Drug, Drug Evaluation, Preclinical, Drug Resistance, Drug Resistance, Multiple, Humans, Mice, Plasmodium falciparum, drug effects, Plasmodium yoelii

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          Abstract

          The high cost and protracted time line of new drug discovery are major roadblocks to creating therapies for neglected diseases. To accelerate drug discovery we created a library of 2,687 existing drugs and screened for inhibitors of the human malaria parasite Plasmodium falciparum. The antihistamine astemizole and its principal human metabolite are promising new inhibitors of chloroquine-sensitive and multidrug-resistant parasites, and they show efficacy in two mouse models of malaria.

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