Abstract
Structural optimization of 3-hydroxy-N'-arylidenepropanehydrazonamides provided new analogs with nanomolar to subnanomolar antiplasmodial activity against asexual blood stages of Plasmodium falciparum, excellent parasite selectivity, and nanomolar activity against the earliest forms of gametocyte development. Particularly, derivatives with a 1,3-dihalo-6-trifluoromethylphenanthrene moiety showed outstanding in vivo properties and demonstrated in part curative activity in the Plasmodium berghei mouse model when administered perorally.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amides / chemical synthesis
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Amides / chemistry*
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Amides / pharmacology
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Animals
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Antimalarials / chemical synthesis
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Antimalarials / chemistry*
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Antimalarials / pharmacology
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Hep G2 Cells
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Humans
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Hydrazones / chemical synthesis
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Hydrazones / chemistry*
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Hydrazones / pharmacology
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Malaria / drug therapy*
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Malaria / parasitology
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Mice
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Phenanthrenes / chemical synthesis
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Phenanthrenes / chemistry*
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Phenanthrenes / pharmacology
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Plasmodium berghei / drug effects*
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Stereoisomerism
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Structure-Activity Relationship
Substances
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Amides
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Antimalarials
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Hydrazones
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Phenanthrenes