Abstract
Screening our in-house compound collection using a cell based Plasmodium falciparum proliferation assay we discovered a known pan-kinase inhibitor scaffold as a hit. Further optimization of this series led us to a novel benzamide scaffold which was devoid of human kinase activity while retaining its antiplasmodial activity. The evolution of this compound series leading to optimized candidates with good cellular potency against multiple strains as well as decent in vivo profile is described in this Letter.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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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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Benzamides / chemical synthesis
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Benzamides / chemistry*
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Benzamides / pharmacology
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Directed Molecular Evolution
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Enzyme Inhibitors / chemical synthesis
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Enzyme Inhibitors / chemistry*
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Enzyme Inhibitors / pharmacology
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Humans
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Mice
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Phosphotransferases / antagonists & inhibitors*
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Plasmodium falciparum / drug effects
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Plasmodium falciparum / enzymology*
Substances
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Antimalarials
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Benzamides
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Enzyme Inhibitors
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Phosphotransferases