Abstract
Cinnamic acid derivatives containing a 4-amino-7-chloroquinoline scaffold (blue) and substituted cinnamoyl building blocks (green) linked through an alkylamine chain (red) were found to have potent (11-59 nM) in vitro activities against erythrocytic chloroquine- resistant Plasmodium falciparum.
Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Antimalarials / chemistry*
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Antimalarials / pharmacology*
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Chloroquine / analogs & derivatives*
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Chloroquine / pharmacology*
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Cinnamates / chemistry*
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Cinnamates / pharmacology*
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Drug Resistance
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Erythrocytes / parasitology
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Humans
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Malaria, Falciparum / drug therapy
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Plasmodium falciparum / drug effects*
Substances
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Antimalarials
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Cinnamates
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cinnamic acid
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Chloroquine