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Antimalarial Properties of Simplified Kalihinol Analogues.


ABSTRACT: Several kalihinol natural products, members of the broader isocyanoterpene family of antimalarial agents, are potent inhibitors of Plasmodium falciparum, the agent of the most severe form of human malaria. Our previous total synthesis of kalihinol B provided a blueprint to generate many analogues within this family, some as complex as the natural product and some much simplified and easier to access. Each analogue was tested for blood-stage antimalarial activity using both drug-sensitive and -resistant P. falciparum strains. Many considerably simpler analogues of the kalihinols retained potent activity, as did a compound with a different decalin scaffold made in only three steps from sclareolide. Finally, one representative compound showed reasonable stability toward microsomal metabolism, suggesting that the isonitrile functional group that is critical for activity is not an inherent liability in these compounds.

SUBMITTER: Daub ME 

PROVIDER: S-EPMC5346982 | biostudies-literature | 2017 Mar

REPOSITORIES: biostudies-literature

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Antimalarial Properties of Simplified Kalihinol Analogues.

Daub Mary Elisabeth ME   Prudhomme Jacques J   Ben Mamoun Choukri C   Le Roch Karine G KG   Vanderwal Christopher D CD  

ACS medicinal chemistry letters 20170216 3


Several kalihinol natural products, members of the broader isocyanoterpene family of antimalarial agents, are potent inhibitors of <i>Plasmodium falciparum</i>, the agent of the most severe form of human malaria. Our previous total synthesis of kalihinol B provided a blueprint to generate many analogues within this family, some as complex as the natural product and some much simplified and easier to access. Each analogue was tested for blood-stage antimalarial activity using both drug-sensitive  ...[more]

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