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Citation
Tags
HERO ID
7175917
Reference Type
Journal Article
Title
Caged Garcinia Xanthones, a Novel Chemical Scaffold with Potent Antimalarial Activity
Author(s)
Ke, H; Morrisey, JM; Qu, S; Chantarasriwong, O; Mather, MW; Theodorakis, EA; Vaidya, AB; ,
Year
2017
Is Peer Reviewed?
Yes
Journal
Antimicrobial Agents and Chemotherapy
ISSN:
0066-4804
EISSN:
1098-6596
Publisher
AMER SOC MICROBIOLOGY
Location
WASHINGTON
PMID
27799215
DOI
10.1128/AAC.01220-16
Web of Science Id
WOS:000394095800013
Abstract
Caged Garcinia xanthones (CGXs) constitute a family of natural products that are produced by tropical/subtropical trees of the genus Garcinia. CGXs have a unique chemical architecture, defined by the presence of a caged scaffold at the C ring of a xanthone moiety, and exhibit a broad range of biological activities. Here we show that synthetic CGXs exhibit antimalarial activity against Plasmodium falciparum, the causative parasite of human malaria, at the intraerythrocytic stages. Their activity can be substantially improved by attaching a triphenylphosphonium group at the A ring of the caged xanthone. Specifically, CR135 and CR142 were found to be highly effective antimalarial inhibitors, with 50% effective concentrations as low as similar to 10 nM. CGXs affect malaria parasites at multiple intraerythrocytic stages, with mature stages (trophozoites and schizonts) being more vulnerable than immature rings. Within hours of CGX treatment, malaria parasites display distinct morphological changes, significant reduction of parasitemia (the percentage of infected red blood cells), and aberrant mitochondrial fragmentation. CGXs do not, however, target the mitochondrial electron transport chain, the target of the drug atovaquone and several preclinical candidates. CGXs are cytotoxic to human HEK293 cells at the low micromolar level, which results in a therapeutic window of around 150-fold for the lead compounds. In summary, we show that CGXs are potent antimalarial compounds with structures distinct from those of previously reported antimalarial inhibitors. Our results highlight the potential to further develop Garcinia natural product derivatives as novel antimalarial agents.
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