Article ID Journal Published Year Pages File Type
1393734 Chemistry & Biology 2012 10 Pages PDF
Abstract

SummaryThe marine natural product symplostatin 4 (Sym4) has been recognized as a potent antimalarial agent. However, its mode of action and, in particular, direct targets have to date remained elusive. We report a chemical synthesis of Sym4 and show that Sym4-treatment of P. falciparum-infected red blood cells (RBCs) results in the generation of a swollen food vacuole phenotype and a reduction of parasitemia at nanomolar concentrations. We furthermore demonstrate that Sym4 is a nanomolar inhibitor of the P. falciparum falcipains in infected RBCs, suggesting inhibition of the hemoglobin degradation pathway as Sym4's mode of action. Finally, we reveal a critical influence of the unusual methyl-methoxypyrrolinone (mmp) group of Sym4 for potent inhibition, indicating that Sym4 derivatives with such a mmp moiety might represent viable lead structures for the development of antimalarial falcipain inhibitors.

Graphical AbstractFigure optionsDownload full-size imageDownload high-quality image (485 K)Download as PowerPoint slideHighlights► A convergent chemical synthesis of symplostatin 4 (Sym4) and Sym4 derivatives is reported ► Sym4 irreversibly inhibits malarial falcipains in infected red blood cells ► Sym4's unusual methyl-methoxypyrrolinone group is required for nanomolar inhibition of falcipains

Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
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