| Literature DB >> 17611943 |
Thomas Kurz1, Katrin Schlüter, Miriam Pein, Christoph Behrendt, Bärbel Bergmann, Rolf D Walter.
Abstract
The synthesis and in-vitro antimalarial activity of conformationally restrained bis(pivaloyloxymethyl) ester analogues of the natural product fosmidomycin is presented. In contrast to alpha-aryl-substituted analogues, conformationally restrained aromatic analogues exhibit only moderate in-vitro antimalarial activity against the chloroquine-sensitive strain 3D7 of Plasmodium falciparum. The most active derivative displays an IC(50) value of 47 microM.Entities:
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Year: 2007 PMID: 17611943 DOI: 10.1002/ardp.200700013
Source DB: PubMed Journal: Arch Pharm (Weinheim) ISSN: 0365-6233 Impact factor: 3.751