Related Experiment Video
Updated: May 29, 2026

CRISPR/Cas9 Gene Editing to Make Conditional Mutants of Human Malaria Parasite P. falciparum
Published on: September 18, 2018
Reverse fosmidomycin derivatives against the antimalarial drug target IspC (Dxr)
Christoph T Behrendt1, Andrea Kunfermann, Victoria Illarionova
1Institut für Pharmazeutische und Medizinische Chemie, Heinrich Heine Universität, Universitätsstrasse 1, 40225 Düsseldorf, Germany.
Abstract:
Reverse hydroxamate-based inhibitors of IspC, a key enzyme of the non-mevalonate pathway of isoprenoid biosynthesis and a validated antimalarial target, were synthesized and biologically evaluated. The binding mode of one derivative in complex with EcIspC and a divalent metal ion was clarified by X-ray analysis. Pilot experiments have demonstrated in vivo potential.
More Related Videos
Related Concept Videos
Anthelminthic Agents
Antiprotozoal Agents

