New antimalarial targets: The example of glucose transport
- 1 January 2008
- journal article
- review article
- Published by Elsevier in Travel Medicine and Infectious Disease
- Vol. 6 (1-2), 58-66
- https://doi.org/10.1016/j.tmaid.2008.01.005
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- Interaction of O-(undec-10-en)-yl-d-glucose derivatives with the Plasmodium falciparum hexose transporter (PfHT)Bioorganic & Medicinal Chemistry Letters, 2007
- High-Throughput Plasmodium falciparum Growth Assay for Malaria Drug DiscoveryAntimicrobial Agents and Chemotherapy, 2007
- Searching for New Antimalarial Therapeutics amongst Known DrugsChemical Biology & Drug Design, 2006
- Probing structure/affinity relationships for the Plasmodium falciparum hexose transporter with glucose derivativesBioorganic & Medicinal Chemistry Letters, 2006
- Inhibition of hexose transport and abrogation of pH homeostasis in the intraerythrocytic malaria parasite by an O‐3‐hexose derivativeFEBS Letters, 2004
- Comparative characterization of hexose transporters of Plasmodium knowlesi, Plasmodium yoelii and Toxoplasma gondii highlights functional differences within the apicomplexan familyBiochemical Journal, 2002
- Hexose Transport in Asexual Stages of Plasmodium falciparum and KinetoplastidaeParasitology Today, 2000
- Glucose and Lactate Kinetics in Children with Severe MalariaJournal of Clinical Endocrinology & Metabolism, 2000
- The structure of lactate dehydrogenase from Plasmodium falciparum reveals a new target for anti-malarial designNature Structural & Molecular Biology, 1996
- Sequence and Structure of a Human Glucose TransporterScience, 1985