Study ID Study Title Species Institute
ST000414Metabolomics-based screening of the Malaria Box reveals both novel and established mechanisms of actionPlasmodium falciparumMonash Institute of Pharmaceutical Sciences
ST000441Metabolomic Profiling of the Malaria Box Reveals Antimalarial Target PathwaysPlasmodium falciparumPennsylvania State University
ST000546Multi-omics based identification of specific biochemical changes associated with PfKelch13-mutant artemisinin resistant PlasmodiumPlasmodium falciparumMonash University
ST000817Dynamics of metabolism, proliferation and differentiation in Toxoplasma gondii mutants deficient in glycolysis and gluconeogenesisToxoplasma gondiiCSIR-National Chemical Laboratory
ST001033Determination of mode of action of anti-malalrial drugs using untargeted metabolomicsPlasmodium falciparumMonash University
ST001149Plasmodium Niemann-Pick Type C1-Related Protein is a Druggable Target Required for Parasite Membrane HomeostasisPlasmodium falciparumPennsylvania State University
ST001175Multi-omics analysis demonstrates unique mode of action of a potent new antimalarial compound, JPC-3210, against Plasmodium falciparumPlasmodium falciparumMonash University
ST001188P. falciparum infected erythrocytesPlasmodium falciparumUniversity of Melbourne
ST001201Peroxide antimalarial treatment timecourse on trophozoite-stage P. falciparum parasitesPlasmodium falciparumMonash University
ST001202Peroxide antimalarial treatment timecourse on ring-stage P. falciparum parasitesPlasmodium falciparumMonash University
ST001204Peroxide antimalarial extended treatment timecourse on trophozoite-stage P. falciparum parasitesPlasmodium falciparumMonash University
ST001205Peroxide antimalarial treatment of K13-mutant and -wildtype P. falciparum parasitesPlasmodium falciparumMonash University
ST001232Combining stage - specificity and metabolomic profiling to advance drug discovery for malariaPlasmodium falciparumPennsylvania State University
ST001238P falciparum asexual metabolomics following drug treatment (part-I)Plasmodium falciparumPennsylvania State University
ST001274Metabolomics-based profiling of the mode of action of Pathogen Box compounds in Trypanosoma brucei (part-I)Trypanosoma bruceiMonash University
ST001275Metabolomics-based profiling of the mode of action of Pathogen Box compounds in Trypanosoma brucei (part-II)Trypanosoma bruceiMonash University
ST001276Development and Characterisation of a Novel Class of Aroyl Guanidine Containing Anti-Trypanosomal CompoundsTrypanosoma bruceiMonash University
ST001279K13 mutations driving artemisinin resistance rewrite Plasmodium falciparum’s programmed intra-erythrocytic development and transform mitochondrial physiologyPlasmodium falciparumPennsylvania State University
ST001304Multi-omics analysis delineates the distinct functions of sub-cellular acetyl-CoA pools in Toxoplasma gondiiToxoplasma gondiiMonash University
ST001315Retargeting azithromycin-like compounds as antimalarials with dual modalityPlasmodium falciparumMonash University
ST001652Atypical Molecular Basis for Drug Resistance to Mitochondrial AQ: A Function Inhibitors in Plasmodium falciparumPlasmodium falciparumU.S. Food & Drug Administration
ST001660Plasmodium falciparum metabolomics as a result of treatment with putative acetyl-CoA synthetase inhibitorsPlasmodium falciparumPennsylvania State University
ST001822The RNA-binding protein RBP42 regulates cellular energy metabolism in mammalian-infective Trypanosoma bruceiTrypanosoma bruceiRutgers University
ST001878Targeted analysis of Babesia divergens merozoitesBlood parasiteUniversidad CEU San Pablo
ST001985Profiling Plasmodium falciparum parasites and human red blood cells after treatment with MMV693183Plasmodium falciparumPennsylvania State University
ST002011The anticancer human mTOR inhibitor MLN0128/Sapanisertib with potent multistage in vitro antiplasmodium activity and in vivo antimalarial efficacy in a humanised mouse model is an inhibitor of multiple Plasmodium falciparum kinases.Plasmodium falciparumPennsylvania State University
ST002024Plasmodium falciparum stable-isotope carbon labeling to explore metabolic consequences of keto–acid dehydrogenase disruptionPlasmodium falciparumPennsylvania State University
ST002051The apicomplexan parasite Toxoplasma gondii forms bradyzoite-containing tissue cysts that cause chronic and drug-tolerant infections.Toxoplasma gondiiRobert Koch-Institute
ST002053Resistance to NaFAc of in vitro maturated Toxoplasma gondii bradyzoites in human myotubes.Toxoplasma gondiiRobert Koch-Institute
ST002078Multiple modes of interfering with the activity of Plasmodium falciparum cytoplasmic isoleucyl-tRNA synthetase illustrate the enzyme is a promising antimalarial target.Plasmodium falciparumPennsylvania State University
ST002106Genetic and chemical validation of Plasmodium falciparum aminopeptidase PfA-M17 as a drug target in the hemoglobin digestion pathway (Part 1)Plasmodium falciparumMonash University
ST002107Genetic and chemical validation of Plasmodium falciparum aminopeptidase PfA-M17 as a drug target in the hemoglobin digestion pathway (Part 2)Plasmodium falciparumMonash University
ST002108Genetic and chemical validation of Plasmodium falciparum aminopeptidase PfA-M17 as a drug target in the hemoglobin digestion pathway (Part 3)Plasmodium falciparumMonash University
ST002181Piperaquine-resistant PfCRT mutations differentially impact drug transport, hemoglobin catabolism and parasite physiology in Plasmodium falciparum asexual blood stages.Plasmodium falciparumPennsylvania State University
ST002309Targeting malaria parasites with novel derivatives of azithromycinPlasmodium falciparumMonash University
ST002698Systemic host inflammation induces stage-specific transcriptomic modification and slower maturation in malaria parasitesPlasmodium bergheiPeter Doherty Institute for Infection and Immunity
ST002792Chemoproteomics validates selective targeting of Plasmodium M1 alanyl aminopeptidase as a cross-species strategy to treat malariaPlasmodium falciparumMonash University
ST002926Multi-“omics” analysis reveals the orphan P. falciparum protein kinase PfPK8 regulates multi-gene family expression Plasmodium falciparumMonash University
ST003144On-target, dual aminopeptidase inhibition provides cross-species antimalarial activityPlasmodium falciparumMonash University
ST003160New class of heterospirocyclic compounds present strong and rapid activity against artemisinin- and multidrug-resistant P. falciparum parasitesPlasmodium falciparumMonash University

Return to search page
  logo