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Abbreviations
ACT: artemisinin-based combination therapy
CG: cycloguanil
CLint: intrinsic clearance
CQ: chloroquine
DDU: Drug Discovery Unit
EC50 : half maximal effective concentration
ED90 : 90% effective dose
GSK: GlaxoSmithKline
hERG: human ether-à-go-go-related gene
HLM: human liver microsome
IC50: half maximal inhibitory concentration
i.p.: intraperitoneally
IVIEWGA: in vitro evolution and whole-genome analysis
IVIVC: in vitro-in vivo correlation
MLEM: Model List of Essential Medicines
MLM: mouse liver microsome
MMV: Medicines for Malaria Venture
MoA: mode/mechanism of action
mRNA: messenger ribonucleic acid
MTX: methotrexate
OSM: Open Source Malaria
P.: Plasmodium
p.o.: (per os) orally
Pb: Plasmodium berghei
Pc: Plasmodium cynomolgi
Pf: Plasmodium falciparum
Pf ATP4: Plasmodium falciparum ATPase transporter
Pf CARL: Plasmodium falciparum cyclic amine resistance locus
Pf CPSF3: Plasmodium falciparum cleavage and polyadenylation specificity factor
Pf DHFR: Plasmodium falciparum dihydrofolate reductase
Pf DHODH: Plasmodium falciparum dihydroorotate dehydrogenase
Pf eEF2: Plasmodium falciparum translational elongation factor 2
Pf PI3K: Plasmodium falciparum phosphatidylinositol-3-kinase
Pf PI4K: Plasmodium falciparum phosphatidylinositol-4-OH kinase
Py : Plasmodium yoelli
PYR: pyrimethamine
q.d.: (quaque die) one a day
RCQ(s): reversed chloroquine(s)
SAR: structure-activity relationship
SCID: severe combined immunodeficiency
STPHI: Swiss Tropical and Public Health Institute
TAP: triaminopyrimidine
TQ: tafenoquine
tRNA: transfer ribonucleic acid
WHO: World Health Organization
Keywords: Malaria, Plasmodium, Mechanism of action, Drug discovery, Drug development
Original online version of this article (DOI: 10.1186/s12936-019-2724-z).