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Affecting Drugs
Drug Name	PubMed Articles (year of publication)
1,2,3,4-tetrahydro-β-carboline derivative	Stereoselective preparation of pyridoxal 1,2,3,4-tetrahydro-ß-carboline derivatives and the influence of their absolute and relative configuration on the proliferation of the malaria parasite Plasmodium falciparum(2014)
1,3-trans-substituted tetrahydro-β-carboline	Stereoselective preparation of pyridoxal 1,2,3,4-tetrahydro-ß-carboline derivatives and the influence of their absolute and relative configuration on the proliferation of the malaria parasite Plasmodium falciparum(2014)
3-aminooxy-1-aminopropane	Screening of potential targets in Plasmodium falciparum using stage-specific metabolic network analysis(2015)
3-aminooxy-2-fluoropropanamine	Screening of potential targets in Plasmodium falciparum using stage-specific metabolic network analysis(2015)
8-methyl-5'-{[(z)-4-aminobut-2-enyl]methylamino}-5'-deoxyadenosine	Novel S-adenosyl-L-methionine decarboxylase inhibitors as potent antiproliferative agents against intraerythrocytic Plasmodium falciparum parasites(2013)
Butane-1,1,4,4-tetraamine	Screening of potential targets in Plasmodium falciparum using stage-specific metabolic network analysis(2015)
Butane-1,1,4-triamine	Screening of potential targets in Plasmodium falciparum using stage-specific metabolic network analysis(2015)
Butane-1,1,4-triamine	Screening of potential targets in Plasmodium falciparum using stage-specific metabolic network analysis(2015)
Cgp 40215a	3-Aminooxy-1-aminopropane and derivatives have an antiproliferative effect on cultured Plasmodium falciparum by decreasing intracellular polyamine concentrations(2005)
Cgp 48664a	3-Aminooxy-1-aminopropane and derivatives have an antiproliferative effect on cultured Plasmodium falciparum by decreasing intracellular polyamine concentrations(2005)
CGP 52622A	3-Aminooxy-1-aminopropane and derivatives have an antiproliferative effect on cultured Plasmodium falciparum by decreasing intracellular polyamine concentrations(2005)
CGP 54169A	3-Aminooxy-1-aminopropane and derivatives have an antiproliferative effect on cultured Plasmodium falciparum by decreasing intracellular polyamine concentrations(2005)
CGP40215A	The Plasmodium falciparum bifunctional ornithine decarboxylase, S-adenosyl-L-methionine decarboxylase, enables a well balanced polyamine synthesis without domain-domain interaction(2001)
CGP52622A	Comparative properties of a three-dimensional model of Plasmodium falciparum ornithine decarboxylase(2003)
CGP52623A	The Plasmodium falciparum bifunctional ornithine decarboxylase, S-adenosyl-L-methionine decarboxylase, enables a well balanced polyamine synthesis without domain-domain interaction(2001)
CGP54169A	Comparative properties of a three-dimensional model of Plasmodium falciparum ornithine decarboxylase(2003) Screening of potential targets in Plasmodium falciparum using stage-specific metabolic network analysis(2015)
difluoromethyl ornithine	Comparative properties of a three-dimensional model of Plasmodium falciparum ornithine decarboxylase(2003) Screening of potential targets in Plasmodium falciparum using stage-specific metabolic network analysis(2015)
Mdl 73811	Effect of drugs inhibiting spermidine biosynthesis and metabolism on the in vitro development of Plasmodium falciparum(2001) Antimalarial drug targets in Plasmodium falciparum predicted by stage-specific metabolic network analysis(2010)
Mdl-73811	Irreversible inhibition of S-adenosylmethionine decarboxylase in Plasmodium falciparum-infected erythrocytes: growth inhibition in vitro(1991)
Molecular charcterization, suggested target	In the human malaria parasite Plasmodium falciparum, polyamines are synthesized by a bifunctional ornithine decarboxylase, S-adenosylmethionine decarboxylase(2000)
O-(3-Amino-2-fluoropropyl)hydroxylamine	Screening of potential targets in Plasmodium falciparum using stage-specific metabolic network analysis(2015)
ornithine	Screening of potential targets in Plasmodium falciparum using stage-specific metabolic network analysis(2015)
putrescine	The Plasmodium falciparum bifunctional ornithine decarboxylase, S-adenosyl-L-methionine decarboxylase, enables a well balanced polyamine synthesis without domain-domain interaction(2001)