3-(n-acetyl-n-hydroxy)aminopropylphosphonic acid has been researched along with Malaria in 10 studies
*Malaria: A protozoan disease caused in humans by four species of the PLASMODIUM genus: PLASMODIUM FALCIPARUM; PLASMODIUM VIVAX; PLASMODIUM OVALE; and PLASMODIUM MALARIAE; and transmitted by the bite of an infected female mosquito of the genus ANOPHELES. Malaria is endemic in parts of Asia, Africa, Central and South America, Oceania, and certain Caribbean islands. It is characterized by extreme exhaustion associated with paroxysms of high FEVER; SWEATING; shaking CHILLS; and ANEMIA. Malaria in ANIMALS is caused by other species of plasmodia. [MeSH]
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (20.00) | 18.2507 |
2000's | 4 (40.00) | 29.6817 |
2010's | 4 (40.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Devreux, V; Jomaa, H; Van Calenbergh, S; Van der Eycken, J; Wiesner, J | 1 |
Cos, P; Maes, L; Van Calenbergh, S; Verbrugghen, T | 1 |
Bacher, A; Behrendt, C; Brücher, K; Fischer, M; Gräwert, T; Held, J; Illarionov, B; Konzuch, S; Kurz, T; Lienau, C; Maes, L; Mordmüller, B; Wittlin, S | 1 |
Calderón, F; Fernández-Álvaro, E; Hong, WD; Nixon, GL; O'Neill, PM | 1 |
DeSieno, MA; Griffin, BM; Johannes, TW; Kelleher, NL; Metcalf, WW; Thomas, PM; Zhao, H | 1 |
Beck, E; Henschker, D; Jomaa, H; Ortmann, R; Reichenberg, A; Schlitzer, M; Wiesner, J | 2 |
Altincicek, B; Beck, E; Eberl, M; Hintz, M; Jomaa, H; Lichtenthaler, HK; Sanderbrand, S; Soldati, D; Türbachova, I; Weidemeyer, C; Wiesner, J; Zeidler, J | 1 |
Ridley, RG | 1 |
Altincicek, B; Beck, E; Dreiseidler, E; Jomaa, H; Reichenberg, A; Sanderbrand, S; Schlitzer, M; Weidemeyer, C; Wiesner, J | 1 |
1 review(s) available for 3-(n-acetyl-n-hydroxy)aminopropylphosphonic acid and Malaria
Article | Year |
---|---|
Antimalarial Chemotherapy: Natural Product Inspired Development of Preclinical and Clinical Candidates with Diverse Mechanisms of Action.
Topics: Antimalarials; Biological Products; Chemistry, Pharmaceutical; Humans; Malaria; Molecular Structure | 2016 |
9 other study(ies) available for 3-(n-acetyl-n-hydroxy)aminopropylphosphonic acid and Malaria
Article | Year |
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Synthesis and evaluation of alpha,beta-unsaturated alpha-aryl-substituted fosmidomycin analogues as DXR inhibitors.
Topics: Aldose-Ketose Isomerases; Animals; Antimalarials; Chemistry, Pharmaceutical; Drug Design; Drug Evaluation, Preclinical; Enzyme Inhibitors; Fosfomycin; Inhibitory Concentration 50; Malaria; Models, Chemical; Molecular Structure; Multienzyme Complexes; Oxidoreductases; Plasmodium falciparum; Structure-Activity Relationship | 2007 |
Synthesis and evaluation of alpha-halogenated analogues of 3-(acetylhydroxyamino)propylphosphonic acid (FR900098) as antimalarials.
Topics: Acute Disease; Animals; Antimalarials; Fosfomycin; Malaria; Mice; Plasmodium berghei; Plasmodium falciparum; Structure-Activity Relationship | 2010 |
Prodrugs of reverse fosmidomycin analogues.
Topics: Animals; Antimalarials; Cell Survival; Disease Models, Animal; Dose-Response Relationship, Drug; Fosfomycin; HeLa Cells; Humans; Malaria; Mice; Mice, SCID; Molecular Structure; Plasmodium berghei; Plasmodium falciparum; Prodrugs; Structure-Activity Relationship | 2015 |
Deciphering the late biosynthetic steps of antimalarial compound FR-900098.
Topics: Antimalarials; Biosynthetic Pathways; Escherichia coli; Escherichia coli Proteins; Fosfomycin; Genes, Bacterial; Humans; Malaria | 2010 |
Acyloxyalkyl ester prodrugs of FR900098 with improved in vivo anti-malarial activity.
Topics: Animals; Antimalarials; Biological Availability; Fosfomycin; Indicators and Reagents; Lysophospholipids; Malaria; Mevalonic Acid; Mice; Mice, Inbred BALB C; Prodrugs | 2003 |
Alkoxycarbonyloxyethyl ester prodrugs of FR900098 with improved in vivo antimalarial activity.
Topics: Administration, Oral; Aldose-Ketose Isomerases; Animals; Antimalarials; Biological Availability; Dose-Response Relationship, Drug; Fosfomycin; Malaria; Mice; Mice, Inbred BALB C; Multienzyme Complexes; Oxidoreductases; Plasmodium; Prodrugs; Quantitative Structure-Activity Relationship | 2005 |
Inhibitors of the nonmevalonate pathway of isoprenoid biosynthesis as antimalarial drugs.
Topics: Aldose-Ketose Isomerases; Amino Acid Sequence; Animals; Antimalarials; Cloning, Molecular; Enzyme Inhibitors; Fosfomycin; Genes, Protozoan; Hemiterpenes; Malaria; Malaria, Falciparum; Mevalonic Acid; Mice; Molecular Sequence Data; Multienzyme Complexes; Organelles; Organophosphorus Compounds; Oxidoreductases; Pentosephosphates; Plasmodium falciparum; Recombinant Proteins; Reverse Transcriptase Polymerase Chain Reaction; Terpenes | 1999 |
Planting the seeds of new antimalarial drugs.
Topics: Aldose-Ketose Isomerases; Animals; Antimalarials; Drug Design; Enzyme Inhibitors; Fosfomycin; Hemiterpenes; Humans; Malaria; Malaria, Falciparum; Mice; Multienzyme Complexes; Organelles; Organophosphorus Compounds; Oxidoreductases; Plasmodium falciparum; Steroids; Transferases | 1999 |
Diaryl ester prodrugs of FR900098 with improved in vivo antimalarial activity.
Topics: Aldose-Ketose Isomerases; Animals; Antimalarials; Disease Models, Animal; Fosfomycin; Malaria; Mice; Multienzyme Complexes; Organophosphonates; Oxidoreductases; Plasmodium; Prodrugs; Treatment Outcome | 2001 |