Results 31 to 40 of about 1,660 (188)
Background The study investigated the pharmacokinetics of fosmidomycin when given alone and in combination with clindamycin in patients with acute uncomplicated falciparum malaria. Methods A total of 15 and 18 patients with acute uncomplicated Plasmodium
Chauemung Anurak +4 more
doaj +1 more source
Pharmacokinetics of fosmidomycin, a new phosphonic acid antibiotic [PDF]
The pharmacokinetics of fosmidomycin was investigated in animals and humans after parenteral and oral dosing. In dogs the serum concentration was 54.8 microgram/ml at 0.25 h after an intravenous dose of 20 mg/kg, and the half-life was 1.14 h. Peak concentration was 41.4 microgram/ml after an intramuscular dose of 20 mg/kg and 16.6 microgram/ml after an
T, Murakawa +4 more
openaire +2 more sources
Exploring the Translational Gap of a Novel Class of Escherichia coli IspE Inhibitors
Challenges in the discovery of selective IspE inhibitors with antibacterial activity and no toxicity: This work sheds light on the molecular properties for balancing enzymatic target and bacterial activities simultaneously as well as new starting points for the development of IspE inhibitors with a predicted new mode of action.
Henni‐Karoliina Ropponen +9 more
wiley +1 more source
Optimization synthesis of phosphorous-containing natural products fosmidomycin and FR900098
Fosmidomycin and its acetyl analogue FR900098 are two phosphorus-containing natural products with inhibitory activity against IspC enzyme in the 2-C-methyl-D-erythritol 4-phosphate (MEP) pathway of isoprenoid biosynthesis in plants and most bacteria ...
Aidong Zhang (87588) +4 more
core +1 more source
Tackling Soil ARG‐Carrying Pathogens with Global‐Scale Metagenomics
The ultimate risk of antibiotic abuse is the spread of antibiotic resistance genes (ARGs) into pathogens. This work reveals that soilborne AP diversity is driven by human activities, climatic variables, and physicochemical properties at the global scale. Specifically, agricultural land has the highest AP richness.
Binhao Wang +11 more
wiley +1 more source
SYNTHESIS AND EVALUATION OF FOSMIDOMYCIN ANALOGUES AS ANTIMALARIAL AGENTS
This Ph.D. study constitutes part of an extensive project dealing with the design and development of new agents with antimalarial activity. The enzyme 1-deoxy-D-xylulose-5-phosphate reductoisomerase (DXR), which is involved in the DOXP pathway for isoprenoid synthesis, was chosen as drug target.
Haemers, Timothy
openaire +3 more sources
Durch Kombination von Tandem‐Massenspektrometrie und Isotopenmarkierung wurde 2‐Methylthio‐1,N6‐ethenoadenosin (ms2ϵA) als neue Nukleosid‐Spezies in bakterieller transfer‐RNA (tRNA) identifiziert. Das seltene Vorkommen auf tRNAs, insbesondere wenn diese in die Translation involviert sind, sowie strukturelle und metabolische Ähnlichkeiten zur bekannten ...
Larissa Bessler +8 more
wiley +1 more source
Boron-Containing Analogs of Fosmidomycin: Benzoxaborole Derivatives Exhibit Promising Activity Against Resistant Pathogens [PDF]
James M. Gamrat +9 more
doaj +2 more sources
Fosmidomycin-induced metabolic imbalance is relieved by mutations in GAPDH.
(A) Schematic showing metabolites upstream and downstream of GAPDH function. Abundance ratios (FSM + / FSM -) are displayed for parent (par) and mutant (mut) strains.
Naomi Ghebremichael (9578319) +6 more
core +1 more source
A New Bacterial Adenosine‐Derived Nucleoside as an Example of RNA Modification Damage
Tandem mass spectrometry combined with stable isotope labelling identified a new nucleoside species, namely 2‐methylthio‐1,N6‐ethenoadenosine (ms2ϵA), in bacterial transfer RNA (tRNA). Its rare occurrence on tRNA, especially when involved in translation, and the structural as well as metabolic relation to the known tRNA modification 2‐methylthio‐N6 ...
Larissa Bessler +8 more
wiley +1 more source

