<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"><channel><title>acetohydroxamic acid</title><link>http://www.unboundmedicine.com/medline/ebm/research/acetohydroxamic_acid</link><description>Unbound MEDLINE is a service provided by Unbound Medicine, Inc. that includes data and services from the U.S. National Library of Medicine's MEDLINE® and PubMed® databases.</description><language>en-us</language><copyright>Unbound Medicine, Inc.</copyright><item><title>Redox Reactions of Pu(IV) and Pu(III) in the Presence of Acetohydroxamic Acid in HNO(3) Solutions.</title><link>http://www.unboundmedicine.com/medline/ebm/record/19904974/full_citation/Redox_Reactions_of_Pu_IV__and_Pu_III__in_the_Presence_of_Acetohydroxamic_Acid_in_HNO_3__Solutions_</link><description>Tkac P, Precek M, Paulenova A <br/><span class="title">Redox Reactions of Pu(IV) and Pu(III) in the Presence of Acetohydroxamic Acid in HNO(3) Solutions. [JOURNAL ARTICLE]</span><br/><span class="source" title="Inorganic chemistry">Inorg Chem 2009 Nov 11.</span><br/> <a href="http://www.unboundmedicine.com/medline/ebm/record/19904974/abstract/Redox_Reactions_of_Pu_IV__and_Pu_III__in_the_Presence_of_Acetohydroxamic_Acid_in_HNO_3__Solutions_">Abstract</a> | <a href="http://www.unboundmedicine.com/medline/ebm/record/19904974/full_citation/Redox_Reactions_of_Pu_IV__and_Pu_III__in_the_Presence_of_Acetohydroxamic_Acid_in_HNO_3__Solutions_">Full Citation</a> | <a rel="nofollow" href="http://www.unboundmedicine.com/medline/ebm/related/19904974/Redox_Reactions_of_Pu_IV__and_Pu_III__in_the_Presence_of_Acetohydroxamic_Acid_in_HNO_3__Solutions_">Find Related Articles</a> </description></item><item><title>Synthesis, molecular docking and biological evaluation of metronidazole derivatives as potent Helicobacter pylori urease inhibitors.</title><link>http://www.unboundmedicine.com/medline/ebm/record/19804978/full_citation/Synthesis_molecular_docking_and_biological_evaluation_of_metronidazole_derivatives_as_potent_Helicobacter_pylori_urease_inhibitors_</link><description>Mao WJ, Lv PC, Shi L, et al. <br/><span class="title">Synthesis, molecular docking and biological evaluation of metronidazole derivatives as potent Helicobacter pylori urease inhibitors. [JOURNAL ARTICLE]</span><br/><span class="source" title="Bioorganic &amp; medicinal chemistry">Bioorg Med Chem 2009 Sep 15.</span><br/> <a href="http://www.unboundmedicine.com/medline/ebm/record/19804978/abstract/Synthesis_molecular_docking_and_biological_evaluation_of_metronidazole_derivatives_as_potent_Helicobacter_pylori_urease_inhibitors_">Abstract</a> | <a href="http://www.unboundmedicine.com/medline/ebm/record/19804978/full_citation/Synthesis_molecular_docking_and_biological_evaluation_of_metronidazole_derivatives_as_potent_Helicobacter_pylori_urease_inhibitors_">Full Citation</a> | <a rel="nofollow" href="http://www.unboundmedicine.com/medline/ebm/related/19804978/Synthesis_molecular_docking_and_biological_evaluation_of_metronidazole_derivatives_as_potent_Helicobacter_pylori_urease_inhibitors_">Find Related Articles</a> </description></item><item><title>Novel half-sandwich Ru(II)-hydroxamate complexes: synthesis, characterization and equilibrium study in aqueous solution.</title><link>http://www.unboundmedicine.com/medline/ebm/record/19771370/full_citation/Novel_half_sandwich_Ru_II__hydroxamate_complexes:_synthesis_characterization_and_equilibrium_study_in_aqueous_solution_</link><description>Buglyó P, Farkas E <br/><span class="title">Novel half-sandwich Ru(II)-hydroxamate complexes: synthesis, characterization and equilibrium study in aqueous solution. [Journal Article, Research Support, Non-U.S. Gov't]</span><br/><span class="source" title="Dalton transactions (Cambridge, England : 2003)">Dalton Trans 2009 Oct 14; (38):8063-70.</span><br/> <a href="http://www.unboundmedicine.com/medline/ebm/record/19771370/abstract/Novel_half_sandwich_Ru_II__hydroxamate_complexes:_synthesis_characterization_and_equilibrium_study_in_aqueous_solution_">Abstract</a> | <a href="http://www.unboundmedicine.com/medline/ebm/record/19771370/full_citation/Novel_half_sandwich_Ru_II__hydroxamate_complexes:_synthesis_characterization_and_equilibrium_study_in_aqueous_solution_">Full Citation</a> | <a href="http://dx.doi.org/10.1039/b908173a">Publisher Full Text</a> | <a rel="nofollow" href="http://www.unboundmedicine.com/medline/ebm/related/19771370/Novel_half_sandwich_Ru_II__hydroxamate_complexes:_synthesis_characterization_and_equilibrium_study_in_aqueous_solution_">Find Related Articles</a> </description></item><item><title>Reactive oxygen species and lipoxygenases regulate the oncogenicity of NPM-ALK-positive anaplastic large cell lymphomas.</title><link>http://www.unboundmedicine.com/medline/ebm/record/19503098/full_citation/Reactive_oxygen_species_and_lipoxygenases_regulate_the_oncogenicity_of_NPM_ALK_positive_anaplastic_large_cell_lymphomas_</link><description>Thornber K, Colomba A, Ceccato L, et al. <br/><span class="title">Reactive oxygen species and lipoxygenases regulate the oncogenicity of NPM-ALK-positive anaplastic large cell lymphomas. [JOURNAL ARTICLE]</span><br/><span class="source" title="Oncogene">Oncogene 2009 Jun 8.</span><br/> <a href="http://www.unboundmedicine.com/medline/ebm/record/19503098/abstract/Reactive_oxygen_species_and_lipoxygenases_regulate_the_oncogenicity_of_NPM_ALK_positive_anaplastic_large_cell_lymphomas_">Abstract</a> | <a href="http://www.unboundmedicine.com/medline/ebm/record/19503098/full_citation/Reactive_oxygen_species_and_lipoxygenases_regulate_the_oncogenicity_of_NPM_ALK_positive_anaplastic_large_cell_lymphomas_">Full Citation</a> | <a rel="nofollow" href="http://www.unboundmedicine.com/medline/ebm/related/19503098/Reactive_oxygen_species_and_lipoxygenases_regulate_the_oncogenicity_of_NPM_ALK_positive_anaplastic_large_cell_lymphomas_">Find Related Articles</a> </description></item><item><title>Structure-Activity Relationship Analysis of the Peptide Deformylase Inhibitor 5-Bromo-1H-indole-3-acetohydroxamic Acid.</title><link>http://www.unboundmedicine.com/medline/ebm/record/19053131/full_citation/Structure_Activity_Relationship_Analysis_of_the_Peptide_Deformylase_Inhibitor_5_Bromo_1H_indole_3_acetohydroxamic_Acid_</link><description>Petit S, Duroc Y, Larue V, et al. <br/><span class="title">Structure-Activity Relationship Analysis of the Peptide Deformylase Inhibitor 5-Bromo-1H-indole-3-acetohydroxamic Acid. [JOURNAL ARTICLE]</span><br/><span class="source" title="ChemMedChem">ChemMedChem 2008 Dec 3.</span><br/> <a href="http://www.unboundmedicine.com/medline/ebm/record/19053131/abstract/Structure_Activity_Relationship_Analysis_of_the_Peptide_Deformylase_Inhibitor_5_Bromo_1H_indole_3_acetohydroxamic_Acid_">Abstract</a> | <a href="http://www.unboundmedicine.com/medline/ebm/record/19053131/full_citation/Structure_Activity_Relationship_Analysis_of_the_Peptide_Deformylase_Inhibitor_5_Bromo_1H_indole_3_acetohydroxamic_Acid_">Full Citation</a></description></item><item><title>Dihydroxamate based siderophore model, piperazine-1,4-bis-(N-methyl-acetohydroxamic acid (PIPDMAHA), as a chelating agent of molybdenum(VI).</title><link>http://www.unboundmedicine.com/medline/ebm/record/18968698/full_citation/Dihydroxamate_based_siderophore_model_piperazine_14_bis__N_methyl_acetohydroxamic_acid__PIPDMAHA__as_a_chelating_agent_of_molybdenum_VI__</link><description>Farkas E, Csóka H, Gama S, et al. <br/><span class="title">Dihydroxamate based siderophore model, piperazine-1,4-bis-(N-methyl-acetohydroxamic acid (PIPDMAHA), as a chelating agent of molybdenum(VI). [Journal Article]</span><br/><span class="source" title="Talanta">Talanta 2002 Jul 3; 57(5):935-43.</span><br/> <a href="http://www.unboundmedicine.com/medline/ebm/record/18968698/abstract/Dihydroxamate_based_siderophore_model_piperazine_14_bis__N_methyl_acetohydroxamic_acid__PIPDMAHA__as_a_chelating_agent_of_molybdenum_VI__">Abstract</a> | <a href="http://www.unboundmedicine.com/medline/ebm/record/18968698/full_citation/Dihydroxamate_based_siderophore_model_piperazine_14_bis__N_methyl_acetohydroxamic_acid__PIPDMAHA__as_a_chelating_agent_of_molybdenum_VI__">Full Citation</a> | <a rel="nofollow" href="http://www.unboundmedicine.com/medline/ebm/related/18968698/Dihydroxamate_based_siderophore_model_piperazine_14_bis__N_methyl_acetohydroxamic_acid__PIPDMAHA__as_a_chelating_agent_of_molybdenum_VI__">Find Related Articles</a> </description></item><item><title>Enzymatic, immunological and phylogenetic characterization of Brucella suis urease.</title><link>http://www.unboundmedicine.com/medline/ebm/record/18638408/full_citation/Enzymatic_immunological_and_phylogenetic_characterization_of_Brucella_suis_urease_</link><description>Contreras-Rodriguez A, Quiroz-Limon J, Martins AM, et al. <br/><span class="title">Enzymatic, immunological and phylogenetic characterization of Brucella suis urease. [JOURNAL ARTICLE]</span><br/><span class="source" title="BMC microbiology">BMC Microbiol 2008 Jul 19; 8(1):121.</span><br/> <a href="http://www.unboundmedicine.com/medline/ebm/record/18638408/abstract/Enzymatic_immunological_and_phylogenetic_characterization_of_Brucella_suis_urease_">Abstract</a> | <a href="http://www.unboundmedicine.com/medline/ebm/record/18638408/full_citation/Enzymatic_immunological_and_phylogenetic_characterization_of_Brucella_suis_urease_">Full Citation</a> | <a rel="nofollow" href="http://www.unboundmedicine.com/medline/ebm/related/18638408/Enzymatic_immunological_and_phylogenetic_characterization_of_Brucella_suis_urease_">Find Related Articles</a> </description></item><item><title>Amines and oximes derived from deoxybenzoins as Helicobacter pylori urease inhibitors.</title><link>http://www.unboundmedicine.com/medline/ebm/record/18625539/full_citation/Amines_and_oximes_derived_from_deoxybenzoins_as_Helicobacter_pylori_urease_inhibitors_</link><description>Li HQ, Xiao ZP, Yin-Luo , et al. <br/><span class="title">Amines and oximes derived from deoxybenzoins as Helicobacter pylori urease inhibitors. [JOURNAL ARTICLE]</span><br/><span class="source" title="European journal of medicinal chemistry">Eur J Med Chem 2008 Jun 11.</span><br/> <a href="http://www.unboundmedicine.com/medline/ebm/record/18625539/abstract/Amines_and_oximes_derived_from_deoxybenzoins_as_Helicobacter_pylori_urease_inhibitors_">Abstract</a> | <a href="http://www.unboundmedicine.com/medline/ebm/record/18625539/full_citation/Amines_and_oximes_derived_from_deoxybenzoins_as_Helicobacter_pylori_urease_inhibitors_">Full Citation</a> | <a rel="nofollow" href="http://www.unboundmedicine.com/medline/ebm/related/18625539/Amines_and_oximes_derived_from_deoxybenzoins_as_Helicobacter_pylori_urease_inhibitors_">Find Related Articles</a> </description></item><item><title>Reduction of Pertechnetate by Acetohydroxamic Acid: Formation of [Tc(II)(NO)(AHA)2(H2O)](+) and Implications for the UREX Process.</title><link>http://www.unboundmedicine.com/medline/ebm/record/18597420/full_citation/Reduction_of_Pertechnetate_by_Acetohydroxamic_Acid:_Formation_of_[Tc_II__NO__AHA_2_H2O_]_+__and_Implications_for_the_UREX_Process_</link><description>Gong CM, Lukens WW, Poineau F, et al. <br/><span class="title">Reduction of Pertechnetate by Acetohydroxamic Acid: Formation of [Tc(II)(NO)(AHA)2(H2O)](+) and Implications for the UREX Process. [JOURNAL ARTICLE]</span><br/><span class="source" title="Inorganic chemistry">Inorg Chem 2008 Jul 2.</span><br/> <a href="http://www.unboundmedicine.com/medline/ebm/record/18597420/abstract/Reduction_of_Pertechnetate_by_Acetohydroxamic_Acid:_Formation_of_[Tc_II__NO__AHA_2_H2O_]_+__and_Implications_for_the_UREX_Process_">Abstract</a> | <a href="http://www.unboundmedicine.com/medline/ebm/record/18597420/full_citation/Reduction_of_Pertechnetate_by_Acetohydroxamic_Acid:_Formation_of_[Tc_II__NO__AHA_2_H2O_]_+__and_Implications_for_the_UREX_Process_">Full Citation</a> | <a rel="nofollow" href="http://www.unboundmedicine.com/medline/ebm/related/18597420/Reduction_of_Pertechnetate_by_Acetohydroxamic_Acid:_Formation_of_[Tc_II__NO__AHA_2_H2O_]_+__and_Implications_for_the_UREX_Process_">Find Related Articles</a> </description></item><item><title>Immobilised metal affinity chromatography for the capture of hydroxamate-containing siderophores and other Fe(III)-binding metabolites directly from bacterial culture supernatants.</title><link>http://www.unboundmedicine.com/medline/ebm/record/18575639/full_citation/Immobilised_metal_affinity_chromatography_for_the_capture_of_hydroxamate_containing_siderophores_and_other_Fe_III__binding_metabolites_directly_from_bacterial_culture_supernatants_</link><description>Braich N, Codd R <br/><span class="title">Immobilised metal affinity chromatography for the capture of hydroxamate-containing siderophores and other Fe(III)-binding metabolites directly from bacterial culture supernatants. [Journal Article, Research Support, Non-U.S. Gov't]</span><br/><span class="source" title="The Analyst">Analyst 2008 Jul; 133(7):877-80.</span><br/> <a href="http://www.unboundmedicine.com/medline/ebm/record/18575639/abstract/Immobilised_metal_affinity_chromatography_for_the_capture_of_hydroxamate_containing_siderophores_and_other_Fe_III__binding_metabolites_directly_from_bacterial_culture_supernatants_">Abstract</a> | <a href="http://www.unboundmedicine.com/medline/ebm/record/18575639/full_citation/Immobilised_metal_affinity_chromatography_for_the_capture_of_hydroxamate_containing_siderophores_and_other_Fe_III__binding_metabolites_directly_from_bacterial_culture_supernatants_">Full Citation</a> | <a href="http://dx.doi.org/10.1039/b802355g">Publisher Full Text</a> | <a rel="nofollow" href="http://www.unboundmedicine.com/medline/ebm/related/18575639/Immobilised_metal_affinity_chromatography_for_the_capture_of_hydroxamate_containing_siderophores_and_other_Fe_III__binding_metabolites_directly_from_bacterial_culture_supernatants_">Find Related Articles</a> </description></item></channel></rss>