Works matching DE "ACETOHYDROXAMIC acid"
Results: 21
Kinetic characterization of 4,4′-biphenylsulfonamides as selective non-zinc binding MMP inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2015, v. 30, n. 6, p. 947, doi. 10.3109/14756366.2014.1000889
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Should metabolic evaluation be performed in patients with struvite stones?
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- Urolithiasis, 2017, v. 45, n. 2, p. 185, doi. 10.1007/s00240-016-0893-6
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Kinetic and thermodynamic characterization of C-N bond rotation by N-methylacetohydroxamic acid in aqueous media.
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- Magnetic Resonance in Chemistry, 2016, v. 54, n. 1, p. 46, doi. 10.1002/mrc.4318
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Kinetics of reductive stripping of Np(VI) by acetohydroxamic acid from 30%TBP/kerosene to nitrate medium using a high-speed stirred cell.
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- Radiochimica Acta, 2015, v. 103, n. 9, p. 627, doi. 10.1515/ract-2014-2375
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Investigations of actinides in the context of final disposal of high-level radioactive waste: trivalent actinides in aqueous solution.
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- Journal of Radioanalytical & Nuclear Chemistry, 2014, v. 300, n. 1, p. 177, doi. 10.1007/s10967-014-3010-8
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An improved PUREX process in technetium separation by stepwise reduction.
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- Journal of Radioanalytical & Nuclear Chemistry, 2014, v. 299, n. 3, p. 1329, doi. 10.1007/s10967-013-2888-x
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Purification of uranium product from plutonium contamination using acetohydroxamic acid (AHA) based process.
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- Journal of Radioanalytical & Nuclear Chemistry, 2013, v. 295, n. 1, p. 191, doi. 10.1007/s10967-012-1855-2
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New data on decomposition of nitric solutions of acetohydroxamic acid.
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- Journal of Radioanalytical & Nuclear Chemistry, 2012, v. 291, n. 3, p. 649, doi. 10.1007/s10967-011-1189-5
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Synthesis, inhibitory activity and molecular docking studies of two Cu(II) complexes against Helicobacter pylori urease.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2012, v. 27, n. 4, p. 528, doi. 10.3109/14756366.2011.599065
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Thermodynamics and Kinetics of Reduction of Fe(III) Acetohydroxamic Acid Complex by Ascorbic Acid.
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- Pakistan Journal of Scientific & Industrial Research Series A: Physical Sciences, 2018, v. 61, n. 1, p. 8
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Pathological effects of vanillic acid on urinary tract in rats with infectious calculi.
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- Journal of Hainan Medical University, 2020, v. 26, n. 8, p. 12
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A kinetic study of the oxidation of hydroxamic acids by compounds I and II of horseradish peroxidase: Effect of transition metal ions.
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- Journal of Coordination Chemistry, 2018, v. 71, n. 11-13, p. 1728, doi. 10.1080/00958972.2018.1493200
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Synthesis, Crystal Structures, Molecular Docking, and Urease Inhibitory Activity of Transition Metal Complexes with 2-[4-(4-Fluorophenyl)piperazin-1-yl]acetic Acid.
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- Acta Chimica Slovenica, 2016, v. 63, n. 1, p. 165, doi. 10.17344/acsi.2015.2109
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Acetamide hydrolyzing activity of Bacillus megaterium F-8 with bioremediation potential: Optimization of production and reaction conditions.
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- Environmental Science & Pollution Research, 2014, v. 21, n. 14, p. 8822, doi. 10.1007/s11356-014-2818-7
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Resistance to AHAS inhibitor herbicides: current understanding.
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- Pest Management Science, 2014, v. 70, n. 9, p. 1340, doi. 10.1002/ps.3710
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Kinetics and Mechanism of Reduction of Fe(III)-Acetohydroxamic Acid by Hydroxylamine Hydrochloride at Acidic pH.
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- Pakistan Journal of Chemistry, 2015, v. 5, n. 1, p. 8, doi. 10.15228/2015.v05.i01.p02
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Inhibition of urease activity in the urinary tract pathogen Staphylococcus saprophyticus.
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- Letters in Applied Microbiology, 2014, v. 58, n. 1, p. 31, doi. 10.1111/lam.12153
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Green synthesis of acetohydroxamic acid by thermophilic amidase of Bacillus smithii IIIMB2907.
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- Indian Journal of Biochemistry & Biophysics, 2019, v. 56, n. 5, p. 373
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Morphological changes in Proteus mirabilis O18 biofilm under the influence of a urease inhibitor and a homoserine lactone derivative.
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- Archives of Microbiology, 2014, v. 196, n. 3, p. 169, doi. 10.1007/s00203-014-0952-8
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Biotransformation of Acetamide to Acetohydroxamic Acid at Bench Scale Using Acyl Transferase Activity of Amidase of Geobacillus pallidus BTP-5x MTCC 9225.
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- Indian Journal of Microbiology, 2012, v. 52, n. 1, p. 76, doi. 10.1007/s12088-011-0211-5
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Lipophilic conformationally constrained spiro carbocyclic 2,6‐diketopiperazine‐1‐acetohydroxamic acid analogues as trypanocidal and leishmanicidal agents: An extended SAR study.
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- Chemical Biology & Drug Design, 2018, v. 91, n. 2, p. 408, doi. 10.1111/cbdd.13088
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