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Journal articles on the topic 'Oxamic acid'

Author: Grafiati

Published: 19 October 2024

Last updated: 26 July 2025

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1

Yang, L., L. Liu, B. A. Olsen, and M. A. Nussbaum. "The determination of oxalic acid, oxamic acid, and oxamide in a drug substance by ion-exclusion chromatography." Journal of Pharmaceutical and Biomedical Analysis 22, no. 3 (2000): 487–93. http://dx.doi.org/10.1016/s0731-7085(00)00230-2.

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2

Nuñez, L., L. Barral, and G. Pilcher. "Enthalpies of combustion of oxamic acid, oxamide, and dithiooxamide." Journal of Chemical Thermodynamics 20, no. 10 (1988): 1211–16. http://dx.doi.org/10.1016/0021-9614(88)90105-x.

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3

Veltsistas, P. G., C. D. Papadimitriou, A. M. Z. Slawin, and J. D. Woollins. "Synthesis, Characterization and X-Ray Structural Determination of the Nine-coordinate Tris-aqua Tetra-oxamato Neodymium(III) Complex [Nd(Hoxm)3(H2oxm)·2.5H2O]n." Journal of Chemical Research 23, no. 3 (1999): 222–23. http://dx.doi.org/10.1177/174751989902300326.

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The reaction of NdIII with oxamic acid yields [Nd(Hoxm)3(H2oxm)·2.5H2O] n 1 (H2oxm = oxamic acid) which contains nine-coordinate Nd centres linked into chains via four-coordinate Hoxm- ligands; the chains are connected via an array of H-bonds.

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4

PETYUNIN, G. P., A. V. CHUBENKO, and KH M. AL'RAKHAVI. "ChemInform Abstract: Reaction of 2-Aminopyridine with Oxalic and Oxamic Acid Esters." ChemInform 27, no. 47 (2010): no. http://dx.doi.org/10.1002/chin.199647149.

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5

Lin, Shu-Kun. "N-(3,4-Dichlorophenyl)methyl Oxamic Acid." Molecules 2, no. 12 (1997): M4. http://dx.doi.org/10.3390/m4.

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6

Orge, C. A., J. L. Faria, and M. F. R. Pereira. "Removal of oxalic acid, oxamic acid and aniline by a combined photolysis and ozonation process." Environmental Technology 36, no. 9 (2014): 1075–83. http://dx.doi.org/10.1080/09593330.2014.974682.

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7

Lan, Yixiang, Chao Wang, Fan Yuan, et al. "Electrochemiluminescence of 3,4,9,10-perylenetetracarboxylic acid/oxamic hydrazide and its application in the detection of tannic acid." Analyst 144, no. 15 (2019): 4493–98. http://dx.doi.org/10.1039/c9an00615j.

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8

Zarzyka, Iwona. "Oligomers with structural elements of imidazolidinetrione obtained from oxamic acid and oxamide: polyurethane foams modified by structural elements of imidazolidinetrione." Journal of Polymer Engineering 35, no. 1 (2015): 1–10. http://dx.doi.org/10.1515/polyeng-2013-0318.

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Abstract Hydroxyalkyl derivatives containing oxamidoester and oxamide fragments have been separately obtained using oxamic acid, oxamide and alkylene carbonates. It has been proven that the presence of oxamidoester and oxamide structural fragments in oligomer structures is responsible for the thermal stability of these products. Rigid, thermally stable polyurethane foams were obtained with the use of oligomers with oxamidoestercarbamidoimide, carbamide, oxamidoester and oxamide groups as polyols components. The properties of these foamed materials were compared with each other and with the pro

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9

DELGADO, G. E., L. M. BELANDRIA, M. GUILLEN, A. J. MORA, and L. E. SEIJAS. "STRUCTURAL CHARACTERIZATION OF 2-AMINO-2-OXOACETIC ACID BY X-RAY POWDER DIFFRACTION AND QUANTUM CHEMISTRY." Periódico Tchê Química 16, no. 33 (2019): 516–23. http://dx.doi.org/10.52571/ptq.v16.n33.2019.531_periodico33_pgs_516_523.pdf.

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2-amino-2-oxoacetic acid, carbamoyl formic acid, or oxamic acid is an active pharmaceutical ingredient (API) of great importance mainly because is an inhibitor of lactic dehydrogenase (LDH). It acts as an inhibitor to the metabolic pathways of the tumor cells and exhibited significant anticancer activity against nasopharyngeal carcinoma (NPC) cells in vitro and can be considered as a potential drug for the treatment of type 2 diabetes. Also, this compound could be used as a building block in the design of supramolecular architectures based on hydrogen bonds through the complimentary hydrogen-b

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10

Volkova, Yulia A., Elena I. Chernoburova, Albina S. Petrova, Alexander A. Shtil, and Igor V. Zavarzin. "Reactions of hydrazones derived from oxamic acid thiohydrazides." Phosphorus, Sulfur, and Silicon and the Related Elements 192, no. 2 (2016): 237–40. http://dx.doi.org/10.1080/10426507.2016.1250759.

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11

Fleischer, Sandra, Stefan C. Weiss, Thomas Lucke, Wolfram Seitz, Wolfgang Schulz, and Walter H. Weber. "Formation of Oxamic Acid During Drinking Water Treatment." Ozone: Science & Engineering 37, no. 5 (2015): 441–49. http://dx.doi.org/10.1080/01919512.2015.1040911.

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12

Komendantova, Anna S., Konstantin A. Lyssenko, Igor V. Zavarzin, and Yulia A. Volkova. "Iodine-promoted synthesis of pyrazoles from 1,3-dicarbonyl compounds and oxamic acid thiohydrazides." Organic Chemistry Frontiers 7, no. 13 (2020): 1640–46. http://dx.doi.org/10.1039/d0qo00476f.

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A novel approach to 3,4-dicarbonyl-substituted pyrazoles from 1,3-dicarbonyl compounds and oxamic acid thiohydrazides was developed via iodine-promoted cascade imination/halogenation/cyclization/ring contraction reaction.

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13

Rodríguez-Páez, Lorena, Miguel Angel Chena-Taboada, Arturo Cabrera-Hernández, Joaquín Cordero-Martínez, and Carlos Wong. "Oxamic acid analogues as LDH-C4-specific competitive inhibitors." Journal of Enzyme Inhibition and Medicinal Chemistry 26, no. 4 (2011): 579–86. http://dx.doi.org/10.3109/14756366.2011.566221.

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14

Pelster, B. "Mechanisms of acid release in isolated gas gland cells of the European eel Anguilla anguilla." American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 269, no. 4 (1995): R793—R799. http://dx.doi.org/10.1152/ajpregu.1995.269.4.r793.

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Mechanisms of acid production and of acid release have been analyzed in isolated gas gland cells of the eel swimbladder using a cytosensor microphysiometer. Incubation of isolated cells with oxamic acid caused a dose-dependent decrease in the rate of proton release. At the highest oxamic acid concentration used (20 mmol/l), proton release was reduced by approximately 40%; incubation with sodium fluoride (10 mmol/l) or removal of glucose from the extracellular medium caused 60 and 80% reduction, respectively. NaCN had little effect on proton secretion. Proton release of isolated gas gland cells

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15

Zarzyka-Niemiec, Iwona. "Hydroxyalkoxy derivatives of oxamic acid: polyol substrates for polyurethane foams." Polymer International 58, no. 4 (2009): 388–95. http://dx.doi.org/10.1002/pi.2543.

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16

Devendra, Kumar, Bhadauria Anupama, and C. Sharma R. "Synthesis, structural and biological studies of some oxamic acids and their CoII, NiII and CuII metal complexes." Journal of Indian Chemical Society Vol. 88, Mar 2011 (2011): 427–30. https://doi.org/10.5281/zenodo.5766048.

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Department of Chemistry, Institute of Basic Sciences, Dr. B. R. Ambedkar University, Khandari Road, Agra-282 002, Uttar Pradesh, India <em>E-mail</em> : dev_kumar26@indiatimes.com Department of Chemistry, Institute of Engineering & Technology, Mangalayatan University, Aligarh-202 001, Uttar Pradesh, India <em>Manuscript received 12 March 2010, revised 21 July 2010, accepted 27 July 2010</em> Six new metal complexes of Co<sup>II</sup> , Nl<sup>II</sup> and Cu<sup>II</sup> with N-(4-methoxyphenyl)oxamic acid and N-(4-carboxyphenyl)oxamic acid have beensynthesized and characterized by element

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17

Choi, Seoung-ryoung, Aaron B. Beeler, Anupam Pradhan, et al. "Generation of Oxamic Acid Libraries: Antimalarials and Inhibitors ofPlasmodium falciparumLactate Dehydrogenase." Journal of Combinatorial Chemistry 9, no. 2 (2007): 292–300. http://dx.doi.org/10.1021/cc060110n.

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18

Krayushkin, M. M., V. N. Yarovenko, and I. V. Zavarzin. "Synthesis of heterocyclic compounds based on oxamic acid monothiooxamides and thiohydrazides." Russian Chemical Bulletin 68, no. 6 (2019): 1143–63. http://dx.doi.org/10.1007/s11172-019-2533-0.

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19

van Alphen, J. "Esters of ethylene-1:2-di-oxamic acid and its derivatives." Recueil des Travaux Chimiques des Pays-Bas 53, no. 12 (2010): 1159–66. http://dx.doi.org/10.1002/recl.19340531217.

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20

Matsumoto, K. "Antitumor activities of platinum blues containing α-pyrrolidone, 3,3-dimethylglutarimide, orotic acid, succinamic acid and oxamic acid". Inorganica Chimica Acta 151, № 1 (1988): 9–10. http://dx.doi.org/10.1016/s0020-1693(00)83475-1.

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21

Bie, Chao, Yun Gao, Jia Su, Yamin Dong, Xiangguang Guo, and Xiaoqi Sun. "The efficient separation of thorium from rare earth using oxamic acid in hydrochloric acid medium." Separation and Purification Technology 251 (November 2020): 117358. http://dx.doi.org/10.1016/j.seppur.2020.117358.

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22

Cowell, A. J., and M. Tremayne. "The co-crystallisation and thermal behaviour of oxamic acid, nicotinamide and isonicotinamide." Acta Crystallographica Section A Foundations of Crystallography 64, a1 (2008): C209. http://dx.doi.org/10.1107/s010876730809329x.

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23

Bazureau, J. P., та M. Le Corre. "New synthesis of protected α-dehydro α-aminoacids from substituted oxamic acid". Tetrahedron Letters 29, № 16 (1988): 1919–20. http://dx.doi.org/10.1016/s0040-4039(00)82078-x.

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24

ZARZYKA-NIEMIEC, IWONA. "Synthesis and application of oligomers obtained from oxamic acid and ethylene carbonate." Polimery 54, no. 02 (2009): 099–105. http://dx.doi.org/10.14314/polimery.2009.099.

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25

Nok, Andrew J., Humphrey C. Nzelibe, and Sarah K. Yako. "Trypanosoma evansi Sialidase: Surface Localization, Properties and Hydrolysis of Ghost Red Blood Cells and Brain Cells-Implications in Trypanosomiasis." Zeitschrift für Naturforschung C 58, no. 7-8 (2003): 594–601. http://dx.doi.org/10.1515/znc-2003-7-825.

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Abstract A membrane-bound sialidase was isolated from blood stream (BS) Trypanosoma evansi partially purified and characterized. The enzyme is a glycosyl phosphatidyl inositol (GPI) membrane anchored protein. It was solubilized from T.evansi cells recovered from infected camel blood by detergent treatment with Triton CF 54 and partially purified by a series of chromatography steps. The enzyme was optimally active at pH 5.5 and 37 °C. It had a Kᴍ and Vmax values of 4.8 x 10-6ᴍ and 3.75 x 10-6 mol/min.mg protein with Neu5Acα2, 3lac as substrate respectively. The Kᴍ and Vmax values with fetuin (4

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26

Yokoyama, Naokata, Gordon N. Walker, Alan J. Main, et al. "Synthesis and Structure-Activity Relationships of Oxamic Acid and Acetic Acid Derivatives Related to L-Thyronine." Journal of Medicinal Chemistry 38, no. 4 (1995): 695–707. http://dx.doi.org/10.1021/jm00004a015.

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27

Tarigan, Simson, Risa Indryani, Darminto ., and Jagoda Ignjatovic. "Purification of neuraminidase from Influenza virus subtype H5N1." Jurnal Ilmu Ternak dan Veteriner 14, no. 1 (2013): 75–82. https://doi.org/10.14334/jitv.v14i1.366.

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Influenza-virus neuraminidase plays vital role in the survival of the organisms. Vaccination of animals with this glycoprotein confers immune responses so that enable it to protect the animals from incoming infection. Supplementation of conventional vaccines with this glycoprotein increases the protection and longevity of the vaccine. Purified neuraminidase can also be used to develop serological tests for differentiation of serologically positive animals due to infection or to vaccination. In this study purification of neuraminidase from influenza virus subtype H5N1 was described. Triton x-10

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28

Corpet, D. E., and G. F. Bories. "[3H]chloramphenicol metabolism in human volunteer: oxamic acid as a new major metabolite." Drug Metabolism and Disposition 15, no. 6 (1987): 925–27. https://doi.org/10.1016/s0090-9556(25)06860-6.

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29

Stanton, James L., Edna Cahill, Ronald Dotson, et al. "Synthesis and biological activity of phenoxyphenyl oxamic acid derivatives related to l-thyronine." Bioorganic & Medicinal Chemistry Letters 10, no. 15 (2000): 1661–63. http://dx.doi.org/10.1016/s0960-894x(00)00309-7.

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30

Sosio, A., I. Caramazza, D. Morelli, and A. Carenzi. "Pharmacological evaluation of Z 1819, a new oxamic acid derivative, as antianaphylactic agent." Pharmacological Research Communications 20 (September 1988): 365. http://dx.doi.org/10.1016/s0031-6989(88)80495-8.

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31

Martinez Belmonte, Marta, and Daniel J. Price. "Strong asymmetric hydrogen bonding in 2-(oxamoylamino)ethylammonium oxamate–oxamic acid (1/1)." Acta Crystallographica Section C Crystal Structure Communications 66, no. 3 (2010): o147—o150. http://dx.doi.org/10.1107/s0108270110004233.

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32

Desseyn, Herman, and Georges Schoeters. "The Vibrational Analysis of the Copper Complexes with Planar Oxamides and Oxamic Acid." Bulletin des Sociétés Chimiques Belges 95, no. 1 (2010): 13–27. http://dx.doi.org/10.1002/bscb.19860950102.

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33

Zarzyka-Niemiec, Iwona. "Hydroxyalkylation of oxamic acid with propylene carbonate: Synthesis, composition, and properties of products." Journal of Applied Polymer Science 110, no. 1 (2008): 66–75. http://dx.doi.org/10.1002/app.28609.

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34

Zhang, Jie, Qing-Xia Liu, A.-Hui Li, Bao-Lin Liu, and Ruo-Jie Tao. "Synthesis, Crystal Structures and Properties of Two Heterometallic Complexes [Cu2M] (M = Cd, Mn) with a Novel Oxamato-bridged Ligand." Zeitschrift für Naturforschung B 69, no. 1 (2014): 49–54. http://dx.doi.org/10.5560/znb.2014-3127.

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Two novel trinuclear oxamato-bridged thiosemicarbazone complexes, [Cu(obte)]2Cd(DMF)2 (2) and [Cu(obte)]2Mn(DMF)2 (3) (H2obte = N-(2-benzaldehyde) oxamic acid ethyl ester thiosemicarbazone (1); DMF=dimethylformamide), have been synthesized and characterized by elemental analysis, IR spectroscopy, thermogravimetric analysis (TGA) and single-crystal X-ray diffraction. Complexes 2 and 3 are isostructural, displaying a trinuclear structure. The luminescence properties of complexes 2 and 3 were investigated in the solid state at room temperature. The ligand 1 and its complex 2 have been evaluated f

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35

Buduru, Prasad, and Sundara Raja Reddy B.C. "Oxamic acid and p-aminobenzoic acid functionalized gold nanoparticles as a probe for colorimetric detection of Fe3+ ion." Sensors and Actuators B: Chemical 237 (December 2016): 935–43. http://dx.doi.org/10.1016/j.snb.2016.06.167.

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36

Kryzhna, S. I., O. M. Litvinova, M. E. Bereznyakova, and G. P. Fomina. "Screening of the diuretic activity from the series of new derivatives of oxamic acid." Klìnìčna farmacìâ 19, no. 1 (2015): 42–45. http://dx.doi.org/10.24959/cphj.15.1318.

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37

Yuan, Ming, Li Chen, Junwei Wang, et al. "Transition-Metal-Free Synthesis of Phenanthridinones from Biaryl-2-oxamic Acid under Radical Conditions." Organic Letters 17, no. 2 (2015): 346–49. http://dx.doi.org/10.1021/ol503459s.

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38

Raczyńska, Ewa D., Małgorzata Hallmann, and Kinga Duczmal. "Quantum-chemical studies of amide–iminol tautomerism for inhibitor of lactate dehydrogenase: Oxamic acid." Computational and Theoretical Chemistry 964, no. 1-3 (2011): 310–17. http://dx.doi.org/10.1016/j.comptc.2011.01.017.

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39

Chiarino, Dario, Giancarlo Grancini, Viviana Frigeni, Ivano Biasini, and Angelo Carenzi. "N-(4-Isoxazolylthiazol-2-yl)oxamic acid derivatives as potent orally active antianaphylactic agents." Journal of Medicinal Chemistry 34, no. 2 (1991): 600–605. http://dx.doi.org/10.1021/jm00106a020.

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40

Molina, P., Ma J. Vilaplana, P. L. Andreu, and J. Møller. "Oxamic acid derivaties in heterocyclic synthesis: Preparation of 1,2,4-triazolo[1,5-a]pyrazine derivatives." Journal of Heterocyclic Chemistry 24, no. 5 (1987): 1281–84. http://dx.doi.org/10.1002/jhet.5570240509.

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41

Meena and D. Gupta O. "Electrode kinetics and formation constants of complexes of CuII with N-substituted derivatives of oxamic acid in aqueous media at DME." Journal of Indian Chemical Society Vol. 88, Nov 2011 (2011): 1703–8. https://doi.org/10.5281/zenodo.5791640.

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Department of Chemistry, University of Rajasthan, Jaipur-302 055, Rajasthan, India <em>E-mail</em> : gupta_od@yahoo.com <em>Manuscript received 04 November 2009, revised 18 February 2010, accepted 01 April 2011</em> Polarographic technique has been used to evaluate the kinetic parameters and formation constants of Cu<sup>II </sup>complexes with oxamate (OXA), iodooxamate (IOXA), o-toluidinyloxamate (OTOXA) and p-anisidinyloxamate (PAOXA) at pH 6.8-6.9 and constant ionic strength (j.L = 0.25 M) in aqueous medium at DME. The reduction of all these complexes is found to be quasi-reversible a

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42

Vansant, Christoffel, Herman O. Desseyn, and Spyros P. Perlepes. "The synthesis, spectroscopic and thermal study of oxamic acid compounds of some metal(II) ions." Transition Metal Chemistry 20, no. 5 (1995): 454–59. http://dx.doi.org/10.1007/bf00141516.

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43

Stanton, James L., Edna Cahill, Ronald Dotson, et al. "ChemInform Abstract: Synthesis and Biological Activity of Phenoxyphenyl Oxamic Acid Derivatives Related to L-Thyronine." ChemInform 31, no. 44 (2000): no. http://dx.doi.org/10.1002/chin.200044207.

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44

Tarigan, Simson, R. Indriani, and D. Hewajuli. "Purification and production of monospecific antibody to the hemagglutinin from Subtype H5N1 influenza virus." Jurnal Ilmu Ternak dan Veteriner 15, no. 4 (2012): 308–14. https://doi.org/10.14334/jitv.v15i4.670.

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The purpose of this study was to purify the hemagglutinin from H5N1 virus and to generate monospecific antibody appropriate for production of sensitive and specific immunoassay for H5N1 avian influenza. For this purpose, a local isolate H5N1 virus (A/Ck/West Java/Hamd/2006) was propagated in chicken embryos. The viral pellet was dissolved in a Triton-X-100 solution, undissolved viral particles were pelleted by ultracentrifuge, and the supernatant containing viral surface glycoproteins (Hemagglutinin and neuraminidase) was collected. The neuraminidase in the supernatant was absorbed by passing

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45

Morozov, Vitaly A., Denis G. Samsonenko, and Kira E. Vostrikova. "A Unique Trinuclear, Triangular Ni(II) Complex Composed of Two tri-Anionic bis-Oxamates and Capping Nitroxyl Radicals." Inorganics 13, no. 7 (2025): 214. https://doi.org/10.3390/inorganics13070214.

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Phenylene-based bis-oxamate polydentate ligands offer a unique opportunity for creating a large variety of coordination compounds, in which paramagnetic metal ions are strongly magnetically coupled. The employment of imino nitroxyl (IN) radicals as supplementary ligands confers numerous benefits, including the strong ferromagnetic interaction between Ni and IN. Furthermore, the chelating IN can act as a capping ligand, thereby impeding the formation of coordination polymers. In this study, we present the molecular and crystal structure and experimental and theoretical magnetic behavior of an e

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46

Michaelides, A., and S. Skoulika. "Gel growth of single crystals of complexes of oxamic acid with divalent metals (Pb2+, Ca2+, Cd2+." Journal of Crystal Growth 94, no. 1 (1989): 208–12. http://dx.doi.org/10.1016/0022-0248(89)90620-9.

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47

Halasa, Anna, Leszek Lapinski, Hanna Rostkowska, Igor Reva, and Maciej J. Nowak. "Tunable Diode Lasers as a Tool for Conformational Control: The Case of Matrix-Isolated Oxamic Acid." Journal of Physical Chemistry A 119, no. 11 (2014): 2203–10. http://dx.doi.org/10.1021/jp501448m.

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48

CHIARINO, D., G. GRANCINI, V. FRIGENI, I. BIASINI, and A. CARENZI. "ChemInform Abstract: N-(4-Isoxazolylthiazol-2-yl)oxamic Acid Derivatives as Potent Orally Active Antianaphylactic Agents." ChemInform 22, no. 38 (2010): no. http://dx.doi.org/10.1002/chin.199138157.

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49

Orge, Carla A., O. Salomé G. P. Soares, Patrícia S. F. Ramalho, M. Fernando R. Pereira, and Joaquim L. Faria. "Magnetic Nanoparticles for Photocatalytic Ozonation of Organic Pollutants." Catalysts 9, no. 9 (2019): 703. http://dx.doi.org/10.3390/catal9090703.

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Magnetic nanoparticles (MNP) composed of iron oxide (or other metal–FeO cores) coated with carbon produced by chemical vapour decomposition (CVD) were used in the photocatalytic ozonation of oxamic acid (OMA) which we selected as a model pollutant. The incorporation of Ag and Cu on FeO enhanced the efficiency of the process. The carbon phase significantly increased the photocatalytic activity towards the conversion of OMA. As for the synthesis process, raising the temperature of CVD improved the performance of the produced photocatalysts. The obtained results suggested that the carbon phase is

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50

Ruddraraju, Kasi Viswanatharaju, Devesh Aggarwal, Congwei Niu, et al. "Highly Potent and Selective N-Aryl Oxamic Acid-Based Inhibitors for Mycobacterium tuberculosis Protein Tyrosine Phosphatase B." Journal of Medicinal Chemistry 63, no. 17 (2020): 9212–27. http://dx.doi.org/10.1021/acs.jmedchem.0c00302.

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