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Journal articles on the topic 'Hydroxynicotinic'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Hoveyda, H. R., Veranja Karunaratne, Christopher J. Nichols, Steven J. Rettig, Ashley KW Stephens, and Chris Orvig. "Tripodal trisamides based on nicotinic and picolinic acid derivatives." Canadian Journal of Chemistry 76, no. 4 (1998): 414–25. http://dx.doi.org/10.1139/v98-030.

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A number of polydentate arylamide ligands have been prepared by coupling various acyclic tripodal or linear polyamines with derivatives of nicotinic and picolinic acids. Two synthetic procedures were utilized; tris{[(2-hydroxynicotinyl)carbonyl]-2-aminoethyl}amine (H3NICTREN) was prepared by Method A, the HOSu/DCC method, and the other arylamides in this study were prepared by Method B, the CDI method. Method A involved the reaction of N-hydroxysuccinimide with 2-hydroxynicotinic acid (in the presence of dicyclohexylcarbodiimide (DCC) as a dehydrative coupling reagent) to form the succinimide

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2

Santos, Rui C., Rita M. B. B. M. Figueira, M. Fátima M. Piedade, Hermínio P. Diogo, and Manuel E. Minas da Piedade. "Energetics and Structure of Hydroxynicotinic Acids. Crystal Structures of 2-, 4-, 6-Hydroxynicotinic and 5-Chloro-6-hydroxynicotinic Acids." Journal of Physical Chemistry B 113, no. 43 (2009): 14291–309. http://dx.doi.org/10.1021/jp906908n.

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3

Gero, Thomas W., Larry W. Jaques, Richard P. Mays, Debra H. Reid, Dwight A. Shamblee, and Young S. Lo. "Halogenation of 2-Hydroxynicotinic Acid." Synthetic Communications 19, no. 3-4 (1989): 553–59. http://dx.doi.org/10.1080/00397918908050699.

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4

Gao, Hong Tao. "Synthesis and Structure Characterization of some Triorganotin Esters of Heteroaromatic Carboxlic Acid and Crystal Structure of Triphenyltin Esters 5-Chloro-6-Hydroxynicotinic Acid." Advanced Materials Research 466-467 (February 2012): 463–68. http://dx.doi.org/10.4028/www.scientific.net/amr.466-467.463.

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Reactions of (R3Sn)2O (R=Ph, 2-ClC6H4CH2, 2-FC6H4CH2, 4-CNC6H4CH2) with 5-chloro-6-hydroxynicotinic acid in 1/2 stoichiometry yielded eight triorganotin compounds. These compounds have been characterized by elemental analysis, IR and NMR spectroscopy. The crystal structures of triphenyltin esters of 5-chloro-6-hydroxynicotinic acid were determined by single crystal X-ray diffraction. In the compound, the tin atoms are rendered five-coordinated in a trigonal bipyramidal structure by coordinating though the three phenyl carbon atoms and two oxygen atoms one from carboxylate and other from the ph

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5

Long, Sihui, Mingtao Zhang, Panpan Zhou, Faquan Yu, Sean Parkin, and Tonglei Li. "Tautomeric Polymorphism of 4-Hydroxynicotinic Acid." Crystal Growth & Design 16, no. 5 (2016): 2573–80. http://dx.doi.org/10.1021/acs.cgd.5b01639.

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6

Joseph, Abhinav, Joana S. Rodrigues Alves, Carlos E. S. Bernardes, M. Fátima M. Piedade, and Manuel E. Minas da Piedade. "Tautomer selection through solvate formation: the case of 5-hydroxynicotinic acid." CrystEngComm 21, no. 13 (2019): 2220–33. http://dx.doi.org/10.1039/c8ce02108b.

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Different 5-hydroxynicotinic acid tautomers were selectively captured through solvate formation. The selectivity is lost once the memory of solvation is erased by removing the solvent from the crystal lattice.

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7

Mirzaei, Masoud, Hossein Eshtiagh-Hosseini, Mahboubeh Alipour, et al. "Hydrothermal synthesis, X-ray structure and DFT and magnetic studies of a (H2SiW12O40)2− based one-dimensional linear coordination polymer." Dalton Transactions 44, no. 19 (2015): 8824–32. http://dx.doi.org/10.1039/c4dt03950e.

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In this paper, we report the synthesis and characterization of a novel POM-based inorganic–organic hybrid with an in situ transformation of pyridine-2,3-dicarboxylic acid into nicotinic acid and 2-hydroxynicotinic acid under hydrothermal conditions.

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8

Poersch-Bortolon, Liane Balvedi, Sandra Maria Mansur Scagliusi, Elene Yamazaki-Lau, and Maria Helena Bodanese-Zanettini. "Androgenic response of Brazilian wheat genotypes to different pretreatments of spikes and to a gelling agent." Pesquisa Agropecuária Brasileira 51, no. 11 (2016): 1839–47. http://dx.doi.org/10.1590/s0100-204x2016001100006.

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Abstract The objective of this work was to analyze the androgenic response of Brazilian wheat genotypes to different pretreatments of the spikes, prior to the culture of isolated microspores, and to the effect of a gelling agent in the induction culture medium. Five genotypes were evaluated for embryo formation, green plant regeneration, and spontaneous chromosome duplication. Wheat spikes were subjected to two pretreatments: cold, at 4ºC for 21 days; and 2-hydroxynicotinic acid, at 32ºC for two days. Culture media were evaluated with or without Ficoll as a gelling agent. Cold produced more em

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9

Johnson, Aidan V., M. Fátima M. Piedade, and Catarina V. Esteves. "pH-Dependent Crystallization of 2-, 4-, 5-, and 6-Hydroxynicotinic Acids in Aqueous Media." Crystals 13, no. 7 (2023): 1062. http://dx.doi.org/10.3390/cryst13071062.

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2-, 4-, 5-, and 6-hydroxynicotinic acids were crystallized in a pH-dependent manner using only water as the preferred solvent. The crystallization outcome was quite diverse: individual crystals of different sizes and shapes, microcrystalline powders, crystalline aggregates, and almost amorphous solids. Such a variety of solid forms demonstrates the relevance of pH control during crystallization processes.

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10

TIBBLES, Peter E., Rudolf MÜLLER, and Franz LINGENS. "Degradation of 5-Chloro-2-hydroxynicotinic Acid byMycobacteriumsp. BA." Biological Chemistry Hoppe-Seyler 370, no. 1 (1989): 601–6. http://dx.doi.org/10.1515/bchm3.1989.370.1.601.

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11

S. Harmata, Alexander. "From 5-Hydroxynicotinic Acid to Nitrogenous (4+3)-Cycloadducts." Organic Syntheses 97 (2020): 139–56. http://dx.doi.org/10.15227/orgsyn.097.0139.

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12

Matias, Elisa P., Carlos E. S. Bernardes, M. Fátima M. Piedade, and Manuel E. Minas da Piedade. "A Robust yet Metastable New Hemihydrate of 4-Hydroxynicotinic Acid." Crystal Growth & Design 11, no. 7 (2011): 2803–10. http://dx.doi.org/10.1021/cg1015687.

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13

Long, Sihui, Panpan Zhou, Kathryn L. Theiss, Maxime A. Siegler, and Tonglei Li. "Solid-state identity of 2-hydroxynicotinic acid and its polymorphism." CrystEngComm 17, no. 28 (2015): 5195–205. http://dx.doi.org/10.1039/c4ce02290d.

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14

van Stipdonk, Michael J., Michael J. Kullman, Giel Berden, and Jos Oomens. "Infrared multiple-photon dissociation spectroscopy of deprotonated 6-hydroxynicotinic acid." Rapid Communications in Mass Spectrometry 28, no. 7 (2014): 691–98. http://dx.doi.org/10.1002/rcm.6829.

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15

Liu, Cai-Ming, and You Song. "An Uneven Chain-like Ferromagnetic Copper(II) Coordination Polymer Displaying Metamagnetic Behavior and Long-Range Magnetic Ordering." Magnetochemistry 8, no. 1 (2021): 2. http://dx.doi.org/10.3390/magnetochemistry8010002.

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Ferromagnetic coupling exists in an uneven chain-like copper(II) complex with both end-on azido and syn-syn carboxylato bridges, (Cu3(L)2(N3)4(H2O)3)n (1, HL = 6-hydroxynicotinic acid). It is the first example of one-dimensional (1D) chain-like copper(II) coordination polymer showing both metamagnetic behavior and long-range magnetic ordering (Tc = 6.7 K), thanks to the interchain hydrogen bonds, which make a three-dimensional (3D) supramolecular array of the entire molecular structure and mediate the interchain antiferromagnetic interaction.

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16

Schwenen, Ludger, Dieter Komoßa, and Wolfgang Barz. "Metabolism and Degradation of Nicotinic Acid in Parsley (Petroselinum hortense) Cell Suspension Cultures and Seedlings." Zeitschrift für Naturforschung C 41, no. 1-2 (1986): 148–57. http://dx.doi.org/10.1515/znc-1986-1-222.

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Abstract Application of [6-14C]-or [7-14C]nicotinic acid to parsley cell suspension cultures led to the accumulation of labelled nicotinamide mononucleotide, nicotinamide adenine dinucleotide, nicotinamide N-riboside, nicotinamide and nicotinic acid, indicating the operation of the pyridine nucleotide cycle in these cells. As main conjugates, nicotinic acid N-glucoside and nicotinic acid glucose ester were found. For nicotinic acid degradation the following sequence is suggested: nicotinic acid → 6-hydroxynicotinic acid → 2,5-dihydroxypyridine → a C4/C3 unit of unknown structure → CO2. In asep

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17

Minazzato, Gabriele, Elisa Marangoni, Carlo Fortunato, et al. "A Versatile Continuous Fluorometric Enzymatic Assay for Targeting Nicotinate Phosphoribosyltransferase." Molecules 28, no. 3 (2023): 961. http://dx.doi.org/10.3390/molecules28030961.

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The maintenance of a proper NAD+ pool is essential for cell survival, and tumor cells are particularly sensitive to changes in coenzyme levels. In this view, the inhibition of NAD+ biosynthesis is considered a promising therapeutic approach. Current research is mostly focused on targeting the enzymes nicotinamide phosphoribosyltransferase (NAMPT) and nicotinate phosphoribosyltransferase (NAPRT), which regulate NAD+ biosynthesis from nicotinamide and nicotinic acid, respectively. In several types of cancer cells, both enzymes are relevant for NAD+ biosynthesis, with NAPRT being responsible for

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18

Wang, Wen-Bing, Shan-Shan Xu та Hong-Ji Chen. "Crystal structure of poly[bis(μ2-5-hydroxynicotinato-κ2N:O3)zinc]". Acta Crystallographica Section E Crystallographic Communications 71, № 2 (2015): m23. http://dx.doi.org/10.1107/s2056989015000249.

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The title coordination polymer, [Zn(C6H4NO3)2]n, was prepared under hydrothermal conditions by the reaction of zinc nitrate with 5-hydroxynicotinic acid in the presence of malonic acid. In the structure, the ZnIIion is coordinated by two carboxylate O atoms and two pyridine N atoms of four 5-hydroxynicotinate ligands in a distorted tetrahedral coordination environment. The μ2-bridging mode of each anion leads to the formation of a three-dimensional framework structure. Intermolecular hydrogen bonds between the hydroxy groups of one anion and the non-coordinating carboxylate O atoms of neighbou

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19

MAGDA, S. SALEH. "Equilibrium Study of the Mixed Complex of Copper(II) with 2-Hydroxynicotinic and Salicylic Acids." Journal of Indian Chemical Society Vol. 70, Mar 1993 (1993): 201–105. https://doi.org/10.5281/zenodo.5913591.

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Department of Chemistry, Faculty of Science, Assiut University, Assiut, Egypt <em>Manuscript received 8 July 1992, revised 22 October 1992, accepted 7 January 1993</em> Tbe complexation equilibria between copper(II), 2-hydroxynicotinic acid (hyna) and salicylic acid (sa) have been studied using spectrophotometric and potentiometric pH-titration methods in ethanol-water medium (50%, v,v ; I =0.1 <em>M</em> NaCIO<sub>4</sub>, 25°). Optimum conditions for the predominance of the complex forming equilibrium : Cu(hyna) + sa \(\rightleftharpoons\) Cu(hyna) (sa) were established. The stabili

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20

Zou, Yanhua, Qing Wei, Zhenling Guo, Sanping Chen, and Shengli Gao. "Syntheses, structures and luminescent properties of lanthanide complexes with 6-hydroxynicotinic acid." Inorganica Chimica Acta 375, no. 1 (2011): 181–86. http://dx.doi.org/10.1016/j.ica.2011.04.045.

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21

Gao, Zhongjun, Handong Yin, and Yajie Kong. "Synthesis and Structure Characterization of Some Triorganotin Esters of Heteroaromatic Carboxylic Acid and Crystal Structure of Triphenyltin Esters of 6-Hydroxynicotinic Acid and 5-Chloro-6-hydroxynicotinic Acid." Journal of Inorganic and Organometallic Polymers and Materials 18, no. 3 (2008): 391–97. http://dx.doi.org/10.1007/s10904-008-9214-z.

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22

Nagasawa, Toru, Byungserk Hurh, and Tsuneo Yamane. "Production of 6-Hydroxynicotinic Acid from Nicotinic Acid by Resting Cells ofPseudomonas fluorescensTN5." Bioscience, Biotechnology, and Biochemistry 58, no. 4 (1994): 665–68. http://dx.doi.org/10.1271/bbb.58.665.

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23

Salahuddin, Salahuddin, Muhammad Hanafi, and Hariyanti Hariyanti. "SYNTHESIS AND ANTICANCER ACTIVITY TEST OF 2-HYDROXY-N-PHENYLNICOTINAMIDE." Indonesian Journal of Chemistry 13, no. 2 (2013): 166–70. http://dx.doi.org/10.22146/ijc.21300.

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The novel compound of 2-hydroxy-N-phenylnicotinamide was synthesized from modification of the UK-3A compound, which was known biologically active to inhibit bacterial and cancer cells growth. Synthesis of this compound was carried out in one-step reaction. Analog UK-3A compound namely 2-hydroxy-N-phenylnicotinamide was synthesized from 2-hydroxynicotinic acid as the starting material using amidation reaction with aniline in presence of DCC/DMAP in pyridine. Analog UK-3A was analyzed and identified using TLC, FT-IR, LC-MS and FT-NMR spectrofotometer. The yield after purification was 42.97%. The

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24

Guragain, Manita, Jamie Jennings-Gee, Natalia Cattelan, et al. "The Transcriptional Regulator BpsR Controls the Growth ofBordetella bronchisepticaby Repressing Genes Involved in Nicotinic Acid Degradation." Journal of Bacteriology 200, no. 12 (2018): e00712-17. http://dx.doi.org/10.1128/jb.00712-17.

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ABSTRACTMany of the pathogenic species of the genusBordetellahave an absolute requirement for nicotinic acid (NA) for laboratory growth. These Gram-negative bacteria also harbor a gene cluster homologous to theniccluster ofPseudomonas putidawhich is involved in the aerobic degradation of NA and its transcriptional control. We report here that BpsR, a negative regulator of biofilm formation and Bps polysaccharide production, controls the growth ofBordetella bronchisepticaby repressing the expression ofnicgenes. The severe growth defect of the ΔbpsRstrain in Stainer-Scholte medium was restored b

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25

Srivastava, Ashish Kumar. "Electrochemical and spectral investigation of copper (II) complexes with various hydroxynicotinic acids in dimethylsulfoxide." Chemical Data Collections 36 (December 2021): 100789. http://dx.doi.org/10.1016/j.cdc.2021.100789.

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26

Dogra, S. K. "Spectral characteristics of 2-hydroxynicotinic acid: effects of solvent and acid or base concentrations." Journal of Molecular Structure 737, no. 2-3 (2005): 189–99. http://dx.doi.org/10.1016/j.molstruc.2004.10.060.

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27

Quintal, Susana M. O., Helena I. S. Nogueira, Vitor Félix, and Michael G. B. Drew. "Coordination modes of 2-hydroxynicotinic acid in second- and third-row transition metal complexes." Polyhedron 21, no. 27-28 (2002): 2783–91. http://dx.doi.org/10.1016/s0277-5387(02)01283-4.

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28

Ueda, Makoto, and Reiko Sashida. "Microbial production of 2-hydroxynicotinic acid from nicotinic acid by intact cells of MCI3289." Journal of Molecular Catalysis B: Enzymatic 4, no. 4 (1998): 199–204. http://dx.doi.org/10.1016/s1381-1177(97)00036-2.

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29

Van Stipdonk, Michael, Michael Kullman, Giel Berden, and Jos Oomens. "IRMPD and DFT study of the loss of water from protonated 2-hydroxynicotinic acid." International Journal of Mass Spectrometry 330-332 (December 2012): 134–43. http://dx.doi.org/10.1016/j.ijms.2012.06.026.

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30

Shiraishi, Sanshiro, Nobuo Sakamoto, Kenji Maeda, et al. "Availability of 6-hydroxynicotinic acid for rapid identification of pseudomonas aeruginosa and serratia marcescens." Journal of Chromatography B: Biomedical Sciences and Applications 338 (January 1985): 51–59. http://dx.doi.org/10.1016/0378-4347(85)80069-4.

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31

Xu, Na, Wei Shi, Dai-Zheng Liao, and Shi-Ping Yan. "1D chain lanthanide coordination polymers with 6-hydroxynicotinic acid: Crystal structures and luminescent properties." Inorganic Chemistry Communications 10, no. 10 (2007): 1218–21. http://dx.doi.org/10.1016/j.inoche.2007.07.016.

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32

Guo, Xingmei, Yingxin Gong, Xiaoting Huang, et al. "Self-assembled microporous lanthanide coordination polymers built by 2-hydroxynicotinic acid and oxalate ligands." Inorganic Chemistry Communications 44 (June 2014): 198–201. http://dx.doi.org/10.1016/j.inoche.2014.03.021.

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33

Stephens, Ashley K. W., and Chris Orvig. "Complexation of gallium(III) by 2-hydroxynicotinic acid and 3-hydroxypicolinic acid in aqueous solution." Inorganica Chimica Acta 273, no. 1-2 (1998): 47–53. http://dx.doi.org/10.1016/s0020-1693(97)06017-9.

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34

He, Yin-Hua, You-Zhao Lan, Cai-Hong Zhan, Yun-Long Feng, and Hong Su. "A stable second-order NLO and luminescent Cd(II) complex based on 6-hydroxynicotinic acid." Inorganica Chimica Acta 362, no. 6 (2009): 1952–56. http://dx.doi.org/10.1016/j.ica.2008.09.031.

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35

Guo, Zhenling, Sanping Chen, Qi Yang, and Shengli Gao. "Syntheses, Structures and Thermal Stabilities of Three Novel Lanthanide Coordination Polymers with 6-Hydroxynicotinic Acid." Chinese Journal of Chemistry 28, no. 3 (2010): 383–87. http://dx.doi.org/10.1002/cjoc.201090083.

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36

Danilenko, L. M., M. V. Pokrovsky, A. P. Dovgan, P. D. Kolesnichenko, A. S. Timokhina, and A. S. Kotelnikova. "Cardioprotective effects of derivatives of heterocyclic amino acids and 5-hydroxynicotinic acid in doxorubicin-induced cardiomyopathy." Regional blood circulation and microcirculation 17, no. 1 (2018): 90–96. http://dx.doi.org/10.24884/1682-6655-2018-17-1-90-96.

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37

Ma, Mingguang, Jing Lu, Ling Wang, et al. "Electrochemiluminescence behavior of 2-Hydroxynicotinic acid and identification of phloxine B by electrochemiluminescence resonance energy transfer." Journal of Electroanalytical Chemistry 895 (August 2021): 115544. http://dx.doi.org/10.1016/j.jelechem.2021.115544.

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38

Singh, Sandeep K., Krishna Srivastava, Rahul Banerjee, and Jagdish Prasad. "Syntheses and single crystal X-ray diffraction studies of hydroxynicotinic acid based complexes involving supramolecular interactions." Polyhedron 133 (September 2017): 222–30. http://dx.doi.org/10.1016/j.poly.2017.05.041.

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39

Hurh, Byungserk, Mikiko Ohshima, Tsuneo Yamane, and Toru Nagasawa. "Microbial production of 6-hydroxynicotinic acid, an important building block for the synthesis of modern insecticides." Journal of Fermentation and Bioengineering 77, no. 4 (1994): 382–85. http://dx.doi.org/10.1016/0922-338x(94)90008-6.

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40

Xu, Na, Chao Wang, Wei Shi, Shi-Ping Yan, Peng Cheng, and Dai-Zheng Liao. "Magnetic and Luminescent Properties of Sm, Eu, Tb, and Dy Coordination Polymers with 2-Hydroxynicotinic Acid." European Journal of Inorganic Chemistry 2011, no. 15 (2011): 2387–93. http://dx.doi.org/10.1002/ejic.201100022.

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41

Xu, Na, Wei Shi, Dai-Zheng Liao, Shi-Ping Yan, and Peng Cheng. "Template Synthesis of Lanthanide (Pr, Nd, Gd) Coordination Polymers with 2-Hydroxynicotinic Acid Exhibiting Ferro-/Antiferromagnetic Interaction." Inorganic Chemistry 47, no. 19 (2008): 8748–56. http://dx.doi.org/10.1021/ic800623v.

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42

Ganguly, Aniruddha, Soumen Ghosh, and Nikhil Guchhait. "Critical assessment of the intramolecular hydrogen bonding (IMHB) interaction in two isomeric hydroxynicotinic acids: A computational approach." Computational and Theoretical Chemistry 1045 (October 2014): 41–46. http://dx.doi.org/10.1016/j.comptc.2014.06.027.

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43

Gao, Zhongjun, Haifeng Zhang, and Jingquan Sha. "Synthesis and crystal structure of the one-dimensional chain triphenyltin compound bridged by 5-chloro-6-hydroxynicotinic acid." IOP Conference Series: Materials Science and Engineering 1040 (January 15, 2021): 012010. http://dx.doi.org/10.1088/1757-899x/1040/1/012010.

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44

Shang, Yu-Ting, Jiufu Qin, Jin-Song Gong, et al. "High-throughput screening of a nicotinate dehydrogenase producing Pseudomonas putida mutant for efficient biosynthesis of 6-hydroxynicotinic acid." Molecular Catalysis 509 (June 2021): 111600. http://dx.doi.org/10.1016/j.mcat.2021.111600.

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45

Torimura, Masaki, Hideto Yoshida, Kenji Kano, Tokuji Ikeda, Toru Nagasawa, and Teruhisa Ueda. "Bioelectrochemically Accelerated Microbial Conversion of Nicotinic Acid to 6-Hydroxynicotinic Acid on Microorganism-immobilized Column Electrolytic Flow System." Chemistry Letters 27, no. 4 (1998): 295–96. http://dx.doi.org/10.1246/cl.1998.295.

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46

Wang, Qian-Ming, and Bing Yan. "Designing a family of luminescent hybrid materials by 3-(triethoxysilyl)-propyl isocyanate grafted 2-hydroxynicotinic acid bridge molecules." Journal of Organometallic Chemistry 691, no. 17 (2006): 3567–73. http://dx.doi.org/10.1016/j.jorganchem.2005.12.061.

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47

Torimura, Masaki, Hideto Yoshida, Kenji Kano, Tokuji Ikeda, Toyokazu Yoshida, and Toru Nagasawa. "Bioelectrochemical transformation of nicotinic acid into 6-hydroxynicotinic acid on Pseudomonas fluorescens TN5-immobilized column electrolytic flow system." Journal of Molecular Catalysis B: Enzymatic 8, no. 4-6 (2000): 265–73. http://dx.doi.org/10.1016/s1381-1177(99)00077-6.

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48

Joseph, Abhinav, Carlos E. S. Bernardes, Ana S. Viana, M. Fátima M. Piedade, and Manuel E. Minas da Piedade. "Kinetics and Mechanism of the Thermal Dehydration of a Robust and Yet Metastable Hemihydrate of 4-Hydroxynicotinic Acid." Crystal Growth & Design 15, no. 7 (2015): 3511–24. http://dx.doi.org/10.1021/acs.cgd.5b00594.

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49

Ghanem, Moustafa S., Irene Caffa, Alberto Del Rio, et al. "Identification of NAPRT Inhibitors with Anti-Cancer Properties by In Silico Drug Discovery." Pharmaceuticals 15, no. 7 (2022): 848. http://dx.doi.org/10.3390/ph15070848.

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Depriving cancer cells of sufficient NAD levels, mainly through interfering with their NAD-producing capacity, has been conceived as a promising anti-cancer strategy. Numerous inhibitors of the NAD-producing enzyme, nicotinamide phosphoribosyltransferase (NAMPT), have been developed over the past two decades. However, their limited anti-cancer activity in clinical trials raised the possibility that cancer cells may also exploit alternative NAD-producing enzymes. Recent studies show the relevance of nicotinic acid phosphoribosyltransferase (NAPRT), the rate-limiting enzyme of the Preiss–Handler

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50

Škugor Rončević, Ivana, Nives Vladislavić, Nabanita Chatterjee, Vesna Sokol, Clive L. Oliver, and Boris-Marko Kukovec. "Structural and Electrochemical Studies of Cobalt(II) and Nickel(II) Coordination Polymers with 6-Oxonicotinate and 4,4′-Bipyridine." Chemosensors 9, no. 12 (2021): 352. http://dx.doi.org/10.3390/chemosensors9120352.

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Abstract:

The 6-oxonicotinate (6-Onic) salts of a one-dimensional cationic cobalt(II) or nickel(II) coordination polymers with 4,4′-bipyridine (4,4′-bpy), namely {[Co(4,4′-bpy)(H2O)4](6-Onic)2·2H2O}n (1) and {[Ni(4,4′-bpy)(H2O)4](6-Onic)2·2H2O}n (2), were prepared hydrothermally by reactions of cobalt(II) nitrate hexahydrate or nickel(II) nitrate hexahydrate, respectively, 6-hydroxynicotinic acid and 4,4′-bipyridine in a mixture of ethanol and water. In the hydrogen-bonded frameworks of 1 and 2, the one-dimensional polymeric chains of {[M(4,4′-bpy)(H2O)4]2+}n (M = Co, Ni), the 6-oxonicotinate anions and

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