Log in

Relevant bibliographies by topics / Dihydroxypyridine / Journal articles

To see the other types of publications on this topic, follow the link: Dihydroxypyridine.

Journal articles on the topic 'Dihydroxypyridine'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 50 journal articles for your research on the topic 'Dihydroxypyridine.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

Shukla, Onkar P., and Shanti M. Kaul. "Microbiological transformation of pyridine N-oxide and pyridine by Nocardia sp." Canadian Journal of Microbiology 32, no. 4 (1986): 330–41. http://dx.doi.org/10.1139/m86-065.

Full text

Abstract:

A Nocardia sp., which utilises pyridine N-oxide (PNO), 2-hydroxypyridine, and pyridine as sole sources of carbon, nitrogen, and energy, has been isolated from soil by enrichment on PNO. PNO-adapted cells rapidly oxidized PNO and 2-hydroxypyridine; pyridine was oxidized very slowly. 2-Hydroxy pyridine- and pyridine-adapted cells oxidized their respective substrates, but PNO was not oxidized. Dihydroxypyridines did not accumulate during growth of the organism, but the formation of blue pigments during fermentation of PNO and 2-hydroxypyridine suggested their transient participation. The pigment

APA, Harvard, Vancouver, ISO, and other styles

2

Ramesh, S., and Ganga Radhakrishnan. "Polyurethane zwitterionomers using 2,3-dihydroxypyridine." European Polymer Journal 32, no. 8 (1996): 993–98. http://dx.doi.org/10.1016/0014-3057(96)00032-8.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Baitsch, Daniel, Cristinel Sandu, Roderich Brandsch, and Gabor L. Igloi. "Gene Cluster on pAO1 of Arthrobacter nicotinovorans Involved in Degradation of the Plant Alkaloid Nicotine: Cloning, Purification, and Characterization of 2,6-Dihydroxypyridine 3-Hydroxylase." Journal of Bacteriology 183, no. 18 (2001): 5262–67. http://dx.doi.org/10.1128/jb.183.18.5262-5267.2001.

Full text

Abstract:

ABSTRACT A 27,690-bp gene cluster involved in the degradation of the plant alkaloid nicotine was characterized from the plasmid pAO1 ofArthrobacter nicotinovorans. The genes of the heterotrimeric, molybdopterin cofactor (MoCo)-, flavin adenine dinucleotide (FAD)-, and [Fe-S] cluster-dependent 6-hydroxypseudooxynicotine (ketone) dehydrogenase (KDH) were identified within this cluster. The gene of the large MoCo subunit of KDH was located 4,266 bp from the FAD and [Fe-S] cluster subunit genes. Deduced functions of proteins encoded by open reading frames (ORFs) of the cluster were correlated to i

APA, Harvard, Vancouver, ISO, and other styles

4

Horáčková, Jaroslava, and Vojeslav Štěrba. "Kinetics of Coupling of 4-Methoxybenzenediazonium Ion with 2,6-Dihydroxypyridine." Collection of Czechoslovak Chemical Communications 61, no. 6 (1996): 951–56. http://dx.doi.org/10.1135/cccc19960951.

Full text

Abstract:

The kinetics of reaction of 4-methoxybenzenediazonium ion (3) with 2,6-dihydroxypyridine (1) has been studied in methoxyacetate, acetate, and phosphate buffers. The rate-limiting step is the formation of the reaction intermediate and not the splitting off of the proton (which was detected in the cases of citrazinic acid and its methyl ester). Therefrom it follows that for 2,6-dihydroxypyridine derivatives the steric hindrance to the formation of the Wheland intermediate exerted by CO2- and CO2CH3 groups represents a necessary condition for the rate-limiting splitting off of the proton and, hen

APA, Harvard, Vancouver, ISO, and other styles

5

Pajares, Adriana, José Gianotti, Guillermo Stettler, et al. "Ionization effects on the sensitized photooxidation of 2,3-dihydroxypyridine and 2,4-dihydroxypyridine: a kinetic study." Journal of Photochemistry and Photobiology A: Chemistry 153, no. 1-3 (2002): 101–7. http://dx.doi.org/10.1016/s1010-6030(02)00268-x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Hallengren, Bengt, Mervyn P. Hegarty, Arne Forsgren, Lars E. Ericson, and Arne Melander. "3,4-Dihydroxypyridine: A potential antithyroid drug." Acta Endocrinologica 114, no. 2 (1987): 305–7. http://dx.doi.org/10.1530/acta.0.1140305.

Full text

Abstract:

Abstract. 3,4-Dihydroxypyridine (3,4-DHP), a goitrogenic derivative of the plant amino acid mimosine, has no SH-group, in contrast to conventional antithyroid agents such as methimazole (MMI) and propylthiouracil (PTU). The current in vitro study shows that 3,4-DHP, like MMI and PTU, inhibits iodination of human thyroglobulin and interferes with mitogenic activation of human lymphocytes. This, together with a very low murine bone marrow toxicity, probably related to the absence of an SH-group, makes 3,4-DHP a potential antithyroid drug.

APA, Harvard, Vancouver, ISO, and other styles

7

pirhayati, Mozhgan, Hojat Veisi, and Ali Kakanejadifard. "Palladium stabilized by 3,4-dihydroxypyridine-functionalized magnetic Fe3O4nanoparticles as a reusable and efficient heterogeneous catalyst for Suzuki reactions." RSC Advances 6, no. 32 (2016): 27252–59. http://dx.doi.org/10.1039/c6ra01734g.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Miller, Samantha J., Talia R. Collier, and Weiming Wu. "Efficient reduction of sulfoxides with 2,6-dihydroxypyridine." Tetrahedron Letters 41, no. 20 (2000): 3781–83. http://dx.doi.org/10.1016/s0040-4039(00)00502-5.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

B., K. SINGH, L. JAIN C., and S. SINDHU R. "Polarographic Estimation of Copper-, Lead- and Zinc(II) in Presence of 2,3-Dihydroxypyridine as Complexing Agent." Journal of Indian Chemical Society Vol. 73, Jun 1996 (1996): 297–99. https://doi.org/10.5281/zenodo.5898035.

Full text

Abstract:

Chemistry Department, Regional College of Education, Bhopal-462 013 <em>Manuscript received 11 March 1994, revised 30 August 1994, accepted 19 October 1994</em> Polarographic Estimation of Copper-, Lead- and Zinc(II) in Presence of 2,3-Dihydroxypyridine as Complexing Agent.

APA, Harvard, Vancouver, ISO, and other styles

10

SHASHI, K. BANSAL, and S. SINDHU R. "Polarographic Behaviour of Xanthate Anions as Salts of 2,3-Dihydroxypyridine and 2-Amino-3-hydroxypyridinebis (cyclopentadienyl) titanium(Iv) and -zirconium(Iv) Chelates." Journal of Indian Chemical Society Vol.71, Jan 1994 (1994): 39–40. https://doi.org/10.5281/zenodo.5891034.

Full text

Abstract:

Chemistry Department, Regional College of Education, A.Jmer-305 004 <em>Manuscrtpt received 18 August 1992, revised 5 April 1993, accepted 13 Apnl 1993</em> Polarographic Behaviour of Xanthate Anions as Salts of 2,3-Dihydroxypyridine and 2-Amino-hydroxypyridinebis(cyclopentadienyl)titanium(Iv) and -zirconium(Iv) Chelates

APA, Harvard, Vancouver, ISO, and other styles

11

Li, Xiao-lin, Hao-ting Zhu, Li Zhan, et al. "A Convenient Synthesis of Gimeracil." Journal of Chemical Research 42, no. 1 (2018): 33–34. http://dx.doi.org/10.3184/174751918x15166150010920.

Full text

Abstract:

A practical three-step synthetic approach to gimeracil in a 68% overall yield is described, using 2,4-dimethoxypyridine as the starting material with 3,5-dichloro-2,4-dimethoxypyridine and 3,5-dichloro-2,4-dihydroxypyridine as intermediates. The advantages of this procedure include short reaction steps, simple operation and good yield.

APA, Harvard, Vancouver, ISO, and other styles

12

Morais, Victor M. F., Margarida S. Miranda, and M. Agostinha R. Matos. "Experimental and computational thermochemistry of the dihydroxypyridine isomers." Journal of Chemical Thermodynamics 38, no. 4 (2006): 450–54. http://dx.doi.org/10.1016/j.jct.2005.06.013.

Full text

APA, Harvard, Vancouver, ISO, and other styles

13

Kolder, C. R., and H. J. den Hertog. "Synthesis and reactivity of 5-chloro-2,4-dihydroxypyridine." Recueil des Travaux Chimiques des Pays-Bas 72, no. 4 (2010): 285–95. http://dx.doi.org/10.1002/recl.19530720404.

Full text

APA, Harvard, Vancouver, ISO, and other styles

14

Sachelaru, Paula, Emile Schiltz, Gabor L. Igloi та Roderich Brandsch. "An α/β-Fold C—C Bond Hydrolase Is Involved in a Central Step of Nicotine Catabolism by Arthrobacter nicotinovorans". Journal of Bacteriology 187, № 24 (2005): 8516–19. http://dx.doi.org/10.1128/jb.187.24.8516-8519.2005.

Full text

Abstract:

ABSTRACT The enzyme catalyzing the hydrolytic cleavage of 2,6-dihydroxypseudooxynicotine to 2,6-dihydroxypyridine and γ-N-methylaminobutyrate was found to be encoded on pAO1 of Arthrobacter nicotinovorans. The new enzyme answers an old question about nicotine catabolism and may be the first C—C bond hydrolase that is involved in the biodegradation of a heterocyclic compound.

APA, Harvard, Vancouver, ISO, and other styles

15

Herdeis, Claus, та Gerhard Bissinger. "Synthesis and Serotonin-Receptor Activity of Substituted 1-Oxo-1,2,3,4-tetrahydro-β-carbolines". Zeitschrift für Naturforschung B 42, № 6 (1987): 785–90. http://dx.doi.org/10.1515/znb-1987-0626.

Full text

Abstract:

Abstract 3-Hydroxy-2-pyridone, Strychnocarpine Derivatives, 5-Hydroxytryptamine Receptor Stimulators 2,3-Dihydroxypyridine is used as a starting material for the synthesis of donor and acceptor substituted l-oxo-l,2,3,4-tetrahydro-/S-carbolines via Fischer indole cyclisation. An alkaloid from Alstonia venenata is prepared. All compounds inclusive strychnocarpine show low affinity to the Serotonine receptor.

APA, Harvard, Vancouver, ISO, and other styles

16

SHASHI, K. BANSAL, TIKKU SHIELLA, S. SINDHU R., and SINGH YOGENDRA. "Synthesis and Characterisation of Halides and Complex Halogeno Anions as Salts of Bis( cyclopentadienyl)zirconium(IV) Chelates formed with 2,3-Dihydroxypyridine and 2-Amino-3-hydroxypyridine." Journal of Indian Chemical Society Vol. 68, Oct 1991 (1991): 556–57. https://doi.org/10.5281/zenodo.6137905.

Full text

Abstract:

Chemistry Department. Regional College of Educn.tion, Ajmer-305 004 Chemistry Department. University of Delhi. Delhi-110 007 <em>Manuscript received 27 February 1990. revised 16 September 1991, accepted 20 September 1991</em> Synthesis and Characterisation of Halides and Complex Halogeno Anions as Salts of Bis( cyclopentadienyl)zirconium(IV) Chelates formed with 2,3-Dihydroxypyridine and 2-Amino-3-hydroxypyridine.

APA, Harvard, Vancouver, ISO, and other styles

17

Behrman, Edward J. "Some Derivatives of 5-hydroxy-2-pyridone(2,5-dihydroxypyridine)." Journal of Chemical Research 38, no. 2 (2014): 121–22. http://dx.doi.org/10.3184/174751914x13896383516701.

Full text

APA, Harvard, Vancouver, ISO, and other styles

18

Grote, Zacharias, Simone Bonazzi, Rosario Scopelliti, and Kay Severin. "Bridged Dihydroxypyridine Ligands for the Synthesis of Expanded Helicates." Journal of the American Chemical Society 128, no. 32 (2006): 10382–83. http://dx.doi.org/10.1021/ja0637806.

Full text

APA, Harvard, Vancouver, ISO, and other styles

19

den Hertog, H. J., and D. J. Buurman. "Tautomerism of hydroxypyridines (I): The structure of 2,4-dihydroxypyridine." Recueil des Travaux Chimiques des Pays-Bas 75, no. 3 (2010): 257–64. http://dx.doi.org/10.1002/recl.19560750304.

Full text

APA, Harvard, Vancouver, ISO, and other styles

20

Miller, Samantha J., Talia R. Collier, and Weiming Wu. "ChemInform Abstract: Efficient Reduction of Sulfoxides with 2,6-Dihydroxypyridine." ChemInform 31, no. 33 (2010): no. http://dx.doi.org/10.1002/chin.200033057.

Full text

APA, Harvard, Vancouver, ISO, and other styles

21

N., K. Gaur, Sharma Rashmi, and S. Sindhu R. "Mixed ligand complexes of iron-, cobalt- and nickel(II) with 2,3-dihydroxypyridine and some nitrogen donors." Journal of Indian Chemical Society Vol. 78, Jan 2001 (2001): 26–27. https://doi.org/10.5281/zenodo.5849362.

Full text

Abstract:

Regional Institute of Education, Bhopal-462 013, India <em>Manuscript received 4 January 2000 revised 27 June 2000, accepted 5 September 2000</em> Fe<sup>II</sup> , Co<sup>II </sup>and Ni <sup>II </sup>mixed ligand complexes of 2,3-dihydroxypyridine (DHP) and some nitrogen donor ligands NH<sub>3</sub>/CH<sub>3</sub>NH<sub>2</sub>/C<sub>2</sub>H<sub>5</sub>NH<sub>2</sub>/ Py have been synthesized.

APA, Harvard, Vancouver, ISO, and other styles

22

Shashi, K. Gupta, Sharma Rashmi, and S. Sindhu R. "Synthesis of some salts of 2,3-dihydroxypyridine and 2-amino-3-hydroxypyridine chelates of bis(cyclopentadienyl)titanium(IV)." Journal of Indian Chemical Society Vol. 78, Apr 2001 (2001): 202–3. https://doi.org/10.5281/zenodo.5872374.

Full text

Abstract:

Regional Institute of Education, Bhopal-462 013, India <em>Manuscript received 21 February 2000, revised 8 June 2000, accepted 30 November 2000</em> A series of [(Cp)<sub>2</sub>TiL]<sup>+</sup>X<sup>-</sup> compound, where X<sup>-</sup> = I<sup>-</sup>,Br<sup>-</sup>, \(ClO_4^-\), \(ZnCl_3^-\), \(CdCl_4^{2-}\), \(HgCl_3^-\) and \(FeCl_4^-\)<sub> </sub>and HL = 2,3- dihydroxypyridine and 2-amino-3-hydroxypyridine, have been synthesized. The studies demonstrate tetrahedral coordination around the titanium atom.

APA, Harvard, Vancouver, ISO, and other styles

23

den Hertog, H. J., and J. C. M. Schogt. "Migration of halogen atoms in halogenoderivatives of 2,4-dihydroxypyridine (I)." Recueil des Travaux Chimiques des Pays-Bas 70, no. 4 (2010): 353–60. http://dx.doi.org/10.1002/recl.19510700410.

Full text

APA, Harvard, Vancouver, ISO, and other styles

24

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

25

Domı́nguez-Bello, M. G., M. Lovera, and M. T. Rincón. "Characteristics of dihydroxypyridine-degrading activity in the rumen bacterium Synergistes jonesii." FEMS Microbiology Ecology 23, no. 4 (2006): 361–65. http://dx.doi.org/10.1111/j.1574-6941.1997.tb00417.x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

26

Domínguez-Bello, M. "Characteristics of dihydroxypyridine-degrading activity in the rumen bacterium Synergistes jonesii." FEMS Microbiology Ecology 23, no. 4 (1997): 361–65. http://dx.doi.org/10.1016/s0168-6496(97)00047-0.

Full text

APA, Harvard, Vancouver, ISO, and other styles

27

Treiber, Nora, and Georg E. Schulz. "Structure of 2,6-Dihydroxypyridine 3-hydroxylase from a Nicotine-degrading Pathway." Journal of Molecular Biology 379, no. 1 (2008): 94–104. http://dx.doi.org/10.1016/j.jmb.2008.03.032.

Full text

APA, Harvard, Vancouver, ISO, and other styles

28

Puchała, R., T. Sahlu, Jennifer J. Davis, and S. P. Hart. "Influence of mineral supplementation on 2,3-dihydroxypyridine toxicity in Angora goats." Animal Feed Science and Technology 55, no. 3-4 (1995): 253–62. http://dx.doi.org/10.1016/0377-8401(95)00794-n.

Full text

APA, Harvard, Vancouver, ISO, and other styles

29

Kolder, C. R., and H. J. den Hertog. "Migration of halogen atoms in halogeno-derivatives of 2,4-dihydroxypyridine (II)." Recueil des Travaux Chimiques des Pays-Bas 72, no. 10 (2010): 853–58. http://dx.doi.org/10.1002/recl.19530721005.

Full text

APA, Harvard, Vancouver, ISO, and other styles

30

Yu, Hao, Hongzhi Tang, Xiongyu Zhu, Yangyang Li, and Ping Xu. "Molecular Mechanism of Nicotine Degradation by a Newly Isolated Strain, Ochrobactrum sp. Strain SJY1." Applied and Environmental Microbiology 81, no. 1 (2014): 272–81. http://dx.doi.org/10.1128/aem.02265-14.

Full text

Abstract:

ABSTRACTA newly isolated strain, SJY1, identified asOchrobactrumsp., utilizes nicotine as a sole source of carbon, nitrogen, and energy. Strain SJY1 could efficiently degrade nicotine via a variant of the pyridine and pyrrolidine pathways (the VPP pathway), which highlights bacterial metabolic diversity in relation to nicotine degradation. A 97-kbp DNA fragment containing six nicotine degradation-related genes was obtained by gap closing from the genome sequence of strain SJY1. Three genes, designatedvppB,vppD, andvppE, in the VPP pathway were cloned and heterologously expressed, and the relat

APA, Harvard, Vancouver, ISO, and other styles

31

Wei, Jingjing, Yijing Wang, Xinyi Li, Xue Zhang, and Yongjun Liu. "Mechanistic Insights into Pyridine Ring Degradation Catalyzed by 2,5-Dihydroxypyridine Dioxygenase NicX." Inorganic Chemistry 61, no. 5 (2022): 2517–29. http://dx.doi.org/10.1021/acs.inorgchem.1c03370.

Full text

APA, Harvard, Vancouver, ISO, and other styles

32

Reis, P. J., R. Puchala, T. Sahlu, and A. L. Goetsch. "Effects of mimosine and 2,3-dihydroxypyridine on fiber shedding in Angora goats." Journal of Animal Science 77, no. 5 (1999): 1224. http://dx.doi.org/10.2527/1999.7751224x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

33

Allison, M. J., A. C. Hammond, and R. J. Jones. "Detection of ruminal bacteria that degrade toxic dihydroxypyridine compounds produced from mimosine." Applied and Environmental Microbiology 56, no. 3 (1990): 590–94. http://dx.doi.org/10.1128/aem.56.3.590-594.1990.

Full text

APA, Harvard, Vancouver, ISO, and other styles

34

Puchala, R., Jennifer J. Davis, and T. Sahlu. "Determination of mimosine and 3,4-dihydroxypyridine in milk and plasma of goats." Journal of Chromatography B: Biomedical Sciences and Applications 685, no. 2 (1996): 375–78. http://dx.doi.org/10.1016/s0378-4347(96)00221-6.

Full text

APA, Harvard, Vancouver, ISO, and other styles

35

Gorantla, Jaggaiah N., Divya Kovval, and Ravi S. Lankalapalli. "An unusual synthesis of 2-pyridone and 3,5-dihydroxypyridine from a carbohydrate." Tetrahedron Letters 54, no. 25 (2013): 3230–32. http://dx.doi.org/10.1016/j.tetlet.2013.03.083.

Full text

APA, Harvard, Vancouver, ISO, and other styles

36

Burilov, A. R., I. R. Knyazeva, M. A. Pudovik, et al. "New phosphorus-containing analog of calix[4]resorcinarene based on 2,6-dihydroxypyridine." Russian Chemical Bulletin 56, no. 2 (2007): 364–66. http://dx.doi.org/10.1007/s11172-007-0060-x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

37

Türkmen, Dervis, Carina Dettenrieder, Pontus Forsberg, et al. "Corrosion Detection by Infrared Attenuated Total Reflection Spectroscopy via Diamond-Like Carbon-Coated Silicon Wafers and Iron-Sensitive Dyes." Sensors 19, no. 15 (2019): 3373. http://dx.doi.org/10.3390/s19153373.

Full text

Abstract:

The durability of metal-based constructions, especially those containing reinforced concrete, is mainly limited by corrosion processes. Diamond-like carbon (DLC)-coated silicon (Si) wafers provide a chemically inert and mechanically robust sensing interface for application in aggressive environments. In this study, iron-sensitive dyes, i.e., 2,3-dihydroxypyridine (DHP) and 1,2-dihydroxybenzol (DHB), were coated onto DLC-modified Si wafers for evaluating the potential of detecting corrosion processes via evanescent field absorption spectroscopy using Fourier-transform infrared spectroscopy. The

APA, Harvard, Vancouver, ISO, and other styles

38

Tatsumi, Kunihiko, Takeshi Yamauchi, Kunihiko Kiyono, et al. "3-Cyano-2, 6-Dihydroxypyridine (CNDP), a New Potent Inhibitor of Dihydrouracil Dehydrogenase." Journal of Biochemistry 114, no. 6 (1993): 912–18. http://dx.doi.org/10.1093/oxfordjournals.jbchem.a124276.

Full text

APA, Harvard, Vancouver, ISO, and other styles

39

Mostafa, Sahar I. "Synthesis, characterization and antineoplastic activity of 5-chloro-2,3-dihydroxypyridine transition metal complexes." Journal of Coordination Chemistry 61, no. 10 (2008): 1553–67. http://dx.doi.org/10.1080/00958970701598977.

Full text

APA, Harvard, Vancouver, ISO, and other styles

40

Sahlu, T., R. Puchala, P. J. Reis, et al. "Technical note: tissue residues of mimosine and 2,3-dihydroxypyridine after intravenous infusion in goats." Journal of Animal Science 73, no. 1 (1995): 172. http://dx.doi.org/10.2527/1995.731172x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

41

Oprea, Stefan, and Violeta Otilia Potolinca. "Synthesis and characterization of photoactive polyurethane elastomers with 2,3-dihydroxypyridine in the main chain." Journal of Materials Science 47, no. 2 (2011): 677–84. http://dx.doi.org/10.1007/s10853-011-5838-4.

Full text

APA, Harvard, Vancouver, ISO, and other styles

42

Pepato, Maria T., Mayara F. Alberconi, Michelle C. da Rocha, et al. "Synthesis, characterization and biological analysis of the complex [VO(Hdhp)2] (H2dhp = 2,3-dihydroxypyridine)." Transition Metal Chemistry 33, no. 3 (2007): 301–9. http://dx.doi.org/10.1007/s11243-007-9003-5.

Full text

APA, Harvard, Vancouver, ISO, and other styles

43

Gorantla, Jaggaiah N., Divya Kovval, and Ravi S. Lankalapalli. "ChemInform Abstract: An Unusual Synthesis of 2-Pyridone and 3,5-Dihydroxypyridine from a Carbohydrate." ChemInform 44, no. 40 (2013): no. http://dx.doi.org/10.1002/chin.201340156.

Full text

APA, Harvard, Vancouver, ISO, and other styles

44

Kontoghiorghes, G. J., S. Chambers, and A. V. Hoffbrand. "Comparative study of iron mobilization from haemosiderin, ferritin and iron(III) precipitates by chelators." Biochemical Journal 241, no. 1 (1987): 87–92. http://dx.doi.org/10.1042/bj2410087.

Full text

Abstract:

The heteroaromatic chelators 1,2-dimethyl-3-hydroxypyrid-4-one, maltol, mimosine and 2,4-dihydroxypyridine-N-oxide, have been shown to mobilize iron from human spleen haemosiderin, ferritin and also from iron(III) precipitates, all containing equal amounts of iron, at physiological pH. In the case of almost every chelator, the least-solubilized polynuclear iron form was ferritin, whereas haemosiderin was more soluble and the iron(III) precipitate the most soluble of all. Most of the chelators were more efficient than desferrioxamine at releasing iron from ferritin, but less efficient in the re

APA, Harvard, Vancouver, ISO, and other styles

45

Jiménez, José Ignacio, Iván Acebrón, José Luis García, Eduardo Díaz, and José Miguel Mancheño. "A preliminary crystallographic study of recombinant NicX, an Fe2+-dependent 2,5-dihydroxypyridine dioxygenase fromPseudomonas putidaKT2440." Acta Crystallographica Section F Structural Biology and Crystallization Communications 66, no. 5 (2010): 549–53. http://dx.doi.org/10.1107/s174430911001119x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

46

Varmaghani, Fahimeh, and Davood Nematollahi. "Electrochemically induced oxidative cyclization of 2,3-dihydroxypyridine. Synthesis of a novel highly oxygenated heterocyclic compound." Journal of Physical Organic Chemistry 25, no. 6 (2011): 511–14. http://dx.doi.org/10.1002/poc.1947.

Full text

APA, Harvard, Vancouver, ISO, and other styles

47

Ziegler, Kevin, Dris Ihiawakrim, Ovidiu Ersen, et al. "Electrodeposition of dihydroxypyridine-based films: Strong influence of the used isomer on the film structure." Colloids and Surfaces A: Physicochemical and Engineering Aspects 716 (July 2025): 136743. https://doi.org/10.1016/j.colsurfa.2025.136743.

Full text

APA, Harvard, Vancouver, ISO, and other styles

48

Dong, Caiwen, Yadong Zheng, Hongzhi Tang, et al. "Highly Efficient Synthesis of 2,5-Dihydroxypyridine using Pseudomonas sp. ZZ-5 Nicotine Hydroxylase Immobilized on Immobead 150." Catalysts 8, no. 11 (2018): 548. http://dx.doi.org/10.3390/catal8110548.

Full text

Abstract:

In this report, the use of immobilized nicotine hydroxylase from Pseudomonas sp. ZZ-5 (HSPHZZ) for the production of 2,5-dihydroxypyridine (2,5-DHP) from 6-hydroxy-3-succinoylpyridine (HSP) in the presence of nicotinamide adenine dinucleotide (NADH) and flavin adenine dinucleotide (FAD) is described. HSPHZZ was covalently immobilized on Immobead 150 (ImmHSPHZZ). ImmHSPHZZ (obtained with 5–30 mg of protein per gram of support) catalyzed the hydrolysis of HSP to 2,5-DHP. At a protein loading of 15 mg g−1, ImmHSPHZZ converted 93.6% of HSP to 2,5-DHP in 6 h. The activity of ImmHSPHZZ was compared

APA, Harvard, Vancouver, ISO, and other styles

49

Dominguez-Bello, M. Gloria, and C. S. Stewart. "Characteristics of a Rumen Clostridium Capable of Degrading Mimosine, 3(OH)-4-(1H)-Pyridone and 2,3 Dihydroxypyridine." Systematic and Applied Microbiology 14, no. 1 (1991): 67–71. http://dx.doi.org/10.1016/s0723-2020(11)80363-2.

Full text

APA, Harvard, Vancouver, ISO, and other styles

50

Zuo, Jian. "Crystal structure of catena-poly[diaqua-bis(di(N2,N6-dihydroxypyridine-2,6-dicarboxamide))potassium(I)]tetrahydrate, C14H25N6O14K." Zeitschrift für Kristallographie - New Crystal Structures 233, no. 3 (2018): 445–46. http://dx.doi.org/10.1515/ncrs-2017-0338.

Full text

Abstract:

AbstractC14H25N6O14K, triclinic, P1̅ (no. 2), a = 6.9630(15) Å, b = 9.2770(17) Å, c = 9.6100(18) Å, α = 69.822(2)°, β = 87.225(2)°, γ = 85.559(2)°, V = 580.8(2) Å3, Z = 1, Rgt(F) = 0.0366, wRref(F2) = 0.1052, T = 293(2) K.

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!