Relevant bibliographies by topics / Dihydroxypyridine

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Academic literature on the topic 'Dihydroxypyridine'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Dihydroxypyridine"

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.

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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
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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.

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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.

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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
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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.

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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
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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.

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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.

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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.
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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.

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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.

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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.

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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.
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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.

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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
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Book chapters on the topic "Dihydroxypyridine"

1

Schomburg, Dietmar, and Dörte Stephan. "2,5-Dihydroxypyridine 5,6-dioxygenase." In Enzyme Handbook. Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-57942-4_8.

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2

Schomburg, Dietmar, and Dörte Stephan. "2,6-Dihydroxypyridine 3-monooxygenase." In Enzyme Handbook. Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-57942-4_92.

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3

Pardasani, R. T., and P. Pardasani. "Magnetic properties of vanadium(IV) complex with 2,3-dihydroxypyridine." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 7. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65895-6_7.

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