Статті в журналах з теми "Analogues biomimétiques de nicotinamide"
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Lipka, Pawel, Andrzej Zatorski, Kyoichi A. Watanabe, and Krzysztof W. Pankeiwicz. "Synthesis of Methylene-Bridged Analogues of Nicotinamide Riboside, Nicotinamide Mononucleotide and Nicotinamide Adenine Dinucleotide." Nucleosides and Nucleotides 15, no. 1-3 (January 1996): 149–67. http://dx.doi.org/10.1080/07328319608002377.
Повний текст джерелаPankiewicz, Krzysztof W., Marek M. Kabat, Elzbieta Sochacka, Lech Ciszewski, Joanna Zeidler, and Kyoichi A. Watanabe. "C-Nucleoside Analogues of Nicotinamide Mononucleotide (NMN)." Nucleosides and Nucleotides 7, no. 5-6 (October 1988): 589–93. http://dx.doi.org/10.1080/07328318808056291.
Повний текст джерелаCampbell, P. I., M. I. Abraham, and S. A. Kempson. "Increased cAMP in proximal tubules is acute effect of nicotinamide analogues." American Journal of Physiology-Renal Physiology 257, no. 6 (December 1, 1989): F1021—F1026. http://dx.doi.org/10.1152/ajprenal.1989.257.6.f1021.
Повний текст джерелаPankiewicz, K. W., A. Zatorski, and K. A. Watanabe. "NAD-analogues as potential anticancer agents: conformational restrictions as basis for selectivity." Acta Biochimica Polonica 43, no. 1 (March 31, 1996): 183–93. http://dx.doi.org/10.18388/abp.1996_4552.
Повний текст джерелаGoulioukina, Natasha, Johny Wehbe, Damien Marchand, Roger Busson, Eveline Lescrinier, Dieter Heindl, and Piet Herdewijn. "Synthesis of Nicotinamide Adenine Dinucleotide (NAD) Analogues with a Sugar Modified Nicotinamide Moiety." Helvetica Chimica Acta 90, no. 7 (July 2007): 1266–78. http://dx.doi.org/10.1002/hlca.200790127.
Повний текст джерелаMigaud, Marie, Philip Redpath, Jolanta Haluszczak, and Simon Macdonald. "Nicotinamide Benzimidazolide Dinucleotides, Non-Cyclisable Analogues of NAD+." Synlett 25, no. 16 (August 26, 2014): 2331–36. http://dx.doi.org/10.1055/s-0034-1379000.
Повний текст джерелаHocková, Dana, and Antonín Holý. "Synthesis of Some "Abbreviated" NAD+ Analogues." Collection of Czechoslovak Chemical Communications 62, no. 6 (1997): 948–56. http://dx.doi.org/10.1135/cccc19970948.
Повний текст джерелаKongmuang, Somlak. "Hydrotropic Solubilization of Riboflavin by Urea, Nicotinamide and Nicotinamide Analogues in Aqueous Systems(การละลายในนํ้าฃองไรโบฟลาวินโดยสารไฮโดรโทรปิค: ยูเ..." Thai Journal of Pharmaceutical Sciences 26, № 1 (1 січня 2002): 61–68. http://dx.doi.org/10.56808/3027-7922.2288.
Повний текст джерелаRöllig, Robert, Caroline E. Paul, Magalie Claeys-Bruno, Katia Duquesne, Selin Kara, and Véronique Alphand. "Divorce in the two-component BVMO family: the single oxygenase for enantioselective chemo-enzymatic Baeyer–Villiger oxidations." Organic & Biomolecular Chemistry 19, no. 15 (2021): 3441–50. http://dx.doi.org/10.1039/d1ob00015b.
Повний текст джерелаPankiewicz, Krzysztof, Kyoichi Watanabe, Krystyna Lesiak-Watanabe, Barry Goldstein, and Hiremagalur Jayaram. "The Chemistry of Nicotinamide Adenine Dinucleotide (NAD) Analogues Containing C-Nucleosides Related to Nicotinamide Riboside [1]." Current Medicinal Chemistry 9, no. 7 (April 1, 2002): 733–41. http://dx.doi.org/10.2174/0929867024606920.
Повний текст джерелаPetrelli, Riccardo, Yuk Yin Sham, Liqiang Chen, Krzysztof Felczak, Eric Bennett, Daniel Wilson, Courtney Aldrich, et al. "Selective inhibition of nicotinamide adenine dinucleotide kinases by dinucleoside disulfide mimics of nicotinamide adenine dinucleotide analogues." Bioorganic & Medicinal Chemistry 17, no. 15 (August 2009): 5656–64. http://dx.doi.org/10.1016/j.bmc.2009.06.013.
Повний текст джерелаHocková, Dana, Milena Masojídková, and Antonín Holý. ""Abbreviated" NAD+ Analogues Containinga Phosphonate Function." Collection of Czechoslovak Chemical Communications 61, no. 10 (1996): 1538–48. http://dx.doi.org/10.1135/cccc19961538.
Повний текст джерелаSicsic, Sames, Mohamed Ikbal, and François Le Goffic. "Chemoenzymatic approach to carbocyclic analogues of ribonucleosides and nicotinamide ribose." Tetrahedron Letters 28, no. 17 (January 1987): 1887–88. http://dx.doi.org/10.1016/s0040-4039(00)96001-5.
Повний текст джерелаTanimori, Shinji, Takeshi Ohta, and Mitsunori Kirihata. "An efficient chemical synthesis of nicotinamide riboside (NAR) and analogues." Bioorganic & Medicinal Chemistry Letters 12, no. 8 (April 2002): 1135–37. http://dx.doi.org/10.1016/s0960-894x(02)00125-7.
Повний текст джерелаPaul, Caroline E., Isabel W. C. E. Arends, and Frank Hollmann. "Is Simpler Better? Synthetic Nicotinamide Cofactor Analogues for Redox Chemistry." ACS Catalysis 4, no. 3 (February 5, 2014): 788–97. http://dx.doi.org/10.1021/cs4011056.
Повний текст джерелаPankiewicz, K. W., K. Malinowski, H. N. Jayaram, K. Lesiak Watanabe, and K. A. Watanabe. "Novel Mycophenolic Adenine Bis{phosphonate)s as Potential Immunosuppressants." Current Medicinal Chemistry 6, no. 7 (July 1999): 629–34. http://dx.doi.org/10.2174/092986730607220401124820.
Повний текст джерелаMakarov, Mikhail V., та Marie E. Migaud. "Syntheses and chemical properties of β-nicotinamide riboside and its analogues and derivatives". Beilstein Journal of Organic Chemistry 15 (13 лютого 2019): 401–30. http://dx.doi.org/10.3762/bjoc.15.36.
Повний текст джерелаArora, Mandeep Kumar, Parul Grover, Syed Mohammed Basheeruddin Asdaq, Lovekesh Mehta, Ritu Tomar, Mohd Imran, Anuj Pathak, et al. "Potential role of nicotinamide analogues against SARS-COV-2 target proteins." Saudi Journal of Biological Sciences 28, no. 12 (December 2021): 7567–74. http://dx.doi.org/10.1016/j.sjbs.2021.09.072.
Повний текст джерелаLarocque, Elizabeth, Elizabeth Fei Yin Chu, Nimmashetti Naganna, and Herman O. Sintim. "Nicotinamide–Ponatinib Analogues as Potent Anti-CML and Anti-AML Compounds." ACS Omega 5, no. 6 (February 4, 2020): 2690–98. http://dx.doi.org/10.1021/acsomega.9b03223.
Повний текст джерелаNashawi, Asma A., and Richard Hartley. "New Vitamin E Analogues." Journal of King Abdulaziz University - Medical Sciences 23, no. 4 (December 31, 2016): 25–42. http://dx.doi.org/10.4197/med.23-4.4.
Повний текст джерелаLee, H. J., and G. G. Chang. "Interactions of nicotinamide-adenine dinucleotide phosphate analogues and fragments with pigeon liver malic enzyme. Synergistic effect between the nicotinamide and adenine moieties." Biochemical Journal 245, no. 2 (July 15, 1987): 407–14. http://dx.doi.org/10.1042/bj2450407.
Повний текст джерелаBrown, J. M., M. J. Lemmon, M. R. Horsman, and W. W. Lee. "Structure–activity Relationships for Tumour Radiosensitization by Analogues of Nicotinamide and Benzamide." International Journal of Radiation Biology 59, no. 3 (January 1991): 739–48. http://dx.doi.org/10.1080/09553009114550651.
Повний текст джерелаHargenrader, George N., Ravindra B. Weerasooriya, Stefan Ilic, Jens Niklas, Oleg G. Poluektov, and Ksenija D. Glusac. "Photoregeneration of Biomimetic Nicotinamide Adenine Dinucleotide Analogues via a Dye-Sensitized Approach." ACS Applied Energy Materials 2, no. 1 (November 26, 2018): 80–91. http://dx.doi.org/10.1021/acsaem.8b01574.
Повний текст джерелаBatoux, Nathalie E., Francesca Paradisi, Paul C. Engel, and Marie E. Migaud. "Novel nicotinamide adenine dinucleotide analogues as selective inhibitors of NAD+-dependent enzymes." Tetrahedron 60, no. 31 (July 2004): 6609–17. http://dx.doi.org/10.1016/j.tet.2004.05.091.
Повний текст джерелаPaul, Caroline E., Isabel W. C. E. Arends, and Frank Hollmann. "ChemInform Abstract: Is Simpler Better? Synthetic Nicotinamide Cofactor Analogues for Redox Chemistry." ChemInform 45, no. 18 (April 17, 2014): no. http://dx.doi.org/10.1002/chin.201418274.
Повний текст джерелаKROHN, K., H. HEINS, and K. WIELCKENS. "ChemInform Abstract: Synthesis and Cytotoxic Activity of C-Glycosidic Nicotinamide Riboside Analogues." ChemInform 23, no. 23 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199223265.
Повний текст джерелаTanimori, Shinji, Takeshi Ohta, and Mitsunori Kirihata. "ChemInform Abstract: An Efficient Chemical Synthesis of Nicotinamide Riboside (NAR) and Analogues." ChemInform 33, no. 33 (May 20, 2010): no. http://dx.doi.org/10.1002/chin.200233231.
Повний текст джерелаKolbin, A. S., A. A. Kurylev, Yu Ye Balykina, M. A. Proskurin, and S. A. Mishinova. "Pharmacoeconomic analysis of insulin aspart+nicotinamide versus insulin aspart in patients with diabetes mellitus." Pharmacoeconomics: theory and practice 9, no. 4 (December 15, 2021): 5–11. http://dx.doi.org/10.30809/phe.4.2021.1.
Повний текст джерелаBezsudnova, Ekaterina Yu, Tatiana E. Petrova, Natalia V. Artemova, Konstantin M. Boyko, Ivan G. Shabalin, Tatiana V. Rakitina, Konstantin M. Polyakov, and Vladimir O. Popov. "NADP-Dependent Aldehyde Dehydrogenase from Archaeon Pyrobaculum sp.1860: Structural and Functional Features." Archaea 2016 (2016): 1–14. http://dx.doi.org/10.1155/2016/9127857.
Повний текст джерелаChen, Dongxing, Linjie Li, Krystal Diaz, Iredia D. Iyamu, Ravi Yadav, Nicholas Noinaj, and Rong Huang. "Novel Propargyl-Linked Bisubstrate Analogues as Tight-Binding Inhibitors for Nicotinamide N-Methyltransferase." Journal of Medicinal Chemistry 62, no. 23 (November 14, 2019): 10783–97. http://dx.doi.org/10.1021/acs.jmedchem.9b01255.
Повний текст джерелаWALL, Katherine A., Mariola KLIS, John KORNET, Donna COYLE, Jean-Christophe AMÉ, Myron K. JACOBSON, and James T. SLAMA. "Inhibition of the intrinsic NAD+ glycohydrolase activity of CD38 by carbocyclic NAD analogues." Biochemical Journal 335, no. 3 (November 1, 1998): 631–36. http://dx.doi.org/10.1042/bj3350631.
Повний текст джерелаPankiewicz, Krzysztof W., and Krzysztof Felczak. "From ribavirin to NAD analogues and back to ribavirin in search for anticancer agents." Heterocyclic Communications 21, no. 5 (October 1, 2015): 249–57. http://dx.doi.org/10.1515/hc-2015-0133.
Повний текст джерелаNayak, Yogendra, Venkatachalam Hillemane, Vijay Kumar Daroji, B. S. Jayashree, and M. K. Unnikrishnan. "Antidiabetic Activity of Benzopyrone Analogues in Nicotinamide-Streptozotocin Induced Type 2 Diabetes in Rats." Scientific World Journal 2014 (2014): 1–12. http://dx.doi.org/10.1155/2014/854267.
Повний текст джерелаWang, Lei, Bin Liu, Yuxue Liu, Yue Sun, Wujun Liu, Dayu Yu, and Zongbao K. Zhao. "Escherichia coli Strain Designed for Characterizing in Vivo Functions of Nicotinamide Adenine Dinucleotide Analogues." Organic Letters 21, no. 9 (April 17, 2019): 3218–22. http://dx.doi.org/10.1021/acs.orglett.9b00935.
Повний текст джерелаKam, Bernard L., Olaf Malver, Thomas M. Marschner, and Norman J. Oppenheimer. "Pyridine coenzyme analogues. Synthesis and characterization of .alpha.- and .beta.-nicotinamide arabinoside adenine dinucleotides." Biochemistry 26, no. 12 (June 16, 1987): 3453–61. http://dx.doi.org/10.1021/bi00386a031.
Повний текст джерелаSLEATH, P. R., A. L. HANDLON, and N. J. OPPENHEIMER. "ChemInform Abstract: Pyridine Coenzyme Analogues. Part 3. Synthesis of Three NAD+ Analogues Containing a 2′-Deoxy-2′-Substituted Nicotinamide Arabinofuranosyl Moiety." ChemInform 22, no. 41 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199141250.
Повний текст джерелаZIEGLER, Mathias, Dierk JORCKE, and Manfred SCHWEIGER. "Identification of bovine liver mitochondrial NAD+ glycohydrolase as ADP-ribosyl cyclase." Biochemical Journal 326, no. 2 (September 1, 1997): 401–5. http://dx.doi.org/10.1042/bj3260401.
Повний текст джерелаConforti, Irene, Andrea Benzi, Irene Caffa, Santina Bruzzone, Alessio Nencioni, and Alberto Marra. "Iminosugar-Based Nicotinamide Phosphoribosyltransferase (NAMPT) Inhibitors as Potential Anti-Pancreatic Cancer Agents." Pharmaceutics 15, no. 5 (May 11, 2023): 1472. http://dx.doi.org/10.3390/pharmaceutics15051472.
Повний текст джерелаFelczak, Krzysztof, and Krzysztof W. Pankiewicz. "Synthesis of Methylenebis(Phosphonate) Analogues of 2-, 4-, and 6-Pyridones of Nicotinamide Adenine Dinucleotide." Nucleosides, Nucleotides and Nucleic Acids 30, no. 7-8 (July 2011): 512–23. http://dx.doi.org/10.1080/15257770.2011.575909.
Повний текст джерелаOHTA, Tatuya, Syuhei ISHIKURA, Syunichi SHINTANI, Noriyuki USAMI та Akira HARA. "Kinetic alteration of a human dihydrodiol/3α-hydroxysteroid dehydrogenase isoenzyme, AKR1C4, by replacement of histidine-216 with tyrosine or phenylalanine". Biochemical Journal 352, № 3 (8 грудня 2000): 685–91. http://dx.doi.org/10.1042/bj3520685.
Повний текст джерелаGalloway, T. S., and S. van Heyningen. "Binding of NAD+ by cholera toxin." Biochemical Journal 244, no. 1 (May 15, 1987): 225–30. http://dx.doi.org/10.1042/bj2440225.
Повний текст джерелаZhang, Liangren, Anna Ka Yee Kwong, Zhenjun Yang, Zhe Chen, Hon Cheung Lee, and Lihe Zhang. "Studies on the Synthesis of Nicotinamide Nucleoside and Nucleotide Analogues and Their Inhibitions towards CD38 NADase." HETEROCYCLES 83, no. 12 (2011): 2837. http://dx.doi.org/10.3987/com-11-12361.
Повний текст джерелаTanuma, Sei-ichi, Kiyotaka Katsuragi, Takahiro Oyama, Atsushi Yoshimori, Yuri Shibasaki, Yasunobu Asawa, Hiroaki Yamazaki, et al. "Structural Basis of Beneficial Design for Effective Nicotinamide Phosphoribosyltransferase Inhibitors." Molecules 25, no. 16 (August 10, 2020): 3633. http://dx.doi.org/10.3390/molecules25163633.
Повний текст джерелаCzarnecka, Kamila, Małgorzata Girek, Paweł Kręcisz, Robert Skibiński, Kamil Łątka, Jakub Jończyk, Marek Bajda, et al. "Discovery of New Cyclopentaquinoline Analogues as Multifunctional Agents for the Treatment of Alzheimer’s Disease." International Journal of Molecular Sciences 20, no. 3 (January 24, 2019): 498. http://dx.doi.org/10.3390/ijms20030498.
Повний текст джерелаGalloway, T. S., R. M. Tait, and S. van Heyningen. "Photolabelling of cholera toxin by NAD+." Biochemical Journal 242, no. 3 (March 15, 1987): 927–30. http://dx.doi.org/10.1042/bj2420927.
Повний текст джерелаJiang, Jie, Hongjun Kang, Xiaoliang Song, Sichao Huang, Sha Li, and Jun Xu. "A Model of Interaction between Nicotinamide Adenine Dinucleotide Phosphate (NADPH) Oxidase and Apocynin Analogues by Docking Method." International Journal of Molecular Sciences 14, no. 1 (January 4, 2013): 807–17. http://dx.doi.org/10.3390/ijms14010807.
Повний текст джерелаPankiewicz, Krzysztof W. "Novel nicotinamide adenine dinucleotide analogues as potential anticancer agents: Quest for specific inhibition of inosine monophosphate dehydrogenase." Pharmacology & Therapeutics 76, no. 1-3 (October 1997): 89–100. http://dx.doi.org/10.1016/s0163-7258(97)00092-2.
Повний текст джерелаWhyte, B. J., and W. T. Griffiths. "8-vinyl reduction and chlorophyll a biosynthesis in higher plants." Biochemical Journal 291, no. 3 (May 1, 1993): 939–44. http://dx.doi.org/10.1042/bj2910939.
Повний текст джерелаChen, Zhe, Anna Ka Yee Kwong, Zhenjun Yang, Liangren Zhang, Hon Cheung Lee, and Lihe Zhang. "ChemInform Abstract: Studies of the Synthesis of Nicotinamide Nucleoside and Nucleotide Analogues and Their Inhibitions Towards CD38 NADase." ChemInform 43, no. 15 (March 15, 2012): no. http://dx.doi.org/10.1002/chin.201215205.
Повний текст джерелаZhang, Yanmin, Arnaud Chevalier, Omar Khdour, Larisa Soto, and Sidney Hecht. "Inhibition of Human Cancer Cell Growth by Analogues of Antimycin A." Planta Medica 83, no. 18 (June 8, 2017): 1377–83. http://dx.doi.org/10.1055/s-0043-112343.
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