Artykuły w czasopismach na temat „Quinone”
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Weiss, Sophie A., i Lars J. C. Jeuken. "Electrodes modified with lipid membranes to study quinone oxidoreductases". Biochemical Society Transactions 37, nr 4 (22.07.2009): 707–12. http://dx.doi.org/10.1042/bst0370707.
Pełny tekst źródłaWang, Zhen-Hua, Xiao-Hui Fu, Qun Li, Yong You, Lei Yang, Jian-Qiang Zhao, Yan-Ping Zhang i Wei-Cheng Yuan. "Recent Advances in the Domino Annulation Reaction of Quinone Imines". Molecules 29, nr 11 (24.05.2024): 2481. http://dx.doi.org/10.3390/molecules29112481.
Pełny tekst źródłaJensen,, Kenneth A., Zachary C. Ryan, Amber Vanden Wymelenberg, Daniel Cullen i Kenneth E. Hammel. "An NADH:Quinone Oxidoreductase Active during Biodegradation by the Brown-Rot Basidiomycete Gloeophyllum trabeum". Applied and Environmental Microbiology 68, nr 6 (czerwiec 2002): 2699–703. http://dx.doi.org/10.1128/aem.68.6.2699-2703.2002.
Pełny tekst źródłaMiseviciene, Lina, Zilvinas Anusevicius, Jonas Sarlauskas, Richard J. Harris, Nigel S. Scrutton i Narimantas Cenas. "Two-electron reduction of quinones by Enterobacter cloacae PB2 pentaerythritol tetranitrate reductase: quantitative structure-activity relationships." Acta Biochimica Polonica 54, nr 2 (4.06.2007): 379–85. http://dx.doi.org/10.18388/abp.2007_3260.
Pełny tekst źródłaVienozinskis, J., A. Butkus, N. Cenas i J. Kulys. "The mechanism of the quinone reductase reaction of pig heart lipoamide dehydrogenase". Biochemical Journal 269, nr 1 (1.07.1990): 101–5. http://dx.doi.org/10.1042/bj2690101.
Pełny tekst źródłaGiulivi, C., i E. Cadenas. "One- and two-electron reduction of 2-methyl-1,4-naphthoquinone bioreductive alkylating agents: kinetic studies, free-radical production, thiol oxidation and DNA-strand-break formation". Biochemical Journal 301, nr 1 (1.07.1994): 21–30. http://dx.doi.org/10.1042/bj3010021.
Pełny tekst źródłaBreker, Johannes, Reinhard Schmutzler, Bernd Dorbath i Markus Wieber. "Reaktionen von unsymmetrischen λ5P – λ3P-Diphosphorverbindungen und von Diphosphinen (λ3P – λ3P) mit o-Chinonen / Reactions of Unsymmetrical λ5Ρ – λ3Ρ Diphosphorus Compounds and of Diphosphines (λ3P – λ3P) with o-Quinones". Zeitschrift für Naturforschung B 45, nr 8 (1.08.1990): 1177–86. http://dx.doi.org/10.1515/znb-1990-0812.
Pełny tekst źródłaMonks, Terrence, i Douglas Jones. "The Metabolism and Toxicity of Quinones, Quinonimines, Quinone Methides, and Quinone-Thioethers". Current Drug Metabolism 3, nr 4 (1.08.2002): 425–38. http://dx.doi.org/10.2174/1389200023337388.
Pełny tekst źródłaFlynn, Noah R., Michael D. Ward, Mary A. Schleiff, Corentine M. C. Laurin, Rohit Farmer, Stuart J. Conway, Gunnar Boysen, S. Joshua Swamidass i Grover P. Miller. "Bioactivation of Isoxazole-Containing Bromodomain and Extra-Terminal Domain (BET) Inhibitors". Metabolites 11, nr 6 (15.06.2021): 390. http://dx.doi.org/10.3390/metabo11060390.
Pełny tekst źródłaXu, Wei, William R. Dolbier, Jian-Xin Duan, Yian Zhai, Katsu Ogawa, Merle A. Battiste i Ion Ghiviriga. "Octafluoro[2.2]paracyclophane (AF4) Quinone". Collection of Czechoslovak Chemical Communications 73, nr 12 (2008): 1764–76. http://dx.doi.org/10.1135/cccc20081764.
Pełny tekst źródłaGready, JE, K. Hata, S. Sternhell i CW Tansey. "N.M.R.-Study of Bond Orders in o- and p-Quinone". Australian Journal of Chemistry 43, nr 3 (1990): 593. http://dx.doi.org/10.1071/ch9900593.
Pełny tekst źródłaLi, Jin, Kattesh V. Katti, Ronald G. Cavell, A. Alan Pinkerton i Herbert Nar. "Synthesis and characterization of phosphinimine-substituted trifluoro- or trichloro-p-benzoquinones and their cationic Rh(I) complexes. The crystal and molecular structure of 3,5,6-trichloro-2-(triphenylphosphinimino)-p-benzoquinone". Canadian Journal of Chemistry 74, nr 11 (1.11.1996): 2378–85. http://dx.doi.org/10.1139/v96-265.
Pełny tekst źródłaEllis, Jessie, Xueyan Fu, J. Philip Karl, Patrick Radcliffe, Jason Soares, Laurel Doherty, Christopher Hernandez, Joel Mason, Angela Oliverio i Sarah Booth. "Investigation of Vitamin K Quinone Metabolism by Human Gut Bacteria". Current Developments in Nutrition 4, Supplement_2 (29.05.2020): 392. http://dx.doi.org/10.1093/cdn/nzaa045_025.
Pełny tekst źródłaBegleiter, Asher. "The contribution of alkylation to the activity of quinone antitumor agents". Canadian Journal of Physiology and Pharmacology 64, nr 5 (1.05.1986): 581–85. http://dx.doi.org/10.1139/y86-096.
Pełny tekst źródłaLima, Larissa S., Luiz Cláudio de A. Barbosa, Elson S. de Alvarenga, Antônio J. Demuner i Antônio A. da Silva. "Synthesis and Phytotoxicity Evaluation of Substituted para-Benzoquinones". Australian Journal of Chemistry 56, nr 6 (2003): 625. http://dx.doi.org/10.1071/ch02032.
Pełny tekst źródłaRussell, RA, BA Pilley, RW Irvine i RN Warrener. "Anthracyclines. XVI. Further Comments Concerning the Phthalide Anion Annelation of Quinone Monoacetals". Australian Journal of Chemistry 40, nr 2 (1987): 311. http://dx.doi.org/10.1071/ch9870311.
Pełny tekst źródłaJuliasih, Ni Luh Gede Ratna, Lee Chang Yuan, Yuki Sago, Yoichi Atsuta i Hiroyuki Daimon. "Supercritical Fluid Extraction of Quinones from Compost for Microbial Community Analysis". Journal of Chemistry 2015 (2015): 1–7. http://dx.doi.org/10.1155/2015/717616.
Pełny tekst źródłaIto, Shosuke, Manickam Sugumaran i Kazumasa Wakamatsu. "Chemical Reactivities of ortho-Quinones Produced in Living Organisms: Fate of Quinonoid Products Formed by Tyrosinase and Phenoloxidase Action on Phenols and Catechols". International Journal of Molecular Sciences 21, nr 17 (24.08.2020): 6080. http://dx.doi.org/10.3390/ijms21176080.
Pełny tekst źródłaKhetan, Abhishek. "High-Throughput Virtual Screening of Quinones for Aqueous Redox Flow Batteries: Status and Perspectives". Batteries 9, nr 1 (28.12.2022): 24. http://dx.doi.org/10.3390/batteries9010024.
Pełny tekst źródłaNorkov, Sergey V., Anton V. Cherkasov, Andrey S. Shavyrin, Maxim V. Arsenyev, Viacheslav A. Kuropatov i Vladimir K. Cherkasov. "Annulation of a 1,3-dithiole ring to a sterically hindered o-quinone core. Novel ditopic redox-active ligands". Beilstein Journal of Organic Chemistry 17 (27.01.2021): 273–82. http://dx.doi.org/10.3762/bjoc.17.26.
Pełny tekst źródłaWiraswati, Hesti L., Fida M. Warganegara, Akhmaloka Akhmaloka i Muhamad A. Martoprawiro. "Molecular Docking Studies of ROS Agent from Quinone Family to Reductase Enzymes:Implication in Finding Anticancer Drug Candidate". Biomedical and Pharmacology Journal 14, nr 02 (30.06.2021): 681–89. http://dx.doi.org/10.13005/bpj/2170.
Pełny tekst źródłaKass, G. E., S. K. Duddy i S. Orrenius. "Activation of hepatocyte protein kinase C by redox-cycling quinones". Biochemical Journal 260, nr 2 (1.06.1989): 499–507. http://dx.doi.org/10.1042/bj2600499.
Pełny tekst źródłaLuo, Yu Jiao, Ling Feng Qiu, Yi Ming Chen i Jian Zhang. "Preliminary Discussion on the Activity of Denitrifying Phosphorus-Removing Bacteria in Sequencing Batch Reactors by Quinone Profile Analysis". Advanced Materials Research 518-523 (maj 2012): 440–43. http://dx.doi.org/10.4028/www.scientific.net/amr.518-523.440.
Pełny tekst źródłaOliveira, Joyce C., Renato L. de Carvalho, Hugo G. S. Sampaio, João Honorato, Javier A. Ellena, Felipe T. Martins, João V. M. Pereira i in. "It Takes Two to Tango, Part II: Synthesis of A-Ring Functionalised Quinones Containing Two Redox-Active Centres with Antitumour Activities". Molecules 28, nr 5 (27.02.2023): 2222. http://dx.doi.org/10.3390/molecules28052222.
Pełny tekst źródłaMacDonald, Michael J. "Stimulation of insulin release from pancreatic islets by quinones". Bioscience Reports 11, nr 3 (1.06.1991): 165–70. http://dx.doi.org/10.1007/bf01182485.
Pełny tekst źródłaLian, Xiao-Lei, Alafate Adili, Bin Liu, Zhong-Lin Tao i Zhi-Yong Han. "Enantioselective [4 + 1] cycloaddition of ortho-quinone methides and bromomalonates under phase-transfer catalysis". Organic & Biomolecular Chemistry 15, nr 17 (2017): 3670–73. http://dx.doi.org/10.1039/c7ob00484b.
Pełny tekst źródłaWebster, Richard David. "Utilizing Redox Transformations of Quinones to Modulate Weak Donor and Acceptor Bonding Interactions with H2o and CO2 in Organic Solvents". ECS Meeting Abstracts MA2023-01, nr 41 (28.08.2023): 2335. http://dx.doi.org/10.1149/ma2023-01412335mtgabs.
Pełny tekst źródłaLaatsch, Hartmut. "Methylierung 3,3′-dihydroxylierter 2,2′-Binaphthyl-1,4;1′,4′-dichinone / Methylation of 3,3′-Dihydroxylated 2,2′-Binaphtho-1,4;1′,4′-quinones". Zeitschrift für Naturforschung B 45, nr 3 (1.03.1990): 393–400. http://dx.doi.org/10.1515/znb-1990-0316.
Pełny tekst źródłaTsou, Yun-Jie, Ren-You Guan i Jeng-Liang Han. "Enantioselective organocatalytic vinylogous aldol-cyclization cascade reaction of 3-alkylidene oxindoles with o-quinones". Organic & Biomolecular Chemistry 19, nr 26 (2021): 5836–43. http://dx.doi.org/10.1039/d1ob00888a.
Pełny tekst źródłaJovanovic, S. V., K. Kónya i J. C. Scaiano. "Redox reactions of 3,5-di-tert-butyl-1,2-benzoquinone. Implications for reversal of paper yellowing". Canadian Journal of Chemistry 73, nr 11 (1.11.1995): 1803–10. http://dx.doi.org/10.1139/v95-222.
Pełny tekst źródłaField, J. A., F. J. Cervantes, F. P. van der Zee i G. Lettinga. "Role of quinones in the biodegradation of priority pollutants: a review". Water Science and Technology 42, nr 5-6 (1.09.2000): 215–22. http://dx.doi.org/10.2166/wst.2000.0516.
Pełny tekst źródłaSekulic, Tatjana, Lj V. Vujisic, B. P. M. Curcic, B. M. Mandic, D. Z. Antic, Snezana Trifunovic, D. M. Godjevac, Vlatka Vajs, V. T. Tomic i S. E. Makarov. "Quinones and non-quinones from the defensive secretion of Unciger transsilvanicus (Verhoeff, 1899) (Diplopoda, Julida, Julidae), from Serbia". Archives of Biological Sciences 66, nr 1 (2014): 385–90. http://dx.doi.org/10.2298/abs1401385s.
Pełny tekst źródłaHu, H. Y., B. R. Lim, N. Goto, V. K. Bhupathiraju i K. Fujie. "Characterization of microbial community in an activated sludge process treating domestic wastewater using quinone profiles". Water Science and Technology 43, nr 1 (1.01.2001): 99–106. http://dx.doi.org/10.2166/wst.2001.0024.
Pełny tekst źródłaElgawish, Mohamed Saleh, Naoya Kishikawa, Mohamed A. Helal, Kaname Ohyama i Naotaka Kuroda. "Molecular modeling and spectroscopic study of quinone–protein adducts: insight into toxicity, selectivity, and reversibility". Toxicology Research 4, nr 4 (2015): 843–47. http://dx.doi.org/10.1039/c5tx00098j.
Pełny tekst źródłaNozawa, Mamie, Hong-Ying Hu, Koichi Fujie, Tomohiko Tsuchida i Kohei Urano. "Population dynamics of chromate reducing bacteria in a bioreactor system developed for the treatment of chromate wastewater". Water Science and Technology 37, nr 4-5 (1.02.1998): 109–12. http://dx.doi.org/10.2166/wst.1998.0595.
Pełny tekst źródłaBaxter, Ryan, Akil Hamsath i Jordan Galloway. "Quinone C–H Alkylations via Oxidative Radical Processes". Synthesis 50, nr 15 (6.06.2018): 2915–23. http://dx.doi.org/10.1055/s-0037-1610005.
Pełny tekst źródłaFujie, Koichi, Hong-Ying Hu, Hajime Tanaka i Kohei Urano. "Ecological Studies of Aerobic Submerged Biofilter on the Basis of Respiratory Quinone Profiles". Water Science and Technology 29, nr 7 (1.04.1994): 373–76. http://dx.doi.org/10.2166/wst.1994.0364.
Pełny tekst źródłaSladic, Dusan, Irena Novakovic, Zoran Vujcic, Tatjana Bozic, Natasa Bozic, Dragan Milic, Bogdan Solaja i Miroslav Gasic. "Protein covalent modification of biologically active quinones". Journal of the Serbian Chemical Society 69, nr 11 (2004): 901–7. http://dx.doi.org/10.2298/jsc0411901s.
Pełny tekst źródłaGutiérrez, Isela, Sonia G. Bertolotti, M. A. Biasutti, Arnaldo T. Soltermann i Norman A. García. "Quinones and hydroxyquinones as generators and quenchers of singlet molecular oxygen". Canadian Journal of Chemistry 75, nr 4 (1.04.1997): 423–28. http://dx.doi.org/10.1139/v97-048.
Pełny tekst źródłaKianmehr, Ebrahim, Mehran Rezazadeh Khalkhali, Masoud Rezaeefard, Khalid Mohammed Khan i Seik Weng Ng. "Pd-Catalyzed Dehydrogenative Cross-Coupling of 1,4-Quinones with N,N′-Dialkyluracils". Australian Journal of Chemistry 68, nr 1 (2015): 165. http://dx.doi.org/10.1071/ch14412.
Pełny tekst źródłaSugumaran, M., H. Dali i V. Semensi. "Mechanistic studies on tyrosinase-catalysed oxidative decarboxylation of 3,4-dihydroxymandelic acid". Biochemical Journal 281, nr 2 (15.01.1992): 353–57. http://dx.doi.org/10.1042/bj2810353.
Pełny tekst źródłaGrushevskaya, H. V., i N. G. Krylova. "Carbon Nanotubes as A High-Performance Platform for Target Delivery of Anticancer Quinones". Current Pharmaceutical Design 24, nr 43 (28.03.2019): 5207–18. http://dx.doi.org/10.2174/1381612825666190117095132.
Pełny tekst źródłaHiraishi, Akira, Taichi Umezawa, Hiroyuki Yamamoto, Kenji Kato i Yonosuke Maki. "Changes in Quinone Profiles of Hot Spring Microbial Mats with a Thermal Gradient". Applied and Environmental Microbiology 65, nr 1 (1.01.1999): 198–205. http://dx.doi.org/10.1128/aem.65.1.198-205.1999.
Pełny tekst źródłaHui, Pan, Mathieu Branca, Benoît Limoges i François Mavré. "An autocatalytic organic reaction network based on cross-catalysis". Chemical Communications 57, nr 86 (2021): 11374–77. http://dx.doi.org/10.1039/d1cc05121k.
Pełny tekst źródłaLi, Zhi, i Xiao-Long Xu. "Deciphering the Redox Chain Mechanism in the Catalytic Alkylation of Quinones". Synlett 29, nr 14 (14.05.2018): 1807–13. http://dx.doi.org/10.1055/s-0037-1610125.
Pełny tekst źródłaCaldwell, Sharon L., Joe B. Gilroy, Rajsapan Jain, Evan Crawford, Brian O. Patrick i Robin G. Hicks. "Synthesis and redox properties of a phosphine-subsituted para-dioxolene and its bimetallic palladium complex". Canadian Journal of Chemistry 86, nr 10 (1.10.2008): 976–81. http://dx.doi.org/10.1139/v08-127.
Pełny tekst źródłaSilva, Raquel L., Daniel P. Demarque, Renata G. Dusi, João Paulo B. Sousa, Lorena C. Albernaz i Laila S. Espindola. "Residual Larvicidal Activity of Quinones against Aedes aegypti". Molecules 25, nr 17 (31.08.2020): 3978. http://dx.doi.org/10.3390/molecules25173978.
Pełny tekst źródłaAgalidis, I., E. Rivas i F. Reiss-Husson. "Characterization of Reaction Center-B875 Complex of Rhodocyclus gelatinosus: QB Site Properties Derived from Reconstitution Experiments". Zeitschrift für Naturforschung C 46, nr 1-2 (1.02.1991): 99–105. http://dx.doi.org/10.1515/znc-1991-1-216.
Pełny tekst źródłaMoullet, O., i J. L. Dreyer. "Selective inhibition of adenylate cyclase in bovine cortex by quinones: a novel cellular substrate for quinone cytotoxicity". Biochemical Journal 300, nr 1 (15.05.1994): 99–106. http://dx.doi.org/10.1042/bj3000099.
Pełny tekst źródłaMas y mas, Sarah, Cécile Giustini, Jean-Luc Ferrer, Norbert Rolland, Gilles Curien i David Cobessi. "Analytical ultracentrifugation and preliminary X-ray studies of the chloroplast envelope quinone oxidoreductase homologue fromArabidopsis thaliana". Acta Crystallographica Section F Structural Biology Communications 71, nr 4 (20.03.2015): 455–58. http://dx.doi.org/10.1107/s2053230x1500480x.
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