Artículos de revistas sobre el tema "Quinone"
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Weiss, Sophie A. y Lars J. C. Jeuken. "Electrodes modified with lipid membranes to study quinone oxidoreductases". Biochemical Society Transactions 37, n.º 4 (22 de julio de 2009): 707–12. http://dx.doi.org/10.1042/bst0370707.
Texto completoWang, Zhen-Hua, Xiao-Hui Fu, Qun Li, Yong You, Lei Yang, Jian-Qiang Zhao, Yan-Ping Zhang y Wei-Cheng Yuan. "Recent Advances in the Domino Annulation Reaction of Quinone Imines". Molecules 29, n.º 11 (24 de mayo de 2024): 2481. http://dx.doi.org/10.3390/molecules29112481.
Texto completoJensen,, Kenneth A., Zachary C. Ryan, Amber Vanden Wymelenberg, Daniel Cullen y Kenneth E. Hammel. "An NADH:Quinone Oxidoreductase Active during Biodegradation by the Brown-Rot Basidiomycete Gloeophyllum trabeum". Applied and Environmental Microbiology 68, n.º 6 (junio de 2002): 2699–703. http://dx.doi.org/10.1128/aem.68.6.2699-2703.2002.
Texto completoMiseviciene, Lina, Zilvinas Anusevicius, Jonas Sarlauskas, Richard J. Harris, Nigel S. Scrutton y Narimantas Cenas. "Two-electron reduction of quinones by Enterobacter cloacae PB2 pentaerythritol tetranitrate reductase: quantitative structure-activity relationships." Acta Biochimica Polonica 54, n.º 2 (4 de junio de 2007): 379–85. http://dx.doi.org/10.18388/abp.2007_3260.
Texto completoVienozinskis, J., A. Butkus, N. Cenas y J. Kulys. "The mechanism of the quinone reductase reaction of pig heart lipoamide dehydrogenase". Biochemical Journal 269, n.º 1 (1 de julio de 1990): 101–5. http://dx.doi.org/10.1042/bj2690101.
Texto completoGiulivi, C. y 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, n.º 1 (1 de julio de 1994): 21–30. http://dx.doi.org/10.1042/bj3010021.
Texto completoBreker, Johannes, Reinhard Schmutzler, Bernd Dorbath y 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, n.º 8 (1 de agosto de 1990): 1177–86. http://dx.doi.org/10.1515/znb-1990-0812.
Texto completoMonks, Terrence y Douglas Jones. "The Metabolism and Toxicity of Quinones, Quinonimines, Quinone Methides, and Quinone-Thioethers". Current Drug Metabolism 3, n.º 4 (1 de agosto de 2002): 425–38. http://dx.doi.org/10.2174/1389200023337388.
Texto completoFlynn, Noah R., Michael D. Ward, Mary A. Schleiff, Corentine M. C. Laurin, Rohit Farmer, Stuart J. Conway, Gunnar Boysen, S. Joshua Swamidass y Grover P. Miller. "Bioactivation of Isoxazole-Containing Bromodomain and Extra-Terminal Domain (BET) Inhibitors". Metabolites 11, n.º 6 (15 de junio de 2021): 390. http://dx.doi.org/10.3390/metabo11060390.
Texto completoXu, Wei, William R. Dolbier, Jian-Xin Duan, Yian Zhai, Katsu Ogawa, Merle A. Battiste y Ion Ghiviriga. "Octafluoro[2.2]paracyclophane (AF4) Quinone". Collection of Czechoslovak Chemical Communications 73, n.º 12 (2008): 1764–76. http://dx.doi.org/10.1135/cccc20081764.
Texto completoGready, JE, K. Hata, S. Sternhell y CW Tansey. "N.M.R.-Study of Bond Orders in o- and p-Quinone". Australian Journal of Chemistry 43, n.º 3 (1990): 593. http://dx.doi.org/10.1071/ch9900593.
Texto completoLi, Jin, Kattesh V. Katti, Ronald G. Cavell, A. Alan Pinkerton y 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, n.º 11 (1 de noviembre de 1996): 2378–85. http://dx.doi.org/10.1139/v96-265.
Texto completoEllis, Jessie, Xueyan Fu, J. Philip Karl, Patrick Radcliffe, Jason Soares, Laurel Doherty, Christopher Hernandez, Joel Mason, Angela Oliverio y Sarah Booth. "Investigation of Vitamin K Quinone Metabolism by Human Gut Bacteria". Current Developments in Nutrition 4, Supplement_2 (29 de mayo de 2020): 392. http://dx.doi.org/10.1093/cdn/nzaa045_025.
Texto completoBegleiter, Asher. "The contribution of alkylation to the activity of quinone antitumor agents". Canadian Journal of Physiology and Pharmacology 64, n.º 5 (1 de mayo de 1986): 581–85. http://dx.doi.org/10.1139/y86-096.
Texto completoLima, Larissa S., Luiz Cláudio de A. Barbosa, Elson S. de Alvarenga, Antônio J. Demuner y Antônio A. da Silva. "Synthesis and Phytotoxicity Evaluation of Substituted para-Benzoquinones". Australian Journal of Chemistry 56, n.º 6 (2003): 625. http://dx.doi.org/10.1071/ch02032.
Texto completoRussell, RA, BA Pilley, RW Irvine y RN Warrener. "Anthracyclines. XVI. Further Comments Concerning the Phthalide Anion Annelation of Quinone Monoacetals". Australian Journal of Chemistry 40, n.º 2 (1987): 311. http://dx.doi.org/10.1071/ch9870311.
Texto completoJuliasih, Ni Luh Gede Ratna, Lee Chang Yuan, Yuki Sago, Yoichi Atsuta y 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.
Texto completoIto, Shosuke, Manickam Sugumaran y 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, n.º 17 (24 de agosto de 2020): 6080. http://dx.doi.org/10.3390/ijms21176080.
Texto completoKhetan, Abhishek. "High-Throughput Virtual Screening of Quinones for Aqueous Redox Flow Batteries: Status and Perspectives". Batteries 9, n.º 1 (28 de diciembre de 2022): 24. http://dx.doi.org/10.3390/batteries9010024.
Texto completoNorkov, Sergey V., Anton V. Cherkasov, Andrey S. Shavyrin, Maxim V. Arsenyev, Viacheslav A. Kuropatov y 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 de enero de 2021): 273–82. http://dx.doi.org/10.3762/bjoc.17.26.
Texto completoWiraswati, Hesti L., Fida M. Warganegara, Akhmaloka Akhmaloka y 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, n.º 02 (30 de junio de 2021): 681–89. http://dx.doi.org/10.13005/bpj/2170.
Texto completoKass, G. E., S. K. Duddy y S. Orrenius. "Activation of hepatocyte protein kinase C by redox-cycling quinones". Biochemical Journal 260, n.º 2 (1 de junio de 1989): 499–507. http://dx.doi.org/10.1042/bj2600499.
Texto completoLuo, Yu Jiao, Ling Feng Qiu, Yi Ming Chen y 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 (mayo de 2012): 440–43. http://dx.doi.org/10.4028/www.scientific.net/amr.518-523.440.
Texto completoOliveira, Joyce C., Renato L. de Carvalho, Hugo G. S. Sampaio, João Honorato, Javier A. Ellena, Felipe T. Martins, João V. M. Pereira et al. "It Takes Two to Tango, Part II: Synthesis of A-Ring Functionalised Quinones Containing Two Redox-Active Centres with Antitumour Activities". Molecules 28, n.º 5 (27 de febrero de 2023): 2222. http://dx.doi.org/10.3390/molecules28052222.
Texto completoMacDonald, Michael J. "Stimulation of insulin release from pancreatic islets by quinones". Bioscience Reports 11, n.º 3 (1 de junio de 1991): 165–70. http://dx.doi.org/10.1007/bf01182485.
Texto completoLian, Xiao-Lei, Alafate Adili, Bin Liu, Zhong-Lin Tao y Zhi-Yong Han. "Enantioselective [4 + 1] cycloaddition of ortho-quinone methides and bromomalonates under phase-transfer catalysis". Organic & Biomolecular Chemistry 15, n.º 17 (2017): 3670–73. http://dx.doi.org/10.1039/c7ob00484b.
Texto completoWebster, 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, n.º 41 (28 de agosto de 2023): 2335. http://dx.doi.org/10.1149/ma2023-01412335mtgabs.
Texto completoLaatsch, 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, n.º 3 (1 de marzo de 1990): 393–400. http://dx.doi.org/10.1515/znb-1990-0316.
Texto completoTsou, Yun-Jie, Ren-You Guan y Jeng-Liang Han. "Enantioselective organocatalytic vinylogous aldol-cyclization cascade reaction of 3-alkylidene oxindoles with o-quinones". Organic & Biomolecular Chemistry 19, n.º 26 (2021): 5836–43. http://dx.doi.org/10.1039/d1ob00888a.
Texto completoJovanovic, S. V., K. Kónya y 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, n.º 11 (1 de noviembre de 1995): 1803–10. http://dx.doi.org/10.1139/v95-222.
Texto completoField, J. A., F. J. Cervantes, F. P. van der Zee y G. Lettinga. "Role of quinones in the biodegradation of priority pollutants: a review". Water Science and Technology 42, n.º 5-6 (1 de septiembre de 2000): 215–22. http://dx.doi.org/10.2166/wst.2000.0516.
Texto completoSekulic, Tatjana, Lj V. Vujisic, B. P. M. Curcic, B. M. Mandic, D. Z. Antic, Snezana Trifunovic, D. M. Godjevac, Vlatka Vajs, V. T. Tomic y 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, n.º 1 (2014): 385–90. http://dx.doi.org/10.2298/abs1401385s.
Texto completoHu, H. Y., B. R. Lim, N. Goto, V. K. Bhupathiraju y K. Fujie. "Characterization of microbial community in an activated sludge process treating domestic wastewater using quinone profiles". Water Science and Technology 43, n.º 1 (1 de enero de 2001): 99–106. http://dx.doi.org/10.2166/wst.2001.0024.
Texto completoElgawish, Mohamed Saleh, Naoya Kishikawa, Mohamed A. Helal, Kaname Ohyama y Naotaka Kuroda. "Molecular modeling and spectroscopic study of quinone–protein adducts: insight into toxicity, selectivity, and reversibility". Toxicology Research 4, n.º 4 (2015): 843–47. http://dx.doi.org/10.1039/c5tx00098j.
Texto completoNozawa, Mamie, Hong-Ying Hu, Koichi Fujie, Tomohiko Tsuchida y Kohei Urano. "Population dynamics of chromate reducing bacteria in a bioreactor system developed for the treatment of chromate wastewater". Water Science and Technology 37, n.º 4-5 (1 de febrero de 1998): 109–12. http://dx.doi.org/10.2166/wst.1998.0595.
Texto completoBaxter, Ryan, Akil Hamsath y Jordan Galloway. "Quinone C–H Alkylations via Oxidative Radical Processes". Synthesis 50, n.º 15 (6 de junio de 2018): 2915–23. http://dx.doi.org/10.1055/s-0037-1610005.
Texto completoFujie, Koichi, Hong-Ying Hu, Hajime Tanaka y Kohei Urano. "Ecological Studies of Aerobic Submerged Biofilter on the Basis of Respiratory Quinone Profiles". Water Science and Technology 29, n.º 7 (1 de abril de 1994): 373–76. http://dx.doi.org/10.2166/wst.1994.0364.
Texto completoSladic, Dusan, Irena Novakovic, Zoran Vujcic, Tatjana Bozic, Natasa Bozic, Dragan Milic, Bogdan Solaja y Miroslav Gasic. "Protein covalent modification of biologically active quinones". Journal of the Serbian Chemical Society 69, n.º 11 (2004): 901–7. http://dx.doi.org/10.2298/jsc0411901s.
Texto completoGutiérrez, Isela, Sonia G. Bertolotti, M. A. Biasutti, Arnaldo T. Soltermann y Norman A. García. "Quinones and hydroxyquinones as generators and quenchers of singlet molecular oxygen". Canadian Journal of Chemistry 75, n.º 4 (1 de abril de 1997): 423–28. http://dx.doi.org/10.1139/v97-048.
Texto completoKianmehr, Ebrahim, Mehran Rezazadeh Khalkhali, Masoud Rezaeefard, Khalid Mohammed Khan y Seik Weng Ng. "Pd-Catalyzed Dehydrogenative Cross-Coupling of 1,4-Quinones with N,N′-Dialkyluracils". Australian Journal of Chemistry 68, n.º 1 (2015): 165. http://dx.doi.org/10.1071/ch14412.
Texto completoSugumaran, M., H. Dali y V. Semensi. "Mechanistic studies on tyrosinase-catalysed oxidative decarboxylation of 3,4-dihydroxymandelic acid". Biochemical Journal 281, n.º 2 (15 de enero de 1992): 353–57. http://dx.doi.org/10.1042/bj2810353.
Texto completoGrushevskaya, H. V. y N. G. Krylova. "Carbon Nanotubes as A High-Performance Platform for Target Delivery of Anticancer Quinones". Current Pharmaceutical Design 24, n.º 43 (28 de marzo de 2019): 5207–18. http://dx.doi.org/10.2174/1381612825666190117095132.
Texto completoHiraishi, Akira, Taichi Umezawa, Hiroyuki Yamamoto, Kenji Kato y Yonosuke Maki. "Changes in Quinone Profiles of Hot Spring Microbial Mats with a Thermal Gradient". Applied and Environmental Microbiology 65, n.º 1 (1 de enero de 1999): 198–205. http://dx.doi.org/10.1128/aem.65.1.198-205.1999.
Texto completoHui, Pan, Mathieu Branca, Benoît Limoges y François Mavré. "An autocatalytic organic reaction network based on cross-catalysis". Chemical Communications 57, n.º 86 (2021): 11374–77. http://dx.doi.org/10.1039/d1cc05121k.
Texto completoLi, Zhi y Xiao-Long Xu. "Deciphering the Redox Chain Mechanism in the Catalytic Alkylation of Quinones". Synlett 29, n.º 14 (14 de mayo de 2018): 1807–13. http://dx.doi.org/10.1055/s-0037-1610125.
Texto completoCaldwell, Sharon L., Joe B. Gilroy, Rajsapan Jain, Evan Crawford, Brian O. Patrick y Robin G. Hicks. "Synthesis and redox properties of a phosphine-subsituted para-dioxolene and its bimetallic palladium complex". Canadian Journal of Chemistry 86, n.º 10 (1 de octubre de 2008): 976–81. http://dx.doi.org/10.1139/v08-127.
Texto completoSilva, Raquel L., Daniel P. Demarque, Renata G. Dusi, João Paulo B. Sousa, Lorena C. Albernaz y Laila S. Espindola. "Residual Larvicidal Activity of Quinones against Aedes aegypti". Molecules 25, n.º 17 (31 de agosto de 2020): 3978. http://dx.doi.org/10.3390/molecules25173978.
Texto completoAgalidis, I., E. Rivas y F. Reiss-Husson. "Characterization of Reaction Center-B875 Complex of Rhodocyclus gelatinosus: QB Site Properties Derived from Reconstitution Experiments". Zeitschrift für Naturforschung C 46, n.º 1-2 (1 de febrero de 1991): 99–105. http://dx.doi.org/10.1515/znc-1991-1-216.
Texto completoMoullet, O. y J. L. Dreyer. "Selective inhibition of adenylate cyclase in bovine cortex by quinones: a novel cellular substrate for quinone cytotoxicity". Biochemical Journal 300, n.º 1 (15 de mayo de 1994): 99–106. http://dx.doi.org/10.1042/bj3000099.
Texto completoMas y mas, Sarah, Cécile Giustini, Jean-Luc Ferrer, Norbert Rolland, Gilles Curien y 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, n.º 4 (20 de marzo de 2015): 455–58. http://dx.doi.org/10.1107/s2053230x1500480x.
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