Добірка наукової літератури з теми "Quinone"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся зі списками актуальних статей, книг, дисертацій, тез та інших наукових джерел на тему "Quinone".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Статті в журналах з теми "Quinone"
Weiss, Sophie A., and Lars J. C. Jeuken. "Electrodes modified with lipid membranes to study quinone oxidoreductases." Biochemical Society Transactions 37, no. 4 (July 22, 2009): 707–12. http://dx.doi.org/10.1042/bst0370707.
Повний текст джерелаJensen,, Kenneth A., Zachary C. Ryan, Amber Vanden Wymelenberg, Daniel Cullen, and Kenneth E. Hammel. "An NADH:Quinone Oxidoreductase Active during Biodegradation by the Brown-Rot Basidiomycete Gloeophyllum trabeum." Applied and Environmental Microbiology 68, no. 6 (June 2002): 2699–703. http://dx.doi.org/10.1128/aem.68.6.2699-2703.2002.
Повний текст джерелаWang, Zhen-Hua, Xiao-Hui Fu, Qun Li, Yong You, Lei Yang, Jian-Qiang Zhao, Yan-Ping Zhang, and Wei-Cheng Yuan. "Recent Advances in the Domino Annulation Reaction of Quinone Imines." Molecules 29, no. 11 (May 24, 2024): 2481. http://dx.doi.org/10.3390/molecules29112481.
Повний текст джерелаMiseviciene, Lina, Zilvinas Anusevicius, Jonas Sarlauskas, Richard J. Harris, Nigel S. Scrutton, and Narimantas Cenas. "Two-electron reduction of quinones by Enterobacter cloacae PB2 pentaerythritol tetranitrate reductase: quantitative structure-activity relationships." Acta Biochimica Polonica 54, no. 2 (June 4, 2007): 379–85. http://dx.doi.org/10.18388/abp.2007_3260.
Повний текст джерелаVienozinskis, J., A. Butkus, N. Cenas, and J. Kulys. "The mechanism of the quinone reductase reaction of pig heart lipoamide dehydrogenase." Biochemical Journal 269, no. 1 (July 1, 1990): 101–5. http://dx.doi.org/10.1042/bj2690101.
Повний текст джерелаGiulivi, C., and 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, no. 1 (July 1, 1994): 21–30. http://dx.doi.org/10.1042/bj3010021.
Повний текст джерелаBreker, Johannes, Reinhard Schmutzler, Bernd Dorbath та 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, № 8 (1 серпня 1990): 1177–86. http://dx.doi.org/10.1515/znb-1990-0812.
Повний текст джерелаMonks, Terrence, and Douglas Jones. "The Metabolism and Toxicity of Quinones, Quinonimines, Quinone Methides, and Quinone-Thioethers." Current Drug Metabolism 3, no. 4 (August 1, 2002): 425–38. http://dx.doi.org/10.2174/1389200023337388.
Повний текст джерелаFlynn, Noah R., Michael D. Ward, Mary A. Schleiff, Corentine M. C. Laurin, Rohit Farmer, Stuart J. Conway, Gunnar Boysen, S. Joshua Swamidass, and Grover P. Miller. "Bioactivation of Isoxazole-Containing Bromodomain and Extra-Terminal Domain (BET) Inhibitors." Metabolites 11, no. 6 (June 15, 2021): 390. http://dx.doi.org/10.3390/metabo11060390.
Повний текст джерелаXu, Wei, William R. Dolbier, Jian-Xin Duan, Yian Zhai, Katsu Ogawa, Merle A. Battiste, and Ion Ghiviriga. "Octafluoro[2.2]paracyclophane (AF4) Quinone." Collection of Czechoslovak Chemical Communications 73, no. 12 (2008): 1764–76. http://dx.doi.org/10.1135/cccc20081764.
Повний текст джерелаДисертації з теми "Quinone"
Oosthuizen, Francois Jacobus. "Syntheses of the enantiopure quinones A and A' and their C-1 epimers." Thesis, Oosthuizen, Francois Jacobus (2002) Syntheses of the enantiopure quinones A and A' and their C-1 epimers. PhD thesis, Murdoch University, 2002. https://researchrepository.murdoch.edu.au/id/eprint/234/.
Повний текст джерелаOosthuizen, Francois Jacobus. "Syntheses of the Enantiopure Quinones A and A' and Their C-1 Epimers." Murdoch University, 2002. http://wwwlib.murdoch.edu.au/adt/browse/view/adt-MU20040820.123649.
Повний текст джерелаCassagnes, Laure-Estelle. "Cycle redox quinone-quinone réductase 2 et conséquences sur la production d'espèces oxygénées réactives dans le contexte cellulaire." Thesis, Toulouse 3, 2015. http://www.theses.fr/2015TOU30148/document.
Повний текст джерелаQuinone reductase 2 or QR2 is an enzyme that, like its counterpart QR1, plays a role in detoxification of the highly reactives quinones by reducing them into hydroquinones. On one hand, it has been observed at the cellular and tissue level that the activity of this flavoprotein could have deleterious effects by triggering an overproduction of reactive oxygen species (ROS). On the other hand, overexpression or under expression of QR2 has been observed in some neurodegenerative diseases such as Parkinson's disease and Alzheimer's disease. In this context, this work focused on the study of reactive oxygen species produced during the quinone / QR2 redox cycle and their variations depending on the nature of the quinone, on both purified protein and cell models, in comparison to QR1. The redox properties of the substrates, co-substrates and inhibitors ok QR2 studied by electrochemistry allowed to classify them according to their capacity to be reduced. The enzymatic activity of the protein, either purified or intracellular, was followed by various methodologies (electron paramagnetic resonance, UV-visible and fluorescence spectroscopy, U(H)PLC-MS, confocal fluorescence microscopy). Production of superoxide radical is observed in the presence of cell lines overexpressing or not QR1 and QR2. Quinones are reduced enzymatically to form hydroquinones via the activity of quinone reductase (QR1 and QR2) and semiquinone via the activity of one electron reductases (e.g. CytP540 reductase). Reoxidation of these products is responsible for a greater or lesser production of the superoxide radical, according to the initial structure of the quinone and the affinity for different reductases. Menadione causes a higher production of cellular superoxide in the absence of QR1 and QR2. These analyzes have also shown that, like its counterpart QR1, QR2 is capable of reducing ortho-quinones including catecholquinones (aminochrome, dopachrome, adrenochrome) known for their neuronal toxicity
Minhas, Gurdeep Singh. "Interaction of quinone and quinone-like inhibitors with Thermus thermophilus complex I." Thesis, University of Cambridge, 2014. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.707994.
Повний текст джерелаChauncey, Marek Anthony. "Reactions heterocyclic quinone methides." Thesis, University of Ulster, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.328193.
Повний текст джерелаChhour, Monivan. "Etude de la métabolisation intracellulaire de quinones, du stress oxydant généré et des processus de détoxification associés." Thesis, Toulouse 3, 2020. http://www.theses.fr/2020TOU30004.
Повний текст джерелаQuinones are ubiquitous compounds in nature. They are also one of the essential elements in living organisms. However, their metabolisms are considered as toxic because there are highly reactive. Their structure is easily reduced by one or two electrons. The intracellular metabolism of these quinones via one-electron reduction such as cytochrome P450 reductase or others flavoproteins generates an unstable semiquinones which leads to a burst of free radical production that results in oxidative stress. On the other hand, quinone-reductases 1 and 2 (QR1 and QR2) catalyze quinone reduction via two electrons to form hydroquinones that chemically more stable. This property is well-known as the detoxifying character of quinone-reductase enzymes. However, previous analyses have shown that this detoxifying effect was appeared only for certain types of quinones and depended, in particular, on the type of cells. Thus, in order to better understand the mechanisms leading to the generation of reactive species and in consideration to those links that were mentioned in the literature between QR2 and neurodegeneration, studies were conducted on primary neurons and neuroblastoma cells genetically modified to overexpress in QR2. These studies have shown, by various analytical techniques such as electron paramagnetic resonance or LC-MS, an increase in the toxicity of menadione but also of adrenochrome in the presence of quinone- reductase 2. In order to explain the contradictory characteristics of QR2 from one cell to another, we proposed a hypothesis that a cooperation with another conjugating enzyme, which could react with the unstable reduced form that prevent its reoxidation, is needed to effectively detoxify quinones. Additional analyses (RPE, LCMS, fluorescence) conducted on neuroblastoma cells overexpressing both QR2 and a para-hydroquinone specific conjugation enzyme (UGT) have shown a decrease in oxidative stress when both enzymes are co-expressed
Colucci, Marie A. "Quinone based inhibitors of NQ01." Thesis, University of Nottingham, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.478964.
Повний текст джерелаSunassee, Suthananda Naidu. "Studies in marine quinone chemistry." Thesis, Rhodes University, 2011. http://hdl.handle.net/10962/d1005020.
Повний текст джерелаFerreira, Janaina Gomes. "Estudo de compostos quinônicos com potencial atividade contra a doença de Chagas." Universidade de São Paulo, 2008. http://www.teses.usp.br/teses/disponiveis/75/75131/tde-23062008-163355/.
Повний текст джерелаThis work presents the structure determined by X-ray analyses for two naphthoquinone compounds 3,4-dihydro-2,2-dimethyl-2H-naphtho[1,2-b]pyran-5,6- dione and dimethyl-1,4-naphthoquinone. The crystal packing of these compounds showed the existence of intermolecular hydrogen bonds of the type CH...0. These intermolecular forces are responsible for the self-assembly in three-dimensional supramolecular structure. A set of 29 naphthoimidazoles, derived from β-lapachone, that has shown activity against T. cruzi, the agent of Chagas disease, were modeled. From these structures electronic, geometric, topological, etc, properties were calculated to be used in the investigation by statistic analysis, using the partial least squares method (PLS). After reduction of the number of variables, the best PLS model found was the one obtained with the following variables: Morp17p, X4a, piPC09, RDF065v, BELp6, RDF060p, R4u, RDF035m and RCI. For the PLS model, the lower error of validation was obtained using 3 factors with the coefficients R=0.71 and Q=0.82. Two sets of compounds, naphtoquinones and naphthoimidazoles, were studied by docking method. The results showed that, for both, naphtoquinones and naphthoimidazoles and both trypanothione and glutathione reductase, the compounds have low probability to bind in the active site, and are more likely to bind in the interface site, especially in the interface site of the human protein.
Cardoso, Mariana Filomena do Carmo. "Síntese de derivados 5-amino-1H-pirazólicos da nor-β-lapachona com potencial perfil anticancerígeno". Niterói, 2017. https://app.uff.br/riuff/handle/1/3283.
Повний текст джерелаMade available in DSpace on 2017-04-04T18:00:06Z (GMT). No. of bitstreams: 1 Cardoso, Mariana Filomena do Carmo [Dissertação, 2012].pdf: 7461706 bytes, checksum: 1ba99c29719229ef773ca5d72b10c91f (MD5)
Esse trabalho descreve uma nova metodologia sintética de novos derivados pirazólicos análogos a 2,2-dimetil-2,3-di-hidronafto[1,2-b]furan-4,5-diona (nor-β-lapachona), através da inserção do núcleo pirazólico a posição C-3 da nor-β-lapachona. Nesta dissertação foram sintetizados 16 (dezesseis) substâncias inéditas, sendo oito da família 3-pirazolil-2,2-dimetil-2,3-di-hidronafto[1,2-b]furan-4,5-diona contendo o núcleo pirazólico acoplado à naftoquinona os quais foram submetidos a testes biológicos para avaliação de suas atividades citotóxicas in vitro contra quatro linhagens de células tumorais humanas e uma linhagem de células normais humanas. Todas as amostras mostraram-se ativas para as linhagens tumorais e não apresentaram hemólise. A metodologia clássica para a substituição nucleofílica no carbono 3 da nor-β-lapachona desenvolvida pelo nosso grupo de pesquisa mostrou-se pouco eficaz, levando a baixos rendimentos com formação de vários produtos colaterais. Desta forma, realizou-se um estudo metodológico a fim de se viabilizar a síntese de uma família de 3-pirazolil-nor-β-lapachonas com rendimentos satisfatórios. Assim, após várias modificações nos parâmetros reacionais, observou-se que o melhor intermediário sintético era o 3-hidroxi-2,2-dimetil-2,3-di-hidronafto[1,2-b]furan-4,5-diona
This paper describes a new synthetic methodology to new pyrazole derivatives analogous to the 2,2-dimethyl-2,3-dihidronaphtho-[1,2-b]-furan-4 ,5-dione (nor-β-lapachone) by inserting the core pyrazolic on the C-3 position of the nor-β-lapachone. In this essay were synthesized 16 (sixteen) new compounds, being eight 3-pyrazolyl-2,2-dimethyl-2,3-dihidronaphtho [1,2-b]-furan-4 ,5-dione family containing core pyrazolic naphthoquinone attached to which were submitted to biological tests to evaluate their in vitro cytotoxic activities against four human tumor cell lines and normal human cell line. All samples were active for tumor cell lines and showed no hemolysis. The classical methodology for the nucleophilic substitution at carbon 3 of the nor-β-lapachone developed by our research group proved to be ineffective, leading to low yields with the formation of various side products. Thus, there was a methodological study in order to facilitate the synthesis of a family of 3-pyrazolyl-nor-β-lapachones with satisfactory yields. Then, after the various modifications on the reaction parameters, it was found that the better synthetic intermediate was the 3-hydroxy-2,2-dimethyl-2,3-dihidronaphtho-[1,2-b]-furan-4 ,5-dione
Книги з теми "Quinone"
1942-, Sies H., and Packer Lester, eds. Quinones and quinone enzymes. Amsterdam: Elsevier Academic Press, 2004.
Знайти повний текст джерелаRokita, Steven E., ed. Quinone Methides. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2009. http://dx.doi.org/10.1002/9780470452882.
Повний текст джерелаChauncey, Mark Anthony. Reactions of heterocyclic quinone methides. [s.l: The Author], 1988.
Знайти повний текст джерелаRobertson, Peter K. J. Photoelectrochemical reductions using quinone radical anions. [s.l: The Author], 1989.
Знайти повний текст джерелаThomson, R. H. Naturally occurring quinones III: Recent advances. 3rd ed. London: Chapman and Hall, 1987.
Знайти повний текст джерелаKleef, Mario van. The biosynthesis of the cofactor pyrroloquinoline quinone. Meppel: Drucker:] Krips Repro, 1988.
Знайти повний текст джерелаL, Ernster, and Kungl Svenska vetenskapsakademien, eds. DT diaphorase: A quinone reductase with special functions in cell metabolism and detoxication : proceedings of an international conference held at the Arrhenius Laboratory, University of Stockholm, 1-4 June, 1986. Cambridge: Published on behalf of the Royal Swedish Academy of Sciences by Cambridge University Press, 1987.
Знайти повний текст джерелаThomson, R. H. Naturally occurring quinones IV: Recent advances. 4th ed. London: Blackie Academic & Professional, 1997.
Знайти повний текст джерелаThomson, R. H. Naturally occurring quinones IV: Recent advances. 4th ed. London: Blackie Academic & Professional, 1997.
Знайти повний текст джерелаDeLuca, Dan A. The optimal production of the enzyme cofactor pyrroloquinoline quinone (PQQ) by different species of pseudomonas. Sudbury, Ont: Laurentian University, 1993.
Знайти повний текст джерелаЧастини книг з теми "Quinone"
Schomburg, Dietmar, and Ida Schomburg. "quinate dehydrogenase (quinone) 1.1.5.8." In Class 1 Oxidoreductases, 155–59. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-36265-1_24.
Повний текст джерелаSchomburg, Dietmar, and Dörte Stephan. "Quinate dehydrogenase (pyrroloquinoline-quinone)." In Enzyme Handbook 10, 603–5. Berlin, Heidelberg: Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-642-57756-7_154.
Повний текст джерелаGooch, Jan W. "Quinone." In Encyclopedic Dictionary of Polymers, 604. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_9709.
Повний текст джерелаGooch, Jan W. "Quinone." In Encyclopedic Dictionary of Polymers, 919. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_14632.
Повний текст джерелаDavidson, Victor L. "Quinone Cofactors." In Encyclopedia of Biophysics, 1–4. Berlin, Heidelberg: Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-642-35943-9_46-1.
Повний текст джерелаMatsuoka, Masaru. "Quinone Dyes." In Infrared Absorbing Dyes, 35–43. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4899-2046-1_4.
Повний текст джерелаDavidson, Victor L. "Quinone Cofactors." In Encyclopedia of Biophysics, 2166–68. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-16712-6_46.
Повний текст джерелаSchomburg, Dietmar, and Dörte Stephan. "Cellobiose dehydrogenase (quinone)." In Enzyme Handbook 10, 496–99. Berlin, Heidelberg: Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-642-57756-7_130.
Повний текст джерелаSchomburg, D., M. Salzmann, and D. Stephan. "NADH dehydrogenase (quinone)." In Enzyme Handbook 7, 403–5. Berlin, Heidelberg: Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-78521-4_78.
Повний текст джерелаSchomburg, D., M. Salzmann, and D. Stephan. "NADPH dehydrogenase (quinone)." In Enzyme Handbook 7, 407–9. Berlin, Heidelberg: Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-78521-4_79.
Повний текст джерелаТези доповідей конференцій з теми "Quinone"
Rangel-Rojo, Raul, Hiro Matsuda, K. Kimura, Miguel A. Mendez-Rojas, and William H. Watson. "Wavelength-resolved nonlinearity on triazole-quinone derivatives." In Optical Science and Technology, SPIE's 48th Annual Meeting, edited by Mark G. Kuzyk, Manfred Eich, and Robert A. Norwood. SPIE, 2003. http://dx.doi.org/10.1117/12.502502.
Повний текст джерелаRangel-Rojo, Raul, L. Stranges, Ajoy K. Kar, M. A. Mendez-Rojas, and W. H. Watson. "Near-resonance nonlinearities in triazole-quinone derivatives." In IV Iberoamerican Meeting of Optics and the VII Latin American Meeting of Optics, Lasers and Their Applications, edited by Vera L. Brudny, Silvia A. Ledesma, and Mario C. Marconi. SPIE, 2001. http://dx.doi.org/10.1117/12.437064.
Повний текст джерелаPooja, Harish Mudila, and Anil Kumar. "Quinone based conducting materials for efficient energy storage." In THE FOURTH SCIENTIFIC CONFERENCE FOR ELECTRICAL ENGINEERING TECHNIQUES RESEARCH (EETR2022). AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0162875.
Повний текст джерелаJerrg-Li Liang and D. E. Nikles. "Amine-Quinone Polyurethanes As Binders For Metal Particle Tape." In 1993 Digests of International Magnetics Conference. IEEE, 1993. http://dx.doi.org/10.1109/intmag.1993.642050.
Повний текст джерелаBezsonova, E., M. Dubar, D. Melekhina, К. Evdokimov, V. Klochkov, and E. Sokolova. "3-ARYLIDENE-2-OXINDOLES AS QUINONE REDUCTASE II INHIBITORS." In MedChem-Russia 2021. 5-я Российская конференция по медицинской химии с международным участием «МедХим-Россия 2021». Издательство Волгоградского государственного медицинского университета, 2021. http://dx.doi.org/10.19163/medchemrussia2021-2021-392.
Повний текст джерелаYoshimura, Motomu, Tetsuya Nishimura, Eiji Yagyu, Noriaki Tsukada, and Tetsu Takeyama. "Hole Multiplexing in Quinone Derivative Photochemical Hole Burning Systems." In Persistent Spectral Hole Burning: Science and Applications. Washington, D.C.: Optica Publishing Group, 1991. http://dx.doi.org/10.1364/pshb.1991.the9.
Повний текст джерелаBudiawan, B., S. Handayani, I. C. Dani, R. Bakri, S. Hannaa, and F. Irawati. "In vitro study of DNA adduct 8-hidroxy-2’-deoxyguanosine (8-OHdG) formation through Fenton-like reaction with butylated hydroxytoluene quinone (BHT quinone)." In PROCEEDINGS OF THE 3RD INTERNATIONAL SYMPOSIUM ON CURRENT PROGRESS IN MATHEMATICS AND SCIENCES 2017 (ISCPMS2017). Author(s), 2018. http://dx.doi.org/10.1063/1.5064057.
Повний текст джерелаXiao Hong Yin, K. Kobayashi, T. Kawai, M. Ozaki, K. Yoshino, and Qingquan Lei. "Electrical properties of polymer composites: conducting polymerpolyacene quinone radical polymer." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835422.
Повний текст джерелаYang, XuePeng, Panpan Li, Fangfang Wang, Jianbin Ye, Ke Ma, and Duobin Mao. "An Efficient Separation of Pyrroloquinoline Quinone Using Chemical Complexation Extraction." In International Conference on Chemical,Material and Food Engineering. Paris, France: Atlantis Press, 2015. http://dx.doi.org/10.2991/cmfe-15.2015.20.
Повний текст джерелаYano, J., Y. Matsufuji, and K. Ogura. "Multicolor-expressible ECD materials consisted of polyanilines, and an anionic quinone." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.836068.
Повний текст джерелаЗвіти організацій з теми "Quinone"
Waite, J. H. Polymerization of Quinone-Crosslinked Marine Bioadhesive Protein. Fort Belvoir, VA: Defense Technical Information Center, October 1988. http://dx.doi.org/10.21236/ada200224.
Повний текст джерелаCordingley, John S. The Molecular and Cellular Mechanisms of Quinone Tanning of Proteins. Fort Belvoir, VA: Defense Technical Information Center, June 1994. http://dx.doi.org/10.21236/ada303501.
Повний текст джерелаGalleguillos, R., M. Litt, and S. E. Rickert. Friedel Craft's synthesis and characterization of some acene quinone compounds. Office of Scientific and Technical Information (OSTI), January 1987. http://dx.doi.org/10.2172/6631885.
Повний текст джерелаClark, Catherine D. Examining the Role of Quinone Moieties in the Photochemistry of Colored Dissolved Organic Matter in Coastal Waters. Fort Belvoir, VA: Defense Technical Information Center, September 2002. http://dx.doi.org/10.21236/ada628919.
Повний текст джерелаClark, Catherine D. Examining the Role of Quinone Moieties in the Photochemistry of Colored Dissolved Organic Matter in Coastal Waters. Fort Belvoir, VA: Defense Technical Information Center, August 2001. http://dx.doi.org/10.21236/ada627292.
Повний текст джерелаGust, D., and T. A. Moore. Artificial photosynthesis using chlorophyll based carotenoid quinone triads: A brief synopsis of research progress as of 31 December 1986. Office of Scientific and Technical Information (OSTI), December 1986. http://dx.doi.org/10.2172/5693588.
Повний текст джерелаHanson, D. K., and M. Schiffer. Symmetry-related mutants in the quinone binding sites of the reaction center -- The effects of changes in charge distribution. Office of Scientific and Technical Information (OSTI), September 1997. http://dx.doi.org/10.2172/563250.
Повний текст джерелаSteele, W., and R. Chirico. Thermodynamics of the hydrodenitrogenation of quinoline. Office of Scientific and Technical Information (OSTI), June 1990. http://dx.doi.org/10.2172/6958305.
Повний текст джерелаGunsaru, Bornface. Simplified Reversed Chloroquines to Overcome Malaria Resistance to Quinoline-based Drugs. Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.400.
Повний текст джерелаWang, Hong, Eric Wolfe, Edgar Lara-Curzio, Marco Martinez, and Tracie Lowe. Study on Electrostatic Separation of Quinoline Insolubles from Coal Tar Pitch. Office of Scientific and Technical Information (OSTI), March 2023. http://dx.doi.org/10.2172/1960688.
Повний текст джерела