Статті в журналах з теми "Biological oxidations of sulfur compounds"
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Echizen, Honami, Eita Sasaki, and Kenjiro Hanaoka. "Recent Advances in Detection, Isolation, and Imaging Techniques for Sulfane Sulfur-Containing Biomolecules." Biomolecules 11, no. 11 (October 20, 2021): 1553. http://dx.doi.org/10.3390/biom11111553.
Повний текст джерелаAlbelda Berenguer, Magdalena, Mathilde Monachon, Clémentine Jacquet, Pilar Junier, Céline Rémazeilles, Eleanor J. Schofield, and Edith Joseph. "Biological oxidation of sulfur compounds in artificially degraded wood." International Biodeterioration & Biodegradation 141 (July 2019): 62–70. http://dx.doi.org/10.1016/j.ibiod.2018.06.009.
Повний текст джерелаAbedinzadeh, Z. "Sulfur-centered reactive intermediates derived from the oxidation of sulfur compounds of biological interest." Canadian Journal of Physiology and Pharmacology 79, no. 2 (February 1, 2001): 166–70. http://dx.doi.org/10.1139/y00-085.
Повний текст джерелаFdz-Polanco, F., M. Fdz-Polanco, N. Fernández, M. A. Urueña, P. A. García, and S. Villaverde. "Combining the biological nitrogen and sulfur cycles in anaerobic conditions." Water Science and Technology 44, no. 8 (October 1, 2001): 77–84. http://dx.doi.org/10.2166/wst.2001.0469.
Повний текст джерелаFrancioso, Antonio, Alessia Baseggio Conrado, Luciana Mosca, and Mario Fontana. "Chemistry and Biochemistry of Sulfur Natural Compounds: Key Intermediates of Metabolism and Redox Biology." Oxidative Medicine and Cellular Longevity 2020 (September 29, 2020): 1–27. http://dx.doi.org/10.1155/2020/8294158.
Повний текст джерелаYuen, Pong Kau, and Cheng Man Diana Lau. "New approach for assigning mean oxidation number of carbons to organonitrogen and organosulfur compounds." Chemistry Teacher International 4, no. 1 (October 8, 2021): 1–13. http://dx.doi.org/10.1515/cti-2021-0015.
Повний текст джерелаDvořáková, M., I. Weingartová, J. Nevoral, D. Němeček, and T. Krejčová. "Garlic Sulfur Compounds Suppress Cancerogenesis and Oxidative Stress: a Review." Scientia Agriculturae Bohemica 46, no. 2 (June 1, 2015): 65–72. http://dx.doi.org/10.1515/sab-2015-0018.
Повний текст джерелаEgbujor, Melford Chuka, Maria Petrosino, Karim Zuhra, and Luciano Saso. "The Role of Organosulfur Compounds as Nrf2 Activators and Their Antioxidant Effects." Antioxidants 11, no. 7 (June 26, 2022): 1255. http://dx.doi.org/10.3390/antiox11071255.
Повний текст джерелаShiri, Lotfi, Arash Ghorbani-Choghamarani, and Mosstafa Kazemi. "S–S Bond Formation: Nanocatalysts in the Oxidative Coupling of Thiols." Australian Journal of Chemistry 70, no. 1 (2017): 9. http://dx.doi.org/10.1071/ch16318.
Повний текст джерелаArdón-Muñoz, Luis G., and Jeanne L. Bolliger. "Synthesis of Benzo[4,5]thiazolo[2,3-c][1,2,4]triazole Derivatives via C-H Bond Functionalization of Disulfide Intermediates." Molecules 27, no. 5 (February 22, 2022): 1464. http://dx.doi.org/10.3390/molecules27051464.
Повний текст джерелаStewart, Frank J. "Dissimilatory sulfur cycling in oxygen minimum zones: an emerging metagenomics perspective." Biochemical Society Transactions 39, no. 6 (November 21, 2011): 1859–63. http://dx.doi.org/10.1042/bst20110708.
Повний текст джерелаRudelle, E. A., J. Vollertsen, T. Hvitved-Jacobsen, and A. H. Nielsen. "Kinetics of aerobic oxidation of volatile sulfur compounds in wastewater and biofilm from sewers." Water Science and Technology 68, no. 11 (October 24, 2013): 2330–36. http://dx.doi.org/10.2166/wst.2013.471.
Повний текст джерелаRoman, Pawel, Martijn F. M. Bijmans, and Albert J. H. Janssen. "Quantification of individual polysulfides in lab-scale and full-scale desulfurisation bioreactors." Environmental Chemistry 11, no. 6 (2014): 702. http://dx.doi.org/10.1071/en14128.
Повний текст джерелаLin, Binle, R. Yamaguchi, M. Hosomi, and A. Murakami. "A new treatment process for photo-processing waste using a sulfur-oxidizing bacteria/granular activated carbon system followed by Fenton oxidation." Water Science and Technology 38, no. 4-5 (August 1, 1998): 163–70. http://dx.doi.org/10.2166/wst.1998.0609.
Повний текст джерелаTomkiel, Aneta M., Dorota Czajkowska-Szczykowska, Ewa Olchowik-Grabarek, Lucie Rárová, Szymon Sękowski, and Jacek W. Morzycki. "A Study on the Chemistry and Biological Activity of 26-Sulfur Analogs of Diosgenin: Synthesis of 26-Thiodiosgenin S-Mono- and Dioxides, and Their Alkyl Derivatives." Molecules 28, no. 1 (December 26, 2022): 189. http://dx.doi.org/10.3390/molecules28010189.
Повний текст джерелаMoroz, O. M., S. O. Hnatush, O. V. Tarabas, C. I. Bohoslavets, G. V. Yavorska, and B. M. Borsukevych. "Sulfidogenic activity of sulfate and sulfur reducing bacteria under the influence of metal compounds." Biosystems Diversity 26, no. 1 (April 5, 2018): 3–10. http://dx.doi.org/10.15421/011801.
Повний текст джерелаPehlivan, Özge, Mateusz Waliczek, Monika Kijewska, and Piotr Stefanowicz. "Selenium in Peptide Chemistry." Molecules 28, no. 7 (April 4, 2023): 3198. http://dx.doi.org/10.3390/molecules28073198.
Повний текст джерелаLabischinski, Harald, Dieter Naumann, Gerhard Barnickel, Wolfgang Dreißig, Wojciech Gruszecki, Andreas Hofer, and Hans Bradaczek. "Comparison between the Molecular and Crystal Structures of a Benzylpenicillin Ester and its Corresponding Sulfoxide with Drastically Reduced Biological Activity." Zeitschrift für Naturforschung B 42, no. 3 (March 1, 1987): 367–75. http://dx.doi.org/10.1515/znb-1987-0320.
Повний текст джерелаMilet, G. M. D., and S. J. B. Duff. "Treatment of kraft condensates in a feedback-controlled sequencing batch reactor." Water Science and Technology 38, no. 4-5 (August 1, 1998): 263–71. http://dx.doi.org/10.2166/wst.1998.0642.
Повний текст джерелаKhabibrakhmanova, Alsu M., Roza G. Faizova, Olga A. Lodochnikova, Regina R. Zamalieva, Liliya Z. Latypova, Elena Y. Trizna, Andrey G. Porfiryev, et al. "The Novel Chiral 2(5H)-Furanone Sulfones Possessing Terpene Moiety: Synthesis and Biological Activity." Molecules 28, no. 6 (March 10, 2023): 2543. http://dx.doi.org/10.3390/molecules28062543.
Повний текст джерелаHiguchi, Ohki, Koutaro Tateshita, and Hiroyuki Nishimura. "Antioxidative Activity of Sulfur-Containing Compounds inAlliumSpecies for Human Low-Density Lipoprotein (LDL) Oxidation in Vitro." Journal of Agricultural and Food Chemistry 51, no. 24 (November 2003): 7208–14. http://dx.doi.org/10.1021/jf034294u.
Повний текст джерелаSchippers, Axel, and Dagmar Kock. "Geomicrobiology of Sulfidic Mine Dumps: A Short Review." Advanced Materials Research 71-73 (May 2009): 37–41. http://dx.doi.org/10.4028/www.scientific.net/amr.71-73.37.
Повний текст джерелаTm, Kaplaushenko, Panasenko Oi, and Kucheryavy Yu. "RESEARCH OF THE SYNTHETIC, PHYSICAL AND CHEMICAL PROPERTIES OF 3-ALKYLSULFONYL-5-(CHINOLINE-2-YL, 2-HYDROXYCHINOLINE-4-YL)-4-R -2,4-DIHYDRO3N-1,2,4-TRIAZOLES 1." Asian Journal of Pharmaceutical and Clinical Research 10, no. 1 (January 1, 2016): 81. http://dx.doi.org/10.22159/ajpcr.2017.v10i1.14096.
Повний текст джерелаJanik-Hazuka, Małgorzata, Kamil Kamiński, Marta Kaczor-Kamińska, Joanna Szafraniec-Szczęsny, Aleksandra Kmak, Hassan Kassassir, Cezary Watała, Maria Wróbel, and Szczepan Zapotoczny. "Hyaluronic Acid-Based Nanocapsules as Efficient Delivery Systems of Garlic Oil Active Components with Anticancer Activity." Nanomaterials 11, no. 5 (May 20, 2021): 1354. http://dx.doi.org/10.3390/nano11051354.
Повний текст джерелаFan, Xuetong, Christopher H. Sommers, and Kimberly J. B. Sokorai. "Ionizing Radiation and Antioxidants Affect Volatile Sulfur Compounds, Lipid Oxidation, and Color of Ready-to-Eat Turkey Bologna." Journal of Agricultural and Food Chemistry 52, no. 11 (June 2004): 3509–15. http://dx.doi.org/10.1021/jf035357b.
Повний текст джерелаBeinart, R. A., A. Gartman, J. G. Sanders, G. W. Luther, and P. R. Girguis. "The uptake and excretion of partially oxidized sulfur expands the repertoire of energy resources metabolized by hydrothermal vent symbioses." Proceedings of the Royal Society B: Biological Sciences 282, no. 1806 (May 7, 2015): 20142811. http://dx.doi.org/10.1098/rspb.2014.2811.
Повний текст джерелаLuo, Huiyu, Junbin Chen, Chuhong Su, and Longying Zha. "Advances in the Bioactivities of Phytochemical Saponins in the Prevention and Treatment of Atherosclerosis." Nutrients 14, no. 23 (November 24, 2022): 4998. http://dx.doi.org/10.3390/nu14234998.
Повний текст джерелаHuergo, J., C. Bernardelli, M. Viera, Wolfgang Sand, and Edgardo R. Donati. "FISH Analysis of Bacterial Attachment to Copper Sulfides in Bioleaching Processes." Advanced Materials Research 71-73 (May 2009): 329–32. http://dx.doi.org/10.4028/www.scientific.net/amr.71-73.329.
Повний текст джерелаJang, Sehyun, Ki-Tae Park, Kitack Lee, Young Jun Yoon, Kitae Kim, Hyun Young Chung, Eunho Jang, et al. "Large seasonal and interannual variations of biogenic sulfur compounds in the Arctic atmosphere (Svalbard; 78.9° N, 11.9° E)." Atmospheric Chemistry and Physics 21, no. 12 (June 29, 2021): 9761–77. http://dx.doi.org/10.5194/acp-21-9761-2021.
Повний текст джерелаDotsenko, Victor V., Nawras T. Jassim, Azamat Z. Temerdashev, Zainab R. Abdul-Hussein, Nicolai A. Aksenov, and Inna V. Aksenova. "New 6′-Amino-5′-cyano-2-oxo-1,2-dihydro-1′H-spiro[indole-3,4′-pyridine]-3′-carboxamides: Synthesis, Reactions, Molecular Docking Studies and Biological Activity." Molecules 28, no. 7 (April 2, 2023): 3161. http://dx.doi.org/10.3390/molecules28073161.
Повний текст джерелаSkaff, Ojia, David I. Pattison, Philip E. Morgan, Rushad Bachana, Vimal K. Jain, K. Indira Priyadarsini, and Michael J. Davies. "Selenium-containing amino acids are targets for myeloperoxidase-derived hypothiocyanous acid: determination of absolute rate constants and implications for biological damage." Biochemical Journal 441, no. 1 (December 14, 2011): 305–16. http://dx.doi.org/10.1042/bj20101762.
Повний текст джерелаArshad, Mohammed F., Aftab Alam, Abdullah Ayed Alshammari, Mohammed Bader Alhazza, Ibrahim Mohammed Alzimam, Md Anish Alam, Gulam Mustafa, et al. "Thiazole: A Versatile Standalone Moiety Contributing to the Development of Various Drugs and Biologically Active Agents." Molecules 27, no. 13 (June 21, 2022): 3994. http://dx.doi.org/10.3390/molecules27133994.
Повний текст джерелаTuin, B. J. W., and A. A. C. M. Bos. "Ozone treatment and biodegradation of industrial wastewater containing thioethers." Water Science and Technology 49, no. 4 (February 1, 2004): 279–85. http://dx.doi.org/10.2166/wst.2004.0284.
Повний текст джерелаNasir, H. M., T. A. Saki, and M. Y. Al-Luaibi. "Synthesis, identification and thermal study of some new inorganic polymers based on bis-dithiocarbamate ligands with silicone, tellurium and some transition metals." Innovaciencia Facultad de Ciencias Exactas Físicas y Naturales 7, no. 1 (October 25, 2019): 1–13. http://dx.doi.org/10.15649/2346075x.507.
Повний текст джерелаGałązka, Anna, Anna Marzec-Grządziel, Milan Varsadiya, Jacek Niedźwiecki, Karolina Gawryjołek, Karolina Furtak, Marcin Przybyś, and Jarosław Grządziel. "Biodiversity and Metabolic Potential of Bacteria in Bulk Soil from the Peri-Root Zone of Black Alder (Alnus glutinosa), Silver Birch (Betula pendula) and Scots Pine (Pinus sylvestris)." International Journal of Molecular Sciences 23, no. 5 (February 27, 2022): 2633. http://dx.doi.org/10.3390/ijms23052633.
Повний текст джерелаSaunders, Jaclyn K., Clara A. Fuchsman, Cedar McKay, and Gabrielle Rocap. "Complete arsenic-based respiratory cycle in the marine microbial communities of pelagic oxygen-deficient zones." Proceedings of the National Academy of Sciences 116, no. 20 (April 29, 2019): 9925–30. http://dx.doi.org/10.1073/pnas.1818349116.
Повний текст джерелаSirota, T. V. "Effect of the sulfur-containing compounds on the quinoid process of adrenaline autoxidation; potential neuroprotectors." Biomeditsinskaya Khimiya 65, no. 4 (2019): 316–23. http://dx.doi.org/10.18097/pbmc20196504316.
Повний текст джерелаPeñéñory, Alicia B., Juan E. Argüello, and Marcelo Puiatti. "Novel Model Sulfur Compounds as Mechanistic Probes for Enzymatic and Biomimetic Oxidations." European Journal of Organic Chemistry 2005, no. 1 (December 20, 2004): 114–22. http://dx.doi.org/10.1002/ejoc.200400382.
Повний текст джерелаKulik, Katarzyna, Klaudia Sadowska, Ewelina Wielgus, Barbara Pacholczyk-Sienicka, Elzbieta Sochacka, and Barbara Nawrot. "Different Oxidation Pathways of 2-Selenouracil and 2-Thiouracil, Natural Components of Transfer RNA." International Journal of Molecular Sciences 21, no. 17 (August 19, 2020): 5956. http://dx.doi.org/10.3390/ijms21175956.
Повний текст джерелаVaniushenkova, Anna A., Elina E. Dosadina, Anna A. Hanafina, Sergey V. Kalenov, Nikolay S. Markvichev, and Alexey A. Belov. "Synthesis and study of the properties of composite materials based on cellulose and chitosan containing various therapeutic agents. Part 3. Hydrolytic destruction of dressings based on dialdehydecellulose." Butlerov Communications 59, no. 8 (August 31, 2019): 47–59. http://dx.doi.org/10.37952/roi-jbc-01/19-59-8-47.
Повний текст джерелаMohammed Al bratty, Mohammed Al bratty, Neelaveni Thangavel Neelaveni Thangavel, Hassan Ahmad Alhazmi Hassan Ahmad Alhazmi, Asim Najmi Asim Najmi, Amani Ali Jebril Shar Amani Ali Jebril Shar, Bshoor Ali Farhan Alhabsi Bshoor Ali Farhan Alhabsi, Sumaiya Mosa Suliman Ghazwani Sumaiya Mosa Suliman Ghazwani, Safeena Eranhiyil Ashraf Safeena Eranhiyil Ashraf, and Ziaur Rehman Ziaur Rehman. "Gas Chromatography-Mass Spectrometry-based Phytochemical Analysis and In-Vitro Anti-Lipid Peroxidation, Cyclooxygenase Inhibition Activities of Saudi Eruca sativa Leaves." Journal of the chemical society of pakistan 44, no. 2 (2022): 175. http://dx.doi.org/10.52568/001001/jcsp/44.02.2022.
Повний текст джерелаSchenk, Wolfdieter A., Juergen Frisch, Waldemar Adam, and Frank Prechtl. "Sulfur(IV) compounds as ligands. Part 15. Ligand-centered oxidations of organometallic thiolates using dimethyldioxirane." Inorganic Chemistry 31, no. 15 (July 1992): 3329–31. http://dx.doi.org/10.1021/ic00041a032.
Повний текст джерелаGörbitz, Carl Henrik, Vladimir Levchenko, Jevgenijs Semjonovs, and Mohamed Yusuf Sharif. "Crystal structure of seleno-L-cystine dihydrochloride." Acta Crystallographica Section E Crystallographic Communications 71, no. 6 (May 30, 2015): 726–29. http://dx.doi.org/10.1107/s205698901501021x.
Повний текст джерелаKvasnica, Miroslav, Iva Tišlerová, Jan Šarek, Jan Sejbal та Ivana Císařová. "Preparation of New Oxidized 18-α-Oleanane Derivatives". Collection of Czechoslovak Chemical Communications 70, № 9 (2005): 1447–64. http://dx.doi.org/10.1135/cccc20051447.
Повний текст джерелаBortoli, Marco, Matteo Bruschi, Marcel Swart, and Laura Orian. "Sequential oxidations of phenylchalcogenides by H2O2: insights into the redox behavior of selenium via DFT analysis." New Journal of Chemistry 44, no. 17 (2020): 6724–31. http://dx.doi.org/10.1039/c9nj06449d.
Повний текст джерелаBarce Ferro, Criscieli Taynara, Beatriz Fuzinato dos Santos, Caren Daniele Galeano da Silva, George Brand, Beatriz Amaral Lopes da Silva, and Nelson Luís de Campos Domingues. "Review of the Syntheses and Activities of Some Sulfur-Containing Drugs." Current Organic Synthesis 17, no. 3 (June 9, 2020): 192–210. http://dx.doi.org/10.2174/1570179417666200212113412.
Повний текст джерелаMyles, Daniel J. T., M’hamed Chahma, and Robin G. Hicks. "Synthesis and properties of end-capped bis(oligothienyl) sulfides." Canadian Journal of Chemistry 86, no. 10 (October 1, 2008): 982–91. http://dx.doi.org/10.1139/v08-128.
Повний текст джерелаRose, Peter, Philip Keith Moore, Matthew Whiteman, and Yi-Zhun Zhu. "An Appraisal of Developments in Allium Sulfur Chemistry: Expanding the Pharmacopeia of Garlic." Molecules 24, no. 21 (November 5, 2019): 4006. http://dx.doi.org/10.3390/molecules24214006.
Повний текст джерелаBolton, Sarah G., and Michael D. Pluth. "Modified cyclodextrins solubilize elemental sulfur in water and enable biological sulfane sulfur delivery." Chemical Science 11, no. 43 (2020): 11777–84. http://dx.doi.org/10.1039/d0sc04137h.
Повний текст джерелаProshin, A. N., M. A. Orlova, and T. P. Trofimova. "Biological activity of some sulfur- and selenium-containing spiro compounds." Russian Chemical Bulletin 66, no. 10 (October 2017): 1931–33. http://dx.doi.org/10.1007/s11172-017-1968-4.
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