Статті в журналах з теми "Active chlorine compound"
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Pratskova, Svetlana E., and Oksana E. Sirenko. "Spectrophotometric determination of active chlorine by the color of indophenolic compounds." Butlerov Communications 57, no. 3 (2019): 93–98. http://dx.doi.org/10.37952/roi-jbc-01/19-57-3-93.
Повний текст джерелаFedorova, Lyudmila S., and Anastasia V. Ilyakova. "Comparative evaluation of disinfectant efficacy against biofilm-residing microorganisms." Journal of microbiology, epidemiology and immunobiology 100, no. 5 (2023): 302–9. http://dx.doi.org/10.36233/0372-9311-422.
Повний текст джерелаLe, Giang Truong, Nguyen Thuy Ta, Trung Quoc Pham, and Yen Hai Dao. "Response Surface Analysis of Fenobucarb Removal by Electrochemically Generated Chlorine." Water 11, no. 5 (2019): 899. http://dx.doi.org/10.3390/w11050899.
Повний текст джерелаUsri, Siti Nur Khalidah, Zuhair Jamain, and Mohamad Zul Hilmey Makmud. "A Review on Synthesis, Structural, Flame Retardancy and Dielectric Properties of Hexasubstituted Cyclotriphosphazene." Polymers 13, no. 17 (2021): 2916. http://dx.doi.org/10.3390/polym13172916.
Повний текст джерелаZalaru, Christina, Florea Dumitrascu, Constantin Draghici, et al. "Synthesis, Spectroscopic Characterization, Structural Analysis, and Evaluation of Anti-Tumor, Antimicrobial, and Antibiofilm Activities of Halogenoaminopyrazoles Derivatives." Antibiotics 13, no. 12 (2024): 1119. http://dx.doi.org/10.3390/antibiotics13121119.
Повний текст джерелаLiu, Manli, Mengyao Ren, Yani Zhang, et al. "Antiviral Activity of Benzoheterocyclic Compounds from Soil-Derived Streptomyces jiujiangensis NBERC-24992." Molecules 28, no. 2 (2023): 878. http://dx.doi.org/10.3390/molecules28020878.
Повний текст джерелаKovač, Bruno, Kaća Piletić, Nikolina Kovačević Ganić, and Ivana Gobin. "The Effectiveness of Benzalkonium Chloride as an Active Compound on Selected Foodborne Pathogens Biofilm." Hygiene 2, no. 4 (2022): 226–35. http://dx.doi.org/10.3390/hygiene2040020.
Повний текст джерелаAbdul-Redah Muhsin, Fulath. "Relationship between Combined Chlorine (inactive chlorine) and Thermotolerant (Faecal) Coliforms Bacteria in Drinking Water among some Neighborhoods of Al-Najaf City." Al-Kufa University Journal for Biology 10, no. 2 (2018): 58–66. http://dx.doi.org/10.36320/ajb/v10.i2.8129.
Повний текст джерелаBarakat, Assem, Mohammad Shahidul Islam, M. Ali, et al. "Regio- and Stereoselective Synthesis of a New Series of Spirooxindole Pyrrolidine Grafted Thiochromene Scaffolds as Potential Anticancer Agents." Symmetry 13, no. 8 (2021): 1426. http://dx.doi.org/10.3390/sym13081426.
Повний текст джерелаKrasnov, Victor P., Vera V. Musiyak, Galina L. Levit, et al. "Synthesis of Pyrimidine Conjugates with 4-(6-Amino-hexanoyl)-7,8-difluoro-3,4-dihydro-3-methyl-2H-[1,4]benzoxazine and Evaluation of Their Antiviral Activity." Molecules 27, no. 13 (2022): 4236. http://dx.doi.org/10.3390/molecules27134236.
Повний текст джерелаDesideri, N., C. Conti, I. Sestili, P. Tomao, M. L. Stein, and N. Orsi. "Synthesis and Evaluation of Anti-Rhinovirus 1B Activity of Oxazolinyl-Isoflavans and -3(2H)-Isoflavenes." Antiviral Chemistry and Chemotherapy 3, no. 4 (1992): 195–202. http://dx.doi.org/10.1177/095632029200300402.
Повний текст джерелаGomelya, Mykola, Yana Kryzhanovska, Iryna Makarenko, Tetyana Shabliy, and Oleksandr Kyrylyuk. "Evaluation of the efficiency of the processing of sodium chloride solutions by electrodialysis in a three-chamber electrolyzer using a high-basic anionite." Proceedings of the NTUU “Igor Sikorsky KPI”. Series: Chemical engineering, ecology and resource saving, no. 2 (June 30, 2025): 60–69. https://doi.org/10.20535/2617-9741.2.2025.333975.
Повний текст джерелаSkrzypek, Alicja, Monika Karpińska, Małgorzata Juszczak, et al. "Cholinesterases Inhibition, Anticancer and Antioxidant Activity of Novel Benzoxazole and Naphthoxazole Analogs." Molecules 27, no. 23 (2022): 8511. http://dx.doi.org/10.3390/molecules27238511.
Повний текст джерелаPark, Hyunwoong, Chad D. Vecitis, and Michael R. Hoffmann. "Electrochemical Water Splitting Coupled with Organic Compound Oxidation: The Role of Active Chlorine Species." Journal of Physical Chemistry C 113, no. 18 (2009): 7935–45. http://dx.doi.org/10.1021/jp810331w.
Повний текст джерелаVeljović, Elma, Selma Špirtović-Halilović, Samija Muratović, et al. "Antiproliferative and genotoxic potential of xanthen-3-one derivatives." Acta Pharmaceutica 69, no. 4 (2019): 683–94. http://dx.doi.org/10.2478/acph-2019-0044.
Повний текст джерелаVassilyeva, Olga Yu, Elena A. Buvaylo, Vladimir N. Kokozay, Andrii K. Melnyk, and Brian W. Skelton. "Crystal structure and characterization of a new copper(II) chloride dimer with methyl(pyridin-2-ylmethylidene)amine." Acta Crystallographica Section E Crystallographic Communications 76, no. 6 (2020): 790–93. http://dx.doi.org/10.1107/s2056989020005903.
Повний текст джерелаNyati, Hilda, Tjakko Abeea, Rijkelt Beumera, der Veena Stijn van, and Wilma Hazelegera. "Influence of Organic Material and Biofilms on Disinfectant Efficacy Against Listeria monocytogenes." International Journal of Food Studies I 1 (April 18, 2012): 76–84. https://doi.org/10.5281/zenodo.2593162.
Повний текст джерелаKrawczyk, Przemysław, Beata Jędrzejewska, Joanna Cytarska, Klaudia Seklecka, and Krzysztof Z. Łączkowski. "Synthesis of Carbazole–Thiazole Dyes via One-Pot Tricomponent Reaction: Exploring Photophysical Properties, Tyrosinase Inhibition, and Molecular Docking." Sensors 24, no. 19 (2024): 6368. http://dx.doi.org/10.3390/s24196368.
Повний текст джерелаGardner, Gary, James R. Sanborn, and John R. Goss. "N-Alkylaryltriazine Herbicides: A Possible Link Between Triazines and Phenylureas." Weed Science 35, no. 6 (1987): 763–69. http://dx.doi.org/10.1017/s0043174500079303.
Повний текст джерелаTănase, Drăghici, Hanganu, et al. "New HSV-1 Anti-Viral 1′-Homocarbocyclic Nucleoside Analogs with an Optically Active Substituted Bicyclo[2.2.1]Heptane Fragment as a Glycoside Moiety." Molecules 24, no. 13 (2019): 2446. http://dx.doi.org/10.3390/molecules24132446.
Повний текст джерелаMan, Dariusz, and Marian Podolak. "Tin Compounds Interaction with Membranes of Egg Lecithin Liposomes." Zeitschrift für Naturforschung C 62, no. 5-6 (2007): 427–32. http://dx.doi.org/10.1515/znc-2007-5-617.
Повний текст джерелаGladkikh, Boris P., Dmitry V. Danilov, Vladimir S. D’yachenko, and Gennady M. Butov. "1,3-Dichloroadamantyl-Containing Ureas as Potential Triple Inhibitors of Soluble Epoxide Hydrolase, p38 MAPK and c-Raf." International Journal of Molecular Sciences 25, no. 1 (2023): 338. http://dx.doi.org/10.3390/ijms25010338.
Повний текст джерелаDi Filippo, Ester Sara, Letizia Giampietro, Barbara De Filippis, et al. "Synthesis and Biological Evaluation of Halogenated E-Stilbenols as Promising Antiaging Agents." Molecules 25, no. 23 (2020): 5770. http://dx.doi.org/10.3390/molecules25235770.
Повний текст джерелаVidaillac, Céline, Jean Guillon, Corinne Arpin, et al. "Synthesis of Omeprazole Analogues and Evaluation of These as Potential Inhibitors of the Multidrug Efflux Pump NorA of Staphylococcus aureus." Antimicrobial Agents and Chemotherapy 51, no. 3 (2006): 831–38. http://dx.doi.org/10.1128/aac.01306-05.
Повний текст джерелаBhagwat D, Mali, Akuskar Deepak S., and Jivane Deepak M. "Separation and Detection of Nux Vomika Alkaloids by Thin-Layer Chromatography." Journal of Forensic Chemistry and Toxicology 3, no. 2 (2017): 95–97. http://dx.doi.org/10.21088/jfct.2454.9363.3217.4.
Повний текст джерелаД.А., Кулагина,, Чикина, М.В., Алексеева, Н.А., and Сысолятин, С.В. "REACTIVITY OF 4,10-DI(CHLOROACETYL)-2,6,8,12-TETRACETYL-2,4,6,8,10,12-HEXAAZAISOWURTZITANe IN THE REACTION WITH AMINES." Южно-Сибирский научный вестник, no. 6(46) (December 20, 2022): 296–99. http://dx.doi.org/10.25699/sssb.2022.46.6.046.
Повний текст джерелаMantzanidou, Martha, Eleni Pontiki, and Dimitra Hadjipavlou-Litina. "Pyrazoles and Pyrazolines as Anti-Inflammatory Agents." Molecules 26, no. 11 (2021): 3439. http://dx.doi.org/10.3390/molecules26113439.
Повний текст джерелаGottardi, Waldemar, Dmitri Debabov, and Markus Nagl. "N-Chloramines, a Promising Class of Well-Tolerated Topical Anti-Infectives." Antimicrobial Agents and Chemotherapy 57, no. 3 (2013): 1107–14. http://dx.doi.org/10.1128/aac.02132-12.
Повний текст джерелаFejzagić, Alexander Veljko, Jan Gebauer, Nikolai Huwa, and Thomas Classen. "Halogenating Enzymes for Active Agent Synthesis: First Steps Are Done and Many Have to Follow." Molecules 24, no. 21 (2019): 4008. http://dx.doi.org/10.3390/molecules24214008.
Повний текст джерелаStaniszewska, Monika, Łukasz Kuryk, Aleksander Gryciuk, et al. "The Antifungal Action Mode of N-Phenacyldibromobenzimidazoles." Molecules 26, no. 18 (2021): 5463. http://dx.doi.org/10.3390/molecules26185463.
Повний текст джерелаCacciatore, Federica, Marina Amici, Giulia Romanelli, et al. "Disinfection By-Products (DBPs) in Seawaters, Sediments and Biota near a Marine Terminal for Regasifying Liquefied Natural Gas (LNG) in the Northern Adriatic Sea (Italy)." Processes 9, no. 12 (2021): 2175. http://dx.doi.org/10.3390/pr9122175.
Повний текст джерелаKharchenko, Vyacheslav A. "Getters in silicon." Modern Electronic Materials 5, no. 1 (2019): 1–11. http://dx.doi.org/10.3897/j.moem.5.1.38575.
Повний текст джерелаNogueira, Thais Cristina Mendonça, Lucas dos Santos Cruz, Maria Cristina Lourenço, and Marcus Vinicius Nora de Souza. "Design, Synthesis and Anti-tuberculosis Activity of Hydrazones and N-acylhydrazones Containing Vitamin B6 and Different Heteroaromatic Nucleus." Letters in Drug Design & Discovery 16, no. 7 (2019): 792–98. http://dx.doi.org/10.2174/1570180815666180627122055.
Повний текст джерелаMarkowicz-Piasecka, Magdalena, Ibrahim Komeil, Johanna Huttunen, Joanna Sikora, and Kristiina M. Huttunen. "Effective Cellular Transport of Ortho-Halogenated Sulfonamide Derivatives of Metformin Is Related to Improved Antiproliferative Activity and Apoptosis Induction in MCF-7 Cells." International Journal of Molecular Sciences 21, no. 7 (2020): 2389. http://dx.doi.org/10.3390/ijms21072389.
Повний текст джерелаRoman, Roxana, Lucia Pintilie, Diana Camelia Nuță, et al. "Contribution to the Synthesis, Characterization, Separation and Quantification of New N-Acyl Thiourea Derivatives with Antimicrobial and Antioxidant Potential." Pharmaceutics 15, no. 10 (2023): 2501. http://dx.doi.org/10.3390/pharmaceutics15102501.
Повний текст джерелаGalm, Ute, Stefanie Heller, Stuart Shapiro, Malcolm Page, Shu-Ming Li, and Lutz Heide. "Antimicrobial and DNA Gyrase-Inhibitory Activities of Novel Clorobiocin Derivatives Produced by Mutasynthesis." Antimicrobial Agents and Chemotherapy 48, no. 4 (2004): 1307–12. http://dx.doi.org/10.1128/aac.48.4.1307-1312.2004.
Повний текст джерелаGupta, Akhilesh. "SYNTHESIS OF NOVEL METHOXY SUBSTITUTED BENZOTHIAZOLE DERIVATIVES AND ANTIBACTERIAL ACTIVITY AGAINST ESCHERICHIA COLI." Asian Journal of Pharmaceutical and Clinical Research 11, no. 9 (2018): 416. http://dx.doi.org/10.22159/ajpcr.2018.v11i9.28095.
Повний текст джерелаKastbjerg, Vicky G., Marianne Halberg Larsen, Lone Gram, and Hanne Ingmer. "Influence of Sublethal Concentrations of Common Disinfectants on Expression of Virulence Genes in Listeria monocytogenes." Applied and Environmental Microbiology 76, no. 1 (2009): 303–9. http://dx.doi.org/10.1128/aem.00925-09.
Повний текст джерелаKharchenko, Vyacheslav A. "Getters in silicon." Modern Electronic Materials 5, no. (1) (2019): 1–11. https://doi.org/10.3897/j.moem.5.1.38575.
Повний текст джерелаvan Ommen, B., J. H. T. M. Ploemen, J. J. P. Bogaards, T. J. Monks, S. S. Gau, and P. J. van Bladeren. "Irreversible inhibition of rat glutathione S-transferase 1-1 by quinones and their glutathione conjugates. Structure-activity relationship and mechanism." Biochemical Journal 276, no. 3 (1991): 661–66. http://dx.doi.org/10.1042/bj2760661.
Повний текст джерелаBrito, Tiago O., Lethícia O. Abreu, Karen M. Gomes, et al. "Benzoylthioureas: Design, Synthesis and Antimycobacterial Evaluation." Medicinal Chemistry 16, no. 1 (2020): 93–103. http://dx.doi.org/10.2174/1573406415666181208110753.
Повний текст джерелаNamyatova, K. V., S. S. Zykova, D. S. Ovchinnikov, and S. N. Shurov. "Synthesis and Antihypoxic Activity of 2-aryl-7,7-dimethyl-5-oxo-5,6,7,8-tetrahydroquinoline-4-carboxylic Acids and Their Reaction Products with Substituted Hydrazines." Drug development & registration 12, no. 4 (2023): 28–33. http://dx.doi.org/10.33380/2305-2066-2023-12-4(1)-1654.
Повний текст джерелаSavinova, Ekaterina A., Tatiana A. Salimova, Elena V. Proskurnina, et al. "Effect of Water-Soluble Chlorine-Containing Buckminsterfullerene Derivative on the Metabolism of Reactive Oxygen Species in Human Embryonic Lung Fibroblasts." Oxygen 3, no. 1 (2022): 1–19. http://dx.doi.org/10.3390/oxygen3010001.
Повний текст джерелаRen, Tian, Mingyu Qiao, Lei Zhang, Jean Weese, Tung-Shi Huang, and Xuehong Ren. "Antimicrobial Activity of N-Halamine–Coated Materials in Broiler Chicken Houses." Journal of Food Protection 81, no. 2 (2018): 195–201. http://dx.doi.org/10.4315/0362-028x.jfp-17-176.
Повний текст джерелаHalfacre, John W., Jordan Stewart, Scott C. Herndon, et al. "Using tunable infrared laser direct absorption spectroscopy for ambient hydrogen chloride detection: HCl-TILDAS." Atmospheric Measurement Techniques 16, no. 5 (2023): 1407–29. http://dx.doi.org/10.5194/amt-16-1407-2023.
Повний текст джерелаSachkovska, V. I., O. Yu Zinchenko, B. S. Zhukov, and S. S. Kravets. "EVALUATION OF THE EFFICACY OF CHLORINE-CONTAINING COMMERCIAL PRODUCTS FOR WATER DECONTAMINATION AGAINST COLIFORM BACTERIA." Odesa National University Herald. Biology 29, no. 1(54) (2024): 67–78. http://dx.doi.org/10.18524/2077-1746.2024.1(54).309039.
Повний текст джерелаBrown, Paula N., Michael Chan, Chuck Chang, et al. "Detection of Undeclared Halogen Substituted Drug Compound in a Natural Health Product." Journal of Natural Health Product Research 2, no. 1 (2020): 11–22. https://doi.org/10.1515/jnhpr-2020-020102.
Повний текст джерелаWang, Chen, Yury I. Bauman, Ilya V. Mishakov, Vladimir O. Stoyanovskii, Ekaterina V. Shelepova, and Aleksey A. Vedyagin. "Scaling up the Process of Catalytic Decomposition of Chlorinated Hydrocarbons with the Formation of Carbon Nanostructures." Processes 10, no. 3 (2022): 506. http://dx.doi.org/10.3390/pr10030506.
Повний текст джерелаDi Santo, R., R. Costi, M. Artico, et al. "1,2,5-Benzothiadiazepine and Pyrrolo[2,1-d]-[1,2,5]Benzothiadiazepine Derivatives with Specific Anti-Human Immunodeficiency Virus Type 1 Activity." Antiviral Chemistry and Chemotherapy 9, no. 2 (1998): 127–37. http://dx.doi.org/10.1177/095632029800900204.
Повний текст джерелаAmmann, CExperimental Orthopaedics Innsbruck Medical University Innsbruck Austriahristoph G., Manfred Fille, Johann Hausdorfer, Michael Nogler, Markus Nagl, and Débora Coraça-Huber. "Influence of poly-N-acetylglucosamine in the extracellular matrix on N-chlorotaurine mediated killing of Staphylococcus epidermidis." New Microbiologica 37 (December 12, 2017): 361–64. https://doi.org/10.5281/zenodo.1110704.
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