Статті в журналах з теми "Novel reactive intermediates"
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Hemberger, Patrick, Jeroen A. van Bokhoven, Javier Pérez-Ramírez, and Andras Bodi. "New analytical tools for advanced mechanistic studies in catalysis: photoionization and photoelectron photoion coincidence spectroscopy." Catalysis Science & Technology 10, no. 7 (2020): 1975–90. http://dx.doi.org/10.1039/c9cy02587a.
Повний текст джерелаDamsten, Micaela C., Jon S. B. de Vlieger, Wilfried M. A. Niessen, Hubertus Irth, Nico P. E. Vermeulen, and Jan N. M. Commandeur. "Trimethoprim: Novel Reactive Intermediates and Bioactivation Pathways by Cytochrome P450s." Chemical Research in Toxicology 21, no. 11 (November 17, 2008): 2181–87. http://dx.doi.org/10.1021/tx8002593.
Повний текст джерелаKessar, S. V. "Lewis acid complexed azacarbanions: Novel reactive intermediates of wide synthetic utility." Pure and Applied Chemistry 68, no. 3 (January 1, 1996): 509–14. http://dx.doi.org/10.1351/pac199668030509.
Повний текст джерелаHansel, Colleen M., Timothy G. Ferdelman, and Bradley M. Tebo. "Cryptic Cross-Linkages Among Biogeochemical Cycles: Novel Insights from Reactive Intermediates." Elements 11, no. 6 (November 30, 2015): 409–14. http://dx.doi.org/10.2113/gselements.11.6.409.
Повний текст джерелаGreen, Justin L., and Gregory A. Reed. "Benzo[a]pyrene bay-region sulfonates, a novel class of reactive intermediates." Chemical Research in Toxicology 3, no. 1 (January 1990): 59–64. http://dx.doi.org/10.1021/tx00013a010.
Повний текст джерелаThome, Ulrich, Ahmed Lazrak, Lan Chen, Marion C. Kirk, Michael J. Thomas, Henry Jay Forman, and Sadis Matalon. "Novel SIN-1 reactive intermediates modulate chloride secretion across murine airway cells." Free Radical Biology and Medicine 35, no. 6 (September 2003): 662–75. http://dx.doi.org/10.1016/s0891-5849(03)00392-7.
Повний текст джерелаAttwa, Mohamed W., Adnan A. Kadi, and Hany W. Darwish. "Belizatinib: Novel reactive intermediates and bioactivation pathways characterized by LC–MS/MS." Journal of Pharmaceutical and Biomedical Analysis 171 (July 2019): 132–47. http://dx.doi.org/10.1016/j.jpba.2019.04.006.
Повний текст джерелаGroves, John T. "Cytochrome P450 enzymes: understanding the biochemical hieroglyphs." F1000Research 4 (July 1, 2015): 178. http://dx.doi.org/10.12688/f1000research.6314.1.
Повний текст джерелаHe, Chao, Galiya R. Galimova, Yuheng Luo, Long Zhao, André K. Eckhardt, Rui Sun, Alexander M. Mebel, and Ralf I. Kaiser. "A chemical dynamics study on the gas-phase formation of triplet and singlet C5H2carbenes." Proceedings of the National Academy of Sciences 117, no. 48 (November 16, 2020): 30142–50. http://dx.doi.org/10.1073/pnas.2019257117.
Повний текст джерелаKotuniak, Radosław, and Wojciech Bal. "Kinetics of Cu(ii) complexation by ATCUN/NTS and related peptides: a gold mine of novel ideas for copper biology." Dalton Transactions 51, no. 1 (2022): 14–26. http://dx.doi.org/10.1039/d1dt02878b.
Повний текст джерелаDerevianko, A., T. Graeber, and H. Simms. "REACTIVE OXYGEN INTERMEDIATES (ROI) - A NOVEL ROLE AS SECOND MESSENGERS IN CYTOKINE STIMULATED PMN." Shock 5 (June 1996): 49. http://dx.doi.org/10.1097/00024382-199606002-00157.
Повний текст джерелаScheer, Manfred, Eva Leiner, Peter Kramkowski, Michael Schiffer, and Gerhard Baum. "A Novel Synthetic Approach to Highly Reactive Intermediates Containing a Metal-Phosphorus Triple Bond." Chemistry - A European Journal 4, no. 10 (October 2, 1998): 1917–23. http://dx.doi.org/10.1002/(sici)1521-3765(19981002)4:10<1917::aid-chem1917>3.0.co;2-9.
Повний текст джерелаAlRabiah, Haitham, Adnan A. Kadi, Mohamed W. Attwa, Ali S. Abdelhameed, and Gamal A. E. Mostafa. "Reactive intermediates in copanlisib metabolism identified by LC-MS/MS: phase I metabolic profiling." RSC Advances 9, no. 11 (2019): 6409–18. http://dx.doi.org/10.1039/c8ra10322d.
Повний текст джерелаRuan, Jia, Gregory St. John, Sabine Ehrt, Lee Riley, and Carl Nathan. "noxR3, a Novel Gene fromMycobacterium tuberculosis, Protects Salmonella typhimurium from Nitrosative and Oxidative Stress." Infection and Immunity 67, no. 7 (July 1, 1999): 3276–83. http://dx.doi.org/10.1128/iai.67.7.3276-3283.1999.
Повний текст джерелаSchneider, Thomas, Michael Keim, Bianca Seitz, and Gerhard Maas. "Reactions of 3-aryl-1-(trifluoromethyl)prop-2-yn-1-iminium salts with 1,3-dienes and styrenes." Beilstein Journal of Organic Chemistry 16 (August 24, 2020): 2064–72. http://dx.doi.org/10.3762/bjoc.16.173.
Повний текст джерелаChen, Mei, Guoyan Zhang, Xiao Liang, Wanshu Zhang, Le Zhou, Baofeng He, Ping Song, et al. "Thermally stable transparent sol–gel based active siloxane–oligomer materials with tunable high refractive index and dual reactive groups." RSC Advances 6, no. 75 (2016): 70825–31. http://dx.doi.org/10.1039/c6ra13164f.
Повний текст джерелаRay, César, Andrés García-Sampedro, Christopher Schad, Edurne Avellanal-Zaballa, Florencio Moreno, María J. Ortiz, Jorge Bañuelos, et al. "Alkynyl N-BODIPYs as Reactive Intermediates for the Development of Dyes for Biophotonics." Chemistry Proceedings 3, no. 1 (November 14, 2020): 15. http://dx.doi.org/10.3390/ecsoc-24-08374.
Повний текст джерелаOrhan, Hilmi, and Nico P.E. Vermeulen. "Conventional and Novel Approaches in Generating and Characterization of Reactive Intermediates from Drugs/Drug Candidates." Current Drug Metabolism 12, no. 4 (May 1, 2011): 383–94. http://dx.doi.org/10.2174/138920011795202974.
Повний текст джерелаOng, Voon, Grayson Hough, Michael Schlosser, Ken Bartizal, James M. Balkovec, Kenneth D. James, and B. Radha Krishnan. "Preclinical Evaluation of the Stability, Safety, and Efficacy of CD101, a Novel Echinocandin." Antimicrobial Agents and Chemotherapy 60, no. 11 (September 12, 2016): 6872–79. http://dx.doi.org/10.1128/aac.00701-16.
Повний текст джерелаChen, Lu Yi, Jian Gang Chen, Xin Hui Ruan, Su Xin Xu, Yi Qi Yang, and Bi Jia Wang. "Sustainable Reactive Dyeing of Cotton Fabric in Green Non-Aqueous Medium: A Density Function Theory (DFT) Modeling Study." Key Engineering Materials 671 (November 2015): 139–48. http://dx.doi.org/10.4028/www.scientific.net/kem.671.139.
Повний текст джерелаEhrt, Sabine, Michael U. Shiloh, Jia Ruan, Michael Choi, Stuart Gunzburg, Carl Nathan, Qiao-wen Xie, and Lee W. Riley. "A Novel Antioxidant Gene from Mycobacterium tuberculosis." Journal of Experimental Medicine 186, no. 11 (December 1, 1997): 1885–96. http://dx.doi.org/10.1084/jem.186.11.1885.
Повний текст джерелаZhiqiang, Wang, Hwang Seung Hwan, and Lim Soon Sung. "Effect of Novel Synthesised Policosanyl Phenolates on Lipid Oxidation." Czech Journal of Food Sciences 34, No. 5 (November 1, 2016): 414–21. http://dx.doi.org/10.17221/530/2015-cjfs.
Повний текст джерелаAbdelhameed, Ali S., Mohamed W. Attwa, and Adnan A. Kadi. "Liquid chromatography–tandem mass spectrometry metabolic profiling of nazartinib reveals the formation of unexpected reactive metabolites." Royal Society Open Science 6, no. 8 (August 2019): 190852. http://dx.doi.org/10.1098/rsos.190852.
Повний текст джерелаPetrič, Andrej, Tatjana Špes, and Jorge R. Barrio. "Novel Fluorescent Reactive Dyes as Intermediates for the Preparation of UV and Vis Wavelength Fluorescent Probes." Monatshefte für Chemie / Chemical Monthly 129, no. 8-9 (September 1998): 777–86. http://dx.doi.org/10.1007/pl00013476.
Повний текст джерелаAdams, Nicholas J., Joachim Bargon, John M. Brown, Edward J. Farrington, Erwan Galardon, Ralf Giernoth, Hanjo Heinrich, Benjamin D. John, and Kenji Maeda. "Interplay of synthesis and mechanism in asymmetric homogeneous catalysis." Pure and Applied Chemistry 73, no. 2 (January 1, 2001): 343–46. http://dx.doi.org/10.1351/pac200173020343.
Повний текст джерелаSkariah, Sini, Robert B. Bednarczyk, Matthew K. McIntyre, Gregory A. Taylor, and Dana G. Mordue. "Discovery of a Novel Toxoplasma gondii Conoid-Associated Protein Important for Parasite Resistance to Reactive Nitrogen Intermediates." Journal of Immunology 188, no. 7 (March 2, 2012): 3404–15. http://dx.doi.org/10.4049/jimmunol.1101425.
Повний текст джерелаPETRIC, A., T. SPES, and J. R. BARRIO. "ChemInform Abstract: Novel Fluorescent Reactive Dyes as Intermediates for the Preparation of UV and Vis Wavelength Fluorescent Probes." ChemInform 29, no. 52 (June 18, 2010): no. http://dx.doi.org/10.1002/chin.199852214.
Повний текст джерелаYe, Jianhuai, Jonathan P. D. Abbatt, and Arthur W. H. Chan. "Novel pathway of SO<sub>2</sub> oxidation in the atmosphere: reactions with monoterpene ozonolysis intermediates and secondary organic aerosol." Atmospheric Chemistry and Physics 18, no. 8 (April 24, 2018): 5549–65. http://dx.doi.org/10.5194/acp-18-5549-2018.
Повний текст джерелаSpotte-Smith, Evan Walter Clark, Samuel M. Blau, and Kristin A. Persson. "GPS for the SEI: Charting Electrochemical Mechanisms with Reaction Networks." ECS Meeting Abstracts MA2022-01, no. 4 (July 7, 2022): 518. http://dx.doi.org/10.1149/ma2022-014518mtgabs.
Повний текст джерелаGuo, Shuang, Xiwen Cheng, Jun-Hee Lim, Yu Liu, and Hung-Ying Kao. "Control of antioxidative response by the tumor suppressor protein PML through regulating Nrf2 activity." Molecular Biology of the Cell 25, no. 16 (August 15, 2014): 2485–98. http://dx.doi.org/10.1091/mbc.e13-11-0692.
Повний текст джерелаKatayev, Evgeny A., Herman V. Lavrov, and Victor N. Khrustalev. "Deprotonation induced dioxygen activation and ligand oxidation by dipyrromethane-palladium complexes." Journal of Porphyrins and Phthalocyanines 12, no. 11 (November 2008): 1137–45. http://dx.doi.org/10.1142/s1088424608000509.
Повний текст джерелаBarton, Derek H. R., and Shyamal I. Parekh. "Novel selenium-oxygen and silane-nitrogen bond metatheses. Mechanistic probes, spectroscopic studies, and structural evidence for reactive oligomeric selenoazyl intermediates." Journal of the American Chemical Society 115, no. 3 (February 1993): 948–55. http://dx.doi.org/10.1021/ja00056a019.
Повний текст джерелаShen, Chieh-Yu, Cheng-Hsun Lu, Cheng-Han Wu, Ko-Jen Li, Yu-Min Kuo, Song-Chou Hsieh, and Chia-Li Yu. "The Development of Maillard Reaction, and Advanced Glycation End Product (AGE)-Receptor for AGE (RAGE) Signaling Inhibitors as Novel Therapeutic Strategies for Patients with AGE-Related Diseases." Molecules 25, no. 23 (November 27, 2020): 5591. http://dx.doi.org/10.3390/molecules25235591.
Повний текст джерелаMus, Florence, Hsin-Hua Wu, Alexander B. Alleman, Krista A. Shisler, Oleg A. Zadvornyy, Brian Bothner, Jennifer L. Dubois, and John W. Peters. "Insights into the unique carboxylation reactions in the metabolism of propylene and acetone." Biochemical Journal 477, no. 11 (June 4, 2020): 2027–38. http://dx.doi.org/10.1042/bcj20200174.
Повний текст джерелаColussi, Agustín, and Shinichi Enami. "Detecting Intermediates and Products of Fast Heterogeneous Reactions on Liquid Surfaces via Online Mass Spectrometry." Atmosphere 10, no. 2 (January 26, 2019): 47. http://dx.doi.org/10.3390/atmos10020047.
Повний текст джерелаYang, Xiaojuan, Jing Song, and Liang-Jun Yan. "Chronic Inhibition of Mitochondrial Dihydrolipoamide Dehydrogenase (DLDH) as an Approach to Managing Diabetic Oxidative Stress." Antioxidants 8, no. 2 (February 2, 2019): 32. http://dx.doi.org/10.3390/antiox8020032.
Повний текст джерелаRahman, Md Motiar, Mst Gulshan Ara, Md Sohanur Rahman, Md Sahab Uddin, May N. Bin-Jumah, and Mohammed M. Abdel-Daim. "Recent Development of Catalytic Materials for Ethylbenzene Oxidation." Journal of Nanomaterials 2020 (February 25, 2020): 1–20. http://dx.doi.org/10.1155/2020/7532767.
Повний текст джерелаKassaee, M. Z., S. M. Musavi, M. Ghambarian, and M. R. Khalili Zanjani. "Switching of global minima of novel germylenic reactive intermediates via halogens (X): C2GeH2 vs. C2GeHX at ab initio and DFT levels." Journal of Organometallic Chemistry 691, no. 13 (June 2006): 2933–44. http://dx.doi.org/10.1016/j.jorganchem.2006.02.038.
Повний текст джерелаYin, Guochuan, Andrew M. Danby, David Kitko, John D. Carter, William M. Scheper, and Daryle H. Busch. "Olefin Epoxidation by Alkyl Hydroperoxide with a Novel Cross-Bridged Cyclam Manganese Complex: Demonstration of Oxygenation by Two Distinct Reactive Intermediates." Inorganic Chemistry 46, no. 12 (June 2007): 5125–26. http://dx.doi.org/10.1021/ic700886v.
Повний текст джерелаZhang, Xini, and Peter Ulrich. "Directed approaches to reactive maillard intermediates: Formation of a novel 3-alkylamino-2-hydroxy-4-hydroxymethyl-2-cyclopenten-1-one (“Cypentodine”)." Tetrahedron Letters 37, no. 27 (July 1996): 4667–70. http://dx.doi.org/10.1016/0040-4039(96)00959-8.
Повний текст джерелаYin, Guochuan, Andrew M. Danby, David Kitko, John D. Carter, William M. Scheper, and Daryle H. Busch. "Olefin Epoxidation by Alkyl Hydroperoxide with a Novel Cross-Bridged Cyclam Manganese Complex: Demonstration of Oxygenation by Two Distinct Reactive Intermediates." Inorganic Chemistry 46, no. 6 (March 2007): 2173–80. http://dx.doi.org/10.1021/ic061957r.
Повний текст джерелаAtiakshin, Dmitry A., Victoria Shishkina, Dmitry I. Esaulenko, Evgeniy S. Ovsyannikov, Lyubov N. Antakova, Olga A. Gerasimova, Tatiana V. Samoilenko, Pavel Yu Andreev, Sara T. Magerramova, and Sofia A. Budnevskaya. "Mast Cells as the Target of the Biological Effects of Molecular Hydrogen in the Specific Tissue Microenvironment." International Journal of Biomedicine 12, no. 2 (June 5, 2022): 183–87. http://dx.doi.org/10.21103/article12(2)_ra2.
Повний текст джерелаWang, Xuefeng, Lester Andrews, and Gary P. Kushto. "ChemInform Abstract: Infrared Spectra of the Novel Ge2H2 and Ge2H4 Species and the Reactive GeH1,2,3 Intermediates in Solid Neon, Deuterium and Argon." ChemInform 33, no. 37 (September 17, 2002): no. http://dx.doi.org/10.1002/chin.200237002.
Повний текст джерелаWang, Xuefeng, Lester Andrews, George V. Chertihin, and P. F. Souter. "ChemInform Abstract: Infrared Spectra of the Novel Sn2H2 Species and the Reactive SnH1,2,3 and PbH1,2,3 Intermediates in Solid Neon, Deuterium, and Argon." ChemInform 33, no. 39 (May 19, 2010): no. http://dx.doi.org/10.1002/chin.200239005.
Повний текст джерелаHasanpour, Fatemeh, Javad Saien, and Omid Norouzi. "Catalytic Activation of Hydrogen Peroxide Using Highly Porous Hydrothermally Modified Manganese Catalysts for Removal of Azithromycin Antibiotic from Aqueous Solution." Catalysts 13, no. 1 (December 30, 2022): 77. http://dx.doi.org/10.3390/catal13010077.
Повний текст джерелаThompson, David M., Jason McLeod, and Michael C. Baird. "New methods for the synthesis of transition-metal fullerene complexes." Pure and Applied Chemistry 73, no. 2 (January 1, 2001): 287–89. http://dx.doi.org/10.1351/pac200173020287.
Повний текст джерелаThorsell, Annika, Emre Isin, and Ulrik Jurva. "Characterization of peptide adducts formed via novel reactive intermediates of the CB1 antagonist rimonabant in a model electrochemical system and human liver microsomes." Toxicology Letters 229 (September 2014): S248. http://dx.doi.org/10.1016/j.toxlet.2014.06.835.
Повний текст джерелаZHANG, X., and P. ULRICH. "ChemInform Abstract: Directed Approaches to Reactive Maillard Intermediates: Formation of a Novel 3-Alkylamino-2-hydroxy-4-hydroxymethyl-2-cyclopenten-1-one (“ Cypentodine”)." ChemInform 27, no. 41 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199641079.
Повний текст джерелаSaito, A., та H. Sinohara. "Rabbit α-1-antiproteinase E: a novel recombinant serpin which does not inhibit proteinases". Biochemical Journal 307, № 2 (15 квітня 1995): 369–75. http://dx.doi.org/10.1042/bj3070369.
Повний текст джерелаPan, Yi, Kyle D. Mansfield, Cara C. Bertozzi, Viktoriya Rudenko, Denise A. Chan, Amato J. Giaccia, and M. Celeste Simon. "Multiple Factors Affecting Cellular Redox Status and Energy Metabolism Modulate Hypoxia-Inducible Factor Prolyl Hydroxylase Activity In Vivo and In Vitro." Molecular and Cellular Biology 27, no. 3 (November 13, 2006): 912–25. http://dx.doi.org/10.1128/mcb.01223-06.
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