Artigos de revistas sobre o tema "Thiols"
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Zelli, Renaud, Pascal Dumy, and Alberto Marra. "Metal-free synthesis of imino-disaccharides and calix-iminosugars by photoinduced radical thiol–ene coupling (TEC)." Organic & Biomolecular Chemistry 18, no. 13 (2020): 2392–97. http://dx.doi.org/10.1039/d0ob00198h.
Texto completo da fonteYILMAZ, Yücel, Şaban KELEŞOĞLU, Kemal TEKİN, et al. "A New Biomarker in The Distinction Between Stable Coronary Artery Disease and Acute Coronary Syndrome:Thiols." Journal of Contemporary Medicine 12, no. 4 (2022): 1–6. http://dx.doi.org/10.16899/jcm.981853.
Texto completo da fonteKalyanaraman, B. "Thiyl radicals in biological systems: significant or trivial?" Biochemical Society Symposia 61 (November 1, 1995): 55–63. http://dx.doi.org/10.1042/bss0610055.
Texto completo da fonteSkalska, Jolanta, Paul S. Brookes, S. M. Nadtochy, et al. "Modulation of Cell Surface Protein Free Thiols; A Potential Novel Mechanism of Action of the Sesquiterpene Lactone Parthenolide in Non-Hodgkin's Lymphoma." Blood 114, no. 22 (2009): 3774. http://dx.doi.org/10.1182/blood.v114.22.3774.3774.
Texto completo da fonteSawada, K., B. C. W. Hummel, and P. G. Walfish. "Intermediate Mr cytosolic components potentiate hepatic 5′-deiodinase activation by thiols." Biochemical Journal 238, no. 3 (1986): 787–91. http://dx.doi.org/10.1042/bj2380787.
Texto completo da fonteMANDAL, G., S. WYLLIE, N. SINGH, S. SUNDAR, A. H. FAIRLAMB, and M. CHATTERJEE. "Increased levels of thiols protect antimony unresponsive Leishmania donovani field isolates against reactive oxygen species generated by trivalent antimony." Parasitology 134, no. 12 (2007): 1679–87. http://dx.doi.org/10.1017/s0031182007003150.
Texto completo da fonteFolikumah, Makafui Y., Marc Behl, and Andreas Lendlein. "Reaction behaviour of peptide-based single thiol-thioesters exchange reaction substrate in the presence of externally added thiols." MRS Communications 11, no. 4 (2021): 402–10. http://dx.doi.org/10.1557/s43579-021-00041-z.
Texto completo da fonteSteenkamp, D. J. "Simple methods for the detection and quantification of thiols from Crithidia fasciculata and for the isolation of trypanothione." Biochemical Journal 292, no. 1 (1993): 295–301. http://dx.doi.org/10.1042/bj2920295.
Texto completo da fonteLiu, Zhengkun, Qianqian Wang, Hao Wang, Wenting Su, and Shouliang Dong. "A FRET Based Two-Photon Fluorescent Probe for Visualizing Mitochondrial Thiols of Living Cells and Tissues." Sensors 20, no. 6 (2020): 1746. http://dx.doi.org/10.3390/s20061746.
Texto completo da fonteCavalli, Federica, Lies De Keer, Birgit Huber, Paul H. M. Van Steenberge, Dagmar R. D'hooge, and Leonie Barner. "A kinetic study on the para-fluoro-thiol reaction in view of its use in materials design." Polymer Chemistry 10, no. 22 (2019): 2781–91. http://dx.doi.org/10.1039/c9py00435a.
Texto completo da fonteCopper, Alexander Willem, Cassandra Collins, Susan E. P. Bastian, Trent E. Johnson, and Dimitra L. Capone. "Preliminary investigation of potent thiols in Cypriot wines made from indigenous grape varieties Xynisteri, Maratheftiko and Giannoudhi." OENO One 55, no. 1 (2021): 223–34. http://dx.doi.org/10.20870/oeno-one.2021.55.1.4516.
Texto completo da fonteJaschke, M., H. Wolf, H. Schönherr, H. Ringsdorf, E. Bamberg, and H. J. Butt. "The molecular structure of thiol-monolayers on gold imaged with an Atomic Force Microscope." Proceedings, annual meeting, Electron Microscopy Society of America 53 (August 13, 1995): 714–15. http://dx.doi.org/10.1017/s0424820100139949.
Texto completo da fonteAmir, Roey, Assaf Harnoy, Nitsan Papo, and Gadi Slor. "Mixing End Groups in Thiol-Ene/Yne Reactions as a Simple Approach toward Multienzyme-Responsive Polymeric Amphiphiles." Synlett 29, no. 19 (2018): 2582–87. http://dx.doi.org/10.1055/s-0037-1611340.
Texto completo da fonteMafata, Mpho, Maria Stander, Baptiste Thomachot, and Astrid Buica. "Measuring Thiols in Single Cultivar South African Red Wines Using 4,4-Dithiodipyridine (DTDP) Derivatization and Ultraperformance Convergence Chromatography-Tandem Mass Spectrometry." Foods 7, no. 9 (2018): 138. http://dx.doi.org/10.3390/foods7090138.
Texto completo da fonteP., Pullaiah, Suchitra M. M., and Siddhartha Kumar B. "Protein carbonyls and protein thiols in rheumatoid arthritis." International Journal of Research in Medical Sciences 6, no. 5 (2018): 1738. http://dx.doi.org/10.18203/2320-6012.ijrms20181770.
Texto completo da fonteBoekhoud, Lisanne, Jacqueline Koeze, Elisabeth C. van der Slikke, et al. "Acute Kidney Injury is Associated with Lowered Plasma-Free Thiol Levels." Antioxidants 9, no. 11 (2020): 1135. http://dx.doi.org/10.3390/antiox9111135.
Texto completo da fonteYamamoto, Hiroki, Takuya Fujiwara, Takashi Funatsu, and Makoto Tsunoda. "Quantification of Intracellular Thiols by HPLC-Fluorescence Detection." Molecules 26, no. 8 (2021): 2365. http://dx.doi.org/10.3390/molecules26082365.
Texto completo da fonteChen, Liang, Dimitra L. Capone, and David W. Jeffery. "Analysis of Potent Odour-Active Volatile Thiols in Foods and Beverages with a Focus on Wine." Molecules 24, no. 13 (2019): 2472. http://dx.doi.org/10.3390/molecules24132472.
Texto completo da fonteLangford, C. R., D. W. Johnson, and N. R. Cameron. "Chemical functionalization of emulsion-templated porous polymers by thiol–ene “click” chemistry." Polym. Chem. 5, no. 21 (2014): 6200–6206. http://dx.doi.org/10.1039/c4py00713a.
Texto completo da fonteCrmarić, Dora, and Elvira Bura-Nakić. "Interaction between Cu and Thiols of Biological and Environmental Importance: Case Study Using Combined Spectrophotometric/Bathocuproine Sulfonate Disodium Salt Hydrate (BCS) Assay." Molecules 28, no. 13 (2023): 5065. http://dx.doi.org/10.3390/molecules28135065.
Texto completo da fonteHong, Seung-Mo, Oh Young Kim, and Seok-Ho Hwang. "Chemistry of Polythiols and Their Industrial Applications." Materials 17, no. 6 (2024): 1343. http://dx.doi.org/10.3390/ma17061343.
Texto completo da fonteGupta, Pradeep, and Chandra Maurya. "Phosphorus Pentasulfide Mediated Conversion of Primary Carbamates into Thiols." Synlett 28, no. 13 (2017): 1649–51. http://dx.doi.org/10.1055/s-0036-1589026.
Texto completo da fonteLiszewska, F., A. Blaszczyk, and A. Sirko. "Modification of non-protein thiols contents in transgenic tobacco plants producing bacterial enzymes of cysteine biosynthesis pathway." Acta Biochimica Polonica 48, no. 3 (2001): 647–56. http://dx.doi.org/10.18388/abp.2001_3899.
Texto completo da fonteWarangkar, Suchita C., and Chandrahas N. Khobragade. "Purification, Characterization, and Effect of Thiol Compounds on Activity of the Erwinia carotovora L-Asparaginase." Enzyme Research 2010 (November 1, 2010): 1–10. http://dx.doi.org/10.4061/2010/165878.
Texto completo da fonteOvchinnikova, S. N., and T. P. Aleksandrova. "Effect of solution composition on the desorption behavior of self-assembled monolayers of alkanethiols with different terminal groups." Èlektrohimiâ 60, no. 4 (2024): 300–308. http://dx.doi.org/10.31857/s0424857024040042.
Texto completo da fonteAli, Nura A., Mona A. Atwa, Radwa El-Sayed Marie, and Asmaa K. Abdelmaogood. "Assessment of serum levels of total thiol, thiol-disulfide, and total thiol/thiol-disulfide ratio in patients with vitiligo before and after narrowband ultraviolet B therapy." Egyptian Journal of Dermatology and Venereology 45, no. 1 (2025): 76–85. https://doi.org/10.4103/ejdv.ejdv_27_24.
Texto completo da fonteWang, Shenggang, Yue Huang, and Xiangming Guan. "Fluorescent Probes for Live Cell Thiol Detection." Molecules 26, no. 12 (2021): 3575. http://dx.doi.org/10.3390/molecules26123575.
Texto completo da fonteBourgonje, Arno R., Amaal Eman Abdulle, Areej M. Al-Rawas, et al. "Systemic Oxidative Stress Is Increased in Postmenopausal Women and Independently Associates with Homocysteine Levels." International Journal of Molecular Sciences 21, no. 1 (2020): 314. http://dx.doi.org/10.3390/ijms21010314.
Texto completo da fonteAndersson, A., A. Lindgren, and B. Hultberg. "Effect of thiol oxidation and thiol export from erythrocytes on determination of redox status of homocysteine and other thiols in plasma from healthy subjects and patients with cerebral infarction." Clinical Chemistry 41, no. 3 (1995): 361–66. http://dx.doi.org/10.1093/clinchem/41.3.361.
Texto completo da fonteAkdogan, Muberra, Yasemin Ustundag, Arzu Akdağ, Salim Neselioglu, and Ozcan Erel. "The Thiol-Disulfide Homeostasis and Coenzyme Q10 in Conjunction with Vitamin E Effect on Retinopathy Prematurity." Open Ophthalmology Journal 13, no. 1 (2019): 23–28. http://dx.doi.org/10.2174/1874364101913010023.
Texto completo da fonteOlson, Kenneth R., Kasey J. Clear, Yan Gao, et al. "Redox and Nucleophilic Reactions of Naphthoquinones with Small Thiols and Their Effects on Oxidization of H2S to Inorganic and Organic Hydropolysulfides and Thiosulfate." International Journal of Molecular Sciences 24, no. 8 (2023): 7516. http://dx.doi.org/10.3390/ijms24087516.
Texto completo da fonteRovati, Davide, Benedetta Albini, Pietro Galinetto, et al. "High Stability Thiol-Coated Gold Nanostars Monolayers with Photo-Thermal Antibacterial Activity and Wettability Control." Nanomaterials 9, no. 9 (2019): 1288. http://dx.doi.org/10.3390/nano9091288.
Texto completo da fonteGhosh, Tamashree, Abhishek Santra, and Anup Kumar Misra. "Appel-reagent-mediated transformation of glycosyl hemiacetal derivatives into thioglycosides and glycosyl thiols." Beilstein Journal of Organic Chemistry 9 (May 22, 2013): 974–82. http://dx.doi.org/10.3762/bjoc.9.112.
Texto completo da fontePeddinti, Rama, and Pallavi Singh. "Waste-Free Swift Synthesis of Symmetrical and Unsymmetrical Diarylmethyl Thioethers from Diaryl Carbinols." Synthesis 49, no. 16 (2017): 3633–42. http://dx.doi.org/10.1055/s-0036-1589022.
Texto completo da fonteBednářová, Eva, Simona Hybelbauerová та Jindřich Jindřich. "Optimized methods for preparation of 6I-(ω-sulfanyl-alkylene-sulfanyl)-β-cyclodextrin derivatives". Beilstein Journal of Organic Chemistry 12 (24 лютого 2016): 349–52. http://dx.doi.org/10.3762/bjoc.12.38.
Texto completo da fonteAl-Humadi, Nabil H., Joseph KH Ma, Daniel M. Lewis, Jane YC Ma, Mark W. Barger, and Paul D. Siegel. "Dose-dependent thiol and immune responses to ovalbumin challenge in Brown Norway rats." Toxicology and Industrial Health 18, no. 7 (2002): 343–52. http://dx.doi.org/10.1191/0748233702th155oa.
Texto completo da fonteBramanti, Emilia, Cecilia Vecoli, Danilo Neglia, Maria Paola Pellegrini, Giorgio Raspi, and Renata Barsacchi. "Speciation and Quantification of Thiols by Reversed-Phase Chromatography Coupled with On-Line Chemical Vapor Generation and Atomic Fluorescence Spectrometric Detection: Method Validation and Preliminary Application for Glutathione Measurements in Human Whole Blood." Clinical Chemistry 51, no. 6 (2005): 1007–13. http://dx.doi.org/10.1373/clinchem.2004.045443.
Texto completo da fontePellom, Samuel, Ryan Michalek, and Jason Grayson. "Regulation of Surface Free Thiol Levels During CD8+ T Cell Activation, Proliferation and Differentiation (132.7)." Journal of Immunology 184, no. 1_Supplement (2010): 132.7. http://dx.doi.org/10.4049/jimmunol.184.supp.132.7.
Texto completo da fonteWessig, Pablo, Tanja Schulze, Alexandra Pfennig, Steffen M. Weidner, Sascha Prentzel, and Helmut Schlaad. "Thiol–ene polymerization of oligospiroketal rods." Polymer Chemistry 8, no. 44 (2017): 6879–85. http://dx.doi.org/10.1039/c7py01569k.
Texto completo da fonteMartínez-Blanco, Gilberto Josué, and Jannu Casanova-Moreno. "Characterization of the Reductive Desorption of Self-Assembled Monolayers on Platinum Surfaces." ECS Meeting Abstracts MA2022-01, no. 45 (2022): 1936. http://dx.doi.org/10.1149/ma2022-01451936mtgabs.
Texto completo da fonteGeorgescu, Simona Roxana, Cristina Iulia Mitran, Madalina Irina Mitran, et al. "Thiol-Disulfide Homeostasis in Skin Diseases." Journal of Clinical Medicine 11, no. 6 (2022): 1507. http://dx.doi.org/10.3390/jcm11061507.
Texto completo da fonteSen, Chandan K. "Update on Thiol Status and Supplements in Physical Exercise." Canadian Journal of Applied Physiology 26, S1 (2001): S4—S12. http://dx.doi.org/10.1139/h2001-037.
Texto completo da fonteTong, Ka-Chung, Chun-Nam Lok, Pui-Ki Wan, et al. "An anticancer gold(III)-activated porphyrin scaffold that covalently modifies protein cysteine thiols." Proceedings of the National Academy of Sciences 117, no. 3 (2020): 1321–29. http://dx.doi.org/10.1073/pnas.1915202117.
Texto completo da fonteAkinloye, D. I., R. N. Ugbaja, A. J. Akamo, et al. "Effects of alcohol-graded concentrations on total thiols and some thiol utilizing enzymes." Bayero Journal of Pure and Applied Sciences 15, no. 1 (2022): 202–9. http://dx.doi.org/10.4314/bajopas.v15i1.29.
Texto completo da fonteCesarini, Lucia, Flavia Grignaffini, Anna Alisi, and Anna Pastore. "Alterations in Glutathione Redox Homeostasis in Metabolic Dysfunction-Associated Fatty Liver Disease: A Systematic Review." Antioxidants 13, no. 12 (2024): 1461. http://dx.doi.org/10.3390/antiox13121461.
Texto completo da fonteJain, Surbhi, Lori W. McGinnes, and Trudy G. Morrison. "Overexpression of Thiol/Disulfide Isomerases Enhances Membrane Fusion Directed by the Newcastle Disease Virus Fusion Protein." Journal of Virology 82, no. 24 (2008): 12039–48. http://dx.doi.org/10.1128/jvi.01406-08.
Texto completo da fonteRawat, Mamta, and Julie A. Maupin-Furlow. "Redox and Thiols in Archaea." Antioxidants 9, no. 5 (2020): 381. http://dx.doi.org/10.3390/antiox9050381.
Texto completo da fontevan Eijk, Larissa E., Adriana Tami, Jan-Luuk Hillebrands, et al. "Mild Coronavirus Disease 2019 (COVID-19) Is Marked by Systemic Oxidative Stress: A Pilot Study." Antioxidants 10, no. 12 (2021): 2022. http://dx.doi.org/10.3390/antiox10122022.
Texto completo da fonteSun, Jinyu, Liangwei Zhang, Xiaolong Zhang, Yuesong Hu, Chunpo Ge, and Jianguo Fang. "An ultrafast turn-on thiol probe for protein labeling and bioimaging." Analyst 141, no. 6 (2016): 2009–15. http://dx.doi.org/10.1039/c5an02347e.
Texto completo da fonteBourgonje, Arno R., Ruben Y. Gabriëls, Martin H. de Borst, et al. "Serum Free Thiols Are Superior to Fecal Calprotectin in Reflecting Endoscopic Disease Activity in Inflammatory Bowel Disease." Antioxidants 8, no. 9 (2019): 351. http://dx.doi.org/10.3390/antiox8090351.
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