Статті в журналах з теми "Guanidinium groups"
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Malinska, Maura, Miroslawa Dauter, and Zbigniew Dauter. "Geometry of guanidinium groups in arginines." Protein Science 25, no. 9 (July 4, 2016): 1753–56. http://dx.doi.org/10.1002/pro.2970.
Повний текст джерелаGalukhin, Andrey, Ilnaz Imatdinov, and Yuri Osin. "p-tert-Butylthiacalix[4]arenes equipped with guanidinium fragments: aggregation, cytotoxicity, and DNA binding abilities." RSC Advances 6, no. 39 (2016): 32722–26. http://dx.doi.org/10.1039/c6ra04733e.
Повний текст джерелаBalos, V., M. Bonn, and J. Hunger. "Quantifying transient interactions between amide groups and the guanidinium cation." Physical Chemistry Chemical Physics 17, no. 43 (2015): 28539–43. http://dx.doi.org/10.1039/c5cp04619j.
Повний текст джерелаSzabo, Jan, and Gerhard Maas. "Derivatives of the triaminoguanidinium ion, 4. O-Sulfonylation of N,N′,N″-tris(hydroxybenzylidenamino)guanidinium ions." Zeitschrift für Naturforschung B 71, no. 6 (June 1, 2016): 697–703. http://dx.doi.org/10.1515/znb-2016-0035.
Повний текст джерелаHanke, Marcel, Niklas Hansen, Emilia Tomm, Guido Grundmeier, and Adrian Keller. "Time-Dependent DNA Origami Denaturation by Guanidinium Chloride, Guanidinium Sulfate, and Guanidinium Thiocyanate." International Journal of Molecular Sciences 23, no. 15 (August 1, 2022): 8547. http://dx.doi.org/10.3390/ijms23158547.
Повний текст джерелаMatulková, Irena, Jan Fábry, Václav Eigner, Michal Dušek, Jan Kroupa, and Ivan Němec. "Isostructural Crystals of Bis(Guanidinium) Trioxofluoro-Phosphate/Phosphite in the Ratio 1/0, 0.716/0.284, 0.501/0.499, 0.268/0.732, 0/1—Crystal Structures, Vibrational Spectra and Second Harmonic Generation." Crystals 12, no. 12 (November 23, 2022): 1694. http://dx.doi.org/10.3390/cryst12121694.
Повний текст джерелаBalos, V., M. Bonn, and J. Hunger. "Correction: Quantifying transient interactions between amide groups and the guanidinium cation." Physical Chemistry Chemical Physics 18, no. 2 (2016): 1346–47. http://dx.doi.org/10.1039/c5cp90226f.
Повний текст джерелаCui, Yu Fang, Jin Yan Du, Yu Ming Shang, Yao Wu Wang, Jin Hai Wang, Ya Fei Lv, and Shu Bo Wang. "Novel Anion Exchange Membranes from Poly(aryl ether)s with Quaternary Guanidinium Groups." Advanced Materials Research 560-561 (August 2012): 864–68. http://dx.doi.org/10.4028/www.scientific.net/amr.560-561.864.
Повний текст джерелаDu, Shanshan, Yang Li, Zhilong Chai, Weiguo Shi, and Junlin He. "Site-specific functionalization with amino, guanidinium, and imidazolyl groups enabling the activation of 10–23 DNAzyme." RSC Advances 10, no. 32 (2020): 19067–75. http://dx.doi.org/10.1039/d0ra02226h.
Повний текст джерелаTiritiris, Ioannis. "N,N,N′,N′,N′′-Pentamethyl-N′′-[3-(trimethylazaniumyl)propyl]guanidinium bis(tetraphenylborate)." Acta Crystallographica Section E Structure Reports Online 69, no. 2 (January 26, 2013): o292. http://dx.doi.org/10.1107/s1600536813001992.
Повний текст джерелаKanvah, Sriram, and Gary B. Schuster. "Effect of positively charged backbone groups on radical cation migration and reaction in duplex DNA." Canadian Journal of Chemistry 89, no. 3 (February 2011): 326–30. http://dx.doi.org/10.1139/v10-145.
Повний текст джерелаSauer, Sven, Sarmenio Saliba, Stefan Tussetschläger, Angelika Baro, Wolfgang Frey, Frank Giesselmann, Sabine Laschat, and Willi Kantlehner. "p-Alkoxybiphenyls with guanidinium head groups displaying smectic mesophases." Liquid Crystals 36, no. 3 (May 22, 2009): 275–99. http://dx.doi.org/10.1080/02678290902850027.
Повний текст джерелаRobichon, Alain, and Jean Claude Marie. "Chemical modification of guanidinium groups of vasoactive intestinal peptide." Biochimica et Biophysica Acta (BBA) - General Subjects 923, no. 2 (February 1987): 250–56. http://dx.doi.org/10.1016/0304-4165(87)90010-9.
Повний текст джерелаMüller, Gerhard, Jürgen Riede, and Franz Peter Schmidtchen. "Host-Guest Bonding of Oxoanions to Guanidinium Anchor Groups." Angewandte Chemie International Edition in English 27, no. 11 (November 1988): 1516–18. http://dx.doi.org/10.1002/anie.198815161.
Повний текст джерелаRussell, V. A., and M. D. Ward. "Solid-state structure of a layered hydrogen-bonded salt: guanidinium 5-benzoyl-4-hydroxy-2-methoxybenzenesulfonate methanol solvate." Acta Crystallographica Section B Structural Science 52, no. 1 (February 1, 1996): 209–14. http://dx.doi.org/10.1107/s0108768195009980.
Повний текст джерелаKantlehner, Willi, Jochen Mezger, Ralf Kreß, Horst Hartmann, Thorsten Moschny, Ioannis Tiritiris, Boyan Iliev та ін. "Orthoamide, LXIX [1]. Beiträge zur Synthese N,N,N´,N´,N´´-peralkylierter Guanidine und N,N,N´,N´,N´´䞲,N´´-persubstituierter Guanidiniumsalze / Orthoamides, LXIX [1]. Contributions to the Synthesis of N, N, N´, N´, N´-peralkylated Guanidines and N, N, N´, N´, N´´, N´´-persubstituted Guanidinium Salts". Zeitschrift für Naturforschung B 65, № 7 (1 липня 2010): 873–906. http://dx.doi.org/10.1515/znb-2010-0712.
Повний текст джерелаWei, Bin. "Dimethylammonium guanidinium naphthalene-1,5-disulfonate." Acta Crystallographica Section E Structure Reports Online 68, no. 4 (March 21, 2012): o1123. http://dx.doi.org/10.1107/s1600536812011099.
Повний текст джерелаVortman, M. Ya, Zh P. Kopteva, A. E. Kopteva, D. R. Abdulina, Yu B. Pysmenna, G. O. Iutynska, A. V. Rudenko, V. V. Tretyak, V. N. Lemeshko, and V. V. Shevchenko. "Antibacterial and Fungicidal Activity of Guanidinium Oligomers." Mikrobiolohichnyi Zhurnal 83, no. 4 (August 17, 2021): 86–97. http://dx.doi.org/10.15407/microbiolj83.04.086.
Повний текст джерелаTabujew, Ilja, Ceren Cokca, Leon Zartner, Ulrich S. Schubert, Ivo Nischang, Dagmar Fischer, and Kalina Peneva. "The influence of gradient and statistical arrangements of guanidinium or primary amine groups in poly(methacrylate) copolymers on their DNA binding affinity." Journal of Materials Chemistry B 7, no. 39 (2019): 5920–29. http://dx.doi.org/10.1039/c9tb01269a.
Повний текст джерелаMetzger, A., W. Peschke, and F. P. Schmidtchen. "A Convenient Access to Chiral Monofunctionalized Bicyclic Guanidinium Receptor Groups." Synthesis 1995, no. 05 (May 1995): 566–70. http://dx.doi.org/10.1055/s-1995-3953.
Повний текст джерелаSapse, Anne-Marie, Robert Rothchild, and Kyu Rhee. "An ab initio study of the guanidinium groups in saxitoxin." Journal of Molecular Modeling 12, no. 2 (November 8, 2005): 140–45. http://dx.doi.org/10.1007/s00894-005-0005-y.
Повний текст джерелаLi, Shouchuan, Chunyu Chen, Zhengdong Zhang, Dong Wang, and Shanshan Lv. "Illustration and application of enhancing effect of arginine on interactions between nano-clays: self-healing hydrogels." Soft Matter 15, no. 2 (2019): 303–11. http://dx.doi.org/10.1039/c8sm02188k.
Повний текст джерелаGalukhin, Andrey, Anton Erokhin, Ilnaz Imatdinov, and Yuri Osin. "Investigation of DNA binding abilities of solid lipid nanoparticles based on p-tert-butylthiacalix[4]arene platform." RSC Advances 5, no. 42 (2015): 33351–55. http://dx.doi.org/10.1039/c5ra03814f.
Повний текст джерелаTiritiris, Ioannis, and Willi Kantlehner. "Crystal structure ofN′′-benzyl-N′′-[3-(benzyldimethylazaniumyl)propyl]-N,N,N′,N′-tetramethylguanidinium bis(tetraphenylborate)." Acta Crystallographica Section E Crystallographic Communications 71, no. 12 (December 1, 2015): o1086—o1087. http://dx.doi.org/10.1107/s2056989015024639.
Повний текст джерелаRichter, Friederike, Liam Martin, Katharina Leer, Elisabeth Moek, Franziska Hausig, Johannes C. Brendel, and Anja Traeger. "Tuning of endosomal escape and gene expression by functional groups, molecular weight and transfection medium: a structure–activity relationship study." Journal of Materials Chemistry B 8, no. 23 (2020): 5026–41. http://dx.doi.org/10.1039/d0tb00340a.
Повний текст джерелаCastaneda, C. H., M. J. Scuderi, T. G. Edwards, G. D. Harris Jr., C. M. Dupureur, K. J. Koeller, C. Fisher, and J. K. Bashkin. "Improved antiviral activity of a polyamide against high-risk human papillomavirus via N-terminal guanidinium substitution." MedChemComm 7, no. 11 (2016): 2076–82. http://dx.doi.org/10.1039/c6md00371k.
Повний текст джерелаSalama, Ahmed, Mohamed Hasanin, and Peter Hesemann. "Synthesis and antimicrobial properties of new chitosan derivatives containing guanidinium groups." Carbohydrate Polymers 241 (August 2020): 116363. http://dx.doi.org/10.1016/j.carbpol.2020.116363.
Повний текст джерелаZhu, Xuzhi, Jie Yang, and Kirk S. Schanze. "Conjugated polyelectrolytes with guanidinium side groups. Synthesis, photophysics and pyrophosphate sensing." Photochem. Photobiol. Sci. 13, no. 2 (2014): 293–300. http://dx.doi.org/10.1039/c3pp50288k.
Повний текст джерелаSCHMIDTCHEN, F. P., M. BERGER, A. METZGER, K. GLOE, and H. STEPHAN. "ChemInform Abstract: Foldable Anion Hosts Based on Bicyclic Guanidinium Anchor Groups." ChemInform 28, no. 51 (August 2, 2010): no. http://dx.doi.org/10.1002/chin.199751316.
Повний текст джерелаTanaka, Masato, Hans-Ullrich Siehl, Tillmann Viefhaus, Wolfgang Frey, and Willi Kantlehner. "An ONIOM Study of a Guanidinium Salt Ionic Liquid. Experimental and Computational Characterization of N,N,N`,N`,N``-Pentabutyl-N``-benzylguanidinium Bromide." Zeitschrift für Naturforschung B 64, no. 6 (June 1, 2009): 765–72. http://dx.doi.org/10.1515/znb-2009-0624.
Повний текст джерелаGrogg, Marcel, Donald Hilvert, Albert Beck, and Dieter Seebach. "Syntheses of Cyanophycin Segments for Investigations of Cell-Penetration." Synthesis 51, no. 01 (June 28, 2018): 31–39. http://dx.doi.org/10.1055/s-0037-1610202.
Повний текст джерелаMETZGER, A., W. PESCHKE, and F. P. SCHMIDTCHEN. "ChemInform Abstract: A Convenient Access to Chiral Monofunctionalized Bicyclic Guanidinium Receptor Groups." ChemInform 26, no. 49 (August 17, 2010): no. http://dx.doi.org/10.1002/chin.199549189.
Повний текст джерелаZhou, Zhe, Cansu Ergene, and Edmund F. Palermo. "Guanidinium-Functionalized Photodynamic Antibacterial Oligo(Thiophene)s." MRS Advances 4, no. 59-60 (2019): 3223–31. http://dx.doi.org/10.1557/adv.2019.359.
Повний текст джерелаXue, Boxin, Fen Wang, Jifu Zheng, Shenghai Li, and Suobo Zhang. "Highly stable polysulfone anion exchange membranes incorporated with bulky alkyl substituted guanidinium cations." Molecular Systems Design & Engineering 4, no. 5 (2019): 1039–47. http://dx.doi.org/10.1039/c9me00064j.
Повний текст джерелаHildebrandt, Peter, Roman S. Czernuszewicz, Christine A. Grygon, and Thomas G. Spiro. "Ultraviolet resonance Raman enhancement of the carboxylate and guanidinium groups in amino acids." Journal of Raman Spectroscopy 20, no. 10 (October 1989): 645–50. http://dx.doi.org/10.1002/jrs.1250201003.
Повний текст джерелаSong, Yongbo, Hongyan Zheng, Yulan Niu, Ying Yao, and Rongqian Meng. "Synthesis and Properties of Alkyl Bis-Guanidinium Acetates Surfactants." Tenside Surfactants Detergents 58, no. 2 (March 1, 2021): 127–35. http://dx.doi.org/10.1515/tsd-2019-2241.
Повний текст джерелаKurzmeier, H., and F. P. Schmidtchen. "Abiotic anion receptor functions. A facile and dependable access to chiral guanidinium anchor groups." Journal of Organic Chemistry 55, no. 12 (June 1990): 3749–55. http://dx.doi.org/10.1021/jo00299a013.
Повний текст джерелаChen, Xiaoqiang, Jingyun Wang, Shiguo Sun, Jiangli Fan, Song Wu, Jianfeng Liu, Saijian Ma, Lizhu Zhang, and Xiaojun Peng. "Efficient enhancement of DNA cleavage activity by introducing guanidinium groups into diiron(III) complex." Bioorganic & Medicinal Chemistry Letters 18, no. 1 (January 2008): 109–13. http://dx.doi.org/10.1016/j.bmcl.2007.11.001.
Повний текст джерелаLiu, Fang, Yanhua Wang, and Guo-Yuan Lu. "Bilayer Vesicle Formation in Ethanol from Calix[4]arene Derivative with Two Guanidinium Groups." Chemistry Letters 34, no. 10 (October 2005): 1450–51. http://dx.doi.org/10.1246/cl.2005.1450.
Повний текст джерелаSuresh, J., R. V. Krishnakumar, and S. Natarajan. "L-Argininium trifluoroacetate." Acta Crystallographica Section E Structure Reports Online 62, no. 7 (June 30, 2006): o3127—o3129. http://dx.doi.org/10.1107/s1600536806024743.
Повний текст джерелаSchug, Kevin A., and Wolfgang Lindner. "Noncovalent Binding between Guanidinium and Anionic Groups: Focus on Biological- and Synthetic-Based Arginine/Guanidinium Interactions with Phosph[on]ate and Sulf[on]ate Residues." Chemical Reviews 105, no. 1 (January 2005): 67–114. http://dx.doi.org/10.1021/cr040603j.
Повний текст джерелаWang, Sheng Qin, Mohit Sharma, and Yew Wei Leong. "Polyamide 11/Clay Nanocomposite Using Polyhedral Oligomeric Silsesquioxane Surfactants." Advanced Materials Research 1110 (June 2015): 65–68. http://dx.doi.org/10.4028/www.scientific.net/amr.1110.65.
Повний текст джерелаMORILLAS, Manuel, Martin L. GOBLE, and Richard VIRDEN. "The kinetics of acylation and deacylation of penicillin acylase from Escherichia coli ATCC 11105: evidence for lowered pKa values of groups near the catalytic centre." Biochemical Journal 338, no. 1 (February 8, 1999): 235–39. http://dx.doi.org/10.1042/bj3380235.
Повний текст джерелаGrijalvo, Santiago, Montserrat Terrazas, Anna Aviñó, and Ramón Eritja. "Stepwise synthesis of oligonucleotide–peptide conjugates containing guanidinium and lipophilic groups in their 3′-termini." Bioorganic & Medicinal Chemistry Letters 20, no. 7 (April 2010): 2144–47. http://dx.doi.org/10.1016/j.bmcl.2010.02.049.
Повний текст джерелаAndreyko, Elena A., Joshua B. Puplampu, Patricia A. Ignacio-De Leon, Ilya Zharov, and Ivan I. Stoikov. "p-tert-Butylthiacalix[4]arenes containing guanidinium groups: synthesis and self-assembly into nanoscale aggregates." Supramolecular Chemistry 31, no. 7 (June 16, 2019): 473–83. http://dx.doi.org/10.1080/10610278.2019.1628231.
Повний текст джерелаAït-Haddou, Hassan, Jun Sumaoka, Sheryl L. Wiskur, J. Frantz Folmer-Andersen, and Eric V. Anslyn. "Remarkable Cooperativity between a ZnII Ion and Guanidinium/Ammonium Groups in the Hydrolysis of RNA." Angewandte Chemie International Edition 41, no. 21 (November 4, 2002): 4013–16. http://dx.doi.org/10.1002/1521-3773(20021104)41:21<4013::aid-anie4013>3.0.co;2-y.
Повний текст джерелаVORTMAN, M. YA, V. N. LEMESHKO, L. A. GONCHARENKO, S. M. KOBYLINSKIY, V. V. SHEVCHENKO, and S. N. OSTAPIUK. "OLIGOMERIC GUANIDINE-CONTAINING PROTON CATIONIC IONIC LIQUID." Polymer journal 43, no. 4 (November 26, 2021): 304–10. http://dx.doi.org/10.15407/polymerj.43.04.304.
Повний текст джерелаRoig, Victoria, and Ulysse Asseline. "Oligo-2‘-deoxyribonucleotides Containing Uracil Modified at the 5-Position with Linkers Ending with Guanidinium Groups." Journal of the American Chemical Society 125, no. 15 (April 2003): 4416–17. http://dx.doi.org/10.1021/ja029467v.
Повний текст джерелаPerreault, Denise M., Larry A. Cabell, and Eric V. Anslyn. "Using guanidinium groups for the recognition of RNA and as catalysts for the hydrolysis of RNA." Bioorganic & Medicinal Chemistry 5, no. 6 (June 1997): 1209–20. http://dx.doi.org/10.1016/s0968-0896(97)00051-5.
Повний текст джерелаDeng, Qiliang, Jianhua Wu, Yang Chen, Zhijun Zhang, Yang Wang, Guozhen Fang, Shuo Wang, and Yukui Zhang. "Guanidinium functionalized superparamagnetic silica spheres for selective enrichment of phosphopeptides and intact phosphoproteins from complex mixtures." J. Mater. Chem. B 2, no. 8 (2014): 1048–58. http://dx.doi.org/10.1039/c3tb21540g.
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