Literatura científica selecionada sobre o tema "Caged ligands"
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Artigos de revistas sobre o assunto "Caged ligands"
Tadevosyan, Artavazd, Louis R. Villeneuve, Alain Fournier, David Chatenet, Stanley Nattel e Bruce G. Allen. "Caged ligands to study the role of intracellular GPCRs". Methods 92 (janeiro de 2016): 72–77. http://dx.doi.org/10.1016/j.ymeth.2015.07.005.
Texto completo da fontevan de Graaff, Michel J., Timo Oosenbrug, Mikkel H. S. Marqvorsen, Clarissa R. Nascimento, Mark A. R. de Geus, Bénédicte Manoury, Maaike E. Ressing e Sander I. van Kasteren. "Conditionally Controlling Human TLR2 Activity via Trans-Cyclooctene Caged Ligands". Bioconjugate Chemistry 31, n.º 6 (8 de junho de 2020): 1685–92. http://dx.doi.org/10.1021/acs.bioconjchem.0c00237.
Texto completo da fonteIsa, Masayuki, Shigeyuki Namiki, Daisuke Asanuma e Kenzo Hirose. "Spatiotemporal Control of Receptor Tyrosine Kinase Activity by Caged Ligands". Chemistry Letters 44, n.º 2 (5 de fevereiro de 2015): 150–51. http://dx.doi.org/10.1246/cl.140901.
Texto completo da fonteMayer, Günter, Jens Müller, Timo Mack, Daniel F. Freitag, Thomas Höver, Bernd Pötzsch e Alexander Heckel. "Differential Regulation of Protein Subdomain Activity with Caged Bivalent Ligands". ChemBioChem 10, n.º 4 (2 de fevereiro de 2009): 654–57. http://dx.doi.org/10.1002/cbic.200800814.
Texto completo da fonteSansalone, Lorenzo, Joshua Bratsch-Prince, Sicheng Tang, Burjor Captain, David D. Mott e Françisco M. Raymo. "Photopotentiation of the GABAA receptor with caged diazepam". Proceedings of the National Academy of Sciences 116, n.º 42 (1 de outubro de 2019): 21176–84. http://dx.doi.org/10.1073/pnas.1902383116.
Texto completo da fonteSpecht, Alexandre, Maurice Goeldner, Jakob Wirz e Ling Peng. "Characterization of Caged Cholinergic Ligands; Sulfonated Calix[4]arene Inclusion Complexes". Synlett 1999, Sup. 1 (31 de dezembro de 1999): 981–83. http://dx.doi.org/10.1055/s-1999-3108.
Texto completo da fonteNielson, Alastair J., Chaohong Shen e Joyce M. Waters. "A zirconium zwitterion containing a caged amine H atom". Acta Crystallographica Section C Crystal Structure Communications 59, n.º 11 (31 de outubro de 2003): m494—m496. http://dx.doi.org/10.1107/s0108270103022595.
Texto completo da fonteSTEVENSON, Thirza H., Aldo F. GUTIERREZ, Wendy K. ALDERTON, Lu-yun LIAN e Nigel S. SCRUTTON. "Kinetics of CO binding to the haem domain of murine inducible nitric oxide synthase: differential effects of haem domain ligands". Biochemical Journal 358, n.º 1 (8 de agosto de 2001): 201–8. http://dx.doi.org/10.1042/bj3580201.
Texto completo da fonteMaier, Wolfgang, John E. T. Corrie, George Papageorgiou, Bodo Laube e Christof Grewer. "Comparative analysis of inhibitory effects of caged ligands for the NMDA receptor". Journal of Neuroscience Methods 142, n.º 1 (março de 2005): 1–9. http://dx.doi.org/10.1016/j.jneumeth.2004.07.006.
Texto completo da fonteSlocik, Joseph M., Richard A. Kortes e Rex E. Shepherd. "Developing Carrier Complexes for “Caged NO”: RuCl3(NO)(H2O)2 Complexes of Dipyridylamine, (dpaH), N,N,N'N'-Tetrakis (2-Pyridyl) Adipamide, (tpada), and (2-Pyridylmethyl) Iminodiacetate, (pida2-)". Metal-Based Drugs 7, n.º 2 (1 de janeiro de 2000): 67–75. http://dx.doi.org/10.1155/mbd.2000.67.
Texto completo da fonteTeses / dissertações sobre o assunto "Caged ligands"
Oshige, Eric Stephen. "Photorelease of caged alcohols from artificial metalloenzymes /". Electronic thesis, 2007. http://etd.wfu.edu/theses/available/etd-06102007-193011/.
Texto completo da fonteDiao, Donglin. "Bioinspired complexes engaged within hemicryptophane cage-ligands for O2 activation and C-H bond functionalization in confined space". Electronic Thesis or Diss., Ecole centrale de Marseille, 2022. http://www.theses.fr/2022ECDM0007.
Texto completo da fonteThis thesis aims at developing new hemicryptophane cage-ligands to obtain confined metal-based catalysts for bioinspired O2 activation and C-H bond functionalization in confined space. The design of the targeted cages aims at introducing ligands inspired from metalloproteins active sites, for coordination of biorelevant metals (Cu, Fe, Zn). Importantly, the hemicryptophane structure provide a hydrophobic cavity around the active metal core. This structure aims at stabilizing highly reactive intermediates and reaching different reactivity compare to open model complexes, devoid of cavity. In this context, a major objective of this work was to reach Cu-based bioinspired catalysts able to activate molecular oxygen for challenging C-H bond functionalization. The first part of the thesis consists in a comprehensive literature survey on (i) background of previous applications of hemicryptophane cages and (ii) recent advances in caged bioinspired complexes. The application of our open and caged Cu-complex, based on the tris(pyridyl)amine (TPA) ligand is next described. These catalysts have been used for O2 activation and unusual intramolecular C-H bond functionalization. We then prepare and studied a new TPA-hemicryptophane cage equipped with a C(triazole)-H hydrogen bonding cavity. This functionalized cavity aims at reproducing the binding cavities found in metalloproteins. Finally, hemicryptophane cages based on the triazacyclononane (TACN) ligand have been prepared for the first time. The goal of these cage-ligands is to develop new bioinspired Cu and Fe complexes that could be, for instance, used as O2 activating catalysts
Lee, Ted. "Triggerable ligand presentation using caged-RGD". Diss., Georgia Institute of Technology, 2013. http://hdl.handle.net/1853/52943.
Texto completo da fonteZampese, Jennifer Ann. "Molecular Cages of Controlled Size and Shape". Thesis, University of Canterbury. Chemistry, 2007. http://hdl.handle.net/10092/3370.
Texto completo da fonteHightower, Sean E. "Preparative and computational studies of metal complexes containing molecular cages". Laramie, Wyo. : University of Wyoming, 2007. http://proquest.umi.com/pqdweb?did=1400962461&sid=1&Fmt=2&clientId=18949&RQT=309&VName=PQD.
Texto completo da fonteVersäumer, Marina. "Supramolecular coordination cages based on bispyridyl-ligands with redox properties". Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2016. http://hdl.handle.net/11858/00-1735-0000-002B-7C2F-E.
Texto completo da fonteCherdo, Stéphanie. "Des complexes cage aux nanoparticules, nouveaux catalyseurs pour la production du dihydrogène". Phd thesis, Université Paris Sud - Paris XI, 2013. http://tel.archives-ouvertes.fr/tel-01071035.
Texto completo da fonteLengkeek, Nigel Andrew. "Functional cage-amine complexes : polymerisable metallomonomers and multi-cage complexes". University of Western Australia. School of Biomedical, Biomolecular and Chemical Sciences, 2008. http://theses.library.uwa.edu.au/adt-WU2008.0138.
Texto completo da fonteSañudo, E. Lozano. "Coordination polymers and cages based on phosphine ligands and silver (I)". Thesis, Queen's University Belfast, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.273114.
Texto completo da fonteLaplace, Annabelle. "Complexation et micellisation d'une molécule cage tensioactive". Versailles-St Quentin en Yvelines, 1999. http://www.theses.fr/1999VERS0019.
Texto completo da fonteCapítulos de livros sobre o assunto "Caged ligands"
Peng, Ling, e Maurice Goeldner. "Caged Cholinergic Ligands and Photoregulation of Cholinesterase Activities". In Structure and Function of Cholinesterases and Related Proteins, 253–54. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4899-1540-5_77.
Texto completo da fonteMerlen, Clémence, Louis R. Villeneuve e Bruce G. Allen. "Using Caged Ligands to Study Intracrine Endothelin Signaling in Intact Cardiac Myocytes". In Methods in Molecular Biology, 31–41. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-1755-6_4.
Texto completo da fonteWarmuth, R., B. Gersch, F. Kastenholz, J. M. Lehn, E. Bamberg e E. Grell. "Caged Na+ and K+ ligands: photochemical properties, application for membrane transport studies and selective fluorimetric detection of alkali ions". In The Sodium Pump, 621–24. Heidelberg: Steinkopff, 1994. http://dx.doi.org/10.1007/978-3-642-72511-1_111.
Texto completo da fontePardasani, R. T., e P. Pardasani. "Magnetic properties of dodecanuclear chromium(III) cage with carboxylate ligand". In Magnetic Properties of Paramagnetic Compounds, 1069–70. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49202-4_524.
Texto completo da fonteAnelli, P. L., T. Beringhelli, H. Molinari, F. Montanari e S. Quici. "13C and 1H NMR Characterization of a Na+ClO4 - Complex of a New Lipophilic Cage Ligand". In Advanced Magnetic Resonance Techniques in Systems of High Molecular Complexity, 135–39. Boston, MA: Birkhäuser Boston, 1986. http://dx.doi.org/10.1007/978-1-4615-8521-3_12.
Texto completo da fonteFässler, Thomas F. "Relationships Between Soluble Zintl Anions, Ligand-Stabilized Cage Compounds, and Intermetalloid Clusters of Tetrel (Si–Pb) and Pentel (P–Bi) Elements". In Zintl Ions, 91–131. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/430_2010_33.
Texto completo da fonteGupta, Anita. "Cage Structured Compounds". In Thermoelectric Polymers, 81–98. Materials Research Forum LLC, 2024. http://dx.doi.org/10.21741/9781644903018-5.
Texto completo da fontePeng, Ling, e Maurice Goeldner. "[15] Photoregulation of cholinesterase activities with caged cholinergic ligands". In Methods in Enzymology, 265–78. Elsevier, 1998. http://dx.doi.org/10.1016/s0076-6879(98)91018-7.
Texto completo da fonteHess, George P., e Christof Grewer. "[25] Development and application of caged ligands for neurotransmitter receptors in transient kinetic and neuronal circuit mapping studies". In Methods in Enzymology, 443–73. Elsevier, 1998. http://dx.doi.org/10.1016/s0076-6879(98)91028-x.
Texto completo da fonteHousecroft, Catherine E. "Clusters with metal-metal bonds". In The Heavier d-Block Metals. Oxford University Press, 1999. http://dx.doi.org/10.1093/hesc/9780198501039.003.0007.
Texto completo da fonteTrabalhos de conferências sobre o assunto "Caged ligands"
Sabbatini, Nanda, Massimo Guardigli, Ilse Manet, Raymond Ziessel e Rocco Ungaro. "Lanthanide complexes of cage-type ligands as luminescent labels in fluoroimmunoassays". In Photonics West '95, editado por Joseph R. Lakowicz. SPIE, 1995. http://dx.doi.org/10.1117/12.208524.
Texto completo da fonteCorrêa, Patricia Leal Azevedo. "Sobre o conceito de blank form: uma leitura minimalista de Duchamp". In Encontro da História da Arte. Universidade Estadual de Campinas, 2008. http://dx.doi.org/10.20396/eha.4.2008.3806.
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