Literatura académica sobre el tema "Small Molecular Organic Ligands"
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Artículos de revistas sobre el tema "Small Molecular Organic Ligands"
Nilsson, K. Peter R. "Small organic probes as amyloid specific ligands - Past and recent molecular scaffolds". FEBS Letters 583, n.º 16 (17 de abril de 2009): 2593–99. http://dx.doi.org/10.1016/j.febslet.2009.04.016.
Texto completoPolowin, Joel, Robert Poe y Michael C. Baird. "Extensions of the applicability of the MMX molecular modelling system to determination of barriers to rotation of π-bonded ligands". Canadian Journal of Chemistry 73, n.º 7 (1 de julio de 1995): 1078–83. http://dx.doi.org/10.1139/v95-133.
Texto completoMilanesi, Eva, Paola Costantini, Alberto Gambalunga, Raffaele Colonna, Valeria Petronilli, Anna Cabrelle, Gianpietro Semenzato, Andrea M. Cesura, Emmanuel Pinard y Paolo Bernardi. "The Mitochondrial Effects of Small Organic Ligands of BCL-2". Journal of Biological Chemistry 281, n.º 15 (14 de febrero de 2006): 10066–72. http://dx.doi.org/10.1074/jbc.m513708200.
Texto completoNorel, R., H. J. Wolfson y R. Nussinov. "Small Molecule Recognition: Solid Angles Surface Representation and Molecular Shape Complementarity". Combinatorial Chemistry & High Throughput Screening 2, n.º 4 (agosto de 1999): 223–36. http://dx.doi.org/10.2174/1386207302666220204193837.
Texto completoPeterson, Leif. "Small Molecule Docking of DNA Repair Proteins Associated with Cancer Survival Following PCNA Metagene Adjustment: A Potential Novel Class of Repair Inhibitors". Molecules 24, n.º 3 (12 de febrero de 2019): 645. http://dx.doi.org/10.3390/molecules24030645.
Texto completoSchwarz, Benjamin y Carsten Streb. "Architectural control of urea in supramolecular 1D strontium vanadium oxide chains". Dalton Transactions 44, n.º 9 (2015): 4195–99. http://dx.doi.org/10.1039/c4dt03691c.
Texto completoTatikonda, Rajendhraprasad, Evgeny Bulatov, Zülal Özdemir, Nonappa Nonappa y Matti Haukka. "Infinite coordination polymer networks: metallogelation of aminopyridine conjugates and in situ silver nanoparticle formation". Soft Matter 15, n.º 3 (2019): 442–51. http://dx.doi.org/10.1039/c8sm02006j.
Texto completoCho, Yeon-Jin, Sun-Hye Choi, Rami Lee, Hongik Hwang, Hyewhon Rhim, Ik-Hyun Cho, Hyoung-Chun Kim, Jeong-Ik Lee, Sung-Hee Hwang y Seung-Yeol Nah. "Ginseng Gintonin Contains Ligands for GPR40 and GPR55". Molecules 25, n.º 5 (2 de marzo de 2020): 1102. http://dx.doi.org/10.3390/molecules25051102.
Texto completoComess, Kenneth M., Mark E. Schurdak, Martin J. Voorbach, Michael Coen, Jonathan D. Trumbull, Houjun Yang, Lan Gao et al. "An Ultraefficient Affinity-Based High-Throughout Screening Process: Application to Bacterial Cell Wall Biosynthesis Enzyme MurF". Journal of Biomolecular Screening 11, n.º 7 (14 de septiembre de 2006): 743–54. http://dx.doi.org/10.1177/1087057106289971.
Texto completoShahroz, Mir Mohammad, Hemant Kumar Sharma, Abdulmalik S. A. Altamimi, Mubarak A. Alamri, Abuzer Ali, Amena Ali, Safar Alqahtani et al. "Novel and Potential Small Molecule Scaffolds as DYRK1A Inhibitors by Integrated Molecular Docking-Based Virtual Screening and Dynamics Simulation Study". Molecules 27, n.º 4 (9 de febrero de 2022): 1159. http://dx.doi.org/10.3390/molecules27041159.
Texto completoTesis sobre el tema "Small Molecular Organic Ligands"
Charmant, Jonathan Paul Henry. "Reactivity of the #mu#3-benzyne ligand towards small organic molecules". Thesis, University of Bristol, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.238905.
Texto completoSoules, Régis. "Proprietes cooperatives de complexes polymetalliques des ligands squarate et thiosquarate". Toulouse 3, 1987. http://www.theses.fr/1987TOU30178.
Texto completoAshoka, Sahadevan Suchithra. "Anilate-based molecular building blocks for metal-organic frameworks and molecular conductors Conducting Anilate-Based Mixed-Valence Fe(II)Fe(III) Coordination Polymer: Small-Polaron Hopping Model for Oxalate-Type Fe(II)Fe(III) 2D Networks Nanosheets of Two-Dimensional Neutral Coordination Polymers Based on Near-Infrared-Emitting Lanthanides and a Chlorocyananilate Ligand". Thesis, Angers, 2019. http://bu.univ-angers.fr/Contact.
Texto completoThis work reports on the design, synthesis and characterization of novel anilate-based functional molecular materials showing luminescent, magnetic and/or conducting properties. The family of anilate ligands comprises several derivatives obtained by introducing various substituents (H, F, Cl, Br, I, CN, etc.) at the 3 and 6 positions of the common 2,5-dihydroxy-1,4-benzoquinone framework. Among the anilate ligands, the only known heterosubstituted anilate with Cl/CN substituents at the 3,6 positions, ClCNAn2-, have been selected for preparing a novel family of 2D layered coordination polymers (2D CP) with both 3d metal ions and 4f lanthanide ions, through a general and straightforward synthetic strategy. i) Mixed-valence FeIIFeIII 2D CP, formulated as [TAG][FeIIFeIII(ClCNAn)3], containing, the tris(amino)-guanidinium (TAG) cation for the first time in such 2D networks has been synthesized and thoroughly characterized. ii) 2D CPs based on NIR-emitting lanthanides (YbIII, NdIII, ErIII) and the ClCNAn2- ligand, have been prepared and characterized. These layered compounds were exfoliated to nanosheets, by sonication-assisted solution synthesis. Time-resolved photoluminescence studies performed on both the bulk and nanosheets are also highlighted. iii) Novel family of heteroleptic 2D CPs based on NIR-emitting lanthanides and mixed ligands (ClCNAn2- and carboxylate ligands (DOBDC and F4-BDC)), were prepared and characterized. vi) Novel family of 2D CPs based on DyIII and ClCNAn2- were prepared in order to investigate their magnetic properties. v) Furthermore, the ability of anilate ligands to work as components of BEDT-TTF- based molecular conductors have been demonstrated through the synthesis, via electrocrystallization technique. vi) П-d hybrid multifunctional paramagnetic molecular conductors BEDT-TTF and [Fe(ClCNAn)3]3-) were also studied
Hui, Yu 1977. "Heterjunctions of small molecular weight organic semiconductors". Thesis, McGill University, 2004. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=81540.
Texto completoCIARAMELLI, CARLOTTA. "Synthesis and characterization of new small-molecule ligands of LPS binding proteins". Doctoral thesis, Università degli Studi di Milano-Bicocca, 2015. http://hdl.handle.net/10281/77016.
Texto completoThe purpose of this work is the design, synthesis and characterization of new small molecules, active as ligands of two different lipopolysaccharide (LPS)-binding proteins. LPS, or bacterial endotoxin, is an amphiphilic macromolecule ubiquitous on the outer membrane of Gram-negative bacteria. The LPS binding proteins studied during this thesis project belong to two classes: the bacterial proteins of the Lpt transport machinery and the mammalian TLR4 receptor system, including the co-receptors LBP, CD14, MD-2. Lpt proteins, and in particular the protein LptC, are responsible for the export mechanism of LPS to the cell surface of Gram negative bacteria, which is a fundamental step of the LPS biosynthetic pathway. Therefore, the LPS biogenesis represents an ideal target for development of novel antibiotics against Gram-negative bacteria. Moreover, the structures of Lpt proteins have been elucidated, but very little is known about the mechanism of LPS transport. In this thesis work different techniques were used to study the interaction between LPS and LptC, particularly NMR binding studies. Moreover, a new fluorescent LPS was produced and it was used as a tool to perform LPS-LptC interaction studies with fluorescence techniques. Some new synthetic molecules were also developed during this thesis. Glycolipidic small molecules were designed and synthesized in order to obtain LptC ligands and, in perspective, potential antibiotics against Gram-negative bacteria. Toll-like receptor 4 (TLR4), the innate immunity receptor, recognizes LPS, helped by other proteins (LBP, CD14 and MD-2), and it is responsible for the induction of inflammatory responses. Synthetic small molecules able to modulate innate immunity receptors activity are a powerful mean to study the TLR4 receptor system and have great pharmacological interest as vaccine adjuvants (agonists), antisepsis and anti-inflammatory agents (antagonists). Antagonist activity on TLR4 receptor system of amino glycolipids (IAXO-102) was clearly demonstrated by our research group. The synthesis of molecules derived from IAXO-102 which retain the biological activity of the precursor was a target of this work. In particular, the synthesis of fluorescent probes, used for binding studies, zwitterionic derivatives and dimeric molecules were performed. Anionic TLR4 antagonists with a chemical structure more similar to Lipid A were also obtained in our labs. The aim of this work was the evaluation via NMR binding experiments of their ability to bind the innate immunity co-receptor MD-2. The amphiphilic character of the synthetic lipid A analogues synthesized so far is often associated with low water solubility and poor bioavailability. In this respect, the natural TLR4-active compounds have better solubility and bioavailability. The chemical modification of these structures is very helpful to modulate their biological activity and to enhance target specificity. Consequently, in a later stage of this work, the synthesis of new small molecules with chemical structures inspired to natural TLR4 modulators was pursued. Very recently it was found that some phenolic compounds from olive oil extracts presented a good activity as TLR4 antagonists. The synthesis of some analogues of these molecules was performed to obtain new potential TLR4 antagonists with better water solubility and reduced toxicity.
Rooney, Timothy Patrick Christopher. "Development of small molecule inhibitors of the bromodomain-histone interaction". Thesis, University of Oxford, 2014. http://ora.ox.ac.uk/objects/uuid:dfe22076-befc-4881-8433-b563a9329478.
Texto completoKueh, Alona Swee Hua. "Molecular imprinting of small, poorly functionalised organic compounds". The University of Waikato, 2008. http://hdl.handle.net/10289/2264.
Texto completoCamuñas, i. Soler Joan. "Force-spectroscopy of small ligands binding to nucleic acids". Doctoral thesis, Universitat de Barcelona, 2015. http://hdl.handle.net/10803/286597.
Texto completoLes tècniques de molècula individual permeten seguir les reaccions biomoleculars amb una resolució sense precedents, proveint als científics d’una sèrie d’instruments per a mesurar magnituds físiques i investigar sistemes experimentals difícilment accessibles amb les tradicionals mesures en volum (és a dir a on les mesures es realitzen amb mols de reactiu). Particularment, les pinces òptiques permeten manipular i aplicar forces a molècules individuals i determinar-ne així les seves propietats elàstiques i termodinàmiques. L’atrapament òptic es basa en l’ús d’un feix làser focalitzat per exercir una força òptica a les microesferes (diàmetre ~ 3 µm), que queden confinades a prop del punt focal a causa de la conservació del moment lineal. Els experiments de micromanipulació es realitzen unint els extrems de la molècula que es vol estudiar a la superfícies de dues microesferes diferents, podent així aplicar forces a la molècula quan desplacem una microesfera respecte de l’altra. Per ancorar les molècules a la superfície de les microesferes s’utilitzen unions moleculars que tenen una alta a.nitat (p.ex. enllaç biotina-estreptavidina). Típicament els experiments amb pinces òptiques consisteixen en la micromanipulació d’àcids nucleics (ADN, ARN) o proteïnes de forma individual. Per exemple, una molècula d’ADN pot ésser estirada per a estudiar-ne les propietats elàstiques, o oberta mecànicament (separant les dues cadenes que formen la doble hèlix) per a mesurar les energies lliures d’aparellament entre bases. Un gran nombre d’agents anticancerígens tenen com a diana els àcids nucleics, a on s’hi uneixen afi i efecte de dur a terme la seva acció citotòxica (p. ex. interferint amb processos cel·lulars essencials com són la replicació, la transcripció o els mecanismes de reparació). Per entendre el seu mecanisme d’acció és important conéixer en quines posicions, amb quina a.nitat, i amb quina cinètica s’uneixen a diferents seqüències d’ADN. Els experiments de molècula individual amb pinces òptiques permeten determinar la termodinàmica i cinètica d’unió de molts d’aquests lligands, especialment aquells difícils de caracteritzar mitjançant mesures en volum. És per això que un dels objectius principals d’aquesta tesi ha estat aprofitar les potencialitats de les mesures de molècula individual per a caracteritzar pèptids anticancerígens poc solubles i difícils d’estudiar amb tècniques alternatives: des de la cinètica i termodinàmica d’unió, a l’especi.citat en seqüència i la cinètica d’autoacoblament.
Savard, Didier. "The Versatile Chemistry of Aryl Substituted 1,2,4-triazole Ligands in Molecular Magnetism". Thesis, University of Ottawa (Canada), 2010. http://hdl.handle.net/10393/28677.
Texto completoHassan, Mohammad Rokib y University of Lethbridge Faculty of Arts and Science. "Self-assembled molecular rods and squares with chalcogenadiazole framework ligands". Thesis, Lethbridge, Alta. : University of Lethbridge, Dept. of Chemistry and Biochemistry, c2010, 2010. http://hdl.handle.net/10133/2639.
Texto completoxvii, 152 leaves : ill. (some col.) ; 29 cm
Libros sobre el tema "Small Molecular Organic Ligands"
Keiller, B. T. The vibrational spectra of metal cluster compounds containing small organic ligands. Norwich: University of East Anglia, 1988.
Buscar texto completoJulius, Rebek. Hydrogen-bonded capsules: Molecular behavior in small spaces. Hackensack, NJ: World Scientific, 2015.
Buscar texto completoM, Villalgordo José, ed. Solid-supported combinatorial and parallel synthesis of small-molecular-weight compound libraries. [New York]: Pergamon, 1998.
Buscar texto completoNino, Russo, Salahub Dennis R. 1946-, Witko Malgorzata y North Atlantic Treaty Organization. Scientific Affairs Division., eds. Metal-ligand interactions: Molecular-, nano-, micro-, and macro-systems in complex environments. Dordrecht: Kluwer Academic Publishers, 2003.
Buscar texto completoJr, Rebek Julius. Hydrogen-Bonded Capsules: Molecular Behavior in Small Spaces. World Scientific Publishing Co Pte Ltd, 2015.
Buscar texto completoObrecht, D. y J. M. Villalgordo. Solid-Supported Combinatorial and Parallel Synthesis of Small-Molecular-Weight Compound Libraries. Elsevier Science & Technology Books, 1998.
Buscar texto completoObrecht, D. y J. M. Villalgordo. Solid-Supported Combinatorial and Parallel Synthesis of Small-Molecular-Weight Compound Libraries. Elsevier Science & Technology Books, 1998.
Buscar texto completoTavassoli, Ali. Inhibitors of Protein-Protein Interactions: Small Molecules, Cyclic Peptides, Macrocycles and Antibodies. Royal Society of Chemistry, The, 2020.
Buscar texto completoTavassoli, Ali. Inhibitors of Protein-Protein Interactions: Small Molecules, Cyclic Peptides, Macrocycles and Antibodies. Royal Society of Chemistry, The, 2020.
Buscar texto completo(Editor), N. Russo, Dennis R. Salahub (Editor) y Malgorzata Witko (Editor), eds. Metal-Ligand Interactions Molecular-, Nano-, Micro-systems in Complex Environments (NATO Science Series II: Mathematics, Physics and Chemistry). Springer, 2003.
Buscar texto completoCapítulos de libros sobre el tema "Small Molecular Organic Ligands"
Rehder, Dieter. "Polyoxovanadates with Organic Ligands". En Topics in Molecular Organization and Engineering, 157–66. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-0920-8_11.
Texto completoDickinson, Helena, Melanie Lukasser, Günter Mayer y Alexander Hüttenhofer. "Cell-SELEX: In Vitro Selection of Synthetic Small Specific Ligands". En Methods in Molecular Biology, 213–24. New York, NY: Springer New York, 2015. http://dx.doi.org/10.1007/978-1-4939-2547-6_20.
Texto completoChhajed, Santosh S., Sandeep S. Sonanwane, Harshala Chaudhari y Aarti Sonar. "Drug Interactions: Highlights of Adverse Effects of Low Molecular Weight Ligands". En Biologically Active Small Molecules, 333–48. New York: Apple Academic Press, 2022. http://dx.doi.org/10.1201/9781003283119-18.
Texto completoPuschnig, Peter, Georg Koller, Claudia Draxl y Michael G. Ramsey. "The Structure of Molecular Orbitals Investigated by Angle-Resolved Photoemission". En Small Organic Molecules on Surfaces, 3–23. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-33848-9_1.
Texto completoPozharski, Edwin, Marc C. Deller y Bernhard Rupp. "Validation of Protein–Ligand Crystal Structure Models: Small Molecule and Peptide Ligands". En Methods in Molecular Biology, 611–25. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7000-1_25.
Texto completoChhajed, Santosh S. y Parag A. Pathade. "High-Throughput Screening Technique: Role in the Drug Discovery of Low Molecular Weight Ligands". En Biologically Active Small Molecules, 259–71. New York: Apple Academic Press, 2022. http://dx.doi.org/10.1201/9781003283119-14.
Texto completoLathan, W. A., L. A. Curtiss, W. J. Hehre, J. B. Lisle y J. A. Pople. "Molecular Orbital Structures for Small Organic Molecules and Cations". En Progress in Physical Organic Chemistry, 175–261. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470171905.ch3.
Texto completoDay, Christopher J. y Victoria Korolik. "Identification of Specific Ligands for Sensory Receptors by Small-Molecule Ligand Arrays and Surface Plasmon Resonance". En Methods in Molecular Biology, 303–17. New York, NY: Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-7577-8_24.
Texto completoTayeb-Fligelman, Einav y Meytal Landau. "X-Ray Structural Study of Amyloid-Like Fibrils of Tau Peptides Bound to Small-Molecule Ligands". En Methods in Molecular Biology, 89–100. New York, NY: Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-6598-4_5.
Texto completoHoffer, Laurent, Philippe Roche y Xavier Morelli. "Rational Design of PDZ Domain Inhibitors: Discovery of Small Organic Compounds Targeting PDZ Domains". En Methods in Molecular Biology, 277–89. New York, NY: Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1166-1_16.
Texto completoActas de conferencias sobre el tema "Small Molecular Organic Ligands"
Nicolau, Ioana, Alexandra Bumbacaru, Codruta Badescu Singureanu, Niculina Hadade y Mihaela Matache. "Design and synthesis of multidentate organic ligands for protein-based supra molecular constructs". En RAD Conference. RAD Centre, 2023. http://dx.doi.org/10.21175/rad.abstr.book.2023.2.7.
Texto completoBorota, Ana, Simona Funar-Timofei y Luminita Crisan. "MOLECULAR DOCKING STUDY OF THE INTERACTIONS OF PROSTANOID EP4 RECEPTOR WITH POTENT LIGANDS". En The 21st International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2017. http://dx.doi.org/10.3390/ecsoc-21-04747.
Texto completoLee, Yi-Ting, Yung-Ting Chang, Chin-Ti Chen y Chao-Tsen Chen. "Solution processable small molecular host materials for blue and white phosphorescence OLEDs". En SPIE Organic Photonics + Electronics, editado por Franky So y Chihaya Adachi. SPIE, 2013. http://dx.doi.org/10.1117/12.2021451.
Texto completoFleetham, Tyler, Barry O'Brien, John P. Mudrick, Jiangeng Xue y Jian Li. "Efficiency enhancement in small molecular organic photovoltaic devices employing dual anode interfacial layers". En SPIE Organic Photonics + Electronics, editado por Zakya H. Kafafi y Paul A. Lane. SPIE, 2013. http://dx.doi.org/10.1117/12.2023679.
Texto completoIslam, Mohammad K., David E. Thurston y Khondaker M. Rahman. "Abstract B204: Targeting key DNA/RNA heteroduplex of telomerase by small-molecule ligands." En Abstracts: AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics--Oct 19-23, 2013; Boston, MA. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1535-7163.targ-13-b204.
Texto completoSavvate'ev, Vadim, J. H. Friedl, L. Zou, K. Christensen, W. Oldham, Lewis J. Rothberg, Zoe Chen-Esterlit, Raoul Kopelman y Joseph Shinar. "Transient electroluminescence from multilayer small organic molecular light-emitting devices". En International Symposium on Optical Science and Technology, editado por Zakya H. Kafafi. SPIE, 2001. http://dx.doi.org/10.1117/12.416898.
Texto completoZhang, Xuan, Wenge Guo, Ming Li, Wentao Ma y Sen Meng. "Advances in simulation study on organic small molecular solar cells". En The International Conference on Photonics and Optical Engineering and the Annual West China Photonics Conference (icPOE 2014), editado por Ailing Tian, Anand Asundi, Weiguo Liu y Chunmin Zhang. SPIE, 2015. http://dx.doi.org/10.1117/12.2075692.
Texto completoShim, Hyun-Sub, Hyo Jung Kim, Ji Whan Kim, Sei-Yong Kim, Won-Ik Jeong, Tae-Min Kim y Jang-Joo Kim. "Enhanced sensitivity to near-infrared with high fill factor in small molecular organic solar cells". En SPIE Organic Photonics + Electronics, editado por Zakya H. Kafafi, Christoph J. Brabec y Paul A. Lane. SPIE, 2012. http://dx.doi.org/10.1117/12.930244.
Texto completoTsang, Sai Wing. "Exciton binding energy and dielectric effect in small molecular and polymeric photovoltaic materials (Conference Presentation)". En Organic, Hybrid, and Perovskite Photovoltaics XX, editado por Kwanghee Lee, Zakya H. Kafafi, Paul A. Lane y Ana Flávia Nogueira. SPIE, 2019. http://dx.doi.org/10.1117/12.2528570.
Texto completoDatta, Supriyo, Weidong Tian y Clifford P. Kubiak. "”Resistance” of a molecular wire". En Chemistry and Physics of Small-Scale Structures. Washington, D.C.: Optica Publishing Group, 1997. http://dx.doi.org/10.1364/cps.1997.ctub.2.
Texto completoInformes sobre el tema "Small Molecular Organic Ligands"
Cheon, Kwang-Ohk. The Electric and Optical Properties of Doped Small Molecular Organic Light-Emitting Devices. Office of Scientific and Technical Information (OSTI), enero de 2003. http://dx.doi.org/10.2172/816444.
Texto completoBanin, Amos, Joseph Stucki y Joel Kostka. Redox Processes in Soils Irrigated with Reclaimed Sewage Effluents: Field Cycles and Basic Mechanism. United States Department of Agriculture, julio de 2004. http://dx.doi.org/10.32747/2004.7695870.bard.
Texto completoAltstein, Miriam y Ronald J. Nachman. Rational Design of Insect Control Agent Prototypes Based on Pyrokinin/PBAN Neuropeptide Antagonists. United States Department of Agriculture, agosto de 2013. http://dx.doi.org/10.32747/2013.7593398.bard.
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