Статті в журналах з теми "Caged ligands"
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Tadevosyan, Artavazd, Louis R. Villeneuve, Alain Fournier, David Chatenet, Stanley Nattel, and Bruce G. Allen. "Caged ligands to study the role of intracellular GPCRs." Methods 92 (January 2016): 72–77. http://dx.doi.org/10.1016/j.ymeth.2015.07.005.
Повний текст джерелаvan de Graaff, Michel J., Timo Oosenbrug, Mikkel H. S. Marqvorsen, Clarissa R. Nascimento, Mark A. R. de Geus, Bénédicte Manoury, Maaike E. Ressing, and Sander I. van Kasteren. "Conditionally Controlling Human TLR2 Activity via Trans-Cyclooctene Caged Ligands." Bioconjugate Chemistry 31, no. 6 (June 8, 2020): 1685–92. http://dx.doi.org/10.1021/acs.bioconjchem.0c00237.
Повний текст джерелаIsa, Masayuki, Shigeyuki Namiki, Daisuke Asanuma, and Kenzo Hirose. "Spatiotemporal Control of Receptor Tyrosine Kinase Activity by Caged Ligands." Chemistry Letters 44, no. 2 (February 5, 2015): 150–51. http://dx.doi.org/10.1246/cl.140901.
Повний текст джерелаMayer, Günter, Jens Müller, Timo Mack, Daniel F. Freitag, Thomas Höver, Bernd Pötzsch, and Alexander Heckel. "Differential Regulation of Protein Subdomain Activity with Caged Bivalent Ligands." ChemBioChem 10, no. 4 (February 2, 2009): 654–57. http://dx.doi.org/10.1002/cbic.200800814.
Повний текст джерелаSansalone, Lorenzo, Joshua Bratsch-Prince, Sicheng Tang, Burjor Captain, David D. Mott, and Françisco M. Raymo. "Photopotentiation of the GABAA receptor with caged diazepam." Proceedings of the National Academy of Sciences 116, no. 42 (October 1, 2019): 21176–84. http://dx.doi.org/10.1073/pnas.1902383116.
Повний текст джерелаSpecht, Alexandre, Maurice Goeldner, Jakob Wirz, and Ling Peng. "Characterization of Caged Cholinergic Ligands; Sulfonated Calix[4]arene Inclusion Complexes." Synlett 1999, Sup. 1 (December 31, 1999): 981–83. http://dx.doi.org/10.1055/s-1999-3108.
Повний текст джерелаNielson, Alastair J., Chaohong Shen, and Joyce M. Waters. "A zirconium zwitterion containing a caged amine H atom." Acta Crystallographica Section C Crystal Structure Communications 59, no. 11 (October 31, 2003): m494—m496. http://dx.doi.org/10.1107/s0108270103022595.
Повний текст джерелаSTEVENSON, Thirza H., Aldo F. GUTIERREZ, Wendy K. ALDERTON, Lu-yun LIAN, and 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, no. 1 (August 8, 2001): 201–8. http://dx.doi.org/10.1042/bj3580201.
Повний текст джерелаMaier, Wolfgang, John E. T. Corrie, George Papageorgiou, Bodo Laube, and Christof Grewer. "Comparative analysis of inhibitory effects of caged ligands for the NMDA receptor." Journal of Neuroscience Methods 142, no. 1 (March 2005): 1–9. http://dx.doi.org/10.1016/j.jneumeth.2004.07.006.
Повний текст джерелаSlocik, Joseph M., Richard A. Kortes, and 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, no. 2 (January 1, 2000): 67–75. http://dx.doi.org/10.1155/mbd.2000.67.
Повний текст джерелаSainlos, Matthieu, Wendy S. Iskenderian-Epps, Nelson B. Olivier, Daniel Choquet, and Barbara Imperiali. "Caged Mono- and Divalent Ligands for Light-Assisted Disruption of PDZ Domain-Mediated Interactions." Journal of the American Chemical Society 135, no. 12 (March 13, 2013): 4580–83. http://dx.doi.org/10.1021/ja309870q.
Повний текст джерелаZhao, Jun, Tony D. Gover, Sukumaran Muralidharan, Darryl A. Auston, Daniel Weinreich, and Joseph P. Y. Kao. "Caged Vanilloid Ligands for Activation of TRPV1 Receptors by 1- and 2-Photon Excitation†." Biochemistry 45, no. 15 (April 2006): 4915–26. http://dx.doi.org/10.1021/bi052082f.
Повний текст джерелаBoer, Stephanie A., Winnie Cao, Bianca K. Glascott, and David R. Turner. "Towards a Generalized Synthetic Strategy for Variable Sized Enantiopure M4L4 Helicates." Chemistry 2, no. 3 (June 28, 2020): 613–25. http://dx.doi.org/10.3390/chemistry2030038.
Повний текст джерелаCheng, Weiyan, Shasha Li, Siyuan Han, Ruoyang Miao, Suhua Wang, Chunxia Liu, Han Wei, Xin Tian, and Xiaojian Zhang. "Design, synthesis and biological evaluation of the tumor hypoxia-activated PROTACs bearing caged CRBN E3 ligase ligands." Bioorganic & Medicinal Chemistry 82 (March 2023): 117237. http://dx.doi.org/10.1016/j.bmc.2023.117237.
Повний текст джерелаJackson, Garrett D., Max B. Tipping, Christopher G. P. Taylor, Jerico R. Piper, Callum Pritchard, Cristina Mozaceanu, and Michael D. Ward. "A Family of Externally-Functionalised Coordination Cages." Chemistry 3, no. 4 (October 14, 2021): 1203–14. http://dx.doi.org/10.3390/chemistry3040088.
Повний текст джерелаPichugin, Alexander, Lindsey Ehrler, Sharvan Sehrawat, Theresa Funk, Cate Speake, Patrick Duffy, Hidde Ploegh, and Urszula Krzych. "Identification of Plasmodium berghei novel liver stage CD8 T cell epitopes by caged MHC class I tetramer technology (43.30)." Journal of Immunology 188, no. 1_Supplement (May 1, 2012): 43.30. http://dx.doi.org/10.4049/jimmunol.188.supp.43.30.
Повний текст джерелаReyzer, Michelle L., Jennifer S. Brodbelt, Alan P. Marchand, Zhibing Chen, Zilin Huang, and I. N. N. Namboothiri. "Determination of alkali metal binding selectivities of caged crown ligands by electrospray ionization quadrupole ion trap mass spectrometry." International Journal of Mass Spectrometry 204, no. 1-3 (February 2001): 133–42. http://dx.doi.org/10.1016/s1387-3806(00)00332-8.
Повний текст джерелаPetit, Morgane, Guillaume Bort, Bich-Thuy Doan, Cécile Sicard, David Ogden, Daniel Scherman, Clotilde Ferroud, and Peter I. Dalko. "X-ray Photolysis To Release Ligands from Caged Reagents by an Intramolecular Antenna Sensitive to Magnetic Resonance Imaging." Angewandte Chemie International Edition 50, no. 41 (July 21, 2011): 9708–11. http://dx.doi.org/10.1002/anie.201102948.
Повний текст джерелаPetit, Morgane, Guillaume Bort, Bich-Thuy Doan, Cécile Sicard, David Ogden, Daniel Scherman, Clotilde Ferroud, and Peter I. Dalko. "X-ray Photolysis To Release Ligands from Caged Reagents by an Intramolecular Antenna Sensitive to Magnetic Resonance Imaging." Angewandte Chemie 123, no. 41 (July 21, 2011): 9882–85. http://dx.doi.org/10.1002/ange.201102948.
Повний текст джерелаBlair, Sheryl M., Jennifer S. Brodbelt, Alan P. Marchand, Kaipenchery A. Kumar, and Hyun-Soon Chong. "Evaluation of Binding Selectivities of Caged Crown Ligands toward Heavy Metals by Electrospray Ionization/Quadrupole Ion Trap Mass Spectrometry." Analytical Chemistry 72, no. 11 (June 2000): 2433–45. http://dx.doi.org/10.1021/ac991125t.
Повний текст джерелаFinazzi, Ilaria, Ioannis Bratsos, Teresa Gianferrara, Alberta Bergamo, Nicola Demitri, Gabriele Balducci, and Enzo Alessio. "Photolabile RuIIHalf-Sandwich Complexes Suitable for Developing “Caged” Compounds: Chemical Investigation and Unexpected Dinuclear Species with Bridging Diamine Ligands." European Journal of Inorganic Chemistry 2013, no. 27 (August 2, 2013): 4743–53. http://dx.doi.org/10.1002/ejic.201300792.
Повний текст джерелаBlair, Sheryl M., Jennifer S. Brodbelt, Alan P. Marchand, Hyun-Soon Chong, and Sulejman Alihodžić. "Evaluation of alkali metal binding selectivities of caged aza-crown ether ligands by microelectrospray ionization/quadrupole ion trap mass spectrometry." Journal of the American Society for Mass Spectrometry 11, no. 10 (October 2000): 884–91. http://dx.doi.org/10.1016/s1044-0305(00)00166-5.
Повний текст джерелаYang, Yang, Yanfang Yang, Xiangyang Xie, Xingshi Cai, and Xingguo Mei. "Synergistic targeted delivery of payload into cancer cells using liposomes co-modified with photolabile-caged cell-penetrating peptides and targeting ligands." Journal of Controlled Release 213 (September 2015): e128. http://dx.doi.org/10.1016/j.jconrel.2015.05.216.
Повний текст джерелаNamanga, Jude E., Niels Gerlitzki, Volodymyr Smetana, and Anja-Verena Mudring. "Supramolecularly Caged Green-Emitting Ionic Ir(III)-Based Complex with Fluorinated C^N Ligands and Its Application in Light-Emitting Electrochemical Cells." ACS Applied Materials & Interfaces 10, no. 13 (November 30, 2017): 11026–36. http://dx.doi.org/10.1021/acsami.7b18159.
Повний текст джерелаLuo, Y., R. Cooke, and E. Pate. "A model of stress relaxation in cross-bridge systems: effect of a series elastic element." American Journal of Physiology-Cell Physiology 265, no. 1 (July 1, 1993): C279—C288. http://dx.doi.org/10.1152/ajpcell.1993.265.1.c279.
Повний текст джерелаPetit, Morgane, Guillaume Bort, Bich-Thuy Doan, Cécile Sicard, David Ogden, Daniel Scherman, Clotilde Ferroud, and Peter I. Dalko. "Innentitelbild: X-ray Photolysis To Release Ligands from Caged Reagents by an Intramolecular Antenna Sensitive to Magnetic Resonance Imaging (Angew. Chem. 41/2011)." Angewandte Chemie 123, no. 41 (August 30, 2011): 9682. http://dx.doi.org/10.1002/ange.201105350.
Повний текст джерелаPetit, Morgane, Guillaume Bort, Bich-Thuy Doan, Cécile Sicard, David Ogden, Daniel Scherman, Clotilde Ferroud, and Peter I. Dalko. "Inside Cover: X-ray Photolysis To Release Ligands from Caged Reagents by an Intramolecular Antenna Sensitive to Magnetic Resonance Imaging (Angew. Chem. Int. Ed. 41/2011)." Angewandte Chemie International Edition 50, no. 41 (August 30, 2011): 9510. http://dx.doi.org/10.1002/anie.201105350.
Повний текст джерелаRosair, Georgina M., Greig Scott та Alan J. Welch. "The exopolyhedral ligand orientation (ELO) in 3-(nitrato-κO)-3,3-bis(triphenylphosphane-κP)-3-rhoda-1,2-dicarba-closo-dodecaborane(11) dichloromethane 2.2-solvate". Acta Crystallographica Section C Structural Chemistry 71, № 6 (13 травня 2015): 461–64. http://dx.doi.org/10.1107/s2053229615008724.
Повний текст джерелаFrank, Marina, Lennard Krause, Regine Herbst-Irmer, Dietmar Stalke, and Guido H. Clever. "Narcissistic self-sorting vs. statistic ligand shuffling within a series of phenothiazine-based coordination cages." Dalton Trans. 43, no. 11 (2014): 4587–92. http://dx.doi.org/10.1039/c3dt53243g.
Повний текст джерелаAstakhov, Grigorii, Mikhail Levitsky, Alexander Korlyukov, Lidia Shul’pina, Elena Shubina, Nikolay Ikonnikov, Anna Vologzhanina, et al. "New Cu4Na4- and Cu5-Based Phenylsilsesquioxanes. Synthesis via Complexation with 1,10-Phenanthroline, Structures and High Catalytic Activity in Alkane Oxidations with Peroxides in Acetonitrile." Catalysts 9, no. 9 (August 21, 2019): 701. http://dx.doi.org/10.3390/catal9090701.
Повний текст джерелаMejuto, Carmen, Gregorio Guisado-Barrios, Dmitry Gusev, and Eduardo Peris. "First homoleptic MIC and heteroleptic NHC–MIC coordination cages from 1,3,5-triphenylbenzene-bridged tris-MIC and tris-NHC ligands." Chemical Communications 51, no. 73 (2015): 13914–17. http://dx.doi.org/10.1039/c5cc05114b.
Повний текст джерелаPozzi, Cecilia, Flavio Di Pisa, Daniela Lalli, Camilla Rosa, Elizabeth Theil, Paola Turano, and Stefano Mangani. "Time-lapse anomalous X-ray diffraction shows how Fe2+substrate ions move through ferritin protein nanocages to oxidoreductase sites." Acta Crystallographica Section D Biological Crystallography 71, no. 4 (March 27, 2015): 941–53. http://dx.doi.org/10.1107/s1399004715002333.
Повний текст джерелаHailu, Solomon Legese, Balachandran Unni Nair, Mesfin Redi-Abshiro, Rathinam Aravindhan, Isabel Diaz, and Merid Tessema. "Experimental and computational studies on zeolite-Y encapsulated iron(iii) and nickel(ii) complexes containing mixed-ligands of 2,2′-bipyridine and 1,10-phenanthroline." RSC Advances 5, no. 108 (2015): 88636–45. http://dx.doi.org/10.1039/c5ra14954a.
Повний текст джерелаLi, Qiang. "A three-dimensional anionic metal–dicyanamide network in poly[ethyltriphenylphosphonium [tri-μ2-dicyanamidato-cadmium(II)]]". Acta Crystallographica Section C Structural Chemistry 71, № 1 (1 січня 2015): 65–68. http://dx.doi.org/10.1107/s2053229614027090.
Повний текст джерелаLiu, Jing-Jing, Yue-Jian Lin, Zhen-Hua Li, and Guo-Xin Jin. "Self-assembled half-sandwich polyhedral cages via flexible Schiff-base ligands: an unusual macrocycle-to-cage conversion." Dalton Transactions 45, no. 35 (2016): 13675–79. http://dx.doi.org/10.1039/c6dt02393b.
Повний текст джерелаMin, Hyunsung, Alexander R. Craze, Takahiro Taira, Matthew J. Wallis, Mohan M. Bhadbhade, Ruoming Tian, Daniel J. Fanna, et al. "Self-Assembly of a Rare High Spin FeII/PdII Tetradecanuclear Cubic Cage Constructed via the Metalloligand Approach." Chemistry 4, no. 2 (May 26, 2022): 535–47. http://dx.doi.org/10.3390/chemistry4020038.
Повний текст джерелаRangarajan, Shalini, Owen A. Beaumont, Maravanji S. Balakrishna, Glen B. Deacon, and Victoria L. Blair. "Synthesis and Characterisation of Novel Bis(diphenylphosphane oxide)methanidoytterbium(III) Complexes." Molecules 27, no. 22 (November 9, 2022): 7704. http://dx.doi.org/10.3390/molecules27227704.
Повний текст джерелаDang, Li-Long, Tian Chen, Ting-Ting Zhang, Ting-Ting Li, Jun-Liang Song, Ke-Jia Zhang, and Lu-Fang Ma. "Size-Induced Highly Selective Synthesis of Organometallic Rectangular Macrocycles and Heterometallic Cage Based on Half-Sandwich Rhodium Building Block." Molecules 27, no. 12 (June 10, 2022): 3756. http://dx.doi.org/10.3390/molecules27123756.
Повний текст джерелаFerrara, Skylar J., Bo Wang, and James P. Donahue. "An S4-symmetric mixed-valent decacopper cage comprised of [CuII(L-S2N2)] complexes bridged by CuI(MeCN)n (n = 1 or 2) cations." Dalton Transactions 45, no. 7 (2016): 2997–3002. http://dx.doi.org/10.1039/c5dt04359j.
Повний текст джерелаCuello-Garibo, Jordi-Amat, Michael S. Meijer, and Sylvestre Bonnet. "To cage or to be caged? The cytotoxic species in ruthenium-based photoactivated chemotherapy is not always the metal." Chemical Communications 53, no. 50 (2017): 6768–71. http://dx.doi.org/10.1039/c7cc03469e.
Повний текст джерелаZhao, Yibo, Yunfeng Lu, Ao Liu, Zhi-Yuan Zhang, Chunju Li, and Andrew C. H. Sue. "Macrocycle with Equatorial Coordination Sites Provides New Opportunity for Structure-Diverse Metallacages." Molecules 28, no. 6 (March 10, 2023): 2537. http://dx.doi.org/10.3390/molecules28062537.
Повний текст джерелаSamantray, Sagarika, Sreenivasulu Bandi, and Dillip K. Chand. "Design of a double-decker coordination cage revisited to make new cages and exemplify ligand isomerism." Beilstein Journal of Organic Chemistry 15 (May 21, 2019): 1129–40. http://dx.doi.org/10.3762/bjoc.15.109.
Повний текст джерелаGrobe, Joseph, Kai Lütke-Brochtrup, Bernt Krebs, Mechtild Läge, Hans-Hermann Niemeyer, and Ernst-Ulrich Würthwein. "Alternativ-Liganden XXXVIII. [1] Neue Versuche zur Synthese von Pd(0)- und Pt(0)-Komplexen des Tripod-Phosphanliganden FSi(CH2CH2PMe2)3 / Alternative Ligands XXXVIII. [1] Further Attempts to Synthesize Pd(0) and Pt(0) Complexes with the Tripod Phosphane Ligand FSi(CH2CH2PMe2)3." Zeitschrift für Naturforschung B 62, no. 1 (January 1, 2007): 55–65. http://dx.doi.org/10.1515/znb-2007-0109.
Повний текст джерелаAl Rasbi, Nawal K., and Michael D. Ward. "Synthesis and crystal structure of an M 4 L 6 tetrahedral cage with outward-facing pockets from a substituted pyrazolyl–pyridine ligand." Acta Crystallographica Section C Structural Chemistry 74, no. 8 (July 24, 2018): 961–66. http://dx.doi.org/10.1107/s2053229618009683.
Повний текст джерелаSimon, Cory M., Efrem Braun, Carlo Carraro, and Berend Smit. "Statistical mechanical model of gas adsorption in porous crystals with dynamic moieties." Proceedings of the National Academy of Sciences 114, no. 3 (January 3, 2017): E287—E296. http://dx.doi.org/10.1073/pnas.1613874114.
Повний текст джерелаAvramov, Pavel V., Alex A. Kuzubov, Seiji Sakai, Manabu Ohtomo, Shiro Entani, Yoshihiro Matsumoto, Natalia S. Eleseeva, Vladimir A. Pomogaev, and Hiroshi Naramoto. "Atomic structure and physical properties of fused porphyrin nanoclusters." Journal of Porphyrins and Phthalocyanines 18, no. 07 (July 2014): 552–68. http://dx.doi.org/10.1142/s1088424614500291.
Повний текст джерелаBoer, Stephanie A., and David R. Turner. "Self-selecting homochiral quadruple-stranded helicates and control of supramolecular chirality." Chemical Communications 51, no. 98 (2015): 17375–78. http://dx.doi.org/10.1039/c5cc07422c.
Повний текст джерелаSuzuki, Mitsuaki. "Open-cage Fullerenes as Ligands." Journal of Synthetic Organic Chemistry, Japan 79, no. 10 (October 1, 2021): 968–70. http://dx.doi.org/10.5059/yukigoseikyokaishi.79.968.
Повний текст джерелаHarrowfield, Jack, and Pierre Thuéry. "Uranyl Ion Complexes of Polycarboxylates: Steps towards Isolated Photoactive Cavities." Chemistry 2, no. 1 (February 20, 2020): 63–79. http://dx.doi.org/10.3390/chemistry2010007.
Повний текст джерелаLuise, Chiara, Dina Robaa, and Wolfgang Sippl. "Exploring aromatic cage flexibility of the histone methyllysine reader protein Spindlin1 and its impact on binding mode prediction: an in silico study." Journal of Computer-Aided Molecular Design 35, no. 6 (June 2021): 695–706. http://dx.doi.org/10.1007/s10822-021-00391-9.
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