Статті в журналах з теми "KP1019"
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Alessio, Enzo, and Luigi Messori. "NAMI-A and KP1019/1339, Two Iconic Ruthenium Anticancer Drug Candidates Face-to-Face: A Case Story in Medicinal Inorganic Chemistry." Molecules 24, no. 10 (May 24, 2019): 1995. http://dx.doi.org/10.3390/molecules24101995.
Повний текст джерелаHeffeter, Petra, Katharina Böck, Bihter Atil, Mir Ali Reza Hoda, Wilfried Körner, Caroline Bartel, Ute Jungwirth, et al. "Intracellular protein binding patterns of the anticancer ruthenium drugs KP1019 and KP1339." JBIC Journal of Biological Inorganic Chemistry 15, no. 5 (March 11, 2010): 737–48. http://dx.doi.org/10.1007/s00775-010-0642-1.
Повний текст джерелаStultz, Laura K., Alexandra Hunsucker, Sydney Middleton, Evan Grovenstein, Jacob O’Leary, Eliot Blatt, Mary Miller, James Mobley, and Pamela K. Hanson. "Proteomic analysis of the S. cerevisiae response to the anticancer ruthenium complex KP1019." Metallomics 12, no. 6 (2020): 876–90. http://dx.doi.org/10.1039/d0mt00008f.
Повний текст джерелаBergamo, A., A. Masi, M. A. Jakupec, B. K. Keppler, and G. Sava. "Inhibitory Effects of the Ruthenium Complex KP1019 in Models of Mammary Cancer Cell Migration and Invasion." Metal-Based Drugs 2009 (September 17, 2009): 1–9. http://dx.doi.org/10.1155/2009/681270.
Повний текст джерелаKuhn, P. S., V. Pichler, A. Roller, M. Hejl, M. A. Jakupec, W. Kandioller, and B. K. Keppler. "Improved reaction conditions for the synthesis of new NKP-1339 derivatives and preliminary investigations on their anticancer potential." Dalton Transactions 44, no. 2 (2015): 659–68. http://dx.doi.org/10.1039/c4dt01645a.
Повний текст джерелаCirri, Damiano, Tiziano Marzo, Iogann Tolbatov, Alessandro Marrone, Francesco Saladini, Ilaria Vicenti, Filippo Dragoni, Adele Boccuto, and Luigi Messori. "In Vitro Anti-SARS-CoV-2 Activity of Selected Metal Compounds and Potential Molecular Basis for Their Actions Based on Computational Study." Biomolecules 11, no. 12 (December 10, 2021): 1858. http://dx.doi.org/10.3390/biom11121858.
Повний текст джерелаLevina, Aviva, Anthony R. M. Chetcuti, and Peter A. Lay. "Controversial Role of Transferrin in the Transport of Ruthenium Anticancer Drugs." Biomolecules 12, no. 9 (September 18, 2022): 1319. http://dx.doi.org/10.3390/biom12091319.
Повний текст джерелаJuszczak, Michał, Magdalena Kluska, Daniel Wysokiński, and Katarzyna Woźniak. "Anti-cancer properties of ruthenium compounds: NAMI-A and KP1019." Postępy Higieny i Medycyny Doświadczalnej 74 (February 19, 2020): 12–19. http://dx.doi.org/10.5604/01.3001.0013.8549.
Повний текст джерелаGransbury, Gemma K., Peter Kappen, Chris J. Glover, James N. Hughes, Aviva Levina, Peter A. Lay, Ian F. Musgrave, and Hugh H. Harris. "Comparison of KP1019 and NAMI-A in tumour-mimetic environments." Metallomics 8, no. 8 (2016): 762–73. http://dx.doi.org/10.1039/c6mt00145a.
Повний текст джерелаHeffeter, P., M. A. Jakupec, M. Pongratz, P. Chiba, M. Micksche, W. Körner, M. Hauses, B. Marian, B. K. Keppler, and W. Berger. "630 Molecular mechanisms of resistance against the ruthenium compound KP1019." European Journal of Cancer Supplements 2, no. 8 (September 2004): 190–91. http://dx.doi.org/10.1016/s1359-6349(04)80638-4.
Повний текст джерелаHeffeter, P., A. Riabtseva, Y. Senkiv, C. R. Kowol, W. Körner, U. Jungwith, N. Mitina, et al. "Nanoformulation Improves Activity of the (pre)Clinical Anticancer Ruthenium Complex KP1019." Journal of Biomedical Nanotechnology 10, no. 5 (May 1, 2014): 877–84. http://dx.doi.org/10.1166/jbn.2014.1763.
Повний текст джерелаDömötör, Orsolya, Christian G. Hartinger, Anna K. Bytzek, Tamás Kiss, Bernhard K. Keppler, and Eva A. Enyedy. "Characterization of the binding sites of the anticancer ruthenium(III) complexes KP1019 and KP1339 on human serum albumin via competition studies." JBIC Journal of Biological Inorganic Chemistry 18, no. 1 (October 18, 2012): 9–17. http://dx.doi.org/10.1007/s00775-012-0944-6.
Повний текст джерелаDwyer, Brendan G., Emily Johnson, Efren Cazares, Karen L. McFarlane Holman, and Sarah R. Kirk. "Ruthenium anticancer agent KP1019 binds more tightly than NAMI-A to tRNAPhe." Journal of Inorganic Biochemistry 182 (May 2018): 177–83. http://dx.doi.org/10.1016/j.jinorgbio.2018.02.019.
Повний текст джерелаJones, Michael R., Changhua Mu, Michael C. P. Wang, Michael I. Webb, Charles J. Walsby та Tim Storr. "Modulation of the Aβ peptide aggregation pathway by KP1019 limits Aβ-associated neurotoxicity". Metallomics 7, № 1 (2015): 129–35. http://dx.doi.org/10.1039/c4mt00252k.
Повний текст джерелаBartel, Caroline, Alexander E. Egger, Michael A. Jakupec, Petra Heffeter, Markus Galanski, Walter Berger, and Bernhard K. Keppler. "Influence of ascorbic acid on the activity of the investigational anticancer drug KP1019." JBIC Journal of Biological Inorganic Chemistry 16, no. 8 (June 26, 2011): 1205–15. http://dx.doi.org/10.1007/s00775-011-0809-4.
Повний текст джерелаSingh, Vikash, Gajendra Kumar Azad, Amarendar Reddy M., Shivani Baranwal, and Raghuvir S. Tomar. "Anti-cancer drug KP1019 induces Hog1 phosphorylation and protein ubiquitylation in Saccharomyces cerevisiae." European Journal of Pharmacology 736 (August 2014): 77–85. http://dx.doi.org/10.1016/j.ejphar.2014.04.032.
Повний текст джерелаJakupec, M. A., V. B. Arion, S. Kapitza, E. Reisner, A. Eichinger, M. Pongratz, B. Marian, N. Graf v. Keyserlingk, and B. K. Keppler. "KP1019 (FFC14A) from bench to bedside: preclinical and early clinical development ? an overview." Int. Journal of Clinical Pharmacology and Therapeutics 43, no. 12 (December 1, 2005): 595–96. http://dx.doi.org/10.5414/cpp43595.
Повний текст джерелаSingh, Vikash, Gajendra Kumar Azad, Papita Mandal, M. Amarendar Reddy, and Raghuvir S. Tomar. "Anti-cancer drug KP1019 modulates epigenetics and induces DNA damage response inSaccharomyces cerevisiae." FEBS Letters 588, no. 6 (February 20, 2014): 1044–52. http://dx.doi.org/10.1016/j.febslet.2014.02.017.
Повний текст джерелаCetinbas, Naniye, Michael I. Webb, Joshua A. Dubland, and Charles J. Walsby. "Serum-protein interactions with anticancer Ru(III) complexes KP1019 and KP418 characterized by EPR." JBIC Journal of Biological Inorganic Chemistry 15, no. 2 (August 26, 2009): 131–45. http://dx.doi.org/10.1007/s00775-009-0578-5.
Повний текст джерелаŚpiewak, Klaudyna, Sylwia Świątek, Barbara Jachimska, and Małgorzata Brindell. "Induction of transferrin aggregation by indazolium [tetrachlorobis(1H-indazole)ruthenate(iii)] (KP1019) and its biological function." New Journal of Chemistry 43, no. 28 (2019): 11296–306. http://dx.doi.org/10.1039/c9nj01342c.
Повний текст джерелаFischer, Britta, Petra Heffeter, Kushtrim Kryeziu, Lars Gille, Samuel M. Meier, Walter Berger, Christian R. Kowol, and Bernhard K. Keppler. "Poly(lactic acid) nanoparticles of the lead anticancer ruthenium compound KP1019 and its surfactant-mediated activation." Dalton Trans. 43, no. 3 (2014): 1096–104. http://dx.doi.org/10.1039/c3dt52388h.
Повний текст джерелаLentz, Frederike, Anne Drescher, Andreas Lindauer, Magdalena Henke, Ralf A. Hilger, Christian G. Hartinger, Max E. Scheulen, Christian Dittrich, Bernhard K. Keppler, and Ulrich Jaehde. "Pharmacokinetics of a novel anticancer ruthenium complex (KP1019, FFC14A) in a phase I dose-escalation study." Anti-Cancer Drugs 20, no. 2 (February 2009): 97–103. http://dx.doi.org/10.1097/cad.0b013e328322fbc5.
Повний текст джерелаBierle, Lindsey A., Kira L. Reich, Braden E. Taylor, Eliot B. Blatt, Sydney M. Middleton, Shawnecca D. Burke, Laura K. Stultz, Pamela K. Hanson, Janet F. Partridge, and Mary E. Miller. "DNA Damage Response Checkpoint Activation Drives KP1019 Dependent Pre-Anaphase Cell Cycle Delay in S. cerevisiae." PLOS ONE 10, no. 9 (September 16, 2015): e0138085. http://dx.doi.org/10.1371/journal.pone.0138085.
Повний текст джерелаGolla, Upendarrao, Swati Swagatika, Sakshi Chauhan, and Raghuvir Singh Tomar. "A systematic assessment of chemical, genetic, and epigenetic factors influencing the activity of anticancer drug KP1019 (FFC14A)." Oncotarget 8, no. 58 (September 30, 2017): 98426–54. http://dx.doi.org/10.18632/oncotarget.21416.
Повний текст джерелаRichert, Monika, Grzegorz Trykowski, Mariusz Walczyk, Marcin J. Cieślak, Julia Kaźmierczak-Barańska, Karolina Królewska-Golińska, Janusz W. Sobczak, and Stanisław Biniak. "Modification of multiwalled carbon nanotubes with a ruthenium drug candidate—indazolium[tetrachlorobis(1H-indazole)ruthenate(iii)] (KP1019 )." Dalton Transactions 49, no. 46 (2020): 16791–800. http://dx.doi.org/10.1039/d0dt03528a.
Повний текст джерелаAitken, Jade B., Sumy Antony, Claire M. Weekley, Barry Lai, Leone Spiccia, and Hugh H. Harris. "Distinct cellular fates for KP1019 and NAMI-A determined by X-ray fluorescence imaging of single cells." Metallomics 4, no. 10 (2012): 1051. http://dx.doi.org/10.1039/c2mt20072d.
Повний текст джерелаKapitza, Susanne, Michael A. Jakupec, Maria Uhl, Bernhard K. Keppler, and Brigitte Marian. "The heterocyclic ruthenium(III) complex KP1019 (FFC14A) causes DNA damage and oxidative stress in colorectal tumor cells." Cancer Letters 226, no. 2 (August 2005): 115–21. http://dx.doi.org/10.1016/j.canlet.2005.01.002.
Повний текст джерелаShah, Pramod Kumar, and P. K. Shukla. "A DFT study of reactions of Ru(III) anticancer drug KP1019 with 8-oxoguanine and 8-oxoadenine." Structural Chemistry 31, no. 5 (June 16, 2020): 2087–92. http://dx.doi.org/10.1007/s11224-020-01563-3.
Повний текст джерелаBüchel, Gabriel E., Iryna N. Stepanenko, Michaela Hejl, Michael A. Jakupec, Bernhard K. Keppler, and Vladimir B. Arion. "En Route to Osmium Analogues of KP1019: Synthesis, Structure, Spectroscopic Properties and Antiproliferative Activity oftrans-[OsIVCl4(Hazole)2]." Inorganic Chemistry 50, no. 16 (August 15, 2011): 7690–97. http://dx.doi.org/10.1021/ic200728b.
Повний текст джерелаHartinger, C. G., S. Hann, G. Koellensperger, M. Sulyok, M. Groessl, A. R. Timerbaev, A. V. Rudnev, G. Stingeder, and B. K. Keppler. "Interactions of a novel ruthenium-based anticancer drug (KP1019 or FFC14a) with serum proteins ? significance for the patient." Int. Journal of Clinical Pharmacology and Therapeutics 43, no. 12 (December 1, 2005): 583–85. http://dx.doi.org/10.5414/cpp43583.
Повний текст джерелаMotswainyana, William M., and Peter A. Ajibade. "Anticancer Activities of Mononuclear Ruthenium(II) Coordination Complexes." Advances in Chemistry 2015 (February 19, 2015): 1–21. http://dx.doi.org/10.1155/2015/859730.
Повний текст джерелаStevens, Shannon K., Amy P. Strehle, Rebecca L. Miller, Sarah H. Gammons, Kyle J. Hoffman, John T. McCarty, Mary E. Miller, Laura K. Stultz, and Pamela K. Hanson. "The Anticancer Ruthenium Complex KP1019 Induces DNA Damage, Leading to Cell Cycle Delay and Cell Death in Saccharomyces cerevisiae." Molecular Pharmacology 83, no. 1 (October 22, 2012): 225–34. http://dx.doi.org/10.1124/mol.112.079657.
Повний текст джерелаKuhn, Paul-Steffen, Gabriel E. Büchel, Katarina K. Jovanović, Lana Filipović, Siniša Radulović, Peter Rapta, and Vladimir B. Arion. "Osmium(III) Analogues of KP1019: Electrochemical and Chemical Synthesis, Spectroscopic Characterization, X-ray Crystallography, Hydrolytic Stability, and Antiproliferative Activity." Inorganic Chemistry 53, no. 20 (October 7, 2014): 11130–39. http://dx.doi.org/10.1021/ic501710k.
Повний текст джерелаHeffeter, P., M. Pongratz, E. Steiner, P. Chiba, M. A. Jakupec, L. Elbling, B. Marian, et al. "Intrinsic and Acquired Forms of Resistance against the Anticancer Ruthenium Compound KP1019 [Indazolium trans-[tetrachlorobis(1H-indazole)ruthenate (III)] (FFC14A)." Journal of Pharmacology and Experimental Therapeutics 312, no. 1 (August 26, 2004): 281–89. http://dx.doi.org/10.1124/jpet.104.073395.
Повний текст джерелаHartinger, Christian G, Michael A Jakupec, Stefanie Zorbas-Seifried, Michael Groessl, Alexander Egger, Walter Berger, Haralabos Zorbas, Paul J Dyson, and Bernhard K Keppler. "KP1019, A New Redox-Active Anticancer Agent - Preclinical Development and Results of a Clinical Phase I Study in Tumor Patients." Chemistry & Biodiversity 5, no. 10 (October 2008): 2140–55. http://dx.doi.org/10.1002/cbdv.200890195.
Повний текст джерелаAvramovic, Natasa, Nikola Ignjatovic, and Aleksandar Savic. "Platinum and ruthenium complexes as promising molecules in cancer therapy." Srpski arhiv za celokupno lekarstvo 147, no. 1-2 (2019): 105–9. http://dx.doi.org/10.2298/sarh180706075a.
Повний текст джерелаFerraro, Maria Grazia, Marialuisa Piccolo, Gabriella Misso, Francesco Maione, Daniela Montesarchio, Michele Caraglia, Luigi Paduano, Rita Santamaria, and Carlo Irace. "Breast Cancer Chemotherapeutic Options: A General Overview on the Preclinical Validation of a Multi-Target Ruthenium(III) Complex Lodged in Nucleolipid Nanosystems." Cells 9, no. 6 (June 5, 2020): 1412. http://dx.doi.org/10.3390/cells9061412.
Повний текст джерелаChang, Stephanie W., Andrew R. Lewis, Kathleen E. Prosser, John R. Thompson, Margarita Gladkikh, Marcel B. Bally, Jeffrey J. Warren, and Charles J. Walsby. "CF3Derivatives of the Anticancer Ru(III) Complexes KP1019, NKP-1339, and Their Imidazole and Pyridine Analogues Show Enhanced Lipophilicity, Albumin Interactions, and Cytotoxicity." Inorganic Chemistry 55, no. 10 (May 4, 2016): 4850–63. http://dx.doi.org/10.1021/acs.inorgchem.6b00359.
Повний текст джерелаHartinger, Christian G., Stefanie Zorbas-Seifried, Michael A. Jakupec, Bernd Kynast, Haralabos Zorbas, and Bernhard K. Keppler. "From bench to bedside – preclinical and early clinical development of the anticancer agent indazolium trans-[tetrachlorobis(1H-indazole)ruthenate(III)] (KP1019 or FFC14A)." Journal of Inorganic Biochemistry 100, no. 5-6 (May 2006): 891–904. http://dx.doi.org/10.1016/j.jinorgbio.2006.02.013.
Повний текст джерелаPongratz, Martina, Petra Schluga, Michael A. Jakupec, Vladimir B. Arion, Christian G. Hartinger, G�nter Allmaier, and Bernhard K. Keppler. "Transferrin binding and transferrin-mediated cellular uptake of the ruthenium coordination compound KP1019, studied by means of AAS, ESI-MS and CD spectroscopy." Journal of Analytical Atomic Spectrometry 19, no. 1 (2004): 46. http://dx.doi.org/10.1039/b309160k.
Повний текст джерелаHummer, Alfred A., Petra Heffeter, Walter Berger, Martin Filipits, David Batchelor, Gabriel E. Büchel, Michael A. Jakupec, Bernhard K. Keppler, and Annette Rompel. "X-ray Absorption Near Edge Structure Spectroscopy to Resolve the in Vivo Chemistry of the Redox-Active Indazolium trans-[Tetrachlorobis(1H-indazole)ruthenate(III)] (KP1019)." Journal of Medicinal Chemistry 56, no. 3 (January 31, 2013): 1182–96. http://dx.doi.org/10.1021/jm301648f.
Повний текст джерелаBučinský, Lukas, Gabriel E. Büchel, Robert Ponec, Peter Rapta, Martin Breza, Jozef Kožíšek, Marian Gall, et al. "On the Electronic Structure ofmer,trans-[RuCl3(1H-indazole)2(NO)], a Hypothetical Metabolite of the Antitumor Drug Candidate KP1019: An Experimental and DFT Study." European Journal of Inorganic Chemistry 2013, no. 14 (April 4, 2013): 2505–19. http://dx.doi.org/10.1002/ejic.201201526.
Повний текст джерелаBüchel, Gabriel E., Susanne Kossatz, Ahmad Sadique, Peter Rapta, Michal Zalibera, Lukas Bucinsky, Stanislav Komorovsky, et al. "cis-Tetrachlorido-bis(indazole)osmium(iv) and its osmium(iii) analogues: paving the way towards the cis-isomer of the ruthenium anticancer drugs KP1019 and/or NKP1339." Dalton Transactions 46, no. 35 (2017): 11925–41. http://dx.doi.org/10.1039/c7dt02194a.
Повний текст джерелаBijelic, Aleksandar, Sarah Theiner, Bernhard K. Keppler, and Annette Rompel. "X-ray Structure Analysis of Indazoliumtrans-[Tetrachlorobis(1H-indazole)ruthenate(III)] (KP1019) Bound to Human Serum Albumin Reveals Two Ruthenium Binding Sites and Provides Insights into the Drug Binding Mechanism." Journal of Medicinal Chemistry 59, no. 12 (June 7, 2016): 5894–903. http://dx.doi.org/10.1021/acs.jmedchem.6b00600.
Повний текст джерелаPeng, Chunte Sam, Bogdan I. Fedeles, Vipender Singh, Deyu Li, Tiffany Amariuta, John M. Essigmann, and Andrei Tokmakoff. "Two-dimensional IR spectroscopy of the anti-HIV agent KP1212 reveals protonated and neutral tautomers that influence pH-dependent mutagenicity." Proceedings of the National Academy of Sciences 112, no. 11 (March 2, 2015): 3229–34. http://dx.doi.org/10.1073/pnas.1415974112.
Повний текст джерелаDíaz, Daniel Barón, Anke Neumann, and Habibu Aliyu. "Thermophilic Water Gas Shift Reaction at High Carbon Monoxide and Hydrogen Partial Pressures in Parageobacillus thermoglucosidasius KP1013." Fermentation 8, no. 11 (November 1, 2022): 596. http://dx.doi.org/10.3390/fermentation8110596.
Повний текст джерелаEgger, Alexander E., Sarah Theiner, Christoph Kornauth, Petra Heffeter, Walter Berger, Bernhard K. Keppler, and Christian G. Hartinger. "Quantitative bioimaging by LA-ICP-MS: a methodological study on the distribution of Pt and Ru in viscera originating from cisplatin- and KP1339-treated mice." Metallomics 6, no. 9 (2014): 1616–25. http://dx.doi.org/10.1039/c4mt00072b.
Повний текст джерелаHu, Hui-Chao, Xin-Sheng Chai, Chun-Yun Zhang, Li-Min Fu, Donald Barnes, Liulian Huang, and Lihui Chen. "Experimental data and kinetic models in terms of methanol formation during oxygen delignification processes of alkaline pulps." Holzforschung 69, no. 8 (October 1, 2015): 933–42. http://dx.doi.org/10.1515/hf-2014-0246.
Повний текст джерелаKomadel, P., J. Hrobáriková, L’ Smrčok, and B. Koppelhuber-Bitschnau. "Hydration of reduced-charge montmorillonite." Clay Minerals 37, no. 3 (September 2002): 543–50. http://dx.doi.org/10.1180/0009855023730057.
Повний текст джерелаBailey, Victoria N., Jennifer L. Sones, Caroline M. Camp, and Erin L. Oberhaus. "72 Endocrine and ovarian responses to combined estradiol benzoate-sulpiride in anestrous mares treated with kisspeptin." Journal of Animal Science 98, Supplement_2 (November 1, 2020): 36. http://dx.doi.org/10.1093/jas/skz397.082.
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