Artículos de revistas sobre el tema "Organoruthenium compounds"
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Trobec, Tomaž, Kristina Sepčić, Monika Cecilija Žužek, Jerneja Kladnik, Nina Podjed, Catarina Cardoso Páscoa, Iztok Turel y Robert Frangež. "Fine Tuning of Cholinesterase and Glutathione-S-Transferase Activities by Organoruthenium(II) Complexes". Biomedicines 9, n.º 9 (16 de septiembre de 2021): 1243. http://dx.doi.org/10.3390/biomedicines9091243.
Texto completoChow, Mun Juinn, Cynthia Licona, Giorgia Pastorin, Georg Mellitzer, Wee Han Ang y Christian Gaiddon. "Structural tuning of organoruthenium compounds allows oxidative switch to control ER stress pathways and bypass multidrug resistance". Chemical Science 7, n.º 7 (2016): 4117–24. http://dx.doi.org/10.1039/c6sc00268d.
Texto completoShakil, Md Salman, Shahida Parveen, Zohaib Rana, Fearghal Walsh, Sanam Movassaghi, Tilo Söhnel, Mayur Azam et al. "High Antiproliferative Activity of Hydroxythiopyridones over Hydroxypyridones and Their Organoruthenium Complexes". Biomedicines 9, n.º 2 (27 de enero de 2021): 123. http://dx.doi.org/10.3390/biomedicines9020123.
Texto completoMondal, Ashaparna y Priyankar Paira. "Synthesis and Biological Evaluations of Organoruthenium Scaffolds: A Comprehensive Update". Current Organic Synthesis 15, n.º 2 (24 de abril de 2018): 179–207. http://dx.doi.org/10.2174/1570179414666170703143049.
Texto completoNogueira, Luciano J., Maria A. de Resende, Sheila R. Oliveira, Maria Helena de Araújo, Thais F. F. Magalhães, Milena B. de Oliveira, Cleide V. B. Martins, Miriam T. P. Lopes, Ana C. Araújo e Silva y Claudio L. Donnici. "In vitro susceptibility of Aspergillus spp. to dithiocarbamate organoruthenium compounds". Mycoses 54, n.º 5 (14 de junio de 2010): e323-e329. http://dx.doi.org/10.1111/j.1439-0507.2010.01914.x.
Texto completoParveen, Shahida, Kelvin K. H. Tong, Muhammad Khawar Rauf, Mario Kubanik, Muhammad Ashraf Shaheen, Tilo Söhnel, Stephen M. F. Jamieson, Muhammad Hanif y Christian G. Hartinger. "Coordination Chemistry of Organoruthenium Compounds with Benzoylthiourea Ligands and their Biological Properties". Chemistry – An Asian Journal 14, n.º 8 (14 de febrero de 2019): 1262–70. http://dx.doi.org/10.1002/asia.201801798.
Texto completoNagy, Eszter Marta y Dolores Fregona. "Critical comment on: ‘In vitro susceptibility of Aspergillus spp. to dithiocarbamate organoruthenium compounds’". Mycoses 55, n.º 1 (8 de agosto de 2011): 101. http://dx.doi.org/10.1111/j.1439-0507.2011.02085.x.
Texto completoGomathi, Asaithambi, Paranthaman Vijayan, Periasamy Viswanathamurthi, Shanmugam Suresh, Raju Nandhakumar y Takeshi Hashimoto. "Organoruthenium(II) compounds with pyridyl benzoxazole/benzthiazole moiety: studies on DNA/protein binding and enzyme mimetic activities". Journal of Coordination Chemistry 70, n.º 10 (30 de marzo de 2017): 1645–66. http://dx.doi.org/10.1080/00958972.2017.1309649.
Texto completoCuccioloni, Massimiliano, Valentina Cecarini, Laura Bonfili, Riccardo Pettinari, Alessia Tombesi, Noemi Pagliaricci, Laura Petetta, Mauro Angeletti y Anna Maria Eleuteri. "Enhancing the Amyloid-β Anti-Aggregation Properties of Curcumin via Arene-Ruthenium(II) Derivatization". International Journal of Molecular Sciences 23, n.º 15 (5 de agosto de 2022): 8710. http://dx.doi.org/10.3390/ijms23158710.
Texto completoMovassaghi, Sanam, Euphemia Leung, Muhammad Hanif, Betty Y. T. Lee, Hannah U. Holtkamp, Jason K. Y. Tu, Tilo Söhnel, Stephen M. F. Jamieson y Christian G. Hartinger. "A Bioactive l-Phenylalanine-Derived Arene in Multitargeted Organoruthenium Compounds: Impact on the Antiproliferative Activity and Mode of Action". Inorganic Chemistry 57, n.º 14 (27 de junio de 2018): 8521–29. http://dx.doi.org/10.1021/acs.inorgchem.8b01187.
Texto completoHiraki, Katsuma, Naoyuki Ochi, Yoko Sasada, Hideki Hayashida, Yoshio Fuchita y Shunichiro Yamanaka. "Organoruthenium(II) complexes formed by insertion reactions of some vinyl compounds and conjugated dienes into a hydrido–ruthenium bond". J. Chem. Soc., Dalton Trans., n.º 5 (1985): 873–77. http://dx.doi.org/10.1039/dt9850000873.
Texto completoWieteck, Marcel, Mie Højer Larsen née Vilhelmsen, Pascal Nösel, Jürgen Schulmeister, Frank Rominger, Matthias Rudolph, Markus Pernpointner y A. Stephen K. Hashmi. "Conjugated Vinylgold(I)-Vinylideneruthenium(II) Complexes and Related Organoruthenium Compounds: Stable Analogues of Intermediates Proposed in Dual Gold Catalysis". Advanced Synthesis & Catalysis 358, n.º 9 (27 de abril de 2016): 1449–62. http://dx.doi.org/10.1002/adsc.201600255.
Texto completoBryndza, Henry E., Peter J. Domaille, Wilson Tam, Lawrence K. Fong, Rocco A. Paciello y John E. Bercaw. "Comparison of metal-hydrogen, -oxygen, -nitrogen and -carbon bond strengths and evaluation of functional group additivity principles for organoruthenium and organoplatinum compounds". Polyhedron 7, n.º 16-17 (enero de 1988): 1441–52. http://dx.doi.org/10.1016/s0277-5387(00)81773-8.
Texto completoPavlović, Marijana, Stefan Nikolić, Nevenka Gligorijević, Biljana Dojčinović, Sandra Aranđelović, Sanja Grgurić-Šipka y Siniša Radulović. "New organoruthenium compounds with pyrido[2′,3′:5,6]pyrazino[2,3-f][1, 10]phenanthroline: synthesis, characterization, cytotoxicity, and investigation of mechanism of action". JBIC Journal of Biological Inorganic Chemistry 24, n.º 2 (14 de febrero de 2019): 297–310. http://dx.doi.org/10.1007/s00775-019-01647-4.
Texto completoBryndza, Henry E., Lawrence K. Fong, Rocco A. Paciello, Wilson Tam y John E. Bercaw. "Relative metal-hydrogen, -oxygen, -nitrogen, and -carbon bond strengths for organoruthenium and organoplatinum compounds; equilibrium studies of Cp*(PMe3)2RuX and (DPPE)MePtX systems". Journal of the American Chemical Society 109, n.º 5 (marzo de 1987): 1444–56. http://dx.doi.org/10.1021/ja00239a026.
Texto completoMarques, F., L. Corte-Real, A. P. Alves de Matos, I. Alho, T. S. Morais, A. I. Tomaz, M. H. Garcia y M. P. Bicho. "Intracellular distribution of antitumor Ru (II) compounds: The lysosome and the lysosomal enzymes as targets for anticancer metal-based drugs". Microscopy and Microanalysis 19, S4 (agosto de 2013): 9–10. http://dx.doi.org/10.1017/s1431927613000664.
Texto completoKljun, Jakob, Renata Pavlič, Eva Hafner, Tanja Lipec, Sara Moreno-Da Silva, Primož Tič, Iztok Turel, Tomaž Büdefeld, Jure Stojan y Tea Lanišnik Rižner. "Ruthenium complexes show potent inhibition of AKR1C1, AKR1C2, and AKR1C3 enzymes and anti-proliferative action against chemoresistant ovarian cancer cell line". Frontiers in Pharmacology 13 (11 de agosto de 2022). http://dx.doi.org/10.3389/fphar.2022.920379.
Texto completoRiisom, Mie, Liam Eade, William D. J. Tremlett y Christian G. Hartinger. "The aqueous stability and interactions of organoruthenium compounds with serum proteins, cell culture medium and human serum". Metallomics, 25 de junio de 2022. http://dx.doi.org/10.1093/mtomcs/mfac043.
Texto completoHIRAKI, K., N. OCHI, Y. SASADA, H. HAYASHIDA, Y. FUCHITA y S. YAMANAKA. "ChemInform Abstract: ORGANORUTHENIUM(II) COMPLEXES FORMED BY INSERTION REACTIONS OF SOME VINYL COMPOUNDS AND CONJUGATED DIENES INTO A HYDRIDO-RUTHENIUM BOND". Chemischer Informationsdienst 16, n.º 37 (17 de septiembre de 1985). http://dx.doi.org/10.1002/chin.198537275.
Texto completoBRYNDZA, H. E., P. J. DOMAILLE, W. TAM, L. K. FONG, R. A. PACIELLO y J. E. BERCAW. "ChemInform Abstract: Comparison of Metal-Hydrogen, -Oxygen, -Nitrogen and -Carbon Bond Strengths and Evaluation of Functional Group Additivity Principles for Organoruthenium and Organoplatinum Compounds." ChemInform 20, n.º 4 (24 de enero de 1989). http://dx.doi.org/10.1002/chin.198904098.
Texto completoBRYNDZA, H. E., L. K. FONG, R. A. PACIELLO, W. TAM y J. E. BERCAW. "ChemInform Abstract: Relative Metal-Hydrogen, -Oxygen, -Nitrogen, and -Carbon Bond Strengths for Organoruthenium and Organoplatinum Compounds; Equilibrium Studies of Cp*(PMe3)2RuX and (DPPE)MePtX Systems". ChemInform 18, n.º 28 (14 de julio de 1987). http://dx.doi.org/10.1002/chin.198728091.
Texto completoMeier-Menches, Samuel M., Benjamin Neuditschko, Lukas Janker, Marlene C. Gerner, Klaus G. Schmetterer, Albrecht Reichle y Christopher Gerner. "A Proteomic Platform Enables to Test for AML Normalization In Vitro". Frontiers in Chemistry 10 (1 de febrero de 2022). http://dx.doi.org/10.3389/fchem.2022.826346.
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