2014 – PhD in Bioorganic chemistry (Faculty of Pharmacy, Charles University, Czech Republic),
2009 – Engineer (Faculty of Chemical and Biotechnology, Saint-Petersburg State Institute of Technology (Technical University), Russian Federation)
Since 2014 – Research fellow (FaF UK, Department of Organic and Bioorganic Chemistry)
Since 2016 – teaching of Chemical Laboratory Techniques (practical classes) and General and Inorganic Chemistry (seminars) (Czech language, FaF UK)
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V. Keresteš, J. Kubeš, L. Applová, P. Kollárová, O. Lenčová-Popelová, I. Melnikova, G. Karabanovich, M. M Khazeem, H. Bavlovič-Piskáčková, P. Štěrbová-Kovaříková, C. A Austin, J. Roh, M. Štěrba, T. Šimůnek, A. Jirkovská. Exploring the effects of topoisomerase II inhibitor XK469 on anthracycline cardiotoxicity and DNA damage. Toxicological Sciences, 2024; kfae008, https://doi.org/10.1093/toxsci/kfae008 (IF2023 = 3.8)
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G. Karabanovich, V. Fabiánová, A. Vocat, J. Dušek, L. Valášková, J. Stolaříková, R. R. A. Kitson, P. Pávek, K. Vávrová, K. Djaout, K. Mikušová, A. R. Baulard, S. T. Cole, J. Korduláková, J. Roh. Both nitro groups are essential for high antitubercular activity of 3,5-dinitrobenzylsulfanyl tetrazoles and 1,3,4-oxadiazoles through the deazaflavin-dependent nitroreductase activation pathway. J. Med. Chem. 2024, 67, 81-109. (IF2022 = 7.3)
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E. Jirkovský, A. Jirkovská, H. Bavlovič-Piskáčková, V. Skalická, Z. Pokorná, G. Karabanovich, P. Kollárová-Brázdová, J. Kubeš, O. Lenčová-Popelová, Y. Mazurová, M. Adamcová, A. R. Lyon, J. Roh, T. Šimůnek, P. Štěrbová-Kovaříková, M. Štěrba. Clinically Translatable Prevention of Anthracycline Cardiotoxicity by Dexrazoxane Is Mediated by Topoisomerase II Beta and Not Metal Chelation. Circ Heart Fail. 2021;14: e008209. (IF2021 = 10.447)
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P. Kollarova-Brazdova, A. Jirkovska, G. Karabanovich, Z. Pokorna, H. B. Piskackova, E. Jirkovsky, J. Kubes, O. Lencova-Popelova, Y. Mazurova, M. Adamcova, V. Skalicka, P. Sterbova-Kovarikova, J. Roh, T. Simunek, M. Sterba. Investigation of Structure-Activity Relationships of Dexrazoxane Analogs Reveals Topoisomerase II beta Interaction as a Prerequisite for Effective Protection against Anthracycline Cardiotoxicity. J. Pharmacol Exp Ther., 2020, 373 (3), 402-415 (IF2020 = 4.03)
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A. Jirkovská, G. Karabanovich, J. Kubeš, V. Skalická, I. Melnikova, J. Korábečný, T. Kučera, E. Jirkovský, L. Nováková, H. Bavlovič Piskáčková, J. Škoda, M. Štěrba, C. A. Austin, T. Šimůnek, J. Roh. Structure−Activity Relationship Study of Dexrazoxane Analogues Reveals ICRF-193 as the Most Potent Bisdioxopiperazine against Anthracycline Toxicity to Cardiomyocytes Due to Its Strong Topoisomerase IIβ Interactions. J. Med. Chem. 2021, 64, 3997-4019. (IF2021 = 8.039)
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G. Karabanovich, J. Dušek, K. Savková, O. Pavliš, I. Pávková, J. Korabecny, T. Kučera, H. Kočová Vlčková, S. Huszár, Z. Konyariková, K. Konečná, O. Jandourek, J. Stolaříková, J. Korduláková, K. Vávrová, P. Pavek, V. Klimešová, A. Hrabalek, K. Mikušová, J. Roh. Development of 3,5-Dinitrophenyl-Containing 1,2,4-Triazoles and their Trifluoromethyl Analogues as Highly Efficient Antitubercular Agents Inhibiting Decaprenylphosphoryl-β-D-ribofuranose 2′-Oxidase. J. Med. Chem. 2019, 62, 8115-8139. (IF2019 = 6.205)
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G. Karabanovich, J. Zemanová, T. Smutný, R. Székely, M. Šarkan, I. Centárová, A. Vocat, I. Pávková, P. Čonka, J. Němeček, J. Stolaříková, M. Vejsová, K. Vávrová, V. Klimešová, A. Hrabálek, P. Pávek, S. T. Cole, K. Mikušová, J. Roh. Development of 3,5-Dinitrobenzylsulfanyl-1,3,4-Oxadiazoles and Thiadiazoles as Selective Antitubercular Agents Active Against Replicating and Nonreplicating Mycobacterium tuberculosis. J. Med. Chem. 2016; 59 (6): 2362-2380 (IF2016 = 6.259).