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)
Gordon Research Conference: Tuberculosis Drug Discovery & Development, 2023, Barcelona, Spain
EMBO Workshop on Tuberculosis, 2022, Institut Pasteur, Paris, France
Gordon Research Conference: Tuberculosis Drug Discovery & Development, 2017, Lucca, Italy
2023 – 2025: Member of the research team of Czech science foundation project 23-06558S - The role of signaling associated with DNA damage in development of anthracycline cardiotoxicity and its pharmacological impact
2021 – 2024: Member of the research team of the Czech Health Research Council project NU21-05-00446 "From hit-to-lead candidate - development of novel agents to combat tuberculosis"
2021 – 2023: Member of the research team of Czech science foundation project 21-16195S - Chemical biology approach to study anthracycline cardiotoxicity and pharmacological cardioprotection with focus on topoisomerase II beta
2018 – 2020: Member of the research team of Czech science foundation project 18-08169S - Study of individual topoisomerase II isoforms in anticancer and cardiotoxic effects of anthracyclines and their modulations by bisdioxopiperazines
2014 – 2017: Member of the research teams of the University project UNCE 204019/304019/2012 and Czech science foundation projects GA13-15008S and GA14-08423S, Department of Organic and Bioorganic Chemistry, Faculty of Pharmacy in Hradec Kralove, Charles University
2010 – 2012: Principal Investigator of grant of the Grant Agency of Charles University 55610/2010 "Synthesis and properties of selenium analogues of sulfur antituberculosis drugs"
Synthesis and structure-activity relationships of potential antitubercular agents
Synthesis and structure-activity relationships of topoisomerase II inhibitors and dexrazoxane analogues
total number of publications (2009-2024): 20
total number of citations including self-citations: 433; without self-citations: 380
H-index: 13
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)
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)
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)
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)
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)
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)
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).
PCT patent application: WO2021/144746 A1 (PCT/IB2021/050285). Roh J., Štěrba M., Šimůnek T., Štěrbová P., Karabanovich G., Jirkovská A., Jirkovský E., Bavlovič Piskáčková H., Kubeš J., Jansová H., Kollárová P. Use of ICRF-193 derivatives and pharmaceutical preparations containing thereof for the prevention of chronic cumulative cardiotoxicity caused by therapy with anthracycline anticancer drugs.
Czech patent CZ 308557 B6. Roh J., Karabanovich G., Pavek P., Hrabálek A.: Substituovaný 1,2,4-oxadiazol, jeho použití a farmaceutický přípravek ho obsahující (Substituted 1,2,4-oxadiazole, its use and pharmaceutical preparation containing the same). bought by Svenox Pharmaceuticals LLC