Short CV/Education and training

  • I obtained my PhD in Bioorganic Chemistry in 2018 at Eötvös Loránd University, in the MTA-ELTE Research Group of Peptide Chemistry, Budapest, Hungary. During my studies, I have broadened my research experience in several foreign institutions (Germany, Czech Republic, Peru, Japan). My PhD work involved the synthesis and biological evaluation of antimycobacterial agents and drug-peptide conjugates for targeted drug delivery. After my PhD, I worked on the development of drug-peptide conjugates against glioblastoma in the same group. Currently, I am working in the Aragón Materials Science Institute (ICMA), a joint research institute of Spanish National Research Council (CSIC) and the University of Zaragoza, in Spain as a Marie Skłodowska-Curie postdoctoral fellow. My current project focuses on the development of targeted intracellular delivery of antitubercular agents by functionalized nanocapsules.

Selected publications

  • Krátký, M., Janďourek, O., Baranyai, Zs., Novotná, E., Stolaříková, J., Bősze, Sz., Vinšová, J., Phenolic N-monosubstituted carbamates: Antitubercular and toxicity evaluation of multi-targeting compounds, Eur. J. Med. Chem., 2019, 181, 111578.

  • Baranyai, Zs., Krátký, M., Vosátka, R., Szabó, E., Senoner, Zs., Dávid, S., Stolaříková, J., Vinšová, J., Bősze, Sz., In vitro biological evaluation of new antimycobacterial salicylanilide-tuftsin conjugates, Eur. J. Med. Chem., 2017, 133, 152-173.

  • Krátký, M., Bősze, Sz., Baranyai, Zs., Stolaříková, J., Vinšová, J., Synthesis and biological evolution of hydrazones derived from 4-(trifluoromethyl)benzohydrazide, Bioorg. Med. Chem. Lett., 2017, 27, 5185-5189.

  • Ábrahám, Á.*, Baranyai, Zs.*, Gyulai, G., Pári, E., Horváti, K., Bősze, Sz., Kiss, É., Comparative analysis of new peptide conjugates of antitubercular drug candidates − model membrane and in vitro studies, Colloid. Surface. B., 2016, 147, 106-115. * equal contribution authorship

  • Baranyai, Zs., Krátký, M., Vinšová, J., Szabó, N., Senoner, Zs., Horváti, K., Stolaříková J., Dávid, S., Bősze, Sz., Combating highly resistant emerging pathogen Mycobacterium abscessus and Mycobacterium tuberculosis with novel salicylanilide esters and carbamates, Eur. J. Med. Chem., 2015, 101, 692-704.

  • Krátký, M., Bősze, Sz., Baranyai, Zs., Szabó, I., Stolaríková, J., Paraskevopoulos, G., Vinšová, J., Synthesis and in vitro biological evaluation of 2-(phenylcarbamoyl)phenyl 4-substituted benzoates, Bioorg. Med. Chem., 2015, 23, 868-875.

  • Cserép, G.*, Baranyai, Zs.*, Komáromy, D., Horváti, K., Bősze, Sz., Kele, P., Fluorogenic tagging of peptides via Cys residues using thiol-specific vinyl sulfone affinity tags, Tetrahedron, 2014, 70, 5961-5965. * equal contribution authorship

  • Manea, M., Leurs, U., Orbán, E., Baranyai, Zs., Öhlschläger, P., Marquardt, A., Schulcz, Á., Tejeda, M., Kapuvári, B., Tóvári, J., Mező, G., Enhanced enzymatic stability and antitumor activity of daunorubicin-GnRH-III bioconjugates modified in position 4, Bioconjug. Chem., 2011, 22, 1320-1329.

  • Lente, G., Kalmár, J., Baranyai, Zs., Kun, A., Kék, I., Bajusz, D., Takács, M., Veres, L., Fábián, I., One- versus two-electron oxidation with peroxomonosulfate ion: reactions with iron(II), vanadium(IV), halide ions, and photoreaction with cerium(III), Inorg. Chem., 2009, 48, 1763-1773.



Complete list of publications

Selected projects

  • Marie Skłodowska-Curie Actions Individual Fellowship (MSCA-IF ID: 842652, TBNANO)

Membership in scientific bodies/juries

  • Hungarian Chemical Society

  • European Peptide Society

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