Tudóstér: Szűcs Zsolt publikációi

Szűcs, Z., Bereczki, I., Fenyvesi, F., Herczegh, P., Ostorházi, E., Borbás, A.: Synthesis of an amphiphilic vancomycin aglycone derivative inspired by polymyxins: overcoming glycopeptide resistance in Gram-positive and Gram-negative bacteria in synergy with teicoplanin in vitro.
Sci. Rep. 12 (1), 1-14, 2022.

Bereczki, I., Szűcs, Z., Batta, G., Nagy, T., Ostorházi, E., Kövér, K., Borbás, A., Herczegh, P.: The First Dimeric Derivatives of the Glycopeptide Antibiotic Teicoplanin.
Pharmaceuticals (Basel). 15 (1), 1-17, 2022.

Vimberg, V., Zieglerova, L., Mazumdar, A., Szűcs, Z., Borbás, A., Herczegh, P., Balikova Novotna, G.: Two Novel Semisynthetic Lipoglycopeptides Active against Staphylococcus aureus Biofilms and Cells in Late Stationary Growth Phase.
Pharmaceuticals (Basel). 14 (11), 1-12, 2021.

Szűcs, Z., Bereczki, I., Rőth, E., Milánkovits, M., Ostorházi, E., Batta, G., Nagy, L., Dombrádi, Z., Borbás, A., Herczegh, P.: N-Terminal guanidine derivatives of teicoplanin antibiotics strongly active against glycopeptide resistant Enterococcus faecium.
J. Antibiot. 73 (9), 603-614, 2020.

Szűcs, Z., Naesens, L., Stevaert, A., Ostorházi, E., Batta, G., Herczegh, P., Borbás, A.: Reprogramming of the Antibacterial Drug Vancomycin Results in Potent Antiviral Agents Devoid of Antibacterial Activity.
Pharmaceuticals (Basel). 13 (7), 1-15, 2020.

Bereczki, I., Csávás, M., Szűcs, Z., Rőth, E., Batta, G., Ostorházi, E., Naesens, L., Borbás, A., Herczegh, P.: Synthesis of Antiviral Perfluoroalkyl Derivatives of Teicoplanin and Vancomycin.
ChemMedChem. 15 (17), 1661-1671, 2020.

Szűcs, Z., Ostorházi, E., Kicsák, M., Nagy, L., Borbás, A., Herczegh, P.: New semisynthetic teicoplanin derivatives have comparable in vitro activity to that of oritavancin against clinical isolates of VRE.
J. Antibiot. 72 (7), 524-534, 2019.

Tevyashova, A., Bychkova, E., Korolev, A., Isakova, E., Mirchink, E., Osterman, I., Erdei, R., Szűcs, Z., Batta, G.: Synthesis and evaluation of biological activity for dual-acting antibiotics on the basis of azithromycin and glycopeptides.
Bioorg. Med. Chem. Lett. 29 (2), 276-280, 2019.

Vimberg, V., Gazak, R., Szűcs, Z., Borbás, A., Herczegh, P., Cavanagh, J., Zieglerova, L., Závora, J., Adámková, V., Balikova Novotna, G.: Fluorescence assay to predict activity of the glycopeptide antibiotics.
J. Antibiot. 72 (2), 114-117, 2018.

Szűcs, Z., Kelemen, V., Le Thai, S., Csávás, M., Rőth, E., Batta, G., Stevaert, A., Vanderlinden, E., Naesens, L., Herczegh, P., Borbás, A.: Structure-activity relationship studies of lipophilic teicoplanin pseudoaglycon derivatives as new anti-influenza virus agents.
Eur. J. Med. Chem. 157 1017-1030, 2018.

Szűcs, Z., Bereczki, I., Csávás, M., Rőth, E., Borbás, A., Batta, G., Ostorházi, E., Szatmári, R., Herczegh, P.: Lipophilic teicoplanin pseudoaglycon derivatives are active against vancomycin- and teicoplanin-resistant enterococci.
J. Antibiot. 70 (5), 664-670, 2017.

Szűcs, Z., Csávás, M., Rőth, E., Borbás, A., Batta, G., Perret, F., Ostorházi, E., Szatmári, R., Vanderlinden, E., Naesens, L., Herczegh, P.: Synthesis and biological evaluation of lipophilic teicoplanin pseudoaglycon derivatives containing a substituted triazole function.
J. Antibiot. 70 (2), 152-157, 2017.

Csávás, M., Miskovics, A., Szűcs, Z., Rőth, E., Nagy, Z., Bereczki, I., Herczeg, M., Batta, G., Nemes-Nikodém, É., Ostorházi, E., Rozgonyi, F., Borbás, A., Herczegh, P.: Synthesis and antibacterial evaluation of some teicoplanin pseudoaglycon derivatives containing alkyl- and arylthiosubstituted maleimides.
J. Antibiot. 68 (9), 579-585, 2015.