Publications


Scientific publication by Targetex:
Bereczki, I., Vimberg, V., Lőrincz, E., Papp, H., Nagy, L., Kéki, S., Batta, G., Mitrović, A., Kos, J., Zsigmond, Á., Hajdú, I., Lőrincz, Z., Bajusz, D., Petri, L., Hodek, J., Jakab, F., Keserű, G M., Weber, J., Naesens, L., Herczegh, P., Borbás, A. (2022)
Semisynthetic teicoplanin derivatives with dual antimicrobial activity against SARS-CoV-2 and multiresistant bacteria.
Sci. Rep. 2022 12(1), p.16001 IF = 4.379
https://www.nature.com/articles/s41598-022-20182-y
Stern N, Gacs A, Tátrai E, Flachner B, Hajdú I, Dobi K, Bágyi I, Dormán G, Lőrincz Z, Cseh S, Kígyós A, Tóvári J, Goldblum A. (2022)
Dual Inhibitors of AChE and BACE-1 for Reducing Aβ in Alzheimerʼs Disease: From In Silico to In Vivo
Int. J. Mol. Sci. 2022 23(22), p.13908 IF = 6.208
https://www.mdpi.com/1422-0067/23/21/13098
Flachner B, Dobi K, Benedek A, Cseh S, Lőrincz Z, Hajdú I (2022)
Robust Recombinant Expression of Human Placental Ribonuclease Inhibitor in Insect Cells.
Biomolecules 2022 12(2), p.273 IF = 6.064
https://www.mdpi.com/2218-273X/12/2/273
Pape VF, Palkó R, Tóth S, Szabó MJ, Sessler J, Dormán G, Enyedy EA, Soós T, Szatmári I, Szakács G.(2022)
Structure–Activity Relationships of 8-Hydroxyquinoline-Derived Mannich Bases with Tertiary Amines Targeting Multidrug-Resistant Cancer.
J. Med. Chem. 2022 May 25. IF = 7.446
https://pubs.acs.org/doi/full/10.1021/acs.jmedchem.2c00076
Bereczki I, Papp H, Kuczmog A, Madai M, Nagy V, Agócs A, Batta G, Milánkovits M, Ostorházi E, Mitrović A, Kos J, Zsigmond Á, Hajdú I, Lőrincz Z, Bajusz D, Keserű GM, Hodek J, Weber J, Jakab F, Herczegh P, Borbás A. (2021)
Natural Apocarotenoids and Their Synthetic Glycopeptide Conjugates Inhibit SARS-CoV-2 Replication
Pharmaceuticals, 14(11), 1111. IF = 5.83
https://www.mdpi.com/1424-8247/14/11/1111
Szilágyi K, Flachner B, Hajdú I, Szaszkó M, Dobi K, Lőrincz Z, Cseh S, Dormán G. (2021)
Rapid Identification of Potential Drug Candidates from Multi-Million Compounds’ Repositories. Combination of 2D Similarity Search with 3D Ligand/Structure Based Methods and In Vitro Screening.
Molecules. 26:E5593 IF: 4,41
https://www.mdpi.com/1420-3049/26/18/5593
Dormán G, Flachner B, Hajdú I, András C. (2021)
Target identification and polypharmacology of nutraceuticals.
In: Nutraceuticals: Efficacy, Safety and Toxicity (Ed. R. Gupta, A. Lall, R. Srivastava), Academic Press, pp. 315-343.
https://www.sciencedirect.com/science/article/pii/B9780128210383000239
Gömöri K, Szabados T, Kenyeres É, Pipis J, Földesi I, Siska A, Dormán G, Ferdinandy P, Görbe A, Bencsik P. (2020)
Cardioprotective Effect of Novel Matrix Metalloproteinase Inhibitors.
Int. J. Mol. Sci. 21, 6990. IF=5.923
https://www.mdpi.com/1422-0067/21/19/6990
Szilágyi K, Hajdú I, Flachner B, Lőrincz Z, Balczer J, Gál P, Závodszky P, Pirli C, Balogh B, Mándity IM, Cseh S, Dormán G. (2019)
Design and Selection of Novel C1s Inhibitors by In Silico and In Vitro Approaches.
Molecules. 24:E3641 IF: 3,267
https://www.mdpi.com/1420-3049/24/20/3641
Hajdú I, Kardos J, Major B, Fabó G, Lőrincz Z, Cseh S, Dormán G. (2018)
Inhibition of the LOX enzyme family members with old and new ligands. Selectivity analysis revisited.
Bioorg Med Chem Lett. 28, 3113-3118. IF: 2,448
https://www.sciencedirect.com/science/article/pii/S0960894X18305535
Bencsik P, Kupai K, Görbe A, Kenyeres É, Varga ZV, Pálóczi J, Gáspár R, Kovács L, Weber L, Takács F, Hajdú I, Fabó G, Cseh S, Barna L, Csont T, Csonka C, Dormán G, Ferdinandy P. (2018)
Development of Matrix Metalloproteinase-2 Inhibitors for Cardioprotection.
Front Pharmacol, 9,296 IF: 3,845
https://www.frontiersin.org/articles/10.3389/fphar.2018.00296/full
Szaszkó, M., Hajdú, I., Flachner, B., Dobi, K., Magyar, C., Simon, I., Lőrincz, Z., Kapui, Z., Pázmány, T., Cseh, S., Dormán, G. (2017)
Identification of potential glutaminyl cyclase inhibitors from lead-like libraries by in silico and in vitro fragment-based screening
Molecular Diversity, 21, 175-86. IF:2,229
https://link.springer.com/article/10.1007%2Fs11030-016-9717-4
Dormán G, Nakamura H, Pulsipher A, Prestwich GD. (2016)
The Life of Pi Star: Exploring the Exciting and Forbidden Worlds of the Benzophenone Photophore.
Chem Rev. 116, 15284-15398. IF:47,928
https://pubs.acs.org/doi/10.1021/acs.chemrev.6b00342
Kelemen ÁA, Kiss R, Ferenczy GG, Kovács L, Flachner B, Lőrincz Z, Keserű GM.
Structure-Based Consensus Scoring Scheme for Selecting Class A Aminergic GPCR Fragments. (2016)
J Chem Inf Model. 56, 412-22. IF: 3,760
https://pubs.acs.org/doi/10.1021/acs.jcim.5b00598
Dobi, K., Flachner, B., Pukáncsik, M., Máthé, E., Bognár, M., Szaszkõ, M., Magyar, C., Hajdú, I., Lorincz, Z., Simon, I., Fülöp, F., Cseh, S., Dormán, G. (2015)
Combination of Pharmacophore Matching, 2D Similarity Search, and in Vitro Biological Assays in the Selection of Potential 5-HT6 Antagonists from Large Commercial Repositories
Chemical Biology and Drug Design, 86, 864-80. IF: 2,802
https://onlinelibrary.wiley.com/doi/full/10.1111/cbdd.12563
Dobi, K., Hajdú, I., Flachner, B., Fabó, G., Szaszkó, M., Bognár, M., Magyar, C., Simon, I., Szisz, D., Lõrincz, Z., Cseh, S., Dormán, G. (2014)
Combination of 2D/3D ligand-based similarity search in rapid virtual screening from multimillion compound repositories. Selection and biological evaluation of potential PDE4 and PDE5 inhibitors
Molecules, 19, 7008-39. IF: 2,416
https://www.mdpi.com/1420-3049/19/6/7008
Hajdú, I., Flachner, B., Bognár, M., Végh, B.M., Dobi, K., Lorincz, Z., Lázár, J., Cseh, S., Takács, L., Kurucz, I. (2014)
Monoclonal antibody proteomics: Use of antibody mimotope displaying phages and the relevant synthetic peptides for mAb scouting
Immunology Letters, 160, 172-7. IF: 2,512
https://www.sciencedirect.com/science/article/pii/S0165247814000236
Flachner, B., Tömöri, T., Hajdú, I., Dobi, K., Lorincz, Z., Cseh, S., Dormán, G. (2014)
Rapid in silico selection of an MCHR1 antagonists’ focused library from multi-million compounds’ repositories: Biological evaluation
Medicinal Chemistry Research, 23, 1234-47. IF: 1,402
https://link.springer.com/article/10.1007/s00044-013-0695-0
Flachner B, Lörincz Z, Carotti A, Nicolotti O, Kuchipudi P, Remez N, Sanz F, Tóvári J, Szabó MJ, Bertók B, Cseh S, Mestres J, Dormán G. (2012)
A chemocentric approach to the identification of cancer targets.
PLoS One. 7, e35582 IF:3,730
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0035582
Tömöri T, Hajdú I, Barna L, Lőrincz Z, Cseh S and Dormán G (2012)
Combining 2D and 3D in silico methods for rapid selection of potential PDE5 inhibitors from multimillion compounds’ repositories: biological evaluation.
Mol Divers. 16, 59-72 IF: 2,861
https://link.springer.com/article/10.1007/s11030-011-9335-0
Berta J1, Kenessey I, Dobos J, Tovari J, Klepetko W, Jan Ankersmit H, Hegedus B, Renyi-Vamos F, Varga J, Lorincz Z, Paku S, Ostoros G, Rozsas A, Timar J, Dome B. (2010)
Apelin expression in human non-small cell lung cancer: role in angiogenesis and prognosis.
J Thorac Oncol. 5, 1120-9. IF: 4,040
https://www.sciencedirect.com/science/article/pii/S1556086415305694
Kenessey I, Keszthelyi M, Krámer Z, Berta J, Adám A, Dobos J, Mildner M, Flachner B, Cseh S, Barna G, Szokol B, Orfi L, Kéri G, Döme B, Klepetko W, Tímár J, Tóvári J. (2010)
Inhibition of c-Met with the specific small molecule tyrosine kinase inhibitor SU11274 decreases growth and metastasis formation of experimental human melanoma.
Curr Cancer Drug Targets 10, 332-42 IF:4,771
https://www.eurekaselect.com/69470/article
Kupai K, Szucs G, Cseh S, Hajdu I, Csonka C, Csont T and Ferdinandy P (2010)
Matrix metalloproteinase activity assays: Importance of zymography.
J Pharmacol Toxicol Methods 61, 205-9
https://www.sciencedirect.com/science/article/pii/S1056871910000274
Dormán G, Cseh S, Hajdú I, Barna L, Kónya D, Kupai K, Kovács L and Ferdinandy P (2010)
Matrix metalloproteinase inhibitors: a critical appraisal of design principles and proposed therapeutic utility
Drugs 70, 949-64 IF: 3,738
https://link.springer.com/article/10.2165/11318390-000000000-00000
Vass L1, Kelemen JZ, Fehér LZ, Lorincz Z, Kulin S, Cseh S, Dormán G, Puskás LG. (2009)
Toxicogenomics screening of small molecules using high-density, nanocapillary real-time PCR.
Int J Mol Med. 23, 65-74 IF: 1,980
https://www.spandidos-publications.com/ijmm/23/1/65
Decornez H, Gulyás-Forró A, Papp A, Szabó M, Sármay G, Hajdú I, Cseh S, Dormán G, Kitchen DB. (2009)
Design, selection, and evaluation of a general kinase-focused library.
ChemMedChem. 4,1273-1278. IF:3,150
https://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/cmdc.200900164
Book chapter
Dormán, G., Flachner, B., Hajdú, I., András, C.D.
Target identification and polypharmacology of nutraceuticals
(2016) Nutraceuticals: Efficacy, Safety and Toxicity, pp. 263-286.
https://www.sciencedirect.com/science/article/pii/B9780128021477000218

Publication with Recomgenex affiliation
Molnár L, Keseru GM, Papp A, Lorincz Z, Ambrus G, Darvas F (2006)
A neural network based classification scheme for cytotoxicity predictions:Validation on 30,000 compounds.
Bioorg Med Chem Lett.16, 1037-9. IF: 2,538
https://www.sciencedirect.com/science/article/pii/S0960894X05013752?via%3Dihub
Darvas F, Dormán G, Krajcsi P, Puskás LG, Kovári Z, Lörincz Z, Urge L. (2004)
Recent advances in chemical genomics.
Curr Med Chem. 11, 3119-45. IF: 4,382
https://www.eurekaselect.com/53907/chapter/recent-advances-in-chemical-genomics
Address
TargetEx Ltd.
H-2120 Dunakeszi Madách Imre u 31/2.
Hungary
Zsolt Lőrincz, PhD
Chief Executive Officer
Phone
Tel.: +36-30-352-9529