Szokol B - Search Results

1

Discovery and optimization of novel benzothiophene-3-carboxamides as highly potent inhibitors of Aurora kinases A and B.

Gyulavári P, Szokol B, Szabadkai I, Brauswetter D, Bánhegyi P, Varga A, Markó P, Boros S, Illyés E, Szántai-Kis C, Krekó M, Czudor Z, Őrfi L. Gyulavári P, et al. Among authors: szokol b. Bioorg Med Chem Lett. 2018 Oct 15;28(19):3265-3270. doi: 10.1016/j.bmcl.2018.05.064. Epub 2018 Jun 1. Bioorg Med Chem Lett. 2018. PMID: 30143423

2

A novel drug discovery concept for tuberculosis: inhibition of bacterial and host cell signalling.

Székely R, Wáczek F, Szabadkai I, Németh G, Hegymegi-Barakonyi B, Eros D, Szokol B, Pató J, Hafenbradl D, Satchell J, Saint-Joanis B, Cole ST, Orfi L, Klebl BM, Kéri G. Székely R, et al. Among authors: szokol b. Immunol Lett. 2008 Mar 15;116(2):225-31. doi: 10.1016/j.imlet.2007.12.005. Epub 2008 Jan 8. Immunol Lett. 2008. PMID: 18258308

3

A closer look at the structure of sterically stabilized liposomes: a small-angle X-ray scattering study.

Varga Z, Berényi S, Szokol B, Orfi L, Kéri G, Peták I, Hoell A, Bóta A. Varga Z, et al. Among authors: szokol b. J Phys Chem B. 2010 May 27;114(20):6850-4. doi: 10.1021/jp9109207. J Phys Chem B. 2010. PMID: 20429570

4

Development of a cell-selective and intrinsically active multikinase inhibitor bioconjugate.

Harmsen S, Dolman ME, Nemes Z, Lacombe M, Szokol B, Pató J, Kéri G, Orfi L, Storm G, Hennink WE, Kok RJ. Harmsen S, et al. Among authors: szokol b. Bioconjug Chem. 2011 Apr 20;22(4):540-5. doi: 10.1021/bc1005637. Epub 2011 Mar 31. Bioconjug Chem. 2011. PMID: 21443263

5

Developing FGFR4 inhibitors as potential anti-cancer agents via in silico design, supported by in vitro and cell-based testing.

Ho HK, Németh G, Ng YR, Pang E, Szántai-Kis C, Zsákai L, Breza N, Greff Z, Horváth Z, Pató J, Szabadkai I, Szokol B, Baska F, Őrfî L, Ullrich A, Kéri G, Chua BT. Ho HK, et al. Among authors: szokol b. Curr Med Chem. 2013;20(10):1203-17. doi: 10.2174/0929867311320100001. Curr Med Chem. 2013. PMID: 23409720

6

[Developing FGFR inhibitors as potential anti-cancer agents].

Zsákai L, Németh G, Szántai-Kis C, Greff Z, Horváth Z, Szokol B, Baska F, Boon TC, Orfi L, Kéri G. Zsákai L, et al. Among authors: szokol b. Acta Pharm Hung. 2013;83(2):47-56. Acta Pharm Hung. 2013. PMID: 23926649 Hungarian.

7

[Development and biochemical characterization of EGFR/c-Met dual inhibitors].

Szokol B, Gyulavári P, Baska F, Ibolya K, Greff Z, Szántai KC, Zoltán O, Peták I, Axel U, Vantus T, Kéri G, Orfi L. Szokol B, et al. Acta Pharm Hung. 2013;83(4):121-33. Acta Pharm Hung. 2013. PMID: 24575658 Hungarian.

8

Discovery and Biological Evaluation of Novel Dual EGFR/c-Met Inhibitors.

Szokol B, Gyulavári P, Kurkó I, Baska F, Szántai-Kis C, Greff Z, Orfi Z, Peták I, Pénzes K, Torka R, Ullrich A, Orfi L, Vántus T, Kéri G. Szokol B, et al. ACS Med Chem Lett. 2014 Jan 30;5(4):298-303. doi: 10.1021/ml4003309. eCollection 2014 Apr 10. ACS Med Chem Lett. 2014. PMID: 24900830 Free PMC article.

9

Development of a 3D Tissue Culture-Based High-Content Screening Platform That Uses Phenotypic Profiling to Discriminate Selective Inhibitors of Receptor Tyrosine Kinases.

Booij TH, Klop MJ, Yan K, Szántai-Kis C, Szokol B, Orfi L, van de Water B, Keri G, Price LS. Booij TH, et al. Among authors: szokol b. J Biomol Screen. 2016 Oct;21(9):912-22. doi: 10.1177/1087057116657269. Epub 2016 Jul 7. J Biomol Screen. 2016. PMID: 27412535 Free PMC article.

10

Novel compounds with potent CDK9 inhibitory activity for the treatment of myeloma.

Czudor Z, Balogh M, Bánhegyi P, Boros S, Breza N, Dobos J, Fábián M, Horváth Z, Illyés E, Markó P, Sipos A, Szántai-Kis C, Szokol B, Őrfi L. Czudor Z, et al. Among authors: szokol b. Bioorg Med Chem Lett. 2018 Feb 15;28(4):769-773. doi: 10.1016/j.bmcl.2018.01.002. Epub 2018 Jan 2. Bioorg Med Chem Lett. 2018. PMID: 29329658

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