Illyés E - 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: illyes e. 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

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: illyes e. 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

3

Discovery of N-[4-(Quinolin-4-yloxy)phenyl]benzenesulfonamides as Novel AXL Kinase Inhibitors.

Szabadkai I, Torka R, Garamvölgyi R, Baska F, Gyulavári P, Boros S, Illyés E, Choidas A, Ullrich A, Őrfi L. Szabadkai I, et al. Among authors: illyes e. J Med Chem. 2018 Jul 26;61(14):6277-6292. doi: 10.1021/acs.jmedchem.8b00672. Epub 2018 Jul 9. J Med Chem. 2018. PMID: 29928803

4

Synthesis and characterization of amino acid substituted sunitinib analogues for the treatment of AML.

Nemes Z, Takács-Novák K, Völgyi G, Valko K, Béni S, Horváth Z, Szokol B, Breza N, Dobos J, Szántai-Kis C, Illyés E, Boros S, Kok RJ, Őrfi L. Nemes Z, et al. Among authors: illyes e. Bioorg Med Chem Lett. 2018 Aug 1;28(14):2391-2398. doi: 10.1016/j.bmcl.2018.06.026. Epub 2018 Jun 18. Bioorg Med Chem Lett. 2018. PMID: 29935772

5

Design and synthesis of new imidazo[1,2-a]pyridine and imidazo[1,2-a]pyrazine derivatives with antiproliferative activity against melanoma cells.

Garamvölgyi R, Dobos J, Sipos A, Boros S, Illyés E, Baska F, Kékesi L, Szabadkai I, Szántai-Kis C, Kéri G, Őrfi L. Garamvölgyi R, et al. Among authors: illyes e. Eur J Med Chem. 2016 Jan 27;108:623-643. doi: 10.1016/j.ejmech.2015.12.001. Epub 2015 Dec 12. Eur J Med Chem. 2016. PMID: 26724730

6

Synthesis and Structure-Activity relationship of 1-(5-isoquinolinesulfonyl)piperazine analogues as inhibitors of Mycobacterium tuberculosis IMPDH.

Singh V, Pacitto A, Donini S, Ferraris DM, Boros S, Illyés E, Szokol B, Rizzi M, Blundell TL, Ascher DB, Pato J, Mizrahi V. Singh V, et al. Among authors: illyes e. Eur J Med Chem. 2019 Jul 15;174:309-329. doi: 10.1016/j.ejmech.2019.04.027. Epub 2019 Apr 15. Eur J Med Chem. 2019. PMID: 31055147 Free PMC article.

7

[Pyrido[2,3-b]pyrazines inhibiting both erlotinib-sensitive and erlotinib-resistant cell lines, and their preparation via regioselective condensation reaction].

Kékesi L, Sipos A, Németh G, Dancsó A, Illyés E, Boros S, Breza N, Nemes Z, Hegymegi-Barakonyi B, Pató J, Greff Z, Kéri G, Őrfi L. Kékesi L, et al. Among authors: illyes e. Acta Pharm Hung. 2014;84(3):91-104. Acta Pharm Hung. 2014. PMID: 25470976 Hungarian.

8

Characterization of chemotactic ability of peptides containing N-formyl-methionyl residues in Tetrahymena fMLP as a targeting ligand.

Kohidai L, Török K, Illyés E, Tamási J, Sebestyén F, Láng O, Csaba G, Hudecz F. Kohidai L, et al. Among authors: illyes e. Cell Biol Int. 2003;27(8):695-700. doi: 10.1016/s1065-6995(03)00126-4. Cell Biol Int. 2003. PMID: 12867161

9

Synthesis of oligopeptides with the sequence SXWS and their chemotactic effects on a ciliated protozoan Tetrahymena pyriformis.

Illyés E, Hudecz F, Köhidai L, Láng O, Szabó P, Sebestyén F. Illyés E, et al. J Pept Sci. 2002 Jan;8(1):13-22. doi: 10.1002/psc.363. J Pept Sci. 2002. PMID: 11831559

10

Coloured peptides: synthesis, properties and use in preparation of peptide sub-library kits.

Sebestyén F, Szendrei G, Mák M, Dóda M, Illyés E, Szókán G, Kindla K, Rapp W, Szegö P, Câmpian E, Furka A. Sebestyén F, et al. Among authors: illyes e. J Pept Sci. 1998 Jun;4(4):294-9. doi: 10.1002/(sici)1099-1387(199806)4:4<294::aid-psc147>3.0.co;2-3. J Pept Sci. 1998. PMID: 9680063 Review.

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