Mernyák E - Search Results

1

Transition metal-catalysed A-ring C-H activations and C(sp²)-C(sp²) couplings in the 13α-oestrone series and in vitro evaluation of antiproliferative properties.

Traj P, Abdolkhaliq AH, Németh A, Dajcs ST, Tömösi F, Lanisnik-Rizner T, Zupkó I, Mernyák E. Traj P, et al. Among authors: mernyak e. J Enzyme Inhib Med Chem. 2021 Dec;36(1):895-902. doi: 10.1080/14756366.2021.1900165. J Enzyme Inhib Med Chem. 2021. PMID: 33771084 Free PMC article.

2

Antiproliferative effect of normal and 13-epi-D-homoestrone and their 3-methyl ethers on human reproductive cancer cell lines.

Minorics R, Bózsity N, Wölfling J, Mernyák E, Schneider G, Márki A, Falkay G, Ocsovszki I, Zupkó I. Minorics R, et al. Among authors: mernyak e. J Steroid Biochem Mol Biol. 2012 Oct;132(1-2):168-75. doi: 10.1016/j.jsbmb.2012.04.009. Epub 2012 May 17. J Steroid Biochem Mol Biol. 2012. PMID: 22609630

3

Synthesis and investigation of the anticancer effects of estrone-16-oxime ethers in vitro.

Berényi Á, Minorics R, Iványi Z, Ocsovszki I, Ducza E, Thole H, Messinger J, Wölfling J, Mótyán G, Mernyák E, Frank É, Schneider G, Zupkó I. Berényi Á, et al. Among authors: mernyak e. Steroids. 2013 Jan;78(1):69-78. doi: 10.1016/j.steroids.2012.10.009. Epub 2012 Nov 2. Steroids. 2013. PMID: 23127813

4

Cycloaddition of steroidal cyclic nitrones to C=N dipolarophiles: stereoselective synthesis and antiproliferative effects of oxadiazolidinones in the estrone series.

Mernyák E, Huber J, Szabó J, Schneider G, Hetényi A, Márk L, Maász G, Berényi Á, Kovács I, Minorics R, Zupkó I, Wölfling J. Mernyák E, et al. Steroids. 2013 Oct;78(10):1021-8. doi: 10.1016/j.steroids.2013.06.009. Epub 2013 Jul 4. Steroids. 2013. PMID: 23831783

5

Syntheses and antiproliferative effects of D-homo- and D-secoestrones.

Mernyák E, Szabó J, Bacsa I, Huber J, Schneider G, Minorics R, Bózsity N, Zupkó I, Varga M, Bikádi Z, Hazai E, Wölfling J. Mernyák E, et al. Steroids. 2014 Sep;87:128-36. doi: 10.1016/j.steroids.2014.05.015. Epub 2014 Jun 10. Steroids. 2014. PMID: 24928727

6

Synthesis and in vitro antiproliferative evaluation of d-secooxime derivatives of 13β- and 13α-estrone.

Mernyák E, Fiser G, Szabó J, Bodnár B, Schneider G, Kovács I, Ocsovszki I, Zupkó I, Wölfling J. Mernyák E, et al. Steroids. 2014 Nov;89:47-55. doi: 10.1016/j.steroids.2014.08.015. Epub 2014 Aug 20. Steroids. 2014. PMID: 25150017

7

Synthesis of novel 17-(5'-iodo)triazolyl-3-methoxyestrane epimers via Cu(I)-catalyzed azide-alkyne cycloadditon, and an evaluation of their cytotoxic activity in vitro.

Schneider G, Görbe T, Mernyák E, Wölfling J, Holczbauer T, Czugler M, Sohár P, Minorics R, Zupkó I. Schneider G, et al. Among authors: mernyak e. Steroids. 2015 Jun;98:153-65. doi: 10.1016/j.steroids.2015.02.018. Epub 2015 Feb 28. Steroids. 2015. PMID: 25732071

8

Synthesis of methoxycarbonylpyrazolylandrostene derivatives, and their potential inhibitory effect on androgen biosynthesis and cell proliferation.

Szabó N, Iványi Z, Szécsi M, Julesz J, Mernyák E, Huber J, Wölfling J, Minorics R, Zupkó I, Schneider G. Szabó N, et al. Among authors: mernyak e. Steroids. 2015 Jun;98:143-52. doi: 10.1016/j.steroids.2015.03.008. Epub 2015 Mar 21. Steroids. 2015. PMID: 25804762

9

Synthesis of trans-16-triazolyl-13α-methyl-17-estradiol diastereomers and the effects of structural modifications on their in vitro antiproliferative activities.

Mernyák E, Kovács I, Minorics R, Sere P, Czégány D, Sinka I, Wölfling J, Schneider G, Újfaludi Z, Boros I, Ocsovszki I, Varga M, Zupkó I. Mernyák E, et al. J Steroid Biochem Mol Biol. 2015 Jun;150:123-34. doi: 10.1016/j.jsbmb.2015.04.001. Epub 2015 Apr 3. J Steroid Biochem Mol Biol. 2015. PMID: 25845933

10

Synthesis of antiproliferative 13α-d-homoestrones via Lewis acid-promoted one-pot Prins-Ritter reactions of d-secosteroidal δ-alkenyl-aldehydes.

Huber J, Wölfling J, Schneider G, Ocsovszki I, Varga M, Zupkó I, Mernyák E. Huber J, et al. Among authors: mernyak e. Steroids. 2015 Oct;102:76-84. doi: 10.1016/j.steroids.2015.07.004. Epub 2015 Jul 22. Steroids. 2015. PMID: 26210211

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