These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

127 related articles for article (PubMed ID: 26210211)

  • 1. 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
    Steroids; 2015 Oct; 102():76-84. PubMed ID: 26210211
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    Steroids; 2014 Nov; 89():47-55. PubMed ID: 25150017
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Synthesis and biological evaluation of 13α-estrone derivatives as potential antiproliferative agents.
    Szabó J; Pataki Z; Wölfling J; Schneider G; Bózsity N; Minorics R; Zupkó I; Mernyák E
    Steroids; 2016 Sep; 113():14-21. PubMed ID: 27263437
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    J Steroid Biochem Mol Biol; 2015 Jun; 150():123-34. PubMed ID: 25845933
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Stereoselective synthesis of the four 16-hydroxymethyl-3-methoxy- and 16-hydroxymethyl-3-benzyloxy-13α-estra-1,3,5(10)-trien-17-ol isomers and their antiproliferative activities.
    Kiss A; Mernyák E; Wölfling J; Sinka I; Zupkó I; Schneider G
    Steroids; 2018 Jun; 134():67-77. PubMed ID: 29501755
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Synthesis of Estrone Heterodimers and Evaluation of Their In Vitro Antiproliferative Activity.
    Bózsity N; Nagy V; Szabó J; Pálházi B; Kele Z; Resch V; Paragi G; Zupkó I; Minorics R; Mernyák E
    Int J Mol Sci; 2024 Apr; 25(8):. PubMed ID: 38673860
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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
    Steroids; 2014 Sep; 87():128-36. PubMed ID: 24928727
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Synthesis and in vitro pharmacological evaluation of N-[(1-benzyl-1,2,3-triazol-4-yl)methyl]-carboxamides on d-secoestrone scaffolds.
    Szabó J; Bacsa I; Wölfling J; Schneider G; Zupkó I; Varga M; Herman BE; Kalmár L; Szécsi M; Mernyák E
    J Enzyme Inhib Med Chem; 2016 Aug; 31(4):574-9. PubMed ID: 26360618
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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
    J Steroid Biochem Mol Biol; 2012 Oct; 132(1-2):168-75. PubMed ID: 22609630
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Synthesis and Antiproliferative Activity of Steroidal Diaryl Ethers.
    Kovács É; Ali H; Minorics R; Traj P; Resch V; Paragi G; Bruszel B; Zupkó I; Mernyák E
    Molecules; 2023 Jan; 28(3):. PubMed ID: 36770863
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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
    Steroids; 2013 Oct; 78(10):1021-8. PubMed ID: 23831783
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Synthesis and in Vitro Antiproliferative Evaluation of C-13 Epimers of Triazolyl-d-Secoestrone Alcohols: The First Potent 13α-d-Secoestrone Derivative.
    Szabó J; Jerkovics N; Schneider G; Wölfling J; Bózsity N; Minorics R; Zupkó I; Mernyák E
    Molecules; 2016 May; 21(5):. PubMed ID: 27187336
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Synthesis and Biological Evaluation of Triazolyl 13α-Estrone-Nucleoside Bioconjugates.
    Bodnár B; Mernyák E; Wölfling J; Schneider G; Herman BE; Szécsi M; Sinka I; Zupkó I; Kupihár Z; Kovács L
    Molecules; 2016 Sep; 21(9):. PubMed ID: 27626395
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Novel preparation of substituted oxazolines condensed to d-ring of estrane skeleton and characterization of their antiproliferative properties.
    Kiss A; Jójárt R; Mernyák E; Bartha S; Minorics R; Zupkó I; Schneider G
    Steroids; 2021 Dec; 176():108911. PubMed ID: 34499930
    [TBL] [Abstract][Full Text] [Related]  

  • 15. One-pot synthesis and antiproliferative activity of novel 2,4-diaminopyrimidine derivatives bearing piperidine and piperazine moieties.
    Ma WF; Yang HK; Hu MJ; Li Q; Ma TZ; Zhou ZZ; Liu RY; You WW; Zhao PL
    Eur J Med Chem; 2014 Sep; 84():127-34. PubMed ID: 25016234
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A click approach to novel D-ring-substituted 16α-triazolylestrone derivatives and characterization of their antiproliferative properties.
    Molnár J; Frank É; Minorics R; Kádár Z; Ocsovszki I; Schönecker B; Wölfling J; Zupkó I
    PLoS One; 2015; 10(2):e0118104. PubMed ID: 25692552
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Stereoselective synthesis of new type of estradiol hybrid molecules and their antiproliferative activities.
    Kiss A; Wölfling J; Mernyák E; Frank É; Gyovai A; Kulmány Á; Zupkó I; Schneider G
    Steroids; 2019 Aug; 148():63-72. PubMed ID: 31085213
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Synthesis and biological evaluation of novel pyrano[3,2-c]carbazole derivatives as anti-tumor agents inducing apoptosis via tubulin polymerization inhibition.
    Padmaja P; Koteswara Rao G; Indrasena A; Subba Reddy BV; Patel N; Shaik AB; Reddy N; Dubey PK; Bhadra MP
    Org Biomol Chem; 2015 Feb; 13(5):1404-14. PubMed ID: 25467166
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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
    Steroids; 2015 Jun; 98():143-52. PubMed ID: 25804762
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Novel 13β- and 13α-D-homo steroids: 17a-carboxamido-D-homoestra-1,3,5(10),17-tetraene derivatives via palladium-catalyzed aminocarbonylations.
    Takács A; Acs P; Berente Z; Wölfling J; Schneider G; Kollár L
    Steroids; 2010 Dec; 75(13-14):1075-81. PubMed ID: 20633571
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.