1.
JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY 31 : 4 pp. 574-579. , 6 p. (2016)
Közlemény:2939481 Egyeztetett Forrás Idéző Folyóiratcikk (Szakcikk ) Nyilvános idézők összesen: 18 Független: 3 Függő: 15 Idézett közlemények száma: 14
Folyóiratcikk/Szakcikk (Folyóiratcikk)/Tudományos[2939481] [Érvényesített]
Független idéző: 3, Függő idéző: 15, Nem vizsgált idéző: 0, Összes idéző: 18
  1. * Bacsa I et al. Synthesis of A-ring halogenated 13alpha-estrone derivatives as potential 17beta-HSD1 inhibitors. (2015) STEROIDS 0039-128X 1878-5867 104 230-236
  2. * Herman BE et al. Comparative investigation of the in vitro inhibitory potencies of 13-epimeric estrones and D-secoestrones towards 17β-hydroxysteroid dehydrogenase type 1. (2016) JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY 1475-6366 31 Suppl. 3 61-69
  3. * Klisurić OR et al. Structural analysis and biomedical potential of novel salicyloyloxy estrane derivatives synthesized by microwave irradiation. (2016) STRUCTURAL CHEMISTRY 1040-0400 1572-9001 27 947-960
  4. * Brigitta Bodnár et al. Synthesis and biological evaluation of triazolyl 13α-estrone–nucleoside bioconjugates. (2016) MOLECULES 1420-3049 1420-3049 21 9
  5. * Szabo J et al. Synthesis and in Vitro Antiproliferative Evaluation of C-13 Epimers of Triazolyl-d-Secoestrone Alcohols: The First Potent 13α-D-Secoestrone Derivative. (2016) MOLECULES 1420-3049 1420-3049 21 5
  6. * Zóka Johanna. Biológiailag aktív konjugátumok szintézise módosított ösztrán vázon. (2017)
  7. Xie Tian-Peng et al. Structural Modification for Antitumor Nitrogenous Steroids. (2017) CHINESE JOURNAL OF STRUCTURAL CHEMISTRY 0254-5861 36 12 2007-2019
  8. * Brigitta Bodnár et al. Synthesis and in vitro investigation of potential antiproliferative monosaccharide-D-secoestrone bioconjugates. (2017) BIOORGANIC & MEDICINAL CHEMISTRY LETTERS 0960-894X 1464-3405 27 9 1938-1942
  9. * Bacsa I et al. Synthesis of novel 13 alpha-estrone derivatives by Sonogashira coupling as potential 17 beta-HSD1 inhibitors. (2017) BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY 1860-5397 13 1303-1309
  10. Amr AE-GE et al. In vitro and in vivo anti-breast cancer activities of some synthesized pyrazolinyl-estran-17-one candidates. (2018) MOLECULES 1420-3049 23 7
  11. * Bacsa Ildikó. Ösztrán vázas vegyületek A- és D-gyűrűben történő módosítása. (2018)
  12. * Minorics R et al. Steroidal anticancer agents: an overview of estradiol-related compounds. (2018) ANTI-CANCER AGENTS IN MEDICINAL CHEMISTRY 1871-5206 1875-5992 18 5 652-666
  13. * Bacsa Ildikó et al. Synthesis and structure–activity relationships of 2- and/or 4-halogenated 13β- and 13α-estrone derivatives as enzyme inhibitors of estrogen biosynthesis. (2018) JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY 1475-6366 33 1 1271-1282
  14. * Bodnár Brigitta. Synthesis of monosaccharide and nucleoside conjugates of estrone derivatives. (2018)
  15. * Bacsa I et al. Synthesis of Novel C-2-or C-15-Labeled BODIPY-Estrone Conjugates. (2018) MOLECULES 1420-3049 1420-3049 23 4
  16. El-Naggar Mohamed et al. Potent Anti-Ovarian Cancer with Inhibitor Activities on Both Topoisomerase II and V600EBRAF of Synthesized Substituted Estrone Candidates. (2019) MOLECULES 1420-3049 24 11 p. 2054
  17. * Herman Bianka Edina et al. Synthesis of substituted 15β-alkoxy estrone derivatives and their cofactor-dependent inhibitory effect on 17β-HSD1. (2019) JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY 1475-6366 34 1 1271-1286
  18. * Herman Bianka Edina et al. Steroidal ferrocenes as potential enzyme inhibitors of the estrogen biosynthesis. (2020) BIOLOGIA FUTURA 2676-8615 2676-8607
2020-10-23 13:42