1.
Bacsa, I ; Jojart, R ; Wolfling, J ; Schneider, G ; Herman, BE ; Szecsi, M ; Mernyak, E ✉
Synthesis of novel 13 alpha-estrone derivatives by Sonogashira coupling as potential 17 beta-HSD1 inhibitors
BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY 13 pp. 1303-1309. , 7 p. (2017)
DOI WoS Scopus PubMed SZTE Publicatio
Közlemény:3251236 Egyeztetett Forrás Idéző Folyóiratcikk (Szakcikk ) Tudományos
Nyilvános idéző összesen: 8 | Független: 3 | Függő: 5 | Nem jelölt: 0 | WoS jelölt: 8 | Scopus jelölt: 7 | DOI jelölt: 8
Folyóiratcikk/Szakcikk (Folyóiratcikk)/Tudományos[3251236] [Egyeztetett]
Nyilvános idéző összesen: 8, Független: 3, Függő: 5, Nem jelölt: 0
  1. Dewan Anindita et al. Greener Biogenic Approach for the Synthesis of Palladium Nanoparticles Using Papaya Peel: An Eco-Friendly Catalyst for C-C Coupling Reaction. (2018) ACS OMEGA 2470-1343 3 5 5327-5335
  2. 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 1420-3049 23 7
  3. * Jójárt R. et al. Pd-Catalyzed microwave-assisted synthesis of phosphonated 13α-estrones as potential OATP2B1, 17β-HSD1 and/or STS inhibitors. (2018) BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY 1860-5397 14 2838-2845
  4. * Bacsa I et al. Synthesis of Novel C-2-or C-15-Labeled BODIPY-Estrone Conjugates. (2018) MOLECULES 1420-3049 1420-3049 23 4
  5. * Ildikó Bacsa et al. The first Pd-catalyzed Buchwald-Hartwig aminations at C-2 or C-4 in the estrone series. (2018) BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY 1860-5397 14 998-1003
  6. * Laczkó-Rigó Réka et al. Structural dissection of 13-epiestrones based on the interaction with human Organic anion-transporting polypeptide, OATP2B1.. (2020) JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY 0960-0760 1879-1220 200
  7. * Nagymihály Zoltán et al. Synthesis of 2‐Methylresorcinol‐Based Deepened Cavitands with Chiral Inlet Bearing Steroidal Moieties on the Upper Rim. (2020) CHEMISTRYSELECT 2365-6549 5 23 6933-6938
  8. Cheng Yating et al. The Curcumin Derivative, H10, Suppresses Hormone-Dependent Prostate Cancer by Inhibiting 17 beta-Hydroxysteroid Dehydrogenase Type 3. (2020) FRONTIERS IN PHARMACOLOGY 1663-9812 11
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