Synthesis of trans-16-triazolyl-13α-methyl-17-estradiol diastereomers and the effects of structural modifications on their in vitro antiproliferative activities
Abstract Novel 16-triazoles in the 13α-estrone series were synthesized via Cu(I)-catalyzed azide–alkyne cycloaddition of the two diastereomeric (on C-16 and on C-17) 16-azido-13α-estra-1,3,5(10)-trien-17-ol 3-benzyl ethers with substituted phenylacetylenes. The new heterocyclic derivatives were eval...
Elmentve itt :
Szerzők: |
Mernyák Erzsébet Kovács Ida Minorics Renáta Sere Péter Czégány Dóra Sinka Izabella Wölfling János Schneider Gyula Újfaludi Zsuzsanna Boros Imre Miklós Ocsovszki Imre Varga Mónika Zupkó István |
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Dokumentumtípus: | Cikk |
Megjelent: |
2015
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Sorozat: | JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY
150 No. 0 |
doi: | 10.1016/j.jsbmb.2015.04.001 |
mtmt: | 2878758 |
Online Access: | http://publicatio.bibl.u-szeged.hu/6931 |
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