
Journal of Medicinal Chemistry p. 883 - 887 (2009)
Update date:2022-07-29
Topics:
Agouridas, Vangelis
Magnier, Emmanuel
Blazejewski, Jean-Claude
La?os, Ioanna
Cleeren, Anny
Nonclercq, Denis
Laurent, Guy
Leclercq, Guy
We describe the synthesis of an 11/β isomer 3 of the steroidal antiestrogen fulvestrant 2. Partial fluorination of the 11β side chain in 3 leads to 4, which still shows strong antiproliferative activity on MCF-7 cells. However, unlike 2 and 3, compound 4
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