Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1370343 | Bioorganic & Medicinal Chemistry Letters | 2013 | 4 Pages |
Abstract
The design and synthesis of 11 fluorinated derivatives of tamoxifen are described. Growth inhibition values (GI50) on human HT-29, M21, MCF7, and MDA-MB-231 tumor cells are also reported. In general, the GI50 values are similar or slightly higher than tamoxifen with the most active compound on MCF7 cell line having a GI50 = 3.6 μM. Surprisingly, as opposed to tamoxifen, both geometrical isomers behave similarly. We hypothesize that this behavior is due to in vitro isomerization of the compounds.
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Related Topics
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Organic Chemistry
Authors
Bianca Malo-Forest, Grégory Landelle, Jessye-Ann Roy, Jacques Lacroix, René C. Gaudreault, Jean-François Paquin,