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RU 58668

Known as: RU 58 668, RU-58668 
 
National Institutes of Health

Papers overview

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2011
2011
AbstractThe roots of licorice (Glycyrrhiza glabra) are a rich source of flavonoids, in particular, prenylated flavonoids, such as… Expand
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2006
2006
In most of multiple myeloma (MM) cells, the "pure" antiestrogen (AE) RU 58668 (RU) induced either a G1-arrest (LP-1, OPM-2, NCI… Expand
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2006
2006
Previous studies have shown that 17beta-estradiol (E2) induces antidepressant-like actions per se and potentiates those produced… Expand
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2004
2004
AbstractPurpose. The pure antiestrogen RU58668 (RU) was encapsulated within nanospheres (NS) and nanocapsules (NC) prepared from… Expand
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Highly Cited
2003
Highly Cited
2003
Estrogen receptor-alpha (ER) is down-regulated in the presence of its cognate ligand, estradiol (E2), as well as in the presence… Expand
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1998
1998
The in vivo interaction of estrogen receptor (ER) and Hsp90, demonstrated in the absence of hormone by a nuclear cotranslocation… Expand
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1998
1998
This work tested the hypothesis that gonadal steroid receptor activation was necessary for the restoration of several sociosexual… Expand
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1997
1997
The purpose of this study was to determine if injections of the 11 beta-substituted steroidal antioestrogen, RU 58668, would… Expand
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1996
1996
Previous studies with the pure antiestrogen RU 58668 showed that this compound proved to be highly antiproliferative in vitro… Expand
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1994
1994
RU 58,668, a new steroidal antiestrogen, has been synthesized. Its in vitro and in vivo pharmacological activities have been… Expand
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