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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
Highly Cited
2004
Highly Cited
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
Highly Cited
1998
Highly Cited
1998
The in vivo interaction of estrogen receptor (ER) and Hsp90, demonstrated in the absence of hormone by a nuclear cotranslocation… Expand
Highly Cited
1998
Highly Cited
1998
This work tested the hypothesis that gonadal steroid receptor activation was necessary for the restoration of several sociosexual… Expand
1997
1997
The purpose of this study was to determine if injections of the 11ß‐substituted steroidal antioestrogen, RU 58668, would block… Expand
1996
1996
Previous studies with the pure antiestrogen RU 58668 showed that this compound proved to be highly antiproliferative in vitro… Expand
1995
1995
The recently described pure antiestrogen RU 58668 displayed potent antiproliferative activities in vitro on several ER+ human… Expand
Highly Cited
1994
Highly Cited
1994
RU 58,668, a new steroidal antiestrogen, has been synthesized. Its in vitro and in vivo pharmacological activities have been… Expand