Design, synthesis and structure–activity relationship of novel RXR-selective modulators
摘要:
The synthesis and in vitro characterization of novel RXR-selective ligands possessing various substituted 1-benzofuran or 1-benzothiophene moieties are described. (C) 2004 Elsevier Ltd. All rights reserved.
Design, synthesis and structure–activity relationship of novel RXR-selective modulators
摘要:
The synthesis and in vitro characterization of novel RXR-selective ligands possessing various substituted 1-benzofuran or 1-benzothiophene moieties are described. (C) 2004 Elsevier Ltd. All rights reserved.
The present invention is directed to compounds represented by Structural Formula (I) and pharmaceutically acceptable salts, solvates and hydrates thereof: (I). The invention is also directed to pharmaceutical compositions, methods of use and methods of making compounds represented by Structural Formula (I) and pharmaceutically acceptable salts, solvates and hydrates thereof.
The present invention is directed to compounds represented by Structural Formula (I) and pharmaceutically acceptable salts, solvates and hydrates thereof: (I). The invention is also directed to pharmaceutical compositions, methods of use and methods of making compounds represented by Structural Formula (I) and pharmaceutically acceptable salts, solvates and hydrates thereof.
Design, synthesis and structure–activity relationship of novel RXR-selective modulators
作者:Pierre-Yves Michellys、Jennifer D'Arrigo、Timothy A. Grese、Donald S. Karanewsky、Mark D. Leibowitz、Dale A. Mais、Christopher M. Mapes、Anne Reifel-Miller、Deepa Rungta、Marcus F. Boehm
DOI:10.1016/j.bmcl.2003.12.089
日期:2004.3
The synthesis and in vitro characterization of novel RXR-selective ligands possessing various substituted 1-benzofuran or 1-benzothiophene moieties are described. (C) 2004 Elsevier Ltd. All rights reserved.