作者:Alan T. Johnson、Liming Wang、Samuel J. Gillett、Roshantha A.S. Chandraratna
DOI:10.1016/s0960-894x(99)00047-5
日期:1999.2
A series of high affinity retinoic acid receptor (RAR) antagonists were prepared based upon the known antagonist AGN 193109 (2). Introduction of various phenyl groups revealed a preference for substitution at the para-position relative to the meta-site. Antagonists with the highest affinities for the RARs possessed hydrophobic groups, however, the presence of polar functionality was also well tolerated. (C) 1999 Elsevier Science Ltd. All rights reserved.