Structure–activity relationships of SERMs optimized for uterine antagonism and ovarian safety
摘要:
Structure-activity relationship studies are described, which led to the discovery of novel selective estrogen receptor modulators (SERMs) for the potential treatment of uterine fibroids. The SAR studies focused on limiting brain exposure and were guided by computational properties. Compounds with limited impact on the HPO axis were selected using serum estrogen levels as a biomarker for ovarian stimulation. (c) 2007 Elsevier Ltd. All rights reserved.
Structure–activity relationships of SERMs optimized for uterine antagonism and ovarian safety
摘要:
Structure-activity relationship studies are described, which led to the discovery of novel selective estrogen receptor modulators (SERMs) for the potential treatment of uterine fibroids. The SAR studies focused on limiting brain exposure and were guided by computational properties. Compounds with limited impact on the HPO axis were selected using serum estrogen levels as a biomarker for ovarian stimulation. (c) 2007 Elsevier Ltd. All rights reserved.
Selective estrogen receptor modulators containing a phenylsulfonyl group
申请人:Eli Lilly & Company
公开号:EP1782810A2
公开(公告)日:2007-05-09
The present invention relates to a selective estrogen receptor modulator of formula I:
or a pharmaceutical acid addition salt thereof; useful, e.g., for treating endometriosis and/or uterine leiomyoma/leiomyomata.
本发明涉及一种式 I 的选择性雌激素受体调节剂:
或其药用酸加成盐;可用于治疗子宫内膜异位症和/或子宫白肌瘤/卵巢白肌瘤。