Discovery of a New Class of Liver Receptor Homolog-1 (LRH-1) Antagonists: Virtual Screening, Synthesis and Biological Evaluation
作者:Jullien Rey、Haipeng Hu、Fiona Kyle、Chun-Fui Lai、Laki Buluwela、R. Charles Coombes、Eric A. Ortlund、Simak Ali、James P. Snyder、Anthony G. M. Barrett
DOI:10.1002/cmdc.201200307
日期:2012.11
Targeting LRH‐1: Virtual screening and molecular modeling were used to identify novel antagonists of liver receptor homolog‐1 (LRH‐1), an emerging therapeutic target for breast cancer. Hit compounds were synthesized and biologically assayed, and the preliminary results suggest that raloxifene‐based analogues, substituted at the position C‐7 of the benzothiophene ring, might generate an inactive protein
靶向 LRH-1:使用虚拟筛选和分子建模来确定肝受体同源物 1 (LRH-1) 的新型拮抗剂,这是一种新兴的乳腺癌治疗靶点。合成命中化合物并进行生物学分析,初步结果表明,在苯并噻吩环的 C-7 位取代的基于雷洛昔芬的类似物可能通过结合产生无活性的蛋白质构象,从而拮抗这种核受体。