F Hoffmann-La Roche AG, Grenzacherstrasse, CH-4070 Basel, Switzerland.
Bioorg Med Chem Lett. 2011 Jan 1;21(1):191-4. doi: 10.1016/j.bmcl.2010.11.039. Epub 2010 Nov 12.
Herein we describe the synthesis and structure activity relationship of a new class of FXR agonists identified from a high-throughput screening campaign. Further optimization of the original hits led to molecules that were highly active in an LDL-receptor KO model for dyslipidemia. The most promising candidate is discussed in more detail.
在此,我们描述了一类新型 FXR 激动剂的合成和构效关系,该激动剂是从高通量筛选活动中鉴定出来的。对原始命中化合物的进一步优化导致了在 LDL 受体 KO 血脂异常模型中具有高活性的分子。最有前途的候选物将进行更详细的讨论。