Sookmyung Women's University, Department of Biological Sciences, Yongsan-gu, Seoul, Republic of Korea.
Bioorg Med Chem. 2010 Dec 1;18(23):8315-23. doi: 10.1016/j.bmc.2010.09.068. Epub 2010 Oct 26.
A new series of PPARγ partial agonists, 1,3-diphenyl-1H-pyrazole derivatives, were identified using an improved virtual screening scheme combining ligand-centric and receptor-centric methods. An in vitro assay confirmed the nanomolar binding affinity of 1,3-diphenyl-1H-pyrazole derivatives such as SP3415. We also characterized the competitive antagonism of SP3415 against rosiglitazone at micromolar concentrations. They showed a PPARγ partial agonistic activity similar to that of a known PPARγ drug, pioglitazone, in a cell-based transactivation assay. Furthermore, the structure-activity relationships of the pyrazole derivatives were investigated through comparative molecular field analysis and binding mode analysis, which provided new insight concerning their partial agonistic effect on PPARγ.
采用改进的配体中心和受体中心相结合的虚拟筛选方案,发现了一系列新的 PPARγ 部分激动剂 1,3-二苯基-1H-吡唑衍生物。体外测定证实了 1,3-二苯基-1H-吡唑衍生物如 SP3415 的纳摩尔结合亲和力。我们还在微摩尔浓度下对 SP3415 与罗格列酮的竞争性拮抗作用进行了表征。在基于细胞的转激活测定中,它们表现出与已知的 PPARγ 药物吡格列酮相似的 PPARγ 部分激动活性。此外,通过比较分子场分析和结合模式分析研究了吡唑衍生物的结构-活性关系,为其对 PPARγ 的部分激动作用提供了新的见解。