Discovering potent inhibitors against c-Met kinase: molecular design, organic synthesis and bioassay

作者：Liang Zhongjie; Ding Xiao; Ai Jing; Kong Xiangqian; Chen Limin; Chen Liang; Luo Cheng^*; Geng Meiyu; Liu Hong; Chen Kaixian; Jiang Hualiang

来源：Organic and Biomolecular Chemistry, 2012, 10(2): 421-430.

DOI：10.1039/c1ob06186k

The receptor tyrosine kinase c-Met is an attractive target for therapeutic treatment of cancers nowadays. The discovery of small molecule inhibitors is of special interest in the blockade of the c-Met kinase pathway. Here, we initiated our study from compound 1a, a novel inhibitor against c-Met kinase. A substructure similarity search against the SPECS database and chemical synthesis methods were performed to obtain a series of pyrazolidine-3,5-dione derivatives. Through the enzyme-based assay against c-Met kinase, 4 compounds (1c, 1e, 1m and 1o) showed potential inhibitory activity, with IC50 values mostly less than 10 mu M. Based on the structure-activity relationship (SAR) and binding mode analysis, a focused combinatorial library was designed by the LD1.0 program. Taking into account ADMET properties and synthesis accessibility, seven candidate compounds (5a-g) were successfully synthesized. The activity of the most potent compounds 5b (IC50 = 0.46 mu M) was 20 fold higher than that of the lead 1a. Taken together, our findings identified the pyrazolidine-3,5-dione derivatives as potent inhibitors against c-Met kinase and demonstrated the efficiency of the strategy in the development of small molecules against c-Met kinase.

• 单位
  中国科学院上海药物研究所