Discovery and optimization of selective inhibitors of protein arginine methyltransferase 5 by docking-based virtual screening. Issue 17 (11th April 2017)

• Record Type: Journal Article
• Authors: Ye, Yan; Zhang, Bidong; Mao, Ruifeng; Zhang, Chenhua; Wang, Yulan; Xing, Jing; Liu, Yu-Chih; Luo, Xiaomin; Ding, Hong; Yang, Yaxi; Zhou, Bing; Jiang, Hualiang; Chen, Kaixian; Luo, Cheng; Zheng, Mingyue
• Is Part Of: Organic & biomolecular chemistry. Volume 15:Issue 17(2017)
• Page Start: 3648
• Page End: 3661
• Publication Date: 2017-04-11
• Subjects: Chemistry, Organic -- Periodicals; Bioorganic chemistry -- Periodicals; Chemistry, Physical organic -- Periodicals; 547
• DOI: 10.1039/c7ob00070g
• Languages: English
• ISSNs: 1477-0520

Abstract

Abstract : A series of highly selective and potent inhibitors against PRMT5 have been achieved using virtual screening and medicinal chemistry approaches. Abstract : Protein arginine methyltransferase 5 (PRMT5) is a type II PRMT enzyme critical for diverse cellular processes and different types of cancers. Many efforts have been made to discover novel scaffold PRMT5 inhibitors. Herein, we report the discovery of DC_P33 as a hit compound of PRMT5 inhibitor, identified by molecular docking based virtual screening and 3 H-labeled radioactive methylation assays. Structure–activity relationship (SAR) analysis was performed on the analogs of DC_P33 and then structural modifications were done to improve its activity. Among the derivatives, the compoundDC_C01 displayed an IC50 value of 2.8 μM, and good selectivity toward PRMT1, EZH2 and DNMT3A. Moreover, DC_C01 exhibited anti-proliferation activities against Z-138, Maver-1, and Jeko-1 cancer cells with EC50 values of 12 μM, 12 μM, and 10.5 μM, respectively. Taken together, these results contribute to the development of specific inhibitors against PRMT5 and cancer therapy.