Advances in the 1-phenanthryl-tetrahydroisoquinoline series of PAK4 inhibitors: potent agents restrain tumor cell growth and invasion. Issue 32 (25th July 2016)

• Record Type: Journal Article
• Authors: Hao, Chenzhou; Li, Xiaodong; Song, Shuai; Guo, Bingyu; Guo, Jing; Zhang, Jian; Zhang, Qiaoling; Huang, Wanxu; Wang, Jian; Lin, Bin; Cheng, Maosheng; Li, Feng; Zhao, Dongmei
• Is Part Of: Organic & biomolecular chemistry. Volume 14:Issue 32(2016)
• Page Start: 7676
• Page End: 7690
• Publication Date: 2016-07-25
• Subjects: Chemistry, Organic -- Periodicals; Bioorganic chemistry -- Periodicals; Chemistry, Physical organic -- Periodicals; 547
• DOI: 10.1039/c6ob01072e
• Languages: English
• ISSNs: 1477-0520

Abstract

Abstract : Discovery of a new class of natural product-inspired PAK4 inhibitors as potent anti-cancer agents. Abstract : A new series of novel 1-phenanthryl-tetrahydroisoquinoline derivatives were designed, synthesized and biologically evaluated for their PAK4 inhibitory activities and anti-proliferative effects against three cancer cell lines A549, MCF-7 and HT-1080. Among them, compound12a exhibited the most potent inhibitory activity against PAK4 with an IC50 value of 0.42 μM. Moreover, this compound inhibited the invasion of A549 tumor cells by regulating the PAK4–LIMK1–cofilin signaling pathway in vitro, and exhibited anti-tumor activity in vivo in the A549 tumor xenograft model. To further evaluate the binding mode of12a with PAK4, the biotinylated12a derivative has been synthesized and it was used for immunoprecipitation assay. Intriguingly, our observations suggest that12a interacts with both the N- and C-termini of PAK4.