1570052-89-9Relevant academic research and scientific papers
Design, synthesis and biological evaluation of bromophenol-thiazolylhydrazone hybrids inhibiting the interaction of translation initiation factors eIF4E/eIF4G as multifunctional agents for cancer treatment
Wang, Lijun,Guo, Chuanlong,Li, Xiuxue,Yu, Xuemin,Li, Xiangqian,Xu, Kuo,Jiang, Bo,Jia, Xiaoling,Li, Chao,Shi, Dayong
, p. 153 - 170 (2019)
The eukaryotic initiation factor 4E (eIF4E)is an emerging anticancer drug target for specific anticancer therapy as a promising approach to overcome drug resistance and promote chemotherapy antitumor efficacy. A series of bromophenol-thiazolylhydrazone hybrids were designed, synthesized and evaluated for their antitumor activities. Among of them, the most potent compound 3e (EGPI-1)could inhibit the eIF4E/eIF4G interaction. Further mechanism study demonstrated EGPI-1 played an antitumor role in multiple modes of action including regulating the activity of eIF4E by inhibiting the phosphorylation of eIF4E and 4EBP1, disrupting mitochondrial function through the mTOR/4EBP1 signaling pathway, and inducing autophagy, apoptosis and ROS generation. Moreover, EGPI-1 showed good safety and favorable pharmacokinetic properties in vivo. These observations demonstrate that EGPI-1 may serve as an excellent lead compound for the development of new anticancer drugs that target the eIF4E/eIF4G interface and as a chemical genetic probe to investigate the role of the eIF4E in biological processes and human diseases.
Synthesis and structural characterization of fluorinated thiosemicarbazones
Bautista, Juan L.,Flores-Alamo, Marcos,Tiburcio, Jorge,Vieto, Rebeca,Torrens, Hugo
, p. 13111 - 13123 (2013/11/06)
Six new fluorinated thiosemicarbazones R-C(R′)=N-NH-C(S)NH 2 (R = 2,4-C6H3F2, R′ = H (1); R = 2,5-C6H3F2, R′ = H (2); R = 2,6-C6H3F2, R′ = H (3);
