Discovery of a head-to-tail cyclic peptide as the Keap1-Nrf2 protein-protein interaction inhibitor with high cell potency

2018 ◽  
Vol 143 ◽  
pp. 1578-1589 ◽  
Author(s):  
Meng-Chen Lu ◽  
Qiong Jiao ◽  
Tian Liu ◽  
Shi-Jie Tan ◽  
Hai-Shan Zhou ◽  
...  
2020 ◽  
Vol 28 (21) ◽  
pp. 115738
Author(s):  
Stefania Colarusso ◽  
Daniele De Simone ◽  
Tommaso Frattarelli ◽  
Matteo Andreini ◽  
Mauro Cerretani ◽  
...  

2019 ◽  
Vol 20 (18) ◽  
pp. 4445 ◽  
Author(s):  
Chung-Hang Leung ◽  
Jia-Tong Zhang ◽  
Guan-Jun Yang ◽  
Hao Liu ◽  
Quan-Bin Han ◽  
...  

Due to role of the Keap1–Nrf2 protein–protein interaction (PPI) in protecting cells from oxidative stress, the development of small molecule inhibitors that inhibit this interaction has arisen as a viable approach to combat maladies caused by oxidative stress, such as cancers, neurodegenerative disease and diabetes. To obtain specific and genuine Keap1–Nrf2 inhibitors, many efforts have been made towards developing new screening approaches. However, there is no inhibitor for this target entering the clinic for the treatment of human diseases. New strategies to identify novel bioactive compounds from large molecular databases and accelerate the developmental process of the clinical application of Keap1–Nrf2 protein–protein interaction inhibitors are greatly needed. In this review, we have summarized virtual screening and other methods for discovering new lead compounds against the Keap1–Nrf2 protein–protein interaction. We also discuss the advantages and limitations of different strategies, and the potential of this PPI as a drug target in disease therapy.


2018 ◽  
Vol 117 ◽  
pp. 228-237 ◽  
Author(s):  
Ning Meng ◽  
Hua Tang ◽  
Hao Zhang ◽  
Chengshi Jiang ◽  
Li Su ◽  
...  

2019 ◽  
Vol 14 (9) ◽  
pp. 1874-1878 ◽  
Author(s):  
Katherine R. Lennard ◽  
Reece M. Gardner ◽  
Cyrielle Doigneaux ◽  
Francisco Castillo ◽  
Ali Tavassoli

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