Article
Author: Suo, Yanrui ; Zhang, Xu ; Jin, Rui ; Wang, Xingyu ; Li, Kaige ; Mu, Baiyang ; Song, Weixiao ; Duan, Zhiqiang ; Shen, Aijun ; Hong, Yu ; Lu, Weiwei ; Wen, Xin ; Zhu, Jian ; Hu, Hangchen ; Lu, Xiaojie ; Meng, Linghua ; Zhang, Minmin
The DNA-encoded library (DEL) is a powerful hit-generation tool in drug discovery. This study describes a new DEL with a privileged scaffold quinazolin-4(3H)-one developed by a robust DNA-compatible multicomponent reaction and a series of novel glutathione S-transferase (GST) inhibitors that were identified through affinity-mediated DEL selection. A novel inhibitor 16 was subsequently verified with an inhibitory potency value of 1.55 ± 0.02 μM against SjGST and 2.02 ± 0.20 μM against hGSTM2. Further optimization was carried out via various structure-activity relationship studies. And especially, the co-crystal structure of the compound 16 with the SjGST was unveiled, which clearly demonstrated its binding mode was quite different from the known GSH-like compounds. This new type of probe is likely to play a different role compared with the GSH, which may provide new opportunities to discover more potent GST inhibitors.