针脚1
化学
肽基脯氨酰异构酶
癌症研究
异构酶
计算生物学
癌症
药理学
内科学
酶
生物化学
医学
生物
作者
Chuan Liu,Zhonghui Chen,Lei Chen,Hongmei Song,Jianbo Shen,Xiaoxi Yuan,Shuai Xia,Бо Лю,Qiuxia Chen,Qiang Tian,Xiaoyun Meng,Han Zhu,Xiaofei Dong,Jing Wang,Longying Cai,Xue‐Min Cheng,Yangyang Jia,Guansai Liu,Jin Li,Junyou Ge,Dengfeng Dou
标识
DOI:10.1021/acs.jmedchem.4c01412
摘要
Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 (PIN1) has emerged as a promising therapeutic target for cancer treatment. However, the current PIN1 inhibitors have shown limited efficacy in animal models, leaving the question of whether PIN1 is a proper oncologic target still unanswered. By screening a 1 trillion DNA-encoded library (DEL), we identified novel nonacidic compounds. Among resynthesized DEL compounds,
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