化学
嘧啶
激酶
蛋白激酶A
酶
酶抑制剂
癌症
立体化学
生物化学
内科学
医学
作者
Kaizhao Hu,Yong‐Qiang Luo,Peipei Miao,Lidan Zhao,Bing Zhao,Xiaojing Shi,H Liu
标识
DOI:10.1021/acs.jmedchem.4c01283
摘要
Skp1-CUL1-ROC1-F-box E3 ubiquitin ligases' main component S-phase kinase-associated protein 2 (Skp2) is responsible for specifically recognizing ubiquitination-modified substrates to be degraded such as p27 and p21 in the case of binding with adaptor protein Cks1. Pharmacological inhibition of Skp2 has exhibited promising antitumor activity. Herein, we present the design and optimization of a series of [1,2,4]triazolo[1,5-
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