化学
吉非替尼
泛素连接酶
泛素
体内
小分子
蛋白酶体
计算生物学
表皮生长因子受体
生物化学
基因
受体
生物技术
生物
作者
Ma Lan,Kun Zhang,Ziqi Huang,Yuda Guo,Ning Liu,Jia Chen,Xinyue Wang,Ying Liu,Mei Li,Jiating Li,Cheng Yang,Shuangwei Liu,Guang Yang
标识
DOI:10.1021/acs.jmedchem.4c02273
摘要
disrupts EGFR stability by dissociating the EGFR-HSP90 complex and recruiting E3 ligase, RNF149. More importantly, the potent and selective PD-L1 and BTK degraders were discovered successfully by utilizing the SiHyT strategy. The development of these innovative SiHyT compounds could broaden the repertoire of HyTs, enhancing the future design of TPD agents.
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