泛素连接酶
雄激素受体
双功能
药物发现
化学
DNA连接酶
泛素
RNF4型
细胞生物学
计算生物学
生物物理学
生物化学
生物
医学
酶
内科学
前列腺癌
癌症
基因
催化作用
作者
Duncan E. Scott,Timothy P. C. Rooney,Elliott D. Bayle,Tashfina Mirza,Henriëtte M. G. Willems,Jonathan H. Clarke,Stephen P. Andrews,John Skidmore
标识
DOI:10.1021/acsmedchemlett.0c00194
摘要
Bifunctional molecules known as PROTACs simultaneously bind an E3 ligase and a protein of interest to direct ubiquitination and clearance of that protein, and they have emerged in the past decade as an exciting new paradigm in drug discovery. In order to investigate the permeability and properties of these large molecules, we synthesized two panels of PROTAC molecules, constructed from a range of protein-target ligands, linkers, and E3 ligase ligands. The androgen receptor, which is a well-studied protein in the PROTAC field was used as a model system. The physicochemical properties and permeability of PROTACs are discussed.
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