药物发现
计算生物学
小分子
生物利用度
生化工程
计算机科学
生物
药理学
生物信息学
遗传学
工程类
作者
Carina Cantrill,Prasoon Chaturvedi,Caroline Rynn,Jeannine Petrig Schaffland,Isabelle Walter,Matthias Wittwer
标识
DOI:10.1016/j.drudis.2020.03.012
摘要
Targeted protein degraders are an emerging modality. Their properties fall outside the traditional small-molecule property space and are in the 'beyond rule of 5' space. Consequently, drug discovery programs focused on developing orally bioavailable degraders are expected to face complex drug metabolism and pharmacokinetics (DMPK) challenges compared with traditional small molecules. Nevertheless, little information is available on the DMPK optimization of oral degraders. Therefore, in this review, we discuss our experience of these DMPK optimization challenges and present methodologies and strategies to overcome the hurdles dealing with this new small-molecule modality, specifically in developing oral degraders to treat cancer.
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