化学
敌手
雄激素
雄激素受体
药理学
对偶(语法数字)
生物活性
睾酮(贴片)
结构-活动关系
内分泌学
抗雄激素
内科学
癌症研究
兴奋剂
酶抑制剂
体外
生物化学
作者
Deborah S. Mortensen,Surendra Nayak,Veronique Plantevin-Krenitsky,Evan J. Horn,Joseph Meiring,Samantha Reiss,Kimberly Peacock,Jingjing Zhao,Xiaochu Ba,Stephen Norris,Matthew D. Alexander,Matthew Correa,Dehua Huang,Jean-François Brazeau,John Sapienza,Lida Tehrani,Mark Nagy,Brandon Whitefield,Patrick Papa,Roy Harris
标识
DOI:10.1021/acs.jmedchem.6c01590
摘要
Androgen receptor (AR) signaling is central to the progression of prostate cancer, including castration-resistant disease. Targeted protein degradation, particularly through heterobifunctional compounds, represents a significant advancement in eliminating disease-causing proteins beyond traditional inhibition. Here, we describe the medicinal chemistry discovery of BMS-986365, a novel dual-function AR degrader and an antagonist. BMS-986365 selectively and efficiently degrades both wild-type and clinically relevant mutant ARs while also antagonizing residual AR activity. This dual mechanism results in the robust inhibition of AR-driven pathways and prostate cancer cell growth. The development of BMS-986365 highlights the potential of targeted protein degradation strategies to overcome resistance and improve therapeutic outcomes in prostate cancer.
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