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Journal of medicinal chemistry · 2026

Discovery of Potential First-in-Class Dual Ligand-Directed Degrader and Antagonist of the Androgen Receptor: BMS-986365.

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Mortensen Deborah S, Nayak Surendra, Plantevin-Krenitsky Veronique, Horn Evan J, Meiring Joseph, Reiss Samantha, Peacock Kimberly, Zhao Jingjing, Ba Xiaochu, Norris Stephen, Alexander Matt, Correa Matthew, Huang Dehua, Brazeau Jean-Francois, Sapienza John, Tehrani Lida, Nagy Mark, Whitefield Brandon, Papa Patrick, Harris Roy, Grant Virginia, Norris John D, Ammirante Massimo, Rychak Emily, Wardell Suzanne E, Tsuji Toshiya, Havens Courtney G, Liu Ken, Piccotti Joseph R, Dalvie Deepak, Tang Yang, Guerrero Nadia, Sapinoso Lisa, Baughman Joshua, Cathers Brian E, Rolfe Mark, Hamann Lawrence G, McDonnell Donald P, Narla Rama Krishna, Hansen Joshua D, Xu Shuichan

Аннотация

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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