We report herein the discovery of exceptionally potent and orally bioavailable PROTAC AR degraders with ARD-2585 being the most promising compound. ARD-2585 achieves DC(50) values of â¤0.1 nM in the VCaP cell line with AR gene amplification and in the LNCaP cell line carrying an AR mutation. It potently inhibits cell growth with IC(50) values of 1.5 and 16.2 nM in the VCaP and LNCaP cell lines, respectively, and achieves excellent pharmacokinetics and 51% of oral bioavailability in mice. It is more efficacious than enzalutamide in inhibition of VCaP tumor growth and does not cause any sign of toxicity in mice. ARD-2585 is a promising AR degrader for extensive investigations for the treatment of advanced prostate cancer.
Discovery of ARD-2585 as an Exceptionally Potent and Orally Active PROTAC Degrader of Androgen Receptor for the Treatment of Advanced Prostate Cancer.
发现 ARD-2585 是一种效力极强且口服有效的 PROTAC 雄激素受体降解剂,可用于治疗晚期前列腺癌
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作者:Xiang Weiguo, Zhao Lijie, Han Xin, Qin Chong, Miao Bukeyan, McEachern Donna, Wang Yu, Metwally Hoda, Kirchhoff Paul D, Wang Lu, Matvekas Aleksas, He Miao, Wen Bo, Sun Duxin, Wang Shaomeng
| 期刊: | Journal of Medicinal Chemistry | 影响因子: | 6.800 |
| 时间: | 2021 | 起止号: | 2021 Sep 23; 64(18):13487-13509 |
| doi: | 10.1021/acs.jmedchem.1c00900 | 研究方向: | 肿瘤 |
| 疾病类型: | 前列腺癌 | ||
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