LNCaP公司
恩扎鲁胺
前列腺癌
生物利用度
药代动力学
雄激素受体
化学
前列腺
内科学
癌症研究
药理学
医学
癌症
肿瘤科
生物
作者
Weiguo Xiang,Lijie Zhao,Xin Han,Chong Qin,Bukeyan Miao,Donna McEachern,Yu Wang,Hoda Metwally,Paul D. Kirchhoff,Lu Wang,Aleksas Matvekas,Miao He,Bo Wen,Duxin Sun,Shaomeng Wang
标识
DOI:10.1021/acs.jmedchem.1c00900
摘要
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 DC50 values of ≤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 IC50 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.
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