| Literature DB >> 34473519 |
Weiguo Xiang1,2, Lijie Zhao1,2, Xin Han1,2, Chong Qin1,2, Bukeyan Miao1,2, Donna McEachern1,2, Yu Wang1,2, Hoda Metwally1,2, Paul D Kirchhoff1,2, Lu Wang3, Aleksas Matvekas3, Miao He3, Bo Wen3, Duxin Sun3, Shaomeng Wang1,2,4,5.
Abstract
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.Entities:
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Year: 2021 PMID: 34473519 PMCID: PMC8855934 DOI: 10.1021/acs.jmedchem.1c00900
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446