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Discovery of ARD-2051 as a Potent and Orally Efficacious Proteolysis Targeting Chimera (PROTAC) Degrader of Androgen Receptor for the Treatment of Advanced Prostate Cancer.


ABSTRACT: We report the discovery of ARD-2051 as a potent and orally efficacious androgen receptor (AR) proteolysis-targeting chimera degrader. ARD-2051 achieves DC50 values of 0.6 nM and Dmax >90% in inducing AR protein degradation in both the LNCaP and VCaP prostate cancer cell lines, potently and effectively suppresses AR-regulated genes, and inhibits cancer cell growth. ARD-2051 achieves a good oral bioavailability and pharmacokinetic profile in mouse, rat, and dog. A single oral dose of ARD-2051 strongly reduces AR protein and suppresses AR-regulated gene expression in the VCaP xenograft tumor tissue in mice. Oral administration of ARD-2051 effectively inhibits VCaP tumor growth and causes no signs of toxicity in mice. ARD-2051 is a promising AR degrader for advanced preclinical development for the treatment of AR+ human cancers.

SUBMITTER: Han X 

PROVIDER: S-EPMC10568492 | biostudies-literature | 2023 Jul

REPOSITORIES: biostudies-literature

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Discovery of ARD-2051 as a Potent and Orally Efficacious Proteolysis Targeting Chimera (PROTAC) Degrader of Androgen Receptor for the Treatment of Advanced Prostate Cancer.

Han Xin X   Zhao Lijie L   Xiang Weiguo W   Miao Bukeyan B   Qin Chong C   Wang Mi M   Xu Tianfeng T   McEachern Donna D   Lu Jianfeng J   Wang Yu Y   Metwally Hoda H   Yang Chao-Yie CY   Kirchhoff Paul D PD   Wang Lu L   Matvekas Aleksas A   Takyi-Williams John J   Wen Bo B   Sun Duxin D   Ator Mark M   Mckean Robert R   Wang Shaomeng S  

Journal of medicinal chemistry 20230629 13


We report the discovery of ARD-2051 as a potent and orally efficacious androgen receptor (AR) proteolysis-targeting chimera degrader. ARD-2051 achieves DC<sub>50</sub> values of 0.6 nM and <i>D</i><sub>max</sub> >90% in inducing AR protein degradation in both the LNCaP and VCaP prostate cancer cell lines, potently and effectively suppresses AR-regulated genes, and inhibits cancer cell growth. ARD-2051 achieves a good oral bioavailability and pharmacokinetic profile in mouse, rat, and dog. A sing  ...[more]

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