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Discovery of A031 as effective proteolysis targeting chimera (PROTAC) androgen receptor (AR) degrader for the treatment of prostate cancer.
Chen, Linrong; Han, Liuquan; Mao, Shujun; Xu, Ping; Xu, Xinxin; Zhao, Ruibo; Wu, Zhihua; Zhong, Kai; Yu, Guangliang; Wang, Xiaolei.
Affiliation
  • Chen L; State Key Laboratory of Applied Organic Chemistry, Department of Chemistry, Lanzhou University, 222 S. Tianshui Rd, Lanzhou, 730000, PR China.
  • Han L; Suzhou Degen Bio-medical Co., Ltd, No.1 Huayun Road, SIP, Suzhou, 215000, PR China.
  • Mao S; Suzhou Degen Bio-medical Co., Ltd, No.1 Huayun Road, SIP, Suzhou, 215000, PR China.
  • Xu P; Suzhou Degen Bio-medical Co., Ltd, No.1 Huayun Road, SIP, Suzhou, 215000, PR China.
  • Xu X; Suzhou Degen Bio-medical Co., Ltd, No.1 Huayun Road, SIP, Suzhou, 215000, PR China.
  • Zhao R; State Key Laboratory of Applied Organic Chemistry, Department of Chemistry, Lanzhou University, 222 S. Tianshui Rd, Lanzhou, 730000, PR China.
  • Wu Z; School of Pharmacy, Lanzhou University, 222 S. Tianshui Rd, Lanzhou, 730000, PR China.
  • Zhong K; Suzhou Degen Bio-medical Co., Ltd, No.1 Huayun Road, SIP, Suzhou, 215000, PR China. Electronic address: 28328681@qq.com.
  • Yu G; Suzhou Degen Bio-medical Co., Ltd, No.1 Huayun Road, SIP, Suzhou, 215000, PR China. Electronic address: 41250230@qq.com.
  • Wang X; State Key Laboratory of Applied Organic Chemistry, Department of Chemistry, Lanzhou University, 222 S. Tianshui Rd, Lanzhou, 730000, PR China. Electronic address: Wangxiaolei@lzu.edu.cn.
Eur J Med Chem ; 216: 113307, 2021 Apr 15.
Article in En | MEDLINE | ID: mdl-33652354
ABSTRACT
Androgen receptor (AR) is an effective therapeutic target for the treatment of prostate cancer. We report herein the design, synthesis, and biological evaluation of highly effective proteolysis targeting chimeras (PROTAC) androgen receptor (AR) degraders, such as compound A031. It could induce the degradation of AR protein in VCaP cell lines in a time-dependent manner, achieving the IC 50 value of less than 0.25 µM. The A031 is 5 times less toxic than EZLA and works with an appropriate half-life (t 1/2) or clearance rate (Cl). Also, it has a significant inhibitory effect on tumor growth in zebrafish transplanted with human prostate cancer (VCaP). Therefore, A031 provides a further idea of developing novel drugs for prostate cancer.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Receptors, Androgen / Androgen Receptor Antagonists Limits: Animals / Humans / Male Language: En Journal: Eur J Med Chem Year: 2021 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Receptors, Androgen / Androgen Receptor Antagonists Limits: Animals / Humans / Male Language: En Journal: Eur J Med Chem Year: 2021 Document type: Article