| Literature DB >> 33652354 |
Linrong Chen1, Liuquan Han2, Shujun Mao2, Ping Xu2, Xinxin Xu2, Ruibo Zhao1, Zhihua Wu3, Kai Zhong4, Guangliang Yu5, Xiaolei Wang6.
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.Entities:
Keywords: Androgen receptor; E3 ligand; Human prostate cancer; PROTAC; VHL ligand
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Year: 2021 PMID: 33652354 DOI: 10.1016/j.ejmech.2021.113307
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514