化学
口服活性
雄激素受体
药理学
结构-活动关系
雄激素
化学合成
立体化学
生物化学
内科学
体外
激素
医学
癌症
前列腺癌
作者
Jianing Liao,Chenxian Hu,Weitao Fu,Jinbiao Liao,Xin Chai,Luhu Shan,Xiaohong Xu,Tingjun Hou,Rong Sheng,Dan Li
标识
DOI:10.1021/acs.jmedchem.4c01464
摘要
Androgen receptor (AR) is an important therapeutic target for prostate cancer (PCa) treatment, but prolonged use of AR antagonists has led to variant drug-resistant mutations. Since all marketed AR antagonists target the ligand binding pocket (LBP) of AR, to mitigate cross-resistance, a new drug pocket named Dimer Interface Pocket was discovered and a novel AR antagonist M17-B15 was identified. M17-B15 showed strong in vitro efficacy against PCa but had poor pharmacokinetic properties in vivo. In this study, through rational design and structure-activity relationship exploration, a series of thiadiazoleamide derivatives represented by N29 (IC50 = 0.018 μM) were identified with dominant AR antagonistic activity and remarkable anti-PCa activity in vitro. Furthermore, N29 effectively inhibited a series of typical drug-resistant AR mutants. The improved oral bioavailability of N29 facilitated its efficacy via oral administration, significantly inhibiting LNCaP xenograft tumor in vivo, presenting a promising therapeutic application for PCa.
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