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
前列腺癌
癌症
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
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