化学
前列腺癌
雄激素受体
前列腺
生物利用度
癌症
雄激素
系列(地层学)
雄激素受体拮抗剂
药理学
内科学
生物化学
激素
医学
古生物学
生物
作者
Sharan K. Bagal,Peter C. Astles,C. R. Diène,Argyrides Argyrou,Claire Crafter,Doyle J. Cassar,Charlene Fallan,Andreas Hock,Thomas C. Jones,Kévin Moreau,Gillian M. Lamont,Scott Lamont,Chrysiis Michaloglou,Martin J. Packer,Andy Pike,Antonio Ramos‐Montoya,James S. Scott,Joseph Shaw,Ziyanda Shologu
标识
DOI:10.1021/acs.jmedchem.4c00269
摘要
Androgen receptor (AR) signaling plays a key role in the progression of prostate cancer. This study describes the discovery and optimization of a novel series of AR PROTAC degraders that recruit the Cereblon (CRBN) E3 ligase. Having identified a series of AR ligands based on 4-(4-phenyl-1-piperidyl)-2-(trifluoromethyl)benzonitrile, our PROTAC optimization strategy focused on linker connectivity and CRBN ligand SAR to deliver potent degradation of AR in LNCaP cells. This work culminated in compounds
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