首页 | 本学科首页   官方微博 | 高级检索  
     


Design,syntheses, and characterization of piperazine based chemokine receptor CCR5 antagonists as anti prostate cancer agents
Affiliation:1. Deparment of Medical Oncology, Fox Chase Cancer Center, Philadelphia, PA, USA;2. Department of Biostatistics and Bioinformatics, Fox Chase Cancer Center, Philadelphia, PA, USA;3. Department of General Internal Medicine, Temple University Hospital, Philadelphia, PA, USA;4. Bryn Mawr Medical Associates, Bryn Mawr, PA, USA
Abstract:Chemokine receptor CCR5 plays an important role in the pro-inflammatory environment that aids in the proliferation of prostate cancer cells. Previously, a series of CCR5 antagonists containing a piperidine ring core skeleton were designed based upon the proposed CCR5 antagonist pharmacophore from molecular modeling studies. The developed CCR5 antagonists were able to antagonize CCR5 at a micromolar level and inhibit the proliferation of metastatic prostate cancer cell lines. In order to further explore the structure–activity-relationship of the pharmacophore identified, the molecular scaffold was expanded to contain a piperazine ring as the core. A number of compounds that were synthesized showed promising anti prostate cancer activity and reasonable cytotoxicity profiles based on the biological characterization.
Keywords:CCR5  Antagonists  Prostate cancer  Piperazine ring
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号