Design,syntheses, and characterization of piperazine based chemokine receptor CCR5 antagonists as anti prostate cancer agents |
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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 |
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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. |
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Keywords: | CCR5 Antagonists Prostate cancer Piperazine ring |
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