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Synthesis and Antitumor Activity of Novel Arylpiperazine Derivatives Containing the Saccharin Moiety

Prostate cancer is a major public health problem worldwide. For the development of potential anti-prostate cancer agents, a series of novel arylpiperazine derivatives containing the saccharin moiety based on previous studies was designed, synthesized, and evaluated in prostate (PC-3, LNCaP, and DU14...

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Detalles Bibliográficos
Autores principales: Chen, Hong, Xu, Bing-Bing, Sun, Tao, Zhou, Zhan, Ya, Hui-Yuan, Yuan, Mu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6150201/
https://www.ncbi.nlm.nih.gov/pubmed/29109383
http://dx.doi.org/10.3390/molecules22111857
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author Chen, Hong
Xu, Bing-Bing
Sun, Tao
Zhou, Zhan
Ya, Hui-Yuan
Yuan, Mu
author_facet Chen, Hong
Xu, Bing-Bing
Sun, Tao
Zhou, Zhan
Ya, Hui-Yuan
Yuan, Mu
author_sort Chen, Hong
collection PubMed
description Prostate cancer is a major public health problem worldwide. For the development of potential anti-prostate cancer agents, a series of novel arylpiperazine derivatives containing the saccharin moiety based on previous studies was designed, synthesized, and evaluated in prostate (PC-3, LNCaP, and DU145) cancer cell lines for their anticancer activities. The majority of the compounds exhibited excellent selective activity for the tested cancer cells. Compounds 4 and 12 exhibited strong cytotoxic activities against DU145 cells (half maximal inhibitory concentration (IC(50)) < 2 μM). The structure–activity relationship (SAR) of these arylpiperazine derivatives was also discussed based on the obtained experimental data. This work provides a potential lead compound for anticancer agent development focusing on prostate cancer therapy.
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spelling pubmed-61502012018-11-13 Synthesis and Antitumor Activity of Novel Arylpiperazine Derivatives Containing the Saccharin Moiety Chen, Hong Xu, Bing-Bing Sun, Tao Zhou, Zhan Ya, Hui-Yuan Yuan, Mu Molecules Article Prostate cancer is a major public health problem worldwide. For the development of potential anti-prostate cancer agents, a series of novel arylpiperazine derivatives containing the saccharin moiety based on previous studies was designed, synthesized, and evaluated in prostate (PC-3, LNCaP, and DU145) cancer cell lines for their anticancer activities. The majority of the compounds exhibited excellent selective activity for the tested cancer cells. Compounds 4 and 12 exhibited strong cytotoxic activities against DU145 cells (half maximal inhibitory concentration (IC(50)) < 2 μM). The structure–activity relationship (SAR) of these arylpiperazine derivatives was also discussed based on the obtained experimental data. This work provides a potential lead compound for anticancer agent development focusing on prostate cancer therapy. MDPI 2017-10-29 /pmc/articles/PMC6150201/ /pubmed/29109383 http://dx.doi.org/10.3390/molecules22111857 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chen, Hong
Xu, Bing-Bing
Sun, Tao
Zhou, Zhan
Ya, Hui-Yuan
Yuan, Mu
Synthesis and Antitumor Activity of Novel Arylpiperazine Derivatives Containing the Saccharin Moiety
title Synthesis and Antitumor Activity of Novel Arylpiperazine Derivatives Containing the Saccharin Moiety
title_full Synthesis and Antitumor Activity of Novel Arylpiperazine Derivatives Containing the Saccharin Moiety
title_fullStr Synthesis and Antitumor Activity of Novel Arylpiperazine Derivatives Containing the Saccharin Moiety
title_full_unstemmed Synthesis and Antitumor Activity of Novel Arylpiperazine Derivatives Containing the Saccharin Moiety
title_short Synthesis and Antitumor Activity of Novel Arylpiperazine Derivatives Containing the Saccharin Moiety
title_sort synthesis and antitumor activity of novel arylpiperazine derivatives containing the saccharin moiety
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6150201/
https://www.ncbi.nlm.nih.gov/pubmed/29109383
http://dx.doi.org/10.3390/molecules22111857
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