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New Mild and Simple Approach to Isothiocyanates: A Class of Potent Anticancer Agents
In our current work, acetyl chloride-mediated synthesis of phenethyl isothiocyanate (PEITC) derivatives proves to be convenient and provides the expected products at good to excellent yields. Biological evaluation and structure-activity relationship analysis found that the novel compound 7 showed th...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6152774/ https://www.ncbi.nlm.nih.gov/pubmed/28587167 http://dx.doi.org/10.3390/molecules22060773 |
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author | Luo, Bingling Wang, Jiankang Li, Xiaobing Lu, Wenhua Yang, Jing Hu, Yumin Huang, Peng Wen, Shijun |
author_facet | Luo, Bingling Wang, Jiankang Li, Xiaobing Lu, Wenhua Yang, Jing Hu, Yumin Huang, Peng Wen, Shijun |
author_sort | Luo, Bingling |
collection | PubMed |
description | In our current work, acetyl chloride-mediated synthesis of phenethyl isothiocyanate (PEITC) derivatives proves to be convenient and provides the expected products at good to excellent yields. Biological evaluation and structure-activity relationship analysis found that the novel compound 7 showed the best anticancer activity against human cancer cell line Panc1 and HGC27 compared with PEITC. Compounds 6 and 7 induced more apoptosis in pancreatic cancer cells but less toxicity in non-cancer cells. Further biological study demonstrated that 7 substantially increased intracellular reactive oxygen species (ROS) and depleted glutathione (GSH), leading to an oxidative stress to kill cancer cell. |
format | Online Article Text |
id | pubmed-6152774 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61527742018-11-13 New Mild and Simple Approach to Isothiocyanates: A Class of Potent Anticancer Agents Luo, Bingling Wang, Jiankang Li, Xiaobing Lu, Wenhua Yang, Jing Hu, Yumin Huang, Peng Wen, Shijun Molecules Article In our current work, acetyl chloride-mediated synthesis of phenethyl isothiocyanate (PEITC) derivatives proves to be convenient and provides the expected products at good to excellent yields. Biological evaluation and structure-activity relationship analysis found that the novel compound 7 showed the best anticancer activity against human cancer cell line Panc1 and HGC27 compared with PEITC. Compounds 6 and 7 induced more apoptosis in pancreatic cancer cells but less toxicity in non-cancer cells. Further biological study demonstrated that 7 substantially increased intracellular reactive oxygen species (ROS) and depleted glutathione (GSH), leading to an oxidative stress to kill cancer cell. MDPI 2017-06-01 /pmc/articles/PMC6152774/ /pubmed/28587167 http://dx.doi.org/10.3390/molecules22060773 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 Luo, Bingling Wang, Jiankang Li, Xiaobing Lu, Wenhua Yang, Jing Hu, Yumin Huang, Peng Wen, Shijun New Mild and Simple Approach to Isothiocyanates: A Class of Potent Anticancer Agents |
title | New Mild and Simple Approach to Isothiocyanates: A Class of Potent Anticancer Agents |
title_full | New Mild and Simple Approach to Isothiocyanates: A Class of Potent Anticancer Agents |
title_fullStr | New Mild and Simple Approach to Isothiocyanates: A Class of Potent Anticancer Agents |
title_full_unstemmed | New Mild and Simple Approach to Isothiocyanates: A Class of Potent Anticancer Agents |
title_short | New Mild and Simple Approach to Isothiocyanates: A Class of Potent Anticancer Agents |
title_sort | new mild and simple approach to isothiocyanates: a class of potent anticancer agents |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6152774/ https://www.ncbi.nlm.nih.gov/pubmed/28587167 http://dx.doi.org/10.3390/molecules22060773 |
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