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Synthesis and Cytotoxicity Evaluation of Naphthalimide Derived N-Mustards
A series of N-mustards, which was conjugated to mono- or bis-naphthalimides with a flexible amine link, were synthesized and evaluated for cytotoxicity against five cancer cell lines (HCT-116, PC-3, U87 MG, Hep G2 and SK-OV-3). Several compounds displayed better activities than the control compound...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271267/ https://www.ncbi.nlm.nih.gov/pubmed/24968335 http://dx.doi.org/10.3390/molecules19078803 |
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author | Lou, Qinghua Ji, Liyan Zhong, Wenhe Li, Shasha Yu, Siwang Li, Zhongjun Meng, Xiangbao |
author_facet | Lou, Qinghua Ji, Liyan Zhong, Wenhe Li, Shasha Yu, Siwang Li, Zhongjun Meng, Xiangbao |
author_sort | Lou, Qinghua |
collection | PubMed |
description | A series of N-mustards, which was conjugated to mono- or bis-naphthalimides with a flexible amine link, were synthesized and evaluated for cytotoxicity against five cancer cell lines (HCT-116, PC-3, U87 MG, Hep G2 and SK-OV-3). Several compounds displayed better activities than the control compound amonafide. Further evaluations by fluorescence spectroscopy studies and DNA-interstrand cross-linking assays revealed that the derivatives showed both alkylating and intercalating properties. Among the derivatives, the bis-naphthalimide N-mustard derivative 11b was found to exhibit the highest cytotoxic activity and DNA cross-linking ability. Both 11b and 7b induce HCT-116 cell apoptosis by S phase arrest. |
format | Online Article Text |
id | pubmed-6271267 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62712672018-12-21 Synthesis and Cytotoxicity Evaluation of Naphthalimide Derived N-Mustards Lou, Qinghua Ji, Liyan Zhong, Wenhe Li, Shasha Yu, Siwang Li, Zhongjun Meng, Xiangbao Molecules Article A series of N-mustards, which was conjugated to mono- or bis-naphthalimides with a flexible amine link, were synthesized and evaluated for cytotoxicity against five cancer cell lines (HCT-116, PC-3, U87 MG, Hep G2 and SK-OV-3). Several compounds displayed better activities than the control compound amonafide. Further evaluations by fluorescence spectroscopy studies and DNA-interstrand cross-linking assays revealed that the derivatives showed both alkylating and intercalating properties. Among the derivatives, the bis-naphthalimide N-mustard derivative 11b was found to exhibit the highest cytotoxic activity and DNA cross-linking ability. Both 11b and 7b induce HCT-116 cell apoptosis by S phase arrest. MDPI 2014-06-25 /pmc/articles/PMC6271267/ /pubmed/24968335 http://dx.doi.org/10.3390/molecules19078803 Text en © 2014 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 license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Lou, Qinghua Ji, Liyan Zhong, Wenhe Li, Shasha Yu, Siwang Li, Zhongjun Meng, Xiangbao Synthesis and Cytotoxicity Evaluation of Naphthalimide Derived N-Mustards |
title | Synthesis and Cytotoxicity Evaluation of Naphthalimide Derived N-Mustards |
title_full | Synthesis and Cytotoxicity Evaluation of Naphthalimide Derived N-Mustards |
title_fullStr | Synthesis and Cytotoxicity Evaluation of Naphthalimide Derived N-Mustards |
title_full_unstemmed | Synthesis and Cytotoxicity Evaluation of Naphthalimide Derived N-Mustards |
title_short | Synthesis and Cytotoxicity Evaluation of Naphthalimide Derived N-Mustards |
title_sort | synthesis and cytotoxicity evaluation of naphthalimide derived n-mustards |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271267/ https://www.ncbi.nlm.nih.gov/pubmed/24968335 http://dx.doi.org/10.3390/molecules19078803 |
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