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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...

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Autores principales: Lou, Qinghua, Ji, Liyan, Zhong, Wenhe, Li, Shasha, Yu, Siwang, Li, Zhongjun, Meng, Xiangbao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
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.
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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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