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Cytotoxicity Evaluation of a New Set of 2-Aminobenzo[de]iso-quinoline-1,3-diones
A new series of 2-amino-benzo[de]isoquinoline-1,3-diones was synthesized and fully characterized in our previous paper. Here, their cytotoxic effects have been evaluated in vitro in relation to colon HCT-116, hepatocellular Hep-G2 and breast MCF-7 cancer cell lines, using a crystal violet viability...
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/PMC4284720/ https://www.ncbi.nlm.nih.gov/pubmed/25486059 http://dx.doi.org/10.3390/ijms151222483 |
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author | Al-Salahi, Rashad Alswaidan, Ibrahim Marzouk, Mohamed |
author_facet | Al-Salahi, Rashad Alswaidan, Ibrahim Marzouk, Mohamed |
author_sort | Al-Salahi, Rashad |
collection | PubMed |
description | A new series of 2-amino-benzo[de]isoquinoline-1,3-diones was synthesized and fully characterized in our previous paper. Here, their cytotoxic effects have been evaluated in vitro in relation to colon HCT-116, hepatocellular Hep-G2 and breast MCF-7 cancer cell lines, using a crystal violet viability assay. The IC(50)-values of the target compounds are reported in µg/mL, using doxorubicin as a reference drug. The findings revealed that compounds 14, 15, 16, 21 and 22 had significant cytotoxic effects against HCT-116, MCF-7 and Hep-G2 cell lines. Their IC(50) values ranged between 1.3 and 8.3 μg/mL in relation to doxorubicin (IC(50) ≈ 0.45–0.89 μg/mL). Therefore, these compounds could be used as templates for furthering the development and design of more potent antitumor agents through structural modification. |
format | Online Article Text |
id | pubmed-4284720 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-42847202015-01-21 Cytotoxicity Evaluation of a New Set of 2-Aminobenzo[de]iso-quinoline-1,3-diones Al-Salahi, Rashad Alswaidan, Ibrahim Marzouk, Mohamed Int J Mol Sci Article A new series of 2-amino-benzo[de]isoquinoline-1,3-diones was synthesized and fully characterized in our previous paper. Here, their cytotoxic effects have been evaluated in vitro in relation to colon HCT-116, hepatocellular Hep-G2 and breast MCF-7 cancer cell lines, using a crystal violet viability assay. The IC(50)-values of the target compounds are reported in µg/mL, using doxorubicin as a reference drug. The findings revealed that compounds 14, 15, 16, 21 and 22 had significant cytotoxic effects against HCT-116, MCF-7 and Hep-G2 cell lines. Their IC(50) values ranged between 1.3 and 8.3 μg/mL in relation to doxorubicin (IC(50) ≈ 0.45–0.89 μg/mL). Therefore, these compounds could be used as templates for furthering the development and design of more potent antitumor agents through structural modification. MDPI 2014-12-04 /pmc/articles/PMC4284720/ /pubmed/25486059 http://dx.doi.org/10.3390/ijms151222483 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 Al-Salahi, Rashad Alswaidan, Ibrahim Marzouk, Mohamed Cytotoxicity Evaluation of a New Set of 2-Aminobenzo[de]iso-quinoline-1,3-diones |
title | Cytotoxicity Evaluation of a New Set of 2-Aminobenzo[de]iso-quinoline-1,3-diones |
title_full | Cytotoxicity Evaluation of a New Set of 2-Aminobenzo[de]iso-quinoline-1,3-diones |
title_fullStr | Cytotoxicity Evaluation of a New Set of 2-Aminobenzo[de]iso-quinoline-1,3-diones |
title_full_unstemmed | Cytotoxicity Evaluation of a New Set of 2-Aminobenzo[de]iso-quinoline-1,3-diones |
title_short | Cytotoxicity Evaluation of a New Set of 2-Aminobenzo[de]iso-quinoline-1,3-diones |
title_sort | cytotoxicity evaluation of a new set of 2-aminobenzo[de]iso-quinoline-1,3-diones |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4284720/ https://www.ncbi.nlm.nih.gov/pubmed/25486059 http://dx.doi.org/10.3390/ijms151222483 |
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