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Synthesis and cytotoxic activity of organotin(IV) diallyldithiocarbamate compounds as anticancer agent towards colon adenocarcinoma cells (HT-29)
CONTEXT: Diphenyltin(IV) diallyldithiocarbamate compound (Compound 1) and triphenyltin(IV) diallyldithiocarbamate compound (Compound 2) are two newly synthesised compounds of organotin(IV) with diallyldithiocarbamate ligands. OBJECTIVE: To assess the cytotoxic effects of two synthesised compounds ag...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8117248/ https://www.ncbi.nlm.nih.gov/pubmed/34025187 http://dx.doi.org/10.1016/j.sjbs.2021.02.060 |
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author | Haezam, Farah Natasha Awang, Normah Kamaludin, Nurul Farahana Mohamad, Rapidah |
author_facet | Haezam, Farah Natasha Awang, Normah Kamaludin, Nurul Farahana Mohamad, Rapidah |
author_sort | Haezam, Farah Natasha |
collection | PubMed |
description | CONTEXT: Diphenyltin(IV) diallyldithiocarbamate compound (Compound 1) and triphenyltin(IV) diallyldithiocarbamate compound (Compound 2) are two newly synthesised compounds of organotin(IV) with diallyldithiocarbamate ligands. OBJECTIVE: To assess the cytotoxic effects of two synthesised compounds against HT-29 human colon adenocarcinoma cells and human CCD-18Co normal colon cells. MATERIALS AND METHODS: Two successfully synthesised compounds were characterised using elemental (carbon, hydrogen, nitrogen, and sulphur) analysis, Fourier-Transform Infrared (FTIR), and (1)H, (13)C (119)Sn Nucleus Magnetic Resonance (NMR) spectroscopies. The single-crystal structure of both compounds was determined by X-ray single-crystal analysis. The cytotoxicity of the compounds was assessed using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazholium bromide (MTT) assay upon 24 h of treatment. While the mode of cell death was determined based on the externalisation of phosphatidylserine using a flow cytometer. RESULTS: The elemental analysis data of the two compounds showed an agreement with the suggested formula of (C(6)H(5))(2)Sn[S(2)CN(C(3)H(5))(2)](2) for Compound 1 and (C(6)H(5))(3)Sn[S(2)CN(C(3)H(5))(2)] for Compound 2. The two major peaks of infrared absorbance, i.e., ν(C = N) and ν(C = S) were detected at the range of 1475–1479 cm(−1) and 972–977 cm(−1), respectively. The chemical shift of carbon in NCS(2) group for Compound 1 and 2 were found at 200.82 and 197.79 ppm. The crystal structure of Compound 1 showed that it is six coordinated and crystallised in monoclinic, P2(1)/c space group. While the crystal structure of Compound 2 is five coordinated and crystallised in monoclinic, P2(1)/c space group. The cytotoxicity (IC(50)) of the two compounds against HT-29 cell were 2.36 μM and 0.39 μM. Meanwhile, the percentage of cell death modes between 60% and 75% for compound 1 and compound 2 were mainly due to apoptosis, suggesting that both compounds induced growth arrest. CONCLUSION: Our study concluded that the synthesised compounds showed potent cytotoxicity towards HT-29 cell, with the triphenyltin(IV) compound showing the highest effect compared to diphenyltin(IV). |
format | Online Article Text |
id | pubmed-8117248 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-81172482021-05-20 Synthesis and cytotoxic activity of organotin(IV) diallyldithiocarbamate compounds as anticancer agent towards colon adenocarcinoma cells (HT-29) Haezam, Farah Natasha Awang, Normah Kamaludin, Nurul Farahana Mohamad, Rapidah Saudi J Biol Sci Original Article CONTEXT: Diphenyltin(IV) diallyldithiocarbamate compound (Compound 1) and triphenyltin(IV) diallyldithiocarbamate compound (Compound 2) are two newly synthesised compounds of organotin(IV) with diallyldithiocarbamate ligands. OBJECTIVE: To assess the cytotoxic effects of two synthesised compounds against HT-29 human colon adenocarcinoma cells and human CCD-18Co normal colon cells. MATERIALS AND METHODS: Two successfully synthesised compounds were characterised using elemental (carbon, hydrogen, nitrogen, and sulphur) analysis, Fourier-Transform Infrared (FTIR), and (1)H, (13)C (119)Sn Nucleus Magnetic Resonance (NMR) spectroscopies. The single-crystal structure of both compounds was determined by X-ray single-crystal analysis. The cytotoxicity of the compounds was assessed using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazholium bromide (MTT) assay upon 24 h of treatment. While the mode of cell death was determined based on the externalisation of phosphatidylserine using a flow cytometer. RESULTS: The elemental analysis data of the two compounds showed an agreement with the suggested formula of (C(6)H(5))(2)Sn[S(2)CN(C(3)H(5))(2)](2) for Compound 1 and (C(6)H(5))(3)Sn[S(2)CN(C(3)H(5))(2)] for Compound 2. The two major peaks of infrared absorbance, i.e., ν(C = N) and ν(C = S) were detected at the range of 1475–1479 cm(−1) and 972–977 cm(−1), respectively. The chemical shift of carbon in NCS(2) group for Compound 1 and 2 were found at 200.82 and 197.79 ppm. The crystal structure of Compound 1 showed that it is six coordinated and crystallised in monoclinic, P2(1)/c space group. While the crystal structure of Compound 2 is five coordinated and crystallised in monoclinic, P2(1)/c space group. The cytotoxicity (IC(50)) of the two compounds against HT-29 cell were 2.36 μM and 0.39 μM. Meanwhile, the percentage of cell death modes between 60% and 75% for compound 1 and compound 2 were mainly due to apoptosis, suggesting that both compounds induced growth arrest. CONCLUSION: Our study concluded that the synthesised compounds showed potent cytotoxicity towards HT-29 cell, with the triphenyltin(IV) compound showing the highest effect compared to diphenyltin(IV). Elsevier 2021-05 2021-02-24 /pmc/articles/PMC8117248/ /pubmed/34025187 http://dx.doi.org/10.1016/j.sjbs.2021.02.060 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Haezam, Farah Natasha Awang, Normah Kamaludin, Nurul Farahana Mohamad, Rapidah Synthesis and cytotoxic activity of organotin(IV) diallyldithiocarbamate compounds as anticancer agent towards colon adenocarcinoma cells (HT-29) |
title | Synthesis and cytotoxic activity of organotin(IV) diallyldithiocarbamate compounds as anticancer agent towards colon adenocarcinoma cells (HT-29) |
title_full | Synthesis and cytotoxic activity of organotin(IV) diallyldithiocarbamate compounds as anticancer agent towards colon adenocarcinoma cells (HT-29) |
title_fullStr | Synthesis and cytotoxic activity of organotin(IV) diallyldithiocarbamate compounds as anticancer agent towards colon adenocarcinoma cells (HT-29) |
title_full_unstemmed | Synthesis and cytotoxic activity of organotin(IV) diallyldithiocarbamate compounds as anticancer agent towards colon adenocarcinoma cells (HT-29) |
title_short | Synthesis and cytotoxic activity of organotin(IV) diallyldithiocarbamate compounds as anticancer agent towards colon adenocarcinoma cells (HT-29) |
title_sort | synthesis and cytotoxic activity of organotin(iv) diallyldithiocarbamate compounds as anticancer agent towards colon adenocarcinoma cells (ht-29) |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8117248/ https://www.ncbi.nlm.nih.gov/pubmed/34025187 http://dx.doi.org/10.1016/j.sjbs.2021.02.060 |
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