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A New Complex Design of Fe (II) Isoleucine Dithiocarbamate as a Novel Anticancer and Antivirus against SARSCOV-2 (COVID-19)

BACKGROUND: This study was carried out to synthesize a new complex of Fe(II) with isoleucine dithiocarbamate ligand and to determine its potential as an anticancer and antiviral agent for SARSCOV-2. METHODS: The synthesized complexes were then characterized by UV-vis and FT-IR spectroscopy and their...

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Autores principales: Irfandi, Rizal, Riswandi, Riswandi, Raya, Indah, Ahmad, Ahyar, Fudholi, Ahmad, Jarre, Sulistiani, Sari, Dewi Ratih Tirto, Santi, Santi, Wijaya, Ronald Ivan, Prihantono, Prihantono
Formato: Online Artículo Texto
Lenguaje:English
Publicado: West Asia Organization for Cancer Prevention 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9810283/
https://www.ncbi.nlm.nih.gov/pubmed/36172674
http://dx.doi.org/10.31557/APJCP.2022.23.9.3113
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author Irfandi, Rizal
Riswandi, Riswandi
Raya, Indah
Ahmad, Ahyar
Fudholi, Ahmad
Jarre, Sulistiani
Sari, Dewi Ratih Tirto
Santi, Santi
Wijaya, Ronald Ivan
Prihantono, Prihantono
author_facet Irfandi, Rizal
Riswandi, Riswandi
Raya, Indah
Ahmad, Ahyar
Fudholi, Ahmad
Jarre, Sulistiani
Sari, Dewi Ratih Tirto
Santi, Santi
Wijaya, Ronald Ivan
Prihantono, Prihantono
author_sort Irfandi, Rizal
collection PubMed
description BACKGROUND: This study was carried out to synthesize a new complex of Fe(II) with isoleucine dithiocarbamate ligand and to determine its potential as an anticancer and antiviral agent for SARSCOV-2. METHODS: The synthesized complexes were then characterized by UV-vis and FT-IR spectroscopy and their melting points. The value of the conductivity of the complex compound is also determined. Anti-cancer activity was tested in vitro and molecular docking. Its potential as an antiviral against SARSCOV-2 was also carried out by molecular docking. Pharmacokinetics/ADMET properties were also carried out on the complex. RESULT: Spectral results showed the successful synthesis of Fe(II) isoleucine dithiocarbamate complex. The complex produced UV-vis spectra at 268 and 575 nm, and the IR data at 399–599 cm-1 showed the coordination between the Fe(II) atoms with sulphur, nitrogen and oxygen of the isoleucine dithiocarbamate ligand. Fe(II) isoleucine dithiocarbamate had a cytotoxicity effect on the MCF-7 cell line (IC(50) =613 µg/mL). The complex significantly caused morphological changes in the breast cancer cell line, finally leading to cell apoptosis. CONCLUSION: Cytotoxic test of Fe(II) isoleucine dithiocarbamate showed moderate anticancer activity on MCF-7 cancer cells and showed antiviral activity against SARSCOV-2 by interfering with spike glycoprotein –ACE2 receptors, and inhibiting major proteases and 3Clpro.
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spelling pubmed-98102832023-01-06 A New Complex Design of Fe (II) Isoleucine Dithiocarbamate as a Novel Anticancer and Antivirus against SARSCOV-2 (COVID-19) Irfandi, Rizal Riswandi, Riswandi Raya, Indah Ahmad, Ahyar Fudholi, Ahmad Jarre, Sulistiani Sari, Dewi Ratih Tirto Santi, Santi Wijaya, Ronald Ivan Prihantono, Prihantono Asian Pac J Cancer Prev Research Article BACKGROUND: This study was carried out to synthesize a new complex of Fe(II) with isoleucine dithiocarbamate ligand and to determine its potential as an anticancer and antiviral agent for SARSCOV-2. METHODS: The synthesized complexes were then characterized by UV-vis and FT-IR spectroscopy and their melting points. The value of the conductivity of the complex compound is also determined. Anti-cancer activity was tested in vitro and molecular docking. Its potential as an antiviral against SARSCOV-2 was also carried out by molecular docking. Pharmacokinetics/ADMET properties were also carried out on the complex. RESULT: Spectral results showed the successful synthesis of Fe(II) isoleucine dithiocarbamate complex. The complex produced UV-vis spectra at 268 and 575 nm, and the IR data at 399–599 cm-1 showed the coordination between the Fe(II) atoms with sulphur, nitrogen and oxygen of the isoleucine dithiocarbamate ligand. Fe(II) isoleucine dithiocarbamate had a cytotoxicity effect on the MCF-7 cell line (IC(50) =613 µg/mL). The complex significantly caused morphological changes in the breast cancer cell line, finally leading to cell apoptosis. CONCLUSION: Cytotoxic test of Fe(II) isoleucine dithiocarbamate showed moderate anticancer activity on MCF-7 cancer cells and showed antiviral activity against SARSCOV-2 by interfering with spike glycoprotein –ACE2 receptors, and inhibiting major proteases and 3Clpro. West Asia Organization for Cancer Prevention 2022-09 /pmc/articles/PMC9810283/ /pubmed/36172674 http://dx.doi.org/10.31557/APJCP.2022.23.9.3113 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-Non Commercial 4.0 International License. https://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Research Article
Irfandi, Rizal
Riswandi, Riswandi
Raya, Indah
Ahmad, Ahyar
Fudholi, Ahmad
Jarre, Sulistiani
Sari, Dewi Ratih Tirto
Santi, Santi
Wijaya, Ronald Ivan
Prihantono, Prihantono
A New Complex Design of Fe (II) Isoleucine Dithiocarbamate as a Novel Anticancer and Antivirus against SARSCOV-2 (COVID-19)
title A New Complex Design of Fe (II) Isoleucine Dithiocarbamate as a Novel Anticancer and Antivirus against SARSCOV-2 (COVID-19)
title_full A New Complex Design of Fe (II) Isoleucine Dithiocarbamate as a Novel Anticancer and Antivirus against SARSCOV-2 (COVID-19)
title_fullStr A New Complex Design of Fe (II) Isoleucine Dithiocarbamate as a Novel Anticancer and Antivirus against SARSCOV-2 (COVID-19)
title_full_unstemmed A New Complex Design of Fe (II) Isoleucine Dithiocarbamate as a Novel Anticancer and Antivirus against SARSCOV-2 (COVID-19)
title_short A New Complex Design of Fe (II) Isoleucine Dithiocarbamate as a Novel Anticancer and Antivirus against SARSCOV-2 (COVID-19)
title_sort new complex design of fe (ii) isoleucine dithiocarbamate as a novel anticancer and antivirus against sarscov-2 (covid-19)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9810283/
https://www.ncbi.nlm.nih.gov/pubmed/36172674
http://dx.doi.org/10.31557/APJCP.2022.23.9.3113
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