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An efficient 2-aminothiazolesalicylaldehyde fluorescent chemosensor for Fe(2+) ion detection and a potential inhibitor of NUDT5 signaling hormone for breast cancer cell and molecular keypad lock application

A novel thiazole phenol conjugate, 2-aminothiazolesalicylaldehyde (receptor1) was designed and synthesized for the first time through a single step process via Schiff base condensation reaction. The formation of receptor1 was confirmed by FTIR, (13)C NMR, and (1)H NMR. The IR spectra confirmed the p...

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Autores principales: Basha, Summaya Banu, Charles, Immanuel David, Raju, Nandhakumar, Manokaran, Sakthivel, Kuzhandaivel, Hemalatha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Versita 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9362492/
https://www.ncbi.nlm.nih.gov/pubmed/35966345
http://dx.doi.org/10.1007/s11696-022-02373-z
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author Basha, Summaya Banu
Charles, Immanuel David
Raju, Nandhakumar
Manokaran, Sakthivel
Kuzhandaivel, Hemalatha
author_facet Basha, Summaya Banu
Charles, Immanuel David
Raju, Nandhakumar
Manokaran, Sakthivel
Kuzhandaivel, Hemalatha
author_sort Basha, Summaya Banu
collection PubMed
description A novel thiazole phenol conjugate, 2-aminothiazolesalicylaldehyde (receptor1) was designed and synthesized for the first time through a single step process via Schiff base condensation reaction. The formation of receptor1 was confirmed by FTIR, (13)C NMR, and (1)H NMR. The IR spectra confirmed the presence of the aldimine formation. It is further supported by the proton NMR, showing the disappearance of aldehyde peaks and the formation of a new imine peak. This is further corroborated by the (13)C NMR. The receptor1 complexing with various metal ions were studied through fluorescence spectroscopy showed its selectivity toward Fe(2+) ion following a reverse photoinduced electron transfer (PET) process compared to all other potentially competing ions. The receptor1 was applied as a sensor to sense Fe(2+) ion in water samples. The detection limit for Fe(2+) ion in drinking water was substantially lower (0.003 µM) than the EPA (environmental protection agency) recommendation (5.37 M). The capability of receptor1 in recovering Fe(2+) ion in bore water, tap water, and drinking water was up to 99.5%. The receptor1 was also used as a chelating ligand (receptor1) in molecular docking and it was assessed as a potential inhibitor of NUDT5, a silence hormone signaling for breast cancer. The test compound (PDB: 5NWH) showed good affinity toward the target receptor1 with the binding energy of – 5.23 kcal mol(−1). Furthermore, the receptor1 showed excellent reversibility property on adding EDTA solution. Due to the marvelous reversible property, a molecular-scale sequential information processing circuit is designed for the multi-task behavior such as ‘Writing-Reading-Erasing-Reading’ in the form of binary logic gate. The consecutive addition of Fe(2+) ion and EDTA solution to receptor1 paves a way for the construction of INHIBIT logic gate. Additionally, the receptor1 showed the mimicking behavior of molecular keypad lock. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11696-022-02373-z.
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spelling pubmed-93624922022-08-10 An efficient 2-aminothiazolesalicylaldehyde fluorescent chemosensor for Fe(2+) ion detection and a potential inhibitor of NUDT5 signaling hormone for breast cancer cell and molecular keypad lock application Basha, Summaya Banu Charles, Immanuel David Raju, Nandhakumar Manokaran, Sakthivel Kuzhandaivel, Hemalatha Chem Zvesti Original Paper A novel thiazole phenol conjugate, 2-aminothiazolesalicylaldehyde (receptor1) was designed and synthesized for the first time through a single step process via Schiff base condensation reaction. The formation of receptor1 was confirmed by FTIR, (13)C NMR, and (1)H NMR. The IR spectra confirmed the presence of the aldimine formation. It is further supported by the proton NMR, showing the disappearance of aldehyde peaks and the formation of a new imine peak. This is further corroborated by the (13)C NMR. The receptor1 complexing with various metal ions were studied through fluorescence spectroscopy showed its selectivity toward Fe(2+) ion following a reverse photoinduced electron transfer (PET) process compared to all other potentially competing ions. The receptor1 was applied as a sensor to sense Fe(2+) ion in water samples. The detection limit for Fe(2+) ion in drinking water was substantially lower (0.003 µM) than the EPA (environmental protection agency) recommendation (5.37 M). The capability of receptor1 in recovering Fe(2+) ion in bore water, tap water, and drinking water was up to 99.5%. The receptor1 was also used as a chelating ligand (receptor1) in molecular docking and it was assessed as a potential inhibitor of NUDT5, a silence hormone signaling for breast cancer. The test compound (PDB: 5NWH) showed good affinity toward the target receptor1 with the binding energy of – 5.23 kcal mol(−1). Furthermore, the receptor1 showed excellent reversibility property on adding EDTA solution. Due to the marvelous reversible property, a molecular-scale sequential information processing circuit is designed for the multi-task behavior such as ‘Writing-Reading-Erasing-Reading’ in the form of binary logic gate. The consecutive addition of Fe(2+) ion and EDTA solution to receptor1 paves a way for the construction of INHIBIT logic gate. Additionally, the receptor1 showed the mimicking behavior of molecular keypad lock. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11696-022-02373-z. Versita 2022-08-04 2022 /pmc/articles/PMC9362492/ /pubmed/35966345 http://dx.doi.org/10.1007/s11696-022-02373-z Text en © Institute of Chemistry, Slovak Academy of Sciences 2022, Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Original Paper
Basha, Summaya Banu
Charles, Immanuel David
Raju, Nandhakumar
Manokaran, Sakthivel
Kuzhandaivel, Hemalatha
An efficient 2-aminothiazolesalicylaldehyde fluorescent chemosensor for Fe(2+) ion detection and a potential inhibitor of NUDT5 signaling hormone for breast cancer cell and molecular keypad lock application
title An efficient 2-aminothiazolesalicylaldehyde fluorescent chemosensor for Fe(2+) ion detection and a potential inhibitor of NUDT5 signaling hormone for breast cancer cell and molecular keypad lock application
title_full An efficient 2-aminothiazolesalicylaldehyde fluorescent chemosensor for Fe(2+) ion detection and a potential inhibitor of NUDT5 signaling hormone for breast cancer cell and molecular keypad lock application
title_fullStr An efficient 2-aminothiazolesalicylaldehyde fluorescent chemosensor for Fe(2+) ion detection and a potential inhibitor of NUDT5 signaling hormone for breast cancer cell and molecular keypad lock application
title_full_unstemmed An efficient 2-aminothiazolesalicylaldehyde fluorescent chemosensor for Fe(2+) ion detection and a potential inhibitor of NUDT5 signaling hormone for breast cancer cell and molecular keypad lock application
title_short An efficient 2-aminothiazolesalicylaldehyde fluorescent chemosensor for Fe(2+) ion detection and a potential inhibitor of NUDT5 signaling hormone for breast cancer cell and molecular keypad lock application
title_sort efficient 2-aminothiazolesalicylaldehyde fluorescent chemosensor for fe(2+) ion detection and a potential inhibitor of nudt5 signaling hormone for breast cancer cell and molecular keypad lock application
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9362492/
https://www.ncbi.nlm.nih.gov/pubmed/35966345
http://dx.doi.org/10.1007/s11696-022-02373-z
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