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Synthesis, Characterization, Antibacterial, Antifungal and Anticorrosion Activities of 1,2,4-Triazolo[1,5-a]quinazolinone
The synthesis of 5,6,7,8-tetrahydro-[1,2,4]triazolo[5,1-b]quinazolin-9(4H)-one (THTQ), a potentially biologically active compound, was pursued, and its structure was determined through a sequence of spectral analysis, including (1)H-NMR, (13)C-NMR, IR, and HRMS. Four bacterial and four fungal strain...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10385296/ https://www.ncbi.nlm.nih.gov/pubmed/37513216 http://dx.doi.org/10.3390/molecules28145340 |
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author | Ettahiri, Walid Salim, Rajae Adardour, Mohamed Ech-chihbi, Elhachmia Yunusa, Ismaeel Alanazi, Mohammed M. Lahmidi, Sanae Barnossi, Azeddin El Merzouki, Oussama Iraqi Housseini, Abdelilah Rais, Zakia Baouid, Abdesselam Taleb, Mustapha |
author_facet | Ettahiri, Walid Salim, Rajae Adardour, Mohamed Ech-chihbi, Elhachmia Yunusa, Ismaeel Alanazi, Mohammed M. Lahmidi, Sanae Barnossi, Azeddin El Merzouki, Oussama Iraqi Housseini, Abdelilah Rais, Zakia Baouid, Abdesselam Taleb, Mustapha |
author_sort | Ettahiri, Walid |
collection | PubMed |
description | The synthesis of 5,6,7,8-tetrahydro-[1,2,4]triazolo[5,1-b]quinazolin-9(4H)-one (THTQ), a potentially biologically active compound, was pursued, and its structure was determined through a sequence of spectral analysis, including (1)H-NMR, (13)C-NMR, IR, and HRMS. Four bacterial and four fungal strains were evaluated for their susceptibility to the antibacterial and antifungal properties of the THTQ compound using the well diffusion method. The impact of THTQ on the corrosion of mild steel in a 1 M HCl solution was evaluated using various methods such as weight loss, potentiodynamic polarization (PDP), electrochemical impedance spectroscopy (EIS), and scanning electron microscopy (SEM) analysis. The study revealed that the effectiveness of THTQ as an inhibitor increased with the concentration but decreased with temperature. The PDP analysis suggested that THTQ acted as a mixed-type inhibitor, whereas the EIS data showed that it created a protective layer on the steel surface. This protective layer occurs due to the adsorption behavior of THTQ following Langmuir’s adsorption isotherm. The inhibition potential of THTQ is also predicted theoretically using DFT at B3LYP and Monte Carlo simulation. |
format | Online Article Text |
id | pubmed-10385296 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-103852962023-07-30 Synthesis, Characterization, Antibacterial, Antifungal and Anticorrosion Activities of 1,2,4-Triazolo[1,5-a]quinazolinone Ettahiri, Walid Salim, Rajae Adardour, Mohamed Ech-chihbi, Elhachmia Yunusa, Ismaeel Alanazi, Mohammed M. Lahmidi, Sanae Barnossi, Azeddin El Merzouki, Oussama Iraqi Housseini, Abdelilah Rais, Zakia Baouid, Abdesselam Taleb, Mustapha Molecules Article The synthesis of 5,6,7,8-tetrahydro-[1,2,4]triazolo[5,1-b]quinazolin-9(4H)-one (THTQ), a potentially biologically active compound, was pursued, and its structure was determined through a sequence of spectral analysis, including (1)H-NMR, (13)C-NMR, IR, and HRMS. Four bacterial and four fungal strains were evaluated for their susceptibility to the antibacterial and antifungal properties of the THTQ compound using the well diffusion method. The impact of THTQ on the corrosion of mild steel in a 1 M HCl solution was evaluated using various methods such as weight loss, potentiodynamic polarization (PDP), electrochemical impedance spectroscopy (EIS), and scanning electron microscopy (SEM) analysis. The study revealed that the effectiveness of THTQ as an inhibitor increased with the concentration but decreased with temperature. The PDP analysis suggested that THTQ acted as a mixed-type inhibitor, whereas the EIS data showed that it created a protective layer on the steel surface. This protective layer occurs due to the adsorption behavior of THTQ following Langmuir’s adsorption isotherm. The inhibition potential of THTQ is also predicted theoretically using DFT at B3LYP and Monte Carlo simulation. MDPI 2023-07-11 /pmc/articles/PMC10385296/ /pubmed/37513216 http://dx.doi.org/10.3390/molecules28145340 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ettahiri, Walid Salim, Rajae Adardour, Mohamed Ech-chihbi, Elhachmia Yunusa, Ismaeel Alanazi, Mohammed M. Lahmidi, Sanae Barnossi, Azeddin El Merzouki, Oussama Iraqi Housseini, Abdelilah Rais, Zakia Baouid, Abdesselam Taleb, Mustapha Synthesis, Characterization, Antibacterial, Antifungal and Anticorrosion Activities of 1,2,4-Triazolo[1,5-a]quinazolinone |
title | Synthesis, Characterization, Antibacterial, Antifungal and Anticorrosion Activities of 1,2,4-Triazolo[1,5-a]quinazolinone |
title_full | Synthesis, Characterization, Antibacterial, Antifungal and Anticorrosion Activities of 1,2,4-Triazolo[1,5-a]quinazolinone |
title_fullStr | Synthesis, Characterization, Antibacterial, Antifungal and Anticorrosion Activities of 1,2,4-Triazolo[1,5-a]quinazolinone |
title_full_unstemmed | Synthesis, Characterization, Antibacterial, Antifungal and Anticorrosion Activities of 1,2,4-Triazolo[1,5-a]quinazolinone |
title_short | Synthesis, Characterization, Antibacterial, Antifungal and Anticorrosion Activities of 1,2,4-Triazolo[1,5-a]quinazolinone |
title_sort | synthesis, characterization, antibacterial, antifungal and anticorrosion activities of 1,2,4-triazolo[1,5-a]quinazolinone |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10385296/ https://www.ncbi.nlm.nih.gov/pubmed/37513216 http://dx.doi.org/10.3390/molecules28145340 |
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