Synthesis and Biological Evaluation of Coumarin Bearing Thiourea Derivative as Potential Antibacterial Agent
In this study, a series of thiourea-substituted coumarin was synthesized in a four-step reaction from a precursor, 2-oxo-2H-chromene-3-carboxylic acid. The structures of all synthesized compounds were confirmed using NMR and LCMS. All synthesized compounds were screened for their antibacterial activ...
Published in: | RUSSIAN JOURNAL OF ORGANIC CHEMISTRY |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
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MAIK NAUKA/INTERPERIODICA/SPRINGER
2024
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Online Access: | https://www-webofscience-com.uitm.idm.oclc.org/wos/woscc/full-record/WOS:001396042400024 |
author |
Alsukor Alim; Inayatsyah Nurul Alam; Mohamad Sharifah Aminah Syed; Ridhwan Mohamad Jemain Mohamad; Rasol Nurulfazlina Edayah; Imran Syahrul |
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Alsukor Alim; Inayatsyah Nurul Alam; Mohamad Sharifah Aminah Syed; Ridhwan Mohamad Jemain Mohamad; Rasol Nurulfazlina Edayah; Imran Syahrul Synthesis and Biological Evaluation of Coumarin Bearing Thiourea Derivative as Potential Antibacterial Agent Chemistry |
author_facet |
Alsukor Alim; Inayatsyah Nurul Alam; Mohamad Sharifah Aminah Syed; Ridhwan Mohamad Jemain Mohamad; Rasol Nurulfazlina Edayah; Imran Syahrul |
author_sort |
Alsukor |
spelling |
Alsukor, Alim; Inayatsyah, Nurul Alam; Mohamad, Sharifah Aminah Syed; Ridhwan, Mohamad Jemain Mohamad; Rasol, Nurulfazlina Edayah; Imran, Syahrul Synthesis and Biological Evaluation of Coumarin Bearing Thiourea Derivative as Potential Antibacterial Agent RUSSIAN JOURNAL OF ORGANIC CHEMISTRY English Article In this study, a series of thiourea-substituted coumarin was synthesized in a four-step reaction from a precursor, 2-oxo-2H-chromene-3-carboxylic acid. The structures of all synthesized compounds were confirmed using NMR and LCMS. All synthesized compounds were screened for their antibacterial activity against gram-negative (Escherichia coli, Salmonella typhimurium, and Enterobacter aerogenes) and gram-positive (Staphylococcus aureus and Bacillus subtilis) bacteria strains using well diffusion method. Most of the synthesized compounds were found to be susceptible to most of the tested bacterial strains. The structure-activity relationship showed that compounds with substituents at the ortho position had lower overall activity as compared to meta-substituted and para-substituted compounds. Compound 19 was found to be the most effective antibacterial agent against gram-positive S. aureus and B. subtilis, with minimum inhibitory concentration values of 31.25 and 62.50 mu g/mL, respectively. Molecular docking performed on potential compounds revealed significant binding site interaction with S. aureus gyrase residue Asp1083 and Met1121. MAIK NAUKA/INTERPERIODICA/SPRINGER 1070-4280 1608-3393 2024 60 SUPPL1 10.1134/S1070428024130177 Chemistry WOS:001396042400024 https://www-webofscience-com.uitm.idm.oclc.org/wos/woscc/full-record/WOS:001396042400024 |
title |
Synthesis and Biological Evaluation of Coumarin Bearing Thiourea Derivative as Potential Antibacterial Agent |
title_short |
Synthesis and Biological Evaluation of Coumarin Bearing Thiourea Derivative as Potential Antibacterial Agent |
title_full |
Synthesis and Biological Evaluation of Coumarin Bearing Thiourea Derivative as Potential Antibacterial Agent |
title_fullStr |
Synthesis and Biological Evaluation of Coumarin Bearing Thiourea Derivative as Potential Antibacterial Agent |
title_full_unstemmed |
Synthesis and Biological Evaluation of Coumarin Bearing Thiourea Derivative as Potential Antibacterial Agent |
title_sort |
Synthesis and Biological Evaluation of Coumarin Bearing Thiourea Derivative as Potential Antibacterial Agent |
container_title |
RUSSIAN JOURNAL OF ORGANIC CHEMISTRY |
language |
English |
format |
Article |
description |
In this study, a series of thiourea-substituted coumarin was synthesized in a four-step reaction from a precursor, 2-oxo-2H-chromene-3-carboxylic acid. The structures of all synthesized compounds were confirmed using NMR and LCMS. All synthesized compounds were screened for their antibacterial activity against gram-negative (Escherichia coli, Salmonella typhimurium, and Enterobacter aerogenes) and gram-positive (Staphylococcus aureus and Bacillus subtilis) bacteria strains using well diffusion method. Most of the synthesized compounds were found to be susceptible to most of the tested bacterial strains. The structure-activity relationship showed that compounds with substituents at the ortho position had lower overall activity as compared to meta-substituted and para-substituted compounds. Compound 19 was found to be the most effective antibacterial agent against gram-positive S. aureus and B. subtilis, with minimum inhibitory concentration values of 31.25 and 62.50 mu g/mL, respectively. Molecular docking performed on potential compounds revealed significant binding site interaction with S. aureus gyrase residue Asp1083 and Met1121. |
publisher |
MAIK NAUKA/INTERPERIODICA/SPRINGER |
issn |
1070-4280 1608-3393 |
publishDate |
2024 |
container_volume |
60 |
container_issue |
SUPPL1 |
doi_str_mv |
10.1134/S1070428024130177 |
topic |
Chemistry |
topic_facet |
Chemistry |
accesstype |
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id |
WOS:001396042400024 |
url |
https://www-webofscience-com.uitm.idm.oclc.org/wos/woscc/full-record/WOS:001396042400024 |
record_format |
wos |
collection |
Web of Science (WoS) |
_version_ |
1823296085711388672 |