Synthesis and Biological Evaluation of Coumarin Bearing Thiourea Derivative as Potential Antibacterial Agent

Abstract: 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 antibacte...

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Published in:Russian Journal of Organic Chemistry
Main Author: Alsukor A.; Inayatsyah N.A.; Mohamad S.A.S.; Ridhwan M.J.M.; Rasol N.E.; Imran S.
Format: Article
Language:English
Published: Pleiades Publishing 2024
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85217668581&doi=10.1134%2fS1070428024130177&partnerID=40&md5=68b7be1829308a73ac3dc03384f97364
id 2-s2.0-85217668581
spelling 2-s2.0-85217668581
Alsukor A.; Inayatsyah N.A.; Mohamad S.A.S.; Ridhwan M.J.M.; Rasol N.E.; Imran S.
Synthesis and Biological Evaluation of Coumarin Bearing Thiourea Derivative as Potential Antibacterial Agent
2024
Russian Journal of Organic Chemistry
60
Suppl 1
10.1134/S1070428024130177
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85217668581&doi=10.1134%2fS1070428024130177&partnerID=40&md5=68b7be1829308a73ac3dc03384f97364
Abstract: 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 µg/mL, respectively. Molecular docking performed on potential compounds revealed significant binding site interaction with S. aureus gyrase residue Asp1083 and Met1121. © Pleiades Publishing, Ltd. 2024.
Pleiades Publishing
10704280
English
Article

author Alsukor A.; Inayatsyah N.A.; Mohamad S.A.S.; Ridhwan M.J.M.; Rasol N.E.; Imran S.
spellingShingle Alsukor A.; Inayatsyah N.A.; Mohamad S.A.S.; Ridhwan M.J.M.; Rasol N.E.; Imran S.
Synthesis and Biological Evaluation of Coumarin Bearing Thiourea Derivative as Potential Antibacterial Agent
author_facet Alsukor A.; Inayatsyah N.A.; Mohamad S.A.S.; Ridhwan M.J.M.; Rasol N.E.; Imran S.
author_sort Alsukor A.; Inayatsyah N.A.; Mohamad S.A.S.; Ridhwan M.J.M.; Rasol N.E.; Imran S.
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
publishDate 2024
container_title Russian Journal of Organic Chemistry
container_volume 60
container_issue Suppl 1
doi_str_mv 10.1134/S1070428024130177
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-85217668581&doi=10.1134%2fS1070428024130177&partnerID=40&md5=68b7be1829308a73ac3dc03384f97364
description Abstract: 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 µg/mL, respectively. Molecular docking performed on potential compounds revealed significant binding site interaction with S. aureus gyrase residue Asp1083 and Met1121. © Pleiades Publishing, Ltd. 2024.
publisher Pleiades Publishing
issn 10704280
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