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...

Full description

Bibliographic Details
Published in:RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
Main Authors: Alsukor, Alim; Inayatsyah, Nurul Alam; Mohamad, Sharifah Aminah Syed; Ridhwan, Mohamad Jemain Mohamad; Rasol, Nurulfazlina Edayah; Imran, Syahrul
Format: Article
Language:English
Published: MAIK NAUKA/INTERPERIODICA/SPRINGER 2024
Subjects:
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
spellingShingle 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
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