Design, Characterization, Antimicrobial Activity,and <i>In Silico</i> Studies of TheinothiazoloquinazolineDerivatives Bearing Thiazinone, Tetrazole, and Triazole Moieties

The pressing demand for novel antibiotics to counter drug-resistant bacteria, such as methicillin-resistant Staphylococcus aureus (MRSA), underscores the serious public health threat posed by antibiotic resistance. To address this issue, novel quinazoline-4-one derivatives were developed, synthesized, and evaluated <i>in vitro</i> against a range of pathogens, including fungi like Aspergillus fumigatus (RCMB 002008), Gram-negative bacteria like Escherichia coli (ATCC 25922), and Gram-positive bacteria like Staphylococcus aureus (ATCC 25923) and MRSA (USA300). Notably, the thieno-thiazolo-quinazoline compounds <b>4</b> and <b>5</b> demonstrated a strong ability to inhibit and disrupt MRSA USA300 biofilm formation across all tested concentrations. Furthermore, in an <i>in vivo</i> MRSA skin infection model, these compounds effectively reduced bacterial counts compared to both vehicle-treated and untreated control groups. To enhance understanding and provide deeper insights, ADMET and docking simulations were also conducted.

Publication Details

Journal
Figshare
Published
2025-03-01
DOI
https://doi.org/10.1021/acsomega.4c11076.s001
Primary Topic
Quinazolinone synthesis and applications
Type
article
Field-Weighted Citation Impact
0.00
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article

Design, Characterization, Antimicrobial Activity,and In Silico Studies of TheinothiazoloquinazolineDerivatives Bearing Thiazinone, Tetrazole, and Triazole Moieties

Figshare
Quinazolinone synthesis and applications
article

Design, Characterization, Antimicrobial Activity,and In Silico Studies of TheinothiazoloquinazolineDerivatives Bearing Thiazinone, Tetrazole, and Triazole Moieties

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Abstract

The pressing demand for novel antibiotics to counter drug-resistant bacteria, such as methicillin-resistant Staphylococcus aureus (MRSA), underscores the serious public health threat posed by antibiotic resistance. To address this issue, novel quinazoline-4-one derivatives were developed, synthesized, and evaluated <i>in vitro</i> against a range of pathogens, including fungi like Aspergillus fumigatus (RCMB 002008), Gram-negative bacteria like Escherichia coli (ATCC 25922), and Gram-positive bacteria like Staphylococcus aureus (ATCC 25923) and MRSA (USA300). Notably, the thieno-thiazolo-quinazoline compounds <b>4</b> and <b>5</b> demonstrated a strong ability to inhibit and disrupt MRSA USA300 biofilm formation across all tested concentrations. Furthermore, in an <i>in vivo</i> MRSA skin infection model, these compounds effectively reduced bacterial counts compared to both vehicle-treated and untreated control groups. To enhance understanding and provide deeper insights, ADMET and docking simulations were also conducted.

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Quinazolinone synthesis and applications
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