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<title>Saudi Pharmaceutical Journal March 2024</title>
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<place><placeTerm type="text">Arab Saudi</placeTerm></place>
<publisher>University of Jeddah</publisher>
<dateIssued>2024</dateIssued>
<issuance>monographic</issuance>
<edition>March 2024</edition>
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<languageTerm type="text">Indonesia</languageTerm>
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<note>ABSTRACT
Background: Tetrazole-based derivatives and their electronic structures have displayed interesting antimicrobial
activity.
Methods: The tetrazole-based hybrids linked with thiazole, thiophene and thiadiazole ring systems have been
synthesized through various chemical reactions. The computational method DFT/B3LYP has been utilized to
calculate their electronic properties. The antimicrobial effectiveness was investigated against representative
bacterial and fungal strains. Additionally, the synthesized derivatives binding interaction was stimulated by
docking program against PDB ID: 4URO as a model of the ATP binding domain of S. aureus DNA Gyrase subunit
B.
Results: The structures of the synthesized tetrazole-based derivatives were confirmed by IR, NMR, and Mass
spectroscopic data. The DFT/B3LYP method showed that the thiadiazole derivatives 9a&ndash;c had lower &Delta;EH-L than
the thiophenes 7a&ndash;c and thiazoles 5a&ndash;c. The hybrids 5b, 5c, and 7b exhibited proper antibacterial activity
against Gram&rsquo;s +ve bacterial strains (S. aureus and S. pneumonia), while 9a displayed potent activity towards
Gram&rsquo;s -ve bacterial strains (S. typhimurium and E. coli). Meanwhile, derivatives 5a-b, 7a, 7c, and 9c showed
good effectiveness towards fungal strain (C. albicans).
Conclusion: The study provides valuable tetrazole core-linked heterocyclic rings and opens the door to further

research on their electrical characteristics and applications. Tetrazoles and thiazoles have antibacterial prop-
erties in pharmacological frameworks, making these hybrids potential lead molecules for drug development. The

conclusion summarizes the data and suggests that the synthesized chemicals&rsquo; interaction with a particular protein domain suggests focused biological activity.</note>
<subject authority=""><topic>DNA Gyrase</topic></subject>
<subject authority=""><topic>Tetrazole-thiophene hybrids</topic></subject>
<subject authority=""><topic>Docking</topic></subject>
<subject authority=""><topic>DFT modelling</topic></subject>
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<physicalLocation>PERPUSTAKAAN SEKOLAH TINGGI ILMU KESEHATAN SAMARINDA REPOSITORY</physicalLocation>
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<numerationAndChronology type="1">JIN178</numerationAndChronology>
<sublocation>Perpus.Akfarsam (Jurnal Farmasi Internasional)</sublocation>
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