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Synthesis and Characterization of Some New 1,3,4-thiadiazole Compounds Derived from 3,4-(Methylenedioxy)cinnamic Acid and their Antimicrobial Activities

dc.contributor.authorMuglu, Halit
dc.contributor.authorGur, Mahmut
dc.contributor.authorBen Hsin, Maesm Ahmed Mohamed
dc.contributor.authorSener, Nesrin
dc.contributor.authorOzkinali, Sevil
dc.contributor.authorOzkan, Osman Emre
dc.contributor.authorSener, Izzet
dc.date.accessioned2026-01-05T23:13:47Z
dc.date.issued2019-08-23
dc.description.abstractSome new 1,3,4-thiadiazole compounds derived from 3,4-(methylenedioxy)cinnamic acid were synthesized in this study. Their structures were determined using UV-Vis, IR, 1H-NMR, and 13C-NMR spectroscopy. Moreover, the antibacterial activities of the new 1,3,4-thiadiazole derivatives were tested against Gram positive (Enterococcus durans, Bacillus subtilis, and Staphylococcus aureus) and gram negative (Salmonella typhimurium, Escherichia coli, Salmonella enteritidis, Salmonella infantis, Salmonella kentucky, Enterobacter aerogenes) bacteria using the disk diffusion method. Furthermore, their antifungal activity was tested against Candida albicans using the disk diffusion method. Some of the synthesized compounds (V, VII, XIII, and XIV) showed antibacterial activity against S. aureus. Also, one synthesized compound (VIII) showed antibacterial activity against E. coli, exhibiting 8 and 9 mm inhibition zones using 50 and 80 µL. One compound (IX) showed antibacterial activity against E. aerogenes, exhibiting a 12 mm inhibition zone using 80 µL. One compound (XIII) showed antibacterial activity against S. kentucky, exhibiting an inhibition zone of about 9 mm using 80 µL. Also, one compound (VII) showed antibacterial activity against E. durans, exhibiting 7, 7, and 8 mm inhibition zones using 30, 50, and 80 µL. None of the compounds (I-XV) showed antifungal activity against C. albicans. These results showed that some of the synthesized compounds could be used as antibacterial agents.
dc.description.urihttps://doi.org/10.2174/1570178616666190118153815
dc.description.urihttps://dx.doi.org/10.2174/1570178616666190118153815
dc.description.urihttps://hdl.handle.net/11491/6822
dc.identifier.doi10.2174/1570178616666190118153815
dc.identifier.endpage836
dc.identifier.issn1570-1786
dc.identifier.openairedoi_dedup___::8eb6c0e3db7960f5a7c04648bbce8b51
dc.identifier.orcid0000-0001-9942-6324
dc.identifier.orcid0000-0003-0540-7523
dc.identifier.scopus2-s2.0-85074061151
dc.identifier.startpage825
dc.identifier.urihttps://hdl.handle.net/20.500.12597/43654
dc.identifier.volume16
dc.identifier.wos000483301600006
dc.language.isoeng
dc.publisherBentham Science Publishers Ltd.
dc.relation.ispartofLetters in Organic Chemistry
dc.rightsCLOSED
dc.subjectantimicrobial activity
dc.subjectIR and NMR spectroscopy
dc.subjectgram positive
dc.subject,3,4-Thiadiazole
dc.subjectantibacterial activities
dc.subjectgram-negative bacteria
dc.subject.sdg3. Good health
dc.titleSynthesis and Characterization of Some New 1,3,4-thiadiazole Compounds Derived from 3,4-(Methylenedioxy)cinnamic Acid and their Antimicrobial Activities
dc.typeArticle
dspace.entity.typePublication
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