Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/58619
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dc.contributor.authorCetin, Dogan-
dc.contributor.authorKonus, Metin-
dc.contributor.authorYilmaz, Can-
dc.contributor.authorArslan, Sevki-
dc.contributor.authorAbdelsalam, Aminehafis-
dc.contributor.authorHutanu, Elena Daniela-
dc.contributor.authorKivrak, Arif-
dc.date.accessioned2025-01-22T17:12:03Z-
dc.date.available2025-01-22T17:12:03Z-
dc.date.issued2024-
dc.identifier.issn2365-6549-
dc.identifier.urihttps://doi.org/10.1002/slct.202404367-
dc.identifier.urihttps://hdl.handle.net/11499/58619-
dc.description.abstractIn this study, antioxidants, anticancer, and antimicrobial properties of four newly synthesized thiophene derivatives were investigated. In addition, basic ADME properties were calculated in silico. According to the study's findings, tested compounds antioxidant activity was weaker than the standards in both the FRAP and ABTS assays. The MTT analysis revealed that the chemicals 3 and 4 were cytotoxic to every cancer cell line that was tested. 3 and 4 increased the rate of apoptosis in the tested cancer cells at levels close to that in the positive control group. The gene expression levels of apoptotic markers (BAX, Bcl-2, Casp-3, -8, and -9) detected at all cell lines after incubation with 3 and 4 were changed as expected for apoptotic agents, except Bcl-2 of HT-29. It was concluded that the addition of bromine to C2 of thiophene cycle of 3, resulted 4 with greater apoptotic potential probably because of a change in molecular conformation and ligand exchange kinetics. Compound 3 was found to have antifungal activity against Aspergillus niger, while 4 was found to have antibacterial activity on gram-positive bacteria. In silico ADME/T analysis revealed that 3 and 4 were able to pass through the gastrointestinal tract lumen and blood-brain barrier.en_US
dc.description.sponsorshipVan Yuzuencue Yimath;l University [FBA-2023-10372, FBA-2021-9723]; TUEBITAK BIDEBen_US
dc.description.sponsorshipThe authors thank to Van Yuezuencue Y & imath;l University (FBA-2023-10372 and FBA-2021-9723) for financial supporting of reactant and reagents. D. Cetin thanks to TUEBITAK BIDEB within the scope of 2211-A General Domestic PhD for scholarships.en_US
dc.language.isoenen_US
dc.publisherWiley-v C H verlag Gmbhen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAnticancer Activityen_US
dc.subjectAntioxidanten_US
dc.subjectAntimicrobialen_US
dc.subjectApoptosisen_US
dc.subjectThiophene Derivativesen_US
dc.titleDetermination of Antioxidant, Antimicrobial and Anticancer Properties of Newly Synthesized 2-Methoxyphenyl Thiophene Derivativesen_US
dc.typeArticleen_US
dc.identifier.volume9en_US
dc.identifier.issue47en_US
dc.departmentPamukkale Universityen_US
dc.identifier.doi10.1002/slct.202404367-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid57216928891-
dc.authorscopusid56387553800-
dc.authorscopusid57221517895-
dc.authorscopusid8684142100-
dc.authorscopusid57285719100-
dc.authorscopusid59470446300-
dc.authorscopusid57218921206-
dc.authorwosidçetin, doğan/ABQ-1207-2022-
dc.authorwosidKIVRAK, Arif/W-2196-2017-
dc.identifier.scopus2-s2.0-85211945873-
dc.identifier.wosWOS:001376657200001-
dc.identifier.scopusqualityQ3-
dc.description.woscitationindexScience Citation Index Expanded-
dc.identifier.wosqualityQ3-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairetypeArticle-
item.languageiso639-1en-
crisitem.author.dept17.02. Biology-
Appears in Collections:Fen Fakültesi Koleksiyonu
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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