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https://hdl.handle.net/11499/47324
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Yılmaz C. | - |
dc.contributor.author | Othman Pirdawid A. | - |
dc.contributor.author | Fidan Babat C. | - |
dc.contributor.author | Konuş M. | - |
dc.contributor.author | Çetin D. | - |
dc.contributor.author | Kıvrak A. | - |
dc.contributor.author | Algso M.A.S. | - |
dc.contributor.author | Arslan, Sevki | - |
dc.contributor.author | Mutlu, Dogukan | - |
dc.contributor.author | Otur, Cigdem | - |
dc.contributor.author | Kizildogan, Aslihan Kurt | - |
dc.date.accessioned | 2023-01-09T21:23:56Z | - |
dc.date.available | 2023-01-09T21:23:56Z | - |
dc.date.issued | 2022 | - |
dc.identifier.issn | 2365-6549 | - |
dc.identifier.uri | https://doi.org/10.1002/slct.202200784 | - |
dc.identifier.uri | https://hdl.handle.net/11499/47324 | - |
dc.description.abstract | Thiophene derivatives are studied intensively due to their anticancer, antimicrobial, antioxidant and some other clinically important properties. In this study, the biological properties of a new thiophene derivative, so called BMPT, with a moderate drug score of 0.29 were tested. BMPT showed selective cytotoxicity for LnCap, HepG2 and Caco-2 cancer cell lines with EC50 values of 138.573 ?M, 185.931 ?M, and 108.657 ?M, respectively, but not on the control cell line HEK293. The increased expressions were detected for caspase3, caspase8, caspase9 and Bax; but Bcl-2 expressions were decreased at cancer cell lines. BMPT decreased the total thiol content and total GST activities at HepG2 47 % and 40 %, respectively, and, molecular docking supported inhibitory models for GSTP1-1, GSTA1-1 and GSTM2-2 were mixed, uncompetitive and uncompetitive, respectively. BMPT also showed potent antibacterial activity against Staphylococcus aureus. Related with its selective inhibition on GST activities, BMPT is proposed to have significant apoptotic effect leaded by changes, especially, in caspase 3, Bcl-2 and Bax expressions. © 2022 Wiley-VCH GmbH. | en_US |
dc.description.sponsorship | European Cooperation in Science and Technology, COST: CA17104, CM1407; Ondokuz Mayis Üniversitesi: PYO.ZRT.1904.20.010; Pamukkale Üniversitesi, PAÜ: PAU?BAP?2018?KRM?011; Türkiye Bilimsel ve Teknolojik Araştirma Kurumu, TÜBITAK: 115Z020, FBA?2021?9723, FYL?2019?7938 | en_US |
dc.description.sponsorship | . The authors thank to The Scientific and Technological Research Council of Turkey (Project No: 115Z020). Authors, also, thank to Van Yüzüncü Yıl University Scientific Research Projects Department for supporting this work by project numbers FBA?2021?9723 and FYL?2019?7938. Authors thank to Pamukkale University (PAU?BAP?2018?KRM?011) and Ondokuz Mayıs University (PYO.ZRT.1904.20.010) for financial supporting of reactant and reagents. The author(s) A. K., C. Y., A. K. K and M. K. would like to acknowledge networking contribution by the COST Action CM1407 “Challenging organic syntheses inspired by nature from natural products chemistry to drug discovery”. A. Kivrak. also would like to acknowledge networking contribution by the COST Action CA17104 “New diagnostic and therapeutic tools against multidrug resistant tumours” | en_US |
dc.description.sponsorship | The authors thank to The Scientific and Technological Research Council of Turkey (Project No: 115Z020). Authors, also, thank to Van Yüzüncü Yıl University Scientific Research Projects Department for supporting this work by project numbers FBA-2021-9723 and FYL-2019-7938. Authors thank to Pamukkale University (PAU-BAP-2018-KRM-011) and Ondokuz Mayıs University (PYO.ZRT.1904.20.010) for financial supporting of reactant and reagents. The author(s) A. K., C. Y., A. K. K and M. K. would like to acknowledge networking contribution by the COST Action CM1407 “Challenging organic syntheses inspired by nature from natural products chemistry to drug discovery”. A. Kivrak. also would like to acknowledge networking contribution by the COST Action CA17104 “New diagnostic and therapeutic tools against multidrug resistant tumours”. | en_US |
dc.language.iso | en | en_US |
dc.publisher | John Wiley and Sons Inc | en_US |
dc.relation.ispartof | ChemistrySelect | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | anticancer activity | en_US |
dc.subject | apoptosis | en_US |
dc.subject | biological activity | en_US |
dc.subject | GST inhibition | en_US |
dc.subject | heteroaromatic compounds | en_US |
dc.title | A Thiophene Derivative, 2-Bromo-5-(2-(methylthio)phenyl)thiophene, Has Effective Anticancer Potential with Other Biological Properties | en_US |
dc.type | Article | en_US |
dc.identifier.volume | 7 | en_US |
dc.identifier.issue | 15 | en_US |
dc.identifier.doi | 10.1002/slct.202200784 | - |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.authorscopusid | 57221517895 | - |
dc.authorscopusid | 57607459400 | - |
dc.authorscopusid | 57610120300 | - |
dc.authorscopusid | 56387553800 | - |
dc.authorscopusid | 57216928891 | - |
dc.authorscopusid | 8694518300 | - |
dc.authorscopusid | 57203329350 | - |
dc.identifier.scopus | 2-s2.0-85128664107 | en_US |
dc.identifier.wos | WOS:000783845600001 | en_US |
dc.identifier.scopusquality | Q2 | - |
item.fulltext | No Fulltext | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
item.languageiso639-1 | en | - |
item.openairetype | Article | - |
item.grantfulltext | none | - |
crisitem.author.dept | 17.02. Biology | - |
Appears in Collections: | Fen-Edebiyat Fakültesi Koleksiyonu Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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