Publication:
Synthesis, Biological Evaluation and Molecular Docking of Novel Thiophene-Based Indole Derivatives as Potential Antibacterial, GST Inhibitor and Apoptotic Anticancer Agents

dc.authorscopusid56387553800
dc.authorscopusid57216928891
dc.authorscopusid57221517895
dc.authorscopusid8684142100
dc.authorscopusid57212511655
dc.authorscopusid57192710504
dc.authorscopusid57216929187
dc.contributor.authorKonus, M.
dc.contributor.authorCetin, D.
dc.contributor.authorYılmaz, C.
dc.contributor.authorArslan, S.
dc.contributor.authorMutlu, D.
dc.contributor.authorKurt-Kızıldoğan, A.
dc.contributor.authorOtur, Ç.
dc.date.accessioned2020-06-21T12:17:56Z
dc.date.available2020-06-21T12:17:56Z
dc.date.issued2020
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Konus] Metin, Department of Molecular Biology and Genetics, Van Yüzüncü Yıl Üniversitesi, Van, Turkey; [Cetin] Dogan, Department of Molecular Biology and Genetics, Van Yüzüncü Yıl Üniversitesi, Van, Turkey; [Yılmaz] Can, Department of Molecular Biology and Genetics, Van Yüzüncü Yıl Üniversitesi, Van, Turkey; [Arslan] Şevki, Department of Biology, Science and Arts Faculty, Pamukkale Üniversitesi, Denizli, Denizli, Turkey; [Mutlu] Dogukan, Department of Biology, Science and Arts Faculty, Pamukkale Üniversitesi, Denizli, Denizli, Turkey; [Kurt-Kızıldoğan] Aslıhan, Department of Agricultural Biotechnology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Otur] Çiğdem, Department of Agricultural Biotechnology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Ozok-Arici] Omruye, Department of Molecular Biology and Genetics, Van Yüzüncü Yıl Üniversitesi, Van, Turkey, Department of Chemistry, Van Yüzüncü Yıl Üniversitesi, Van, Turkey; [As Algso] Muheb, Department of Chemistry, Van Yüzüncü Yıl Üniversitesi, Van, Turkey; [Kivrak] Arif, Department of Chemistry, Van Yüzüncü Yıl Üniversitesi, Van, Turkeyen_US
dc.description.abstractHeteroaromatic indoles play a leading role in the development of pharmaceutical, medical, chemical and agricultural fields due to their structural properties. In this study, it was first time that biological properties of (antioxidant, antimicrobial, cytotoxic and apoptotis-induced anticancer) 3-(5-bromothiophen-2-yl)-1-ethyl-2-phenyl-1H-indole 4 and 3-([2,2′-bithiophen]-5-yl)-1-ethyl-2-phenyl-1H-indole 5 were described. According to the overall results, while 4 did not show any significant cytotoxic, antioxidant and antimicrobial activities, 5 showed high reducing activity and very strong antibacterial activity against Enterococcus faecalis. Furthermore, 5 showed dose-dependent cytotoxic effect in all tested cell lines. The EC<inf>50</inf> values of the 5 were found to be 16 μM for CaCo-2, 29 μM for LnCaP, 14 μM for MDA-MB231, 21 μM for HepG2 and 87 μM for HEK293 cells, respectively. 5 also caused induction of apoptosis and promising glutathione S-transferase (GST) enzyme inhibition in HepG2 cells. Consequently, 5 could be also considered as a promising medical agent in cancer treatment. © 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheimen_US
dc.identifier.doi10.1002/slct.202001523
dc.identifier.endpage5814en_US
dc.identifier.issn2365-6549
dc.identifier.issue19en_US
dc.identifier.scopus2-s2.0-85085309087
dc.identifier.scopusqualityQ3
dc.identifier.startpage5809en_US
dc.identifier.urihttps://doi.org/10.1002/slct.202001523
dc.identifier.volume5en_US
dc.identifier.wosWOS:000535017800041
dc.identifier.wosqualityQ3
dc.language.isoenen_US
dc.publisherWiley-Blackwell info@wiley.comen_US
dc.relation.ispartofChemistryselecten_US
dc.relation.journalChemistryselecten_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAntibacterialen_US
dc.subjectApoptotic Anticancer Agenten_US
dc.subjectCytotoxicityen_US
dc.subjectGST Inhibitoren_US
dc.subjectIndoleen_US
dc.subjectThiopheneen_US
dc.titleSynthesis, Biological Evaluation and Molecular Docking of Novel Thiophene-Based Indole Derivatives as Potential Antibacterial, GST Inhibitor and Apoptotic Anticancer Agentsen_US
dc.typeArticleen_US
dspace.entity.typePublication

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