Publication:
Synthesis and Evaluation of Antioxidant, Antimicrobial and Anticancer Properties of 2-(Prop-2-yn-1-yloxy)benzaldehyde Derivatives

dc.authorscopusid56387553800
dc.authorscopusid57516565000
dc.authorscopusid57221517895
dc.authorscopusid8694518300
dc.authorscopusid57192910088
dc.authorscopusid57197758391
dc.contributor.authorKonus, M.
dc.contributor.authorAydemi̇r, S.
dc.contributor.authorYılmaz, C.
dc.contributor.authorKivrak, A.
dc.contributor.authorKizildogan, A.K.
dc.contributor.authorArpaci, P.U.
dc.date.accessioned2020-06-21T13:05:22Z
dc.date.available2020-06-21T13:05:22Z
dc.date.issued2019
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Konus] Metin, Department of Molecular Biology and Genetics, Van Yüzüncü Yıl Üniversitesi, Van, Turkey; [Aydemi̇r] Selahattin, 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; [Kivrak] Arif, Department of Chemistry, Van Yüzüncü Yıl Üniversitesi, Van, Turkey; [Kizildogan] Aslıhan Kurt, Department of Agricultural Biotechnology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Arpaci] Pembegül Uyar, Department of Biotechnology, Selçuk Üniversitesi, Selçuklu, Konya, Turkeyen_US
dc.description.abstract5-bromo-2-(prop-2-yn-1-yloxy)benzaldehyde (compound 3) and 3,5-di-tert-butyl-2-(prop-2- yn-1-yloxy)benzaldehyde (compound 5) were synthesized via nucleophilic substitution reactions. Compound 5 showed higher antioxidant capacity with respect to compound 3 in all the four different antioxidant activity methods used. Moreover, in phosphomolybdenum assay, compound 5, with 1.1 proportion value, showed almost the same total antioxidant capacity compared to universal trolox standard. Furthermore, Broth microdilution method and agar disc diffusion tests demonstrated that the same compound also exhibited good antibacterial activity towards the bacteria Bacillus subtilis. Finally, both of the benzaldehyde compounds showed high antifungal activity against Aspergillus niger. In this study, compound 5 (IC<inf>50</inf>: 54.3 µg/ml) showed significant cytotoxic activity against breast adenocarcinoma cell line MCF-7 with respect to compound 3 (IC50: 173.4 µg/ml). © 2019 Bentham Science Publishers.en_US
dc.identifier.doi10.2174/1570178616666181116100232
dc.identifier.endpage423en_US
dc.identifier.issn1570-1786
dc.identifier.issn1875-6255
dc.identifier.issue5en_US
dc.identifier.scopus2-s2.0-85066089034
dc.identifier.scopusqualityQ4
dc.identifier.startpage415en_US
dc.identifier.urihttps://doi.org/10.2174/1570178616666181116100232
dc.identifier.volume16en_US
dc.identifier.wosWOS:000462832500005
dc.identifier.wosqualityQ4
dc.language.isoenen_US
dc.publisherBentham Science Publishers B.V. P.O. Box 294 Bussum 1400 AGen_US
dc.relation.ispartofLetters in Organic Chemistryen_US
dc.relation.journalLetters in Organic Chemistryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject2-(Prop-2-yn-1-yloxy)Benzaldehydeen_US
dc.subjectAntibacterialen_US
dc.subjectAnticanceren_US
dc.subjectAntifungalen_US
dc.subjectAntioxidanten_US
dc.subjectHuman Breast Carcinomaen_US
dc.titleSynthesis and Evaluation of Antioxidant, Antimicrobial and Anticancer Properties of 2-(Prop-2-yn-1-yloxy)benzaldehyde Derivativesen_US
dc.typeArticleen_US
dspace.entity.typePublication

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