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dc.contributor.authorBaskan, Ceren
dc.contributor.authorErturk, Aliye Gediz
dc.contributor.authorAydin, Birsen
dc.contributor.authorSiriken, Belgin
dc.date.accessioned2024-03-12T19:29:03Z
dc.date.available2024-03-12T19:29:03Z
dc.date.issued2022
dc.identifier.issn0045-2068
dc.identifier.issn1090-2120
dc.identifier.urihttps://doi.org/10.1016/j.bioorg.2021.105517
dc.identifier.urihttps://hdl.handle.net/20.500.12450/2169
dc.description.abstractSulfahydantoins are five-membered rings found in the structure of chemicals that exhibit antibacterial, antiinflammatory, and anticonvulsant properties. They also activate serine protease enzymes that catalyze the hydrolysis of peptide bonds. Five 3-imino sulfahydantoin compounds were synthesized by using Strecker synthesis reaction with minor modifications. We used reflux of various aldehydes with excess sulfamide in 85% methanol in the presence of sodium cyanide. The spectroscopic properties of these compounds were studied in detail. Antibacterial activities of all synthesized new compounds against four Gram-positive (Staphylococcus aureus, Bacillus cereus, Bacillus subtilis, Streptococcus mutans) and four Gram-negative (Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumoniae, Salmonella Enteritidis) bacteria were investigated by disc diffusion and microdilution method. pBR322 plasmid DNA binding abilities of compounds were investigated in vitro by agarose gel electrophoresis. In addition, the cytotoxic activities of the compounds against the human malignant pleural mesothelioma (SPC212) cell line were determined by the MTT method. The remarkable result in this study is that the synthesized compounds, especially 4b, 4d, and 4e, have significant biological activities. It has been demonstrated that these compounds, which cause DNA damage, also have an important antibacterial effect on both Gram-negative and Gram-positive bacteria when results compared with the control group antibiotics. Compound 4e exhibited the highest antibacterial potency against Streptococcus mutans (24.33 +/- 0.57) from Gram-positive bacteria and Pseudomonas aeruginosa (24.66 +/- 1.15) from Gram-negative bacteria. At the same time, MTT results determined that compounds 4b, 4d, and 4e showed cytotoxic activity against the SPC212 cells. In particular, compound 4b had a high cytotoxic effect, and the IC50 value was determined as 6.25 mu M.en_US
dc.description.sponsorshipAmasya University Scientific Research Project [FMB-BAP 19-0430]; Ordu University Scientific Research Project Coordination Department (ODU-BAP), Ordu, TURKEY [TF-1522]en_US
dc.description.sponsorshipThis work was financially supported by the Amasya University Scientific Research Project (Project Number: FMB-BAP 19-0430), Amasya and Ordu University Scientific Research Project Coordination Department (ODU-BAP), Ordu, TURKEY (Grant no. TF-1522). The authors also acknowledge to Central Research and Application Laboratory, in Amasya University.en_US
dc.language.isoengen_US
dc.publisherAcademic Press Inc Elsevier Scienceen_US
dc.relation.ispartofBioorganic Chemistryen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectThiadiazolidine 1en_US
dc.subject1-dioxideen_US
dc.subjectSpectroscopyen_US
dc.subjectAntibacterial activityen_US
dc.subjectDNA bindingen_US
dc.subjectCytotoxic activityen_US
dc.title3-Imino derivative-sulfahydantoins: Synthesis, in vitro antibacterial and cytotoxic activities and their DNA interactionsen_US
dc.typearticleen_US
dc.departmentAmasya Üniversitesien_US
dc.identifier.volume119en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.scopus2-s2.0-85120177593en_US
dc.identifier.doi10.1016/j.bioorg.2021.105517
dc.department-temp[Baskan, Ceren] Amasya Univ, Serefeddin Sabuncuoglu Hlth Serv Vocat Sch, Amasya, Turkey; [Erturk, Aliye Gediz] Ordu Univ, Fac Arts & Sci, Dept Chem, Ordu, Turkey; [Aydin, Birsen] Amasya Univ, Fac Arts & Sci, Dept Biol, Amasya, Turkey; [Siriken, Belgin] Ondokuz Mayis Univ, Fac Vet Med, Dept Aquat Anim Dis, Samsun, Turkeyen_US
dc.identifier.wosWOS:000729024600008en_US
dc.identifier.pmid34861626en_US
dc.authorwosidBaşkan, Ceren/JAC-2851-2023


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