Please use this identifier to cite or link to this item: http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/3588
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dc.contributor.authorBaskan, Ceren-
dc.contributor.authorErturk, Aliye Gediz-
dc.contributor.authorAydin, Birsen-
dc.contributor.authorSiriken, Belgin-
dc.date.accessioned2023-01-06T11:59:33Z-
dc.date.available2023-01-06T11:59:33Z-
dc.date.issued2022-
dc.identifier.citationBaskan, C., Erturk, AG., Aydin, B., Siriken, B. (2022). 3-Imino derivative-sulfahydantoins: Synthesis, in vitro antibacterial and cytotoxic activities and their DNA interactions. Bioorganic Chemistry, 119, -.Doi:10.1016/j.bioorg.2021.105517en_US
dc.identifier.isbn0045-2068-
dc.identifier.isbn1090-2120-
dc.identifier.urihttp://dx.doi.org/10.1016/j.bioorg.2021.105517-
dc.identifier.urihttps://www.webofscience.com/wos/woscc/full-record/WOS:000729024600008-
dc.identifier.urihttps://pubmed.ncbi.nlm.nih.gov/34861626-
dc.identifier.urihttp://earsiv.odu.edu.tr:8080/xmlui/handle/11489/3588-
dc.descriptionWoS Categories : Biochemistry & Molecular Biology; Chemistry, Organic Web of Science Index : Science Citation Index Expanded (SCI-EXPANDED); Index Chemicus (IC) Research Areas : Biochemistry & Molecular Biology; Chemistryen_US
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.sponsorshipFunding Orgs : Amasya University Scientific Research Project [FMB-BAP 19-0430]; Ordu University Scientific Research Project Coordination Department (ODU-BAP), Ordu, TURKEY [TF-1522] Funding Name Preferred : Amasya University Scientific Research Project(Amasya University); Ordu University Scientific Research Project Coordination Department (ODU-BAP), Ordu, TURKEY Funding Text : This 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 auten_US
dc.language.isoengen_US
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE SAN DIEGOen_US
dc.relation.isversionof10.1016/j.bioorg.2021.105517en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subject1,1-DIOXIDES; ARYLATIONen_US
dc.subjectThiadiazolidine 1; 1-dioxide; Spectroscopy; Antibacterial activity; DNA binding; Cytotoxic activityen_US
dc.title3-Imino derivative-sulfahydantoins: Synthesis, in vitro antibacterial and cytotoxic activities and their DNA interactionsen_US
dc.typearticleen_US
dc.relation.journalBIOORGANIC CHEMISTRYen_US
dc.contributor.departmentOrdu Üniversitesien_US
dc.identifier.volume119en_US
Appears in Collections:Moleküler Biyoloji ve Genetik Bölümü

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