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3-Imino derivative-sulfahydantoins: Synthesis, in vitro antibacterial and cytotoxic activities and their DNA interactions

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dc.contributor.author Baskan, Ceren
dc.contributor.author Erturk, Aliye Gediz
dc.contributor.author Aydin, Birsen
dc.contributor.author Siriken, Belgin
dc.date.accessioned 2023-01-06T11:59:33Z
dc.date.available 2023-01-06T11:59:33Z
dc.date.issued 2022
dc.identifier.citation Baskan, 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.2021.105517 en_US
dc.identifier.isbn 0045-2068
dc.identifier.isbn 1090-2120
dc.identifier.uri http://dx.doi.org/10.1016/j.bioorg.2021.105517
dc.identifier.uri https://www.webofscience.com/wos/woscc/full-record/WOS:000729024600008
dc.identifier.uri https://pubmed.ncbi.nlm.nih.gov/34861626
dc.identifier.uri http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/3588
dc.description WoS Categories : Biochemistry & Molecular Biology; Chemistry, Organic Web of Science Index : Science Citation Index Expanded (SCI-EXPANDED); Index Chemicus (IC) Research Areas : Biochemistry & Molecular Biology; Chemistry en_US
dc.description.abstract Sulfahydantoins 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.sponsorship Funding 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 aut en_US
dc.language.iso eng en_US
dc.publisher ACADEMIC PRESS INC ELSEVIER SCIENCE SAN DIEGO en_US
dc.relation.isversionof 10.1016/j.bioorg.2021.105517 en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject 1,1-DIOXIDES; ARYLATION en_US
dc.subject Thiadiazolidine 1; 1-dioxide; Spectroscopy; Antibacterial activity; DNA binding; Cytotoxic activity en_US
dc.title 3-Imino derivative-sulfahydantoins: Synthesis, in vitro antibacterial and cytotoxic activities and their DNA interactions en_US
dc.type article en_US
dc.relation.journal BIOORGANIC CHEMISTRY en_US
dc.contributor.department Ordu Üniversitesi en_US
dc.identifier.volume 119 en_US


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