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Synthesis and antimicrobial activity of electron rich olefin derived cyclic ureas

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dc.contributor.author Çetinkaya, B.
dc.contributor.author Çetinkaya, E.
dc.contributor.author Küçükbay, H.
dc.contributor.author Durmaz, R.
dc.date.accessioned 2022-10-06T09:35:27Z
dc.date.available 2022-10-06T09:35:27Z
dc.date.issued 1996
dc.identifier.issn 00044172 (ISSN)
dc.identifier.uri http://hdl.handle.net/11616/62844
dc.description.abstract Seventeen cyclic ureas containing imidazolidine and benzimidazoline nuclei were synthesised by the reaction of electron-rich olefins with appropriate group 16 elements (O, S, Se, Te). The compounds synthesised were identified by 1H, 13C-NMR, FT-IR and mass spectroscopic techniques and micro analysis. All compounds studied in this work were screened for their in vitro antimicrobial activity against standard strains: Enterococcus faecalis (ATCC 29212), Staphylococcus aureus (ATCC 29213), Escherichia coli (ATCC 25922) and Pseudomonas aeruginosa (ATCC 27853). Eight of the compounds were found effective to inhibit the growth of Gram-positive bacteria (Enterococcus faecalis and Staphylococcus aureus) at MIC values between 25-400 μg/ml. None of the compounds exhibit antimicrobial activity against gram-negative bacteria (Escherichia coli and Pseudmonas aeruginosa) at the concentrations studied (6.25-800 μg/ml).
dc.source Arzneimittel-Forschung/Drug Research
dc.title Synthesis and antimicrobial activity of electron rich olefin derived cyclic ureas


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