Novel eugenol bearing oxypropanolamines: Synthesis, characterization, antibacterial, antidiabetic, and anticholinergic potentials

dc.contributor.authorGenç Bilgiçli, Hayriye
dc.contributor.authorKestane, Ali
dc.contributor.authorTaslimi, Parham
dc.contributor.authorKarabay, Oguz
dc.contributor.authorBytyqi-Damoni, Arlinda
dc.contributor.authorZengin, Mustafa
dc.contributor.authorGülçin, İlhami
dc.contributor.authorTaslimi, Parham
dc.date.accessioned2019-04-29T08:41:42Z
dc.date.available2019-04-29T08:41:42Z
dc.date.created2019
dc.date.issued2019
dc.date.issuedyyyymmdd2019-04-16
dc.departmentFakülteler, Fen Fakültesi, Biyoteknoloji Bölümü
dc.description.abstractFive oxypropanol amine derivatives that four of them are novel have been synthesized with high yields and practical methods. in vitro antibacterial susceptibility of Acinetobacter baumannii, Pseudomonas aeruginosa, Escherichia coli and Staphylococcus aureus strains to synthesized substances were evaluated with agar well-diffusion method by comparison with commercially available drugs. Most of the bacteria were multidrug resistant. It was concluded that these compounds are much more effective than reference drugs. These eugenol bearing oxypropanolamine derivatives were also effective inhibitors against ?-glycosidase, cytosolic carbonic anhydrase I and II isoforms (hCA I and II), and acetylcholinesterase (AChE) enzymes with Ki values in the range of 0.80 ± 0.24–3.52 ± 1.01 µM for hCA I, 1.08 ± 0.15–3.64 ± 0.92 µM for hCA II, 5.18 ± 0.84–12.46 ± 2.08 µM for ?-glycosidase, and 11.33 ± 2.83–32.81 ± 9.73 µM for AChE, respectively
dc.identifier.doi10.1016/j.bioorg.2019.102931
dc.identifier.otherhttps://doi.org/10.1016/j.bioorg.2019.102931
dc.identifier.pmid31015178
dc.identifier.scopus2-s2.0-85064440937
dc.identifier.scopusqualityQ2
dc.identifier.urihttps://hdl.handle.net/11772/1133
dc.identifier.urihttps://doi.org/10.1016/j.bioorg.2019.102931
dc.identifier.volume88
dc.identifier.wosWOS:000475378400025
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherElsevier
dc.relation.ispartofBioorganic Chemistry
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectEugenol
dc.subjectAntibacterial effects
dc.subject?-glycosidase
dc.subjectCarbonic anhydrase
dc.subjectAcetylcholinesterase
dc.subjectEnzyme inhibition
dc.titleNovel eugenol bearing oxypropanolamines: Synthesis, characterization, antibacterial, antidiabetic, and anticholinergic potentials
dc.typeArticle
dspace.entity.typePublication
relation.isAuthorOfPublicationdadfa319-65b8-4543-92b4-bea49e0139e9
relation.isAuthorOfPublication.latestForDiscoverydadfa319-65b8-4543-92b4-bea49e0139e9

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