Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/823
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dc.contributor.authorBožić, Bojanen_US
dc.contributor.authorRogan, Jelenaen_US
dc.contributor.authorPoleti, Dejanen_US
dc.contributor.authorRančić, Milicaen_US
dc.contributor.authorTrišović, Nemanjaen_US
dc.contributor.authorBožić, Biljanaen_US
dc.contributor.authorUšćumlić, Gordanaen_US
dc.date.accessioned2019-07-12T20:59:06Z-
dc.date.available2019-07-12T20:59:06Z-
dc.date.issued2017-05-01-
dc.identifier.issn1878-5352-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/823-
dc.description.abstract© 2013 King Saud University A series of six novel 2-(5-arylidene-2,4-dioxotetrahydrothiazole-3-yl)propanoic acids and six corresponding methyl esters were synthesized. All compounds were characterized by melting points, elemental analysis, FT-IR, 1H and 13C NMR spectroscopy. Crystal structure of methyl-2-(5-(4-methoxybenzylidene)-2,4–dioxotetrahydrothiazole-3-yl)propionate was confirmed by X-ray analysis. The antiproliferative activity of all synthesized compounds against human colon cancer, breast cancer and myelogenous leukemia cell lines, i.e. HCT-116, MDA-231 and K562, respectively, was evaluated. The results indicate that antiproliferative activity of the synthesized esters is better than the activity of the corresponding acids. All synthesized compounds showed significant antiproliferative effects against HCT116 cells in all tested concentrations (0.01–100 μM). Moreover, in vitro antimicrobial activity against a wide range of tested microorganisms was examined.en_US
dc.relation.ispartofArabian Journal of Chemistryen_US
dc.subject2,4-Thiazolidinedioneen_US
dc.subjectAntimicrobial activityen_US
dc.subjectAntiproliferative activityen_US
dc.subjectPropanoic acid derivativeen_US
dc.subjectX-ray analysisen_US
dc.titleSynthesis, characterization and biological activity of 2-(5-arylidene-2,4-dioxotetrahydrothiazole-3-yl)propanoic acid derivativesen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.arabjc.2013.10.002-
dc.identifier.scopus2-s2.0-84885487028-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/84885487028-
dc.description.rankM21en_US
dc.description.impact4.553en_US
dc.description.startpageS2637en_US
dc.description.endpageS2643en_US
dc.description.volume10en_US
dc.description.issuesup2en_US
item.cerifentitytypePublications-
item.openairetypeArticle-
item.fulltextWith Fulltext-
item.grantfulltextrestricted-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptChair of General Physiology and Biophysics-
crisitem.author.deptChair of General Physiology and Biophysics-
crisitem.author.orcid0000-0001-9910-2741-
crisitem.author.orcid0000-0002-1238-1731-
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