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dc.creatorBožić, Bojan
dc.creatorRogan, Jelena
dc.creatorPoleti, Dejan
dc.creatorRančić, Milica
dc.creatorTrišović, Nemanja
dc.creatorBožić, Biljana
dc.creatorUšćumlić, Gordana
dc.date.accessioned2021-03-10T13:25:20Z
dc.date.available2021-03-10T13:25:20Z
dc.date.issued2017
dc.identifier.issn1878-5352
dc.identifier.urihttp://TechnoRep.tmf.bg.ac.rs/handle/123456789/3607
dc.description.abstractA 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, H-1 and C-13 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 lM). Moreover, in vitro antimicrobial activity against a wide range of tested microorganisms was examined.en
dc.publisherElsevier Science Bv, Amsterdam
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172013/RS//
dc.relationinfo:eu-repo/grantAgreement/MESTD/Integrated and Interdisciplinary Research (IIR or III)/45007/RS//
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceArabian Journal of Chemistry
dc.subjectPropanoic acid derivativeen
dc.subject2,4-Thiazolidinedioneen
dc.subjectX-ray analysisen
dc.subjectAntiproliferative activityen
dc.subjectAntimicrobial activityen
dc.titleSynthesis, characterization and biological activity of 2-(5-arylidene-2,4-dioxotetrahydrothiazole-3-yl) propanoic acid derivativesen
dc.typearticle
dc.rights.licenseBY-NC-ND
dc.citation.epageS2643
dc.citation.other10: S2637-S2643
dc.citation.rankM22
dc.citation.spageS2637
dc.citation.volume10
dc.identifier.doi10.1016/j.arabjc.2013.10.002
dc.identifier.fulltexthttp://TechnoRep.tmf.bg.ac.rs/bitstream/id/1457/3604.pdf
dc.identifier.scopus2-s2.0-84885487028
dc.identifier.wos000418897900039
dc.type.versionpublishedVersion


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Приказ основних података о документу