Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/1230
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dc.contributor.authorHmuda, Sleemen_US
dc.contributor.authorTrišović, Nemanjaen_US
dc.contributor.authorRogan, Jelenaen_US
dc.contributor.authorPoleti, Dejanen_US
dc.contributor.authorVitnik, Željkoen_US
dc.contributor.authorVitnik, Vesnaen_US
dc.contributor.authorValentić, Natašaen_US
dc.contributor.authorBožić, Biljanaen_US
dc.contributor.authorUšćumlić, Gordanaen_US
dc.date.accessioned2019-09-09T12:00:34Z-
dc.date.available2019-09-09T12:00:34Z-
dc.date.issued2014-01-01-
dc.identifier.issn0026-9247-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/1230-
dc.description.abstractTwo new series of hydantoin derivatives, 3-(4-substituted benzyl)-5,5-diphenyl- and 3-(4-substituted benzyl)-5-ethyl-5-phenylhydantoins, were synthesized and their antiproliferative activity was tested against human colon cancer HCT-116 and breast cancer MDA-MB-231 cell lines. The presence of different substituents on both hydantoin and benzyl moieties changed the antiproliferative activity of the investigated hydantoins, whereby most of the compounds showed superior antiproliferative activity against MDA-MB-231 than against the HCT-116 cell line. The structure of three compounds was studied by single-crystal X-ray diffraction. The general structural characteristic is the presence of N-H···O hydrogen bonds in crystal packings. The molecular geometry and bonding features of the investigated hydantoins in the ground states were calculated using the density functional method. The relationship between structure and antiproliferative activity was discussed. The data presented in this investigation afford guidelines for the preparation of new hydantoin derivatives with greater antiproliferative activity. Graphical Abstract: [Figure not available: see fulltext.] © 2014 Springer-Verlag Wien.en_US
dc.relation.ispartofMonatshefte fur Chemieen_US
dc.subjectAntiproliferative activityen_US
dc.subjectHydantoinen_US
dc.subjectNatural bond orbital analysisen_US
dc.subjectQuantum chemical calculationsen_US
dc.subjectX-ray structure determinationen_US
dc.titleNew derivatives of hydantoin as potential antiproliferative agents: Biological and structural characterization in combination with quantum chemical calculationsen_US
dc.typeArticleen_US
dc.identifier.doi10.1007/s00706-013-1149-6-
dc.identifier.scopus2-s2.0-84899649174-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/84899649174-
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.orcid0000-0002-1238-1731-
Appears in Collections:Journal Article
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