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dc.creatorLudwig, Gerd
dc.creatorMojić, Marija
dc.creatorBulatović, Mirna
dc.creatorMijatović, Sanja
dc.creatorMaksimović-Ivanić, Danijela
dc.creatorSteinborn, Dirk
dc.creatorKaluđerović, Goran N
dc.date.accessioned2020-07-31T08:40:04Z
dc.date.available2900-01-01
dc.date.issued2016
dc.identifier.issn1871-5206
dc.identifier.urihttps://radar.ibiss.bg.ac.rs/handle/123456789/3827
dc.description.abstractIn vitro studies with the ruthenium(II) and analogous iridium(III) complexes [Ru(η6- p-cymene)Cl2{Ph2PCH2CH2CH2S(O)xPh-κP}], [Ru(η6-p-cymene)Cl{Ph2PCH2CH2CH2S(O)xPh- κP,κS}][PF6] (1-4), [Ir(η5-C5Me5)Cl2{Ph2PCH2CH2CH2S(O)xPh-κP}] and [Ir(η5-C5Me5)Cl{Ph2 PCH2CH2CH2S(O)xPh-κP,κS}][PF6] (5-8; x = 0, 1) revealed the high selectivity toward the 8505C, A253, MCF-7, SW480 and 518A2 cancer cell lines. Thus, the cationic ruthenium complex 4 proved to be the most selective one. In case of the neutral and cationic ruthenium complexes 1-4 the caspase-dependent apoptotic cell death was proven as the main cause of the drug's tumoricidal action on 8505C cell line.en
dc.language.isoensr
dc.publisherSharjah: Bentham Science Publisherssr
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/173013/RS//sr
dc.rightsrestrictedAccesssr
dc.sourceAnti-Cancer Agents in Medicinal Chemistrysr
dc.subjectApoptosissr
dc.subjectAutophagysr
dc.subjectCaspasesr
dc.subjectCisplatinsr
dc.subjectIridium(III) complexessr
dc.subjectRuthenium(II) complexessr
dc.titleBiological Potential of Halfsandwich Ruthenium(II) and Iridium (III) Complexesen
dc.typearticlesr
dc.rights.licenseARRsr
dcterms.abstractСтеинборн, Дирк; Калуђеровић, Горан Н; Лудwиг, Герд; Мојић, Марија; Булатовић, Мирна; Мијатовић, Сања; Максимовић-Иванић, Данијела;
dc.rights.holder© 2016 Bentham Science Publisherssr
dc.citation.issue11
dc.citation.volume16
dc.identifier.doi10.2174/1871520615666151029100749
dc.identifier.pmid26510901
dc.identifier.scopus2-s2.0-84992360776
dc.identifier.wos000390325500008
dc.citation.spage1455
dc.citation.epage1460
dc.type.versionpublishedVersionsr
dc.citation.rankM22


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