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dc.creatorSabo, Tibor J.
dc.creatorDinovic, VA
dc.creatorKaluđerović, Goran N.
dc.creatorStanojković, Tatjana P.
dc.creatorBogdanović, Goran A.
dc.creatorJuranic, ZD
dc.date.accessioned2018-03-01T19:37:00Z
dc.date.available2018-03-01T19:37:00Z
dc.date.issued2005
dc.identifier.issn0020-1693
dc.identifier.urihttps://vinar.vin.bg.ac.rs/handle/123456789/2876
dc.description.abstractFour platinum(IV) complexes, trans,trans-dichlorobis(N,N-dimethylglycinato)platinum(IV), trans,trans-[Pt(dmgly)(2)Cl-2] (1) and trans.trans-dibromobis(N,N-dimethylglycinato)platinum(IV), trans,trans-[Pt(dmgly)(2)Br-2] (2), as well as, trans,trans-dichlorobis(N-methylglycinato)platinum(IV), trans,trans-[Pt(sar)(2)Cl-2] (3) and trans,trans-dibromobis(N-methylglycinato)platinum(IV), trans,trans-[Pt(sar)(2)Br-2] (4) (with configuration index for all complexes OC-6-14), were synthesized and characterized by elemental analysis, infrared and H-1 NMR spectroscopy. In the aim to assess the selectivity in the antitumor action of these complexes, the antiproliferative action of these compounds was determined to human adenocarcinoma HeLa cells; to human myelogenous leukemia K562 cells and to normal immunocompetent cells; i.e., on human PBMC. The details of the crystal structure synthesized trans,trans-[Pt(sar)(2)Br-2] complex were also reported here. In the crystal structure of trans, trans-[Pt(sar)(2)Br-2] the Pt(IV) ion had a deformed octahedral coordination with both N-methylglycinates and bromides bonded trans to one another and with the NPt-Br bond angles of 84.1(4) and 95.9(4)degrees. The trans, trans-[Pt(sar)(2)Br-2] complex molecules form 2D-layers with multiple N-H (...) O and C-H (...) O hydrogen bonds. (c) 2005 Elsevier B.V. All rights reserved.en
dc.rightsrestrictedAccessen
dc.sourceInorganica Chimica Actaen
dc.subjectplatinum (IV) complexesen
dc.subjectbidentate ligandsen
dc.subjectsarcosineen
dc.subjectcrystal structureen
dc.subjectneoplastic cellsen
dc.subjectPBMCen
dc.titleSyntheses and activity of some platinum(IV) complexes with N-methyl derivate of glycine and halogeno ligands against HeLa, K562 cell lines and human PBMCen
dc.typearticleen
dcterms.abstractДиновиц, ВA; Јураниц, ЗД; Сабо, ТЈ; Калудеровиц, ГН; Станојковиц, ТП; Богдановић Горан;
dc.citation.volume358
dc.citation.issue7
dc.citation.spage2239
dc.citation.epage2245
dc.identifier.wos000228137700011
dc.identifier.doi10.1016/j.ica.2005.01.007
dc.citation.rankM22
dc.identifier.scopus2-s2.0-15044361609


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