Приказ основних података о документу

dc.creatorMeszaros, Janos P.
dc.creatorPoljarević, Jelena
dc.creatorGal, Tamas G.
dc.creatorMay, Nora V.
dc.creatorSpengler, Gabriella
dc.creatorEnyedy, Eva A.
dc.date.accessioned2019-04-15T16:01:52Z
dc.date.available2021-02-26
dc.date.available2021-02-26
dc.date.issued2019
dc.identifier.issn0162-0134
dc.identifier.urihttps://cherry.chem.bg.ac.rs/handle/123456789/2891
dc.description.abstractHalf-sandwich organometallic complexes of curcumin are extensively investigated as anticancer compounds.Speciation studies were performed to explore the solution stability of curcumin complexes formed with [Rh(η5- C5Me5)(H2O)3]2+. Acetylacetone (Hacac), as the simplest β-diketone ligand bearing (O,O) donor set, was involved for comparison and its Ru(η6‑p‑cymene), Ru(η6‑toluene) complexes were also studied. 1H NMR, UV–visible and pH-potentiometric titrations revealed a clear trend of stability constants of the acac complexes: Ru(η6‑p‑cymene) > Ru(η6‑toluene) > Rh(η5-C5Me5). Despite this order, the highest extent of complex formation is seen for the Rh(η5-C5Me5) complexes at pH 7.4. Formation constant of [Rh(η5-C5Me5)(H2curcumin) (H2O)]+ reveals similar solution stability to that of the acac complex. Additionally, structures of two complexes were determined by X-ray crystallography. The in vitro cytotoxicity of curcumin was not improved by the complexation with these organometallic cations.
dc.publisherElsevier
dc.relationNational Research Development and Innovation Office-NKFIA through projects GINOP-2.3.2-15-2016-00038, FK 124240, K 115762
dc.relationMinistry of Human Capacities, Hungary grant 20391-3/2018/FEKUSTRAT
dc.relationJ. Bolyai Research Scholarship of the Hungarian Academy of Sciences (É.A.E, N.V.M.)
dc.rightsembargoedAccess
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceJournal of Inorganic Biochemistry
dc.subjectCurcumin
dc.subjectCytotoxicity
dc.subjectHalf-sandwich complexes
dc.subjectSolution stability
dc.subjectX-ray crystal structures
dc.titleComparative solution and structural studies of half-sandwich rhodium and ruthenium complexes bearing curcumin and acetylacetone
dc.typearticle
dc.rights.licenseBY-NC-ND
dcterms.abstractМесзарос, Јанос П.; Гал, Тамас Г.; Маy, Нора В.; Спенглер, Габриелла; Енyедy, Ева A.; Пољаревић, Јелена;
dc.citation.volume195
dc.citation.spage91
dc.citation.epage100
dc.identifier.wos000469408500010
dc.identifier.doi10.1016/j.jinorgbio.2019.02.015
dc.citation.rankM21~
dc.description.otherSupplementary material: [http://cherry.chem.bg.ac.rs/handle/123456789/2875]
dc.description.otherThis is the peer-reviewed version of the following article: Meszaros, J. P.; Poljarević, J.; Gal, T. G.; May, N. V.; Spengler, G.; Enyedy, E. A. Comparative Solution and Structural Studies of Half-Sandwich Rhodium and Ruthenium Complexes Bearing Curcumin and Acetylacetone. Journal of Inorganic Biochemistry 2019, 195, 91–100. [https://doi.org/10.1016/j.jinorgbio.2019.02.015]
dc.type.versionacceptedVersion
dc.identifier.scopus2-s2.0-85063508269
dc.identifier.fulltexthttps://cherry.chem.bg.ac.rs/bitstream/id/6698/10.1016@j.jinorgbio.2019.02.015.pdf


Документи

Thumbnail

Овај документ се појављује у следећим колекцијама

Приказ основних података о документу