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One Step Up in Antiproliferative Activity: The Ru-Zn Complex [RuCp(PPh3)2-μ-dmoPTA-1κP:2κ2N,N′-ZnCl2](CF3SO3)
dc.contributor.author | Mendoza, Zenaida | |
dc.contributor.author | Lorenzo-Luis, Pablo | |
dc.contributor.author | Scalambra, Franco | |
dc.contributor.author | Padrón, José M. | |
dc.contributor.author | Romerosa, Antonio | |
dc.date.accessioned | 2019-11-12T07:51:33Z | |
dc.date.available | 2019-11-12T07:51:33Z | |
dc.date.issued | 2018-10-10 | |
dc.identifier.uri | http://hdl.handle.net/10835/7246 | |
dc.description.abstract | The synthesis, characterization and antiproliferative activity of the bimetallic Ru-Zn complex [RuCp(PPh3)2-μ- dmoPTA-1κP:2κ2N,N′-ZnCl2](CF3SO3) (4) and the monometallic Ru complex [RuCp(PPh3)2(dmoPTA-1κP)](CF3SO3) (5) are presented. Against human lung, cervix, breast, and colon solid tumor cell lines, complex 4 showed an enhanced antiproliferative activity (GI50 = 30–83 nM) when compared to its parent complex[RuCp(PPh3)2(HdmoPTA-1κP)](CF3SO3) (2). Additionally, it was significantly more active against the breast cancer cell line T-47D than its sibling cobalt complex [RuCp(PPh3)2-μ-dmoPTA- 1κP:2κ2N,N′-CoCl2](CF3SO3) (3). When evaluated against nontumor human cell line BJ-hTert, complex 4 was 3–8 times less active, indicating a large selectivity for tumor cells, while compound 5 was not selective. | es_ES |
dc.language.iso | en | es_ES |
dc.relation | info:eu-repo/grantAgreement/ES/MINECO/CTQ2015-67384-R/ES/Polímeros poliheteroorganmetálicos fluorecentes solubles en agua/PPFSA | es_ES |
dc.source | Eur. J. Inorg. Chem. 2018, 4684–4688 | es_ES |
dc.title | One Step Up in Antiproliferative Activity: The Ru-Zn Complex [RuCp(PPh3)2-μ-dmoPTA-1κP:2κ2N,N′-ZnCl2](CF3SO3) | es_ES |
dc.type | info:eu-repo/semantics/article | es_ES |
dc.relation.publisherversion | https://onlinelibrary.wiley.com/doi/full/10.1002/ejic.201800857 | es_ES |
dc.rights.accessRights | info:eu-repo/semantics/openAccess | es_ES |
dc.identifier.doi | 10.1002/ejic.201800857 |