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BielawskiChristopher W

Bielawski, Christopher W.
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dc.citation.endPage 1256 -
dc.citation.number 2 -
dc.citation.startPage 1245 -
dc.citation.title CHEMICAL SCIENCE -
dc.citation.volume 7 -
dc.contributor.author Arambula, J. F. -
dc.contributor.author McCall, R. -
dc.contributor.author Sidoran, K. J. -
dc.contributor.author Magda, D. -
dc.contributor.author Mitchell, N. A. -
dc.contributor.author Bielawski, C. W. -
dc.contributor.author Lynch, V. M. -
dc.contributor.author Sessler, J. L. -
dc.contributor.author Arumugam, K. -
dc.date.accessioned 2023-12-22T00:10:19Z -
dc.date.available 2023-12-22T00:10:19Z -
dc.date.created 2016-02-25 -
dc.date.issued 2016-02 -
dc.description.abstract Ferrocene containing N-heterocyclic carbene (NHC) ligated gold(I) complexes of the type [Au(NHC)(2)](+) were prepared and found to be capable of regulating the formation of reactive oxygen species (ROS) via multiple mechanisms. Single crystal X-ray analysis of bis(1-(ferrocenylmethyl)-3-mesitylimidazol-2-ylidene)-gold(I) chloride (5) and bis(1,3-di(ferrocenylmethyl)imidazol-2-ylidene)-gold(I) chloride (6) revealed a quasi-linear geometry around the gold(I) centers (i.e., the C-Au-C bond angle were measured to be similar to 177 degrees and all the Au-C-carbene bonds distances were in the range of 2.00 (7)-2.03 (1) angstrom). A series of cell studies indicated that cell proliferation inhibition and ROS generation were directly proportional to the amount of ferrocene contained within the [Au(NHC)(2)](+) complexes (IC50 of 6 < 5 < bis(1-benzyl-3-mesitylimidazol-2-ylidene)-gold(I) chloride (4)). Complexes 4-6 were also confirmed to inhibit thioredoxin reductase as inferred from lipoate reduction assays and increased chelatable intracellular zinc concentrations. RNA microarray gene expression assays revealed that 6 induces endoplasmic reticulum stress response pathways as a result of ROS increase -
dc.identifier.bibliographicCitation CHEMICAL SCIENCE, v.7, no.2, pp.1245 - 1256 -
dc.identifier.doi 10.1039/c5sc03519h -
dc.identifier.issn 2041-6520 -
dc.identifier.scopusid 2-s2.0-84961383314 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/18591 -
dc.identifier.url http://pubs.rsc.org/en/Content/ArticleLanding/2016/SC/C5SC03519H#!divAbstract -
dc.identifier.wosid 000368835300051 -
dc.language 영어 -
dc.publisher ROYAL SOC CHEMISTRY -
dc.title Targeting antioxidant pathways with ferrocenylated N-heterocyclic carbene supported gold(I) complexes in A549 lung cancer cells -
dc.type Article -
dc.description.isOpenAccess TRUE -
dc.relation.journalWebOfScienceCategory Chemistry, Multidisciplinary -
dc.relation.journalResearchArea Chemistry -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordPlus INDUCE OXIDATIVE STRESS -
dc.subject.keywordPlus THIOREDOXIN REDUCTASE -
dc.subject.keywordPlus MOTEXAFIN GADOLINIUM -
dc.subject.keywordPlus ANTITUMOR-ACTIVITY -
dc.subject.keywordPlus ANTIPROLIFERATIVE ACTIVITY -
dc.subject.keywordPlus FERROCENIUM DERIVATIVES -
dc.subject.keywordPlus PALLADIUM COMPLEXES -
dc.subject.keywordPlus IONIZING-RADIATION -
dc.subject.keywordPlus SANDWICH COMPLEXES -
dc.subject.keywordPlus ANTICANCER AGENTS SYNTHESIS -

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