<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chao XJ</submitter><funding>Fundamental Research Funds for the Central Universities</funding><funding>NSF China</funding><funding>Basic Frontier Scientific Research Program</funding><funding>Strategic Priority Research Program of CAS</funding><funding>NIH</funding><pagination>10520-10528</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6847114</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>47(20)</volume><pubmed_abstract>We have found recently that nuclear uptake of the cell-impermeable DNA light-switching Ru(II)-polypyridyl cationic complexes such as [Ru(bpy)2(dppz)]Cl2 was remarkably enhanced by pentachlorophenol (PCP), by forming ion-pairing complexes via a passive diffusion mechanism. However, it is not clear whether the enhanced nuclear uptake of [Ru(bpy)2(dppz)]2+ is only limited to PCP, or it is a general phenomenon for other highly chlorinated phenols (HCPs); and if so, what are the major physicochemical factors in determining nuclear uptake? Here, we found that the nuclear uptake of [Ru(bpy)2(dppz)]2+ can also be facilitated by other two groups of HCPs including three tetrachlorophenol (TeCP) and six trichlorophenol (TCP) isomers. Interestingly and unexpectedly, 2,3,4,5-TeCP was found to be the mo</pubmed_abstract><journal>Nucleic acids research</journal><pubmed_title>Targeted live-cell nuclear delivery of the DNA 'light-switching' Ru(II) complex via ion-pairing with chlorophenolate counter-anions: the critical role of binding stability and lipophilicity of the ion-pairing complexes.</pubmed_title><pmcid>PMC6847114</pmcid><funding_grant_id>ES00210</funding_grant_id><funding_grant_id>21477139</funding_grant_id><funding_grant_id>RR01008</funding_grant_id><funding_grant_id>21621064</funding_grant_id><funding_grant_id>XDB01020300</funding_grant_id><funding_grant_id>ZDBS-LY-SLH027</funding_grant_id><funding_grant_id>2018A030310242</funding_grant_id><funding_grant_id>21407163</funding_grant_id><funding_grant_id>21777180</funding_grant_id><funding_grant_id>18zxxxt38</funding_grant_id><funding_grant_id>21836005</funding_grant_id><funding_grant_id>ES11497</funding_grant_id><funding_grant_id>21577149</funding_grant_id><pubmed_authors>Yan ZY</pubmed_authors><pubmed_authors>Tang M</pubmed_authors><pubmed_authors>Zhu BZ</pubmed_authors><pubmed_authors>Shao J</pubmed_authors><pubmed_authors>Huang CH</pubmed_authors><pubmed_authors>Chao XJ</pubmed_authors><pubmed_authors>Huang R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Targeted live-cell nuclear delivery of the DNA 'light-switching' Ru(II) complex via ion-pairing with chlorophenolate counter-anions: the critical role of binding stability and lipophilicity of the ion-pairing complexes.</name><description>We have found recently that nuclear uptake of the cell-impermeable DNA light-switching Ru(II)-polypyridyl cationic complexes such as [Ru(bpy)2(dppz)]Cl2 was remarkably enhanced by pentachlorophenol (PCP), by forming ion-pairing complexes via a passive diffusion mechanism. However, it is not clear whether the enhanced nuclear uptake of [Ru(bpy)2(dppz)]2+ is only limited to PCP, or it is a general phenomenon for other highly chlorinated phenols (HCPs); and if so, what are the major physicochemical factors in determining nuclear uptake? Here, we found that the nuclear uptake of [Ru(bpy)2(dppz)]2+ can also be facilitated by other two groups of HCPs including three tetrachlorophenol (TeCP) and six trichlorophenol (TCP) isomers. Interestingly and unexpectedly, 2,3,4,5-TeCP was found to be the mo</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Nov</publication><modification>2025-04-04T12:17:58.418Z</modification><creation>2020-05-21T19:06:04Z</creation></dates><accession>S-EPMC6847114</accession><cross_references><pubmed>31584083</pubmed><doi>10.1093/nar/gkz152</doi></cross_references></HashMap>