<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10</volume><submitter>Ma X</submitter><pubmed_abstract>The development of heteronuclear metal complexes as potent anticancer agents has received increasing attention in recent years. In this study, two new heteronuclear Ru(Ⅱ)-Re(Ⅰ) metal complexes, [Ru(bpy)&lt;sub>2&lt;/sub>LRe(CO)&lt;sub>3&lt;/sub>(DIP)](PF&lt;sub>6&lt;/sub>)&lt;sub>3&lt;/sub> and [Ru(phen)&lt;sub>2&lt;/sub>LRe(CO)&lt;sub>3&lt;/sub>(DIP)](PF&lt;sub>6&lt;/sub>)&lt;sub>3&lt;/sub> [&lt;b>RuRe-1&lt;/b> and &lt;b>RuRe-2&lt;/b>, L = 2-(4-pyridinyl)imidazolio[4,5-f][1,10]phenanthroline, bpy = 2,2'-bipyridine, DIP = 4,7-diphenyl-1,10-phenanthroline, phen = 1,10-phenanthroline], were synthesized and characterized. Cytotoxicity assay shows that &lt;b>RuRe-1&lt;/b> and &lt;b>RuRe-2&lt;/b> exhibit higher anticancer activity than cisplatin, and exist certain selectivity toward human cancer cells over normal cells. The anticancer mechanistic studies reveal tha</pubmed_abstract><journal>Frontiers in chemistry</journal><pagination>890925</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9196629</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Synthesis, Characterization and Antitumor Mechanism Investigation of Heterometallic Ru(Ⅱ)-Re(Ⅰ) Complexes.</pubmed_title><pmcid>PMC9196629</pmcid><pubmed_authors>Lu J</pubmed_authors><pubmed_authors>Ye R</pubmed_authors><pubmed_authors>Ma X</pubmed_authors><pubmed_authors>Yang P</pubmed_authors><pubmed_authors>Li R</pubmed_authors><pubmed_authors>Huang B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Synthesis, Characterization and Antitumor Mechanism Investigation of Heterometallic Ru(Ⅱ)-Re(Ⅰ) Complexes.</name><description>The development of heteronuclear metal complexes as potent anticancer agents has received increasing attention in recent years. In this study, two new heteronuclear Ru(Ⅱ)-Re(Ⅰ) metal complexes, [Ru(bpy)&lt;sub>2&lt;/sub>LRe(CO)&lt;sub>3&lt;/sub>(DIP)](PF&lt;sub>6&lt;/sub>)&lt;sub>3&lt;/sub> and [Ru(phen)&lt;sub>2&lt;/sub>LRe(CO)&lt;sub>3&lt;/sub>(DIP)](PF&lt;sub>6&lt;/sub>)&lt;sub>3&lt;/sub> [&lt;b>RuRe-1&lt;/b> and &lt;b>RuRe-2&lt;/b>, L = 2-(4-pyridinyl)imidazolio[4,5-f][1,10]phenanthroline, bpy = 2,2'-bipyridine, DIP = 4,7-diphenyl-1,10-phenanthroline, phen = 1,10-phenanthroline], were synthesized and characterized. Cytotoxicity assay shows that &lt;b>RuRe-1&lt;/b> and &lt;b>RuRe-2&lt;/b> exhibit higher anticancer activity than cisplatin, and exist certain selectivity toward human cancer cells over normal cells. The anticancer mechanistic studies reveal tha</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-22T05:59:25.959Z</modification><creation>2025-04-05T21:32:29.421Z</creation></dates><accession>S-EPMC9196629</accession><cross_references><pubmed>35711955</pubmed><doi>10.3389/fchem.2022.890925</doi></cross_references></HashMap>