Novel ruthenium(ii) N-heterocyclic carbene complexes: Synthesis, characterization, and evaluation of their biological activities
dc.authorid | Gurbuz, Nevin/0000-0003-3201-3597; | |
dc.authorwosid | Mansour, Lamjed/AAD-8613-2019 | |
dc.authorwosid | Gurbuz, Nevin/A-3069-2016 | |
dc.authorwosid | OZDEMIR, ISMAIL/KVY-3420-2024 | |
dc.contributor.author | Jawhari, Ahmed Hussain | |
dc.contributor.author | Amri, Nasser | |
dc.contributor.author | Mukhrish, Yousef E. | |
dc.contributor.author | Gatri, Rafik | |
dc.contributor.author | Ozdemir, Ismail | |
dc.contributor.author | Gurbuz, Nevin | |
dc.contributor.author | Mansour, Lamjed | |
dc.date.accessioned | 2024-08-04T20:54:55Z | |
dc.date.available | 2024-08-04T20:54:55Z | |
dc.date.issued | 2023 | |
dc.department | İnönü Üniversitesi | en_US |
dc.description.abstract | A series of ruthenium(ii) complexes with N-heterocyclic carbene (NHC) ligands of the general type (arene)(NHC)Ru(ii)X-2 (where X = halide) (3a-3d) were synthesized and characterized in order to compare their antibacterial activities with benzimidazolium salts 2. Our comparison revealed that ruthenium(ii) NHC complexes 3 were more active than benzimidazolium salts 2. Furthermore, the two complexes 3b and 3d had a potent inhibitory effect against acetylcholinesterase with an IC50 of 4.52 and 4.04 gmL(-1) and against tyrosinase with an IC50 of 20.77 and 25.84 gmL(-1), respectively. In addition, screening of benzimidazolium salts (2a-2d) and their ruthenium(ii) complexes (3a-3d) against colon carcinoma cell lines (HCT-116) and hepatocellular carcinoma cell lines (HepG-2) were studied. The obtained results revealed that complex 3a is the most active against vinblastines. | en_US |
dc.description.sponsorship | King Saud University, Riyadh, Saudi Arabia [RSP2023R75] | en_US |
dc.description.sponsorship | The authors extend their appreciation to the Researchers Supporting Project (number RSP2023R75), King Saud University, Riyadh, Saudi Arabia. | en_US |
dc.identifier.doi | 10.1515/mgmc-2023-0008 | |
dc.identifier.issn | 0792-1241 | |
dc.identifier.issn | 2191-0219 | |
dc.identifier.issue | 1 | en_US |
dc.identifier.scopus | 2-s2.0-85179054459 | en_US |
dc.identifier.scopusquality | Q3 | en_US |
dc.identifier.uri | https://doi.org/10.1515/mgmc-2023-0008 | |
dc.identifier.uri | https://hdl.handle.net/11616/101707 | |
dc.identifier.volume | 46 | en_US |
dc.identifier.wos | WOS:001109537000001 | en_US |
dc.identifier.wosquality | Q3 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.language.iso | en | en_US |
dc.publisher | De Gruyter Poland Sp Z O O | en_US |
dc.relation.ispartof | Main Group Metal Chemistry | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | biological activity | en_US |
dc.subject | benzimidazolium salts | en_US |
dc.subject | ruthenium complexes | en_US |
dc.subject | silver complexes | en_US |
dc.subject | HCT-116 | en_US |
dc.subject | HepG-2 | en_US |
dc.title | Novel ruthenium(ii) N-heterocyclic carbene complexes: Synthesis, characterization, and evaluation of their biological activities | en_US |
dc.type | Article | en_US |