Biological Activities of NHC-Pd(II) Complexes Based on Benzimidazolylidene N-heterocyclic Carbene (NHC) Ligands Bearing Aryl Substituents
dc.authorid | Yaşar, Sedat/0000-0001-7285-2761 | |
dc.authorid | Özdemir, İsmail/0000-0001-6325-0216 | |
dc.authorid | Touj, Nedra/0000-0001-6071-4361 | |
dc.authorid | Touj, Nedra/0000-0001-6071-4361 | |
dc.authorid | Khan, Tariq Ayub/0000-0001-6184-5929 | |
dc.authorid | AL NASR, IBRAHIM/0000-0003-4690-1050 | |
dc.authorid | Hamdi, Naceur/0000-0003-0110-9588 | |
dc.authorwosid | Yaşar, Sedat/ABG-8356-2020 | |
dc.authorwosid | Özdemir, İsmail/ABI-5192-2020 | |
dc.authorwosid | Touj, Nedra/AAM-2982-2021 | |
dc.authorwosid | Touj, Nedra/G-6828-2019 | |
dc.authorwosid | Nasr, Ibrahim Al/AFP-8105-2022 | |
dc.authorwosid | Hamdi, Naceur/M-3308-2016 | |
dc.contributor.author | Al Nasr, Ibrahim | |
dc.contributor.author | Touj, Nedra | |
dc.contributor.author | Koko, Waleed | |
dc.contributor.author | Khan, Tariq | |
dc.contributor.author | Ozdemir, Ismail | |
dc.contributor.author | Yasar, Sedat | |
dc.contributor.author | Hamdi, Naceur | |
dc.date.accessioned | 2024-08-04T20:49:00Z | |
dc.date.available | 2024-08-04T20:49:00Z | |
dc.date.issued | 2020 | |
dc.department | İnönü Üniversitesi | en_US |
dc.description.abstract | N-heterocyclic carbene (NHC) precursors (2a-i), their pyridine-enhanced precatalyst preparation stabilization and initiation (PEPPSI)-themed palladium N-heterocyclic carbene complexes (3a-i) and palladium N-heterocyclic triphenylphosphines complexes (4a-i) were synthesized and characterized by elemental analysis and H-1 NMR, C-13 NMR, IR, and LC-MS spectroscopic techniques. The (NHC)Pd(II) complexes 3-4 were tested against MCF7 and MDA-MB-231 cancer cells, Escherichia coli, methicillin-resistant Staphylococcus aureus (MRSA), Candida albicans microorganisms, Leishmania major promastigotes and amastigotes, Toxoplasma gondii parasites, and Vero cells in vitro. The biological assays indicated that all compounds are highly active against cancer cells, with an IC50 < 1.5 mu g mL(-1). Eight compounds proved antibacterial and antileishmanial activities, while only three compounds had strong antifungal activities against C. albicans. In our conclusion, compounds 3 (b, f, g, and h) and 4b are the most suitable drug candidates for anticancer, antimicrobial, and antiparasitical. | en_US |
dc.description.sponsorship | Deanship of Scientific Research, Qassim University | en_US |
dc.description.sponsorship | Researchers would like to thank the Deanship of Scientific Research, Qassim University for funding publication of this project. | en_US |
dc.identifier.doi | 10.3390/catal10101190 | |
dc.identifier.issn | 2073-4344 | |
dc.identifier.issue | 10 | en_US |
dc.identifier.scopus | 2-s2.0-85092700333 | en_US |
dc.identifier.scopusquality | Q2 | en_US |
dc.identifier.uri | https://doi.org/10.3390/catal10101190 | |
dc.identifier.uri | https://hdl.handle.net/11616/99590 | |
dc.identifier.volume | 10 | en_US |
dc.identifier.wos | WOS:000584126700001 | en_US |
dc.identifier.wosquality | Q2 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.language.iso | en | en_US |
dc.publisher | Mdpi | en_US |
dc.relation.ispartof | Catalysts | 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 | Pd(II)– N-heterocyclic carbene (NHC) complexes | en_US |
dc.subject | benzimidazolium salts | en_US |
dc.subject | biological activities | en_US |
dc.subject | cytotoxicity | en_US |
dc.title | Biological Activities of NHC-Pd(II) Complexes Based on Benzimidazolylidene N-heterocyclic Carbene (NHC) Ligands Bearing Aryl Substituents | en_US |
dc.type | Article | en_US |