Pregled bibliografske jedinice broj: 924421
Heteroleptic ruthenium bioflavonoid complexes: From synthesis to in vitro biological activity
Heteroleptic ruthenium bioflavonoid complexes: From synthesis to in vitro biological activity // Journal of coordination chemistry, 70 (2017), 24; 4030-4053 doi:10.1080/00958972.2017.1409893 (podatak o recenziji nije dostupan, članak, znanstveni)
CROSBI ID: 924421 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Heteroleptic ruthenium bioflavonoid complexes:
From synthesis to in vitro biological activity
Autori
Zahirović, Adnan ; Kahrović, Emira ; Cindrić, Marina ; Kraljević Pavelić, Sandra ; Hukić, Mirsada ; Harej, Anja ; Turkušić, Emir
Izvornik
Journal of coordination chemistry (0095-8972) 70
(2017), 24;
4030-4053
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
Ruthenium, flavonoid, biomolecules, anticancer, antimicrobial
Sažetak
Heteroleptic ruthenium(II) bioflavonoid complexes of quercetin, morin, chrysin, and 3- hydroxyflavone were prepared and their interaction with CT DNA and BSA along with antioxidant and in vitro anticancer and antimicrobial activities was investigated. The formulation and characterization of complexes were achieved through elemental and thermal analysis, mass spectrometry, 1H NMR spectroscopy along with infrared, electronic absorption, and emission spectroscopy as well as square-wave voltammetry, and magnetic and conductivity measurements. Ruthenium(II) is octahedrally coordinated in cationic complex species to two bidentate diimine ligands (2, 2′- bipyridine or 1, 10-phenanthroline) and one bidentate monobasic flavonoid ligand through 3, 4-site of quercetin, morin, and 3- hydroxyflavone or 4, 5-site of chrysin. Complexes bind CT DNA by intercalation and binding constants comparable to ethidium bromide or 10 times higher. Binding constants of complexes to BSA were several times higher compared to ibuprofen and diazepam, and suggest that the complexes have a strong affinity to BSA. Antioxidant activity tests showed that the complexes are more potent in terms of radical inhibition compared to the parent flavonoids. Cytotoxic testing revealed that the Ru(II) complex of quercetin with 2, 2′-bipyridine co- ligand has good selectivity to breast adenocarcinoma, while the complex of 3- hydroxyflavone with 2, 2′-bipyridine co-ligand showed strong cytotoxicity toward all tested cell lines with IC50 ∼ 1 μM. All complexes showed moderate activity toward Acinetobacter baumannii, while the Ru(II) complex of 3- hydroxyflavone with 2, 2′-bipyridine showed excellent activity toward MRSA and Candida albicans.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Interdisciplinarne prirodne znanosti
POVEZANOST RADA
Ustanove:
Prirodoslovno-matematički fakultet, Zagreb,
Sveučilište u Rijeci - Odjel za biotehnologiju
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
Uključenost u ostale bibliografske baze podataka::
- CA Search (Chemical Abstracts)
- Cambridge Crystallographic Data Centre
- Chimica
- Google Scholar
- Microsoft Academic
- ProQuest