Ni(ii)/Cu(ii)/Zn(ii) 5, 5-diethylbarbiturate complexes with 1, 10-phenanthroline and 2, 2′-dipyridylamine: synthesis, structures, DNA/BSA binding, nuclease activity, molecular docking, cellular uptake, cytotoxicity and the mode of cell death. Issue 25 (6th June 2016)

• Record Type: Journal Article
• Authors: Yilmaz, Veysel T.; Icsel, Ceyda; Suyunova, Feruza; Aygun, Muhittin; Aztopal, Nazlihan; Ulukaya, Engin
• Is Part Of: Dalton transactions. Volume 45:Issue 25(2016)
• Page Start: 10466
• Page End: 10479
• Publication Date: 2016-06-06
• Subjects: Chemistry, Inorganic -- Periodicals; Chemistry, Physical and theoretical -- Periodicals; Chemistry, Inorganic -- Periodicals; 546.05
• DOI: 10.1039/c6dt01726f
• Languages: English
• ISSNs: 1477-9226

Abstract

Abstract : DNA/BSA binding and anticancer properties of new Ni(ii ), Cu(ii ) and Zn(ii ) 5, 5-diethylbarbiturate complexes were evaluated. Abstract : New 5, 5-diethylbarbiturate (barb) complexes of Ni(ii ), Cu(ii ) and Zn(ii ) with 1, 10-phenanthroline (phen) and 2, 2′-dipyridylamine (dpya), namely [Ni(phen-κ N, N ′)3 ]Cl(barb)·7H2 O (1 ), [Cu(barb-κ N )(barb-κ 2 N, O )(phen-κ N, N ′)]·H2 O (2 ), [Cu(barb-κ N )2 (phen-κ N, N ′)] (2a ), [Zn(barb-κ N )2 (phen-κ N, N ′)]·H2 O (3 ), [Ni(barb-κ 2 N, O )(dpya-κ N, N ′)2 ]Cl·2H2 O (4 ), [Cu(barb-κ 2 N, O )2 (dpya-κ N, N ′)]·2H2 O (5 ) and [Zn(barb-κ N )2 (dpya-κ N, N ′)] (6 ), were synthesized and characterized by elemental analysis, UV-vis, FT-IR and ESI-MS. The structures of the complexes were determined by X-ray crystallography. Notably, 3 and6 were fluorescent in MeOH : H2 O at rt. The interaction of the complexes with fish sperm (FS) DNA and bovine serum albumin (BSA) was investigated in detail by various techniques. The complexes exhibited groove binding along with a partial intercalative interaction with DNA, while the hydrogen bonding and hydrophobic interactions played a major role in binding to BSA. It is noteworthy that2 exhibited the highest affinity towards DNA and BSA. Enzyme inhibition assay showed that1–4 show a preference for both A/T and G/C rich sequences in pUC19 DNA, while5 and6 display a binding specificity to the G/C and A/T rich regions, respectively. These findings were further supported by molecular docking. The cellular uptake studies suggested that2 was deposited mostly in the membrane fraction of the cells. Among the present complexes, 2 exhibited a very strong cytotoxic effect on A549, MCF-7, HT-29 and DU-145 cancer cells, being more potent than cisplatin. Moreover, 2 induces cell death through the apoptotic mode obtained by flow cytometry.