Yayın:
Trans-Dichloridopalladium(II) and platinum(II) complexes with 2-(hydroxymethyl)pyridine and 2-(2-hydroxyethyl)pyridine: Synthesis, structural characterization, DNA binding and in vitro cytotoxicity studies

Placeholder

Tarih

Akademik Birimler

Kurum Yazarları

İçsel, Ceyda
Yılmaz, Veysel T.
Arı, Ferda
Ulukaya, Engin

Yazarlar

Harrison, William T. A.

Danışman

Dil

Türü

Yayıncı:

Elsevier France

Dergi Başlığı

Dergi ISSN

Cilt Başlığı

Özet

Four trans-palladium(II)- and trans-platinum(II)-chlorido complexes, trans-[PdCl2(2-hmpy)(2)] (1), trans-[PtCl2(2-hmpy)(2)] (2), trans-[Pdcl(2)(2-hepy)(2)] (3) and trans-[PtCl2(2-hepy)(2)] (4) (2-hmpy = 2-(hydroxymethyl)pyridine and 2-hepy = 2-(2-hydroxyethyl)pyridine), have been synthesized and characterized by elemental analysis, IR, NMR, and X-ray diffraction. The binding properties of these complexes with fish sperm DNA (FS-DNA) were investigated by UV titration, viscosity, thermal denaturation and electrophoresis measurements. The complexes can bind to FS-DNA and complex 4 exhibits the highest binding constant. Gel electrophoresis assay demonstrates that all the complexes can cleave the pCMV-beta gal plasmid DNA to a different degree. The cytotoxic activities of the complexes were tested against four different cancer cell lines. In general, the platinum(II) complexes are more effective than the isostructural palladium(II) complexes. Complex 4 shows high anticancer activity, compared to transplatin, cisplatin, carboplatin and oxaliplatin.

Açıklama

Kaynak:

Anahtar Kelimeler:

Konusu

Pharmacology & pharmacy, Transplatinum complexes, 2-(Hydroxymethyl)pyridine, 2-(2-Hydroxyethyl)pyridine, DNA binding, Cytotoxic activity, Trans geometry, Ethidium-bromide, Metal-complexes, Antitumor, Palladium(II), Pd(II), Ligand, Drugs, Ruthenium(II), Fluorescence

Alıntı

İçsel, C. vd. (2013). "Trans-Dichloridopalladium(II) and platinum(II) complexes with 2-(hydroxymethyl)pyridine and 2-(2-hydroxyethyl)pyridine: Synthesis, structural characterization, DNA binding and in vitro cytotoxicity studies". European Journal of Medicinal Chemistry, 60, 386-394 .

Endorsement

Review

Supplemented By

Referenced By

0

Views

0

Downloads