| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1309347 | Inorganica Chimica Acta | 2014 | 9 Pages |
•Di-n-butyltin(IV) complex of the chiral anti-inflammatory drug.•Structural characterization.•Organotins towards the linoleic acid, the intracellular glutathione and the nuclear CT-DNA.
The already known di-n-butyltin(IV) complex of the chiral anti-inflammatory drug naproxen (Hnapr) of formula [(n-Bu-)2Sn(nap)2] (1), was re-synthesized here with an alternative method and it was used for the assessment of organotins towards the linoleic acid which is located in the cell membrane, the intracellular glutathione and the nuclear CT-DNA. The compound was characterized by melting point (m.p.) 119Sn Mössbauer while its structure was confirmed by X-ray crystallography. The influence of 1, upon the peroxidation of linoleic acid to hydroperoxylinoleic was kinetically studied. The binding affinity of 1 towards the intracellular molecular components CT-DNA and glutathione (GSH) was studied by UV–Vis spectroscopy.
Graphical abstractThe already known di-n-butyltin(IV) complex of the chiral anti-inflammatory drug naproxen (Hnapr) of formula [(n-Bu-)2Sn(nap)2] (1), was re-synthesized here with an alternative method and it was used for the assessment of organotins towards the linoleic acid which is located in the cell m;embrane, the intracellular glutathione and the nuclear CT-DNA.Figure optionsDownload full-size imageDownload as PowerPoint slide
