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Synthesis, structural characterization and biological studies of the triphenyltin(IV) complex with 2-thiobarbituric acid.
- Source :
-
European journal of medicinal chemistry [Eur J Med Chem] 2011 Jul; Vol. 46 (7), pp. 2835-44. Date of Electronic Publication: 2011 Apr 08. - Publication Year :
- 2011
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Abstract
- The reaction between 2-thiobarbituric acid (H(2)TBA), which was treated with an equimolar amount of potassium hydroxide, in a water with triphenytin chloride in methanol, results in the formation of the {[Ph(3)Sn(O-HTBA)]}(n) (1) complex. Crystals of the hydrated 1 with formula {[Ph(3)Sn(O-HTBA)]·0.7(H(2)O)}(n) were growth from methanol/acetonitrile solution, of the white precipitation, filtered off, from the reaction. The crystal structure of complex 1 has been determined by X-ray diffraction at 120 K. Complex 1 is polymeric. The geometry around the tin(IV) ions is trigonal bi-pyramidal with coordination to three C atoms from phenyl groups and one O atom from a de-protonated HTBA ligand. Complex 1 and the already known [(n-Bu)(3)Sn(O-HTBA)·H(2)O] (2) were evaluated for their in vitro cytotoxic activity (cell viability) against human cancer cell lines: HeLa (cervical), OAW-42 (ovarian), MCF-7 (breast, ER positive), MDA-MB-231 (breast, ER negative), A549 (lung), Caki-1 (renal) and additionally, the normal human lung cell line MRC-5 (normal human fetal lung fibroblast cells) and normal immortalized human mammary gland epithelial cell line MTSV17 with a Trypan Blue assay. Moreover complex 1 was evaluated for its in vitro cell growth proliferation activity against leiomyosarcoma cells (LMS), MCF-7 and MRC-5 cells with a Thiazolyl Blue Tetrazolium Bromide (MTT) assay. The type of cell death caused by complexes 1 and 2 was also evaluated by use of flow cytometry assay. The results showed that these compounds mediate a strong cytotoxic response to normal and cancer cell lines tested through apoptosis and induce cell cycle arrest in S phase of the cell cycle, suggesting DNA intercalation (direct or indirect) with the complexes. Finally, the influence of these complexes 1 and 2 upon the catalytic peroxidation of linoleic acid to hydroperoxylinoleic acid by the enzyme lipoxygenase (LOX) was kinetically and theoretically studied.<br /> (Copyright © 2011 Elsevier Masson SAS. All rights reserved.)
- Subjects :
- Antineoplastic Agents pharmacology
Apoptosis drug effects
Cell Line, Tumor
Cell Proliferation drug effects
Coordination Complexes pharmacology
Crystallography, X-Ray
Drug Screening Assays, Antitumor
Fibroblasts cytology
Fibroblasts drug effects
HeLa Cells
Humans
Hydroxides chemistry
Intercalating Agents pharmacology
Linoleic Acid chemistry
Lipoxygenase chemistry
MCF-7 Cells
Potassium Compounds chemistry
S Phase Cell Cycle Checkpoints drug effects
Structure-Activity Relationship
Antineoplastic Agents chemical synthesis
Coordination Complexes chemical synthesis
Intercalating Agents chemical synthesis
Organotin Compounds chemistry
Thiobarbiturates chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1768-3254
- Volume :
- 46
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- European journal of medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 21521629
- Full Text :
- https://doi.org/10.1016/j.ejmech.2011.04.005