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Multinuclear NMR spectroscopy and antiproliferative activity in vitro of platinum(II) and palladium(II) complexes with 6-mercaptopurine
A series of Pd(II) and Pt(II) complexes with 6-mercaptopurine (6-Hmp) of formulae Pd(6-Hmp) 2Cl 2 ( 1), Pd(6-mp) 2·2H 2O ( 2), Pt(6-mp) 2·2H 2O ( 3), Pt(6-mp)(dmso)Cl ( 4) was synthesized and studied by IR, far-IR, 1H, 13C, 15N NMR. ( 1) has an ionic character and consists of distinct [Pd(6-Hmp) 2]...
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Published in: | Journal of molecular structure 2004-11, Vol.707 (1), p.241-247 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A series of Pd(II) and Pt(II) complexes with 6-mercaptopurine (6-Hmp) of formulae Pd(6-Hmp)
2Cl
2 (
1), Pd(6-mp)
2·2H
2O (
2), Pt(6-mp)
2·2H
2O (
3), Pt(6-mp)(dmso)Cl (
4) was synthesized and studied by IR, far-IR,
1H,
13C,
15N NMR. (
1) has an ionic character and consists of distinct [Pd(6-Hmp)
2]
2+ cations and uncoordinated Cl
− anions, whereas (
2,3) are neutral species with central atoms bis-chelated by the deprotonated 6-mp
− ligands. NMR studies suggest that S and N(7) are the complexation sites, while far-IR spectra indicate the square-planar geometry of Pd(II) or Pt(II). In (
4) the Pt(II) atom is coordinated by one chelating 6-mp
− anion, S-bonded dmso molecule and a terminal chloride. The antiproliferative activity in vitro of (
2–4) was tested against human leukaemia HL-60 cells, being exhibited for (
2) at the level ca. six times lower than in case of cisplatin. |
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ISSN: | 0022-2860 1872-8014 |
DOI: | 10.1016/j.molstruc.2004.07.027 |