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Antitumour Activity of a pt(III) Derivative of 2-Mercaptopyrimidine

The complex [Pt(2)Cl(2)(Spym)(4)], where Spym = 2-mercaptopyrimidine, was synthesized and analyzed spectroscopically. The presence in the (195)Pt NMR spectrum, of only one signal for the Pt(III) indicates the symmetrical arrangement of the ligands and the identical setting of N, S and Cl atoms, PtS(...

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Detalles Bibliográficos
Autores principales: Cervantes, G., Prieto, M. J., Moreno, V.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 1997
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2365033/
https://www.ncbi.nlm.nih.gov/pubmed/18475760
http://dx.doi.org/10.1155/MBD.1997.9
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author Cervantes, G.
Prieto, M. J.
Moreno, V.
author_facet Cervantes, G.
Prieto, M. J.
Moreno, V.
author_sort Cervantes, G.
collection PubMed
description The complex [Pt(2)Cl(2)(Spym)(4)], where Spym = 2-mercaptopyrimidine, was synthesized and analyzed spectroscopically. The presence in the (195)Pt NMR spectrum, of only one signal for the Pt(III) indicates the symmetrical arrangement of the ligands and the identical setting of N, S and Cl atoms, PtS(2)ClN(2), for the two Pt atoms being different to other compounds described in the literature. The interaction of this complex with DNA was studied by several techniques, including circular dichroism, melting temperature determination, electron microscopy (EM) and atomic force microscopy (TMAFM). Preliminary results show a high activity against HL-60 and HeLa tumour lines for the Pt-2-mercaptopyrimidine complex in comparison with cisplatin activity. Higher values for IC(50) were obtained, while the values of LD(50) were lower than those for cisplatin.
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spelling pubmed-23650332008-05-12 Antitumour Activity of a pt(III) Derivative of 2-Mercaptopyrimidine Cervantes, G. Prieto, M. J. Moreno, V. Met Based Drugs Research Article The complex [Pt(2)Cl(2)(Spym)(4)], where Spym = 2-mercaptopyrimidine, was synthesized and analyzed spectroscopically. The presence in the (195)Pt NMR spectrum, of only one signal for the Pt(III) indicates the symmetrical arrangement of the ligands and the identical setting of N, S and Cl atoms, PtS(2)ClN(2), for the two Pt atoms being different to other compounds described in the literature. The interaction of this complex with DNA was studied by several techniques, including circular dichroism, melting temperature determination, electron microscopy (EM) and atomic force microscopy (TMAFM). Preliminary results show a high activity against HL-60 and HeLa tumour lines for the Pt-2-mercaptopyrimidine complex in comparison with cisplatin activity. Higher values for IC(50) were obtained, while the values of LD(50) were lower than those for cisplatin. Hindawi Publishing Corporation 1997 /pmc/articles/PMC2365033/ /pubmed/18475760 http://dx.doi.org/10.1155/MBD.1997.9 Text en Copyright © 1997 Hindawi Publishing Corporation. http://creativecommons.org/licenses/by/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Cervantes, G.
Prieto, M. J.
Moreno, V.
Antitumour Activity of a pt(III) Derivative of 2-Mercaptopyrimidine
title Antitumour Activity of a pt(III) Derivative of 2-Mercaptopyrimidine
title_full Antitumour Activity of a pt(III) Derivative of 2-Mercaptopyrimidine
title_fullStr Antitumour Activity of a pt(III) Derivative of 2-Mercaptopyrimidine
title_full_unstemmed Antitumour Activity of a pt(III) Derivative of 2-Mercaptopyrimidine
title_short Antitumour Activity of a pt(III) Derivative of 2-Mercaptopyrimidine
title_sort antitumour activity of a pt(iii) derivative of 2-mercaptopyrimidine
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2365033/
https://www.ncbi.nlm.nih.gov/pubmed/18475760
http://dx.doi.org/10.1155/MBD.1997.9
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