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Cytotoxic Phosphinoarsino and Diphosphino Pd(II) Complexes of Thiolate Amino Acids and Glutathione
The novel complexes [Pd(L-L′)(SR)Cl] where L-L′ is Ph(2)PCH(2)CH(2)PPh(2) (dppe) or Ph(2)AsCH(2)CH(2)PPh(2) (dadpe) and RSH is glutathione, L-cysteine, or N-acetyl-L-cysteine, have been prepared and characterised. Their structures in the solid-state and in solution are discussed. The introduction of...
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
1995
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2364951/ https://www.ncbi.nlm.nih.gov/pubmed/18472743 http://dx.doi.org/10.1155/MBD.1995.19 |
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author | Dhubhghaill, Orla M. Ni Sadler, Peter J. Fernandez, Esther Garcia |
author_facet | Dhubhghaill, Orla M. Ni Sadler, Peter J. Fernandez, Esther Garcia |
author_sort | Dhubhghaill, Orla M. Ni |
collection | PubMed |
description | The novel complexes [Pd(L-L′)(SR)Cl] where L-L′ is Ph(2)PCH(2)CH(2)PPh(2) (dppe) or Ph(2)AsCH(2)CH(2)PPh(2) (dadpe) and RSH is glutathione, L-cysteine, or N-acetyl-L-cysteine, have been prepared and characterised. Their structures in the solid-state and in solution are discussed. The introduction of cysteine or glutathione as a ligand in these complexes greatly improved their aqueous solubility compared with the hydrophobic parent dichloro complexes. The cytotoxicities of the glutathione complexes towards the cell-lines L1210, ADJ/PC6 and CH1 were investigated. Their cytotoxicities towards L1210 cells were comparable to those of the parent dichloro complexes. |
format | Text |
id | pubmed-2364951 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1995 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-23649512008-05-12 Cytotoxic Phosphinoarsino and Diphosphino Pd(II) Complexes of Thiolate Amino Acids and Glutathione Dhubhghaill, Orla M. Ni Sadler, Peter J. Fernandez, Esther Garcia Met Based Drugs Research Article The novel complexes [Pd(L-L′)(SR)Cl] where L-L′ is Ph(2)PCH(2)CH(2)PPh(2) (dppe) or Ph(2)AsCH(2)CH(2)PPh(2) (dadpe) and RSH is glutathione, L-cysteine, or N-acetyl-L-cysteine, have been prepared and characterised. Their structures in the solid-state and in solution are discussed. The introduction of cysteine or glutathione as a ligand in these complexes greatly improved their aqueous solubility compared with the hydrophobic parent dichloro complexes. The cytotoxicities of the glutathione complexes towards the cell-lines L1210, ADJ/PC6 and CH1 were investigated. Their cytotoxicities towards L1210 cells were comparable to those of the parent dichloro complexes. Hindawi Publishing Corporation 1995 /pmc/articles/PMC2364951/ /pubmed/18472743 http://dx.doi.org/10.1155/MBD.1995.19 Text en Copyright © 1995 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 Dhubhghaill, Orla M. Ni Sadler, Peter J. Fernandez, Esther Garcia Cytotoxic Phosphinoarsino and Diphosphino Pd(II) Complexes of Thiolate Amino Acids and Glutathione |
title | Cytotoxic Phosphinoarsino and Diphosphino Pd(II) Complexes
of Thiolate Amino Acids and Glutathione |
title_full | Cytotoxic Phosphinoarsino and Diphosphino Pd(II) Complexes
of Thiolate Amino Acids and Glutathione |
title_fullStr | Cytotoxic Phosphinoarsino and Diphosphino Pd(II) Complexes
of Thiolate Amino Acids and Glutathione |
title_full_unstemmed | Cytotoxic Phosphinoarsino and Diphosphino Pd(II) Complexes
of Thiolate Amino Acids and Glutathione |
title_short | Cytotoxic Phosphinoarsino and Diphosphino Pd(II) Complexes
of Thiolate Amino Acids and Glutathione |
title_sort | cytotoxic phosphinoarsino and diphosphino pd(ii) complexes
of thiolate amino acids and glutathione |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2364951/ https://www.ncbi.nlm.nih.gov/pubmed/18472743 http://dx.doi.org/10.1155/MBD.1995.19 |
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