Cargando…
Synthesis, Characterization and Antitumor Activity of cis-bis(acylthioureato) platinum(II) Complexes, cis-[PtL(2)] [HL(1)=N,N-Diphenyl-N'-Benzoylthiourea or HL(2)=N,N-diphenyl-N'-(p-nitrobenzoyl)thiourea]
A low-molecular weight chromium-containing fraction of the material resulting from dichromate reduction by bovine liver homogenate was investigated by NMR and ES-MS. The ES-MS spectrum showed a readily detectable peak at m/z 786.1. The same molecular weight reasonably agreed with the relatively low...
Autores principales: | , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2003
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267062/ https://www.ncbi.nlm.nih.gov/pubmed/18365059 http://dx.doi.org/10.1155/S1565363303000219 |
_version_ | 1782151600988487680 |
---|---|
author | Hernández, Wilfredo Spodine, Evgenia Muñoz, Juan Carlos Beyer, Lothar Schröder, Uwe Ferreira, Jorge Pavani, Mario |
author_facet | Hernández, Wilfredo Spodine, Evgenia Muñoz, Juan Carlos Beyer, Lothar Schröder, Uwe Ferreira, Jorge Pavani, Mario |
author_sort | Hernández, Wilfredo |
collection | PubMed |
description | A low-molecular weight chromium-containing fraction of the material resulting from dichromate reduction by bovine liver homogenate was investigated by NMR and ES-MS. The ES-MS spectrum showed a readily detectable peak at m/z 786.1. The same molecular weight reasonably agreed with the relatively low diffusion coefficient measured by NMR-DOSY experiments on the main species observed in the (1)H NMR spectrum. At least two downfield shifted and broad paramagnetic signals were apparent in the (1)H NMR spectrum. Temperature dependence of chemical shift was exploited in order to estimate the diamagnetic shift of the signals in the diamagnetic region of the spectrum. 2D TOCSY, NOESY, COSY and (1)H-(13)C HMQC spectra revealed the presence of aromatic protons (which were assigned as His residues), Gly and some other short chain amino-acids. Combinations of the molecular masses of such components together with acetate (which is present in the solution) and chromium atoms allowed a tentative proposal of a model for the compound. |
format | Text |
id | pubmed-2267062 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-22670622008-03-24 Synthesis, Characterization and Antitumor Activity of cis-bis(acylthioureato) platinum(II) Complexes, cis-[PtL(2)] [HL(1)=N,N-Diphenyl-N'-Benzoylthiourea or HL(2)=N,N-diphenyl-N'-(p-nitrobenzoyl)thiourea] Hernández, Wilfredo Spodine, Evgenia Muñoz, Juan Carlos Beyer, Lothar Schröder, Uwe Ferreira, Jorge Pavani, Mario Bioinorg Chem Appl Research Article A low-molecular weight chromium-containing fraction of the material resulting from dichromate reduction by bovine liver homogenate was investigated by NMR and ES-MS. The ES-MS spectrum showed a readily detectable peak at m/z 786.1. The same molecular weight reasonably agreed with the relatively low diffusion coefficient measured by NMR-DOSY experiments on the main species observed in the (1)H NMR spectrum. At least two downfield shifted and broad paramagnetic signals were apparent in the (1)H NMR spectrum. Temperature dependence of chemical shift was exploited in order to estimate the diamagnetic shift of the signals in the diamagnetic region of the spectrum. 2D TOCSY, NOESY, COSY and (1)H-(13)C HMQC spectra revealed the presence of aromatic protons (which were assigned as His residues), Gly and some other short chain amino-acids. Combinations of the molecular masses of such components together with acetate (which is present in the solution) and chromium atoms allowed a tentative proposal of a model for the compound. Hindawi Publishing Corporation 2003 /pmc/articles/PMC2267062/ /pubmed/18365059 http://dx.doi.org/10.1155/S1565363303000219 Text en Copyright © 2003 Wilfredo Hernández et al. http://creativecommons.org/licenses/by/2.0 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 Hernández, Wilfredo Spodine, Evgenia Muñoz, Juan Carlos Beyer, Lothar Schröder, Uwe Ferreira, Jorge Pavani, Mario Synthesis, Characterization and Antitumor Activity of cis-bis(acylthioureato) platinum(II) Complexes, cis-[PtL(2)] [HL(1)=N,N-Diphenyl-N'-Benzoylthiourea or HL(2)=N,N-diphenyl-N'-(p-nitrobenzoyl)thiourea] |
title | Synthesis, Characterization and Antitumor Activity of
cis-bis(acylthioureato) platinum(II) Complexes, cis-[PtL(2)] [HL(1)=N,N-Diphenyl-N'-Benzoylthiourea or HL(2)=N,N-diphenyl-N'-(p-nitrobenzoyl)thiourea] |
title_full | Synthesis, Characterization and Antitumor Activity of
cis-bis(acylthioureato) platinum(II) Complexes, cis-[PtL(2)] [HL(1)=N,N-Diphenyl-N'-Benzoylthiourea or HL(2)=N,N-diphenyl-N'-(p-nitrobenzoyl)thiourea] |
title_fullStr | Synthesis, Characterization and Antitumor Activity of
cis-bis(acylthioureato) platinum(II) Complexes, cis-[PtL(2)] [HL(1)=N,N-Diphenyl-N'-Benzoylthiourea or HL(2)=N,N-diphenyl-N'-(p-nitrobenzoyl)thiourea] |
title_full_unstemmed | Synthesis, Characterization and Antitumor Activity of
cis-bis(acylthioureato) platinum(II) Complexes, cis-[PtL(2)] [HL(1)=N,N-Diphenyl-N'-Benzoylthiourea or HL(2)=N,N-diphenyl-N'-(p-nitrobenzoyl)thiourea] |
title_short | Synthesis, Characterization and Antitumor Activity of
cis-bis(acylthioureato) platinum(II) Complexes, cis-[PtL(2)] [HL(1)=N,N-Diphenyl-N'-Benzoylthiourea or HL(2)=N,N-diphenyl-N'-(p-nitrobenzoyl)thiourea] |
title_sort | synthesis, characterization and antitumor activity of
cis-bis(acylthioureato) platinum(ii) complexes, cis-[ptl(2)] [hl(1)=n,n-diphenyl-n'-benzoylthiourea or hl(2)=n,n-diphenyl-n'-(p-nitrobenzoyl)thiourea] |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267062/ https://www.ncbi.nlm.nih.gov/pubmed/18365059 http://dx.doi.org/10.1155/S1565363303000219 |
work_keys_str_mv | AT hernandezwilfredo synthesischaracterizationandantitumoractivityofcisbisacylthioureatoplatinumiicomplexescisptl2hl1nndiphenylnbenzoylthioureaorhl2nndiphenylnpnitrobenzoylthiourea AT spodineevgenia synthesischaracterizationandantitumoractivityofcisbisacylthioureatoplatinumiicomplexescisptl2hl1nndiphenylnbenzoylthioureaorhl2nndiphenylnpnitrobenzoylthiourea AT munozjuancarlos synthesischaracterizationandantitumoractivityofcisbisacylthioureatoplatinumiicomplexescisptl2hl1nndiphenylnbenzoylthioureaorhl2nndiphenylnpnitrobenzoylthiourea AT beyerlothar synthesischaracterizationandantitumoractivityofcisbisacylthioureatoplatinumiicomplexescisptl2hl1nndiphenylnbenzoylthioureaorhl2nndiphenylnpnitrobenzoylthiourea AT schroderuwe synthesischaracterizationandantitumoractivityofcisbisacylthioureatoplatinumiicomplexescisptl2hl1nndiphenylnbenzoylthioureaorhl2nndiphenylnpnitrobenzoylthiourea AT ferreirajorge synthesischaracterizationandantitumoractivityofcisbisacylthioureatoplatinumiicomplexescisptl2hl1nndiphenylnbenzoylthioureaorhl2nndiphenylnpnitrobenzoylthiourea AT pavanimario synthesischaracterizationandantitumoractivityofcisbisacylthioureatoplatinumiicomplexescisptl2hl1nndiphenylnbenzoylthioureaorhl2nndiphenylnpnitrobenzoylthiourea |