Trans platinum complexes design: One novel water soluble oxime derivative that contains aliphatic amines in trans configuration
Autor: | Leticia Cubo, Patricio Aller, Adoración G. Quiroga, Carmen Navarro-Ranninger, Elena de Blas |
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Rok vydání: | 2007 |
Předmět: |
Models
Molecular Platinum complexes Stereochemistry chemistry.chemical_element Platinum Compounds Antitumor drugs Apoptosis Stereoisomerism Crystal structure Biochemistry Cell Line Inorganic Chemistry chemistry.chemical_compound Cell Line Tumor Oximes medicine Animals Humans Molecule Amines Cytotoxicity Cisplatin Molecular Structure Oxime Rats Solubility chemistry Drug Screening Assays Antitumor Platinum Derivative (chemistry) medicine.drug |
Zdroj: | Digital.CSIC. Repositorio Institucional del CSIC instname |
ISSN: | 0162-0134 |
DOI: | 10.1016/j.jinorgbio.2006.08.012 |
Popis: | 7 páginas, 5 figuras, 1 tabla -- PAGS nros. 104-110 In an attempt to design new antitumoral drugs based on transplatin complexes, we determined the experimental conditions for the preparation of trans-[Pt((CH3)2CNOH)((CH3)2CHNH2)Cl2], and solved the crystal structure. The cytotoxicity of the novel complex, the cis counterpart, cisplatin, and a trans complex with aliphatic amines, as well as the capacity of some of these complexes to cause either apoptotic or necrotic cell death, was comparatively examined in NRK-52E rat renal tubular cells and HepG2 human hepatoma cells. The results indicate that the oxime complex with trans geometry, but not the one with cis geometry, causes death by apoptosis, making the complex potentially suitable for therapeutic purposes. However cytotoxicity values are higher in the case of cis geometry than in trans geometry in both tumoral and non-tumoral cell lines Authors thank the Spanish Ministry of Science and Education, Spanish CICYT Grants: SAF2003-01700 and SAF2004-01250 |
Databáze: | OpenAIRE |
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