Abstract
Two homologous trinuclear polyamine chelates with either Pt(II) (Ia) or Pd(II) (Ib) were screened for their anticancer properties. Their growth-inhibition activity towards a human tongue epithelioma (HSC-3) was assessed in vitro, and the effect of the cation alteration was determined (IC50 =32 μM for Ib vs 66 μM for Ia).
Keywords: Pt(II), Pd(II), spermidine, anticancer drugs, squamous tongue epithelioma
Letters in Drug Design & Discovery
Title: Pt(II) vs Pd(II) Polyamine Complexes as New Anticancer Drugs: A Structure- Activity Study
Volume: 3 Issue: 3
Author(s): S. M. Fiuza, A. M. Amado, Paulo J. Oliveira, Vilma A. Sardao, L. A.E.B. de Carvalho and M. P.M. Marques
Affiliation:
Keywords: Pt(II), Pd(II), spermidine, anticancer drugs, squamous tongue epithelioma
Abstract: Two homologous trinuclear polyamine chelates with either Pt(II) (Ia) or Pd(II) (Ib) were screened for their anticancer properties. Their growth-inhibition activity towards a human tongue epithelioma (HSC-3) was assessed in vitro, and the effect of the cation alteration was determined (IC50 =32 μM for Ib vs 66 μM for Ia).
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Cite this article as:
Fiuza M. S., Amado M. A., Oliveira J. Paulo, Sardao A. Vilma, de Carvalho A.E.B. L. and Marques P.M. M., Pt(II) vs Pd(II) Polyamine Complexes as New Anticancer Drugs: A Structure- Activity Study, Letters in Drug Design & Discovery 2006; 3(3) . https://dx.doi.org/10.2174/157018006776286989
DOI https://dx.doi.org/10.2174/157018006776286989 |
Print ISSN 1570-1808 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-628X |

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