Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    ISSN: 0268-2605
    Keywords: palladium ; platinum ; imidazoline ; DNA ; cyclometallated complexes ; cytotoxic activity ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In this paper we describe the synthesis and chemical characterization of three new Pd(II)-imidazoline complexes: [PdCl2 (C6H5-CH2-C3H5N2)2] (2), [PdCl(SEt2) (C6H4-C3H5N2)] (5) and [Pd(C6H4-C3H5N2) (μ-Br)]2 (6). We have also analyzed the DNA modifications and in vitro antileukaemic activity of these compounds and of their previously reported analogs [Pd Cl2 (C6H5-C3H5N2)2] (1), [Pd (C6H4-C3H5N2) (μ-OAc)]2 (3), [Pd (C6H4-C3H5N2) (μ-Cl)]2 (4) and [Pt(C6H4-C3H5N2)(μ-Cl] (7). All these compounds modify the DNA secondary structure since they alter the melting temperature (Tm) of the DNA. Circular dichroism spectra indicated, moreover, that compounds 3, 5 and 6 induced higher modification on the double helix than compounds 1, 2 and 4. While compounds 1, 2 and 5 seem to induce slight changes in the electrophoretic mobility of the open and covalently closed circular forms of pUC8 DNA at high ri (input molar ratio of Pd or Pt to nucleotides), compounds 3, 6 and 7 do not modify at any ri the tertiary structure of the plasmid DNA. Antileukaemic tests suggest that compounds 1, 4 and 7 exhibit important cytotoxic activity since their IC50 values against HL-60 human leukaemic cells were below 10 μg ml-1. © 1997 John Wiley & Sons, Ltd.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...