Solid-phase synthesis and pharmacological evaluation of novel nucleoside-tethered dinuclear platinum(II) complexes

Bioorg Med Chem Lett. 2011 Oct 1;21(19):5835-8. doi: 10.1016/j.bmcl.2011.07.104. Epub 2011 Aug 3.

Abstract

Three novel inosine-based dinuclear platinum complexes have been synthesized via a solid-phase strategy. In these compounds, the metal is linked both to the N-7 of the purine nucleus and to the terminal amine group of a hexylamine side chain installed on N-1. Cis- or trans- diamine as well as ethylenediamine ligands are coordinated to platinum along with a chloride. The synthesised complexes were tested against four different human tumor cell lines. One of these complexes proved to be more cytotoxic than cisplatin against the MCF7 cancer cell line in a short-term exposure assay.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Antimetabolites, Antineoplastic / chemical synthesis*
  • Antimetabolites, Antineoplastic / chemistry
  • Antimetabolites, Antineoplastic / pharmacology*
  • Antimetabolites, Antineoplastic / toxicity
  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology*
  • Antineoplastic Agents / toxicity
  • Cell Line, Tumor
  • Diamines / chemistry
  • Drug Design
  • Drug Screening Assays, Antitumor
  • Female
  • HeLa Cells
  • Humans
  • Inhibitory Concentration 50
  • Inosine / chemistry
  • Molecular Structure
  • Nucleosides / chemistry
  • Platinum / chemistry
  • Solid-Phase Synthesis Techniques*
  • Structure-Activity Relationship
  • Tumor Cells, Cultured

Substances

  • Antimetabolites, Antineoplastic
  • Antineoplastic Agents
  • Diamines
  • Nucleosides
  • Platinum
  • Inosine