Bis(3-hydroxy-4-pyridinone)-EDTA derivative as a potential therapeutic Al-chelating agent. Synthesis, solution studies and biological assays

J Inorg Biochem. 2005 Sep;99(9):1845-52. doi: 10.1016/j.jinorgbio.2005.06.022.

Abstract

The 3-hydroxy-4-pyridinones are chelating agents of current interest due to their high affinity for hard metal ions and potential clinical applications as metal-decorporation agents. A new bis-(3-hydroxy-4-pyridinone) derivative of EDTA have been developed, and herein we describe the results of solution studies to determine the protonation constants and the partition coefficient. Biodistribution studies, performed with 67Ga-overload mice, showed rapid clearance of the radiotracer from the body, thus indicating that the new ligand should be a quite effective agent for the in vivo aluminium removal.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aluminum / chemistry*
  • Animals
  • Chelating Agents / chemical synthesis*
  • Chelating Agents / chemistry
  • Chelating Agents / pharmacokinetics
  • Chelating Agents / pharmacology*
  • Edetic Acid / analogs & derivatives*
  • Edetic Acid / chemical synthesis
  • Edetic Acid / chemistry
  • Edetic Acid / pharmacokinetics
  • Edetic Acid / pharmacology
  • Female
  • Magnetic Resonance Spectroscopy
  • Mice
  • Solutions
  • Tissue Distribution

Substances

  • Chelating Agents
  • Solutions
  • ethylenodiamino-N,N'-bis(acetocarboxyl)-N,N'-bis(acetyl(1-(3'-aminopropyl)-3-hydroxy-2-methyl-4-pyridinone))
  • Edetic Acid
  • Aluminum