Lipoic acid analogs with enhanced pharmacological activity

Bioorg Med Chem. 2014 Jan 1;22(1):505-12. doi: 10.1016/j.bmc.2013.10.057. Epub 2013 Nov 14.

Abstract

Lipoic acid (1,2-dithiolane-3-pentanoic acid) is a pharmacophore with unique antioxidant and cytoprotective properties. We synthesized a library based upon the condensation of natural and unnatural amino acids with the carboxylic acid moiety of lipoic acid. SAR studies were conducted using a cardiac ischemia-reperfusion animal model. Cytoprotective efficacy was associated with the R-enantiomer of the dithiolane. Potency of library compounds was dictated by the acidic strength of the adduct. α-N-[(R)-1,2-dithiolane-3-pentanoyl]-L-glutamyl-L-alanine, designated CMX-2043, was chosen for further pharmacologic evaluation.

Keywords: Amino acids; Ischemia-reperfusion; Lipoic acid; Polymerization; SAR studies.

MeSH terms

  • Animals
  • Dipeptides / pharmacology*
  • Disease Models, Animal
  • Magnetic Resonance Spectroscopy
  • Male
  • Rats
  • Rats, Sprague-Dawley
  • Reperfusion Injury
  • Structure-Activity Relationship
  • Thioctic Acid / analogs & derivatives*
  • Thioctic Acid / pharmacology

Substances

  • Dipeptides
  • alpha-N-(1,2-dithiolane-3-pentanoyl)glutamylalanine
  • Thioctic Acid