Dipeptide boronic acid inhibitors of dipeptidyl peptidase IV: determinants of potency and in vivo efficacy and safety

J Med Chem. 2008 Oct 9;51(19):6005-13. doi: 10.1021/jm800390n. Epub 2008 Sep 11.

Abstract

Dipeptidyl peptidase IV (DPP-IV; E.C. 3.4.14.5), a serine protease that degrades the incretin hormones GLP-1 and GIP, is now a validated target for the treatment of type 2 diabetes. Dipeptide boronic acids, among the first, and still among the most potent DPP-IV inhibitors known, suffer from a concern over their safety. Here we evaluate the potency, in vivo efficacy, and safety of a selected set of these inhibitors. The adverse effects induced by boronic acid-based DPP-IV inhibitors are essentially limited to what has been observed previously for non-boronic acid inhibitors and attributed to cross-reactivity with DPP8/9. While consistent with the DPP8/9 hypothesis, they are also consistent with cross-reactivity with some other intracellular target. The results further show that the potency of simple dipeptide boronic acid-based inhibitors can be combined with selectivity against DPP8/9 in vivo to produce agents with a relatively wide therapeutic index (>500) in rodents.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Animals
  • Blood Glucose / analysis
  • Blood Glucose / metabolism
  • Boronic Acids / administration & dosage*
  • Boronic Acids / chemistry
  • Boronic Acids / pharmacology
  • Cell Line
  • Cloning, Molecular
  • Dipeptides / administration & dosage*
  • Dipeptides / chemistry
  • Dipeptides / pharmacology
  • Dipeptidyl Peptidase 4 / blood
  • Dipeptidyl Peptidase 4 / isolation & purification
  • Dipeptidyl-Peptidase IV Inhibitors
  • Dipeptidyl-Peptidases and Tripeptidyl-Peptidases / antagonists & inhibitors
  • Dipeptidyl-Peptidases and Tripeptidyl-Peptidases / biosynthesis
  • Dose-Response Relationship, Drug
  • Drug Evaluation, Preclinical
  • Drug-Related Side Effects and Adverse Reactions
  • Female
  • Glucose / administration & dosage
  • Glucose Tolerance Test
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Molecular Conformation
  • Peptide Library
  • Rats
  • Rats, Sprague-Dawley
  • Serine Proteinase Inhibitors / administration & dosage*
  • Serine Proteinase Inhibitors / chemistry
  • Serine Proteinase Inhibitors / pharmacology
  • Structure-Activity Relationship
  • Substrate Specificity
  • Time Factors

Substances

  • Blood Glucose
  • Boronic Acids
  • Dipeptides
  • Dipeptidyl-Peptidase IV Inhibitors
  • Peptide Library
  • Serine Proteinase Inhibitors
  • DPP9 protein, human
  • Dipeptidyl-Peptidases and Tripeptidyl-Peptidases
  • Dipeptidyl Peptidase 4
  • Glucose