A new class of potent, slowly reversible dehydropeptidase inhibitors

Biochem Int. 1991 Apr;23(6):1107-15.

Abstract

Dehydrodipeptide analogs whose scissile carboxamide has been replaced with a PO(OH)CH2 group have been found to be potent inhibitors of the zinc protease dehydrodipeptidase 1 (DHP-1, renal dipeptidase, EC 3.4.13.11). The best of these inhibitors, compound 25 (Ki = 0.52 nM), is two hundred times more potent than cilastatin 2 which is used clinically as a component of the broad-spectrum antibiotic combination Primaxin. Compound 25 is a tight binding inhibitor exhibiting slow binding kinetics with a remarkably slow off rate from DHP-1 (half life greater than 8 hours). The kinetics of its binding are consistent with a simple on-off mechanism whereas the less active D-enantiomer 26 appears to bind in an initial loose complex with the enzyme which slowly rearranges to a tighter complex (Ki = 83 nM).

MeSH terms

  • Animals
  • Cilastatin / chemistry
  • Cilastatin / pharmacology
  • Dipeptidases / antagonists & inhibitors*
  • Kinetics
  • Molecular Structure
  • Substrate Specificity
  • Swine

Substances

  • Cilastatin
  • Dipeptidases
  • dipeptidase