Synthesis of potent and highly selective nonguanidine azetidinone inhibitors of human tryptase

Bioorg Med Chem Lett. 2004 May 3;14(9):2227-31. doi: 10.1016/j.bmcl.2004.02.011.

Abstract

Azetidinones such as BMS-363131 (2) and BMS-363130 (3), which contain a guanidine group in the C-3 side chain were previously shown to be very potent inhibitors of human tryptase with high selectivity versus other serine proteases, including trypsin. In this letter, we describe the discovery of a number of potent azetidinone tryptase inhibitors in which the guanidine moiety at the ring C-3 position is replaced with primary or secondary amine or aminopyridine functionality. In particular, BMS-354326 (4) is a highly potent tryptase inhibitor (IC(50)=1.8 nM), which has excellent selectivity against trypsin and most other related serine proteases.

MeSH terms

  • Azetidines / chemical synthesis*
  • Azetidines / chemistry
  • Azetidines / pharmacology
  • Humans
  • Serine Endopeptidases / drug effects*
  • Serine Proteinase Inhibitors / chemical synthesis*
  • Serine Proteinase Inhibitors / chemistry
  • Serine Proteinase Inhibitors / pharmacology
  • Tryptases

Substances

  • Azetidines
  • Serine Proteinase Inhibitors
  • azetidine
  • Serine Endopeptidases
  • Tryptases