Design, modelling, synthesis and biological evaluation of peptidomimetic phosphinates as inhibitors of matrix metalloproteinases MMP-2 and MMP-8

Bioorg Med Chem. 2005 Aug 1;13(15):4740-9. doi: 10.1016/j.bmc.2005.04.079.

Abstract

Three novel peptidomimetic phosphinate inhibitors have been synthesized and evaluated as inhibitors of matrix metalloproteinases MMP-2 and MMP-8. Their IC50 values are in the micromolar range, and one of them showed to be the most effective inhibitor of MMP-2. The differences in binding affinities for MMP-2 and MMP-8 of the three phosphinates have been rationalized by means of modelling studies and molecular dynamics simulations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Drug Design*
  • Inhibitory Concentration 50
  • Matrix Metalloproteinase 2 / metabolism
  • Matrix Metalloproteinase 8 / metabolism
  • Matrix Metalloproteinase Inhibitors*
  • Models, Chemical*
  • Molecular Structure
  • Phosphorous Acids / chemical synthesis
  • Phosphorous Acids / chemistry*
  • Phosphorous Acids / pharmacology
  • Protease Inhibitors / chemical synthesis*
  • Protease Inhibitors / chemistry
  • Protease Inhibitors / pharmacology*

Substances

  • Matrix Metalloproteinase Inhibitors
  • Phosphorous Acids
  • Protease Inhibitors
  • Matrix Metalloproteinase 2
  • Matrix Metalloproteinase 8
  • metaphosphoric acid