Structure-based design and synthesis of a series of hydroxamic acids with a quaternary-hydroxy group in P1 as inhibitors of matrix metalloproteinases

Bioorg Med Chem Lett. 1998 Apr 7;8(7):837-42. doi: 10.1016/s0960-894x(98)00125-5.

Abstract

Examination of the S1 area of the active site of pro-stromelysin has led us to the design of novel and potent inhibitors of matrix metalloproteinases containing constrained quaternary-hydroxy group at P1. The synthesis and biological activity of these compounds with variations at P1', P2', and P3' will be described.

MeSH terms

  • Catalytic Domain
  • Collagenases / chemistry
  • Computer Simulation
  • Drug Design
  • Enzyme Precursors / antagonists & inhibitors
  • Enzyme Precursors / chemistry
  • Hydrogen Bonding
  • Hydroxamic Acids / chemical synthesis
  • Hydroxamic Acids / chemistry*
  • Hydroxamic Acids / pharmacology
  • Indicators and Reagents
  • Matrix Metalloproteinase 1
  • Matrix Metalloproteinase 3 / chemistry
  • Matrix Metalloproteinase Inhibitors
  • Metalloendopeptidases / antagonists & inhibitors*
  • Metalloendopeptidases / chemistry
  • Models, Molecular
  • Molecular Conformation
  • Molecular Structure
  • Protease Inhibitors / chemical synthesis
  • Protease Inhibitors / chemistry*
  • Protease Inhibitors / pharmacology
  • Protein Conformation
  • Structure-Activity Relationship

Substances

  • Enzyme Precursors
  • Hydroxamic Acids
  • Indicators and Reagents
  • Matrix Metalloproteinase Inhibitors
  • Protease Inhibitors
  • Collagenases
  • Metalloendopeptidases
  • prostromelysin
  • Matrix Metalloproteinase 3
  • Matrix Metalloproteinase 1