A novel class of inhibitors of peptide deformylase discovered through high-throughput screening and virtual ligand screening

J Med Chem. 2004 Dec 30;47(27):6669-72. doi: 10.1021/jm049222o.

Abstract

Peptide deformylase (PDF) has been identified as a promising antibacterial and herbicide target. A structurally novel class of inhibitors containing a 2-thioxo-thiazolidin-4-one heterocycle substituted by an arylidene group at the 5-position and a hexanoic acid side chain at the 3-position was discovered independently via high-throughput screening and virtual ligand screening. Data mining and analogue synthesis established a structure--activity relationship for the side chain region that is consistent with the docked structure.

MeSH terms

  • Amidohydrolases / antagonists & inhibitors*
  • Amidohydrolases / chemistry
  • Drug Design
  • Enzyme Inhibitors / chemical synthesis
  • Enzyme Inhibitors / pharmacology*
  • Ligands
  • Structure-Activity Relationship

Substances

  • Enzyme Inhibitors
  • Ligands
  • Amidohydrolases
  • peptide deformylase