Discovery and structure-activity relationship analysis of Staphylococcus aureus sortase A inhibitors

Bioorg Med Chem. 2009 Oct 15;17(20):7174-85. doi: 10.1016/j.bmc.2009.08.067. Epub 2009 Sep 6.

Abstract

Methicillin resistant Staphylococcus aureus (MRSA) is a major health problem that has created a pressing need for new antibiotics. Compounds that inhibit the S. aureus SrtA sortase may function as potent anti-infective agents as this enzyme attaches virulence factors to the cell wall. Using high-throughput screening, we have identified several compounds that inhibit the enzymatic activity of the SrtA. A structure-activity relationship (SAR) analysis led to the identification of several pyridazinone and pyrazolethione analogs that inhibit SrtA with IC(50) values in the sub-micromolar range. Many of these molecules also inhibit the sortase enzyme from Bacillus anthracis suggesting that they may be generalized sortase inhibitors.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aminoacyltransferases / antagonists & inhibitors*
  • Bacterial Proteins / antagonists & inhibitors*
  • Cysteine Endopeptidases
  • Drug Discovery
  • Enzyme Inhibitors / chemistry*
  • Enzyme Inhibitors / pharmacology*
  • Pyridazines / chemistry*
  • Pyridazines / pharmacology*
  • Staphylococcus aureus / enzymology*
  • Staphylococcus aureus / growth & development
  • Structure-Activity Relationship

Substances

  • Bacterial Proteins
  • Enzyme Inhibitors
  • Pyridazines
  • Aminoacyltransferases
  • sortase A
  • Cysteine Endopeptidases