Conformationally restricted analogs of deoxynegamycin

Bioorg Med Chem Lett. 2004 Jun 21;14(12):3103-7. doi: 10.1016/j.bmcl.2004.04.036.

Abstract

Deoxynegamycin (1b) is a protein synthesis inhibitor with activity against Gram-negative (GN) bacteria. A series of conformationally restricted analogs were synthesized to probe its bioactive conformation. Indeed, some of the constrained analogs were found to be equal or better than deoxynegamycin in protein synthesis assay (1b, IC(50)=8.2 microM; 44, IC(50)=6.6 microM; 35e(2), IC(50)=1 microM). However, deoxynegamycin had the best in vitro whole cell antibacterial activity (Escherichia coli, MIC=4-16 microg/mL; Klebsiella pneumoniae, MIC=8 microg/mL) suggesting that other factors such as permeation may also be contributing to the overall whole cell activity. A new finding is that deoxynegamycin is efficacious in an E. coli murine septicemia model (ED(50)=4.8 mg/kg), providing further evidence of the favorable in vivo properties of this class of molecules.

MeSH terms

  • Amino Acids, Diamino / chemistry*
  • Amino Acids, Diamino / pharmacology
  • Animals
  • Escherichia coli / drug effects
  • Escherichia coli / growth & development
  • Klebsiella pneumoniae / drug effects
  • Klebsiella pneumoniae / growth & development
  • Mice
  • Microbial Sensitivity Tests / statistics & numerical data
  • Molecular Conformation

Substances

  • Amino Acids, Diamino
  • negamycin