Discovery of niclosamide and its O-alkylamino-tethered derivatives as potent antibacterial agents against carbapenemase-producing and/or colistin resistant Enterobacteriaceae isolates

Bioorg Med Chem Lett. 2019 Jun 1;29(11):1399-1402. doi: 10.1016/j.bmcl.2019.03.032. Epub 2019 Mar 23.

Abstract

Carbapenemase-producing Enterobacteriaceae (CPE) represents the most worrisome evolution of the antibiotic resistance crisis, which is almost resistant to most of available antibiotics. This situation is getting even worse particularly due to the recent emergence of colistin resistance. Herein, niclosamide, an FDA-approved traditional drug, and its novel O-alkylamino-tethered derivatives were discovered as new and potent antibacterial agents against carbapenemase-producing and/or colistin resistant Enterobacteriaceae isolates. Among these molecules, compound 10 (HJC0431) with 4-aminobutyl moiety showed the broad antibacterial activities, effective against 6 strains. In vitro checkerboard and time-kill course studies demonstrated the synergistic effects of the screened compounds with colistin against the corresponding strains with various degrees.

Keywords: Antibacterial agents; Carbapenemase-producing Enterobacteriaceae; Colistin resistance; Niclosamide derivatives; Synergistic effects.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / chemical synthesis
  • Anti-Bacterial Agents / chemistry
  • Anti-Bacterial Agents / pharmacology*
  • Carbapenem-Resistant Enterobacteriaceae / drug effects*
  • Colistin / pharmacology
  • Dose-Response Relationship, Drug
  • Drug Discovery*
  • Drug Resistance, Bacterial / drug effects*
  • Enterobacteriaceae / drug effects*
  • Humans
  • Microbial Sensitivity Tests
  • Molecular Structure
  • Niclosamide / chemical synthesis
  • Niclosamide / chemistry
  • Niclosamide / pharmacology*
  • Structure-Activity Relationship

Substances

  • Anti-Bacterial Agents
  • Niclosamide
  • Colistin