Studies on the chemical modification of monensin. IV. Synthesis, sodium ion permeability, and biological activity of 7-O-acyl- and 7-O-alkylmonensins

Chem Pharm Bull (Tokyo). 1992 Sep;40(9):2331-7. doi: 10.1248/cpb.40.2331.

Abstract

7-O-Acyl-(4a-e) and 7-O-alkylmonensins (5a-d) were prepared from monensin (1). Their lipophilicity, sodium ion permeability in human erythrocytes, antibacterial activity and effect on rat tail artery were examined. There was a correlation between lipophilicity and sodium ion permeability as well as between lipophilicity and antibacterial activity. We also found that the compound having larger sodium ion permeability, showed stronger contraction of rat tail artery. 7-O-Benzylmonensin (5c) exhibited higher lipophilicity and larger sodium ion permeability than monensin (1) among the tested monensin derivatives. In addition, antibacterial activity and contractile effect on rat tail artery of 5c were comparable to those of 1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Infective Agents / chemical synthesis*
  • Anti-Infective Agents / pharmacology
  • Erythrocytes / drug effects
  • Humans
  • In Vitro Techniques
  • Microbial Sensitivity Tests
  • Monensin / analogs & derivatives*
  • Monensin / chemistry
  • Monensin / pharmacology
  • Muscle, Smooth, Vascular / drug effects
  • Rats
  • Rats, Inbred WKY

Substances

  • Anti-Infective Agents
  • Monensin