Isoplatensimycin: Synthesis and biological evaluation

Bioorg Med Chem Lett. 2009 Aug 15;19(16):4601-2. doi: 10.1016/j.bmcl.2009.06.092. Epub 2009 Jun 27.

Abstract

Isoplatensimycin, a novel analog of platensimycin, was synthesized via intramolecular dipolar cycloaddition of a carbonyl ylide. Isoplatensimycin showed little activities against strains of Staphylococcus aureus, but exhibited activities against some vancomycin-resistant enteroccoci.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adamantane / analogs & derivatives*
  • Adamantane / chemical synthesis
  • Adamantane / chemistry
  • Adamantane / pharmacology
  • Aminobenzoates / chemical synthesis*
  • Aminobenzoates / chemistry
  • Aminobenzoates / pharmacology
  • Anilides / chemical synthesis*
  • Anilides / chemistry
  • Anilides / pharmacology
  • Anti-Bacterial Agents / chemical synthesis*
  • Anti-Bacterial Agents / chemistry
  • Anti-Bacterial Agents / pharmacology
  • Enterococcus / drug effects
  • Methicillin-Resistant Staphylococcus aureus / drug effects
  • Microbial Sensitivity Tests
  • Vancomycin Resistance

Substances

  • Aminobenzoates
  • Anilides
  • Anti-Bacterial Agents
  • isoplatensimycin
  • Adamantane
  • platensimycin