Solid-phase combinatorial synthesis of a lysyl-tRNA synthetase (LysRS) inhibitory library

J Comb Chem. 2008 May-Jun;10(3):391-400. doi: 10.1021/cc700157j. Epub 2008 Apr 22.

Abstract

The solid-phase combinatorial synthesis of a new library with potential inhibitory activity against the cytoplasmic lysyl-tRNA synthetase (LysRS) isoform of Trypanosoma brucei is described. The library has been specifically designed to mimic the lysyl adenylate complex. The design was carried out by dividing the complex into four modular parts. Proline derivatives (cis-gamma-amino-L-proline or trans-gamma-hydroxy-L-proline) were chosen as central scaffolds. After primary screening, three compounds of the library caused in vitro inhibition of the tRNA aminoacylation reaction in the low micromolar range.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aminoacylation / drug effects
  • Animals
  • Antiprotozoal Agents / chemical synthesis*
  • Antiprotozoal Agents / pharmacology
  • Chromatography, High Pressure Liquid / methods
  • Combinatorial Chemistry Techniques*
  • Drug Evaluation, Preclinical
  • Lysine-tRNA Ligase / antagonists & inhibitors*
  • Lysine-tRNA Ligase / chemistry
  • Lysine-tRNA Ligase / isolation & purification
  • Molecular Conformation
  • Proline / analogs & derivatives
  • Proline / chemical synthesis*
  • Proline / pharmacology
  • Stereoisomerism
  • Trypanosoma brucei brucei / enzymology

Substances

  • Antiprotozoal Agents
  • Proline
  • Lysine-tRNA Ligase