Identification of Bis-Cyclic Guanidines as Antiplasmodial Compounds from Positional Scanning Mixture-Based Libraries

Molecules. 2019 Mar 20;24(6):1100. doi: 10.3390/molecules24061100.

Abstract

The screening of more than 30 million compounds derived from 81 small molecule libraries built on 81 distinct scaffolds identified pyrrolidine bis-cyclic guanidine library (TPI-1955) to be one of the most active and selective antiplasmodial libraries. The screening of the positional scanning library TPI-1955 arranged on four sets of sublibraries (26 + 26 + 26 + 40), totaling 120 samples for testing provided information about the most important groups of each variable position in the TPI-1955 library containing 738,192 unique compounds. The parallel synthesis of the individual compounds derived from the deconvolution of the positional scanning library led to the identification of active selective antiplasmodial pyrrolidine bis-cyclic guanidines.

Keywords: antiplasmodial; combinatorial chemistry; guanidines; heterocyclic peptidomimetics; malaria; parallel synthesis; solid-phase synthesis.

MeSH terms

  • Animals
  • Antimalarials / therapeutic use*
  • Combinatorial Chemistry Techniques
  • Guanidines / chemistry*
  • Malaria / drug therapy
  • Mice
  • Plasmodium / drug effects
  • Solid-Phase Synthesis Techniques / methods

Substances

  • Antimalarials
  • Guanidines