Target fishing reveals PfPYK-1 and PfRab6 as potential targets of an antiplasmodial 4-anilino-2-trichloromethylquinazoline hit compound

Bioorg Med Chem. 2024 Mar 15:102:117654. doi: 10.1016/j.bmc.2024.117654. Epub 2024 Feb 28.

Abstract

We present investigations about the mechanism of action of a previously reported 4-anilino-2-trichloromethylquinazoline antiplasmodial hit-compound (Hit A), which did not share a common mechanism of action with established commercial antimalarials and presented a stage-specific effect on the erythrocytic cycle of P. falciparum at 8 < t < 16 h. The target of Hit A was searched by immobilising the molecule on a solid support via a linker and performing affinity chromatography on a plasmodial lysate. Several anchoring positions of the linker (6,7 and 3') and PEG-type linkers were assessed, to obtain a linked-hit molecule displaying in vitro antiplasmodial activity similar to that of unmodified Hit A. This allowed us to identify the PfPYK-1 kinase and the PfRab6 GTP-ase as potential targets of Hit A.

Keywords: 2-trichloromethylquinazoline; Affinity chromatography; Antiplasmodial hit; Drug-linked matrix; PfPYK-1; PfRab6; Target fishing.

MeSH terms

  • Antimalarials* / chemistry
  • Erythrocytes
  • Humans
  • Malaria, Falciparum* / drug therapy
  • Plasmodium falciparum
  • Structure-Activity Relationship

Substances

  • Antimalarials