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Incorporation of an Isohexide Subunit into the Endochin-like Quinolone Scaffold.

Julia SenkinaSpencer Knapp
Published in: Molecules (Basel, Switzerland) (2024)
In order to improve the drug-likeness qualities, the antimalarial endochin-like quinolone (ELQ) scaffold has been modified by replacing the 4-(trifluoromethoxy)phenyl portion with an isoidide unit that is further adjustable by varying the distal O-substituents. As expected, the water solubilities of the new analogs are greatly improved, and the melting points are lower. However, the antimalarial potency of the new analogs is reduced to EC 50 > 1 millimolar, a result ascribable to the hydrophilic nature of the new substitution.
Keyphrases
  • tissue engineering
  • molecular docking
  • plasmodium falciparum
  • high resolution
  • liquid chromatography
  • minimally invasive
  • adverse drug
  • molecular dynamics simulations
  • drug induced
  • electronic health record