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Artefenomel Regioisomer RLA-3107 Is a Promising Lead for the Discovery of Next-Generation Endoperoxide Antimalarials

Brian R. Blank, Jiří Gut, Philip J. Rosenthal, Adam R. Renslo

2023ACS Medicinal Chemistry Letters14 citationsDOIOpen Access PDF

Abstract

High Resolution Image Download MS PowerPoint Slide Clinical development of the antimalarial artefenomel was recently halted due to formulation challenges stemming from the drug’s lipophilicity and low aqueous solubility. The symmetry of organic molecules is known to influence crystal packing energies and by extension solubility and dissolution rates. Here we evaluate RLA-3107, a desymmetrized, regioisomeric form of artefenomel in vitro and in vivo, finding that the regioisomer retains potent antiplasmodial activity while offering improved human microsome stability and aqueous solubility as compared to artefenomel. We also report in vivo efficacy data for artefenomel and its regioisomer across 12 different dosing regimens.

Topics & Concepts

LipophilicitySolubilityStructural isomerChemistryIn vivoCombinatorial chemistryDissolutionAqueous solutionDrug discoveryStereochemistryOrganic chemistryBiochemistryBiologyBiotechnologyMalaria Research and ControlComputational Drug Discovery MethodsSynthesis and Catalytic Reactions
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