Physicochemical Profiling and Comparison of Research Antiplasmodials and Advanced Stage Antimalarials with Oral Drugs
Amritansh Bhanot, Sandeep Sundriyal
Abstract
), aromatic ring counts (#Ar), and hydrogen bond acceptors. Despite both categories being bioavailable, the ASAM molecules are relatively larger and more lipophilic, have a lower polar surface area, and possess a higher count of heteroaromatic rings than oral drugs. Also, antimalarials are found to have a higher proportion of aromatic (#ArN) and basic nitrogen (#BaN) counts, features implicitly used in the design of antimalarial molecules but not well studied hitherto. We also propose using descriptors scaled by the sum of #ArN and #BaN (SBAN) to define an antimalarial property space. Together, these results may have important applications in the identification and optimization of future antimalarials.
Topics & Concepts
Lipinski's rule of fiveChemistryPotencyPolar surface areaBioavailabilityMoleculePartition coefficientOctanolStereochemistryHydrogen bondQuantitative structure–activity relationshipPharmacologyChemical spaceCombinatorial chemistryIn vitroDrug discoveryOrganic chemistryBiochemistryMedicineGeneIn silicoComputational Drug Discovery MethodsMalaria Research and ControlDrug Transport and Resistance Mechanisms