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[1,2,4]Triazolo[1,5-<i>a</i>]pyrimidine Phosphodiesterase 2A Inhibitors: Structure and Free-Energy Perturbation-Guided Exploration

Gary Tresadern, Ingrid Velter, Andrés A. Trabanco, Frans Van den Keybus, Gregor J. Macdonald, Marijke Somers, Greet Vanhoof, Philip M. Leonard, Marieke Lamers, Yves E. M. Van Roosbroeck, Peter Buijnsters

2020Journal of Medicinal Chemistry28 citationsDOIOpen Access PDF

Abstract

We describe the hit-to-lead exploration of a [1,2,4]triazolo[1,5-a]pyrimidine phosphodiesterase 2A (PDE2A) inhibitor arising from high-throughput screening. X-ray crystallography enabled structure-guided design, leading to the identification of preferred substructural components. Further rounds of optimization used relative binding free-energy calculations to prioritize different substituents from the large accessible chemical space. The free-energy perturbation (FEP) calculations were performed for 265 putative PDE2A inhibitors, and 100 compounds were synthesized representing a relatively large prospective application providing unexpectedly active molecules with IC50′s from 2340 to 0.89 nM. Lead compound 46 originating from the FEP calculations showed PDE2A inhibition IC50 of 1.3 ± 0.39 nM, ∼100-fold selectivity versus other PDE enzymes, clean cytochrome P450 profile, in vivo target occupancy, and promise for further lead optimization.

Topics & Concepts

ChemistryFree energy perturbationPyrimidineLead compoundEnzymeIC50PhosphodiesteraseCombinatorial chemistryChemical spaceMoleculeCytidine deaminaseSelectivityStereochemistryIn vivoComputational chemistryBiochemistryDrug discoveryIn vitroOrganic chemistryCatalysisBiologyBiotechnologyPhosphodiesterase function and regulationSynthesis and Catalytic ReactionsPhenothiazines and Benzothiazines Synthesis and Activities
[1,2,4]Triazolo[1,5-<i>a</i>]pyrimidine Phosphodiesterase 2A Inhibitors: Structure and Free-Energy Perturbation-Guided Exploration | Litcius