Arthur Van Aerschot
Leuven, VLG, Belgium
Last Updated: 09/26/2026
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Found 40 publications
Crystal structure of Mycobacterium tuberculosis mycothione reductase in complex with a specific inhibitor reveals competition with NADP(H) binding.
Journal: FEBS letters
Published: December 16, 2025
Rational fragment-based design of compounds targeting the PWWP domain of the HRP family.
Journal: European journal of medicinal chemistry
Published: July 29, 2024
Structural Basis of Cysteine Ligase MshC Inhibition by Cysteinyl-Sulfonamides.
Journal: International journal of molecular sciences
Published: November 11, 2022
Discovery of novel druggable pockets on polyomavirus VP1 through crystallographic fragment-based screening to develop capsid assembly inhibitors.
Journal: RSC chemical biology
Published: February 18, 2022
Towards Novel 3-Aminopyrazinamide-Based Prolyl-tRNA Synthetase Inhibitors: In Silico Modelling, Thermal Shift Assay and Structural Studies.
Journal: International journal of molecular sciences
Published: May 25, 2021
Aminoacyl-tRNA Synthetases as Valuable Targets for Antimicrobial Drug Discovery.
Journal: International journal of molecular sciences
Published: January 18, 2021
Synthesis and Biological Evaluation of 1,3-Dideazapurine-Like 7-Amino-5-Hydroxymethyl-Benzimidazole Ribonucleoside Analogues as Aminoacyl-tRNA Synthetase Inhibitors.
Journal: Molecules (Basel, Switzerland)
Published: September 24, 2020
Synthesis and structure-activity studies of novel anhydrohexitol-based Leucyl-tRNA synthetase inhibitors.
Journal: European journal of medicinal chemistry
Published: August 11, 2020
Synthesis and structural insights into the binding mode of the albomycin δ1 core and its analogues in complex with their target aminoacyl-tRNA synthetase.
Journal: Bioorganic & medicinal chemistry
Published: June 02, 2020
Phenyltriazole-functionalized sulfamate inhibitors targeting tyrosyl- or isoleucyl-tRNA synthetase.
Journal: Bioorganic & medicinal chemistry
Published: March 18, 2020
Last Updated: 09/26/2026