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Chemistryopen|January 31, 2019
A Series of Analogues to the AT2R Prototype Antagonist C38 Allow Fine Tuning of the Previously Reported Antagonist Binding ModeRebecka Isaksson, Jens Lindman, Johan Wannberg, et al.
Scientific Reports|April 27, 2017
The GPR139 reference agonists 1a and 7c, and tryptophan and phenylalanine share a common binding siteAnne Cathrine Nøhr, Willem Jespers, Mohamed A Shehata, et al.
Elife|February 10, 2021
Structure and mechanism of a phage-encoded SAM lyase revises catalytic function of enzyme familyXiaohu Guo, Annika Söderholm, Sandesh Kanchugal P, et al.
Journal of Medicinal Chemistry|August 10, 2017
Effect of Nitrogen Atom Substitution in A3 Adenosine Receptor Binding: N-(4,6-Diarylpyridin-2-yl)acetamides as Potent and Selective AntagonistsJhonny Azuaje, Willem Jespers, Vicente Yaziji, et al.
RSC Medicinal Chemistry|January 22, 2021
Macrocyclic peptidomimetics as inhibitors of insulin-regulated aminopeptidase (IRAP)Nicholas Barlow, Sudarsana Reddy Vanga, Jonas Sävmarker, et al.
Molecular Pharmacology|June 22, 2023
Discovery and In Vitro Characterization of BAY 2686013, an Allosteric Small Molecule Antagonist of the Human Pituitary Adenylate Cyclase-Activating Polypeptide ReceptorGernot Langer, John Scott, Christoffer Lind, et al.
Angewandte Chemie (International Ed. in English)|June 17, 2020
X-Ray Crystallography and Free Energy Calculations Reveal the Binding Mechanism of A2A Adenosine Receptor AntagonistsWillem Jespers, Grégory Verdon, Jhonny Azuaje, et al.
Molecular Pharmacology|January 16, 2016
Binding to and Inhibition of Insulin-Regulated Aminopeptidase by Macrocyclic Disulfides Enhances Spine DensityShanti Diwakarla, Erik Nylander, Alfhild Grönbladh, et al.
ACS Chemical Neuroscience|August 9, 2016
Aryl Sulfonamide Inhibitors of Insulin-Regulated Aminopeptidase Enhance Spine Density in Primary Hippocampal Neuron CulturesShanti Diwakarla, Erik Nylander, Alfhild Grönbladh, et al.
Journal of Medicinal Chemistry|December 29, 2020
3,4-Dihydropyrimidin-2(1H)-ones as Antagonists of the Human A2B Adenosine Receptor: Optimization, Structure-Activity Relationship Studies, and Enantiospecific RecognitionMaría Majellaro, Willem Jespers, Abel Crespo, et al.
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