Area of research
Molecular Biology · Cellular and Molecular Neuroscience
Research interest
Research interests include Chemistry, Receptor, Agonist, Neuropeptide Y receptor, Histamine, and Stereochemistry.
Pandemic Drugs at Pandemic Speed: Infrastructure for Accelerating COVID-19 Drug Discovery with Hybrid Machine Learning- and Physics-based Simulations on High Performance Computers
N-Terminus to Arginine Side-Chain Cyclization of Linear Peptidic Neuropeptide Y Y<sub>4</sub> Receptor Ligands Results in Picomolar Binding Constants
Dibenzodiazepinone-type muscarinic receptor antagonists conjugated to basic peptides: Impact of the linker moiety and unnatural amino acids on M2R selectivity
UR-DEBa242: A Py-5-Labeled Fluorescent Multipurpose Probe for Investigations on the Histamine H<sub>3</sub> and H<sub>4</sub> Receptors
Red-Emitting Dibenzodiazepinone Derivatives as Fluorescent Dualsteric Probes for the Muscarinic Acetylcholine M<sub>2</sub> Receptor
Water-soluble inhibitors of ABCG2 (BCRP) – A fragment-based and computational approach
Oligopeptides as Neuropeptide Y Y<sub>4</sub> Receptor Ligands: Identification of a High-Affinity Tetrapeptide Agonist and a Hexapeptide Antagonist
Argininamide-type neuropeptide Y Y<sub>1</sub> receptor antagonists: the nature of <i>N</i><sup>ω</sup>-carbamoyl substituents determines Y<sub>1</sub>R binding mode and affinity
Universal Activation Index for Class A GPCRs
Conjugation of Short Peptides to Dibenzodiazepinone-Type Muscarinic Acetylcholine Receptor Ligands Determines M<sub>2</sub>R Selectivity
Basal Histamine H<sub>4</sub> Receptor Activation: Agonist Mimicry by the Diphenylalanine Motif
Structure‐Activity Relationship of Hetarylpropylguanidines Aiming at the Development of Selective Histamine Receptor Ligands<sup>†</sup>
Structural basis of ligand binding modes at the neuropeptide Y Y1 receptor
Highly Potent, Stable, and Selective Dimeric Hetarylpropylguanidine-Type Histamine H<sub>2</sub> Receptor Agonists
Radiolabeled Dibenzodiazepinone-Type Antagonists Give Evidence of Dualsteric Binding at the M<sub>2</sub> Muscarinic Acetylcholine Receptor
Mimicking of Arginine by Functionalized<i>N</i><sup>ω</sup>-Carbamoylated Arginine As a New Broadly Applicable Approach to Labeled Bioactive Peptides: High Affinity Angiotensin, Neuropeptide Y, Neuropeptide FF, and Neurotensin Receptor Ligands As Examples
The Extracellular Loop 2 (ECL2) of the Human Histamine H4 Receptor Substantially Contributes to Ligand Binding and Constitutive Activity
Molecular determinants for the high constitutive activity of the human histamine<scp>H</scp><sub>4</sub>receptor: functional studies on orthologues and mutants
Luciferase Reporter Gene Assay on Human, Murine and Rat Histamine H4 Receptor Orthologs: Correlations and Discrepancies between Distal and Proximal Readouts