Dominik Thimm
Bonn, NW 53121, Germany
Last Updated: 09/26/2026
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Found 15 publications
From Inhibitor to Reporter: Nirmatrelvir-Derived Fluorogenic Substrates for the SARS-CoV-2 Main Protease.
Journal: ACS chemical biology
Published: June 16, 2026
Subnanomolar MAS-related G protein-coupled receptor-X2/B2 antagonists with efficacy in human mast cells and disease models.
Journal: Signal transduction and targeted therapy
Published: August 14, 2024
MAS-related G protein-coupled receptors X (MRGPRX): Orphan GPCRs with potential as targets for future drugs.
Journal: Pharmacology & therapeutics
Published: May 30, 2022
A Cellular Assay for the Identification and Characterization of Connexin Gap Junction Modulators.
Journal: International journal of molecular sciences
Published: January 14, 2021
Targeting the Main Protease of SARS-CoV-2: From the Establishment of High Throughput Screening to the Design of Tailored Inhibitors.
Journal: Angewandte Chemie (International ed. in English)
Published: December 21, 2020
A group of cationic amphiphilic drugs activates MRGPRX2 and induces scratching behavior in mice.
Journal: The Journal of allergy and clinical immunology
Published: April 28, 2020
Diindolylmethane Derivatives: Potent Agonists of the Immunostimulatory Orphan G Protein-Coupled Receptor GPR84.
Journal: Journal of medicinal chemistry
Published: April 14, 2017
The 2016 Frontiers in Medicinal Chemistry Conference in Bonn.
Journal: ChemMedChem
Published: January 04, 2017
The nucleobase adenine as a signalling molecule in the kidney.
Journal: Acta physiologica (Oxford, England)
Published: November 13, 2014
6-Bromo-8-(4-[(3)H]methoxybenzamido)-4-oxo-4H-chromene-2-carboxylic Acid: a powerful tool for studying orphan G protein-coupled receptor GPR35.
Journal: Journal of medicinal chemistry
Published: July 30, 2013
8-Benzamidochromen-4-one-2-carboxylic acids: potent and selective agonists for the orphan G protein-coupled receptor GPR35.
Journal: Journal of medicinal chemistry
Published: May 30, 2013
The second extracellular loop of GPCRs determines subtype-selectivity and controls efficacy as evidenced by loop exchange study at A2 adenosine receptors.
Journal: Biochemical pharmacology
Published: January 18, 2013
Last Updated: 09/26/2026