Peter Gmeiner Department of Chemistry and Pharmacy Friedrich-Alexander University Erlangen-Nuernberg Biography Publications Institution JoVE Articles Peter Gmeiner has not added a biography. If you are Peter Gmeiner and would like to personalize this page please email our Author Liaison for assistance. Publications Rational Design of Agonists for Bitter Taste Receptor TAS2R14: from Modeling to Bench and Back Cellular and Molecular Life Sciences : CMLS. Feb, 2020 | Pubmed ID: 31236627 Structure-based Exploration of an Allosteric Binding Pocket in the NTS1 Receptor Using Bitopic NT(8-13) Derivatives and Molecular Dynamics Simulations Journal of Molecular Modeling. Jun, 2019 | Pubmed ID: 31209646 Development of Covalent Antagonists for β1- and β2-adrenergic Receptors Bioorganic & Medicinal Chemistry. Jul, 2019 | Pubmed ID: 31151791 Monitoring of the Dopamine D2 Receptor Agonists Hordenine and N-methyltyramine During the Brewing Process and in Commercial Beer Samples Food Chemistry. Mar, 2019 | Pubmed ID: 30409657 Structure-guided Development of Selective M3 Muscarinic Acetylcholine Receptor Antagonists Proceedings of the National Academy of Sciences of the United States of America. 11, 2018 | Pubmed ID: 30404914 Visualization of Ligand-induced Dopamine D and D Receptor Internalization by TIRF Microscopy Scientific Reports. 09, 2017 | Pubmed ID: 28883522 β-Arrestin Biased Dopamine D2 Receptor Partial Agonists: Synthesis and Pharmacological Evaluation Bioorganic & Medicinal Chemistry. 10, 2017 | Pubmed ID: 28870802 Potent Haloperidol Derivatives Covalently Binding to the Dopamine D2 Receptor Bioorganic & Medicinal Chemistry. 10, 2017 | Pubmed ID: 28666858 Development of Molecular Tools Based on the Dopamine D Receptor Ligand FAUC 329 Showing Inhibiting Effects on Drug and Food Maintained Behavior Bioorganic & Medicinal Chemistry. 07, 2017 | Pubmed ID: 28495386 Hydroxy-Substituted Heteroarylpiperazines: Novel Scaffolds for β-Arrestin-Biased DR Agonists Journal of Medicinal Chemistry. 06, 2017 | Pubmed ID: 28489379 Theranostic Value of Multimers: Lessons Learned from Trimerization of Neurotensin Receptor Ligands and Other Targeting Vectors Pharmaceuticals (Basel, Switzerland). Mar, 2017 | Pubmed ID: 28287433 NTS2-selective Neurotensin Mimetics with Tetrahydrofuran Amino Acids Bioorganic & Medicinal Chemistry. 01, 2017 | Pubmed ID: 27842797 Structure-guided Development of Dual β2 Adrenergic/dopamine D2 Receptor Agonists Bioorganic & Medicinal Chemistry. 06, 2016 | Pubmed ID: 27132867 Arrestin-Bound Rhodopsin: A Molecular Structure and Its Impact on the Development of Biased GPCR Ligands Angewandte Chemie (International Ed. in English). Nov, 2015 | Pubmed ID: 26361376 1,4-Disubstituted Aromatic Piperazines with High 5-HT2A/D2 Selectivity: Quantitative Structure-selectivity Investigations, Docking, Synthesis and Biological Evaluation Bioorganic & Medicinal Chemistry. Sep, 2015 | Pubmed ID: 26299826 Selective GPCR Ligands Bioorganic & Medicinal Chemistry. Jul, 2015 | Pubmed ID: 25818769 Structure-based Evolution of Subtype-selective Neurotensin Receptor Ligands ChemistryOpen. Oct, 2014 | Pubmed ID: 25478316 Synthesis and Binding Profile of Haloperidol-based Bivalent Ligands Targeting Dopamine D(2)-like Receptors Bioorganic & Medicinal Chemistry Letters. Aug, 2014 | Pubmed ID: 25047579 Covalent Agonists for Studying G Protein-coupled Receptor Activation Proceedings of the National Academy of Sciences of the United States of America. Jul, 2014 | Pubmed ID: 25006259 In Vivo Monitoring of the Antiangiogenic Effect of Neurotensin Receptor-mediated Radiotherapy by Small-animal Positron Emission Tomography: a Pilot Study Pharmaceuticals (Basel, Switzerland). Apr, 2014 | Pubmed ID: 24743103 بروتوكول الدوس خطوة بخطوة لزيادة الإنتاجية في مقالات GPCR المستندة إلى المعاوقة الخالية من التسميات Judith A. Stolwijk1, Anne-Kathrin Mildner1, Christian Kade1, Michael Skiba1, Guenther Bernhardt2, Armin Buschauer2, Harald Huebner3, Peter Gmeiner3, Joachim Wegener1,4 1Institute of Analytical Chemistry, Chemo- and Biosensors, University of Regensburg, 2Institute of Pharmacy, University of Regensburg, 3Department of Chemistry and Pharmacy, Friedrich-Alexander University Erlangen-Nuernberg, 4Fraunhofer Research Institution for Microsystems and Solid State Technologies EMFT JoVE 60686 Biochemistry
بروتوكول الدوس خطوة بخطوة لزيادة الإنتاجية في مقالات GPCR المستندة إلى المعاوقة الخالية من التسميات Judith A. Stolwijk1, Anne-Kathrin Mildner1, Christian Kade1, Michael Skiba1, Guenther Bernhardt2, Armin Buschauer2, Harald Huebner3, Peter Gmeiner3, Joachim Wegener1,4 1Institute of Analytical Chemistry, Chemo- and Biosensors, University of Regensburg, 2Institute of Pharmacy, University of Regensburg, 3Department of Chemistry and Pharmacy, Friedrich-Alexander University Erlangen-Nuernberg, 4Fraunhofer Research Institution for Microsystems and Solid State Technologies EMFT JoVE 60686 Biochemistry
