Ligand-Conjugates Targeting an Intracellular Allosteric Site for Neurotensin Receptor-1
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Dissertation, 2024
- Keyword
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Chemische Synthese
Ligand
- Event
-
Veröffentlichung
- (where)
-
Erlangen
- (who)
-
Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)
- (when)
-
2025
- Creator
- Contributor
-
Gmeiner, Peter
Eichler, Jutta
- DOI
-
10.25593/open-fau-1523
- URN
-
urn:nbn:de:101:1-2501100404389.025527031154
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:37 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Shinkwin, Patrick
- Gmeiner, Peter
- Eichler, Jutta
- Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)
Time of origin
- 2025
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Gmeiner, Peter
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Development of a negative allosteric modulator binding to the membrane surface of the β2AR
Targeting the Intracellular Allosteric Binding Site (IABS) of G Protein-Coupled Receptors (GPCRs)
Interactions of Bivalent Ligands with Heterodimers of Dopamine and Neurotensin Receptors
Evaluation of Neurotensin Receptor-1 Antagonists as Potential Radiotracers for the Therapy of Pancreatic Adenocarcinoma
Evaluation of the neurotensin receptor-1 as target for molecular imaging and radiotherapy of pancreatic and prostate cancer
Structure-based design and synthesis of allosteric modulators and chemical tools for the human chemokine receptor CXCR3
Functional Evaluation of Bivalent Ligands at Heterodimers of Dopamine D3 and Neurotensin 1 Receptors
Structure‐Based Evolution of Subtype‐Selective Neurotensin Receptor Ligands
Conformationally Restricted Epinephrine Analogs
Novel selective M3 muscarinic acetylcholine receptor ligands: Design, synthesis, and characterization
Gmeiner, Peter
Gmeiner, Peter
Development of a negative allosteric modulator binding to the membrane surface of the β2AR
Targeting the Intracellular Allosteric Binding Site (IABS) of G Protein-Coupled Receptors (GPCRs)
Interactions of Bivalent Ligands with Heterodimers of Dopamine and Neurotensin Receptors
Evaluation of Neurotensin Receptor-1 Antagonists as Potential Radiotracers for the Therapy of Pancreatic Adenocarcinoma
Evaluation of the neurotensin receptor-1 as target for molecular imaging and radiotherapy of pancreatic and prostate cancer
Structure-based design and synthesis of allosteric modulators and chemical tools for the human chemokine receptor CXCR3
Functional Evaluation of Bivalent Ligands at Heterodimers of Dopamine D3 and Neurotensin 1 Receptors
Structure‐Based Evolution of Subtype‐Selective Neurotensin Receptor Ligands
Conformationally Restricted Epinephrine Analogs