Small Molecule Tools to Study Cellular Target Engagement for the Intracellular Allosteric Binding Site of GPCRs

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: In: Chemistry – A European Journal 29.1 (2023): e202202565

Classification: Medizin, Gesundheit

Event: Veröffentlichung

(where): Erlangen

(who): Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)

(when): 2023

Creator: Huber, Max E.
Toy, Lara
Schmidt, Maximilian F.
Weikert, Dorothee
Schiedel, Matthias

DOI: 10.1002/chem.202202565

URN: urn:nbn:de:bvb:29-opus4-227521

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:47 AM CEST

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Associated

Huber, Max E.
Toy, Lara
Schmidt, Maximilian F.
Weikert, Dorothee
Schiedel, Matthias
Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)

Time of origin

2023

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β-arrestin mediates communication between plasma membrane and intracellular GPCRs to regulate signaling

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Small Molecule Tools to Study Cellular Target Engagement for the Intracellular Allosteric Binding Site of GPCRs

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β-arrestin mediates communication between plasma membrane and intracellular GPCRs to regulate signaling

Hochschulschrift

Investigation of structure and allosteric modulation of family C GPCRs by sequence, structure and ligand based approaches

Investigation of dynamic processes of prototypical class A GPCRs by single-molecule microscopy

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A promising small molecule binding pocket in class B GPCRs: expanding potential for drug development

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Small Molecule Tools to Study Cellular Target Engagement for the Intracellular Allosteric Binding Site of GPCRs

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Other Objects (12)

Small Molecule Tools to Study Cellular Target Engagement for the Intracellular Allosteric Binding Site of GPCRs

Targeting the Intracellular Allosteric Binding Site (IABS) of G Protein-Coupled Receptors (GPCRs)

β-arrestin mediates communication between plasma membrane and intracellular GPCRs to regulate signaling

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Ligand-Conjugates Targeting an Intracellular Allosteric Site for Neurotensin Receptor-1

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A promising small molecule binding pocket in class B GPCRs: expanding potential for drug development

Extracellular and intracellular small-molecule galectin-3 inhibitors

Small Molecule Tools to Study Cellular Target Engagement for the Intracellular Allosteric Binding Site of GPCRs

Targeting the Intracellular Allosteric Binding Site (IABS) of G Protein-Coupled Receptors (GPCRs)

β-arrestin mediates communication between plasma membrane and intracellular GPCRs to regulate signaling

Investigation of structure and allosteric modulation of family C GPCRs by sequence, structure and ligand based approaches

Investigation of dynamic processes of prototypical class A GPCRs by single-molecule microscopy

Ligand-Conjugates Targeting an Intracellular Allosteric Site for Neurotensin Receptor-1

Small molecule inhibitors reveal allosteric regulation of USP14 via steric blockade

Allosteric modulation of the farnesoid X receptor by a small molecule

Small-molecule and mutational analysis of allosteric Eg5 inhibition by monastrol

Allosteric modulation of the farnesoid X receptor by a small molecule

A promising small molecule binding pocket in class B GPCRs: expanding potential for drug development

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Small Molecule Tools to Study Cellular Target Engagement for the Intracellular Allosteric Binding Site of GPCRs

Targeting the Intracellular Allosteric Binding Site (IABS) of G Protein-Coupled Receptors (GPCRs)

β-arrestin mediates communication between plasma membrane and intracellular GPCRs to regulate signaling

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