Allosteric modulation of the farnesoid X receptor by a small molecule

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: In: Scientific reports, 8.2018, Nr. 1, Art. 6846, doi:10.1038/s41598-018-25158-5

Event: Veröffentlichung

(where): Frankfurt am Main

(who): Universitätsbibliothek Johann Christian Senckenberg

(when): 2018

Creator: Gabler, Matthias
Kramer, Jan
Schmidt, Jurema
Pollinger, Julius
Weber, Julia
Kaiser, Astrid
Löhr, Frank
Proschak, Ewgenij
Schubert-Zsilavecz, Manfred
Merk, Daniel

URN: urn:nbn:de:hebis:30:3-472257

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:24 AM CEST

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Associated

Gabler, Matthias
Kramer, Jan
Schmidt, Jurema
Pollinger, Julius
Weber, Julia
Kaiser, Astrid
Löhr, Frank
Proschak, Ewgenij
Schubert-Zsilavecz, Manfred
Merk, Daniel
Universitätsbibliothek Johann Christian Senckenberg

Time of origin

2018

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Allosteric modulation of the farnesoid X receptor by a small molecule

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Hochschulschrift

Virtuelles Screening und De-Novo-Design von PPARα-Agonisten [PPAR-alpha-Agonisten] mit Oberflächen-Deskriptoren

Allosteric modulation of the farnesoid X receptor by a small molecule

Small molecule engagement of kinase complexes in cells

Closantel is an allosteric inhibitor of human Taspase1

Aktivatoren von KNa1.1-Kanälen für die Therapie von Schmerz und Pruritus

Synthesis of macrocyclic kinase inhibitors

Molecular similarity for machine learning in drug development

Multi-target approaches in metabolic syndrome

Synthese und biochemische Charakterisierung von Metallo-β-Lactamasen-Inhibitoren

PocketPicker: analysis of ligand binding-sites with shape descriptors

Targeting reader domains of the epigenetic code

Molecular similarity for machine learning in drug development : poster presentation

Hochschulschrift

Virtuelles Screening und De-Novo-Design von PPARα-Agonisten [PPAR-alpha-Agonisten] mit Oberflächen-Deskriptoren

Allosteric modulation of the farnesoid X receptor by a small molecule

Small molecule engagement of kinase complexes in cells

Closantel is an allosteric inhibitor of human Taspase1

Aktivatoren von KNa1.1-Kanälen für die Therapie von Schmerz und Pruritus

Synthesis of macrocyclic kinase inhibitors

Molecular similarity for machine learning in drug development

Multi-target approaches in metabolic syndrome

Synthese und biochemische Charakterisierung von Metallo-β-Lactamasen-Inhibitoren

PocketPicker: analysis of ligand binding-sites with shape descriptors

Targeting reader domains of the epigenetic code

Molecular similarity for machine learning in drug development : poster presentation

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Allosteric modulation of the farnesoid X receptor by a small molecule

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Other Objects (12)

Virtuelles Screening und De-Novo-Design von PPARα-Agonisten [PPAR-alpha-Agonisten] mit Oberflächen-Deskriptoren

Allosteric modulation of the farnesoid X receptor by a small molecule

Small molecule engagement of kinase complexes in cells

Closantel is an allosteric inhibitor of human Taspase1

Aktivatoren von KNa1.1-Kanälen für die Therapie von Schmerz und Pruritus

Synthesis of macrocyclic kinase inhibitors

Molecular similarity for machine learning in drug development

Multi-target approaches in metabolic syndrome

Synthese und biochemische Charakterisierung von Metallo-β-Lactamasen-Inhibitoren

PocketPicker: analysis of ligand binding-sites with shape descriptors

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Molecular similarity for machine learning in drug development : poster presentation

Virtuelles Screening und De-Novo-Design von PPARα-Agonisten [PPAR-alpha-Agonisten] mit Oberflächen-Deskriptoren

Allosteric modulation of the farnesoid X receptor by a small molecule

Small molecule engagement of kinase complexes in cells

Closantel is an allosteric inhibitor of human Taspase1

Aktivatoren von KNa1.1-Kanälen für die Therapie von Schmerz und Pruritus

Synthesis of macrocyclic kinase inhibitors

Molecular similarity for machine learning in drug development

Multi-target approaches in metabolic syndrome

Synthese und biochemische Charakterisierung von Metallo-β-Lactamasen-Inhibitoren

PocketPicker: analysis of ligand binding-sites with shape descriptors

Targeting reader domains of the epigenetic code

Molecular similarity for machine learning in drug development : poster presentation

Virtuelles Screening und De-Novo-Design von PPARα-Agonisten [PPAR-alpha-Agonisten] mit Oberflächen-Deskriptoren

Allosteric modulation of the farnesoid X receptor by a small molecule

Small molecule engagement of kinase complexes in cells

Closantel is an allosteric inhibitor of human Taspase1

Aktivatoren von KNa1.1-Kanälen für die Therapie von Schmerz und Pruritus

Synthesis of macrocyclic kinase inhibitors

Molecular similarity for machine learning in drug development

Multi-target approaches in metabolic syndrome

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PocketPicker: analysis of ligand binding-sites with shape descriptors

Targeting reader domains of the epigenetic code

Molecular similarity for machine learning in drug development : poster presentation

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