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ACS Chemical Biology
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December 16, 2024
Development of a Class A/B Hybrid GPCR System for the Proximity-Assisted Screening of GPCR Ligands
Monika T Gnatzy, Steffen Hartmann, Felix Hausch
ACS Medicinal Chemistry Letters
|
November 20, 2024
Toward Dual Targeting of Catalytic and Gatekeeper Pockets in Cyclophilins Using a Macrocyclic Scaffold
Johannes K Dreizler, Christian Meyners, Felix Hausch
Expert Opinion on Investigational Drugs
|
March 15, 2011
Corticotropin releasing factor receptor antagonists for major depressive disorder
Marcelo Paez-Pereda, Felix Hausch, Florian Holsboer
Chembiochem : a European Journal of Chemical Biology
|
May 7, 2009
Fluorescent probes to characterise FK506-binding proteins
Christian Kozany, Andreas März, Christoph Kress, et al.
Chemistry & Biology
|
April 3, 2003
Design, synthesis, and evaluation of gluten peptide analogs as selective inhibitors of human tissue transglutaminase
Felix Hausch, Tuula Halttunen, Markku Mäki, et al.
Biomolecules
|
January 24, 2019
The Many Faces of FKBP51
Andreas Hähle, Stephanie Merz, Christian Meyners, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)
|
December 18, 2019
Enantioselective Synthesis of a Tricyclic, sp<sup>3</sup> -Rich Diazatetradecanedione: an Amino Acid-Based Natural Product-Like Scaffold
Matthias Bischoff, Peter Mayer, Christian Meyners, et al.
Organic Letters
|
October 7, 2014
Stereoselective construction of the 5-hydroxy diazabicyclo[4.3.1]decane-2-one scaffold, a privileged motif for FK506-binding proteins
Matthias Bischoff, Claudia Sippel, Andreas Bracher, et al.
Journal of Medicinal Chemistry
|
October 1, 2015
Structure-Affinity Relationship Analysis of Selective FKBP51 Ligands
Xixi Feng, Claudia Sippel, Andreas Bracher, et al.
Biological Chemistry
|
July 17, 2004
Searching for the most effective screening system to identify cell-active inhibitors of beta-secretase
Oliver Middendorp, Urs Lüthi, Felix Hausch, et al.
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Showing results (11-20 of 125) with videos related to
Sort By:
Page
of 13
ACS Chemical Biology
|
December 16, 2024
Development of a Class A/B Hybrid GPCR System for the Proximity-Assisted Screening of GPCR Ligands
Monika T Gnatzy, Steffen Hartmann, Felix Hausch
ACS Medicinal Chemistry Letters
|
November 20, 2024
Toward Dual Targeting of Catalytic and Gatekeeper Pockets in Cyclophilins Using a Macrocyclic Scaffold
Johannes K Dreizler, Christian Meyners, Felix Hausch
Expert Opinion on Investigational Drugs
|
March 15, 2011
Corticotropin releasing factor receptor antagonists for major depressive disorder
Marcelo Paez-Pereda, Felix Hausch, Florian Holsboer
Chembiochem : a European Journal of Chemical Biology
|
May 7, 2009
Fluorescent probes to characterise FK506-binding proteins
Christian Kozany, Andreas März, Christoph Kress, et al.
Chemistry & Biology
|
April 3, 2003
Design, synthesis, and evaluation of gluten peptide analogs as selective inhibitors of human tissue transglutaminase
Felix Hausch, Tuula Halttunen, Markku Mäki, et al.
Biomolecules
|
January 24, 2019
The Many Faces of FKBP51
Andreas Hähle, Stephanie Merz, Christian Meyners, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)
|
December 18, 2019
Enantioselective Synthesis of a Tricyclic, sp<sup>3</sup> -Rich Diazatetradecanedione: an Amino Acid-Based Natural Product-Like Scaffold
Matthias Bischoff, Peter Mayer, Christian Meyners, et al.
Organic Letters
|
October 7, 2014
Stereoselective construction of the 5-hydroxy diazabicyclo[4.3.1]decane-2-one scaffold, a privileged motif for FK506-binding proteins
Matthias Bischoff, Claudia Sippel, Andreas Bracher, et al.
Journal of Medicinal Chemistry
|
October 1, 2015
Structure-Affinity Relationship Analysis of Selective FKBP51 Ligands
Xixi Feng, Claudia Sippel, Andreas Bracher, et al.
Biological Chemistry
|
July 17, 2004
Searching for the most effective screening system to identify cell-active inhibitors of beta-secretase
Oliver Middendorp, Urs Lüthi, Felix Hausch, et al.
Page
of 13