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Jörg Benz

Showing results (11-20 of 64) with videos related to

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Journal of Molecular Biology|February 6, 2010
Structure of the human fatty acid synthase KS-MAT didomain as a framework for inhibitor designGünter Pappenberger, Jörg Benz, Bernard Gsell, et al.
Nature|November 5, 2004
Insight into steroid scaffold formation from the structure of human oxidosqualene cyclaseRalf Thoma, Tanja Schulz-Gasch, Brigitte D'Arcy, et al.
Bioorganic & Medicinal Chemistry Letters|June 2, 2006
Structure-based design of indole propionic acids as novel PPARalpha/gamma co-agonistsBernd Kuhn, Hans Hilpert, Jörg Benz, et al.
Chemmedchem|April 11, 2012
Comparative molecular profiling of the PPARα/γ activator aleglitazar: PPAR selectivity, activity and interaction with cofactorsMichel Dietz, Peter Mohr, Bernd Kuhn, et al.
Bioorganic & Medicinal Chemistry Letters|July 25, 2008
Allosteric FBPase inhibitors gain 10(5) times in potency when simultaneously binding two neighboring AMP sitesPaul Hebeisen, Bernd Kuhn, Philipp Kohler, et al.
ACS Chemical Biology|October 17, 2013
Determination of protein-ligand binding constants of a cooperatively regulated tetrameric enzyme using electrospray mass spectrometryDragana Cubrilovic, Wolfgang Haap, Konstantin Barylyuk, et al.
Journal of Molecular Biology|September 21, 2010
Enhancing the stability and solubility of the glucocorticoid receptor ligand-binding domain by high-throughput library screeningTobias Seitz, Ralf Thoma, Guillaume A Schoch, et al.
Bioorganic & Medicinal Chemistry Letters|August 1, 2006
Synthesis and evaluation of anilinohexafluoroisopropanols as activators/modulators of LXRalpha and betaNarendra Panday, Jörg Benz, Denise Blum-Kaelin, et al.
Chemmedchem|December 20, 2016
Inhibition of the Cysteine Protease Human Cathepsin L by Triazine Nitriles: Amide⋅⋅⋅Heteroarene π-Stacking Interactions and Chalcogen Bonding in the S3 PocketMaude Giroud, Jakov Ivkovic, Mara Martignoni, et al.
Plos One|September 9, 2022
A potent and selective inhibitor for the modulation of MAGL activity in the neurovasculatureAlicia M Kemble, Benoit Hornsperger, Iris Ruf, et al.
Pageof 7

Showing results (11-20 of 64) with videos related to

Sort By:
Pageof 7
Journal of Molecular Biology|February 6, 2010
Structure of the human fatty acid synthase KS-MAT didomain as a framework for inhibitor designGünter Pappenberger, Jörg Benz, Bernard Gsell, et al.
Nature|November 5, 2004
Insight into steroid scaffold formation from the structure of human oxidosqualene cyclaseRalf Thoma, Tanja Schulz-Gasch, Brigitte D'Arcy, et al.
Bioorganic & Medicinal Chemistry Letters|June 2, 2006
Structure-based design of indole propionic acids as novel PPARalpha/gamma co-agonistsBernd Kuhn, Hans Hilpert, Jörg Benz, et al.
Chemmedchem|April 11, 2012
Comparative molecular profiling of the PPARα/γ activator aleglitazar: PPAR selectivity, activity and interaction with cofactorsMichel Dietz, Peter Mohr, Bernd Kuhn, et al.
Bioorganic & Medicinal Chemistry Letters|July 25, 2008
Allosteric FBPase inhibitors gain 10(5) times in potency when simultaneously binding two neighboring AMP sitesPaul Hebeisen, Bernd Kuhn, Philipp Kohler, et al.
ACS Chemical Biology|October 17, 2013
Determination of protein-ligand binding constants of a cooperatively regulated tetrameric enzyme using electrospray mass spectrometryDragana Cubrilovic, Wolfgang Haap, Konstantin Barylyuk, et al.
Journal of Molecular Biology|September 21, 2010
Enhancing the stability and solubility of the glucocorticoid receptor ligand-binding domain by high-throughput library screeningTobias Seitz, Ralf Thoma, Guillaume A Schoch, et al.
Bioorganic & Medicinal Chemistry Letters|August 1, 2006
Synthesis and evaluation of anilinohexafluoroisopropanols as activators/modulators of LXRalpha and betaNarendra Panday, Jörg Benz, Denise Blum-Kaelin, et al.
Chemmedchem|December 20, 2016
Inhibition of the Cysteine Protease Human Cathepsin L by Triazine Nitriles: Amide⋅⋅⋅Heteroarene π-Stacking Interactions and Chalcogen Bonding in the S3 PocketMaude Giroud, Jakov Ivkovic, Mara Martignoni, et al.
Plos One|September 9, 2022
A potent and selective inhibitor for the modulation of MAGL activity in the neurovasculatureAlicia M Kemble, Benoit Hornsperger, Iris Ruf, et al.
Pageof 7