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Journal of Medicinal Chemistry
|
May 16, 2019
Characterization of Covalent Pyrazolopyrimidine-MKK7 Complexes and a Report on a Unique DFG-in/Leu-in Conformation of Mitogen-Activated Protein Kinase Kinase 7 (MKK7)
Patrik Wolle, Julian Engel, Steven Smith, et al.
Nature Chemistry
|
December 19, 2012
Natural-product-derived fragments for fragment-based ligand discovery
Björn Over, Stefan Wetzel, Christian Grütter, et al.
Plos One
|
September 12, 2017
Structure-based design, synthesis and crystallization of 2-arylquinazolines as lipid pocket ligands of p38α MAPK
Mike Bührmann, Bianca M Wiedemann, Matthias P Müller, et al.
Nature Chemical Biology
|
June 30, 2009
Interactive exploration of chemical space with Scaffold Hunter
Stefan Wetzel, Karsten Klein, Steffen Renner, et al.
Biochemical and Biophysical Research Communications
|
March 3, 2019
Co-crystal structure determination and cellular evaluation of 1,4-dihydropyrazolo[4,3-c] [1,2] benzothiazine 5,5-dioxide p38α MAPK inhibitors
Desirée Bartolini, Mike Bührmann, Maria Letizia Barreca, et al.
Bioorganic & Medicinal Chemistry
|
March 7, 2008
ATP competitive inhibitors of D-alanine-D-alanine ligase based on protein kinase inhibitor scaffolds
Gemma Triola, Stefan Wetzel, Bernhard Ellinger, et al.
Journal of Molecular Biology
|
March 18, 2008
Biochemical and structural analysis of substrate promiscuity in plant Mg2+-dependent O-methyltransferases
Jakub G Kopycki, Daniel Rauh, Alexander A Chumanevich, et al.
Journal of the American Chemical Society
|
May 23, 2012
Direct binding assay for the detection of type IV allosteric inhibitors of Abl
Ralf Schneider, Christian Becker, Jeffrey R Simard, et al.
Angewandte Chemie (International Ed. in English)
|
July 16, 2010
Identification of thiazolidinones spiro-fused to indolin-2-ones as potent and selective inhibitors of the Mycobacterium tuberculosis protein tyrosine phosphatase B
Viktor V Vintonyak, Karin Warburg, Holger Kruse, et al.
Bioorganic & Medicinal Chemistry
|
December 7, 2010
Synthesis and biological evaluation of 7-substituted-1-(3-bromophenylamino)isoquinoline-4-carbonitriles as inhibitors of myosin light chain kinase and epidermal growth factor receptor
Haridas B Rode, Martin L Sos, Christian Grütter, et al.
Page
of 16
Search research articles
Search
Showing results (51-60 of 159) with videos related to
Sort By:
Page
of 16
Journal of Medicinal Chemistry
|
May 16, 2019
Characterization of Covalent Pyrazolopyrimidine-MKK7 Complexes and a Report on a Unique DFG-in/Leu-in Conformation of Mitogen-Activated Protein Kinase Kinase 7 (MKK7)
Patrik Wolle, Julian Engel, Steven Smith, et al.
Nature Chemistry
|
December 19, 2012
Natural-product-derived fragments for fragment-based ligand discovery
Björn Over, Stefan Wetzel, Christian Grütter, et al.
Plos One
|
September 12, 2017
Structure-based design, synthesis and crystallization of 2-arylquinazolines as lipid pocket ligands of p38α MAPK
Mike Bührmann, Bianca M Wiedemann, Matthias P Müller, et al.
Nature Chemical Biology
|
June 30, 2009
Interactive exploration of chemical space with Scaffold Hunter
Stefan Wetzel, Karsten Klein, Steffen Renner, et al.
Biochemical and Biophysical Research Communications
|
March 3, 2019
Co-crystal structure determination and cellular evaluation of 1,4-dihydropyrazolo[4,3-c] [1,2] benzothiazine 5,5-dioxide p38α MAPK inhibitors
Desirée Bartolini, Mike Bührmann, Maria Letizia Barreca, et al.
Bioorganic & Medicinal Chemistry
|
March 7, 2008
ATP competitive inhibitors of D-alanine-D-alanine ligase based on protein kinase inhibitor scaffolds
Gemma Triola, Stefan Wetzel, Bernhard Ellinger, et al.
Journal of Molecular Biology
|
March 18, 2008
Biochemical and structural analysis of substrate promiscuity in plant Mg2+-dependent O-methyltransferases
Jakub G Kopycki, Daniel Rauh, Alexander A Chumanevich, et al.
Journal of the American Chemical Society
|
May 23, 2012
Direct binding assay for the detection of type IV allosteric inhibitors of Abl
Ralf Schneider, Christian Becker, Jeffrey R Simard, et al.
Angewandte Chemie (International Ed. in English)
|
July 16, 2010
Identification of thiazolidinones spiro-fused to indolin-2-ones as potent and selective inhibitors of the Mycobacterium tuberculosis protein tyrosine phosphatase B
Viktor V Vintonyak, Karin Warburg, Holger Kruse, et al.
Bioorganic & Medicinal Chemistry
|
December 7, 2010
Synthesis and biological evaluation of 7-substituted-1-(3-bromophenylamino)isoquinoline-4-carbonitriles as inhibitors of myosin light chain kinase and epidermal growth factor receptor
Haridas B Rode, Martin L Sos, Christian Grütter, et al.
Page
of 16