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Daniel Rauh

Showing results (121-130 of 159) with videos related to

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Journal of Medicinal Chemistry|June 19, 2013
Targeting gain of function and resistance mutations in Abl and KIT by hybrid compound designAndré Richters, Julia Ketzer, Matthäus Getlik, et al.
Chemmedchem|February 16, 2022
Covalent Allosteric Inhibitors of Akt Generated Using a Click Fragment ApproachLeandi van der Westhuizen, Jörn Weisner, Abu Taher, et al.
Angewandte Chemie (International Ed. in English)|May 26, 2017
Phenotypic Identification of a Novel Autophagy Inhibitor Chemotype Targeting Lipid Kinase VPS34Lucas Robke, Luca Laraia, Marjorie A Carnero Corrales, et al.
Journal of Medicinal Chemistry|August 24, 2017
Design, Synthesis, and Biological Evaluation of Novel Type I<sup>1</sup>/<sub>2</sub> p38α MAP Kinase Inhibitors with Excellent Selectivity, High Potency, and Prolonged Target Residence Time by Interfering with the R-SpineNiklas M Walter, Heike K Wentsch, Mike Bührmann, et al.
Journal of Medicinal Chemistry|August 31, 2017
Structure-Guided Development of Covalent and Mutant-Selective Pyrazolopyrimidines to Target T790M Drug Resistance in Epidermal Growth Factor ReceptorJulian Engel, Steven Smith, Jonas Lategahn, et al.
Chemical Science|April 19, 2019
Structural and chemical insights into the covalent-allosteric inhibition of the protein kinase AktNiklas Uhlenbrock, Steven Smith, Jörn Weisner, et al.
Angewandte Chemie (International Ed. in English)|June 26, 2015
Covalent-Allosteric Kinase InhibitorsJörn Weisner, Rajesh Gontla, Leandi van der Westhuizen, et al.
Nature Communications|September 7, 2021
Cellular model system to dissect the isoform-selectivity of Akt inhibitorsLena Quambusch, Laura Depta, Ina Landel, et al.
Journal of Medicinal Chemistry|December 4, 2014
Combining X-ray crystallography and molecular modeling toward the optimization of pyrazolo[3,4-d]pyrimidines as potent c-Src inhibitors active in vivo against neuroblastomaCristina Tintori, Anna Lucia Fallacara, Marco Radi, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 29, 2025
Phase 2 trial of ponatinib in patients with metastatic gastrointestinal stromal tumor following failure or intolerance of prior therapy with imatinib (POETIG trial)Johanna Falkenhorst, Phillipp Ivanyi, Tom Schulz, et al.
Pageof 16

Showing results (121-130 of 159) with videos related to

Sort By:
Pageof 16
Journal of Medicinal Chemistry|June 19, 2013
Targeting gain of function and resistance mutations in Abl and KIT by hybrid compound designAndré Richters, Julia Ketzer, Matthäus Getlik, et al.
Chemmedchem|February 16, 2022
Covalent Allosteric Inhibitors of Akt Generated Using a Click Fragment ApproachLeandi van der Westhuizen, Jörn Weisner, Abu Taher, et al.
Angewandte Chemie (International Ed. in English)|May 26, 2017
Phenotypic Identification of a Novel Autophagy Inhibitor Chemotype Targeting Lipid Kinase VPS34Lucas Robke, Luca Laraia, Marjorie A Carnero Corrales, et al.
Journal of Medicinal Chemistry|August 24, 2017
Design, Synthesis, and Biological Evaluation of Novel Type I<sup>1</sup>/<sub>2</sub> p38α MAP Kinase Inhibitors with Excellent Selectivity, High Potency, and Prolonged Target Residence Time by Interfering with the R-SpineNiklas M Walter, Heike K Wentsch, Mike Bührmann, et al.
Journal of Medicinal Chemistry|August 31, 2017
Structure-Guided Development of Covalent and Mutant-Selective Pyrazolopyrimidines to Target T790M Drug Resistance in Epidermal Growth Factor ReceptorJulian Engel, Steven Smith, Jonas Lategahn, et al.
Chemical Science|April 19, 2019
Structural and chemical insights into the covalent-allosteric inhibition of the protein kinase AktNiklas Uhlenbrock, Steven Smith, Jörn Weisner, et al.
Angewandte Chemie (International Ed. in English)|June 26, 2015
Covalent-Allosteric Kinase InhibitorsJörn Weisner, Rajesh Gontla, Leandi van der Westhuizen, et al.
Nature Communications|September 7, 2021
Cellular model system to dissect the isoform-selectivity of Akt inhibitorsLena Quambusch, Laura Depta, Ina Landel, et al.
Journal of Medicinal Chemistry|December 4, 2014
Combining X-ray crystallography and molecular modeling toward the optimization of pyrazolo[3,4-d]pyrimidines as potent c-Src inhibitors active in vivo against neuroblastomaCristina Tintori, Anna Lucia Fallacara, Marco Radi, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 29, 2025
Phase 2 trial of ponatinib in patients with metastatic gastrointestinal stromal tumor following failure or intolerance of prior therapy with imatinib (POETIG trial)Johanna Falkenhorst, Phillipp Ivanyi, Tom Schulz, et al.
Pageof 16