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Daniel Rauh

Showing results (81-90 of 159) with videos related to

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ACS Chemical Biology|December 27, 2014
Identification and further development of potent TBK1 inhibitorsAndré Richters, Debjit Basu, Julian Engel, et al.
ACS Chemical Biology|March 29, 2013
De novo design of protein kinase inhibitors by in silico identification of hinge region-binding fragmentsRobert Urich, Grant Wishart, Michael Kiczun, et al.
ACS Medicinal Chemistry Letters|May 17, 2023
Addressing the Osimertinib Resistance Mutation EGFR-L858R/C797S with Reversible AminopyrimidinesTobias Grabe, Kirujan Jeyakumar, Janina Niggenaber, et al.
European Journal of Medicinal Chemistry|December 14, 2011
Structure-based design, synthesis and biological evaluation of N-pyrazole, N'-thiazole urea inhibitors of MAP kinase p38αMatthäus Getlik, Christian Grütter, Jeffrey R Simard, et al.
Journal of Medicinal Chemistry|August 18, 2012
Targeting the hinge glycine flip and the activation loop: novel approach to potent p38α inhibitorsKathrin E Martz, Angelika Dorn, Benjamin Baur, et al.
Angewandte Chemie (International Ed. in English)|October 5, 2019
Covalent-Allosteric Inhibitors to Achieve Akt Isoform-SelectivityLena Quambusch, Ina Landel, Laura Depta, et al.
ACS Medicinal Chemistry Letters|May 14, 2025
Advancing TET Inhibitor Development: From Structural Insights to Biological EvaluationSuzanne Willems, Lejla Maksumic, Janina Niggenaber, et al.
The Plant Journal : for Cell and Molecular Biology|March 19, 2013
BSKs are partially redundant positive regulators of brassinosteroid signaling in ArabidopsisShivakumar Sreeramulu, Yana Mostizky, Sukumaran Sunitha, et al.
Organic Letters|October 3, 2009
A "cyanine-cyanine" salt exhibiting photovoltaic propertiesPierre-Antoine Bouit, Daniel Rauh, Stefan Neugebauer, et al.
Journal of Medicinal Chemistry|March 13, 2010
Synthesis and biological evaluation of 4-anilinoquinolines as potent inhibitors of epidermal growth factor receptorVijaykumar G Pawar, Martin L Sos, Haridas B Rode, et al.
Pageof 16

Showing results (81-90 of 159) with videos related to

Sort By:
Pageof 16
ACS Chemical Biology|December 27, 2014
Identification and further development of potent TBK1 inhibitorsAndré Richters, Debjit Basu, Julian Engel, et al.
ACS Chemical Biology|March 29, 2013
De novo design of protein kinase inhibitors by in silico identification of hinge region-binding fragmentsRobert Urich, Grant Wishart, Michael Kiczun, et al.
ACS Medicinal Chemistry Letters|May 17, 2023
Addressing the Osimertinib Resistance Mutation EGFR-L858R/C797S with Reversible AminopyrimidinesTobias Grabe, Kirujan Jeyakumar, Janina Niggenaber, et al.
European Journal of Medicinal Chemistry|December 14, 2011
Structure-based design, synthesis and biological evaluation of N-pyrazole, N'-thiazole urea inhibitors of MAP kinase p38αMatthäus Getlik, Christian Grütter, Jeffrey R Simard, et al.
Journal of Medicinal Chemistry|August 18, 2012
Targeting the hinge glycine flip and the activation loop: novel approach to potent p38α inhibitorsKathrin E Martz, Angelika Dorn, Benjamin Baur, et al.
Angewandte Chemie (International Ed. in English)|October 5, 2019
Covalent-Allosteric Inhibitors to Achieve Akt Isoform-SelectivityLena Quambusch, Ina Landel, Laura Depta, et al.
ACS Medicinal Chemistry Letters|May 14, 2025
Advancing TET Inhibitor Development: From Structural Insights to Biological EvaluationSuzanne Willems, Lejla Maksumic, Janina Niggenaber, et al.
The Plant Journal : for Cell and Molecular Biology|March 19, 2013
BSKs are partially redundant positive regulators of brassinosteroid signaling in ArabidopsisShivakumar Sreeramulu, Yana Mostizky, Sukumaran Sunitha, et al.
Organic Letters|October 3, 2009
A "cyanine-cyanine" salt exhibiting photovoltaic propertiesPierre-Antoine Bouit, Daniel Rauh, Stefan Neugebauer, et al.
Journal of Medicinal Chemistry|March 13, 2010
Synthesis and biological evaluation of 4-anilinoquinolines as potent inhibitors of epidermal growth factor receptorVijaykumar G Pawar, Martin L Sos, Haridas B Rode, et al.
Pageof 16