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Alexander Rasch

Showing results (11-20 of 22) with videos related to

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Tissue Engineering. Part C, Methods|December 6, 2019
An <i>Ex Vivo</i> Bone Defect Model to Evaluate Bone Substitutes and Associated Bone Regeneration ProcessesTim Klüter, Rywan Hassan, Alexander Rasch, et al.
Journal of Medicinal Chemistry|August 8, 2024
Novel Small-Molecule Atypical Chemokine Receptor 3 Agonists: Design, Synthesis, and Pharmacological Evaluation for Antiplatelet TherapyAlp Bayrak, Martyna Szpakowska, Valerie Dicenta-Baunach, et al.
Journal of Medicinal Chemistry|May 22, 2025
A "Ligand First" Approach toward Selective, Covalent JNK2/3 InhibitorsValentin R Wydra, Nicole Plank, Stefan Zwirner, et al.
Journal of Medicinal Chemistry|April 11, 2024
Development of Highly Potent and Selective Covalent FGFR4 Inhibitors Based on S<sub>N</sub>Ar ElectrophilesMoritz Schwarz, Maksym Kurkunov, Florian Wittlinger, et al.
RSC Medicinal Chemistry|August 4, 2025
A twist in the tale: shifting from covalent targeting of a tyrosine in JAK3 to a lysine in MK2Laura Hillebrand, Guiqun Wang, Alexander Rasch, et al.
Journal of Medicinal Chemistry|December 16, 2024
Design, Synthesis, and Biochemical Evaluation of Novel MLK3 Inhibitors: A Target Hopping ExamplePascal Sander, Martin P Schwalm, Andreas Krämer, et al.
Research Square|October 4, 2023
Linking ATP and allosteric sites to achieve superadditive binding with bivalent EGFR kinase inhibitorsDavid Heppner, Florian Wittlinger, Blessing Ogboo, et al.
Journal of Medicinal Chemistry|July 13, 2026
Riding toward Selectivity: Optimization of Covalent 7-Azaindole-Based BMX Kinase InhibitorsXiaojun Julia Liang, Claudia Albertini, Thales Kronenberger, et al.
ACS Pharmacology & Translational Science|April 18, 2024
Correction to "Cathepsin-Targeting SARS-CoV-2 Inhibitors: Design, Synthesis, and Biological Activity"Philipp Flury, Julian Breidenbach, Nadine Krüger, et al.
ACS Pharmacology & Translational Science|February 15, 2024
Cathepsin-Targeting SARS-CoV-2 Inhibitors: Design, Synthesis, and Biological ActivityPhilipp Flury, Julian Breidenbach, Nadine Krüger, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Tissue Engineering. Part C, Methods|December 6, 2019
An <i>Ex Vivo</i> Bone Defect Model to Evaluate Bone Substitutes and Associated Bone Regeneration ProcessesTim Klüter, Rywan Hassan, Alexander Rasch, et al.
Journal of Medicinal Chemistry|August 8, 2024
Novel Small-Molecule Atypical Chemokine Receptor 3 Agonists: Design, Synthesis, and Pharmacological Evaluation for Antiplatelet TherapyAlp Bayrak, Martyna Szpakowska, Valerie Dicenta-Baunach, et al.
Journal of Medicinal Chemistry|May 22, 2025
A "Ligand First" Approach toward Selective, Covalent JNK2/3 InhibitorsValentin R Wydra, Nicole Plank, Stefan Zwirner, et al.
Journal of Medicinal Chemistry|April 11, 2024
Development of Highly Potent and Selective Covalent FGFR4 Inhibitors Based on S<sub>N</sub>Ar ElectrophilesMoritz Schwarz, Maksym Kurkunov, Florian Wittlinger, et al.
RSC Medicinal Chemistry|August 4, 2025
A twist in the tale: shifting from covalent targeting of a tyrosine in JAK3 to a lysine in MK2Laura Hillebrand, Guiqun Wang, Alexander Rasch, et al.
Journal of Medicinal Chemistry|December 16, 2024
Design, Synthesis, and Biochemical Evaluation of Novel MLK3 Inhibitors: A Target Hopping ExamplePascal Sander, Martin P Schwalm, Andreas Krämer, et al.
Research Square|October 4, 2023
Linking ATP and allosteric sites to achieve superadditive binding with bivalent EGFR kinase inhibitorsDavid Heppner, Florian Wittlinger, Blessing Ogboo, et al.
Journal of Medicinal Chemistry|July 13, 2026
Riding toward Selectivity: Optimization of Covalent 7-Azaindole-Based BMX Kinase InhibitorsXiaojun Julia Liang, Claudia Albertini, Thales Kronenberger, et al.
ACS Pharmacology & Translational Science|April 18, 2024
Correction to "Cathepsin-Targeting SARS-CoV-2 Inhibitors: Design, Synthesis, and Biological Activity"Philipp Flury, Julian Breidenbach, Nadine Krüger, et al.
ACS Pharmacology & Translational Science|February 15, 2024
Cathepsin-Targeting SARS-CoV-2 Inhibitors: Design, Synthesis, and Biological ActivityPhilipp Flury, Julian Breidenbach, Nadine Krüger, et al.
Pageof 3