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Lewis Elson

Showing results (11-20 of 24) with videos related to

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Biorxiv : the Preprint Server for Biology|May 4, 2026
Macrocyclization of Broad-Spectrum Kinase Inhibitor Bosutinib leads to Potent and Selective Quinoline-based HIPK4 Inhibitor AZ137Athina Zerva, Nicolai D Raig, Zaile Zhuang, et al.
Journal of Medicinal Chemistry|December 21, 2023
Synthesis of Pyrazole-Based Macrocycles Leads to a Highly Selective Inhibitor for MST3Jennifer Alisa Amrhein, Lena Marie Berger, Dimitrios-Ilias Balourdas, et al.
Science Advances|June 4, 2025
Type II kinase inhibitors that target Parkinson's disease-associated LRRK2Nicolai D Raig, Katherine J Surridge, Marta Sanz-Murillo, et al.
European Journal of Medicinal Chemistry|April 24, 2023
Shifting the selectivity of pyrido[2,3-d]pyrimidin-7(8H)-one inhibitors towards the salt-inducible kinase (SIK) subfamilyMarcel Rak, Roberta Tesch, Lena M Berger, et al.
Journal of Medicinal Chemistry|July 19, 2024
Back-Pocket Optimization of 2-Aminopyrimidine-Based Macrocycles Leads to Potent EPHA2/GAK Kinase InhibitorsJoshua Gerninghaus, Rezart Zhubi, Andreas Krämer, et al.
Biorxiv : the Preprint Server for Biology|February 26, 2024
Back-pocket optimization of 2-aminopyrimidine-based macrocycles leads to potent dual EPHA2/GAK kinase inhibitors with antiviral activityJoshua Gerninghaus, Rezart Zhubi, Andreas Krämer, et al.
Journal of Medicinal Chemistry|February 29, 2024
Development of Selective Pyrido[2,3-<i>d</i>]pyrimidin-7(8<i>H</i>)-one-Based Mammalian STE20-Like (MST3/4) Kinase InhibitorsMarcel Rak, Amelie Menge, Roberta Tesch, et al.
ACS Medicinal Chemistry Letters|November 19, 2025
Un-LOK-ing a New Approach for Conformational Selective Targeting of STK10 (LOK)Martina Dettenhöfer, Laura Nadine Tandara, Jennifer Alisa Amrhein, et al.
ACS Chemical Biology|April 14, 2025
Repurposing of the RIPK1-Selective Benzo[1,4]oxazepin-4-one Scaffold for the Development of a Type III LIMK1/2 InhibitorSebastian Mandel, Thomas Hanke, Sebastian Mathea, et al.
Journal of Medicinal Chemistry|June 17, 2026
On the Scope of DCAF1-Recruiting PROTACs Degrading Protein KinasesJanik Weckesser, Nebojša Miletić, Saran Aswathaman Sivashanmugam, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Biorxiv : the Preprint Server for Biology|May 4, 2026
Macrocyclization of Broad-Spectrum Kinase Inhibitor Bosutinib leads to Potent and Selective Quinoline-based HIPK4 Inhibitor AZ137Athina Zerva, Nicolai D Raig, Zaile Zhuang, et al.
Journal of Medicinal Chemistry|December 21, 2023
Synthesis of Pyrazole-Based Macrocycles Leads to a Highly Selective Inhibitor for MST3Jennifer Alisa Amrhein, Lena Marie Berger, Dimitrios-Ilias Balourdas, et al.
Science Advances|June 4, 2025
Type II kinase inhibitors that target Parkinson's disease-associated LRRK2Nicolai D Raig, Katherine J Surridge, Marta Sanz-Murillo, et al.
European Journal of Medicinal Chemistry|April 24, 2023
Shifting the selectivity of pyrido[2,3-d]pyrimidin-7(8H)-one inhibitors towards the salt-inducible kinase (SIK) subfamilyMarcel Rak, Roberta Tesch, Lena M Berger, et al.
Journal of Medicinal Chemistry|July 19, 2024
Back-Pocket Optimization of 2-Aminopyrimidine-Based Macrocycles Leads to Potent EPHA2/GAK Kinase InhibitorsJoshua Gerninghaus, Rezart Zhubi, Andreas Krämer, et al.
Biorxiv : the Preprint Server for Biology|February 26, 2024
Back-pocket optimization of 2-aminopyrimidine-based macrocycles leads to potent dual EPHA2/GAK kinase inhibitors with antiviral activityJoshua Gerninghaus, Rezart Zhubi, Andreas Krämer, et al.
Journal of Medicinal Chemistry|February 29, 2024
Development of Selective Pyrido[2,3-<i>d</i>]pyrimidin-7(8<i>H</i>)-one-Based Mammalian STE20-Like (MST3/4) Kinase InhibitorsMarcel Rak, Amelie Menge, Roberta Tesch, et al.
ACS Medicinal Chemistry Letters|November 19, 2025
Un-LOK-ing a New Approach for Conformational Selective Targeting of STK10 (LOK)Martina Dettenhöfer, Laura Nadine Tandara, Jennifer Alisa Amrhein, et al.
ACS Chemical Biology|April 14, 2025
Repurposing of the RIPK1-Selective Benzo[1,4]oxazepin-4-one Scaffold for the Development of a Type III LIMK1/2 InhibitorSebastian Mandel, Thomas Hanke, Sebastian Mathea, et al.
Journal of Medicinal Chemistry|June 17, 2026
On the Scope of DCAF1-Recruiting PROTACs Degrading Protein KinasesJanik Weckesser, Nebojša Miletić, Saran Aswathaman Sivashanmugam, et al.
Pageof 3