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Journal of Medicinal Chemistry
|
August 6, 2025
Tetrahydropyrazolopyridinones as a Novel Class of Potent and Highly Selective LIMK Inhibitors
Alex G Baldwin, David W Foley, D Heulyn Jones, et al.
Chemmedchem
|
October 27, 2017
Identification and Optimization of 4-Anilinoquinolines as Inhibitors of Cyclin G Associated Kinase
Christopher R M Asquith, Tuomo Laitinen, James M Bennett, et al.
Scientific Reports
|
July 16, 2017
NEK1 kinase domain structure and its dynamic protein interactome after exposure to Cisplatin
Talita D Melo-Hanchuk, Priscila Ferreira Slepicka, Gabriela Vaz Meirelles, et al.
Nature
|
April 4, 2014
Stereospecific targeting of MTH1 by (S)-crizotinib as an anticancer strategy
Kilian V M Huber, Eidarus Salah, Branka Radic, et al.
Scientific Reports
|
November 13, 2019
Binding and structural analyses of potent inhibitors of the human Ca<sup>2+</sup>/calmodulin dependent protein kinase kinase 2 (CAMKK2) identified from a collection of commercially-available kinase inhibitors
Gerson S Profeta, Caio V Dos Reis, André da S Santiago, et al.
ACS Medicinal Chemistry Letters
|
September 19, 2019
Development of Pyridine-based Inhibitors for the Human Vaccinia-related Kinases 1 and 2
Ricardo A M Serafim, Fernando H de Souza Gama, Luiz A Dutra, et al.
Journal of Medicinal Chemistry
|
April 18, 2024
Unexpected Noncovalent Off-Target Activity of Clinical BTK Inhibitors Leads to Discovery of a Dual NUDT5/14 Antagonist
Esra Balıkçı, Anne-Sophie M C Marques, Ludwig G Bauer, et al.
ACS Medicinal Chemistry Letters
|
March 19, 2020
SGC-AAK1-1: A Chemical Probe Targeting AAK1 and BMP2K
Carrow Wells, Rafael M Couñago, Juanita C Limas, et al.
Nature Chemical Biology
|
August 30, 2016
Covalent targeting of remote cysteine residues to develop CDK12 and CDK13 inhibitors
Tinghu Zhang, Nicholas Kwiatkowski, Calla M Olson, et al.
Journal of Medicinal Chemistry
|
February 16, 2019
SGC-GAK-1: A Chemical Probe for Cyclin G Associated Kinase (GAK)
Christopher R M Asquith, Benedict-Tilman Berger, Jing Wan, et al.
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Search research articles
Search
Showing results (61-70 of 78) with videos related to
Sort By:
Page
of 8
Journal of Medicinal Chemistry
|
August 6, 2025
Tetrahydropyrazolopyridinones as a Novel Class of Potent and Highly Selective LIMK Inhibitors
Alex G Baldwin, David W Foley, D Heulyn Jones, et al.
Chemmedchem
|
October 27, 2017
Identification and Optimization of 4-Anilinoquinolines as Inhibitors of Cyclin G Associated Kinase
Christopher R M Asquith, Tuomo Laitinen, James M Bennett, et al.
Scientific Reports
|
July 16, 2017
NEK1 kinase domain structure and its dynamic protein interactome after exposure to Cisplatin
Talita D Melo-Hanchuk, Priscila Ferreira Slepicka, Gabriela Vaz Meirelles, et al.
Nature
|
April 4, 2014
Stereospecific targeting of MTH1 by (S)-crizotinib as an anticancer strategy
Kilian V M Huber, Eidarus Salah, Branka Radic, et al.
Scientific Reports
|
November 13, 2019
Binding and structural analyses of potent inhibitors of the human Ca<sup>2+</sup>/calmodulin dependent protein kinase kinase 2 (CAMKK2) identified from a collection of commercially-available kinase inhibitors
Gerson S Profeta, Caio V Dos Reis, André da S Santiago, et al.
ACS Medicinal Chemistry Letters
|
September 19, 2019
Development of Pyridine-based Inhibitors for the Human Vaccinia-related Kinases 1 and 2
Ricardo A M Serafim, Fernando H de Souza Gama, Luiz A Dutra, et al.
Journal of Medicinal Chemistry
|
April 18, 2024
Unexpected Noncovalent Off-Target Activity of Clinical BTK Inhibitors Leads to Discovery of a Dual NUDT5/14 Antagonist
Esra Balıkçı, Anne-Sophie M C Marques, Ludwig G Bauer, et al.
ACS Medicinal Chemistry Letters
|
March 19, 2020
SGC-AAK1-1: A Chemical Probe Targeting AAK1 and BMP2K
Carrow Wells, Rafael M Couñago, Juanita C Limas, et al.
Nature Chemical Biology
|
August 30, 2016
Covalent targeting of remote cysteine residues to develop CDK12 and CDK13 inhibitors
Tinghu Zhang, Nicholas Kwiatkowski, Calla M Olson, et al.
Journal of Medicinal Chemistry
|
February 16, 2019
SGC-GAK-1: A Chemical Probe for Cyclin G Associated Kinase (GAK)
Christopher R M Asquith, Benedict-Tilman Berger, Jing Wan, et al.
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of 8