SGC-GAK-1 : a chemical probe for cyclin G associated kinase (GAK)
Christopher R. M. Asquith, Benedict-Tilman Berger, Jing Wan, James M. Bennett, Stephen J. Capuzzi, Daniel J. Crona, David H. Drewry, Michael P. East, Jonathan M. Elkins, Oleg Fedorov, Paulo H. Godoi, Debra M. Hunter, Stefan Knapp, Susanne Müller, Chad D. Torrice, Carrow I. Wells, H. Shelton Earp,...
Christopher R. M. Asquith, Benedict-Tilman Berger, Jing Wan, James M. Bennett, Stephen J. Capuzzi, Daniel J. Crona, David H. Drewry, Michael P. East, Jonathan M. Elkins, Oleg Fedorov, Paulo H. Godoi, Debra M. Hunter, Stefan Knapp, Susanne Müller, Chad D. Torrice, Carrow I. Wells, H. Shelton Earp, Timothy M. Willson, William J. Zuercher
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Agradecimentos: The SGC is a registered charity (No. 1097737) that receives funds from AbbVie, Bayer Pharma AG, Boehringer Ingelheim, Canada Foundation for Innovation, Eshelman Institute for Innovation, Genome Canada, Innovative Medicines Initiative (EU/EFPIA) [ULTRA-DD Grant 115766], Janssen, Merck...
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Agradecimentos: The SGC is a registered charity (No. 1097737) that receives funds from AbbVie, Bayer Pharma AG, Boehringer Ingelheim, Canada Foundation for Innovation, Eshelman Institute for Innovation, Genome Canada, Innovative Medicines Initiative (EU/EFPIA) [ULTRA-DD Grant 115766], Janssen, Merck KGaA Darmstadt Germany, MSD, Novartis Pharma AG, Ontario Ministry of Economic Development and Innovation, Pfizer, São Paulo Research Foundation-FAPESP, Takeda, and Wellcome [Grant 106169/ZZ14/Z]. Antti Poso and Tuomo Laitinen (University of Eastern Finland) are thanked for informative discussions. We also thank Dr. Brandie Ehrmann for LC–MS/HRMS support provided by the Mass Spectrometry Core Laboratory at the University of North Carolina at Chapel Hill
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Abstract: We describe SGC-GAK-1 (11), a potent, selective, and cell-active inhibitor of cyclin G-associated kinase (GAK), together with a structurally related negative control SGC-GAK-1N (14). 11 was highly selective in an in vitro kinome-wide screen, but cellular engagement assays defined RIPK2 as...
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Abstract: We describe SGC-GAK-1 (11), a potent, selective, and cell-active inhibitor of cyclin G-associated kinase (GAK), together with a structurally related negative control SGC-GAK-1N (14). 11 was highly selective in an in vitro kinome-wide screen, but cellular engagement assays defined RIPK2 as a collateral target. We identified 18 as a potent RIPK2 inhibitor lacking GAK activity. Together, this chemical probe set can be used to interrogate GAK cellular biology
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SGC-GAK-1 : a chemical probe for cyclin G associated kinase (GAK)
Christopher R. M. Asquith, Benedict-Tilman Berger, Jing Wan, James M. Bennett, Stephen J. Capuzzi, Daniel J. Crona, David H. Drewry, Michael P. East, Jonathan M. Elkins, Oleg Fedorov, Paulo H. Godoi, Debra M. Hunter, Stefan Knapp, Susanne Müller, Chad D. Torrice, Carrow I. Wells, H. Shelton Earp,...
Christopher R. M. Asquith, Benedict-Tilman Berger, Jing Wan, James M. Bennett, Stephen J. Capuzzi, Daniel J. Crona, David H. Drewry, Michael P. East, Jonathan M. Elkins, Oleg Fedorov, Paulo H. Godoi, Debra M. Hunter, Stefan Knapp, Susanne Müller, Chad D. Torrice, Carrow I. Wells, H. Shelton Earp, Timothy M. Willson, William J. Zuercher
SGC-GAK-1 : a chemical probe for cyclin G associated kinase (GAK)
Christopher R. M. Asquith, Benedict-Tilman Berger, Jing Wan, James M. Bennett, Stephen J. Capuzzi, Daniel J. Crona, David H. Drewry, Michael P. East, Jonathan M. Elkins, Oleg Fedorov, Paulo H. Godoi, Debra M. Hunter, Stefan Knapp, Susanne Müller, Chad D. Torrice, Carrow I. Wells, H. Shelton Earp,...
Christopher R. M. Asquith, Benedict-Tilman Berger, Jing Wan, James M. Bennett, Stephen J. Capuzzi, Daniel J. Crona, David H. Drewry, Michael P. East, Jonathan M. Elkins, Oleg Fedorov, Paulo H. Godoi, Debra M. Hunter, Stefan Knapp, Susanne Müller, Chad D. Torrice, Carrow I. Wells, H. Shelton Earp, Timothy M. Willson, William J. Zuercher
Fontes
Journal of medicinal chemistry (Fonte avulsa) |