Fragment Optimization of Reversible Binding to the Switch II Pocket on KRAS Leads to a Potent, In Vivo Active KRAS G12C Inhibitor
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Published in | Journal of medicinal chemistry Vol. 65; no. 21; pp. 14614 - 14629 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
10.11.2022
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Online Access | Get full text |
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Author | Gerstberger, Thomas Krämer, Oliver Little, Andrew Mantoulidis, Andreas Savarese, Fabio Böttcher, Jark Gmaschitz, Gerhard Gollner, Andreas Mayer, Moriz Treu, Matthias Bröker, Joachim Smethurst, Chris Gmachl, Michael Weinstabl, Harald McConnell, Darryl B. Wunberg, Tobias W. Fesik, Stephen Waterson, Alex G. Rudolph, Dorothea Abbott, Jason R. Phan, Jason Arnhof, Heribert Mischerikow, Nikolai Rumpel, Klaus Kessler, Dirk Sun, Qi Herdeis, Lorenz |
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Fesik, Stephen organization: Department of Biochemistry, Vanderbilt University School of Medicine, 2215 Garland Avenue, 607 Light Hall, Nashville, Tennessee 37232-0146, United States |
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Title | Fragment Optimization of Reversible Binding to the Switch II Pocket on KRAS Leads to a Potent, In Vivo Active KRAS G12C Inhibitor |
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