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Nature Structural & Molecular Biology|November 16, 2004
Structures of human MAP kinase kinase 1 (MEK1) and MEK2 describe novel noncompetitive kinase inhibitionJeffrey F Ohren, Huifen Chen, Alexander Pavlovsky, et al.
Bioorganic & Medicinal Chemistry Letters|May 15, 2021
Development of BET inhibitors as potential treatments for cancer: A search for structural diversityMatthew D Hill, Haiquan Fang, John Tokarski, et al.
Bioorganic & Medicinal Chemistry Letters|September 24, 2021
Development of BET inhibitors as potential treatments for cancer: A new carboline chemotypeMatthew D Hill, Claude Quesnelle, John Tokarski, et al.
Journal of Structural Biology|December 19, 2007
Rational protein engineering in action: the first crystal structure of a phenylalanine tRNA synthetase from Staphylococcus haemolyticusArtem G Evdokimov, Marlene Mekel, Kim Hutchings, et al.
Bioorganic & Medicinal Chemistry Letters|August 18, 2020
Discovery of a phenylpyrazole amide ROCK inhibitor as a tool molecule for in vivo studiesZilun Hu, Cailan Wang, Peter W Glunz, et al.
Bioorganic & Medicinal Chemistry Letters|April 13, 2023
Synthesis and biological evaluation of biaryl alkyl ethers as inhibitors of IDO1Jay A Markwalder, Aaron J Balog, David K Williams, et al.
ACS Medicinal Chemistry Letters|February 20, 2020
Discovery of BMS-986260, a Potent, Selective, and Orally Bioavailable TGFβR1 Inhibitor as an Immuno-oncology AgentUpender Velaparthi, Chetan Padmakar Darne, Jayakumar Warrier, et al.
ACS Medicinal Chemistry Letters|July 21, 2022
Development of BET Inhibitors as Potential Treatments for Cancer: Optimization of Pharmacokinetic PropertiesMatthew D Hill, Haiquan Fang, Derek Norris, et al.
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