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Nature Reviews. Drug Discovery|March 17, 2018
Kinase inhibitors: the road aheadFleur M Ferguson, Nathanael S GrayBioorganic & Medicinal Chemistry Letters|August 19, 2017
Characterization of a highly selective inhibitor of the Aurora kinasesFleur M Ferguson, Zainab M Doctor, Apirat Chaikuad, et al.ACS Medicinal Chemistry Letters|October 18, 2019
Dual Inhibition of TAF1 and BET Bromodomains from the BI-2536 Kinase Inhibitor ScaffoldDavid Remillard, Dennis L Buckley, Hyuk-Soo Seo, et al.Bioorganic & Medicinal Chemistry Letters|June 9, 2019
Synthesis and structure activity relationships of a series of 4-amino-1H-pyrazoles as covalent inhibitors of CDK14Fleur M Ferguson, Zainab M Doctor, Scott B Ficarro, et al.Progress in Cell Cycle Research|November 5, 2003
Optimization of experimental antimitotic agents: classical and combinatorial methodsNathanael S GrayACS Medicinal Chemistry Letters|October 25, 2016
Discovery of a Series of 5,11-Dihydro-6H-benzo[e]pyrimido[5,4-b][1,4]diazepin-6-ones as Selective PI3K-δ/γ InhibitorsFleur M Ferguson, Jing Ni, Tinghu Zhang, et al.Current Opinion in Chemical Biology|January 4, 2011
Small molecule modulators of antioxidant response pathwayWooyoung Hur, Nathanael S GrayMethods in Enzymology|November 18, 2014
Discovery of allosteric BCR-ABL inhibitors from phenotypic screen to clinical candidateNathanael S Gray, Doriano FabbroNature Chemical Biology|June 20, 2006
Rational design of inhibitors that bind to inactive kinase conformationsYi Liu, Nathanael S GrayPageof 50