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Bioorganic & Medicinal Chemistry Letters|July 18, 2012
4-Phenyl-7-azaindoles as potent, selective and bioavailable IKK2 inhibitors demonstrating good in vivo efficacyJohn Liddle, Paul Bamborough, Michael D Barker, et al.Bioorganic & Medicinal Chemistry Letters|August 7, 2009
Quinolines as a novel structural class of potent and selective PDE4 inhibitors. Optimisation for inhaled administrationMichael D Woodrow, Stuart P Ballantine, Michael D Barker, et al.Journal of Medicinal Chemistry|January 16, 2016
Cell Penetrant Inhibitors of the KDM4 and KDM5 Families of Histone Lysine Demethylases. 2. Pyrido[3,4-d]pyrimidin-4(3H)-one DerivativesSusan M Westaway, Alex G S Preston, Michael D Barker, et al.Bioorganic & Medicinal Chemistry Letters|September 10, 2011
Discovery of GSK143, a highly potent, selective and orally efficacious spleen tyrosine kinase inhibitorJohn Liddle, Francis L Atkinson, Michael D Barker, et al.Journal of Medicinal Chemistry|January 16, 2016
Cell Penetrant Inhibitors of the KDM4 and KDM5 Families of Histone Lysine Demethylases. 1. 3-Amino-4-pyridine Carboxylate DerivativesSusan M Westaway, Alex G S Preston, Michael D Barker, et al.Nature Chemical Biology|January 27, 2015
Inhibition of PAD4 activity is sufficient to disrupt mouse and human NET formationHuw D Lewis, John Liddle, Jim E Coote, et al.Pageof 3