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Current Topics in Medicinal Chemistry|October 5, 2006
Ligands targeting the excitatory amino acid transporters (EAATs)John Dunlop, John A Butera
Bioorganic & Medicinal Chemistry Letters|May 3, 2005
Synthesis and bladder smooth muscle relaxing properties of substituted 3-amino-4-aryl-(and aralkyl-)cyclobut-3-ene-1,2-dionesJohn A Butera, Douglas J Jenkins, Joseph R Lennox, et al.
Bioorganic & Medicinal Chemistry Letters|March 6, 2010
Identification of pyridazino[4,5-b]indolizines as selective PDE4B inhibitorsAndrew F Donnell, Paul J Dollings, John A Butera, et al.
Biochemical Pharmacology|November 18, 2008
Novel progesterone receptor modulators with gene selective and context-dependent partial agonismThomas J Berrodin, Scott A Jelinsky, Nilsa Graciani, et al.
Bioorganic & Medicinal Chemistry Letters|July 21, 2009
Discovery of a class of potent gap-junction modifiers as novel antiarrhythmic agentsEugene L Piatnitski Chekler, John A Butera, Li Di, et al.
Journal of Medicinal Chemistry|January 23, 2004
Design, synthesis, and biological evaluation of thio-containing compounds with serum HDL-cholesterol-elevating propertiesHassan Elokdah, Theodore S Sulkowski, Magid Abou-Gharbia, et al.
Assay and Drug Development Technologies|May 18, 2010
Ion channel screening plates: design, construction, and maintenanceScott C Mayer, John A Butera, David J Diller, et al.
European Journal of Pharmacology|January 27, 2009
Pharmacological comparison of muscarinic ligands: historical versus more recent muscarinic M1-preferring receptor agonistsJulia N Heinrich, John A Butera, Tikva Carrick, et al.
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