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Bioorganic & Medicinal Chemistry|May 9, 2003
Structural studies on McN-5652-X, a high-affinity ligand for the serotonin transporter in mammalian brainBruce E Maryanoff, David F McComsey, Rina K Dukor, et al.Journal of Lipid Research|July 1, 2014
In vivo efficacy of HDL-like nanolipid particles containing multivalent peptide mimetics of apolipoprotein A-IYannan Zhao, Audrey S Black, David J Bonnet, et al.ACS Central Science|July 11, 2017
Self-Assembling Cyclic d,l-α-Peptides as Modulators of Plasma HDL Function. A Supramolecular Approach toward Antiatherosclerotic AgentsYannan Zhao, Luke J Leman, Debra J Search, et al.Journal of Medicinal Chemistry|March 28, 2008
Carbonic anhydrase-II inhibition. what are the true enzyme-inhibitory properties of the sulfamide cognate of topiramate?Bruce E Maryanoff, David F McComsey, Jung Lee, et al.Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|December 17, 2009
Cooperative antithrombotic effect from the simultaneous inhibition of thrombin and factor XaEdward C Giardino, Barbara J Haertlein, Lawrence de Garavilla, et al.American Journal of Respiratory and Critical Care Medicine|October 31, 2009
Dual inhibition of cathepsin G and chymase is effective in animal models of pulmonary inflammationBruce E Maryanoff, Lawrence de Garavilla, Michael N Greco, et al.Bioorganic & Medicinal Chemistry Letters|July 17, 2012
Pyrimidinopyrimidine inhibitors of ketohexokinase: exploring the ring C2 group that interacts with Asp-27B in the ligand binding pocketBruce E Maryanoff, John C O'Neill, David F McComsey, et al.Biochemical Pharmacology|July 6, 2010
Potency variation of small-molecule chymase inhibitors across speciesJukka Kervinen, Carl Crysler, Shariff Bayoumy, et al.Chemical Biology & Drug Design|August 23, 2006
Exploration of potential prodrugs of RWJ-445167, an oxyguanidine-based dual inhibitor of thrombin and factor XaBruce E Maryanoff, David F McComsey, Michael J Costanzo, et al.Bioorganic & Medicinal Chemistry Letters|June 12, 2003
High-affinity thrombin receptor (PAR-1) ligands: a new generation of indole-based peptide mimetic antagonists with a basic amine at the C-terminusHan Cheng Zhang, Kimberly B White, David F McComsey, et al.Pageof 8