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The Journal of Pharmacology and Experimental Therapeutics|July 21, 2007
Ex vivo occupancy of gamma-secretase inhibitors correlates with brain beta-amyloid peptide reduction in Tg2576 miceMargi E Goldstein, Yang Cao, Tracey Fiedler, et al.
The Journal of Pharmacology and Experimental Therapeutics|September 8, 2021
A Glutamate N-Methyl-d-Aspartate (NMDA) Receptor Subunit 2B-Selective Inhibitor of NMDA Receptor Function with Enhanced Potency at Acidic pH and Oral Bioavailability for Clinical UseScott J Myers, Kamalesh P Ruppa, Lawrence J Wilson, et al.
Bioorganic & Medicinal Chemistry Letters|December 7, 2002
Imidazo[4,5-c]pyridines as corticotropin releasing factor receptor ligandsArgyrios G Arvanitis, Joseph T Rescinito, Charles R Arnold, et al.
Bioorganic & Medicinal Chemistry Letters|May 16, 2007
Design and synthesis of benzoazepinone-derived cyclic malonamides and aminoamides as potent gamma-secretase inhibitorsMichael G Yang, Jian-Liang Shi, Dilip P Modi, et al.
Neuropharmacology|November 3, 2015
Biochemical and behavioral effects of PDE10A inhibitors: Relationship to target site occupancyYu-Wen Li, Matthew A Seager, Trevor Wojcik, et al.
Nuclear Medicine and Biology|May 6, 2014
Synthesis and evaluation of candidate PET radioligands for corticotropin-releasing factor type-1 receptorsNicholas J Lodge, Yu-Wen Li, Frederick T Chin, et al.
Bioorganic & Medicinal Chemistry Letters|December 7, 2002
Imidazo[4,5-b]pyridines as corticotropin releasing factor receptor ligandsArgyrios G Arvanitis, Joseph T Rescinito, Charles R Arnold, et al.
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