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Pain|June 20, 2006
(L)-Phenylglycine, but not necessarily other alpha2delta subunit voltage-gated calcium channel ligands, attenuates neuropathic pain in ratsJames J Lynch, Prisca Honore, David J Anderson, et al.Frontiers in Genetics|November 1, 2012
AhR activation underlies the CYP1A autoinduction by A-998679 in ratsMichael J Liguori, Chih-Hung Lee, Hong Liu, et al.Bioorganic & Medicinal Chemistry Letters|May 6, 2003
Structure-activity relationship of a novel class of naphthyl amide KATP channel openersSean C Turner, William A Carroll, Tammie K White, et al.European Journal of Pharmacology|June 12, 2016
A-306989, an inhibitor of adenosine kinase, is renoprotective in rodent models of podocyte, basement membrane, and obstructive injuryChang Z Zhu, Sujatha Gopalakrishnan, Kelly Doyle, et al.Journal of Neuroscience Methods|July 5, 2011
KCNQ2/3 openers show differential selectivity and site of action across multiple KCNQ channelsDi Zhang, Rama Thimmapaya, Xu-Feng Zhang, et al.Molecular Pharmacology|June 20, 2003
[125I]A-312110, a novel high-affinity 1,4-dihydropyridine ATP-sensitive K+ channel opener: characterization and pharmacology of bindingRachel Davis-Taber, Eduardo J Molinari, Robert J Altenbach, et al.The Journal of Pharmacology and Experimental Therapeutics|July 13, 2007
An allosteric modulator of the alpha7 nicotinic acetylcholine receptor possessing cognition-enhancing properties in vivoDaniel B Timmermann, Jens Halvard Grønlien, Kathy L Kohlhaas, et al.Journal of Medicinal Chemistry|December 13, 2006
Effects of substitution on 9-(3-bromo-4-fluorophenyl)-5,9-dihydro-3H,4H-2,6-dioxa-4- azacyclopenta[b]naphthalene-1,8-dione, a dihydropyridine ATP-sensitive potassium channel openerRobert J Altenbach, Michael E Brune, Steven A Buckner, et al.CNS Neuroscience & Therapeutics|May 17, 2008
Preclinical characterization of A-582941: a novel alpha7 neuronal nicotinic receptor agonist with broad spectrum cognition-enhancing propertiesKarin R Tietje, David J Anderson, R Scott Bitner, et al.Journal of Biomolecular Screening|November 14, 2006
Utility of large-scale transiently transfected cells for cell-based high-throughput screens to identify transient receptor potential channel A1 (TRPA1) antagonistsJun Chen, Marc R Lake, Reza S Sabet, et al.Pageof 10