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Journal of Medicinal Chemistry|April 29, 2008
Structure-activity relationship studies on N'-aryl carbohydrazide P2X7 antagonistsDerek W Nelson, Kathy Sarris, Douglas M Kalvin, et al.Journal of Medicinal Chemistry|April 29, 2009
Discovery and biological evaluation of novel cyanoguanidine P2X(7) antagonists with analgesic activity in a rat model of neuropathic painArturo Perez-Medrano, Diana L Donnelly-Roberts, Prisca Honore, et al.Bioorganic & Medicinal Chemistry Letters|September 24, 2004
Synthesis and activity of 2-[4-(4-[3H]-2-cyanophenyl)piperazinyl]-N-(2,4,6-[3H]3-3-methylphenyl)acetamide: a selective dopamine D4 receptor agonist and radioligandMark A Matulenko, Bruce Surber, Leimin Fan, et al.Bioorganic & Medicinal Chemistry|June 10, 2004
Synthesis and functional activity of (2-aryl-1-piperazinyl)-N-(3-methylphenyl)acetamides: selective dopamine D4 receptor agonistsMark A Matulenko, Ahmed A Hakeem, Teodozyi Kolasa, et al.Journal of Medicinal Chemistry|June 9, 2006
Structure-activity relationship studies on a series of novel, substituted 1-benzyl-5-phenyltetrazole P2X7 antagonistsDerek W Nelson, Robert J Gregg, Michael E Kort, et al.Biochemical Pharmacology|July 28, 2004
Comparative pharmacology of human dopamine D(2)-like receptor stable cell lines coupled to calcium flux through Galpha(qo5)Robert B Moreland, Masaki Nakane, Diana L Donnelly-Roberts, et al.Neuropharmacology|July 5, 2005
2-[4-(3,4-Dimethylphenyl)piperazin-1-ylmethyl]-1H benzoimidazole (A-381393), a selective dopamine D4 receptor antagonistMasaki Nakane, Marlon D Cowart, Gin C Hsieh, et al.The Journal of Pharmacology and Experimental Therapeutics|September 20, 2006
A-740003 [N-(1-{[(cyanoimino)(5-quinolinylamino) methyl]amino}-2,2-dimethylpropyl)-2-(3,4-dimethoxyphenyl)acetamide], a novel and selective P2X7 receptor antagonist, dose-dependently reduces neuropathic pain in the ratPrisca Honore, Diana Donnelly-Roberts, Marian T Namovic, et al.Inflammation Research : Official Journal of the European Histamine Research Society ... [Et Al.]|March 12, 2011
Comparative analysis of inactivated-state block of N-type (Ca(v)2.2) calcium channelsTimothy A Vortherms, Andrew M Swensen, Wende Niforatos, et al.Chembiochem : a European Journal of Chemical Biology|January 10, 2018
Design of Aminobenzothiazole Inhibitors of Rho Kinases 1 and 2 by Using Protein Kinase A as a Structure SurrogateRussell A Judge, Anil Vasudevan, Victoria E Scott, et al.Pageof 3