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Chirality|January 11, 1992
Stereoselective binding and activity of oxotremorine analogs at muscarinic receptors in rat brainW S Messer, D O Ngur, Y F Abuh, et al.Chirality|January 1, 1996
Synthesis and pharmacology of the enantiomers of UH301: opposing interactions with 5-HT1A receptorsS E Hillver, L Björk, B B Höök, et al.Journal of Medicinal Chemistry|April 10, 1999
Characterization of the binding site of the histamine H3 receptor. 1. Various approaches to the synthesis of 2-(1H-imidazol-4-yl)cyclopropylamine and histaminergic activity of (1R,2R)- and (1S,2S)-2-(1H-imidazol-4-yl)-cyclopropylamineI J De Esch, R C Vollinga, K Goubitz, et al.The Journal of Pharmacology and Experimental Therapeutics|September 2, 2005
Intrinsic efficacy of antipsychotics at human D2, D3, and D4 dopamine receptors: identification of the clozapine metabolite N-desmethylclozapine as a D2/D3 partial agonistE S Burstein, J Ma, S Wong, et al.Psychopharmacology|July 20, 2004
The role of M1 muscarinic receptor agonism of N-desmethylclozapine in the unique clinical effects of clozapineD M Weiner, H Y Meltzer, I Veinbergs, et al.The Journal of Pharmacology and Experimental Therapeutics|September 19, 2001
5-hydroxytryptamine2A receptor inverse agonists as antipsychoticsD M Weiner, E S Burstein, N Nash, et al.Pageof 23