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Molecular Pharmacology|September 1, 1994
Cannabinoid receptor binding and agonist activity of amides and esters of arachidonic acidJ C Pinto, F Potié, K C Rice, et al.Drug Design and Discovery|August 31, 1999
Studies of molecular pharmacophore/receptor models for GABAA/benzodiazepine receptor subtypes: binding affinities of substituted beta-carbolines at recombinant alpha x beta 3 gamma 2 subtypes and quantitative structure-activity relationship studies via a comparative molecular field analysisQ Huang, E D Cox, T Gan, et al.Journal of Medicinal Chemistry|May 1, 1984
Biomimetic approach to potential benzodiazepine receptor agonists and antagonistsF Guzman, M Cain, P Larscheid, et al.The Journal of Trauma|December 1, 1990
Traumatic left renal artery stenosis managed with splenorenal bypass: case reportG W Barone, M B Kahn, J M Cook, et al.Journal of Medicinal Chemistry|October 10, 1998
Predictive models for GABAA/benzodiazepine receptor subtypes: studies of quantitative structure-activity relationships for imidazobenzodiazepines at five recombinant GABAA/benzodiazepine receptor subtypes [alphaxbeta3gamma2 (x = 1-3, 5, and 6)] via comparative molecular field analysisQ Huang, R Liu, P Zhang, et al.European Journal of Pharmacology|August 30, 2001
Influence of benzodiazepine binding site ligands on fear-conditioned contextual memoryT M DeLorey, R C Lin, B McBrady, et al.The Journal of Pharmacology and Experimental Therapeutics|September 1, 1986
Metaphit, an acylating ligand for phencyclidine receptors: characterization of in vivo actions in the ratP C Contreras, S Johnson, R Freedman, et al.Journal of Medicinal Chemistry|November 24, 1995
(E)-8-benzylidene derivatives of 2-methyl-5-(3-hydroxyphenyl)morphans: highly selective ligands for the sigma 2 receptor subtypeC M Bertha, B J Vilner, M V Mattson, et al.Pharmacology, Biochemistry, and Behavior|July 12, 2005
The stimulus properties of LSD in C57BL/6 miceJ C Winter, A K Kieres, M D Zimmerman, et al.Synapse (New York, N.Y.)|May 1, 1993
Identification of a GBR12935 homolog, LR1111, which is over 4,000-fold selective for the dopamine transporter, relative to serotonin and norepinephrine transportersR B Rothman, B Lewis, C Dersch, et al.Pageof 48