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The Journal of Pharmacology and Experimental Therapeutics|July 1, 1992
Characterization of the enantiomers of cis-N-[2-(3,4-dichlorophenyl)ethyl]-N-methyl-2-(1- pyrrolidinyl)cyclohexylamine (BD737 and BD738): novel compounds with high affinity, selectivity and biological efficacy at sigma receptorsW D Bowen, J M Walker, B R de Costa, et al.Neuropeptides|February 1, 1985
Local anesthetic properties of opioids and phencyclidines: interaction with the voltage-dependent, batrachotoxin binding site in sodium channelsC R Creveling, E T McNeal, G A Lewandowski, et al.Journal of Medicinal Chemistry|November 2, 2001
Synthesis and biological evaluation of tropane-like 1-[2-[bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazine (GBR 12909) analoguesY Zhang, D B Joseph, W D Bowen, et al.Synapse (New York, N.Y.)|August 1, 1991
[3H]1-[2-(2-thienyl)cyclohexyl]piperidine labels two high-affinity binding sites in human cortex: further evidence for phencyclidine binding sites associated with the biogenic amine reuptake complexH C Akunne, A A Reid, A Thurkauf, et al.FEBS Letters|November 19, 1984
3-[18F]Acetylcyclofoxy: a useful probe for the visualization of opiate receptors in living animalsC B Pert, J A Danks, M A Channing, et al.Journal of Medicinal Chemistry|December 10, 1999
Oxygenated analogues of 1-[2-(Diphenylmethoxy)ethyl]- and 1-[2-[Bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazines (GBR 12935 and GBR 12909) as potential extended-action cocaine-abuse therapeutic agentsD B Lewis, D Matecka, Y Zhang, et al.Synapse (New York, N.Y.)|July 27, 1999
GBR12909 attenuates amphetamine-induced striatal dopamine release as measured by [(11)C]raclopride continuous infusion PET scansV L Villemagne, D F Wong, F Yokoi, et al.Journal of Medicinal Chemistry|February 28, 1997
Heteroaromatic analogs of 1-[2-(diphenylmethoxy)ethyl]- and 1-[2-[bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazines (GBR 12935 and GBR 12909) as high-affinity dopamine reuptake inhibitorsD Matecka, D Lewis, R B Rothman, et al.Neurochemical Research|April 1, 1994
An electrophilic affinity ligand based on (+)-MK801 distinguishes PCP site 1 from PCP site 2H C Akunne, J A Monn, A Thurkauf, et al.Journal of Medicinal Chemistry|April 28, 1995
Probes for narcotic receptor-mediated phenomena. 20. Alteration of opioid receptor subtype selectivity of the 5-(3-hydroxyphenyl)morphans by application of the message-address concept: preparation of delta-opioid receptor ligandsC M Bertha, J L Flippen-Anderson, R B Rothman, et al.Pageof 48