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F I Carroll

Showing results (181-190 of 208) with videos related to

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Bioorganic & Medicinal Chemistry Letters|November 26, 1999
(+/-)-4-[(N-allyl-cis-3-methyl-4-piperidinyl)phenylamino]-N,N-diethylbenzamide displays selective binding for the delta opioid receptorJ B Thomas, X M Herault, R B Rothman, et al.
Nuclear Medicine and Biology|January 15, 1998
Fluoro-norchloroepibatidine: preclinical assessment of acute toxicityP E Molina, Y S Ding, F I Carroll, et al.
Biochemical Pharmacology|August 23, 1996
Effects of sphingosine stereoisomers on P-glycoprotein phosphorylation and vinblastine accumulation in multidrug-resistant MCF-7 cellsC W Sachs, L M Ballas, S W Mascarella, et al.
British Journal of Pharmacology|June 14, 2014
Anti-nociception mediated by a κ opioid receptor agonist is blocked by a δ receptor agonistA M W Taylor, K W Roberts, A A Pradhan, et al.
Journal of Medicinal Chemistry|January 20, 1995
Cocaine and 3 beta-(4'-substituted phenyl)tropane-2 beta-carboxylic acid ester and amide analogues. New high-affinity and selective compounds for the dopamine transporterF I Carroll, P Kotian, A Dehghani, et al.
Synapse (New York, N.Y.)|December 1, 1996
Mapping nicotinic acetylcholine receptors with PETY S Ding, S J Gatley, J S Fowler, et al.
Synapse (New York, N.Y.)|January 1, 1994
RTI-4793-14, a new ligand with high affinity and selectivity for the (+)-MK801-insensitive [3H]1-]1-(2-thienyl)cyclohexyl]piperidine binding site (PCP site 2) of guinea pig brainC B Goodman, D N Thomas, A Pert, et al.
Journal of Medicinal Chemistry|December 1, 1988
Synthesis, absolute configuration, and molecular modeling study of etoxadrol, a potent phencyclidine-like agonistA Thurkauf, P C Zenk, R L Balster, et al.
Translational Psychiatry|July 2, 2014
A thermostable bacterial cocaine esterase rapidly eliminates cocaine from brain in nonhuman primatesL L Howell, J A Nye, J S Stehouwer, et al.
Journal of Medicinal Chemistry|June 20, 1998
Investigation of the N-substituent conformation governing potency and mu receptor subtype-selectivity in (+)-(3R, 4R)-dimethyl-4-(3-hydroxyphenyl)piperidine opioid antagonistsJ B Thomas, S W Mascarella, R B Rothman, et al.
Pageof 21

Showing results (181-190 of 208) with videos related to

Sort By:
Pageof 21
Bioorganic & Medicinal Chemistry Letters|November 26, 1999
(+/-)-4-[(N-allyl-cis-3-methyl-4-piperidinyl)phenylamino]-N,N-diethylbenzamide displays selective binding for the delta opioid receptorJ B Thomas, X M Herault, R B Rothman, et al.
Nuclear Medicine and Biology|January 15, 1998
Fluoro-norchloroepibatidine: preclinical assessment of acute toxicityP E Molina, Y S Ding, F I Carroll, et al.
Biochemical Pharmacology|August 23, 1996
Effects of sphingosine stereoisomers on P-glycoprotein phosphorylation and vinblastine accumulation in multidrug-resistant MCF-7 cellsC W Sachs, L M Ballas, S W Mascarella, et al.
British Journal of Pharmacology|June 14, 2014
Anti-nociception mediated by a κ opioid receptor agonist is blocked by a δ receptor agonistA M W Taylor, K W Roberts, A A Pradhan, et al.
Journal of Medicinal Chemistry|January 20, 1995
Cocaine and 3 beta-(4'-substituted phenyl)tropane-2 beta-carboxylic acid ester and amide analogues. New high-affinity and selective compounds for the dopamine transporterF I Carroll, P Kotian, A Dehghani, et al.
Synapse (New York, N.Y.)|December 1, 1996
Mapping nicotinic acetylcholine receptors with PETY S Ding, S J Gatley, J S Fowler, et al.
Synapse (New York, N.Y.)|January 1, 1994
RTI-4793-14, a new ligand with high affinity and selectivity for the (+)-MK801-insensitive [3H]1-]1-(2-thienyl)cyclohexyl]piperidine binding site (PCP site 2) of guinea pig brainC B Goodman, D N Thomas, A Pert, et al.
Journal of Medicinal Chemistry|December 1, 1988
Synthesis, absolute configuration, and molecular modeling study of etoxadrol, a potent phencyclidine-like agonistA Thurkauf, P C Zenk, R L Balster, et al.
Translational Psychiatry|July 2, 2014
A thermostable bacterial cocaine esterase rapidly eliminates cocaine from brain in nonhuman primatesL L Howell, J A Nye, J S Stehouwer, et al.
Journal of Medicinal Chemistry|June 20, 1998
Investigation of the N-substituent conformation governing potency and mu receptor subtype-selectivity in (+)-(3R, 4R)-dimethyl-4-(3-hydroxyphenyl)piperidine opioid antagonistsJ B Thomas, S W Mascarella, R B Rothman, et al.
Pageof 21