Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

R B Rothman

Showing results (241-250 of 262) with videos related to

Pageof 27
Sort By:
Journal of Medicinal Chemistry|June 1, 1989
Probes for narcotic receptor mediated phenomena. 15. (3S,4S)-(+)-trans-3-methylfentanyl isothiocyanate, a potent site-directed acylating agent for the delta opioid receptors in vitroC H Kim, R B Rothman, A E Jacobson, et al.
Journal of Medicinal Chemistry|November 22, 1996
Development of novel, potent, and selective dopamine reuptake inhibitors through alteration of the piperazine ring of 1-[2-(diphenylmethoxy)ethyl]-and 1-[2-[bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazines (GBR 12935 and GBR 12909)D Matecka, R B Rothman, L Radesca, et al.
Journal of Medicinal Chemistry|November 1, 1990
Synthesis and evaluation of N-substituted cis-N-methyl-2-(1-pyrrolidinyl)cyclohexylamines as high affinity sigma receptor ligands. Identification of a new class of highly potent and selective sigma receptor probesB R de Costa, K C Rice, W D Bowen, 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.
Pharmacology, Biochemistry, and Behavior|November 1, 1994
Lack of evidence for context-dependent cocaine-induced sensitization in humans: preliminary studiesR B Rothman, D A Gorelick, M H Baumann, et al.
The Journal of Pharmacology and Experimental Therapeutics|April 1, 1995
Studies of the biogenic amine transporters. V. Demonstration of two binding sites for the cocaine analog [125I]RTI-55 associated with the 5-HT transporter in rat brain membranesM L Silverthorn, C M Dersch, M H Baumann, et al.
The Journal of Pharmacology and Experimental Therapeutics|July 1, 1995
Studies of the biogenic amine transporters. VI. Characterization of a novel cocaine binding site, identified with [125I]RTI-55, in membranes prepared from whole rat brain minus caudateR B Rothman, M L Silverthorn, M H Baumann, et al.
Synapse (New York, N.Y.)|March 28, 1998
Studies of the biogenic amine transporters. VII. Characterization of a novel cocaine binding site identified with [125I]RTI-55 in membranes prepared from human, monkey and guinea pig caudateR B Rothman, M L Silverthorn, J R Glowa, et al.
The Journal of Pharmacology and Experimental Therapeutics|July 1, 1994
Studies of the biogenic amine transporters. IV. Demonstration of a multiplicity of binding sites in rat caudate membranes for the cocaine analog [125I]RTI-55R B Rothman, J L Cadet, H C Akunne, et al.
The Journal of Pharmacology and Experimental Therapeutics|March 1, 1994
Studies of the biogenic amine transporters. III. Demonstration of two binding sites for [3H]GBR12935 and [3H]BTCP in rat caudate membranesH C Akunne, C M Dersch, J L Cadet, et al.
Pageof 27

Showing results (241-250 of 262) with videos related to

Sort By:
Pageof 27
Journal of Medicinal Chemistry|June 1, 1989
Probes for narcotic receptor mediated phenomena. 15. (3S,4S)-(+)-trans-3-methylfentanyl isothiocyanate, a potent site-directed acylating agent for the delta opioid receptors in vitroC H Kim, R B Rothman, A E Jacobson, et al.
Journal of Medicinal Chemistry|November 22, 1996
Development of novel, potent, and selective dopamine reuptake inhibitors through alteration of the piperazine ring of 1-[2-(diphenylmethoxy)ethyl]-and 1-[2-[bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazines (GBR 12935 and GBR 12909)D Matecka, R B Rothman, L Radesca, et al.
Journal of Medicinal Chemistry|November 1, 1990
Synthesis and evaluation of N-substituted cis-N-methyl-2-(1-pyrrolidinyl)cyclohexylamines as high affinity sigma receptor ligands. Identification of a new class of highly potent and selective sigma receptor probesB R de Costa, K C Rice, W D Bowen, 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.
Pharmacology, Biochemistry, and Behavior|November 1, 1994
Lack of evidence for context-dependent cocaine-induced sensitization in humans: preliminary studiesR B Rothman, D A Gorelick, M H Baumann, et al.
The Journal of Pharmacology and Experimental Therapeutics|April 1, 1995
Studies of the biogenic amine transporters. V. Demonstration of two binding sites for the cocaine analog [125I]RTI-55 associated with the 5-HT transporter in rat brain membranesM L Silverthorn, C M Dersch, M H Baumann, et al.
The Journal of Pharmacology and Experimental Therapeutics|July 1, 1995
Studies of the biogenic amine transporters. VI. Characterization of a novel cocaine binding site, identified with [125I]RTI-55, in membranes prepared from whole rat brain minus caudateR B Rothman, M L Silverthorn, M H Baumann, et al.
Synapse (New York, N.Y.)|March 28, 1998
Studies of the biogenic amine transporters. VII. Characterization of a novel cocaine binding site identified with [125I]RTI-55 in membranes prepared from human, monkey and guinea pig caudateR B Rothman, M L Silverthorn, J R Glowa, et al.
The Journal of Pharmacology and Experimental Therapeutics|July 1, 1994
Studies of the biogenic amine transporters. IV. Demonstration of a multiplicity of binding sites in rat caudate membranes for the cocaine analog [125I]RTI-55R B Rothman, J L Cadet, H C Akunne, et al.
The Journal of Pharmacology and Experimental Therapeutics|March 1, 1994
Studies of the biogenic amine transporters. III. Demonstration of two binding sites for [3H]GBR12935 and [3H]BTCP in rat caudate membranesH C Akunne, C M Dersch, J L Cadet, et al.
Pageof 27