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

Richard B Rothman

Showing results (131-140 of 159) with videos related to

Pageof 16
Sort By:
Bioorganic & Medicinal Chemistry|March 28, 2006
Structure-activity relationships of substituted N-benzyl piperidines in the GBR series: Synthesis of 4-(2-(bis(4-fluorophenyl)methoxy)ethyl)-1-(2-trifluoromethylbenzyl)piperidine, an allosteric modulator of the serotonin transporterTerrence L Boos, Elisabeth Greiner, W Jason Calhoun, et al.
The Journal of Pharmacology and Experimental Therapeutics|September 5, 2003
In vitro characterization of ephedrine-related stereoisomers at biogenic amine transporters and the receptorome reveals selective actions as norepinephrine transporter substratesRichard B Rothman, Nga Vu, John S Partilla, et al.
Brain Research Bulletin|July 22, 2008
Differential effects of opioid agonists on G protein expression in CHO cells expressing cloned human opioid receptorsHeng Xu, Xiaoying Wang, John S Partilla, et al.
Organic Letters|July 1, 2005
Salvinicins A and B, new neoclerodane diterpenes from Salvia divinorumWayne W Harding, Kevin Tidgewell, Matthew Schmidt, et al.
Organic & Biomolecular Chemistry|August 9, 2008
Synthesis and pharmacological effects of the enantiomers of the N-phenethyl analogues of the ortho and para e- and f-oxide-bridged phenylmorphansJosef Zezula, Lisa Singer, Anna K Przybył, et al.
Bioorganic & Medicinal Chemistry|June 21, 2011
Probes for narcotic receptor mediated phenomena. 43. Synthesis of the ortho-a and para-a, and improved synthesis and optical resolution of the ortho-b and para-b oxide-bridged phenylmorphans: compounds with moderate to low opioid-receptor affinityFeng Li, John E Folk, Kejun Cheng, et al.
Journal of Natural Products|June 24, 2006
Synthesis of salvinorin A analogues as opioid receptor probesKevin Tidgewell, Wayne W Harding, Anthony Lozama, et al.
Journal of Medicinal Chemistry|March 5, 2004
Identification of opioid ligands possessing mixed micro agonist/delta antagonist activity among pyridomorphinans derived from naloxone, oxymorphone, and hydromorphone [correction of hydropmorphone]Subramaniam Ananthan, Naveen K Khare, Surendra K Saini, et al.
The Journal of Pharmacology and Experimental Therapeutics|May 5, 2006
Antinociceptive and hypothermic effects of Salvinorin A are abolished in a novel strain of kappa-opioid receptor-1 knockout miceMichael A Ansonoff, Jiwen Zhang, Traci Czyzyk, et al.
Drug and Alcohol Dependence|December 31, 2014
Behavioral, biological, and chemical perspectives on atypical agents targeting the dopamine transporterMaarten E A Reith, Bruce E Blough, Weimin C Hong, et al.
Pageof 16

Showing results (131-140 of 159) with videos related to

Sort By:
Pageof 16
Bioorganic & Medicinal Chemistry|March 28, 2006
Structure-activity relationships of substituted N-benzyl piperidines in the GBR series: Synthesis of 4-(2-(bis(4-fluorophenyl)methoxy)ethyl)-1-(2-trifluoromethylbenzyl)piperidine, an allosteric modulator of the serotonin transporterTerrence L Boos, Elisabeth Greiner, W Jason Calhoun, et al.
The Journal of Pharmacology and Experimental Therapeutics|September 5, 2003
In vitro characterization of ephedrine-related stereoisomers at biogenic amine transporters and the receptorome reveals selective actions as norepinephrine transporter substratesRichard B Rothman, Nga Vu, John S Partilla, et al.
Brain Research Bulletin|July 22, 2008
Differential effects of opioid agonists on G protein expression in CHO cells expressing cloned human opioid receptorsHeng Xu, Xiaoying Wang, John S Partilla, et al.
Organic Letters|July 1, 2005
Salvinicins A and B, new neoclerodane diterpenes from Salvia divinorumWayne W Harding, Kevin Tidgewell, Matthew Schmidt, et al.
Organic & Biomolecular Chemistry|August 9, 2008
Synthesis and pharmacological effects of the enantiomers of the N-phenethyl analogues of the ortho and para e- and f-oxide-bridged phenylmorphansJosef Zezula, Lisa Singer, Anna K Przybył, et al.
Bioorganic & Medicinal Chemistry|June 21, 2011
Probes for narcotic receptor mediated phenomena. 43. Synthesis of the ortho-a and para-a, and improved synthesis and optical resolution of the ortho-b and para-b oxide-bridged phenylmorphans: compounds with moderate to low opioid-receptor affinityFeng Li, John E Folk, Kejun Cheng, et al.
Journal of Natural Products|June 24, 2006
Synthesis of salvinorin A analogues as opioid receptor probesKevin Tidgewell, Wayne W Harding, Anthony Lozama, et al.
Journal of Medicinal Chemistry|March 5, 2004
Identification of opioid ligands possessing mixed micro agonist/delta antagonist activity among pyridomorphinans derived from naloxone, oxymorphone, and hydromorphone [correction of hydropmorphone]Subramaniam Ananthan, Naveen K Khare, Surendra K Saini, et al.
The Journal of Pharmacology and Experimental Therapeutics|May 5, 2006
Antinociceptive and hypothermic effects of Salvinorin A are abolished in a novel strain of kappa-opioid receptor-1 knockout miceMichael A Ansonoff, Jiwen Zhang, Traci Czyzyk, et al.
Drug and Alcohol Dependence|December 31, 2014
Behavioral, biological, and chemical perspectives on atypical agents targeting the dopamine transporterMaarten E A Reith, Bruce E Blough, Weimin C Hong, et al.
Pageof 16