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B Rothman

Showing results (381-390 of 532) with videos related to

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Bioorganic & Medicinal Chemistry Letters|February 5, 2003
Synthesis, opioid receptor binding, and functional activity of 5'-substituted 17-cyclopropylmethylpyrido[2',3':6,7]morphinansSubramaniam Ananthan, Hollis S Kezar, Surendra K Saini, et al.
European Journal of Pharmacology|May 13, 1986
Morphine tolerance increases mu-noncompetitive delta binding sitesR B Rothman, J A Danks, A E Jacobson, et al.
Bioorganic & Medicinal Chemistry|December 17, 2009
Probes for narcotic receptor mediated phenomena. 40. N-substituted cis-4a-ethyl-1,2,3,4,4a,9a-hexahydrobenzofuro[2,3-c]pyridin-8-olsMalliga R Iyer, Yong Sok Lee, Jeffrey R Deschamps, et al.
Synapse (New York, N.Y.)|November 9, 2000
Opioid peptide receptor studies. 14. Stereochemistry determines agonist efficacy and intrinsic efficacy in the [(35)S]GTP-gamma-S functional binding assayH Xu, A Hashimoto, K C Rice, et al.
Bioorganic & Medicinal Chemistry Letters|April 20, 2006
Synthetic studies of neoclerodane diterpenes from Salvia divinorum: selective modification of the furan ringWayne W Harding, Matthew Schmidt, Kevin Tidgewell, et al.
Synapse (New York, N.Y.)|December 8, 2006
A comparison of noninternalizing (herkinorin) and internalizing (DAMGO) mu-opioid agonists on cellular markers related to opioid tolerance and dependenceHeng Xu, John S Partilla, Xiaoying Wang, et al.
Journal of Medicinal Chemistry|July 22, 2005
Neoclerodane diterpenes as a novel scaffold for mu opioid receptor ligandsWayne W Harding, Kevin Tidgewell, Nathan Byrd, et al.
European Journal of Pharmacology|August 29, 1989
Pharmacological activities of optically pure enantiomers of the kappa opioid agonist, U50,488, and its cis diastereomer: evidence for three kappa receptor subtypesR B Rothman, C P France, V Bykov, et al.
Synapse (New York, N.Y.)|September 29, 1999
Opioid peptide receptor studies. 12. Buprenorphine is a potent and selective mu/kappa antagonist in the [35S]-GTP-gamma-S functional binding assayD V Romero, J S Partilla, Q X Zheng, et al.
Peptides|January 8, 1999
Regulation of mu binding sites after chronic administration of antibodies directed against specific anti-opiate peptidesC B Goodman, S Heyliger, B Emilien, et al.
Pageof 54

Showing results (381-390 of 532) with videos related to

Sort By:
Pageof 54
Bioorganic & Medicinal Chemistry Letters|February 5, 2003
Synthesis, opioid receptor binding, and functional activity of 5'-substituted 17-cyclopropylmethylpyrido[2',3':6,7]morphinansSubramaniam Ananthan, Hollis S Kezar, Surendra K Saini, et al.
European Journal of Pharmacology|May 13, 1986
Morphine tolerance increases mu-noncompetitive delta binding sitesR B Rothman, J A Danks, A E Jacobson, et al.
Bioorganic & Medicinal Chemistry|December 17, 2009
Probes for narcotic receptor mediated phenomena. 40. N-substituted cis-4a-ethyl-1,2,3,4,4a,9a-hexahydrobenzofuro[2,3-c]pyridin-8-olsMalliga R Iyer, Yong Sok Lee, Jeffrey R Deschamps, et al.
Synapse (New York, N.Y.)|November 9, 2000
Opioid peptide receptor studies. 14. Stereochemistry determines agonist efficacy and intrinsic efficacy in the [(35)S]GTP-gamma-S functional binding assayH Xu, A Hashimoto, K C Rice, et al.
Bioorganic & Medicinal Chemistry Letters|April 20, 2006
Synthetic studies of neoclerodane diterpenes from Salvia divinorum: selective modification of the furan ringWayne W Harding, Matthew Schmidt, Kevin Tidgewell, et al.
Synapse (New York, N.Y.)|December 8, 2006
A comparison of noninternalizing (herkinorin) and internalizing (DAMGO) mu-opioid agonists on cellular markers related to opioid tolerance and dependenceHeng Xu, John S Partilla, Xiaoying Wang, et al.
Journal of Medicinal Chemistry|July 22, 2005
Neoclerodane diterpenes as a novel scaffold for mu opioid receptor ligandsWayne W Harding, Kevin Tidgewell, Nathan Byrd, et al.
European Journal of Pharmacology|August 29, 1989
Pharmacological activities of optically pure enantiomers of the kappa opioid agonist, U50,488, and its cis diastereomer: evidence for three kappa receptor subtypesR B Rothman, C P France, V Bykov, et al.
Synapse (New York, N.Y.)|September 29, 1999
Opioid peptide receptor studies. 12. Buprenorphine is a potent and selective mu/kappa antagonist in the [35S]-GTP-gamma-S functional binding assayD V Romero, J S Partilla, Q X Zheng, et al.
Peptides|January 8, 1999
Regulation of mu binding sites after chronic administration of antibodies directed against specific anti-opiate peptidesC B Goodman, S Heyliger, B Emilien, et al.
Pageof 54