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Thomas A Munro

Showing results (1-10 of 17) with videos related to

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BMC Biology|October 10, 2023
Reanalysis of a μ opioid receptor crystal structure reveals a covalent adduct with BU72Thomas A Munro
Magnetic Resonance in Chemistry : MRC|July 20, 2007
Confirmation of the NMR assignments of salvinorin AThomas A Munro
Journal of Natural Products|May 24, 2003
Salvinorins D-F, new neoclerodane diterpenoids from Salvia divinorum, and an improved method for the isolation of salvinorin AThomas A Munro, Mark A Rizzacasa
Acta Crystallographica. Section E, Structure Reports Online|January 4, 2013
Salvinorin B meth-oxy-methyl etherThomas A Munro, Douglas M Ho, Bruce M Cohen
Journal of Natural Products|September 27, 2003
Divinatorins A-C, new neoclerodane diterpenoids from the controlled sage Salvia divinorumAndrea K Bigham, Thomas A Munro, Mark A Rizzacasa, et al.
Journal of Medicinal Chemistry|January 22, 2005
Studies toward the pharmacophore of salvinorin A, a potent kappa opioid receptor agonistThomas A Munro, Mark A Rizzacasa, Bryan L Roth, et al.
Beilstein Journal of Organic Chemistry|January 24, 2014
Studies toward bivalent κ opioids derived from salvinorin A: heteromethylation of the furan ring reduces affinityThomas A Munro, Wei Xu, Douglas M Ho, et al.
The Journal of Organic Chemistry|November 19, 2005
Autoxidation of salvinorin A under basic conditionsThomas A Munro, Glenn W Goetchius, Bryan L Roth, et al.
The Journal of Biological Chemistry|June 19, 2013
Functional selectivity of 6'-guanidinonaltrindole (6'-GNTI) at κ-opioid receptors in striatal neuronsCullen L Schmid, John M Streicher, Chad E Groer, et al.
Neuropharmacology|July 14, 2009
Salvinorin A and derivatives: protection from metabolism does not prolong short-term, whole-brain residenceJacob M Hooker, Thomas A Munro, Cécile Béguin, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
BMC Biology|October 10, 2023
Reanalysis of a μ opioid receptor crystal structure reveals a covalent adduct with BU72Thomas A Munro
Magnetic Resonance in Chemistry : MRC|July 20, 2007
Confirmation of the NMR assignments of salvinorin AThomas A Munro
Journal of Natural Products|May 24, 2003
Salvinorins D-F, new neoclerodane diterpenoids from Salvia divinorum, and an improved method for the isolation of salvinorin AThomas A Munro, Mark A Rizzacasa
Acta Crystallographica. Section E, Structure Reports Online|January 4, 2013
Salvinorin B meth-oxy-methyl etherThomas A Munro, Douglas M Ho, Bruce M Cohen
Journal of Natural Products|September 27, 2003
Divinatorins A-C, new neoclerodane diterpenoids from the controlled sage Salvia divinorumAndrea K Bigham, Thomas A Munro, Mark A Rizzacasa, et al.
Journal of Medicinal Chemistry|January 22, 2005
Studies toward the pharmacophore of salvinorin A, a potent kappa opioid receptor agonistThomas A Munro, Mark A Rizzacasa, Bryan L Roth, et al.
Beilstein Journal of Organic Chemistry|January 24, 2014
Studies toward bivalent κ opioids derived from salvinorin A: heteromethylation of the furan ring reduces affinityThomas A Munro, Wei Xu, Douglas M Ho, et al.
The Journal of Organic Chemistry|November 19, 2005
Autoxidation of salvinorin A under basic conditionsThomas A Munro, Glenn W Goetchius, Bryan L Roth, et al.
The Journal of Biological Chemistry|June 19, 2013
Functional selectivity of 6'-guanidinonaltrindole (6'-GNTI) at κ-opioid receptors in striatal neuronsCullen L Schmid, John M Streicher, Chad E Groer, et al.
Neuropharmacology|July 14, 2009
Salvinorin A and derivatives: protection from metabolism does not prolong short-term, whole-brain residenceJacob M Hooker, Thomas A Munro, Cécile Béguin, et al.
Pageof 2