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Munro, Thomas Anthony
thomas a munro
thomas anthony munro
Creation class: 
Creation role: 
Related names: 
Béguin, Cécile
Bigham, Andrea K.
Coyle, Jeremy R.
Dinieri, Jennifer A.
Duncan, Katharine K.
Goetchius, Glenn W.
Harvard University
Hooker, Jacob M.
Lopez, Juan Carlos
McLean Hospital
Mendelson, John E.
Munro, Thomas A.
Munro, Thomas Anthony
Potter, David N.
Rizzacasa, Mark A.
Roth, Bryan L.
Staples, Richard J.
University of Melbourne
Xu, Wei
8-epi-Salvinorin B: crystal structure and affinity at the kappa opioid receptor.
Autoxidation of salvinorin A under basic conditions.
chemistry of Salvia divinorum, The
Confirmation of the NMR assignments of salvinorin A.
Divinatorins A-C, new neoclerodane diterpenoids from the controlled sage Salvia divinorum.
Lack of effect of sublingual salvinorin A, a naturally occurring kappa opioid, in humans: a placebo-controlled trial.
Modification of the furan ring of salvinorin A: identification of a selective partial agonist at the kappa opioid receptor.
N-methylacetamide analog of salvinorin A: a highly potent and selective kappa-opioid receptor agonist with oral efficacy.
Salvinorin A and derivatives: protection from metabolism does not prolong short-term, whole-brain residence.
Salvinorins D-F, new neoclerodane diterpenoids from Salvia divinorum, and an improved method for the isolation of salvinorin A.
Standard protecting groups create potent and selective kappa opioids: salvinorin B alkoxymethyl ethers.
Studies toward the pharmacophore of salvinorin A, a potent kappa opioid receptor agonist.