| scholarly article | Q13442814 |
| P50 | author | Thomas A. Munro | Q42073508 |
| P2093 | author name string | Wei Xu | |
| Bruce M Cohen | |||
| Douglas M Ho | |||
| Lee-Yuan Liu-Chen | |||
| P2860 | cites work | Structure of the human κ-opioid receptor in complex with JDTic | Q24308048 |
| Duration of action of a broad range of selective κ-opioid receptor antagonists is positively correlated with c-Jun N-terminal kinase-1 activation | Q24634808 | ||
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| Standard protecting groups create potent and selective kappa opioids: salvinorin B alkoxymethyl ethers | Q24651427 | ||
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| Structure of the δ-opioid receptor bound to naltrindole | Q27679153 | ||
| International Union of Pharmacology Committee on Receptor Nomenclature and Drug Classification. XXXVIII. Update on terms and symbols in quantitative pharmacology | Q28189543 | ||
| Neuropharmacology of the naturally occurring kappa-opioid hallucinogen salvinorin A | Q30467220 | ||
| Molecular signatures of G-protein-coupled receptors | Q34327700 | ||
| Synthesis and in vitro evaluation of salvinorin A analogues: effect of configuration at C(2) and substitution at C(18). | Q34538561 | ||
| Chemotype-selective modes of action of κ-opioid receptor agonists | Q37348899 | ||
| Salvinorin A and derivatives: protection from metabolism does not prolong short-term, whole-brain residence | Q37349384 | ||
| The best of both worlds? Bitopic orthosteric/allosteric ligands of g protein-coupled receptors | Q37930665 | ||
| Class A G-protein-coupled receptor (GPCR) dimers and bivalent ligands | Q38107222 | ||
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| Modification of the furan ring of salvinorin A: identification of a selective partial agonist at the kappa opioid receptor | Q41872689 | ||
| Salvinorin B methoxymethyl ether | Q42073472 | ||
| Antinociceptive effects of herkinorin, a MOP receptor agonist derived from salvinorin A in the formalin test in rats: new concepts in mu opioid receptor pharmacology: from a symposium on new concepts in mu-opioid pharmacology. | Q42633341 | ||
| Salvinorin A: allosteric interactions at the mu-opioid receptor | Q44332543 | ||
| Toward a structure-based model of salvinorin A recognition of the kappa-opioid receptor | Q44337934 | ||
| Structure-activity relationships of trans-3,4-dimethyl-4-(3-hydroxyphenyl)piperidine antagonists for mu- and kappa-opioid receptors | Q44340510 | ||
| Synthetic studies of neoclerodane diterpenes from Salvia divinorum: selective modification of the furan ring. | Q51808389 | ||
| Salvinorin B derivatives, EOM-Sal B and MOM-Sal B, produce stimulus generalization in male Sprague-Dawley rats trained to discriminate salvinorin A. | Q51858703 | ||
| Allosteric Modulation of G Protein–Coupled Receptors | Q56115675 | ||
| Structure-activity relationships in narcotic antagonists with N-furylmethyl substituents | Q68343293 | ||
| P304 | page(s) | 2916-2924 | |
| P577 | publication date | 2013-12-20 | |
| P1433 | published in | Beilstein Journal of Organic Chemistry | Q2894008 |
| P1476 | title | Studies toward bivalent κ opioids derived from salvinorin A: heteromethylation of the furan ring reduces affinity | |
| P478 | volume | 9 |
| Q34796464 | Synthesis and κ-opioid receptor activity of furan-substituted salvinorin A analogues | cites work | P2860 |
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