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Nalfurafine promotes myelination in vitro and facilitates recovery from cuprizone + rapamycin‐induced demyelination in mice.
- Published in:
- Glia, 2024, v. 72, n. 10, p. 1801, doi. 10.1002/glia.24583
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- Publication type:
- Article
Identification of a novel 'almost neutral' μ-opioid receptor antagonist in CHO cells expressing the cloned human μ-opioid receptor.
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- Synapse, 2010, v. 64, n. 4, p. 280, doi. 10.1002/syn.20723
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- Publication type:
- Article
A comparison of noninternalizing (herkinorin) and internalizing (DAMGO) μ-opioid agonists on cellular markers related to opioid tolerance and dependence.
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- Synapse, 2007, v. 61, n. 3, p. 166, doi. 10.1002/syn.20356
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- Publication type:
- Article
Pharmacokinetics of the plant-derived κ-opioid hallucinogen salvinorin A in nonhuman primates.
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- Synapse, 2005, v. 58, n. 3, p. 208, doi. 10.1002/syn.20191
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- Publication type:
- Article
High-dose fenfluramine administration decreases serotonin transporter binding, but not serotonin transporter protein levels, in rat forebrain (This article is a US Government work and, as such, is in the public domain in the United States of America.).
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- Synapse, 2003, v. 50, n. 3, p. 233, doi. 10.1002/syn.10266
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- Publication type:
- Article
k Opioids as potential treatments for stimulant dependence.
- Published in:
- AAPS Journal, 2005, v. 7, n. 3, p. E592, doi. 10.1208/aapsj070361
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- Publication type:
- Article
Mu opioid receptor activation without arrestin-interactions; a pharmacological approach.
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- FASEB Journal, 2007, v. 21, n. 5, p. A426
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- Publication type:
- Article
Functional Activity of Enantiomeric Oximes and Diastereomeric Amines and Cyano Substituents at C9 in 3-Hydroxy- N -phenethyl-5-phenylmorphans.
- Published in:
- Molecules, 2024, v. 29, n. 9, p. 1926, doi. 10.3390/molecules29091926
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- Publication type:
- Article
Potent MOR Agonists from 2′-Hydroxy-5,9-dimethyl- N -phenethyl Substituted-6,7-benzomorphans and from C8-Hydroxy, Methylene and Methyl Derivatives of N -Phenethylnormetazocine.
- Published in:
- Molecules, 2023, v. 28, n. 23, p. 7709, doi. 10.3390/molecules28237709
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- Publication type:
- Article
A MOR Antagonist with High Potency and Antagonist Efficacy among Diastereomeric C9-Alkyl-Substituted N -Phenethyl-5-(3-hydroxy)phenylmorphans.
- Published in:
- Molecules, 2023, v. 28, n. 14, p. 5411, doi. 10.3390/molecules28145411
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- Publication type:
- Article
The Kappa Opioid Receptor Agonist 16-Bromo Salvinorin A Has Anti-Cocaine Effects without Significant Effects on Locomotion, Food Reward, Learning and Memory, or Anxiety and Depressive-like Behaviors.
- Published in:
- Molecules, 2023, v. 28, n. 12, p. 4848, doi. 10.3390/molecules28124848
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- Publication type:
- Article
Discovery of a Potent Highly Biased MOR Partial Agonist among Diastereomeric C9-Hydroxyalkyl-5-phenylmorphans.
- Published in:
- Molecules, 2023, v. 28, n. 12, p. 4795, doi. 10.3390/molecules28124795
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- Publication type:
- Article
Synthesis and Pharmacological Evaluation of Enantiopure N-Substituted Ortho-c Oxide-Bridged 5-Phenylmorphans.
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- Molecules, 2022, v. 27, n. 24, p. 8808, doi. 10.3390/molecules27248808
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- Publication type:
- Article
A Journey through Diastereomeric Space: The Design, Synthesis, In Vitro and In Vivo Pharmacological Activity, and Molecular Modeling of Novel Potent Diastereomeric MOR Agonists and Antagonists.
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- Molecules, 2022, v. 27, n. 19, p. 6455, doi. 10.3390/molecules27196455
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- Publication type:
- Article
The Intriguing Effects of Substituents in the N-Phenethyl Moiety of Norhydromorphone: A Bifunctional Opioid from a Set of "Tail Wags Dog" Experiments.
- Published in:
- Molecules, 2020, v. 25, n. 11, p. 2640, doi. 10.3390/molecules25112640
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- Publication type:
- Article
Kappa Opioid Receptor Agonist Mesyl Sal B Attenuates Behavioral Sensitization to Cocaine with Fewer Aversive Side-Effects than Salvinorin A in Rodents.
- Published in:
- Molecules, 2018, v. 23, n. 10, p. 2602, doi. 10.3390/molecules23102602
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- Publication type:
- Article
Contingent administration of typical and biased kappa opioid agonists reduces cocaine and oxycodone choice in a drug vs. food choice procedure in male rhesus monkeys.
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- Psychopharmacology, 2024, v. 241, n. 2, p. 305, doi. 10.1007/s00213-023-06486-5
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- Publication type:
- Article
The kappa-opioid receptor agonist, triazole 1.1, reduces oxycodone self-administration and enhances oxycodone-induced thermal antinociception in male rats.
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- Psychopharmacology, 2021, v. 238, n. 12, p. 3463, doi. 10.1007/s00213-021-05965-x
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- Publication type:
- Article
Kappa opioid agonists reduce oxycodone self-administration in male rhesus monkeys.
- Published in:
- Psychopharmacology, 2020, v. 237, n. 5, p. 1471, doi. 10.1007/s00213-020-05473-4
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- Publication type:
- Article
The C-2 derivatives of salvinorin A, ethoxymethyl ether Sal B and β-tetrahydropyran Sal B, have anti-cocaine properties with minimal side effects.
- Published in:
- Psychopharmacology, 2017, v. 234, n. 16, p. 2499, doi. 10.1007/s00213-017-4637-2
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- Publication type:
- Article
Modafinil and its metabolites enhance the anticonvulsant action of classical antiepileptic drugs in the mouse maximal electroshock-induced seizure model.
- Published in:
- Psychopharmacology, 2015, v. 232, n. 14, p. 2463, doi. 10.1007/s00213-015-3884-3
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- Publication type:
- Article
Assessment of the kappa opioid agonist, salvinorin A, as a punisher of drug self-administration in monkeys.
- Published in:
- Psychopharmacology, 2014, v. 231, n. 14, p. 2751, doi. 10.1007/s00213-014-3436-2
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- Publication type:
- Article
The Salvinorin Analogue, Ethoxymethyl Ether Salvinorin B, Promotes Remyelination in Preclinical Models of Multiple Sclerosis.
- Published in:
- Frontiers in Neurology, 2021, v. 12, p. 1, doi. 10.3389/fneur.2021.782190
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- Publication type:
- Article
The unique psychostimulant profile of (±)-modafinil: investigation of behavioral and neurochemical effects in mice.
- Published in:
- European Journal of Neuroscience, 2017, v. 45, n. 1, p. 167, doi. 10.1111/ejn.13376
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- Publication type:
- Article
Rational inhibitor design for Pseudomonas aeruginosa salicylate adenylation enzyme PchD.
- Published in:
- Journal of Biological Inorganic Chemistry (JBIC), 2022, v. 27, n. 6, p. 541, doi. 10.1007/s00775-022-01941-8
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- Publication type:
- Article
Sex Differences in Kappa Opioid Receptor Agonist Mediated Attenuation of Chemotherapy-Induced Neuropathic Pain in Mice.
- Published in:
- Frontiers in Pharmacology, 2022, v. 13, p. 1, doi. 10.3389/fphar.2022.813562
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- Publication type:
- Article
Rapid-Onset Anti-Stress Effects of a Kappa-Opioid Receptor Antagonist, LY2795050, Against Immobility in an Open Space Swim Paradigm in Male and Female Mice.
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- Frontiers in Pharmacology, 2021, v. 12, p. 1, doi. 10.3389/fphar.2021.775317
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- Publication type:
- Article
Enhanced and complementary benefits of a nalfurafine and fingolimod combination to treat immune‐driven demyelination.
- Published in:
- Clinical & Translational Immunology, 2023, v. 12, n. 12, p. 1, doi. 10.1002/cti2.1480
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- Publication type:
- Article
Nalfurafine reduces neuroinflammation and drives remyelination in models of CNS demyelinating disease.
- Published in:
- Clinical & Translational Immunology, 2021, v. 10, n. 1, p. 1, doi. 10.1002/cti2.1234
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- Publication type:
- Article
Dose-related effects of salvinorin A in humans: dissociative, hallucinogenic, and memory effects.
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- Psychopharmacology, 2013, v. 226, n. 2, p. 381, doi. 10.1007/s00213-012-2912-9
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- Publication type:
- Article
The discriminative effects of the κ-opioid hallucinogen salvinorin A in nonhuman primates: dissociation from classic hallucinogen effects.
- Published in:
- Psychopharmacology, 2010, v. 210, n. 2, p. 253, doi. 10.1007/s00213-009-1771-5
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- Publication type:
- Article
Kappa opioids and the modulation of pain.
- Published in:
- Psychopharmacology, 2010, v. 210, n. 1, p. 109, doi. 10.1007/s00213-010-1819-6
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- Publication type:
- Article
Mitochondrial Targeted Coenzyme Q, Superoxide, and Fuel Selectivity in Endothelial Cells.
- Published in:
- PLoS ONE, 2009, v. 4, n. 1, p. 1, doi. 10.1371/journal.pone.0004250
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- Publication type:
- Article
Design, synthesis, and preliminary evaluation of a potential synthetic opioid rescue agent.
- Published in:
- Journal of Biomedical Science, 2021, v. 28, n. 1, p. 1, doi. 10.1186/s12929-021-00758-y
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- Publication type:
- Article
Role of Ventral Subiculum in Context-Induced Relapse to Alcohol Seeking after Punishment-Imposed Abstinence.
- Published in:
- Journal of Neuroscience, 2016, v. 36, n. 11, p. 3281, doi. 10.1523/JNEUROSCI.4299-15.2016
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- Publication type:
- Article
Discriminative-Stimulus Effects of Synthetic Cathinones in Squirrel Monkeys.
- Published in:
- International Journal of Neuropsychopharmacology, 2021, v. 24, n. 8, p. 656, doi. 10.1093/ijnp/pyab017
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- Publication type:
- Article
Evaluation of Biased and Balanced Salvinorin A Analogs in Preclinical Models of Pain.
- Published in:
- Frontiers in Neuroscience, 2020, v. 14, p. 1, doi. 10.3389/fnins.2020.00765
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- Publication type:
- Article
Synthesis and Opioid Activity of Tyr<sup>1</sup>- ψ[( Z)CF=CH]-Gly<sup>2</sup> and Tyr<sup>1</sup>- ψ[( S)/( R)-CF<sub>3</sub>CH-NH]-Gly<sup>2</sup> Leu-enkephalin Fluorinated Peptidomimetics.
- Published in:
- ChemMedChem, 2017, v. 12, n. 8, p. 571, doi. 10.1002/cmdc.201700103
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- Publication type:
- Article
The Acute Effects of the Atypical Dissociative Hallucinogen Salvinorin A on Functional Connectivity in the Human Brain.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41598-020-73216-8
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- Publication type:
- Article
Profile of a short-acting κ-antagonist, LY2795050, on self-grooming behaviors, forced swim test and locomotor activity: sex comparison in mice.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Time course of pharmacokinetic and hormonal effects of inhaled high-dose salvinorin A in humans.
- Published in:
- 2016
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- Publication type:
- journal article