NOR-BINALTORPHIMINE (NOR-BNI) : POTENT AND SELECTIVE KAPPAOPIOID RECEPTOR ANTAGONIST WITH LONG-LASTING ACTIVITY IN VIVO

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Isolation, Purification and Characterization of Cyclomaltooctadecaose (v-Cyclodextrin), Cyclomaltononadecaose (ζ-Cyclodextrin), Cyclomaltoeicosaose (o-Cyclodextrin) and Cyclomaltoheneicosaose (π-Cyclodextrin)
Isolation, Purification, and Characterization of Cyclomaltotetradecaose (ι-Cyclodextrin), Cyclomaltopentadecaose (κ-Cyclodextrin), Cyclomaltohexadecaose (λ-Cyclodextrin), and Cyclomaltoheptadecaose(μ-Cyclodextrin)
Complex Formation of Cyclomaltononaose δ-Cyclodextrin (δ-CD) with Macrocyclic Compounds
Polymorphic Structure of dl-12Hydroxystearic Acid
Crystal Structure of Cyclomaltodecaose(ε-Cyclodextrin)at 203 K
Solubilization of C_ into Water by Complexation with δ-Cyclodextrin
Isolation and Purification of Cyclomaltononaose (δ-CD) from CELDEX SG-30
Isolation, Purification, and Characterization of Cyclomaltodecaose (ε-Cyclodextrin), Cyclomaltoundecaose (ζ-Cyclodextrin) and Cyclomaltotridecaose (θ-Cyclodextrin)
Crystal Structure of DL-12-Hydroxystearic Acid
HPLC Determination of (+)-Pseudoephedrine and (-)-Ephedrine in Japanese Herbal Medicines Containing Ephedra Herb Using Solid-Phase Extraction
Amphidinin B, a New Polyketide Metabolite from Marine Dinoflagellate Amphidinium sp.
Application of Modified Mosher's Method for Primary Alcohols with a Methyl Group at C2 Position
Generalization of NMDA-Receptor Antagonists to the Discriminative Stimulus Effects of κ-Opioid Receptor Agonists U-50,488H, but Not TRK-820 in Rats
Potential Anxiolytic and Antidepressant-Like Activities of SNC80, a Selective δ-Opioid Agonist, in Behavioral Models in Rodents
Lack of μ-Opioid Receptor-Mediated G-Protein Activation in the Spinal Cord of Mice Lacking Exon 1 or Exons 2 and 3 of the MOR-1 Gene
TRK-820, a Selective к-Opioid Agonist, Produces Potent Antinociception in Cynomolgus Monkeys
INTERACTION BETWEEN MU AND KAPPA RECEPTORS IN PHARMACOLOGICAL EFFECTS OF TOLERANCE TO AND DEPENDENCE ON SEVERAL OPIOIDS
The First Example of the Stereoselective Synthesis of 7β-Carbamoyl-4,5α-epoxymorphinan via a Novel and Reactive γ-Lactone
Syntheses of Potential Metabolites of a Potent к-Opioid Receptor Agonist, TRK-820
Syntheses of 10-Oxo, 10α-Hydroxy, and 10β-Hydroxy Derivatives of a Potent к-Opioid Receptor Agonist, TRK-820
Rational Drug Design and Synthesis of a Highly Selective Nonpeptide δ-Opioid Agonist, (4aS^*, 12aR^*)-4a-(3-Hydroxyphenyl)-2-methyl-1,2,3,4,4a, 5,12,12a-octahydropyrido[3,4-b]acridine (TAN-67)
DISCOVERY OF A STRUCTURALLY NOVEL OPIOID K-AGONIST DERIVED FROM 4,5-EPOXYMORPHINAN
NOR-BINALTORPHIMINE (NOR-BNI) : POTENT AND SELECTIVE KAPPAOPIOID RECEPTOR ANTAGONIST WITH LONG-LASTING ACTIVITY IN VIVO
Structural Confirmation of 15-Norlubiminol and 15-Norepilubiminol, Isolated from Solanum aethiopicum, by Chemical Conversion from Lubimin and Epilubimin, and their Antifungal Activity(Organic Chemistry)
P-532 Structure-Antitussive Activity Relationships of Naltrindole Derivatives : Discovery of Novel and Potent Antitussive Agents
Effect of Diabetes on the Morphine-Induced Inhibition of Gastrointestinal Tranist
Information Integration Architecture for Agent-Based Computer Supported Cooperative Work System (Special Issue on Multisensor Fusion and Intergration)
ABNORMAL REACTION OF 4,5-EPOXYDIHYDROMOROHINONES AND ITS APPLICATION TO THE SYNTHESES OF OPIOID RECEPTOR ANTAGONISTS
Effects of κ-Agonist on the Antinociception and Locomotor Enhancing Action Induced by Morphine in Mice
SYNTHESES OF DELTA OPIOID ANTAGONISTS AND THEIR STRUCTURE ACTIVITY RELATIONSHIPS
Potential Anxiolytic and Antidepressant-Like Activities of SNC80, a Selective .DELTA.-Opioid Agonist, in Behavioral Models in Rodents
The Role of Mu- and Kappa-Opioid Receptors in Cocaine-Induced Conditioned Place Preference.
Blockade of .DELTA.-Opioid Receptors Prevents Morphine-Induced Place Preference in Mice.

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