All Stories

  1. Nociceptin/Orphanin FQ Receptor Structure, Signaling, Ligands, Functions, and Interactions with Opioid Systems
  2. Pharmacological stress is required for the anti-alcohol effect of the α3β4* nAChR partial agonist AT-1001
  3. Activation of β2-adrenergic receptor by (R,R′)-4′-methoxy-1-naphthylfenoterol inhibits proliferation and motility of melanoma cells
  4. AT-1001: a high-affinity α3β4 nAChR ligand with novel nicotine-suppressive pharmacology
  5. BU08073 a buprenorphine analogue with partial agonist activity at μ-receptorsin vitrobut long-lasting opioid antagonist activityin vivoin mice
  6. Challenges for opioid receptor nomenclature: IUPHAR Review 9
  7. Tyrosine 308 Is Necessary for Ligand-directed G s Protein-biased Signaling of β 2 -Adrenoceptor
  8. Discovery of a Potent and Selective α3β4 Nicotinic Acetylcholine Receptor Antagonist from an α-Conotoxin Synthetic Combinatorial Library
  9. [125I]AT-1012, a new high affinity radioligand for the α3β4 nicotinic acetylcholine receptors
  10. Comparative molecular field analysis of fenoterol derivatives interacting with an agonist-stabilized form of the β2-adrenergic receptor
  11. Scaffold Ranking and Positional Scanning Utilized in the Discovery of nAChR-Selective Compounds Suitable for Optimization Studies
  12. Designing bifunctional NOP receptor–mu opioid receptor ligands from NOP receptor-selective scaffolds. Part I.
  13. The Use of Bifunctional NOP/Mu and NOP Receptor Selective Compounds for the Treatment of Pain, Drug Abuse, and Psychiatric Disorders
  14. Retrodialysis of N/OFQ into the nucleus accumbens shell blocks cocaine-induced increases in extracellular dopamine and locomotor activity
  15. Sub-anesthetic concentrations of (R,S)-ketamine metabolites inhibit acetylcholine-evoked currents in α7 nicotinic acetylcholine receptors
  16. Pharmacology of Mixed NOP/Mu Ligands
  17. Oxidative folding and preparation of α-conotoxins for use in high-throughput structure-activity relationship studies
  18. Rodent motor and neuropsychological behaviour measured in home cages using the integrated modular platform SmartCage™
  19. Nociceptin/orphanin FQ inhibition with SB612111 ameliorates dextran sodium sulfate-induced colitis
  20. Radiosynthesis of a 125I analog of a highly selective alpha3beta4 nicotinic acetylcholine receptor antagonist ligand for use in autoradiography studies
  21. AT-1001: A High Affinity and Selective α3β4 Nicotinic Acetylcholine Receptor Antagonist Blocks Nicotine Self-Administration in Rats
  22. Structural Determinants of Opioid and NOP Receptor Activity in Derivatives of Buprenorphine
  23. Orphanin FQ/Nociceptin Activates Nuclear Factor Kappa B
  24. Novel ligands interacting with opioid receptors
  25. Effect of fenoterol stereochemistry on the β2 adrenergic receptor system: Ligand-directed chiral recognition
  26. Novel α3β4 Nicotinic Acetylcholine Receptor-Selective Ligands. Discovery, Structure−Activity Studies, and Pharmacological Evaluation
  27. The effect of stereochemistry on the thermodynamic characteristics of the binding of fenoterol stereoisomers to the β2-adrenoceptor
  28. Comparative molecular field analysis of fenoterol derivatives: A platform towards highly selective and effective β2-adrenergic receptor agonists
  29. Activity of new NOP receptor ligands in a rat peripheral mononeuropathy model: Potentiation of morphine anti-allodynic activity by NOP receptor antagonists
  30. Synthesis of Isohasubanan Alkaloids via Enantioselective Ketone Allylation and Discovery of an Unexpected Rearrangement
  31. Paralytic activity of (des-Glu1)conotoxin GI analogs in the mouse diaphragm
  32. Novel μ-selective Met-enkephalinamide analogs with antagonist activity.
  33. Evolutionary Sequence Modeling for Discovery of Peptide Hormones
  34. F.100. Nociceptin/Orphanin FQ Antagonists Ameliorate the Disease Pathogenesis During Inflammatory Bowel Disease
  35. Peptidomics ofCpefat/fatmouse brain regions: implications for neuropeptide processing
  36. Hypocretin/orexin and nociceptin/orphanin FQ coordinately regulate analgesia in a mouse model of stress-induced analgesia
  37. Small-Molecule Agonists and Antagonists of the Opioid Receptor-Like Receptor (ORL1, NOP): Ligand-Based Analysis of Structural Factors Influencing Intrinsic Activity at NOP
  38. Synthesis and antitubercular activity of phenothiazines with reduced binding to dopamine and serotonin receptors
  39. Anti-nociceptive and anti-allodynic effects of a high affinity NOP hexapeptide [Ac-RY(3-Cl)YRWR-NH2] (Syn 1020) in rodents
  40. Evolutionary Sequence Modeling for Discovery of Peptide Hormones
  41. Regulation of the prepronociceptin gene and its effect on neuronal differentiation
  42. Small-molecule agonists and antagonists of the opioid receptor-like receptor (ORL1, NOP): Ligand-based analysis of structural factors influencing intrinsic activity at NOP
  43. Synthesis and in vitro biological evaluation of a carbon glycoside analogue of morphine-6-glucuronide
  44. Design, Chemical Synthesis, and Biological Evaluation of Thiosaccharide Analogues of Morphine- and Codeine-6-Glucuronide
  45. Synthesis and biological evaluation of some 6-arylamidomorphines as analogues of morphine-6-glucuronide
  46. Synthesis, receptor binding and functional studies of mesoridazine stereoisomers
  47. A Novel Series of Piperidin-4-yl-1,3-Dihydroindol-2-ones as Agonist and Antagonist Ligands at the Nociceptin Receptor
  48. The Design and Synthesis of a Novel Quinolizidine Template for Potent Opioid and Opioid Receptor-Like (ORL1, NOP) Receptor Ligands.
  49. The design and synthesis of a novel quinolizidine template for potent opioid and opioid receptor-like (ORL1, NOP) receptor ligands
  50. Regulation of transcription of the human prepronociceptin gene by Sp1
  51. Characterization of opiates, neuroleptics, and synthetic analogs at ORL1 and opioid receptors
  52. Transcriptional Regulation of the Human Prepronociceptin Gene
  53. Species differences in the efficacy of compounds at the nociceptin receptor (ORL1)
  54. Structural Determinants of Opioid Activity in the Orvinols and Related Structures:  Ethers of Orvinol and Isoorvinol
  55. Structural Determinants of Opioid Activity in the Orvinols and Related Structures. Ethers of 7,8-Cyclopenta-Fused Analogs of Buprenorphine
  56. Retinoic acid (RA) receptor transcriptional activation correlates with inhibition of 12-O-tetradecanoylphorbol- 13-acetate-induced ornithine decarboxylase (ODC) activity by retinoids: A potential role fortrans-RA-induced ZBP-89 in ODC inhibition
  57. Characterization of the δ-opioid receptor found in SH-SY5Y neuroblastoma cells
  58. Modulation of enkephalin release by nociceptin (orphanin FQ)
  59. Synthesis and characterization of substituted benzoylhydrazones of naloxone
  60. Desensitization of melanotropin receptors in COS-7 cells
  61. Nociceptin in vitro biotransformation in human blood
  62. Isolation and structure of the endogenous agonist of opioid receptor-like ORL1 receptor
  63. The in vitro pharmacological characterization of naloxone benzoylhydrazone
  64. Characterization of the δ receptor subtype in SH-SY5Y neuroblastoma cells
  65. Evidence for an NMDA receptor subunit in human keratinocytes and rat cardiocytes
  66. Molecular determinants of recognition and activation at the ?-opioid receptor by met-enkephalin-like peptides
  67. Comparison of κ2-opioid receptors in guinea pig brain and guinea pig ileum membranes
  68. The μ-opioid activity of κ-opioid receptor agonist compounds in the guinea pig ileum
  69. Development of peptidomimetic inhibitors of a newly isolated atrial peptide-degrading enzyme
  70. Isolation and characterization of a new atrial peptide-degrading enzyme from bovine kidney
  71. μ-Opioid receptor binding in intact SH-SY5Y neuroblastoma cells
  72. Effects of addition of a 2-methyl group to ethyl nipecotates (.beta.-meperidines) on receptor affinities and opiate agonist/antagonist activities
  73. N-Substituent modulation of opiate agonist/antagonist activity in resolved 3-methyl-3-(m-hydroxyphenyl)piperidines
  74. Inhibition of [3H]captopril binding by peptide analog angiotensin converting enzyme inhibitors
  75. The use of computer analysis in describing multiple opiate receptors
  76. Structure-activity studies of β-carboline analogs
  77. Computer-assisted determination of benzodiazepine receptor heterogeneity
  78. Pyrazolo[1,5-a]pyrimidines: Receptor binding and anxiolytic behavioral studies
  79. Replacement of the peptide-backbone amides connecting Tyr-Gly and Gly-Gly in leucine-enkephalin with ketomethylene groups: synthesis and biological activity
  80. Detailed receptor binding studies of a series of N-substituted ethyl 3-arylnipecotates
  81. Computer-assisted analysis of receptor-binding studies of [3H]-naloxone and [3H]-DADL: A reinterpretation of the Na+ effect
  82. [3H]Doxepin interactions with histamine H1-receptors and other sites in guinea pig and rat brain homogenates
  83. Storage of dopamine and acetylcholine in granules of PC12, a clonal pheochromocytoma cell line
  84. Role of Mg 2+ ion-activated ATPase and a pH gradient in the storage of catecholamines in synaptic vesicles
  85. Energy utilization in the uptake of catecholamines by synaptic vesicles and adrenal chromaffin granules