1
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Antidepressant-like effects of kappa-opioid receptor antagonists in the forced swim test in rats.
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J Pharmacol Exp Ther
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2003
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3.48
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2
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Effects of kappa-opioid receptor ligands on intracranial self-stimulation in rats.
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Psychopharmacology (Berl)
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2004
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2.35
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3
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A heterodimer-selective agonist shows in vivo relevance of G protein-coupled receptor dimers.
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Proc Natl Acad Sci U S A
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2005
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2.31
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4
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Opioid-induced tolerance and dependence in mice is modulated by the distance between pharmacophores in a bivalent ligand series.
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Proc Natl Acad Sci U S A
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2005
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2.29
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5
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A bivalent ligand (KDN-21) reveals spinal delta and kappa opioid receptors are organized as heterodimers that give rise to delta(1) and kappa(2) phenotypes. Selective targeting of delta-kappa heterodimers.
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J Med Chem
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2004
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1.61
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6
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A bivalent ligand (KDAN-18) containing delta-antagonist and kappa-agonist pharmacophores bridges delta2 and kappa1 opioid receptor phenotypes.
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J Med Chem
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2005
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1.41
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7
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Interaction of bivalent ligand KDN21 with heterodimeric delta-kappa opioid receptors in human embryonic kidney 293 cells.
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Mol Pharmacol
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2005
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1.29
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8
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Absence of conditioned place preference or reinstatement with bivalent ligands containing mu-opioid receptor agonist and delta-opioid receptor antagonist pharmacophores.
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Eur J Pharmacol
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2007
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1.22
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9
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Ligands that interact with putative MOR-mGluR5 heteromer in mice with inflammatory pain produce potent antinociception.
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Proc Natl Acad Sci U S A
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2013
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1.22
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10
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Standard opioid agonists activate heteromeric opioid receptors: evidence for morphine and [d-Ala(2)-MePhe(4)-Glyol(5)]enkephalin as selective μ-δ agonists.
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ACS Chem Neurosci
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2009
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1.13
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11
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Kappa opioid antagonist effects of the novel kappa antagonist 5'-guanidinonaltrindole (GNTI) in an assay of schedule-controlled behavior in rhesus monkeys.
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Psychopharmacology (Berl)
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2002
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1.09
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12
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Induced association of mu opioid (MOP) and type 2 cholecystokinin (CCK2) receptors by novel bivalent ligands.
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J Med Chem
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2009
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1.06
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13
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N-naphthoyl-beta-naltrexamine (NNTA), a highly selective and potent activator of μ/kappa-opioid heteromers.
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Proc Natl Acad Sci U S A
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2011
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1.05
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14
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Allosteric interactions between δ and κ opioid receptors in peripheral sensory neurons.
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Mol Pharmacol
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2011
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1.00
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15
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A bivalent ligand (KMN-21) antagonist for mu/kappa heterodimeric opioid receptors.
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Bioorg Med Chem Lett
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2009
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0.94
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16
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Synthesis and in vitro characterization of radioiodinatable benzodiazepines selective for type 1 and type 2 cholecystokinin receptors.
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J Med Chem
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2009
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0.93
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17
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Molecular basis for binding and subtype selectivity of 1,4-benzodiazepine antagonist ligands of the cholecystokinin receptor.
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J Biol Chem
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2012
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0.92
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18
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Naloxone acts as a potent analgesic in transgenic mouse models of sickle cell anemia.
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Proc Natl Acad Sci U S A
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2007
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0.92
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19
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Clinically employed opioid analgesics produce antinociception via μ-δ opioid receptor heteromers in Rhesus monkeys.
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ACS Chem Neurosci
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2012
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0.92
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20
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The FEMA GRAS assessment of cinnamyl derivatives used as flavor ingredients.
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Food Chem Toxicol
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2004
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0.90
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21
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The δ opioid receptor agonist SNC80 selectively activates heteromeric μ-δ opioid receptors.
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ACS Chem Neurosci
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2012
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0.89
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22
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Homology modeling and molecular dynamics simulations of the mu opioid receptor in a membrane-aqueous system.
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Chembiochem
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2005
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0.89
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23
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Selectivity of delta- and kappa-opioid ligands depends on the route of central administration in mice.
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J Pharmacol Exp Ther
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2007
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0.89
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24
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Reduced antinociception of opioids in rats and mice by vaccination with immunogens containing oxycodone and hydrocodone haptens.
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J Med Chem
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2013
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0.86
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25
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Comparison of peptidic and nonpeptidic delta-opioid agonists on guanosine 5'-O-(3-[35S]thio)triphosphate ([35S]GTPgammaS) binding in brain slices from Sprague-Dawley rats.
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J Pharmacol Exp Ther
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2004
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0.85
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26
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Modulation of cell surface expression of nonactivated cholecystokinin receptors using bivalent ligand-induced internalization.
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J Med Chem
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2010
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0.84
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27
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Bivalent ligands that target μ opioid (MOP) and cannabinoid1 (CB1) receptors are potent analgesics devoid of tolerance.
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J Med Chem
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2013
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0.84
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28
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An immunocytochemical-derived correlate for evaluating the bridging of heteromeric mu-delta opioid protomers by bivalent ligands.
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ACS Chem Biol
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2013
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0.83
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29
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Specific cross-linking of Lys233 and Cys235 in the mu opioid receptor by a reporter affinity label.
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Biochemistry
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2005
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0.83
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30
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Consequences of opioid receptor mutation on actions of univalent and bivalent kappa and delta ligands.
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Psychopharmacology (Berl)
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2010
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0.81
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31
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Methadone and heroin antinociception: predominant delta-opioid-receptor responses in methadone-tolerant mice.
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Jpn J Pharmacol
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2002
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0.81
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32
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Characterization of specific opioid binding sites in neural membranes from the myenteric plexus of porcine small intestine.
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J Pharmacol Exp Ther
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2003
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0.79
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33
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Criteria for the safety evaluation of flavoring substances. The Expert Panel of the Flavor and Extract Manufacturers Association.
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Food Chem Toxicol
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2005
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0.78
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34
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Putative kappa opioid heteromers as targets for developing analgesics free of adverse effects.
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J Med Chem
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2014
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0.78
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35
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Opioid activity of spinally selective analogues of N-naphthoyl-β-naltrexamine in HEK-293 cells and mice.
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J Med Chem
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2012
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0.76
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36
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My farewell to the Journal of Medicinal Chemistry.
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J Med Chem
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2011
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0.76
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37
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Modulation of musculoskeletal hyperalgesia by brown adipose tissue activity in mice.
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Pain
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2016
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0.75
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38
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A bivalent ligand that activates mu opioid receptor and antagonizes mGluR5 receptor reduces neuropathic pain in mice.
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Pain
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2017
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0.75
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39
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Naphthalene dicarboxaldehyde as an electrophilic fluorogenic moiety for affinity labeling: application to opioid receptor affinity labels with greatly improved fluorogenic properties.
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J Med Chem
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2002
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0.75
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40
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o-Naphthalenedicarboxaldehyde derivative of 7'-aminonaltrindole as a selective delta-opioid receptor affinity label.
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J Med Chem
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2007
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0.75
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41
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Revision of purity criteria for tested compounds.
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J Med Chem
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2009
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0.75
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