Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
1
|
Structure of the nociceptin/orphanin FQ receptor in complex with a peptide mimetic.
|
Nature
|
2012
|
2.96
|
2
|
Solution structure of the Alzheimer amyloid beta-peptide (1-42) in an apolar microenvironment. Similarity with a virus fusion domain.
|
Eur J Biochem
|
2002
|
1.99
|
3
|
The alpha-to-beta conformational transition of Alzheimer's Abeta-(1-42) peptide in aqueous media is reversible: a step by step conformational analysis suggests the location of beta conformation seeding.
|
Chembiochem
|
2006
|
1.70
|
4
|
Evaluation of the Dmt-Tic pharmacophore: conversion of a potent delta-opioid receptor antagonist into a potent delta agonist and ligands with mixed properties.
|
J Med Chem
|
2002
|
1.40
|
5
|
Potent delta-opioid receptor agonists containing the Dmt-Tic pharmacophore.
|
J Med Chem
|
2002
|
1.23
|
6
|
[Nphe1,Arg14,Lys15]nociceptin-NH2, a novel potent and selective antagonist of the nociceptin/orphanin FQ receptor.
|
Br J Pharmacol
|
2002
|
1.14
|
7
|
Structure-activity studies on neuropeptide S: identification of the amino acid residues crucial for receptor activation.
|
J Biol Chem
|
2006
|
1.13
|
8
|
Anxiolytic-like effect of neuropeptide S in the rat defensive burying.
|
Peptides
|
2008
|
1.08
|
9
|
Blockade of nociceptin/orphanin FQ transmission attenuates symptoms and neurodegeneration associated with Parkinson's disease.
|
J Neurosci
|
2005
|
1.06
|
10
|
Anxiolytic- and antidepressant-like activities of H-Dmt-Tic-NH-CH(CH2-COOH)-Bid (UFP-512), a novel selective delta opioid receptor agonist.
|
Peptides
|
2007
|
1.05
|
11
|
Long-lasting antinociceptive spinal effects in primates of the novel nociceptin/orphanin FQ receptor agonist UFP-112.
|
Pain
|
2009
|
1.05
|
12
|
In vitro and in vivo pharmacological characterization of the neuropeptide s receptor antagonist [D-Cys(tBu)5]neuropeptide S.
|
J Pharmacol Exp Ther
|
2008
|
1.05
|
13
|
Urantide mimics urotensin-II induced calcium release in cells expressing recombinant UT receptors.
|
Eur J Pharmacol
|
2004
|
1.04
|
14
|
Solution structure of amyloid beta-peptide (25-35) in different media.
|
J Med Chem
|
2004
|
1.04
|
15
|
UFP-101, a peptide antagonist selective for the nociceptin/orphanin FQ receptor.
|
CNS Drug Rev
|
2005
|
1.01
|
16
|
Solution structure of ZASP PDZ domain; implications for sarcomere ultrastructure and enigma family redundancy.
|
Structure
|
2004
|
0.99
|
17
|
Further studies on the pharmacological profile of the neuropeptide S receptor antagonist SHA 68.
|
Peptides
|
2010
|
0.97
|
18
|
Direct influence of C-terminally substituted amino acids in the Dmt-Tic pharmacophore on delta-opioid receptor selectivity and antagonism.
|
J Med Chem
|
2004
|
0.96
|
19
|
Synthesis and biological activity of human neuropeptide S analogues modified in position 2.
|
J Med Chem
|
2008
|
0.95
|
20
|
A new ligand for the urotensin II receptor.
|
Br J Pharmacol
|
2002
|
0.95
|
21
|
Pharmacological profile of NOP receptors coupled with calcium signaling via the chimeric protein G alpha qi5.
|
Naunyn Schmiedebergs Arch Pharmacol
|
2009
|
0.95
|
22
|
Interaction of calmodulin with the phosphofructokinase target sequence.
|
FEBS Lett
|
2004
|
0.95
|
23
|
Blockade of nociceptin/orphanin FQ receptor signaling in rat substantia nigra pars reticulata stimulates nigrostriatal dopaminergic transmission and motor behavior.
|
J Neurosci
|
2004
|
0.95
|
24
|
Conformation-activity relationship of neuropeptide S and some structural mutants: helicity affects their interaction with the receptor.
|
J Med Chem
|
2007
|
0.94
|
25
|
In vitro and in vivo studies on UFP-112, a novel potent and long lasting agonist selective for the nociceptin/orphanin FQ receptor.
|
Peptides
|
2007
|
0.93
|
26
|
Pharmacological characterization of the nociceptin/orphanin FQ receptor non peptide antagonist Compound 24.
|
Eur J Pharmacol
|
2009
|
0.92
|
27
|
Central injections of nocistatin or its C-terminal hexapeptide exert anxiogenic-like effect on behaviour of mice in the plus-maze test.
|
Br J Pharmacol
|
2002
|
0.91
|
28
|
Immunosensing by a Synthetic Ligand-Gated Ion Channel Financial support from the board of the Swiss Federal Institutes of Technology (SPP Minast, 7.06) is acknowledged. We thank G. Corradin for numerous discussions and J. Lakey for critical reading of the manuscript.
|
Angew Chem Int Ed Engl
|
2001
|
0.91
|
29
|
Conversion of the potent delta-opioid agonist H-Dmt-Tic-NH-CH(2)-bid into delta-opioid antagonists by N(1)-benzimidazole alkylation(1).
|
J Med Chem
|
2005
|
0.91
|
30
|
Pharmacological characterization of the nociceptin receptor which mediates reduction of alcohol drinking in rats.
|
Peptides
|
2002
|
0.90
|
31
|
Protein-protein interface-binding peptides inhibit the cancer therapy target human thymidylate synthase.
|
Proc Natl Acad Sci U S A
|
2011
|
0.90
|
32
|
In vitro and in vivo pharmacological characterization of the novel UT receptor ligand [Pen5,DTrp7,Dab8]urotensin II(4-11) (UFP-803).
|
Br J Pharmacol
|
2006
|
0.89
|
33
|
The nociceptin/orphanin FQ-NOP receptor antagonist effects on an animal model of sepsis.
|
Intensive Care Med
|
2008
|
0.89
|
34
|
Blockade of nociceptin/orphanin FQ transmission in rat substantia nigra reverses haloperidol-induced akinesia and normalizes nigral glutamate release.
|
J Neurochem
|
2004
|
0.89
|
35
|
Pharmacological profile of nociceptin/orphanin FQ receptors.
|
Clin Exp Pharmacol Physiol
|
2002
|
0.89
|
36
|
Synthesis and opioid activity of N,N-dimethyl-Dmt-Tic-NH-CH(R)-R' analogues: acquisition of potent delta antagonism.
|
Bioorg Med Chem
|
2003
|
0.89
|
37
|
[Arg(14),Lys(15)]nociceptin, a highly potent agonist of the nociceptin/orphanin FQ receptor: in vitro and in vivo studies.
|
J Pharmacol Exp Ther
|
2002
|
0.89
|
38
|
Chronic treatment with the selective NOP receptor antagonist [Nphe 1, Arg 14, Lys 15]N/OFQ-NH 2 (UFP-101) reverses the behavioural and biochemical effects of unpredictable chronic mild stress in rats.
|
Psychopharmacology (Berl)
|
2009
|
0.88
|
39
|
Structure-activity study at positions 3 and 4 of human neuropeptide S.
|
Bioorg Med Chem
|
2008
|
0.88
|
40
|
Hypothalamic neuropeptide S receptor blockade decreases discriminative cue-induced reinstatement of cocaine seeking in the rat.
|
Psychopharmacology (Berl)
|
2012
|
0.88
|
41
|
Copper binding to the neurotoxic peptide PrP106-126: thermodynamic and structural studies.
|
Chembiochem
|
2004
|
0.86
|
42
|
Identification of an achiral analogue of J-113397 as potent nociceptin/orphanin FQ receptor antagonist.
|
Bioorg Med Chem
|
2005
|
0.86
|
43
|
Ligands raise the constraint that limits constitutive activation in G protein-coupled opioid receptors.
|
J Biol Chem
|
2013
|
0.86
|
44
|
Pharmacological characterization of tachykinin tetrabranched derivatives.
|
Br J Pharmacol
|
2014
|
0.86
|
45
|
Synthesis and separation of the enantiomers of the neuropeptide S receptor antagonist (9R/S)-3-oxo-1,1-diphenyl-tetrahydro-oxazolo[3,4-a]pyrazine-7-carboxylic acid 4-fluoro-benzylamide (SHA 68).
|
J Med Chem
|
2011
|
0.86
|
46
|
Neuropeptide S: a novel regulator of pain-related amygdala plasticity and behaviors.
|
J Neurophysiol
|
2013
|
0.86
|
47
|
Proinflammatory and vasodilator effects of nociceptin/orphanin FQ in the rat mesenteric microcirculation are mediated by histamine.
|
Am J Physiol Heart Circ Physiol
|
2007
|
0.85
|
48
|
Structure-activity studies on the nociceptin/orphanin FQ receptor antagonist 1-benzyl-N-{3-[spiroisobenzofuran-1(3H),4'-piperidin-1-yl]propyl} pyrrolidine-2-carboxamide.
|
Bioorg Med Chem
|
2009
|
0.85
|
49
|
Blockade of adenosine A2A receptor counteracts neuropeptide-S-induced hyperlocomotion in mice.
|
Naunyn Schmiedebergs Arch Pharmacol
|
2009
|
0.84
|
50
|
Endogenous nociceptin/orphanin FQ signalling produces opposite spinal antinociceptive and supraspinal pronociceptive effects in the mouse formalin test: pharmacological and genetic evidences.
|
Pain
|
2006
|
0.84
|
51
|
Synthesis and biological activity of nociceptin/orphanin FQ analogues substituted in position 7 or 11 with Calpha,alpha-dialkylated amino acids.
|
Bioorg Med Chem
|
2007
|
0.84
|
52
|
[(pF)Phe4,Arg14,Lys15]N/OFQ-NH2 (UFP-102), a highly potent and selective agonist of the nociceptin/orphanin FQ receptor.
|
J Pharmacol Exp Ther
|
2004
|
0.83
|
53
|
Nociceptin/orphanin FQ receptor agonists attenuate L-DOPA-induced dyskinesias.
|
J Neurosci
|
2012
|
0.83
|
54
|
The paraventricular nucleus of the hypothalamus is a neuroanatomical substrate for the inhibition of palatable food intake by neuropeptide S.
|
Eur J Neurosci
|
2009
|
0.83
|
55
|
The SH3 domain of nebulin binds selectively to type II peptides: theoretical prediction and experimental validation.
|
J Mol Biol
|
2002
|
0.83
|
56
|
Functional selectivity of nociceptin/orphanin FQ peptide receptor partial agonists on cardiovascular and renal function.
|
J Pharmacol Exp Ther
|
2005
|
0.83
|
57
|
Binding of the novel radioligand [(3)H]UFP-101 to recombinant human and native rat nociceptin/orphanin FQ receptors.
|
Naunyn Schmiedebergs Arch Pharmacol
|
2008
|
0.82
|
58
|
The interaction of highly helical structural mutants with the NOP receptor discloses the role of the address domain of nociceptin/orphanin FQ.
|
Chemistry
|
2005
|
0.82
|
59
|
Nociceptin/orphanin FQ receptor activation decreases the airway hyperresponsiveness induced by allergen in sensitized mice.
|
Am J Physiol Lung Cell Mol Physiol
|
2013
|
0.82
|
60
|
Anxiolytic- and panicolytic-like effects of Neuropeptide S in the mouse elevated T-maze.
|
Eur J Neurosci
|
2012
|
0.82
|
61
|
Urotensin II stimulates plasma extravasation in mice via UT receptor activation.
|
Naunyn Schmiedebergs Arch Pharmacol
|
2004
|
0.82
|
62
|
UFP-101 antagonizes the spinal antinociceptive effects of nociceptin/orphanin FQ: behavioral and electrophysiological studies in mice.
|
Peptides
|
2006
|
0.82
|
63
|
CuII binding sites located at His-96 and His-111 of the human prion protein: thermodynamic and spectroscopic studies on model peptides.
|
Dalton Trans
|
2008
|
0.81
|
64
|
Pharmacological profiles of presynaptic nociceptin/orphanin FQ receptors modulating 5-hydroxytryptamine and noradrenaline release in the rat neocortex.
|
Br J Pharmacol
|
2003
|
0.81
|
65
|
Activation of the nociceptin/orphanin FQ receptor reduces bronchoconstriction and microvascular leakage in a rabbit model of gastroesophageal reflux.
|
Br J Pharmacol
|
2005
|
0.81
|
66
|
Effect of neuropeptide S receptor antagonists and partial agonists on palatable food consumption in the rat.
|
Peptides
|
2010
|
0.81
|
67
|
UFP-112 a potent and long-lasting agonist selective for the Nociceptin/Orphanin FQ receptor.
|
CNS Neurosci Ther
|
2010
|
0.81
|
68
|
Unexpected impact of the number of glutamine residues on metal complex stability.
|
Metallomics
|
2013
|
0.81
|
69
|
Effects of nociceptin/orphanin FQ receptor ligands on blood pressure, heart rate, and plasma catecholamine concentrations in guinea pigs.
|
Naunyn Schmiedebergs Arch Pharmacol
|
2003
|
0.81
|
70
|
Modeling of overloaded gradient elution of nociceptin/orphanin FQ in reversed-phase liquid chromatography.
|
J Chromatogr A
|
2005
|
0.81
|
71
|
Cell and tissue responses of a range of Urotensin II analogs at cloned and native urotensin II receptors. Evidence for coupling promiscuity.
|
Naunyn Schmiedebergs Arch Pharmacol
|
2006
|
0.80
|
72
|
Gastrointestinal effects of intracerebroventricularly injected nociceptin/orphaninFQ in rats.
|
Peptides
|
2004
|
0.80
|
73
|
Urodynamic effects of intravesical nociceptin/orphanin FQ in neurogenic detrusor overactivity: a randomized, placebo-controlled, double-blind study.
|
Urology
|
2003
|
0.80
|
74
|
New approaches to high-throughput structure characterization of SH3 complexes: the example of Myosin-3 and Myosin-5 SH3 domains from S. cerevisiae.
|
Protein Sci
|
2006
|
0.80
|
75
|
Peripheral mechanisms involved in gastric mucosal protection by intracerebroventricular and intraperitoneal nociceptin in rats.
|
Endocrinology
|
2005
|
0.80
|
76
|
Mixed tridentate π -donor and monodentate π -acceptor ligands as chelating systems for rhenium-188 and technetium-99m nitrido radiopharmaceuticals.
|
Curr Radiopharm
|
2013
|
0.79
|
77
|
Synthesis and antimicrobial activity of dermaseptin S1 analogues.
|
Bioorg Med Chem
|
2008
|
0.79
|
78
|
Nociceptin modulates bronchoconstriction induced by sensory nerve activation in mouse lung.
|
Am J Respir Cell Mol Biol
|
2009
|
0.79
|
79
|
Role of the ecto-nucleotidases in the cooperative effect of adenosine and neuropeptide-S on locomotor activity in mice.
|
Pharmacol Biochem Behav
|
2011
|
0.79
|
80
|
Effects of [(pF)Phe(4)]nociceptin/orphanin FQ-(1-13)NH(2) on GTPgamma(35)S binding and cAMP formation in Chinese hamster ovary cells expressing the human nociceptin/orphanin FQ receptor.
|
Eur J Pharmacol
|
2002
|
0.79
|
81
|
Nociceptin/orphanin FQ modulates motor behavior and primary motor cortex output through receptors located in substantia nigra reticulata.
|
Neuropsychopharmacology
|
2008
|
0.79
|
82
|
Intrathecal [Nphe1]nociceptin( 1-13)NH2 selectively reduces the spinal inhibitory effect of nociceptin.
|
Life Sci
|
2002
|
0.78
|
83
|
Neuropeptide S inhibits stress-stimulated faecal output in the rat.
|
Pharmacol Res
|
2011
|
0.78
|
84
|
Crystal structures of dipeptides containing the Dmt-Tic pharmacophore.
|
J Med Chem
|
2002
|
0.78
|
85
|
Pharmacological characterisation of [(pX)Phe4]nociceptin(1-13)amide analogues. 1. In vitro studies.
|
Naunyn Schmiedebergs Arch Pharmacol
|
2002
|
0.78
|
86
|
Urotensin II evokes neurotransmitter release from rat cerebrocortical slices.
|
Neurosci Lett
|
2008
|
0.78
|
87
|
Further studies on the pharmacological features of the nociceptin/orphanin FQ receptor ligand ZP120.
|
Peptides
|
2008
|
0.78
|
88
|
Structural and dynamic characterization of copper(II) binding of the human prion protein outside the octarepeat region.
|
Chemistry
|
2007
|
0.78
|
89
|
Internalization and stability of a thymidylate synthase Peptide inhibitor in ovarian cancer cells.
|
J Med Chem
|
2014
|
0.78
|
90
|
Study of synthetic peptides derived from the PKI55 protein, a protein kinase C modulator, in human neutrophils stimulated by the methyl ester derivative of the hydrophobic N-formyl tripeptide for-Met-Leu-Phe-OH.
|
FEBS J
|
2007
|
0.77
|
91
|
Copper-ion interaction with the 106-113 domain of the prion protein: a solution-equilibria study on model peptides.
|
Dalton Trans
|
2005
|
0.77
|
92
|
The nociceptin/orphanin FQ receptor antagonist UFP-101 reduces microvascular inflammation to lipopolysaccharide in vivo.
|
PLoS One
|
2013
|
0.77
|
93
|
Effects of chronic nociceptin/orphanin FQ exposure on cAMP accumulation and receptor density in Chinese hamster ovary cells expressing human nociceptin/orphanin FQ receptors.
|
Eur J Pharmacol
|
2002
|
0.77
|
94
|
Nociceptin/orphanin FQ prevents ethanol-induced gastric lesions in the rat.
|
Regul Pept
|
2005
|
0.77
|
95
|
The coordination of NiII and Cu(II) ions to the polyhistidyl motif of Hpn protein: is it as strong as we think?
|
Chemistry
|
2012
|
0.77
|
96
|
Nociceptin/orphanin FQ inhibits electrically induced contractions of the human bronchus via NOP receptor activation.
|
Peptides
|
2005
|
0.77
|
97
|
Optimization of peptides that target human thymidylate synthase to inhibit ovarian cancer cell growth.
|
J Med Chem
|
2014
|
0.77
|
98
|
Mass spectrometric/bioinformatic identification of a protein subset that characterizes the cellular activity of anticancer peptides.
|
J Proteome Res
|
2014
|
0.77
|
99
|
Daily intravesical instillation of 1 mg nociceptin/orphanin FQ for the control of neurogenic detrusor overactivity: a multicenter, placebo controlled, randomized exploratory study.
|
J Urol
|
2006
|
0.77
|
100
|
In vitro and in vivo pharmacological characterization of the nociceptin/orphanin FQ receptor ligand Ac-RYYRIK-ol.
|
Eur J Pharmacol
|
2006
|
0.76
|
101
|
Desensitisation of native and recombinant human urotensin-II receptors.
|
Naunyn Schmiedebergs Arch Pharmacol
|
2009
|
0.76
|
102
|
[Nphe(1)]N/OFQ-(1-13)-NH(2) is a competitive and selective antagonist at nociceptin/orphanin FQ receptors mediating K(+) channel activation in rat periaqueductal gray slices.
|
Neuropharmacology
|
2002
|
0.76
|
103
|
Proteinase-activated receptor-1 (PAR-1) activation contracts the isolated human renal artery in vitro.
|
Br J Pharmacol
|
2003
|
0.76
|
104
|
Role of nociceptin/orphanin FQ receptors in the decrease of mucosal mast cells caused by acute stress in the rat colon.
|
Life Sci
|
2011
|
0.76
|
105
|
Pharmacological characterisation of [(pX)Phe4]nociceptin(1-13)NH2 analogues. 2. In vivo studies.
|
Naunyn Schmiedebergs Arch Pharmacol
|
2002
|
0.76
|
106
|
GABA(A) signalling is involved in N/OFQ anxiolytic-like effects but not in nocistatin anxiogenic-like action as evaluated in the mouse elevated plus maze.
|
Peptides
|
2008
|
0.76
|
107
|
Functional coupling of the nociceptin/orphanin FQ receptor in dog brain membranes.
|
Brain Res
|
2004
|
0.75
|
108
|
Quantitative study of [(pF)Phe4,Arg14,Lys15]nociceptin/orphanin FQ-NH2 (UFP-102) at NOP receptors in rat periaqueductal gray slices.
|
Eur J Pharmacol
|
2007
|
0.75
|
109
|
Chronic intracerebroventricular infusion of nociceptin/orphanin FQ increases food and ethanol intake in alcohol-preferring rats.
|
Peptides
|
2006
|
0.75
|
110
|
The unusual metal ion binding ability of histidyl tags and their mutated derivatives.
|
Dalton Trans
|
2016
|
0.75
|
111
|
The hypothalamus-pituitary-adrenal axis does not influence the protective effects of nociceptin/orphanin FQ on the rat gastric mucosa.
|
Regul Pept
|
2008
|
0.75
|
112
|
In vitro activity of dermaseptin S1 derivatives against genital pathogens.
|
APMIS
|
2010
|
0.75
|
113
|
Thermodynamic and spectroscopic investigation on the role of Met residues in Cu(II) binding to the non-octarepeat site of the human prion protein.
|
Metallomics
|
2012
|
0.75
|
114
|
Correction to "Mass Spectrometric/Bioinformatic Identification of a Protein Subset That Characterizes the Cellular Activity of Anticancer Peptides".
|
J Proteome Res
|
2016
|
0.75
|
115
|
Structure-activity relationship study of position 4 in the urotensin-II receptor ligand U-II(4-11).
|
Peptides
|
2007
|
0.75
|
116
|
Effects of neuropeptide S on seizures and oxidative damage induced by pentylenetetrazole in mice.
|
Pharmacol Biochem Behav
|
2012
|
0.75
|
117
|
Characterization of nociceptin/orphanin FQ binding sites in dog brain membranes.
|
Anesth Analg
|
2003
|
0.75
|
118
|
[Nphe1,Arg14,Lys15]N/OFQ-NH2 is a competitive antagonist of NOP receptors in the periaqueductal gray.
|
Eur J Pharmacol
|
2005
|
0.75
|
119
|
Solution structure of nociceptin peptides.
|
J Pept Sci
|
2002
|
0.75
|
120
|
Nociceptin/orphanin FQ induces simultaneously anxiolytic and amnesic effects in the mouse elevated T-maze task.
|
Naunyn Schmiedebergs Arch Pharmacol
|
2014
|
0.75
|
121
|
N-carbamidoyl-4-((3-ethyl-2,4,4-trimethylcyclohexyl)methyl)benzamide enhances staurosporine cytotoxic effects likely inhibiting the protective action of Magmas toward cell apoptosis.
|
J Med Chem
|
2014
|
0.75
|
122
|
Nociceptin/orphanin FQ prevents gastric damage induced by cold-restraint stress in the rat by acting in the periphery.
|
Peptides
|
2007
|
0.75
|
123
|
Anti-inflammatory and analgesic effects displayed by peptides derived from PKI55 protein, an endogenous protein kinase C inhibitor.
|
Naunyn Schmiedebergs Arch Pharmacol
|
2010
|
0.75
|
124
|
Structure-activity relationship study on Tyr9 of urotensin-II(4-11): identification of a partial agonist of the UT receptor.
|
Peptides
|
2009
|
0.75
|