| Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
|
1
|
Electrophysiological and in vivo characterization of A-317567, a novel blocker of acid sensing ion channels.
|
Pain
|
2005
|
1.46
|
|
2
|
Molecular determinants of species-specific activation or blockade of TRPA1 channels.
|
J Neurosci
|
2008
|
1.42
|
|
3
|
Transient receptor potential A1 mediates an osmotically activated ion channel.
|
Eur J Neurosci
|
2008
|
1.23
|
|
4
|
TRPV1b overexpression negatively regulates TRPV1 responsiveness to capsaicin, heat and low pH in HEK293 cells.
|
J Neurochem
|
2006
|
1.05
|
|
5
|
Role of central and peripheral mGluR5 receptors in post-operative pain in rats.
|
Pain
|
2005
|
0.96
|
|
6
|
Activation of dopamine D4 receptors by ABT-724 induces penile erection in rats.
|
Proc Natl Acad Sci U S A
|
2004
|
0.96
|
|
7
|
Reconstitution of human corpus cavernosum smooth muscle in vitro and in vivo.
|
Tissue Eng
|
2002
|
0.95
|
|
8
|
Capsaicin causes protein synthesis inhibition and microtubule disassembly through TRPV1 activities both on the plasma membrane and intracellular membranes.
|
Biochem Pharmacol
|
2007
|
0.93
|
|
9
|
Activation of TRPA1 channels by the fatty acid amide hydrolase inhibitor 3'-carbamoylbiphenyl-3-yl cyclohexylcarbamate (URB597).
|
Mol Pharmacol
|
2007
|
0.93
|
|
10
|
Discovery of 2-(4-pyridin-2-ylpiperazin-1-ylmethyl)-1H-benzimidazole (ABT-724), a dopaminergic agent with a novel mode of action for the potential treatment of erectile dysfunction.
|
J Med Chem
|
2004
|
0.92
|
|
11
|
A-412997, a selective dopamine D4 agonist, improves cognitive performance in rats.
|
Pharmacol Biochem Behav
|
2005
|
0.92
|
|
12
|
Structure-activity relationship of triazafluorenone derivatives as potent and selective mGluR1 antagonists.
|
J Med Chem
|
2005
|
0.91
|
|
13
|
Reperfusion of ischemic corporal tissue: physiologic and biochemical changes in an animal model of ischemic priapism.
|
Urology
|
2003
|
0.90
|
|
14
|
Antidepressant-like effect of D(2/3) receptor-, but not D(4) receptor-activation in the rat forced swim test.
|
Neuropsychopharmacology
|
2005
|
0.89
|
|
15
|
Central mechanisms regulating penile erection in conscious rats: the dopaminergic systems related to the proerectile effect of apomorphine.
|
J Pharmacol Exp Ther
|
2003
|
0.88
|
|
16
|
Discovery of 3-methyl-N-(1-oxy-3',4',5',6'-tetrahydro-2'H-[2,4'-bipyridine]-1'-ylmethyl)benzamide (ABT-670), an orally bioavailable dopamine D4 agonist for the treatment of erectile dysfunction.
|
J Med Chem
|
2006
|
0.88
|
|
17
|
YC-1 potentiates the nitric oxide/cyclic GMP pathway in corpus cavernosum and facilitates penile erection in rats.
|
Eur J Pharmacol
|
2003
|
0.87
|
|
18
|
Modulation of human TRPV1 receptor activity by extracellular protons and host cell expression system.
|
Eur J Pharmacol
|
2006
|
0.86
|
|
19
|
A-350619: a novel activator of soluble guanylyl cyclase.
|
Life Sci
|
2003
|
0.85
|
|
20
|
Correlation between brain/plasma ratios and efficacy in neuropathic pain models of selective metabotropic glutamate receptor 1 antagonists.
|
Bioorg Med Chem Lett
|
2006
|
0.85
|
|
21
|
Effects of selective dopamine receptor subtype agonists on cardiac contractility and regional haemodynamics in rats.
|
Clin Exp Pharmacol Physiol
|
2004
|
0.84
|
|
22
|
Quantification of TRPV1 protein levels in rat tissues to understand its physiological roles.
|
J Mol Neurosci
|
2012
|
0.83
|
|
23
|
Dopamine D4 ligands and models of receptor activation: 2-(4-pyridin-2-ylpiperazin-1-ylmethyl)-1H-benzimidazole and related heteroarylmethylarylpiperazines exhibit a substituent effect responsible for additional efficacy tuning.
|
J Med Chem
|
2004
|
0.82
|
|
24
|
Utility of large-scale transiently transfected cells for cell-based high-throughput screens to identify transient receptor potential channel A1 (TRPA1) antagonists.
|
J Biomol Screen
|
2006
|
0.82
|
|
25
|
Dopamine D2, but not D4, receptor agonists are emetogenic in ferrets.
|
Pharmacol Biochem Behav
|
2005
|
0.81
|
|
26
|
A cell-based microarrayed compound screening format for identifying agonists of G-protein-coupled receptors.
|
Anal Biochem
|
2003
|
0.81
|
|
27
|
Discovery of TRPV1 antagonist ABT-116.
|
Bioorg Med Chem Lett
|
2010
|
0.81
|
|
28
|
Analgesic activity of metabotropic glutamate receptor 1 antagonists on spontaneous post-operative pain in rats.
|
Eur J Pharmacol
|
2007
|
0.81
|
|
29
|
1-aryl-3-(4-pyridine-2-ylpiperazin-1-yl)propan-1-one oximes as potent dopamine D4 receptor agonists for the treatment of erectile dysfunction.
|
J Med Chem
|
2006
|
0.81
|
|
30
|
Synthesis and functional activity of (2-aryl-1-piperazinyl)-N-(3-methylphenyl)acetamides: selective dopamine D4 receptor agonists.
|
Bioorg Med Chem
|
2004
|
0.80
|
|
31
|
Application of large-scale transiently transfected cells to functional assays of ion channels: different targets and assay formats.
|
Assay Drug Dev Technol
|
2007
|
0.80
|
|
32
|
Dopamine D4 receptor signaling in the rat paraventricular hypothalamic nucleus: Evidence of natural coupling involving immediate early gene induction and mitogen activated protein kinase phosphorylation.
|
Neuropharmacology
|
2005
|
0.79
|
|
33
|
Expression and purification of human TRPV1 in baculovirus-infected insect cells for structural studies.
|
Protein Expr Purif
|
2008
|
0.78
|
|
34
|
Rapid hit to lead evaluation of pyrazolo[3,4-d]pyrimidin-4-one as selective and orally bioavailable mGluR1 antagonists.
|
Bioorg Med Chem Lett
|
2007
|
0.77
|
|
35
|
Acrylamide analog as a novel nitric oxide-independent soluble guanylyl cyclase activator.
|
J Pharmacol Sci
|
2006
|
0.77
|
|
36
|
Synthesis and evaluation of 3-aryl piperidine analogs as potent and efficacious dopamine D4 receptor agonists.
|
Bioorg Med Chem
|
2005
|
0.77
|
|
37
|
Characterization of A-425619 at native TRPV1 receptors: a comparison between dorsal root ganglia and trigeminal ganglia.
|
Eur J Pharmacol
|
2008
|
0.77
|
|
38
|
[3H]A-778317 [1-((R)-5-tert-butyl-indan-1-yl)-3-isoquinolin-5-yl-urea]: a novel, stereoselective, high-affinity antagonist is a useful radioligand for the human transient receptor potential vanilloid-1 (TRPV1) receptor.
|
J Pharmacol Exp Ther
|
2007
|
0.76
|
|
39
|
2-[4-(3,4-Dimethylphenyl)piperazin-1-ylmethyl]-1H benzoimidazole (A-381393), a selective dopamine D4 receptor antagonist.
|
Neuropharmacology
|
2005
|
0.75
|
|
40
|
Central oxytocinergic and dopaminergic mechanisms regulating penile erection in conscious rats.
|
Pharmacol Biochem Behav
|
2005
|
0.75
|
|
41
|
Development of ELISA to measure TRPV1 protein in rat tissues.
|
J Neurosci Methods
|
2011
|
0.75
|
|
42
|
Synthesis and activity of 2-[4-(4-[3H]-2-cyanophenyl)piperazinyl]-N-(2,4,6-[3H]3-3-methylphenyl)acetamide: a selective dopamine D4 receptor agonist and radioligand.
|
Bioorg Med Chem Lett
|
2004
|
0.75
|