Related references
Note: Only part of the references are listed.The synthetic peptide PnPP-19 induces peripheral antinociception via activation of NO/cGMP/KATP pathway: Role of eNOS and nNOS
A. C. N. Freitas et al.
NITRIC OXIDE-BIOLOGY AND CHEMISTRY (2017)
Identification of a Cyanine-Dye Labeled Peptidic Ligand for Y1R and Y4R, Based upon the Neuropeptide Y C-Terminal Analogue, BVD-15
Mengjie Liu et al.
BIOCONJUGATE CHEMISTRY (2016)
PnPP-19, a spider toxin peptide, induces peripheral antinociception through opioid and cannabinoid receptors and inhibition of neutral endopeptidase
A. C. N. Freitas et al.
BRITISH JOURNAL OF PHARMACOLOGY (2016)
A spider derived peptide, PnPP-19, induces central antinociception mediated by opioid and cannabinoid systems
Daniela da Fonseca Pacheco et al.
JOURNAL OF VENOMOUS ANIMALS AND TOXINS INCLUDING TROPICAL DISEASES (2016)
Structure-based discovery of opioid analgesics with reduced side effects
Aashish Manglik et al.
NATURE (2016)
δ-Ctenitoxin-Pn1a, a Peptide from Phoneutria nigriventer Spider Venom, Shows Antinociceptive Effect Involving Opioid and Cannabinoid Systems, in Rats
Bruna Luiza Emerich et al.
TOXINS (2016)
Voltage-Gated R-Type Calcium Channel Inhibition via Human mu-, delta-, and kappa-opioid Receptors Is Voltage-Independently Mediated by G beta gamma Protein Subunits
Geza Berecki et al.
MOLECULAR PHARMACOLOGY (2016)
PnPP-19, a Synthetic and Nontoxic Peptide Designed from a Phoneutria nigriventer Toxin, Potentiates Erectile Function via NO/cGMP
Carolina Nunes Silva et al.
JOURNAL OF UROLOGY (2015)
Biased agonism of the μ-opioid receptor by TRV130 increases analgesia and reduces on-target adverse effects versus morphine: A randomized, double-blind, placebo-controlled, crossover study in healthy volunteers
David G. Soergel et al.
PAIN (2014)
The Effect of PnTx2-6 Protein From Phoneutria nigriventer Spider Toxin on Improvement of Erectile Dysfunction in a Rat Model of Cavernous Nerve Injury
Ae Ryang Jung et al.
UROLOGY (2014)
A G Protein-Biased Ligand at the μ-Opioid Receptor Is Potently Analgesic with Reduced Gastrointestinal and Respiratory Dysfunction Compared with Morphines
Scott M. DeWire et al.
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS (2013)
Antinociceptive effect of Brazilian armed spider venom toxin Tx3-3 in animal models of neuropathic pain
Gerusa Duarte Dalmolin et al.
PAIN (2011)
Analgesic effect in rodents of native and recombinant Phα1β toxin, a high-voltage-activated calcium channel blocker isolated from armed spider venom
Alessandra H. Souza et al.
PAIN (2008)
Tx2-6 toxin of the Phoneutria nigriventer spider potentiates rat erectile function
K. P. Nunes et al.
TOXICON (2008)
A rational nomenclature for naming peptide toxins from spiders and other venomous animals
Glenn F. King et al.
TOXICON (2008)
Spinal G-protein-gated potassium channels contribute in a dose-dependent manner to the analgesic effect of μ- and δ- but not κ-opioids
CL Marker et al.
JOURNAL OF NEUROSCIENCE (2005)
Morphine side effects in beta-arrestin 2 knockout mice
KM Raehal et al.
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS (2005)
μ-Opioid receptor desensitization by β-arrestin-2 determines morphine tolerance but not dependence
LM Bohn et al.
NATURE (2000)
Changes in GIRK1/GIRK2 deactivation kinetics and basal activity in the presence and absence of RGS4
C Ulens et al.
LIFE SCIENCES (2000)
Share Paper
