Results 141 to 150 of about 62,302 (192)

Peptide toxins that target vertebrate voltage-gated sodium channels underly the painful stings of harvester ants. [PDF]

open access: yesJ Biol Chem
Robinson SD   +9 more
europepmc   +1 more source

<i>N</i>-(4-Bromo-2,5-Dimethoxyphenethyl)-6-(4-Phenylbutoxy)Hexan-1-Amine (XOB): A Novel Phenylalkylamine Antagonist of Serotonin 2A Receptors and Voltage-Gated Sodium Channels. [PDF]

open access: yesMol Pharmacol
Denomme N   +12 more
europepmc   +1 more source

Ubiquitylation of Voltage-Gated Sodium Channels

open access: yes, 2014
Ion channel proteins are regulated by different types of posttranslational modifications. The focus of this review is the regulation of voltage-gated sodium channels (Navs) upon their ubiquitylation. The amiloride-sensitive epithelial sodium channel (ENaC) was the first ion channel shown to be regulated upon ubiquitylation.
Laedermann, Cédric J   +2 more
openaire   +5 more sources

Effects of Benzothiazolamines on Voltage-Gated Sodium Channels

open access: yes, 2017
Benzothiazole is a versatile fused heterocycle that aroused much interest in drug discovery as anticonvulsant, neuroprotective, analgesic, anti-inflammatory, antimicrobial, and anticancer. Two benzothiazolamines, riluzole and lubeluzole, are known blockers of voltage-gated sodium (Nav) channels.
Farinato, Alessandro   +2 more
openaire   +4 more sources

Voltage-gated sodium channels

Current Opinion in Pharmacology, 2015
Voltage-gated sodium channels play a key role in the transmission of sensory information about the status of organs in the periphery. Sensory fibers contain a heterogeneous yet specific distribution of voltage-gated sodium channel isoforms. Major efforts by industry and academic groups are underway to develop medicines that interrupt inappropriate ...
Kevin, Kwong, Michael J, Carr
openaire   +3 more sources

Voltage-gated sodium channels

Current Opinion in Pharmacology, 2001
Increased knowledge of the molecular diversity of sodium channel alpha- and beta-subunits, and their distribution of expression have been highlights of the past year. The development of subtype-specific channel blockers remains elusive, but the discovery of selective inhibitors such as mu-conotoxins promises useful antagonists in the near future.
J N, Wood, M, Baker
openaire   +2 more sources

Voltage-Gated Sodium Channels and Hyperalgesia

Annual Review of Pharmacology and Toxicology, 2004
Physiological and pharmacological evidence both have demonstrated a critical role for voltage-gated sodium channels (VGSCs) in many types of chronic pain syndromes because these channels play a fundamental role in the excitability of neurons in the central and peripheral nervous systems. Alterations in function of these channels appear to be intimately
Josephine, Lai   +3 more
openaire   +2 more sources

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